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Explore every episode of the podcast Arthritis Life

Dive into the complete episode list for Arthritis Life. Each episode is cataloged with detailed descriptions, making it easy to find and explore specific topics. Keep track of all episodes from your favorite podcast and never miss a moment of insightful content.

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TitlePub. DateDuration
What’s it like to be a Doctor with RA and Vasculitis?26 Sep 202401:08:42

Elena also shares her favorite resources for living well with arthritis, including supportive footwear brands, arthritis gadgets, and inspirational books. Shes hares practical tips like finding the right shoes to support your joints, using dictation tools to reduce hand strain, and the importance of accepting that some pain may persist while still being able to live a fulfilling life. 

Throughout the conversation, Dr Elena and Cheryl emphasize the value of prioritizing what's important and showing up for family, work, and health—even when symptoms make things challenging. If you're newly diagnosed with RA, this episode offers comforting, actionable advice and a reminder that you're not alone in navigating this journey.

DISCLAIMER FOR THIS EPISODE:

The views expressed are those of the author and do not reflect the official policy or position of the US Air Force, Department of Defense or the US Government*

Episode Themes:

Personal Challenges and Advice: Elena shares her experience with managing rheumatoid arthritis and vasculitis and discusses practical tips for newly diagnosed individuals.

Useful Products and Tools: Cheryl and Elena discuss favorite footwear brands and how they impact daily comfort and highlight dictation software as a game-changer for writing tasks.

Living Well with Rheumatoid Arthritis: Elena emphasizes focusing on doing what's most important, even with some discomfort, to achieve a fulfilling life.

Inspirational Mantras: Elena shares her favorite motivational sayings and discusses how this perspective helps her manage daily challenges.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.


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The Power of Strength Training for Rheumatoid Arthritis, with Kinesiologist Dr. Jasmin Ma21 Sep 202400:51:19

Dr. Ma advises people with rheumatoid arthritis to start small, listen to their body, and use her "START" guide to gradually build an active routine that feels right for you. She also explains how the START guide is a useful tool for clinicians like physiotherapists and occupational therapists to support patients in developing sustainable strength training routines.

Dr. Ma  also shares her favorite mantra, "control the controllables and enjoy the enjoyables," which is a great reminder to focus on what you can manage and find joy in the little things. Plus, Cheryl and Dr. Ma dive into how having a supportive community—whether it’s big or just a few people—can make a huge difference in thriving with RA! 

Episode Themes:

Physical Activity with RA: Dr. Ma shares how you should listen to your body’s needs and pace yourself to avoid overexertion. Physical activity is more than exercise; it’s about reducing sedentary time and increasing daily activity.

Kinesiologist’s Approach to Movement: Using the 24-Hour Movement Guidelines, Dr. Ma talks about the balance of physical activity, sleep, and reducing sedentary behavior, all while accounting for the challenges posed by RA.

The Importance of Community: Cheryl and Dr. Ma discuss how community is key for thriving with RA, but it looks different for everyone. Whether it’s a large group, one-on-one support, or reaching out to a healthcare professional, connection makes a difference.

Inspirational Mantra: Dr. Ma shares her favorite saying: "Control the controllables and enjoy the enjoyables." Focus on what you can manage and find joy in the present moment.

Empowering Mindset: Cheryl and Dr. Ma discuss how RA management is about becoming your own scientist and finding what works best for you.

Mental Shift on Exercise: Cheryl and Dr. Ma explore the idea of reframing exercise as something empowering, rather than just a necessity, and how staying active can contribute to feeling more in control of your health.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

For full episode details include a transcript and video:

Go to the episode page on the Arthritis Life Website.


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“Bald Girl Big World:” Colleen’s Alopecia Story17 Jun 202401:25:35

What’s it like to suddenly go bald at age 22? In this episode, Cheryl interviews Colleen Kydd, who speaks candidly about living with autoimmune alopecia.  She shares how she went from covering her baldness with wigs to confidently, unapologetically embracing her identity as a “bald girl in a big world!” Colleen shares how she managed her alopecia in the corporate world, dating life, world travels and new role as an entrepreneur.

Throughout the episode, Cheryl and Colleen discuss acceptance, self compassion, and the crucial importance of connecting with others when we’re struggling.  Cheryl and Colleen reflect on the transformative power of  storytelling, and the importance of pursuing a meaningful life amidst the challenges of chronic illness.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now!

For full episode details:

Go to the episode page on the Arthritis Life website for full show notes plus a full transcript, video and more!


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Why do Disability Pride and Disability Representation Matter? “Cursed” novelist and JIA Patient Karol Ruth Silverstein14 Jul 202100:55:46

Episode at a glance:

  • Karol’s experience getting diagnosed with JIA at age 13 and being angry, terrified and grumpy about it
  • The importance of disability representation beyond the cliche “inspirational” story
  • How Karol learned the importance of partnership with a doctor and taking an active role in her care in her 20s
  • Why Karol identifies as disabled, rather than a “person with disability” (including a discussion of the #SayTheWord, #TheWordIsDisabled movement)
  • How both Cheryl and Karol have confronted their internalized ableism
  • Why Karol wishes she had listened to her occupational therapists earlier, and why occupational therapy is so important for people with rheumatic diseases
  • Excerpts from Karol’s award winning young adult novel “Cursed,” about a young woman with JIA who is “frank, funny and full of f-bombs.”
  • The importance of disability pride

Speaker Bios:

Karol Ruth Silverstein is a children's book author and screenwriter. She was diagnosed with juvenile rheumatoid arthritis at 13 and has identified as disabled since 21. Originally from Philadelphia, she now lives in West Hollywood with her two exceptionally fully cats. You can find her website at: https://www.karolruthsilverstein.com/ 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

This episode is brought to you by Rheum to THRIVE, an online support group and educational program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. 

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.\
For full episode links go to:  https://arthritis.theenthusiasticlife.com/2021/07/14/why-do-disability-pride-and-disability-representation-matter-with-cursed-novelist-and-jia-patient-karol-ruth-silverstein/


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How to Prevent and Cope with Rheumatic Disease Flare Ups05 Jul 202100:53:10
Episode at a glance:
  • Introduction and Agenda Review (1:00)
  • Definition of a Flare Up for rheumatic disease (which includes ankylosing spondylitis, psoriatic arthritis and rheumatoid arthritis) (6:30)
  • What causes flare-ups, and why is it so important to discover our own unique flare triggers? (7:40)
  • Focus on Pain: tools to prevent pain and reduce existing pain (25:00)
  • Focus on Fatigue: tools to prevent and reduce fatigue (31:00)
  • Focus on Stress: ways to decrease stress levels & cope with existing stress (37:00)
Medical disclaimer:

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsor

Rheum to THRIVE, an empowerment program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. Learn more here

Speaker Bio:

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

Episode links:

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Tips for Pregnancy and Postpartum with Rheumatoid Arthritis with Mariah Leach17 Jun 202101:04:51

This episode includes discussions about:

  • How to decide whether or not to have children while living with a chronic illness
  • Tips for comfortable sex with chronic pain
  • Frequently Asked Questions about pregnancy with rheumatoid arthritis, including how to find out which medications are safe
  • Cheryl and Mariah’s experiences with childbirth and C-sections
  • How frequent is the postpartum flare-up and how can it be prevented?
  • Advice for feeding a newborn with rheumatoid arthritis, including discussions about ergonomics, breast versus bottle feeding and “fed is best.”
  • Practical tips for managing the physical and energy demands of new babies including diapering, clothing, baby wearing and more!

This is part one of a two part series - later, Mariah and Cheryl will share tips for parenting toddlers / “big kids” and managing mental health as chronically ill parents!

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

This episode is brought to you by Rheum to THRIVE, an online support group and education program Cheryl created to help people with rheumatic disease become more confident, supported and connected. 

Episode links:

For full episode details, including a detailed episode breakdown, go to: https://arthritis.theenthusiasticlife.com/2021/06/17/tips-for-pregnancy-and-postpartum-with-rheumatoid-arthritis/


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Arthritis Poetry Reading Event08 Jun 202100:44:38

Speaker bios in order of appearance:

Kristen Brogan: Kristen has been living with rheumatoid arthritis and Sjogren's since 2018. She is a Board Certified Behavior Analyst and has a PhD in Cognitive and Behavioral Sciences, which she uses to inform behavioral chronic illness coaching that she provides for others living with chronic illness. In her free time, she enjoys writing, yoga, meditation, and spending time with her partner and their three dogs. 

Links: IG handle @WarriorsMoveMountains and my website which is www.WarriorsMoveMountains.WordPress.com

Emma  is a 24 year old living with inflammatory arthritis in Ontario, Canada.

Gittel is a 32-year-old daughter of immigrants from Central America, who was born and raised in downtown Los Angeles. She is a "forever teacher" who is no longer in the workforce due to her diagnosis of ankylosing spondylitis (among others). Currently, she is riding out the pandemic at her parents' and is learning to manage her illness as best she can---one moment at a time. She can be found on IG at @gittie

Melissa McKenzie is a writer from Jamaica who can be found at @pennedbymelissa on Instagram.

Joel Nelson: Writer. Arthritis Advocate. Dad. Sharing my story of Juvenile Idiopathic Arthritis to raise awareness. Specialising in pain, parenting and mental health. Also writes for leading charities and organisations.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

You can find Cheryl at:

Unity Schmidt: Born into a near-death experience, my journey with JRA became official shortly after my 1st birthday; activating my lifepath to move from chronic pain to purpose. As a life coach, author and teacher, I help my clients understand their energy, move through any blocks/challenges, and awaken their inner magic to reach their biggest dreams! Learn practical, magical ways to uplevel your life and choose your adventure with faery godmother life coaching, classes and my "SOS Energy Report" now available online.

Mary (Mimi) Cross, age 27, diagnosed with rheumatoid arthritis 7 years ago, runs Inflammation Vacation and can be found on Instagram at @inflammationvacation.

Ashley Shrum is a physical therapist living with arthritis who can be found on Instagram at @a.shrummer

Effie Koliopoulos is a freelance writer and rheumatoid arthritis patient advocate. She created her blog Rising Above Rheumatoid Arthritis in 2016, after being inspired to share her story more publicly and connect with others after undergoing a total knee replacement.

Currently residing in Chicago, she is working on her debut children’s picture book, enjoys creating video content for her YouTube channel and other projects. Effie’s Blog

This podcast is brought to you Rheum to THRIVE, a membership community Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. Join the waitlist  today!

Arthritis Life links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

  • 01:00 Kristen Brogan: “An Unexpected Rebirth” (Sjogren’s)
  • 05:00 - Emma (inflammatory arthritis)
  • 7:55 - Gittel (AS) - “Being at War with Myself (aka the Rocky Relationship with my Body)”
  • 12:50 - Melissa - “I am More than this Grief”
  • 18:00 - Cheryl Crow - “A Pleasure to Have in Class”
  • 27:00 - Joel Nelson - “The Arthritis Tease” and “The Invisible”
  • 30:10 -  Unity - Croon
  • 33:40 - Gittel - additional biographical info
  • 34:40 - Melissa - “Brain Fog” poem
  • 37:10 - Mimi Cross (Inflammation Vacation)
  • 38:15 - Ashley S “You Say You’ll Never but I do.”
  • 41:25 - Gittel - Second poem
  • 43:00 - Effie - reading from Brenda Klean-Sasser poem (2012) “100 Shades of Blue”

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Chronically Brown: The Importance of Cultural Representation in Chronic Illness Communities, With Sukhjeen Kaur25 May 202100:53:14

Topics covered in this episode include:

  • Stigmas around disability within South Asian communities.
  • Sukhjeen’s personal story with rheumatoid arthritis and how that led her to form the nonprofit Chronically Brown
  • Exploration of medication shaming.
  • Lack of representation of people of color’s voices in online chronic illness communities.
  • Discussion about how South Asian practices (like yoga, herbal remedies and turmeric) are sometimes bashed within the chronic illness community.
  • Dos and Don’ts for when reacting to someone’s chronic illness or disability.
  • What should medical professionals consider when treating someone of South Asian descent?
  • Exploration of white privilege and microaggressions

Speaker Bios:

Sukhjeen Kaur is the Founder of Chronically Brown which aims to address the ableism in South Asian communities. Chronically Brown is a non-profit organisation dedicated to empowering South Asians with invisible & visible disability through education and support. Sukhjeen has lived with rheumatoid arthritis for 2 years.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and enjoyable patient education and self-management resources.

This episode is brought to you by the Rheumatoid Arthritis Roadmap, an self-paced online course Cheryl created that teaches people with RA how to confidently manage their physical, social and emotional life. 

Episode links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Breakdown:

1:00 - Sukhjeen shares her initial difficulty adjusting to her chronic illness due to lack of representation of people of color in online communities. She shares how she learned to accept her condition after connecting with others from her cultural community.

5:30 - Sukhjeen explains how and why she formed the nonprofit Chronically Brown. She shares how she grew up in a predominantly white area and felt her cultural background was erased during her youth. The exclusion and stigmas for people of color with disabilities leads Sukhjeen to form Chronically Brown. 

9:05 - What does “intersectionality” mean and how does that apply to a person of color living with a disability? What does it feel like to be excluded from both your culture and your disability community? 

10:30 - Specific stigmas around disability within South Asian communities, including “What will people say?” Pressure to hide your chronic illness, not use mobility aids, “fix” or cure your illness, maintain an image of perfection and more examples. 

15:00 - How Sukhjeen became comfortable being more outspoken about her experiences with disability. 

20:00 - Sukhjeen explores medication shaming within South Asian communities and the chronic illness community at large. 

22:00 - Exploration of how South Asian cultural treatments (like yoga or herbal remedies or turmeric) are sometimes bashed within the chronic illness community. The importance of the language we chose; “have you tried yoga” can be exclusive or derogatory towards South Asian communities.

26:45 - Exploration of the phrase “herbal medicine” and how that often signifies nonwhite practices versus “Western medicine.” 

28:35 - Recognition of the emotional and energetic labor that goes into educating others about culture. Recognition that not every South Asian person wants to speak about their culture. 

30:30 - Sukhjeen explains her “Dos and Don’ts” when reacting to someone’s chronic illness or disability, and what to say when you don’t know what to say. Why is it so harmful when people say things like “you just need to push through it” or “my friend tried XYZ and they are cured, you should too.”

35:15 - What does Sukhjeen want medical professionals to know about South Asian cultures and disability? 

41:00 - Sukhjeen’s final message: the importance of including South Asians in all efforts around chronic illness and disability, and uplifting the voices of people of color.

44:00 - Reflection on #DisabilityTooWhite. The importance of representation of people of color’s experiences. Cheryl’s reflection as a white person about the importance of recognizing your blind spots and subtle forms of racism and biases. 

46:00 - Sukhjeen’s examples of racial microaggressions when filling her medication and a pharmacist delaying her medication due to his difficulty understanding her name.

50:00 - Cheryl’s reflections on having white privilege, the importance of recognizing it and using it in a helpful way rather than taking advantage of it.

51:30 - Where to follow up with Sukhjeen.


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The Worst Good News: What to do when Test Results are Normal but you Feel Awful? Joel Nelson's Story.13 May 202100:58:10

Topics include:

  • Joel shares what it was like to grow up with juvenile idiopathic arthritis
  • Joel explores the vulnerability of doctor patient interactions and the concern chronic illness patients often have of being perceived as hypochondriacs.
  • Joel and Cheryl discuss the imperfections of our current health systems, and the fact that “No Established Cause doesn’t mean No Problem.”
  • A group Pain Management program helps Joel rewire how he thinks about pain
  • Cheryl & Joel share tips and exercises for mental wellbeing despite chronic illness

Speaker Bios:

Joel Nelson: Writer. Arthritis Advocate. Dad. Sharing my story of Juvenile Idiopathic Arthritis to raise awareness. Specialising in pain, parenting and mental health. Also writes for leading charities and organisations.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

This episode is brought to you by the Rheumatoid Arthritis Roadmap, an self-paced online course Cheryl created that teaches people with RA how to confidently manage their physical, social and emotional life with this condition.

Episode links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

1:00 - Introduction and Joel’s diagnosis story.

3:00-11:30 - Joel reads from his blog post, “No established cause doesn’t mean no problem.”

11:45 - Cheryl & Joel discuss the vulnerability of seeing new specialist doctors. Joel expands on his experiences with the neurologist who had not reviewed his medical chart.

15:15 - Cheryl & Joel discuss being worried about being perceived as a hypochondriac, and the challenges of filtering what information you share with a doctor / medical provider.

22:45 - Joel expands on his emotional response to the test results letter he received from the neurologist with his test results.  Cheryl & Joel discuss the imperfections of our current health system.

28:00 - Cheryl expands on how patients who have difficulty functioning in daily life deserve access to care, for example occupational therapy, even if there is “no known cause.”

30:00 - Joel explains what his GP (primary care) said after his neurological test results were normal. He went through pain management therapy which included disability adjustment training. He made a conscious choice to put his energy into adapting to it and making peace with it, yet continues living in fear that a neurological episode will happen again. 

35:30 - Joel talks about his Pain Management program, which included group therapy, individual therapy, occupational therapy, physical therapy, learning about pain and special wellbeing topics. It helps him “rewire how he thought.” 

40:00 -  Cheryl’s perspective about finding a balance between trying to heal or eliminate pain, and building our capacity to adapt to our life as it is, even including pain.

42:30 - Joel describes a helpful exercise from his pain management program: writing down the biggest issues with your current situation and recognizing that pain wasn’t necessarily the biggest problem, it was partly the spiraling thoughts around it. 

46:30 - Cheryl’s analogy for positive versus negative thoughts - like a radio station you can choose to fight them, try to constantly turn them up or down or drown them out, or we can just acknowledge that they are simply there, sometimes they’re helpful, sometimes not and I can continue going where I want to go despite them. 

48:00 - Joel’s realization that he might not be able to turn “off” the negative thoughts, but he can let them have less power over him. Example of his work as an IT manager and how he struggles with guilt when he takes time off.  

51:30 - Cheryl and Joel reflect on how having to say no and take sick days challenges your sense of self. Discuss the challenges of activity pacing when you are a parent.

55:00- Concluding thoughts - link between physical and mental health. Don’t be afraid to ask your medical providers questions and be involved with decision making.


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Parenting, Faith and Respecting Different Treatment Choices: Conversation with The Rheumatoid Arthritis Mama Renee Anderson04 May 202100:50:33

Episode at a glance:

  • Renee’s diagnosis journey after a decade of mystery symptoms
  • How rheumatoid arthritis has affected Renee’s parenting and homeschooling
  • Renee’s Christian faith helps her cope with challenging times
  • Cheryl and Renee share their different treatment choices (western medicine and natural only approaches) and how important it is to respect each other despite different choices
  • How Renee adopts an anti-inflammatory lifestyle
  • The dark side of focusing on wellness and diet: Renee shares about orthorexia, an unhealthy obsession with healthy food
  • Why Renee started her Rheumatoid Arthritis Mamas Sisterhood Facebook group

Speaker Bios:

Renee is a former middle school teacher turned homeschooling mom of three. She’s been married for 17 years and lives in West Michigan. She started The Rheumatoid Arthritis Mama after her RA diagnosis in late 2017 when she began sharing her journey, faith, and experiences with RA openly and authentically on Instagram and Facebook. 

Since then, Renee has been interviewed by and featured in media outlets such as Healthline, Health Central, CreakyJoints, WEGO Health, Self Magazine, and more. Her Facebook support group, The Rheumatoid Arthritis Mamas Sisterhood, has nearly 2,000 members and she uses the group as a space for all women to come together regardless of their treatment choices to support one another, share their experiences, and connect with other autoimmune disease warriors. 

Renee has a passion to support and encourage other women (especially moms) who are battling autoimmune diseases. Her goal is to provide others with encouragement and hope, feel less alone, and inspire them to live their best lives despite battling autoimmune disease. Her newest endeavor, a podcast called Every Day with Autoimmune, is set to launch during the summer of 2021!

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for eighteen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

This episode is brought to you by the Rheumatoid Arthritis Roadmap, an self-paced online course Cheryl created that teaches people with RA how to confidently manage their physical, social and emotional life with this condition.

Episode links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the detailed show breakdown:

2:14 - Renee’s journey getting her RA diagnosis after a decade of mystery symptoms. 

5:23 - Renee has mixed emotions after her diagnosis: fear and confusion, mixed with relief that she finally had a definitive answer. 

6:45: Discussion about how common it is for people with autoimmune symptoms to be dismissed by medical professionals.

8:30 - How Renee’s three children have become more compassionate and sensitive as a result of mommy’s rheumatoid arthritis. How she initially tried to hide her diagnosis from them, and how she then realized she needed to be open with her children and husband.  

13:15 - Renee opens up about her infertility journey and what she learned about communication, stress management and how to relinquish control.

15:40 - How Renee structures her daily routine to suit her RA needs and her family’s needs.

18:10  - How Renee’s Christian faith and eternal perspective helps her cope with RA.

20:00 - Cheryl reflects on how, despite being an agnostic / atheist now, she carries forward lessons she learned as a child about the importance of unconditional love and the idea that everyone is worthy even if they have a health challenge.

21:55 - Cheryl & Renee discuss how different people have different treatment paths and the divides within the RA community at times between a “natural” and a “western medication” approach. How Renee explored lifestyle and diet and worked with a functional medicine doctor. 

26:35 - While Renee is able to control her RA with lifestyle and diet, she will never fault or judge anyone for taking medication.

27:35 - Cheryl’s perspective as someone on three RA medications. The importance of differentiating as patients between sharing our experiences and then making the leap that *because* it worked for me, it 100% will work for you. Important to remember the current scientific evidence at the population level favors an early aggressive medication approach. 

29:20 - How Renee’ focuses on an overall anti inflammatory lifestyle; an integrative approach - not “either/or” but “both.” 

30:00 - How Renee’s experience with unkindness and negativity in Facebook groups inspired her to start her own group: the Rheumatoid Arthritis Mamas Sisterhood.

34:05 - The dark side to obsessing over “healthy food,” you can become orthorexic - obsessive with eating only healthy or “clean” foods.

36:35 - Patients are the expert on our own patient journeys but that doesn’t mean that we know what will work for another patient. 

37:10  Renee shares the foods that trigger *her* inflammation. 

38:45 - How Renee healed herself from her negative emotions around food and has built a healthy relationship with food through Elizabeth Dahl, a food coach. How to learn food is not the enemy. Learning to be careful about what she eats without being militant has helped her.

43:35 - Discussion of disease-specific Facebook groups, how it’s important to have a place to vent sometimes but it’s also important to find groups that suit your needs, and if you’d like a more supportive and positive place there are groups for that too.

47:25 - Concluding thoughts.


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It's just a bad day, not a bad life: Julie Croner's Psoriatic Arthritis Journey24 Apr 202100:45:43

Specific topics include:

  • Julie’s experience with multiple knee surgeries 
  • Avascular Necrosis leads to Complex Regional Pain Syndrome and Julie is bedriddenfor 6 months
  • How a trip to Disney World led to Julie’s epiphany that she should share her story and start a blog
  • How Julie put her Information Technology (IT) degree to use while tracking her symptoms and discovering her unique inflammation triggers
  • How Julie discovered the most important tools for living a healthy, full life with PSA
  • Julie’s current role as a patient advocate with WEGO health
  • How PSA affected Julie’s dating life and how she met her now husband
  • Julie’s experiences with pregnancy and parenting with PSA

This episode is brought to you by the Rheumatoid Arthritis Roadmap, an self-paced online course Cheryl created that teaches people with RA how to confidently manage their physical, social and emotional life with this condition.

Speaker Bios:

Julie Croner, a psoriatic arthritis patient leader, is on a mission to advocate for ALL advocates. She's the Vice President of the Patient Leader Network at WEGO Health and was named to MM&M's inaugural class of 40 Under 40 in 2020. Julie has been featured by Stanford Medicine X, the National Psoriasis Foundation, Everyday Health, WebMD, HealthLine, and more. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

Episode links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

1:00 - Introduction to Julie.

2:00 - Julie’s winding journey to a psoriatic arthritis diagnosis: knee surgeries / swelling from fifth grade until after college and during work as an Information Technology (IT) consultant.

4:55 - Julie gets the adult diagnosis of psoriatic arthritis (PSA) and her rheumatologist helps get it under control. She’s able to connect the dots of her chronic health issues in retrospect and see how it all relates to psoriatic arthritis (PSA).

8:24 -  Julie also experiences avascular necrosis in the femur bone (leg) which led to complex regional pain syndrome (CRPS). She started connecting to other patients online, got medication for PSA and started exploring diet and lifestyle. 

9:48: Julie researches anti-inflammation lifestyle approaches, and uses her IT consultant skills to make an excel spreadsheet to track everything (food, movement, mood, medications, etc) for 6 months and discovered her unique inflammation and flare  triggers.

 10:55 The BEST thing she did in her journey!

11:20 - Julie discovers that her body is sensitive to food triggers. She discovers that gentle movement, meditation and mindfulness helps her. She continues going on and off medications when needed. 

12:40 - Cheryl reflects on the importance of discovering your own unique triggers and not thinking there is a one size all solution. 

14:00 - Julie’s worst food triggers for joint inflammation. (15:12) 

15:44 - Julie is bedridden for 6 months due to her Avasular Necrosis and is depressed. Her parents take her to DisneyWorld and she has an epiphany after doing a singing competition!  She decides to share her story through starting a blog: “It’s just a bad day not a bad life.”

19:20 - After being on disability for four years, she decides to focus on a career in patient advocacy rather than IT consulting.

20:30 - Julie starts working for WEGO Health, a network of patient leaders. She helps patients and loved ones use their story and get connected to companies wanting their insights.

23:40 - Why Julie thinks it’s so important for patients to share our stories: how she found an answer to her avascular necrosis due to seeing another patient’s story online.

26:50 - How Julie’s health conditions affected her dating life, and how she met her husband. Her husband said, “You talk like you USED to be great, and the person I see IS really great! (28:13)”

30:00 - How did PSA affect her family planning with her spouse who is in the army. When pregnant she felt very nervous and overwhelmed.  She signed up for a MothertoBaby study.

33:45 - During her first pregnancy PSA went into remission, psoriasis in 1st trimester. Second pregnancy didn’t go into remission. 

35:15 - What helped her when babies were little: asking for help, planning ahead, pacing yourself. 

37:15: How Julie copes with big emotions while parenting: Headspace app and Mindful Mamas app. 

39:36 - Julie’s best advice for newly diagnosed patients - empower yourself and be a partner with your medical team.

40:45 - Cheryl and Julie’s advice to patients who are overwhelmed when “doing their own research” - how to evaluate which resources are high quality information and which are low quality or dangerous. Reflections on how to navigate disease-specific Facebook groups.

44:15: Julie’s concluding thoughts: if you are dealing with an autoimmune disease, you are not alone.

 


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From Devastated to Patient Leader: Eileen Davidson’s Rheumatoid Arthritis Story15 Apr 202100:47:48

Episode at a glance:

  • Eileen shares her rocky road to an RA diagnosis when he son was two years old
  • How Eileen's blog led her to patient advocacy and research 
  • How symptom tracking helped Eileen reduce pain and improve fatigue
  • How exercise helps Eileen reduce pain and improve fatigue
  • What it's like to be a single mom with RA
  • Reflections on  mental health while living with chronic illness

Speaker bios:

Eileen Davidson is a rheumatoid arthritis patient advocate from Vancouver British Columbia Canada. She volunteers with the Arthritis Research Canada patient advisory board and the Canadian Institute of Health Research - Institute of Musculoskeletal Health and Arthritis patient engagement research ambassador. When not advocating she is writing about her experience with arthritis through Creaky Joints, Chronic Eileen or can be found being a mom to her son Jacob.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

This episode is brought to you by Rheum to THRIVE, a membership community Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. 

Episode links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

1:40 - Eileen’s diagnosis story: many years of symptoms prior to her diagnosis when her son was two years old. 

5:50 - How Eileen’s symptoms affected her ability to take care of her baby. 

8:16 - Eileen’s devastation after receiving her diagnosis due to seeing her aunt suffer from severe rheumatoid arthritis and pass away the same week.

10:00 - How Eileen learned to trust her medical providers.

11:20 - What helped Eileen learn to cope with her RA and share her story publicly; how others responded to her story and how  writing introduced her to advocacy efforts.

15:00 - How others’ negativity motivated Eileen, and Eileen shares some of the positive responses to her writing.

17:45 - Eileen describes participating in arthritis research on symptom tracking using a FitBit, with a physiotherapist. Through tracking she started seeing patterns between menstrual cycle, sleep, exercise, rest.

22:30 -  Eileen learned the benefits of strength training and helped researchers explore barriers to patients participating in strength training. 

26:00 - Physical activity doesn’t have to look like formal exercise, it can be as simple as gardening, Zumba, yoga, or dancing.

29:00 - How the pandemic affected Eileen’s exercise routine and pain levels.

31:30 - How exercise helps Eileen with fatigue. 

34:00 - Eileen shares her journey with depression and mental health.

36:20- What’s helped Eileen cope with depression and anxiety from rheumatoid arthritis & pain.

38:00 - Eileen’s advice to other parents with rheumatoid arthritis and reflections on what her son has learned from having a mom with a disability.  

41:00 - How her rheumatoid arthritis has made her a better mom and changed her priorities

44:20 - The different forms patient advocacy can take.

46:00 - Eileen’s final message: if you’re interested in getting involved in research, don’t hesitate! 


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Pregnancy and Parenting with Psoriatic Arthritis: Jamie’s Story01 Apr 202101:07:19

In this episode, Cheryl & Jamie discuss:

  • Jamie’s challenging diagnosis journey
  • The difference between her pre-psoriatic arthritis pregnancy and parenting experience and her experience being pregnant with psoriatic arthritis, including a discussion of medications
  • The difficulties of being a young person with rheumatic disease
  • The challenges of family planning with rheumatic disease: whether to have another child or not?
  • What it’s like to live with anxiety along with rheumatic disease
  • Balancing gratitude and grief
  • Learning to overcome “mom guilt”
  • Our children need us to be present not perfect

Speaker bios:

Jamie lives in Gloucestershire, England, with her husband and their two children; Harper aged 4 and Kit who is almost 5 months. She was diagnosed with psoriatic arthritis in early 2019 and is still in the process of “learning” her condition. She is a freelance writer and self proclaimed coffee addict who is passionate about combining traditional and holistic approaches to find the best combination to manage her chronic illness.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Episode links:

Medical disclaimer:

All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

01:00 – Jamie’s introduction and her initial health issues: consistent pain in her fingers, spine, and neck after her first child was around two years old. 

05:00 – Jamie struggles to get treated seriously by doctors. She’s diagnosed with psoriatic arthritis after originally her doctors said she was “too young” for it. 

5:35 - She and Cheryl discuss their similar diagnosis journeys with medical gaslighting, how both of them had to have their parents advocate for them and spend money on additional doctors before they got their diagnoses. 

7:30 - Discussion of anxiety as a result of untreated / undiagnosed chronic illness. Jamie & Cheryl discuss their experiences getting therapy for anxiety and coming to terms with it.

9:45 – Jamie’s first pregnancy without psoriatic arthritis, as compared to her second pregnancy with it. Discussion about medication decisions and how difficult it was to decide whether to have another child or not.

12:08 - What was it like to be pregnant with psoriatic arthritis during COVID19 pandemic (in 2020)? Includes a discussion about the pregnancy-induced remission she experienced. 

14:30 Jamie discusses her experiences breastfeeding and difficult postpartum medication decisions. Cheryl and Jamie discuss how complicated medical decisions are in the context of a family system, not just what’s “best” for the baby. 

16:30 - Jamie discusses comfortable ways to hold the baby during breastfeeding and the ways in which aspects of the newborn process are easier due to lockdown.

18:00 - Jamie discusses her mixed feelings about using adaptive aids or gadgets in the home, as a young person with arthritis.

20:00 - Balancing gratitude and grief as a mom with a disability.

22:00 - The importance of learning how to adapt continuously, rather than seeing your chronic illness as having an “end point.” 

23:15 - How Jamie’s flare up affects her ability to parent her “big kid” (her 4 year old) and her feelings of mom guilt, complicated by the fact that she’s experienced parenting her child prior to her diagnosis.

26:10 - Cheryl and Jamie discuss how difficult it can be to decide whether to have additional children when you have a rheumatic disease, and how to spread out the space between your children. 

34:45 - Cheryl parenting mantra: “My son needs me to be present, not perfect.”

36:00 - Learning to enjoy the simple pleasures with your children.

39:00 - How Cheryl & Jamie explain their conditions to their children and how it’s helped their children develop empathy.

42:00 - Coping with feelings of “unfairness” when you get diagnosed with an autoimmune disease when you had previously been healthy and had healthy behaviors.

45:00 - Fears of passing your autoimmune condition on to your children. 

47:45 - Mamas Facing Forward - resource for moms and moms to be living with chronic illness. Includes books for children about parents that have disabilities.

50:00 - The importance of having clear expectations to your partner and delegating if possible when raising children.

55:00 - The role social media plays in Jamie & Cheryl’s lives; a blessing and a curse. It can be confusing as the diseases differ drastically between people.

58:00 - What the word “progressive” meant to Jamie when diagnosed and how that has changed over time with the modern treatment options and medication. 

1:01:00 - Cheryl’s experience when newly diagnosed, having faith in the medications.

1:05:00 - The importance of considering how representative the stories that you’re looking at on social media are. When things are going well, people aren’t on the disease-specific social media groups.


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Comedy, Chronic Illness, and Coping: Katie’s Inflammatory Arthritis Story04 Jun 202401:10:41

In this episode, Katie reflects on the crucial role that parental and patient advocacy played in her her journey to a diagnosis of juvenile idiopathic arthritis (JIA).  She also shares her college experience, and discusses the roles that comedy and humor have played in helping her cope. Cheryl and Katie express the importance of accepting the need for assistive devices, setting boundaries, believing in oneself, prioritizing needs, and having a support system to thrive with chronic illness.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now!

Episode at a glance:
  • Kate’s Diagnosis Story at age 15: Katie shares her journey of being an active child and being diagnosed juvenile rheumatoid arthritis (juvenile idiopathic arthritis) at age 15 after experiencing symptoms for an extended period of time that were initially dismissed as “growing pains”.
  • Advocacy: Katie emphasizes the crucial role her mother played in advocating for her during medical appointments, highlighting the importance of having a supportive network. Katie shares advice on self-advocacy, encouraging patients to set firm boundaries and prioritize their needs, even if it means challenging expectations.
  • Support: The conversation emphasizes community and connection, and the benefit of having someone in your corner to help advocate with you.
  • Coping Strategies: Practical tips are shared, including the use of specialized tools and gadgets designed to make daily tasks easier for individuals with arthritis. Katie also shares her experience with medical marijuana.
  • Comedy: Katie shares the importance of comedy in her life, and how it helps her cope with her diagnosis and spread awareness of it.
  • Accommodations: Katie and Cheryl discuss access to accommodations, particularly in educational settings, such as extended test time and speech-to-text tools for students with chronic illnesses.
  • Living Authentically: Katie advocates for a balanced approach of embracing realism while maintaining a positive outlook, acknowledging both the challenges and opportunities for growth that come with chronic illness.
  • Advice to Newly Diagnosed Patients: Carry on, stick up for yourself, and believe in yourself. Write down three things that made you  proud each day.
For full episode details:

Go to the episode page on the Arthritis Life website for full show notes plus a full transcript, video and more!


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Can you Live a Normal Life with Rheumatoid Arthritis?27 Mar 202100:31:33

In this episode Cheryl explains how Acceptance and Commitment Therapy (ACT) has been key for her to build a life she loves despite chronic illnesses. She also shares how she’s found a balance between ways to minimize pain and ways to live a good life despite pain. Additionally she urges listeners to ask, “Can I live a good life despite rheumatoid arthritis?” rather than “Can I live a normal life with rheumatoid arthritis?” 

Speaker bio:

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare she say) FUN patient education and self-management resources. 

Links to things discussed in the podcast episode:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Show notes:

  • 1:20 - Why I chose this topic for today’s episode.
  • 3:00 - Does “normal” mean lack of severe joint damage? Research study showed 80% of people with rheumatoid arthritis can live a “normal life.”
  • 5:00 - What is your definition of normal - compared to what?
  • 7:00 Is a “normal life” the exact life I imagined for myself pre-diagnosis?
  • 7:55 - Is a “normal life” one where I can experience things that are important and achieve meaningful goals and life experiences?
  • 10:05 - Can you live a normal life with RA? It depends on what your definition is, and what your hopes and dreams are underneath your concept of normal.
  • 10:35:  You may not get the normal you wanted or expected, but can you find a NEW normal you can learn to love?
  • 12:40 - There is no guarantee for anyone of a pain free life. Confronting that reality head on can free us from pressure and energy to try to achieve a perfectly pain free life, which is impossible for most.
  • 15:00 - How my therapists taught me the futility of trying to avoid pain and anxiety.
  • 15:45: “The hope is that you can still live a good life despite inevitable pain and suffering, that’s the hope, the hope isn’t that you can avoid it, because avoidance is not a long term sustainable strategy .”
  • 16:00 - We can and should gather evidence based tools to manage and minimize our pain and function on a daily basis, however: “If we ONLY focus on the tools to MINIMIZE pain, the problem can be the expectation or belief that we attach to the idea that if we JUST have the right tools we are going to 100% be guaranteed to avoid all pain, and I do wish that were true, but realistically it’s just not true for most people because, pain, physical or mental, is an inevitable part of the human experience.”
  • 17:15 - Difference between pain and suffering.
  • 17:55 - I was dragged “kicking and screaming” into acceptance. If you are confused, you’re not alone!
  • 18:45: True acceptance of the PRESENT moment is completely different than giving up or resignation.
  • 20:10 - When we’ve done everything we can to reduce pain, instead of struggling with that, we can focus on: what can we still do in the present moment?  What can I still DO that ’s important or valuable to me, DESPITE the pain? I eventually learned to let go of the illusion that if I just do the RIGHT THING I could ALWAYS avoid pain, and once I let go, I was  set free.
  • 21:30 - Balancing act between plan A (using tools to minimize symptoms) and plan B (tools to “workaround” symptoms and function despite them).
  • 22:20 - We spend a lot of time running away from pain and running away from our disease, but what if we spent more time running TOWARDS things we can still do that are valuable?
  • 23:05 - What I  dislike about a “normal” life being defined as one without disease -  feels ableist to me
  • 24:15 - My old optimism: if I just find the right solution my pain will go away, RA will have no affect on my life. New optimism: me and people with it can still live rich, meaningful lives DESPITE discomfort.
  • 27:15 - My new mission: finding a balance between controlling symptoms/minimizing symptoms *and* focusing on maximizing our quality of life despite it.
  • 27:30 - Why I developed Rheum to THRIVE membership community and what it stands for.
  • 28:45 - So many people get stuck in this mentality that they have to WAIT until their symptoms are fully controlled before attempting to thrive or live a full life, and I really encourage you to see what is still possible in your life. What can you still do and enjoy and accomplish despite your condition?
  • 29:25: Can you live a normal life with RA? Depends on your definition of normal!
  • 29:45 - The question I like to ask more than “can I live a normal life with RA:” Can I live a GOOD life with RA? Can I be of service to others, can I leave the world better when I leave it than when I found it?  I think YES.

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What do you do when you hit rock bottom from chronic pain? Mindfulness, Acceptance and more with James Allen17 Mar 202101:03:55

James and Cheryl discuss in detail how they manage fluctuating symptoms and pain from chronic rheumatic diseases. James also explains how his patient journey led him to create his innovative 3-D symptom tracker app, Chronic Insights.

Speaker bios:

James Allen is 39, and has lived with ankylosing spondylitis (AS) for 22 years. He likes to think of arthritis as a clumsy housemate who moved in without permission, who he used to hate but over the years he’s grown to kind of like. It forced him to leave his job as an IT consultant, which in retrospect has been a positive development, because now he’s doing something he really loves - developing a symptom diary app called Chronic Insights.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Episode links:

Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

  • 02:30 - James shares his relationship to his Ankylosing Spondylitis (AS), it’s like someone who moves into your house who at first you try to make go away, then you make peace with it.
  • 05:30- Cheryl and James discuss how metaphors and Acceptance and Commitment Therapy (ACT) help them cope with chronic illness.
  • 10:00 - James’ journey getting his initial diagnosis of Ankylosing Spondylitis quickly due to his dad’s help.
  • 12:20 - James’ journey managing his AS; initially it was pushed to the back of his mind, then it gradually worsened over time and he sought therapy to help with the struggle.
  • 17:10 - Cheryl and James’ important lessons/insights about the importance of communicating your pain levels to your providers. How hard it can be to admit you are in a lot of pain.
  • 19:40 - James’ switch to his first biologic, Humira and how it changed his life for the better.
  • 21:00 - Cheryl and James discuss the phenomenon that many patients are scared of medications, and how the risk / benefit analysis is different for each patient.
  • 23:50 - James enjoys activities like running a half marathon while his medication worked.  Then, experiences his medication wearing off after years of success, which was a massive blow mentally.
  • 25:50 -  James starting over with medications, trying different biologics. He experiences progressive deterioration of his health which negatively affects his work life.
  • 30:50 - James’ condition progresses to where he has difficulty getting out of bed and his partner has to help him with daily living tasks. He hits rock bottom.
  • 32:50 - James comes across meditation and mindfulness, leading to breakthroughs in his ability to manage and cope with pain. He learns to be curious about his pain and develops the ability to observe himself and empathize with his experiencing pain, and eventually accept it.
  • 36:50 - Cheryl explains the importance of the developing mental tools to cope with the uncertainties that come with chronic pain and chronic illness.
  • 39:50 - James discovers slow and gentle somatic exercise, which helps him relax and relieves joint stiffness and tension.
  • 41:50 - The benefits of the reclined exercise bike and a sit/standing desk for James’ back and hip pain.
  • 43:50 - How James sometimes allows himself to have a “bad day” and wallow to help his mental wellbeing.
  • 46:50 - Cheryl dives into acceptance and commitment therapy.
  • 48:50 - James’ challenges with difficulty rating his pain on a scale of 1-10, and why that inspired him to create an app for tracking symptoms.
  • 51:20 - Cheryl and James explain the difficulties of rating pain.
  • 53:00 – James elaborating on how he developed his symptom diary app, Chronic Insights, which allows you to draw your symptoms onto an interactive 3-D model.
  • 57:00 - James’ shares the impact of  having a visual representation of your pain (via his app), and shares the feedback from others who’ve been using the app.
  • 1:04:00 - Where you can find James

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How can Lifestyle and Integrative Medicine Help People with Rheumatic Diseases? With Dr. Yu03 Mar 202100:35:47

Speaker biographies: 

Dr. Micah Yu is double board-certified in internal medicine and lifestyle medicine. He obtained his MD from Chicago Medical School and holds a Masters in Healthcare Administration and Biomedical sciences. He completed his internal medicine residency and rheumatology fellowship at Loma Linda University in Southern California. He has been accepted with a full scholarship to the Andrew Weil Integrative Medicine Fellowship at the University of Arizona.   Dr. Yu has a very unique perspective on autoimmune disease and arthritis as he is both a patient with arthritis and a physician.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Links to things discussed in the episode:

Here's the show breakdown:

  •  01:15 - Rheumatologist Dr. Yu’s journey first with gout, then diffuse joint pain while in medical school, then a diagnosis of spondyloarthritis during his fellowship.
  •  4:30 - What made Dr. Yu want to pursue Rheumatology.
  •  6:00 - Dr. Yu pursues Integrative Medicine and the 6 pillars of Lifestyle Medicine with the help of his wife, also a physician. He adopts a whole food, plant based vegan diet and experiences huge improvements shown in lab work, pain levels and overall weight within 2-3 months.  
  • 8:28 - Dr. Yu explains what “Integrative Medicine” is and explains the process he’s going through to get board certified in it, including learning about Chinese medicine, ayurveda, herbal medicine and more.
  • 9:51 - Dr. Yu explains what the newer field of “Lifestyle Medicine” is, and the overlap between the two.
  • 10:30 - How can an appointment with an integrative medicine Rheumatologist differ from an appointment with a typical Rheumatologist? Discussions of nutrition, sleep, stress and whether medications are necessary. 
  • 12:00 - Cheryl and Dr. Yu discuss the importance of each patient’s treatment plan being individualized and customized to them, and how it can be a source of confusion for newly diagnosed patients when they see that someone else with their “same” diagnosis has a different treatment plan. For example, one person with severe disease who is afraid of medication might be confused why another patient (with more mild disease) was told they could avoid meds.
  • 15:08 - Dr. Yu answers some of the most frequently asked questions about diet and rheumatic disease (vegan diet, plant based, Mediterranean, Paleo and more). Explanation of the influence of the gut microbiome on autoimmune disease
  • 18:50 - Dr. Yu explains which supplements can help with rheumatic diseases and inflammation.
  • 20:15- Dr. Yu shares tips for fatigue. 
  • 21:30- Definition of “Functional Medicine” and his recommendations on finding a provider with valid credentials. 
  • 23:35 - Cheryl and Dr. Yu discuss the importance of sleep, ruling out a sleep disorder and how poor sleep contributes to fatigue and inflammation.
  • 24:45 - Dr. Yu discusses evidence for THC and CBD for it’s anti-inflammatory and pain relief properties. 
  • 26:00 - Is it hard being a patient and provider in Rheumatology? How Dr. Yu’s passion pushes him through the long hours!
  • 28:45 - If Dr. Yu could change anything about Medical School, what would he do?
  • 30:00 - Reflections on how the gray areas in between Integrative / Natural medicine and Western Medicine can be difficult for patients who have anxiety about their condition. How Dr. Yu finds a middle ground with his patients - combining medicines and natural alternatives. 
  • 31:30 - Dr. Yu’s message to patients who are afraid of medications.
  • 33:25 - How do you find a Rheumatologist who also has an Integrative Medicine board certification? 
  • 34:45 - Where can people find Dr. Yu online?

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How to Balance Western Medicine and Alternative Medicine Approaches with Dr. Wada25 Feb 202100:52:20

Dr. Kara Wada is an Assistant Clinical Professor and Associate Fellowship Program Director of Allergy/Immunology at the Ohio State University in Columbus, Ohio. She graduated from the University of Illinois College of Medicine and completed her Internal Medicine and Pediatrics Residency and Allergy/Immunology Fellowship at the Ohio State University and Nationwide Children’s Hospital. 

After having completed additional fellowship training in medical education, Dr. Wada is passionate about building meaningful connection and therapeutic relationships with her patients and inspiring future physicians to do the same. She seeks to empower her patients and coaching clients with a naturally-minded and scientifically-grounded approach to care.  She speaks nationally on topics including medical education, allergic and immunologic conditions. Outside of her work, she is an autoimmune patient, a food allergy mom of 2 spunky daughters, and wife to another Dr. Wada.  

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links to things discussed in the episode:

Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

  • 01:25 - Introduction: Dr. Kara’s job as an Allergist Immunologist doctor at an academic medical center, journey with the autoimmune disease Sjogren's syndrome, and her role as a mother to a child with food allergy.
  • 4:10 - Dr. Kara’s experience having to advocate to get the blood testing and labs drawn for Sjogren’s disease while she was a medical intern.
  • 6:30 - Reflections on the power dynamics in physician - patient relationships and the importance of two way communication.
  • 8:38 - Dr. Kara’s tips on how to develop a trusting relationship with a physician.
  • 13:48 - How Dr. Kara uses a shared decision making to work together with patients, rather than the old model where the doctor told patients what to do.
  • 16:28- Dr. Kara explains the difference between an Allergist Immunologist and a Rheumatologist, and explains how allergist immunologists do more than “just” allergies.
  • 20:25 - How Dr. Kara manages her Sjogren’s currently, with an emphasis on the word “and” (western medicine and other “crunchy” alternatives). An explanation of Dr. Kara’s anti-inflammatory living techniques: food, meditation, and most importantly sleep to support health and healing.
  • 25:10 - How Dr. Kara un-learned her perfectionist tendencies, and Cheryl & Dr. Kara reflect on how parenting helped them lean into “progress over perfection.”
  • 26:28: Reflections on how to accept the reality: you can do everything right, and sometimes your body is going to have a mind of its own. How to accept the element of randomness and move on with an empowered and self-compassionate mindset rather than letting it get us down.
  • 27:00 - Dr. Kara explains how she finds a balance between conventional and complementary alternative treatments: “weeding out the woo.”
  • 31:10 - The warning signs to look out for when looking at different complementary alternative treatment options
  • 33:10 - Dr. Kara explains how the supplement industry is not regulated and can be dangerous and shares her own experience of experiencing liver abnormalities after taking a “superfood” supplement.
  • 36:44 - The importance of a personalized care plan and getting a variety of specialists on your care team.
  • 38:43 - Just because it’s natural doesn’t mean that it’s healthy. Dr. Kara and Cheryl dive into the balance between being open minded and skeptical about alternative methods of managing rheumatic diseases like rheumatoid arthritis and Sjogren’s.
  • 41:00 - Dr. Kara and Cheryl’s discuss the importance of an individualized risk / benefit analysis when trying any new approach (including financial risks / investments, time risks / investments and health risks / investments / benefits).
  • 45:02 - Dr. Kara’s recommended resources for patients looking into alternative options: University of Arizona’s Website.
  • 46:55- Dr. Kara’s advice about lab tests that are marketed as “the tests your doctor doesn’t know to give you,” particularly for “food sensitivities” or food intolerances.
  • 48:33 - Cheryl & Dr. Wada reflect on how to still feel empowered when facing the truth that there may be no “magic wand” solution for rheumatic diseases.
  • 49:05 - Importance of making your ordinary routine fun in small ways to add up to larger gains in health over time. Reflections that many people with rheumatic diseases don’t need many supplements.

 


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How can Water Exercise and Aquatic Yoga help people with Arthritis and Rheumatic Diseases?12 Feb 202101:05:55

Christa Fairbrother is a skilled and experienced water aerobics and aqua yoga instructor who also lives with multiple chronic illnesses. For Christa, living with arthritis and teaching yoga are integrated.  She credits her lack of pain to aqua yoga practice.  Being passionate about aqua yoga, she wants to see aqua yoga in more communities worldwide.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Here's the show breakdown:

01:15 - Christa’s diagnosis journey: symptoms of RA and Lupus symptoms started at age 12, initial diagnosis of Mixed Connective Tissue Disease (MCTD) after the birth of her 2nd son.

05:05 - Christa’s MCTD symptoms (including Raynaud’s) and why it’s so hard to get this rare diagnosis.

8:00 - Christa and Cheryl reflect on what it’s like to live with multiple chronic conditions, not knowing at times what is causing which symptom.

10:40 - Christa’s up and down journey managing her conditions over many years.

15:30 - Cheryl and Christa explain what connective tissue and fascia are.

17:33 - Christa’s journey with yoga, which started when she had back pain being a farrier (a craftsperson who trims and shoes horses' hooves). 

19:40 - After 20 years of doing yoga, Christa became a yoga instructor.

22:11 - What is aqua yoga, and how Christa discovered and fell in love with it.

25:33 - The numerous medical benefits of exercise in the water for healthy people and those living with arthritis. 

32:15 - Christa’s explanation of the offloading of gravity in the water due to buoyancy and how it gives your muscles a more balanced effort.

34:55 - Christa discusses how accessible swimming pools are in the US. 

38:55 - Thoughts around safety and germs with aqua yoga and swimming during the COVID-19 pandemic. 

41:55 - Interested in the Arthritis Foundation’s aqua therapy program? Here is how you can find it at a local water center!

44:40 - Christa describes what happens in an aqua aerobics class.  

47:43 - Cheryl and Christa’s insights on why group classes make people feel empowered, especially during COVID-19. 

50:56 - Cheryl and Christa’s views on how the sensory elements of water can help regulate our mood, from prenatal experiences to adulthood.

55:25 - Christa’s advice on what to do if your joints hurt in the water.

1:01:30 - Salt water pools VS. Chlorine pools and water safety advice that you may not be aware of. 

Episode links:

Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.  


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Life with Arthritis is a Marathon, Not a Sprint: Christy Williams’ Story04 Feb 202101:06:57

Christy Williams is a certified health coach, wife, mother of two and endurance athlete/triathlete. She has been living with an autoimmune disease called Sero-negative spondylarthopathy (blood negative inflammatory arthritis) since the age of 24. She is now 48 and has been in remission for 15 years due to a combination of Remicade (a biologic disease modifier) and an active healthy lifestyle. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. She is passionate about helping others with rheumatoid arthritis thrive despite arthritis. She formed the educational company Arthritis Life in 2019 after seeing a need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Episode links:

Show Breakdown: 

  • 01:00 – Christy shares her diagnosis at 24 after the birth of her first child, and her transition into adulthood. 
  • 03:20 – Christy’s tenacious drive to stay active, her journey completing an ironman challenge. 
  • 5:35: How Christy has managed her inflammatory arthritis over the years: it’s a marathon not a sprint! How she went from being in a wheelchair to completing triathalons after figuring out the right medication and lifestyle interventions such as exercise.
  • 8:00 - Christy explains how fatigue still affects her quality of life, and how she copes with it by pacing herself.
  • 13:05– Christy shares why and how she became a health coach for people with autoimmune disease, after she achieved remission. 
  • 20:30 – How having an autoimmune disease sparked Christy and Cheryl to confront their mortality.
  • 23:10 – Christy’s definition of “remission,” and additional reflections on the fact that no two paths towards remission are the same.
  • 30:10 – Cheryl and Christy share different debates and challenges within the chronic illness community, including medication shaming, or shaming of people who celebrate natural methods.
  • 34:40 - Cheryl reflects on how she’s tried to strike a balance between celebrating how well Western medications have worked for her and also respecting others’ choices if they differ, and how patients within the chronic illness community can unite in our common goals and consider the intent of our messages when we communicate our journeys.
  • 36:00 - How Christy & Cheryl cope with unsolicited advice.
  • 38:00 - How Cheryl’s therapy helped her cope with uncertainty and gray areas during treatment for RA.
  • 41:25 – How Christy has managed her attitude and mindset during the ups and downs of life with inflammatory arthritis.
  • 43:38– Cheryl shares how Acceptance and Commitment Therapy transformed her relationship to uncertainty as a chronic illness patient, and how anxiety makes you want black and white answers and certainty.  
  • 50:00 – Common misconceptions and myths around arthritis and remission.
  • 54:27 – Christy’s advice for anyone battling chronic illness and her best coping mechanisms dealing with uncertainty  
  • 57:00 - Christy’s pre-diagnosis challenges with people not believing her.
  • 1:03:00 - The importance of sharing our stories, even if we get criticized or misunderstood! 

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It's Not Just Joint Pain, and 8 other Things Everyone who Loves Someone with Arthritis Should Know21 Jan 202100:39:21
Episode at a Glance:
  • 0:48: Episode intro
  • 2:50: One -  We want you to learn what the disease is and isn’t.
  • 9:55: Two - The fatigue can be just as bad as the pain.
  • 15:48: Three - It doesn’t just affect the body - it also affects the mind and emotions.
  • 20:20**: Four** - It affects EACH person differently.
  • 22:50: Five - Daily symptoms are often unpredictable.
  • 25:45**: Six -** We want credit for how hard we’re fighting, even when we seem “normal.”
  • 27:54: Seven - Sometimes we need problem solving, other times we need empathy.
  • 34:30: Eight - Managing the disease itself is a job that takes time and energy.
  • 35:55: Bonus point: Take care of YOUR needs as the caregiver/friend
  • 37:10: Concluding thoughts
Medical disclaimer:

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

Links to things discussed in this episode:Thank you so much to episode contributors from Instagram:

@Sophialwebb_  , @mhaggerty_ , @mariavgi , @warriorsmovemountains , @worldofOT , @shelly_steele , _brittanbee_ , @theinvisiblemewarriorspbc , @znev.alia , @aimeefb, @mrs_Alix_Naber, @Lailaschneider, @kat.panning, @Annafitandbeautiful, @danicreegs, @floopilicious, @wsmommie, @house_of_spoons, @Bto22, @diana_rosas023,  @chaichat023, @kheartsphotos, @pdxfashionista, @stephanielabonte, @shelly_steele + numerous anonymous contributors!


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Arthritis Storytelling Hour - 13 Patient Stories in 90 Minutes12 Jan 202101:25:50

In December 2020, Arthritis Life hosted an “Arthritis Storytelling Hour” where thirteen patients shared vivid tales from their lives.

Listen and learn about how difficult the diagnosis process is for some, how people with rheumatoid arthritis and ankylosing spondylitis learned to advocate for themselves, how to navigate work life with your condition, what it’s like to be a “spoonie mom,” the importance of mindset, acceptance and self-care, and more! 

Video details:

Topic: basics of life with RA, diagnosis stories, how diagnosis led to career

  • 1:28 - Chloe Umpleby JIA (Juvenile Idiopathic Arthritis) journey
  • 6:21 - Kia Peters: diagnosis of RA (rheumatoid arthritis) during graduate school
  • 11:00 - Sammantha Dorazio: diagnosis led to career as Nurse Practitioner
  • 14:20-Paulina Burzynsk: how RA helped her take better care of your body 

Topic: Advocacy / learning to speak up

  • 24:30 -  Jed Finley example of how he learned how to advocate for himself in the context of medical appointments for his ankylosing spondylitis 
  • 30:00 -  Mimi Cross - how she learned that if something makes you uncomfortable you need to speak up even if that feels awkward

RA’s effect on work

  • 36:13 - Sarah Dillingham - how she became comfortable talking about RA at work
  • 42:30 - Effie Koliopoulos - how RA led her to her passion for writing 

RA’s and family

  • 46:20 - Ushma Sampat - how RA affects family relationships and life partnership / marriage
  • 54:50 - Jes Hosjan  How AS affects her experience as a mom and how she learned to advocate as a “spoonie mom!”

Humor and Mindset

  • 1:03:02 - Cristina Montoya - Humorous take on life with RA
  • 1:10:17 - Krista - Her experience chasing a past life to be the same “pre diagnosis” and how she learned to embrace the present
  • 1:17:44 - Cheryl Crow - My journey to acceptance of discomfort and uncertainty in life, how ACT (acceptance and commitment therapy) and my two therapists helped me!

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Links to speaker pages and websites:

This video is brought to you by the Rheumatoid Arthritis Roadmap, an intensive online education and support program Cheryl Crow created to empower people with tools to confidently manage their social, emotional and physical lives with rheumatoid arthritis.


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How to Survive the Holidays with a Chronic Illness: Interview with Lene Andersen16 Dec 202000:51:34

Photo credit for Lene’s photo: David Govoni. 

Speaker bios:

Lene (pronounced Lena) is an award-winning writer and rheumatoid arthritis advocate living in Toronto, Canada. Born and raised in Denmark, Lene has had autoimmune arthritis since childhood and has used a power wheelchair since her teens. She has a Masters Degree in Social Work and writes books about living well with RA and other types of chronic illness. Lene shares her home with a cat and too many books.  

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links to things discussed in this episode:

 

Here's the show breakdown:

·       01:50 – Lene shares her diagnosis story with Juvenile and Rheumatoid Arthritis

·       02:32 – Lene shares some tips for managing the holidays with a chronic illness. 

·       05:00 – How Lene learned to embrace “imperfect moments” that create the family legends to make the holidays special.

·       11:45 – Lene’s reflections about navigating the holiday season this year during COVID-19. 

·       20:55 – Lene shares her journey of creating her first book while battling major hurdles living with her Juvenile and Rheumatoid Arthritis.

·       26:45 – Anyone battling chronic illness with big aspirations just take it one step at a time – remember: thinking and planning counts as moving in the right direction. 

·       31:40 – Lene gives insight about using her power wheelchair at age sixteen empowered her to live life to the fullest.

·       36:25 – Lene discusses human right principles by understanding employment and accommodations for people with chronic illness.

·       42:40 – Lene’s advice for newly diagnosed patients. 


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How to get your Patient Voice Heard to Improve Healthcare03 Dec 202000:45:44

Jen dives deep into how and why she co-founded Savvy-Co-op, whose mission is to empower patients to co-create new solutions alongside health innovators. This includes a discussion of her PhD studies in human factors. 

Jen walks us through what it’s like for a patient to get their voice heard and provide feedback to healthcare companies and health innovators through Savvy, all while being monetarily compensated for their time. She also explains why it’s crucial for health innovators to seek diverse patient voices. 

Cheryl and Jen  discuss the importance of quality of life (QOL) measures as part of patient-reported outcomes (PROs).

The episode ends with a summary of Jen’s life experiences as a young person with juvenile idiopathic arthritis, and her advice for newly diagnosed patients today.

Speaker bios:

Jen Horonjeff was diagnosed with juvenile arthritis as an infant and now has a laundry list of other conditions and surprises (like a brain tumor). She is passionate about elevating and valuing the patient voice, and went on to become a health outcomes researcher, human factors engineer, FDA Consumer Representative, and, most importantly, a patient advocate. Jen earned a PhD in Environmental Medicine from NYU, and studies patient-centered outcomes at Columbia University Medical Center. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Episode links:

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

  • 1:00 - Jen’s experience getting a phD in Human Factors, accessibility, and patient centered outcomes while balancing her Juvenile Idiopathic Arthritis (JIA). 
  • 4:50 - How Jen formed Savvy Co-op: a patient owned, public benefit co-op that connects health innovators with patients to provide feedback, where patients are co-owners of the company and are often compensated for their time and expertise.
  • 8:00 - Why is it important for health organizations to not only get patient feedback, but also seek diverse patient voices.
  • 10:50 - Jen walks us through what it’s like for a patient to get their voice heard and provide feedback to healthcare companies and health innovators through Savvy, all while being monetarily compensated for their time. 
  • 15:20 - Why it’s important to follow up with the patient after they complete their “gig,” and let the patient know how their voice had an impact.
  • 17:00 - What does “patients are the expert in their care” mean, and what does  “patient centered care” mean?
  • 18:15 - An example of the patient voice changing health systems: patient feedback about the importance of fatigue led to it being incorporated as a “clinical trial outcome set,” or something that’s measured. 
  •  21:50: Jen’s experience serving on the FDA’s Arthritis Advisory Committee, and explanation of why quality of life (QOL) measures are so important. 
  • 25:15 - Chery’s quick plug for occupational therapy in helping patients achieve the best quality of life possible.
  • 26:15 - Are the current quality of life measures still relevant today, and are they sensitive enough to measure what’s truly important to patients?
  • 31:15 - Issues with patient reported outcomes are not specific to rheumatology, they are common across health conditions; Jen’s example: cystic fibrosis. 
  • 32:30 - Cheryl discusses the difference between basic “activities of daily living” (like dressing oneself) and “instrumental activities of daily living” (more time-consuming and cognitively challenging tasks like caring for children, preparing meals, managing finances). 
  • 33:30 - Jen’s personal journey with juvenile idiopathic arthritis (JIA): from gold shots in the 1980s and being told to avoid movement and exercise, to a dance major in college. 
  • 37:25 - Jen’s advice to parents of children with JIA 
  • 38:25 - Why Jen feels her disease DOES define her. 
  • 41:10 - Jen’s message for newly diagnosed patients: take time to reflect and grieve, acknowledge that this will suck sometimes, then try to step back and see that there are still probably ways to get to where you want to go. 
  • 43:00 - where you can follow Jen and Savvy (+ Jen’s cat as a bonus!).

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Creating a Better Future for Autoimmune Care With Rheumission’s Dr. Micah Yu & Bonnie Feldman21 May 202400:52:22

Cheryl, Dr. Yu and Dr. Feldman share their patient experiences and exploring problems with current healthcare systems. They then share how these problems led them to form creative patient programs and services. Cheryl shares the origin story for her Rheum to THRIVE program, and Dr. Yu and Dr. Feldman share how they created Rheumission,  a virtual first integrative Rheumatology and Lifestyle clinic for people living with autoimmune disease. 

Overall, our passion for reimagining autoimmune care shines through as we highlight gaps in current treatment paradigms, and outline visions for a more inclusive, holistic and effective healthcare model that is proactive versus reactive. 

The discussion concludes with an exploration of cutting-edge advancements in telemedicine and personalized medicine, and all speakers share their best advice for newly diagnosed patients. 

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

Episode at a Glance:
  • Importance of personalized care: we discuss the importance of personalized treatment plans tailored to individual needs, rather than one size fits all solutions.
  • Revolutionizing autoimmune care: we explore the potential positive impact of integrating biotech, digital health, and virtual-first approaches to enhance research, diagnostics, and treatment, with Rheumission as an example.
  • Multidisciplinary approach: we highlight the importance of team-based care in rheumatology and autoimmune care, where you can see not only a rheumatologist and rheumatology nurse but also get care from a multidisciplinary team (including registered dietitians, mental health therapists, physical and occupational therapists, etc).
  • Taking a holistic approach:  we explore the interconnectedness of physical and mental health, addressing lifestyle factors, stress management, and environmental influences.
  • Exploring Mental Health: The conversation highlights the well-documented correlation between autoimmune diseases and mental health issues like anxiety and depression.
  • Why is accessibility important: we discuss the problem of long waiting times for rheumatology appointments and possible solutions.
  • Advocacy for patient involvement: Dr. Bonnie emphasizes the importance of empowering patients to take charge of their health and actively participate in decision-making processes.
For full episode details:

Go to the episode page on the Arthritis Life website for full show notes plus a full transcript, video and more!

 


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Adapting is a Superpower: Stefanie’s Journey as a Mom with RA, Coach and Nurse Practitioner24 Nov 202000:49:58

Stefanie is the Rheumatoid Arthritis Coach. She’s a mother, teacher, volunteer, Family Nurse Practitioner, and also has rheumatoid arthritis. She was diagnosed about six years ago after the birth of her  first child. As a medical professional with over ten years of experience at that time, she was completely lost and felt like her world was shattered. The day she was diagnosed she cried for 10 minutes in the car, and then decided: “I’m not only going to take control of MY disease, but I want to help others to do the same!”

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by learning effective tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links:

Here's the show breakdown:

  • 1:00 - Introduction to Stephanie
  • 2:05 - How Stephanie’s background in medicine helped her figure out her Rheumatoid Arthritis diagnosis. 
  • 4:18- How Stephanie took control of her diagnosis and created the 1st arthritis support group in Las Vegas, Nevada through the Arthritis Foundation. 
  • 7:13 - Stephanie’s experience working in critical care (ICU - Intensive Care Unit) as a nurse at the time of her diagnosis and afterwards
  • 9:20 - Stephanie’s choice to leave the ICU setting due to her RA diagnosis
  • 10:17 - Stephanie’s advice to people with RA who are conflicted about whether to switch careers: don’t be afraid to change paths due to your condition, particularly if it helps you manage your stress better.
  • 13:25 - Cheryl & Stefanie discuss the importance of patient education.
  • 14:35 - Cheryl & Stefanie discuss how having RA changed how they practice as health providers: learning to listen better and be more present.
  • 18:50 - Stephanie’s most important tool to manage her RA on a daily basis: the ability to adapt (it’s a super power)!
  • 20:25 - Examples of how Stefanie adapts her daily routines to match her condition and abilities: pants with buttons versus pants without buttons, bar soap versus pump soap, types of cans, and more examples.
  • 24:30 - Cheryl’s examples of how occupational therapists help patients with arthritis adapt their daily routines to what works best for each individual. 
  • 28:09 - Stefanie’s family history of autoimmune diseases.
  • 29:30 - Stephanie’s first big RA flare after her first child was born and her experience with pregnancy and postpartum with her second child was born.
  • 30:35 - Stefanie’s difficulties with breastfeeding after her first pregnancy, versus her second pregnancy where she knew she couldn’t breastfeed due to medications.
  • 31:47 - Cheryl’s experience with chronic mastitis infections while breastfeeding and her views on infant feeding: fed is best! 
  • 34:15 - How Stefanie manages the demands of parenting with young kids: honest communication with your family, and some adaptations like a ramp for her children to get into their own bed.
  • 40:00 - Stefanie’s journey to creating her RA Coaching program
  • 42:30 - More details about Stephanie’s Rheumatoid Arthritis Coach program: diet, symptoms, and medications, individualized medical chart reviews for Rheumatoid Arthritis patients. 
  • 46:50 - Stefanie’s reflections on the importance of individualized care. 

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Staying Safe, Smart, Strong, Sweet and Silly with Spondylitis: Jason's Story11 Nov 202000:45:29

Jason Webb is a 42 year old father of 3 daughters who has lived with inflammatory arthritis for 38 years. He’s also an artist, chef-educator (27 years), stock trading coach, and mentor to other single fathers. 

Jason is a creative with a flair for wit and humor. He understands that  what works for him might not work for you, but he's there to help you through, so don’t be shy to reach out. He is currently working on a culinary education program and children's book series.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

  • Links to things discussed in the podcast episode:
    • Jason’s website: Chefscookies.ca
    • Jason’s Instagram:
    • Jason’s Facebook accounts:
    • Free Handout: Cheryl’s Master Checklist for Managing RA
    • Cheryl’s Facebook group: Arthritis Life Podcast, Practical Tips & Positive, Realistic Support
    • This episode is brought to you by the Rheumatoid Arthritis Roadmap, an intensive online education and support program Cheryl created to empower people with the tools to confidently manage their social, emotional and physical life with rheumatoid arthritis.
    • Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Here's the show breakdown:

  • 1:09- Jason’s diagnosis story (also known as a journey or saga): from juvenile idiopathic arthritis to ankylosing spondylitis.
  • 6:00 - How Jason copes with gray areas and identify his flare triggers.
  • 8:40 - How Jason manages his physical health at this time.
  • 11:18 - What helps Jason manage Ankylosing Spondylitis: staying “safe, smart, strong, sweet and silly,” plus adaptive aids, massage, knowing his flare cycles, knowing diet and food triggers and more.
  • 16:30  – Coping mechanisms for chronic illness and chronic pain 
  • 19:25 -  Cheryl once again brings up Acceptance and Commitment Therapy - ACT
  • 21:30 - How Jason’s challenging upbringing taught him how to be adaptable.
  • 23:45 - How Jason learned the importance of self-education.
  • 26:00 - Jason’s reflections on the positives and challenges of parenting with a chronic illness.
  • 29:30 - Jason’s past experiences as a chef & how he experienced cycles of stress, physical challenge and financial challenges as a single father.
  • 32:30 - Jason’s experience mentoring other single dads on Facebook
  • 32:30 - Jason reads his letter to single dads and others who are struggling.
  • 37:00 - Jason’s advice for newly diagnosed patients: educate yourself about the disease, listen to your body
  • 39:00 - Jason reflects on the connection between his emotional state and physical symptoms, how stress has caused flare-ups for him.
  • 42:00 - Jason & Cheryl’s parenting and stress-management advice

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From Disability to Dance: How Krista Rowan learned to Love Herself Moving28 Oct 202001:08:12

In January 2000, Krista was diagnosed with Rheumatoid Arthritis; a debilitating autoimmune disease affecting her joints, tissues, skin and organs.  Having experienced chronic pain, disability, stress, depression, isolation and hopelessness for years, she relates deeply to the fear and impact to all facets of life when health is deteriorated.

In 2015, Krista began addressing root cause drivers of her inflammation and disease, which not only dramatically improved her quality of life, but led her to become a speaker and certified coach. Today, Krista is on a reMISSION to inspire and empower others to improve their own health and quality of life.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links to things discussed in the podcast episode:

Episode Breakdown:

  • 01:00 - Krista’s introduction and diagnosis story at age 29
  • 05:15 - Krista’s initial fears about what  life with RA would be like
  • 7:00 - How Krista’s diagnosis affected her relationship with her fiance, wedding planning, family planning and all aspects of life
  • 9:20 - Living in “fear, shame, anger and doom” for the first fifteen years of her journey, without revealing her diagnosis at work or publicly
  • 10:52 - Isolating herself from fear of being perceived as weak 
  • 13:45 - Krista’s experience on prednisone, feeling “not broken”
  • 14:50 – Pregnancy challenges due to RA flare
  • 17:19 - Krista’s wedding - home made Keds
  • 19:14 - Krista hits “rock bottom” after 15 years and leaves her 20 year corporate career and decides not to apply for disability.
  •  21:05 - Krista encounters Teri Wahl’s diet and lifestyle journey with MS and the “Wahl’s Protocol”
  • 22:10 – Krista learns about “root cause medicine,” finds hope and goes back to school to become a “holistic nutritionist.” 
  • 26:25 - Krista learns to pay attention to her inflammation triggers (stress, foods, fragrances, sleep)
  • 29:33 - Krist and Cheryl reflect on the importance of hope and mindset
  • 31:23 - The importance of avoiding the “positive thinking” trap and how it’s good to validate your feelings. 
  • 32:35 - Learning to  mentally reframe what was actually happening in her life and address perceptions to stop her stress response.
  • 35:20 - How Cheryl & Krista both learned to curb the urge to be people-pleasers.
  • 36:00 – Krista and Cheryl discuss learning to set boundaries, say no & protect energy.  
  • 40:27– Krista joins TikTok in June 2020, makes “I can’t shuffle but I can Shakira” viral video showing belly dance style moves
  • 44:02 - Krista is surprised by the positive responses to her dance videos
  • 47:50 - Inspiring people to move however you can, “love yourself moving” 
  • 51:20 - Krista starts showing some of her physical limitations in her videos, and realizes that she doesn’t have to hide her RA anymore. 
  • 56:00 - Krista reflects on going from very private to public about her diagnosis
  • 58:20 - How Krista responds to unsolicited advice from people who don’t have a chronic illness
  • 1:00:10 – Krista’s words of wisdom for newly diagnosed patients.
  • 1:03:07 - Krista’s final thoughts: being 50 and being in the best place she’s been in 21 years, learning how to live in the moment even if it’s uncomfortable.

Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.


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How to Take Care of Your Hands: Interview with Corinne McLees, Occupational Therapist21 Oct 202000:58:40

Speaker bios:

Corinne McLees is passionate about helping individuals maximize the function of their upper extremities, as she believes the hands are imperative to doing the things we love most. She graduated from VCU's Master of Science in Occupational Therapy in 2016 and immediately began working in VCU Heath's hand therapy clinic. Corinne and her OT husband launched My Virtual OT - a 100% virtual occupational therapy practice - in order to safely serve clients amidst COVID-19. She has two small children and one on the way, and she and her husband have greatly enjoyed launching this business together.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. She helps others with rheumatoid arthritis determine how to live a full life *despite* arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare she say) FUN patient education and self-management resources. 

Medical disclaimer: All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode breakdown:

01:00 – Corinne’s explanation of what Occupational Therapy is

05:00 – Educating clients about hand therapy

07:00 – The brain interprets our hands as disproportionately important given their size; discussion of the homonculus 

10:00 – How pain affects daily activities

12:42 – Principles of joint protect while living with chronic hand pain

13:00 – How posture alignment awareness protects joints

19:25 – Overuse of exercises, fatigue, and flares 

25:05 – How to better understand human behavior to support behavior change

30:15- Corinne explains what happens during a virtual occupational therapy visit for patients with RA

33:00 – The importance of distinguishing between different tyes of pain

41:10 – How support groups can help keep you accountable 

45:15-  Additional OT treatments: heat and cold, splinting and joint protection


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How can Yoga Help People with Chronic Illness? Paulina's Story.14 Oct 202000:57:42

In this episode, Paulina shares her personal journey of how she discovered the benefits of yoga after her rheumatoid arthritis diagnosis. She explains how it can help people manage stress and feel a better sense of peace about themselves and their lives. 

Paulina also busts some of the top myths about yoga in this episode.

Paulina Burzynska has been a 𝑅ℎ𝑒𝑢𝑚𝑎𝑡𝑜𝑖𝑑 𝐴𝑟𝑡ℎ𝑟𝑖𝑡𝑖𝑠 𝑊𝑎𝑟𝑟𝑖𝑜𝑟 since the age of 18. She has lived with RA for five years, and as a teacher she is dedicated to providing safe, mindful classes for everyone helping them experience the benefits of yoga. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links Discussed in this episode:

 

Episode breakdown:

01:00 - How Paulina was introduced to Yoga while living with rheumatoid arthritis (RA)

05:00 – You don’t necessarily have to modify your yoga routine

07:00 – How yoga can work with your body’s central nervous system

12:24 – Practicing yoga involves breath work to help with stress and getting your mind and body into a healing state

15:00 – The mental aspect of yoga brings mindfulness

17:56 – Cheryl shares her experience taking Pauline yoga class

22:00- Yoga is not about the intensity but about the healing aspect 

26:16 – How people with RA can modify yoga to help work around painful areas

32:00 – Listen to your intuition about your body

35:00 – Top myths around yoga - “I’m Not flexible enough to do yoga”  

39:00 – You don’t need special equipment to practice yoga  

42:00 – Your muscle fibers through physical activity will get weaker or stronger

45:00 – Certain techniques in yoga can help how your body reacts to stressful situations

48:30 – Insecurities that might prevent people from from trying yoga

52:00 – How yoga can support you


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Five Things I Wish I had Known when I was Diagnosed with Rheumatoid Arthritis07 Oct 202000:34:39

Cheryl explains how rheumatoid arthritis affects more than just joints - it affects people’s whole bodies, and whole lives!

She also explores how she learned to tolerate gray areas rather than seeking black and white answers, and how mindfulness and acceptance helped her with the mental side of life with chronic illness.

This episode also includes a discussion about medical gaslighting, and how Cheryl learned to give herself permission to grieve her diagnosis.

It concludes with a discussion about how managing one’s rheumatoid arthritis is like a full time job. 

Episode breakdown:
  • 1:00 - #1 - Rheumatoid Arthritis affects more than just joints.
  • 5:00 - #2 - RA affects your social life in difficult ways (such as misconceptions) and positive ways (such as connections with a chronic illness community)
  • 9:30 - Tips for using websites and social in productive ways
  • 12:40: #3 - Gray areas are the norm for autoimmune disease
  • 16:09: #4 - Living with chronic illness will affect your mental health.
  • 17:49  Cheryl’s experience with allowing herself to grieve her health
  • 19:13 - Medical gaslighting.
  • 22:14 - #5 -  Managing RA is a job but you can learn how to do it!
Medical disclaimer:

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsor

Rheum to THRIVE, an empowerment program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. Learn more here

Speaker Bio:

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. 

She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links discussed in this episode:

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Race, Gender and Rheumatology with Dr. Maggie Cadet30 Sep 202000:59:25

This episode includes a deep dive into:

  • Why Dr. Cadet chose to specialize in Rheumatology
  • What unique issues rheumatology patiences of color face
  • Why racial representation is important for healthcare providers
  • Dr. Cadet’s advice for rheumatology patients for how to get the most out of appointments and build a trusting relationship with your provider

Speaker bios:

Dr. Magdalena “Maggie” Cadet is a well respected board certified clinical rheumatologist in New York City.  She is an Associate Attending at NYU Langone Medical Center.  She has been selected as a 2016,2017, 2018, 2019,2020 Castle Connolly Top Doctor and 2018,2019 Castle Connolly Exceptional Women in Medicine. Dr. Cadet’s interests have always focused on women’s health issues and issues relating to arthritis, autoimmune diseases, sports medicine, and motivating others to live a healthier lifestyle. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Episode links:

  • Dr. Cadet’s Instagram page where she educates patients and shares her journey.
  • Dr. Cadet’s Website
  • Free Handout: Cheryl’s Master Checklist for Managing RA
  • Cheryl’s Facebook group: Arthritis Life Podcast, Practical Tips & Positive, Realistic Support
  • This episode is brought to you by the Rheumatoid Arthritis Roadmap, an intensive online education and support program Cheryl created to empower people with the tools to confidently manage their social, emotional and physical life with rheumatoid arthritis.
  • Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

 

Episode breakdown

02:30  – How Dr. Cadet became a rheumatologist.

05:16 – The importance of being persistent as a doctor.

08:00 – How Dr. Maggie was able to break societal barriers.

012:45 -  Challenges women doctors of color face and how they advocate for themselves.

15:15 – Systemic racial disparities in healthcare among minorities.

19:30 – The importance of racial representation in healthcare for women of color and minorities.

24:00 - The importance of female doctor representation starting in childhood.

27:15– What Dr. Maggie wants rheumatology patients to know.

32:15- Doing your own research as a rheumatology patient is a job in itself. 

34:15 – The importance of being honest with your doctor about your symptoms.

37:15 - Other healthcare professions that help with the management of your disease.

39:20 – Advice for patients to get the most out of their appointments.

43:30 – Fatigue and pain approaches for autoimmune patients.

48:58 – Understanding that physicians are humans too.

54:45 – Additional advice and insights for rheumatology patients.


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Can diet and nutrition help people with arthritis? Separating myth from fact with three experts.23 Sep 202000:56:49

Cristina Montoya, Registered Dietitian and Kia Peters, Nutrition Student weave together their lived experience as rheumatoid arthritis (RA) patients and nutrition experts in this episode, alongside Jenifer Tharani, a Registered Dietitian Nutritionist who specializes in anti-inflammatory eating.

This episode covers:
  • What’s the difference between a “nutritionist” and a “Registered Dietitian” and why is it important?
  • Nutrition and diet “rabbit holes” that patients often fall down, and mistakes to avoid when seeking support for nutrition.
  • Top myths about diet and disease management, including:
    • Can nutrition choices cure the disease?
    • Are dairy, red meat and nighshades bad for everyone?
  • The psychology behind food choices and how food choices give people a sense of control
  • The importance of symptom tracking and food journaling
  • Kia, Cristina and Cheryl’s lived experiences of trying different approaches to food choices and diet at different stages of their disease management.
Medical disclaimer:

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsor

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

Speaker bios:

Cristina Montoya is a Colombian mama living in the land of maple syrup, beavers and hockey, Canada. She is a Registered Dietitian (RD), a member in good standing with the College of Dietitians of Ontario, Dietitians of Canada, and the Arthritis Health Professions Association (AHPA). As a patient advocate, Cristina participates in the Durham Region Sjögren's Syndrome Support Group from the Sjögren's Society of Canada as well as the Online Consumer Panel from the Arthritis Society.

She is passionate about autoimmune rheumatic diseases, medicinal cannabis science, digestive health, Mediterranean diet and anti-inflammatory way of eating, Hispanic heritage foods, home cooking, gluten-free baking, and living one day at a time. 

Jenifer Tharani, MS RD (Registered Dietitian)

Jenifer Tharani has completed master’s in human nutrition from Texas State University, San Marcos TX and training in dietetics from Emory University Hospital, Atlanta, GA. She is a member of College of Dietitians of Ontario and registered with the Commission of Dietetic Registration. 

She is multilingual and fluently speaks second languages like Hindi and has worked in different settings which has given her experience treating people of all ages with different conditions. Jenifer believes that eating healthy does not have to be boring, time consuming or expensive. She is extremely passionate about helping you adopt an anti-inflammatory eating pattern without restrictions. She doesn’t believe in diets, instead in making small sustainable lifestyle changes to help you find a balance in your everyday life, including trying to keep your favorite foods in the mix! Jenifer’s mantra is “Give a Man a Fish, and You Feed Him for a Day. Teach a Man to Fish, and You Feed Him for a Lifetime” and so she gives you a nutrition toolbox to help manage your health condition or live a healthy and good quality life, whatever your goal may be.

About Jenifer's Virtual Nutrition Coaching Services

In today's technologically driven world, Jenifer provides virtual nutrition coaching to help you take charge of your health from the comfort of your home. In her virtual nutrition practice, she focuses on helping clients adopt an anti-inflammatory eating pattern to help with weight loss, prevent and manage chronic illness like diabetes and autoimmune conditions like rheumatoid and osteoarthritis, fibromyalgia, lupus, psoriatic arthritis, and IBD. 

Kia Peters@livewellwithkia is a Nutrition Student who works with Jenifer, RD to educate other chronic illness warriors about anti-inflammatory nutrition without restriction..

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links to things discussed in the episode:

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How to Value Self-Love and Sexual Pleasure when Living with a Disability: an Occupational Therapist’s Approach16 Sep 202001:21:31

Dr. Sakshi Tickoo (she/her/hers) is a Mumbai-based Occupational Therapist, Personal Counselor and Student Mentor specializing in the fields of Sexuality; Mental Health - Wellness and Rehabilitation. She has served a diverse group of people through home healthcare, telehealth, and school-based settings. She is also the founder and owner of Sex, Love, And OT and The OT Shop.

Sex, Love, and OT is an inclusive and comprehensive platform educating and serving healthcare providers and clients who need tools and resources to advocate for sexual rights and liberation through education, centering pleasure, and freedom of occupational engagement in sexuality towards holistic wellness.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links discussed in this episode:

Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode breakdown:

  • 1:00 – Dr. Tickoo’s story: why she became an occupational therapist  
  • 3:25 – How Dr. Tickoo discovered the niche of sex and relationships 
  • 7:46 – How an occupational therapist can facilitate a client’s engagement in sex and relationships
  • 12:19- How to gain occupational therapy clinical knowledge of how to address sex outside of your textbooks 
  • 14:09 – The barriers for people with chronic illnesses face for sexual participation and intimacy 
  • 18:06 – Advice on how to feel sexy while living with chronic illness 
  • 22:26 -   Giving yourself permission to enjoy sex 
  • 26:15 – How sex is taboo in India and what Dr. Tickoo does to be sex positive
  • 33:45 – The difference between physical & emotional intimacy
  • 36:48 – Communication about intimacy with your partner and how to handle power dynamics 
  • 42:00 – The importance of knowing your partner’s love language 
  • 46:00– How adults have sensory regulation needs and how chronic pain affects sensory processing
  • 51:00 – When to mention that you have a chronic condition or disability when dating
  • 54:51- Tips & tricks for intimacy with your partner when you have arthritis: scheduling, connection, experimentation, positioning aids and more
  • 1:06:45 - The importance of client education about the basics of their condition
  • 1:08:45 - How to choose a good lubricant
  • 1:11:00 - Recommended toys
  • 1:13:00 - “Everything can be sexy [including aids] as long as you think it’s sexy.”
  • 1:13:55 - What is pleasure mapping and how can it help?
  • 1:17:00   - Concluding thoughts

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Relationships, Intimacy and Sex with Arthritis09 Sep 202001:13:28

Navigating intimate relationships while managing a chronic illness can be tricky - how and when do you disclose your disability?  How do you experiment with sexual positions without “ruining the mood?” Is it possible to communicate with your partner in a way that’s respectful and empowering?

In this episode, five panelists share their best advice for *all* aspects of romantic and intimate relationships, including: 

  • Communication tips for all stages of relationships, from first dates to marriage
  • How to workaround fatigue that makes it hard to get “in the mood”
  • Positions that work for wrist or hip pain
  • Lubes that work for dryness
  • Workarounds for jaw pain during oral sex
  • How do disabilities or health conditions contribute to power dynamics in relationships
  • The importance of emotional connections
  • The importance of self-love and respect
  • Why STD prevention and protection are particularly important for people on immunosuppressive medications
  • Panelists’ best advice for newly diagnosed patients who might be worried about how their condition will affect their sex life and relationships

*Trigger warning - in minutes 30-40 there are descriptions of pressuring and coercion into sex without protection

**This episode discusses adult topics (sex) and includes explicit language.

Minute by Minute breakdown:

Episode breakdown:

  • 02:00 - Introduction to panelists: Chloe, Jo, Ali, Paulina & Cheryl.
  • 3:20 - (Chloe) How juvenile arthritis affected her relationships 
  • 07:55 – (Jo) How Jo learned the importance of communication
  • 11:42 – (Ali) Learning to experiment with positions and work around fatigue
  • 16:20 - (Paulina) The importance of communication & emotional connection
  • 23:00 - (Cheryl) Reflection on power dynamics in relationships.
  • 24:25 – (Chloe) Strong emotional connections affect vaginal lubrication.
  • 25:22 – (Chloe) How jaw pain affects oral sex & workarounds, + how fatigue affects sex.
  • 33:00 – (Cheryl) The importance of STD testing for partners due to immunosuppression from meds. Experiences feeling pressured in relationships.
  • 36:00 – (Chloe) Experiences feeling pressured in relationships. 
  • 37:45 – (Jo) Tips for positions and lubricants.
  • 39:00– (Ali) Being cautious when dating, how to work around fatigue, tips for positions and communication. 
  • 43:14 - (Paulina) Your partner is not a mind reader. Tips for lubricants for sensitive skin & positions.
  • 51:00– (Ali) Best adult toys to use for arthritis.
  • 53:00- (Chloe) Communication & practicing positions 
  • 55:00 – (Cheryl) How sex is an “Activity of daily living” according to occupational therapy. Reflection on sex education now versus in the early 1990s.
  • 58:30 – (Paulina) Tips to increase sex drive and address your own pleasure.
  • 1:01:00 – (Chloe) Advice for anyone recently diagnosed.
  • 1:04:00 (Jo) – Final thoughts and advice, disclosing when you are dating online
  • 1:06:00 (Ali) – Final thoughts
  • 1:07:00 (Paulina) – Final thoughts and advice

LINKS discussed in the episode

*For full speaker bios, see www.myarthritislife.net


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What’s it like to run Half Marathons with Autoimmune Disease?13 May 202401:20:17

After facing skepticism from some medical professionals who doubted her ability to run, Gretchen defied expectations and has completed over 100 half marathons, all while raising money and awareness for autoimmune causes. 

She and Cheryl also discuss the importance of self compassion in their journeys with chronic autoimmune disease. Gretchen shares why she resonates with progress over perfection and encourages others to be gentle with themselves while navigating life with autoimmune diseases. 

Gretchen shares how she found creative ways to raise awareness about autoimmune diseases, such as running two half-marathons on two coasts in two days to raise funds for autoimmune research at the Benaroya Research Institute. Through her experiences, Gretchen emphasizes the importance of perseverance, self-advocacy, and building a supportive community.  By sharing her story and promoting resilience, Gretchen aims to inspire hope and empower individuals to find purpose and joy in their own health journeys. 

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

For full episode details including a transcript and video:

Go to the episode page on the Arthritis Life Website 


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How to Exercise with Rheumatoid Arthritis: Randi's Story02 Sep 202000:56:00

Randi and Cheryl dive deep into Randi’s diagnosis journey, her career as a track and field athlete at the University of Alabama, her best advice for newly diagnosed patients, her tips for exercise with RA, and even some dating and relationship advice. 

Randi was diagnosed with Rheumatoid Arthritis at the age of 16 after 6 years of trying to find an answer. Randi says: “My journey with RA has not always been easy, but it has been rewarding. I have had to learn what works best for me in controlling my RA because of course not everyone’s RA is the same. I manage my RA with exercise, a moderation diet, a medication, chiropractic care, and plenty of rest. Oddly, I am thankful to have been diagnosed with RA at 16 because I have become the best version of myself as a result of it.”

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to live a full life despite arthritis, by developing tools to navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare she say) FUN patient education and self-management resources. 

Links to things discussed in the podcast episode:

Here's the show breakdown:

  • 01:00 – Randi’s diagnosis story
  • 4:35 – What it was like to be a college athlete with RA, doing the triple jump in track and field.
  • 8:20 – Randi’s sports injury misdiagnosis.
  • 10:20 – Why Randi pursued her personal trainer certification.
  • 12:54 – Why Randi pursued Chiropractic medicine as her career.
  • 18:00 – Randi’s tips for how to exercise with RA: resistance training, muscle building, cardio and more. 
  • 23:10 – How Randi and Cheryl make cardiovascular exercise fun!
  • 28:45 -   Randi’s advice for newly diagnosed patients with RA (hint: there are many sports metaphors in this advice!). 
  • 32:45 – Discussion about combining “natural” approaches for RA versus Western medicine, and how to find common ground and balance.
  • 35:00 - Randi’s tips on how to build a good relationship with your provider.
  • 39:38 – How healthcare quality can differ for people of color. 
  • 45:46 – How Randi and Cheryl learned not to underreport pain to their providers.
  • 48:00 – Randi’s experience dating with RA and love story with her fiance.
  • 55:15 - Bonus content: Cheryl’s favorite dance routine she learned in the 1990s from MTV videos

Medical disclaimer: All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.


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How to Advocate as a Patient25 Aug 202000:39:26

Effie shares many anecdotes and nuggets of wisdom about how she’s learned to advocate for herself over fifteen years of living with rheumatoid arthritis. She also shares examples of finding a good fit with a provider, and how to get involved in legislative advocacy on a national scale.

Effie Koliopoulos is a freelance writer and rheumatoid arthritis patient advocate. She created her blog Rising Above Rheumatoid Arthritis in 2016, after being inspired to share her story more publicly and connect with others after undergoing a total knee replacement. Currently residing in Chicago, she is working on her debut children’s picture book, enjoys creating video content for her YouTube channel and other projects.

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others develop tools to navigate physical, emotional and social challenges so that they can live a full life *despite* arthritis. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources. 

Links discussed in this episode:

Detailed breakdown of show:

  • 01:30 – Effie’s Diagnosis Story.
  • 03:30 – Effie’s advice for students with rheumatoid arthritis.
  • 06:06 – Examples of when Effie has had to advocate for herself and be actively involved in her care during medical appointments.
  • 08:40 – Examples of Effie advocating for her needs when prescription errors occurred. 
  • 13:15 - Effie’s experiences with getting second opinions and finding a good fit with a doctor.
  • 15:30 - General advice for patients to learn to advocate for themselves with medical professionals.
  • 17:14 - How Effie & Cheryl learned not to downplay symptoms, and how they confront fears around changing medications.
  • 21:00 – Effie’s advice for formal legislative advocacy at your state or national capitol, and why personal stories are so important.
  • 27:21 – How Effie has advocated for invisible illnesses, and Effie’s experience being accused of “faking” her disability (including someone calling the cops on her for using the disability placard).
  • 31:00 – What Effie wishes healthcare providers knew or did better.
  • 35:00 - The impotence of getting medical guidance from the doctor rather than the internet sometimes.
  • 36:05 – What Effie wishes the general public knew about rheumatoid arthritis.
  • 38:00 - Effie’s final words to anyone newly diagnosed: take advantage of the community.

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How can Applied Behavior Analysis and Mindfulness help People with Chronic Illness? Kristen’s Story.19 Aug 202000:57:31

Kristen delves deep into the science behind behavior analysis and shares how she has used data to help her track her symptoms such as brain fog and fatigue. She also shares how mindfulness and acceptance based therapies can help people living with chronic illnesses achieve a better quality of life.

Kristen also helps other chronic illness warriors apply the principles of behavior analysis to their unique health and lifestyle management goals through 1:1 behavioral coaching. In addition to being a chronic illness warrior, Kristen is also pursuing a PhD in Cognitive and Behavioral Sciences, she is married to her high school sweetheart, and loves hiking and being outdoors with her partner and three dogs. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. Her life passion is helping others with rheumatoid arthritis figure out how to successfully navigate physical, emotional and social challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare I say) FUN patient education and self-management resources.

Links discussed in this episode:

Time breakdown: 

  • 01:30 – Introduction
  • 03:00 – Kristen’s diagnosis story for Sjogren’s and RA
  • 5:00 - What is Applied Behavior Analysis (ABA) and who are Board Certified Behavior Analysts (BCBAs)? 
  • 6:30 - Explanation of how ABA can be applied across diagnoses
  •  8:45 – Explaining controversy around ABA for neurodiverse populations
  • 12:20  – Examples as Kristen utilizes Behavior Analysis as a patient to track symptoms: CBD tincture for fatigue and brain fog
  • 15:20 - How tracking data can be a powerful tool to combat overwhelm
  • 19:17 - Importance of rest and learning how to rest without guilt
  • 21:40 - How thoughts, behaviors and the environment influence each other 
  • 25:20 - How Kristen balances being a PhD student with her mental health 
  • 27:45: Kristen’s advice for setting boundaries and learn how to say no
  • 29:00 - Cheryl’s experiences having difficulty saying “no” to things when her health is going well and Kristen’s 80% rule
  • 31:20 - Kristen’s experience with going to therapy and how she manages her stress through mindfulness and ACT 
  • 36:00 - What does Kristen’s mindfulness practice look like on an average day
  • 39:00 - How Cheryl & Kristen cope with uncertainty and find acceptance with their conditions. 
  • 43:10 - Behavior Analysis Coaching with Chronic Illness: how does it work?
  • 46:00 - Balancing act between accepting present and tracking data for future
  • 48:00 - Life Coaching vs Certified Health Coaching versus Board Certified Behavior Analysis
  • 51:00 - Final thoughts

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What does a mind body approach to rheumatoid arthritis look like? Vanessa’s Story11 Aug 202001:03:34

Vanessa Cameron and Cheryl Crow delve deep into Vanessa's rheumatoid arthritis journey, which includes significant work she's done on examining the mind-body connection and finding balance in her life through daily mindfulness, EFT and other practices.

Cameron discovered her passion for hacking her mind and body amid a debilitating bout with Rheumatoid Arthritis. After learning about the emerging science of Self-Compassion and the benefits of meditation, EFT (tapping) and NLP (neuro-linguistic programming) she began incorporating daily science-backed practices that boosted her health and happiness. Her passion led her to start and earn master level practitioner certification to teach EFT and NLP. 

Cheryl Crow is an occupational therapist who has lived with rheumatoid arthritis for seventeen years. She is passionately dedicated to helping others with rheumatoid arthritis figure out how to successfully navigate daily challenges so they can live a life they love despite health challenges. She formed the educational company Arthritis Life in 2019 after seeing a huge need for more engaging, accessible, and (dare she say) FUN patient education and self-management resources. 

This interview was conducted in December 2019.

Get More Support at:

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected**.** See all the details and join the program or waitlist now!

MEDICAL DISCLAIMER:

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Links discussed in this episode:Detailed episode breakdown:
  • 3:00 Beginning signs of RA
  • 4:30 - Massive flare up, feeling “stuck” in life overall
  • 7:10 - Vanessa experiments with dietary changes and finds a diet that helps her inflammation
  • 11:00 - Massive flare up leads to confusion.
  • 15:00 - How she found a good fit with her doctor
  • 19:00 - How a trusting relationship with Dr. Mir helped Vanessa accept western medications.
  • 21:33 - Vanessa’s low point after contacting the flu.
  • 22:00 - Recognizing she needs to address emotional scars from her past.
  • 26:30- How Vanessa used Emotional Freedom Technique (EFT) - Tapping + Journaling to work through her emotional scars (such as being told she’s “too emotional”), and learning to take an energy inventory
  • 31:30 - How a daily self-compassion meditation course helped.
  • 33:10 - Summary of the lifestyle changes she made to manage her wellness on a daily basis
  • 38:14 - How RA struggle now seems like a blessing in disguise
  • 39:20 - How joining a Buddhist community sparked resilience.
  • 42:19 - Vanessa’s advice to newly diagnosed patients
  • 44:17 - How RA affected her experiences in the workplace, how she learned to advocate
  • 44:40 - How she explains RA to people who don’t know anything about it
  • 46:00 - How both Cheryl & Vanessa learned to say no!
  • 49:50 - Lifestyle changes, including saying no and managing energy
  • 51:00- Vanessa worked with an autoimmune health coach.
  • 52:20 - Learning to see Pain as a messenger
  • 53:07 - How EFT helped Vanessa get to the root of her emotions
  • 54:30 - Cheryl talks about how ACT helped her manage difficult emotions.
  • 56:00 - Discussion of Tara Brach’s “RAIN of self-compassion”
  • 59:50   - Concluding thoughts about how Cheryl & Vanessa came to terms with being comfortable sharing their RA and emotional stories.

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Can you Live a Full Life with Pain?04 Aug 202001:35:42

Cheryl & Bronnie are both occupational therapists who live with chronically painful conditions. In this episode, Bronnie shares her unique perspective on how one pursue a full life *despite* pain, rather than seeking solely to eliminate pain. This episode is a must listen for both patients and practitioners.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Get More Support: 

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now!

Speaker Bios:

Dr. Bronnie Lennox Thompson is a pain specialist, clinical instructor, and occupational therapist who lives with chronic pain from fibromyalgia.  She has a passion to help people experiencing chronic health problems achieve their potential. She has worked for 20 years in the field of chronic pain management, helping people develop “self management” skills. Bronnie completed her Masters in Psychology in 1999, and recently earned her Doctorate in Psychology in the mid 2010s. 

Cheryl Crow has lived with rheumatoid arthritis for seventeen years and has been an occupational therapist for seven. After originally working in pediatrics, Cheryl formed the online education and empowerment company Arthritis Life to fill a need for accessible, engaging patient education and self-management resources. 

This interview was conducted on May 17, 2020.

For full episode links plus a transcript:

Go to the show page on the Arthritis Life Website here.


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Best Advice for Newly Diagnosed Patients with Rheumatoid Arthritis28 Jul 202000:43:30

This episode including tips for to cope with the initial diagnosis, how to best educate yourself about your condition, ways to utilize social support without getting overwhelmed,  how to best collaborate with your provider and make treatment decisions, and finally how to take care of your mind and manage stress. 

Episode breakdown:
  • 1:10 - Episode Introduction
  • 2:08 - Analogy for those newly diagnosed - a tourist in an unplanned for land
  • 4:08 - Advice for the initial adjustment period
  • 6:30 - Tips for educating yourself about your condition
  • 10:00 - How to best utilize social support, including social media
  • 18:15 - How to best interact with your providers and medical team.
  • 20:15 - How to choose the best treatment ideas for you
  • 31:44 - Tips for managing stress and taking care of your mind
  • 40:00 - Concluding thoughts
Medical disclaimer:

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsor

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

Links discussed in this episode:Thank you so much to those who contributed their words of wisdom!

From Instagram: @hopeamidthepain, @Rheumatoiddiaries, @TheNarcissistGames, @Sje70, @deepa.venkatraman, @drmaggiecadet, @A.shrummer, @Jbayze2018, @worldofot, @boop911, @Kimesue, @Mommywithmctd, @ra.and.me , @Paulaburza, @_chronically_happy_, @warriorsmovemountains, @graceandable_official 

From Facebook: Monica Thomas, Laura Muller, Christopher Vance.


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Pregnancy, Parenting and More with Rheumatoid Arthritis21 Jul 202000:47:57
Episode at a Glance:

The following is a breakdown of the main topics we discussed - scroll to the end to see hyperlinks for resources mentioned in this episode! As a reminder: this episode was originally recorded in 2019.

  • 01:35 - Claire diagnosis journey for rheumatoid arthritis: difficulty being believed by providers through her official diagnosis and her journey towards accepting it
  • 10:30 Claire’s pregnancy and childbirth experience
  • 14:20 - Claires postpartum experience with RA coming back slowly
  • 16:20 - How Claire parents a Toddler with Rheumatoid Arthritis
  • 18:15 Claire’s advice for people with RA who might want to have a child
  • 20:20 - How to Manage Stress and Anxiety with chronic illness, including tips for finding a good fit with a provider (
  • 26:40: Claire’s advice for newly diagnosed patients
  • 30:10: What Claire wishes doctors did better
  • 31:26: Claire’s tips for a good patient-provider relationship and tips for advocating for yourself
  • 35:36: The Difference between living with an invisible illness and living with a visible one when Claire had to wear a splint!
  • 38:55: How RA affected Claire’s choice of work, and her employment
  • 41:42: How RA affected Claire’s relationship with her husband
  • 44:00 - Fatigue and RA
  • 45:44 – How RA affects friendships and relationships in adulthood
Get More Support at:

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected**.** See all the details and join the program or waitlist now!

External resources mentioned in this episode or relevant to it:MEDICAL DISCLAIMER:

All content found on the Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.


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Episode 2: Rheumatology Basics with Dr. Balderia14 Jul 202000:17:51
Episode at a Glance

Cheryl (rheumatoid arthritis patient and occupational therapist) and rheumatologist Dr. Percy Balderia discuss:

  • 1:00-2:00: -  What is Rheumatology?
  • 2:00 -  Why did Dr. Balderia choose to become a Rheumatologist?
  • 04:50- Day in the life of a Rheumatologist
  • 06:45 - How to build a good relationship with your provider & prepare for appointments
  • 11:16- What should patients know about Rheumatology?
  • 13:07- Meeting the mental health needs of people with chronic illnesses
  • 14:02- How to pick the best treatment plan & utilize supports available to you!

This interview was originally conducted in April 2019.

Episode is brought to you by:

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

Additional links relevant to this episode:

Dr. Percy Balderia is a rheumatologist who sees patients at The Polyclinic Madison Center and The Polyclinic Downtown in Seattle, Washington. He has a special interest in rheumatoid arthritis. He trained at the University of Washington and was awarded The Arthritis Foundation fellowship.

Thank you to our podcast interns, Sarieni & Laura from The Modern OTs podcast, for your help in editing this episode!

MEDICAL DISCLAIMER:

All content found on the Arthritis Life Youtube Channel was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have heard on this podcast. Please seek the advice of a physician or other appropriate healthcare provider before putting information from this channel to use. Links to educational content not created by Cheryl Crow of Arthritis Life are taken at your own risk. Reliance on any information provided by Arthritis Life is solely at your own risk.


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Episode 1: Sarah Dillingham07 Jul 202001:19:45
Episode at a Glance

She and Cheryl discuss their best advice for newly diagnosed patients, explore how fatigue can be more debilitating than pain, highlight the importance of mental health treatment for chronic conditions, and dig into the impact of rheumatoid disease on everyday life. 

Sarah's experience designing her own custom wedding day splint (due to not wanting to wear the typical ugly splints available in the current market) led her to form a start-up called Grace and Able, where she's developing more comfortable and aesthetically pleasing wrist braces. She also runs the Women with Rheumatoid Disease Facebook community. 

Here's the show breakdown:
  • 01:25 - Sarah's diagnosis story and brief medical history
  • 08:30 - Highlights and lowlights from Sarah's experience with medical providers
  • 23:34 - Sarah's advice for newly diagnosed patients (includes a discussion on social media)
  • 38:00 - How rheumatoid disease has affected Sarah's experiences at work
  • 42:27 - The effects rheumatoid disease has had on Sarah's friendships and romantic relationships
  • 47:11 - The origin of Sarah's custom wedding day splint, which led her to form Grace & Able.
  • 51:00 - How chronic illness has affected Sarah and Cheryl's mental health.
  • 59:54 - Why fatigue is the hardest part of coping with RA (even more so than pain).
  • 1:07:20 - What to do when there are no more treatment options - how to have this discussion with your doctor and care team.
  • 1:11:41 - Sarah's frustrations with day to day living, and how she's learned much of what she's needed to cope with pain and daily living challenges from other patients and not health professionals.
  • 1:18:00 - The three MOST important parts of Sarah's current management of her condition.
Additional links relevant to this episode:Get more support at:

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected**.** See all the details and join the program or waitlist now!

MEDICAL DISCLAIMER:

All content found on this podcast was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or heard on this channel.


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Welcome to the Arthritis Life Podcast!21 Jun 202000:12:06

This episode is brought to you by Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

Learn more at: 


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How Mindfulness Helped Paulina Reconnect with Her Body and Thrive with RA02 May 202400:59:45

 On episode 125, Paulina Buryzynska shares how self-compassion and mindfulness help her thrive with rheumatoid arthritis. She also highlights the importance of reconnecting with her body after experiencing a period of dissociation as a coping mechanism for pain.  

Cheryl and Paulina discuss the power of non-judgmental awareness and loving curiosity in navigating emotions and thoughts, as well as acceptance. They also emphasize seeking support while navigating the challenges of chronic illness.  

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

For full episode details plus a full transcript and video:

See the episode page on the Arthritis Life website


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What do People with Rheumatoid Arthritis Need to Know about COVID-19 in 2024?22 Apr 202400:53:24

Dr Dave & Dr Campbell answer Cheryl’s burning questions about long COVID, vaccine efficacy and safety for people with autoimmune conditions, and potential links between autoimmunity and long COVID. They also talk about cutting edge research and new therapies including CAR T-cell therapy.

Dr. Campbell encourages participation in research studies to better understand these complex issues. Dr. Dave emphasizes the need for precision medicine approaches in treating autoimmune diseases like RA, where individualized treatment plans can be tailored to each patient's unique needs. Despite the challenges posed by autoimmune diseases and COVID-19, they express optimism about the future of treatment options and the ongoing medical advancements.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

For full episode details including a transcript & video

Go to the episode post on the Arthritis Life Website (page coming soon)! 


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“Disability is not a Dirty Word:” Catherine’s Story of Fierce Hope & Young Patient Advocacy11 Apr 202401:06:39

Through sharing her own story publicly, Catherine learned the importance of disability representation and advocacy for young people. She also delves into why it is crucial to include the voices of young adults in the research and advocacy process. 

Cheryl and Catherine explore the process of dismantling their own internalized ableism and challenging societal norms around what constitutes a "normal" life. They also challenge the idea that disability is necessarily a “bad” word.  They emphasize the importance of self-care and finding joy in everyday activities, even if they require accommodation. For Catherine, participating in activities like surfing, albeit in an accommodated manner, brings fulfillment and contributes to her definition of living a good life with chronic illness. Throughout the conversation, Cheryl and Catherine underscore the values of self-advocacy, self-acceptance, and finding happiness on one's own terms.

Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

For full episode details

For full episode details including hyperlinks to things discussed on this episode, go to the episode page on the Arthritis Life website. 


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Overcoming Denial, Confronting Food Phobia, and Embracing Online Communities: Ray’s AS and OA Story28 Mar 202401:01:51

Trigger warning: orthorexia / eating disorders; fear of foods

In Episode 122, Ray shares the shock and emotional turmoil he experienced upon receiving his diagnoses of rheumatoid arthritis (RA), ankylosing spondylitis (AS), and osteoarthritis (OA). He described the initial denial he felt and the process of coming to terms with his diagnoses, acknowledging the emotional toll it took on him and his family. 

Cheryl and Ray discuss coping strategies, the role of social media, and finding a supportive community online. He also explains the importance of advocating for oneself and seeking out reliable information and resources, taking a proactive approach to managing his conditions, and finding the right balance between pushing through pain and listening to his body's needs.

Episode at a glance:
  • Diagnosis Story: Ray describes his diagnoses and experience living with rheumatoid arthritis (RA), ankylosing spondylitis (AS), and osteoarthritis (OA).
  • Navigating Multiple Conditions: Ray explains the complexities of living with multiple chronic illnesses, including challenges related to symptom management, accessing healthcare, and adjusting to lifestyle changes.
  • Social Support and Connection: Cheryl and Ray discuss the significance of social support networks, in providing connection and understanding for individuals living with rheumatic diseases.
  • Self-Advocacy and Empowerment: Ray emphasizes the importance of self-advocacy and seeking out reliable information and resources to empower oneself in managing chronic illnesses
  • Acceptance and Resilience: Ray shares insights into his journey from feelings of denial to acceptance and living a fulfilling life despite health challenges.
Medical disclaimer: 

All content found on Arthritis Life public channels was created for generalized informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment.

Episode Sponsors

Rheum to THRIVE, an online course and support program Cheryl created to help people with rheumatic disease go from overwhelmed, confused and alone to confident, supported and connected. See all the details and join the program or waitlist now! 

For full episode details including a transcript & video:

Go to the episode page (coming soon) on the Arthritis Life website. 


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