In this first episode of Inflammatory!, brought to you by Inflammatory Arthritis UK, Debbie and Katy look at what is inflammatory arthritis (IA), their motivation behind creating a new patient led charity (Inflammatory Arthritis UK), and their personal diagnoses. 

They explore in more detail their type of inflammatory arthritis; Debbie shares her diagnosis of juvenile idiopathic arthritis and Katy shares being diagnosed with rheumatoid arthritis in her late twenties. They cover their symptoms including the underestimated and misunderstood fatigue that is associated with IA. 

And they speak openly about how their lives have been impacted by inflammatory arthritis, joint health and coping with the ups and downs of living with a chronic fluctuating disease. They also have a light-hearted debate about persuading Katy, who is energetic like a puppy, to get a puppy! 

If you enjoy this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to www.inflammatoryarthritis.org

A Boutique Broadcast production for Inflammatory Arthritis UK

Hosted on Acast. See acast.com/privacy for more information.

In this second episode of Inflammatory! brought to you by Inflammatory Arthritis UK, Debbie and Katy cover the day they were diagnosed and the impact it had on them and their family. It also covers the day Debbie will never forget, the day her eldest daughter was diagnosed with juvenile idiopathic arthritis, the same type of inflammatory arthritis she has.  

They explore in more detail the actual day they were diagnosed, how Katy ended up at the wrong hospital, the symptoms they had and how they felt when they heard the diagnosis. 

They speak openly about the emotional side of diagnosis, how it knocks your confidence and the impact their diagnosis had on their families. Katy’s mum felt guilty due to IA being evident in her side of the family and Debbie shares how her eldest daughter’s diagnosis impacted her youngest daughter. 

They also cover how and why Debbie was piggy backed round France on a school trip by a teacher with most teachers not believing her diagnosis. Whether Katy and Debbie talked about their diagnosis or kept it a secret, how having a supportive employer is vital and they share how they learnt how to cope with it, adapt and not let it take over their life. 

If you enjoy this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

A Boutique Broadcast production for Inflammatory Arthritis UK

Hosted on Acast. See acast.com/privacy for more information.

In this latest episode of Inflammatory! brought to you by Inflammatory Arthritis UK, Debbie and Katy cover the immediate effect their IA diagnosis had on them, their families, the number of hospital appointments, effects of medications and their emotional reaction. 

They explore in more detail the impact on Katy’s work life, having to plan work around the number of appointments. Having conversations with her boyfriend and doctors about whether they wanted children in the future, something they had not even discussed in private. The impact on schooling with Debbie’s diagnosis and that Debbie didn’t realise at the time, how badly her teachers treated her mum and more recently cover an incident at Debbie’s daughter school. 

They discuss openly how Katy took years to process the emotional side of the diagnosis, but her immediate reaction was to sign up to the London Marathon and a dancer at the Olympics games.  Debbie shares the impact her daughter’s diagnosis had on her husband and her youngest child. But even though history was repeating itself as both Debbie and her daughter had to give up gymnastics after their diagnosis, they both found new passions in life. Covered also in Debbie’s blog 

https://inflammatoryarthritis.org/blogs/

Next week’s episode is our first Q&A session, where you can submit questions or leave us a voice note, through our website https://inflammatoryarthritis.org/podcast-2/ They can be IA related or just wanting to get to know us better. 

Also sign up to our newsletter so you are the first to know about upcoming episodes, research opportunities, any events and IA news. 

https://inflammatoryarthritis.org/

If you enjoy this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

A Boutique Broadcast production

Hosted on Acast. See acast.com/privacy for more information.

In this week’s episode, brought to you by Inflammatory Arthritis UK, Debbie and Katy handed the episode over to you, as it is the first Inflammatory! question and answer session. 

Firstly, they cover the impact hormones has on their inflammatory arthritis, whether they flare during their period and what research is that out there or to come.  

They answer questions in more detail on the mental health of side inflammatory arthritis, how they both try to cope and how they differentiate the emotional side of IA to normal day to day living. Cover what JIA is more detail, and how it can be diagnosis for life. 

They discuss openly whether they have tried alternative medicines, to answer a question that came through as a voice note via the website. Does it make a difference, and the importance of taking medication as it can lead to further joint damage, and for scleritis can lead to blindness. 

They also cover what they do to relax, how Katy is not good at it, what Debbie’s go to TV show is and answer whether they would prefer a bellybutton for a nose or a nose for a bellybutton! 

Also sign up to our newsletter so you are the first to know about upcoming episodes, research opportunities, any events and IA news. 

https://inflammatoryarthritis.org/

If you enjoy this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, it really does help us, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

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Welcome to #fuckitland (you’ll need to listen to the episode to have any idea what we mean by this!).

Debbie and Katy come out of their comfort zones and dive into an often-overlooked topic: relationships and sex while living with inflammatory arthritis and sex. 

They take a deep dive to explore the challenges of relationships and intimacy for those living with inflammatory arthritis. Discuss the physical limitations that affect sex, such as pain, stiffness, fatigue, and medication side effects, and emphasise the importance of open communication and setting boundaries with partners. 

They also highlight the emotional impact of the condition, including self-confidence struggles and fears of being a burden. Debbie shares her experiences navigating relationships with arthritis, while also reflecting on how societal attitudes have changed over time. 

They also speak openly about their experiences with the condition and emphasize that those affected are not alone. Katy shares her recent hand therapy session, where she learned about pain management and the importance of mobility, strength, and control. Debbie, on the other hand, talks about a difficult weekend due to an arthritis flare-up that even disrupted her plans with her husband. She also discusses the challenges of parenting, especially during her children's stressful exam period, and her new role as a trustee for an art therapy charity.

The key takeaway is that people with inflammatory arthritis can still have fulfilling relationships and sex lives by embracing self-confidence, being clear about their needs, and surrounding themselves with supportive partners.

Resources & Links:

• Visit inflammatoryarthritis.org for more information and resources.
• Follow us on Instagram, Facebook, Blue Sky, and LinkedIn for updates and community support.

If you enjoyed this episode, please leave a review and subscribe to our newsletter to stay updated on upcoming episodes and research opportunities.

🎧 Listen now and let’s keep the conversation going!

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Trigger warning - this episode contains discussions about suicidal thoughts

In this episode, Debbie and Katy open up about the often-overlooked mental health challenges of living with inflammatory arthritis. 

Firstly, Katy shares that she is in a better mood, helped by her netball team's rare win and the pain in her wrist didn’t turn into an IA flare. Along with the excitement of her son losing his first tooth and the going rate of Tooth Fairies. 

They go on to share their personal experiences with anxiety, depression, and the emotional toll of chronic illness. From the overwhelming fear of their futures made worse by internet searches after diagnosis to the daily struggles of managing pain. They discuss coping strategies, especially in the dark moments including suicidal thoughts, and emphasise small daily victories. 

They also explore the importance of acknowledging mental health alongside physical health, and the role of support systems including loved ones and pets, and strength through connection with others facing similar struggles in finding hope. 

The conversation highlights the need for better mental health resources, reassuring listeners that they are not alone and it is ok to talk about mental health and to seek help.

Key Topics Covered:

• How inflammatory arthritis affects mental health
• Anxiety, depression, and the fear of the unknown after diagnosis
• Personal experiences with dark moments and the struggle to stay positive

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In this episode, hosts Debbie and Katy, or should we say Lara Croft and Donkey (need to listen to understand why this is so) explore the realities of working life whilst living with inflammatory arthritis.  

Next week is the Q&A episode so please do send in your questions, especially voicenotes here https://inflammatoryarthritis.org/contact-us/ so you can be on the next episode of Inflammatory! 

First, they have a light-hearted conversation about pets especially as it was National Love your Pet Day. Please visit Inflammatory Arthritis UK socials to see Whiskey, Debbie’s dog, debut! They also cover humorous personal anecdotes, including some unusual nicknames. 

They both reflect on being made redundant from different jobs and industries last year, highlighting how stress, a known trigger for IA, impacted them and their IA. The ongoing stress of looking for work, discuss what should or shouldn’t be included in your CV and a dive into the evolving workplace landscape. How laptops have moved on, and the sound of dial up still gives Debbie anxiety to this day! Make sure you listen to the end to fully understand. 

They explore what it means for employers to offer flexible working from day 1? Do they like working from home or do they prefer the office? How work provides them with routine and a purpose but discuss how they plan their day so they don’t trigger an IA flare. 

They also cover how employees with IA can advocate for their needs, how communication is key, what their manager should be doing and how being confident and open about your needs really can help. However, there is support out there for people who may have been discriminated against due to their IA? Support can be found here: 

Citizens Advice

ACAS

Equality Advisory and Support Service

Next Episode Teaser:

Please do send us your questions for the next Q&A session. 

🔗 Follow & Connect:

• Subscribe for new episodes every week, via https://inflammatoryarthritis.org/

·       Follow us on social media for updates and community discussions

Facebook

Instagram

Bluesky 

LinkedIn

• Reach out—we’d love to hear your thoughts and experiences! Email info@inflammatoryarthritis.org

🎧 Listen now and remember: You’re not alone in this journey.

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Hosts Debbie and Katy, go through your questions in this second Inflammatory! Q&A episode. 

Next week on Inflammatory! the hosts will be talking about who inspires them to coincide with World Book Day and International Women’s Day. Please do send in details about who has inspired/supported you and the hosts can do their first shout outs in the next episode. You can send them in and via voicenotes here https://inflammatoryarthritis.org/contact-us/ so you can be heard on the podcast. 

The first question Debbie and Katy discuss is one about their own journey with medication. They cover the psychological impact, feelings of fear and denial about starting long term medication and how it can be frustrating to find the right medication straight away.

They then go on to discuss how can family support people living with IA. Is it more annoying to keep asking if you are ok? The conversation covers what not to say but can family do anything right in this situation? 

A question was asked about hand deformity/surgery and again this picks up on emotional side of what the future could hold. Steroid injections are covered and how Debbie felt when her daughter had her injections and that Debbie’s fingers are similar to that of King Charles III. They also briefly cover that everyone has a comment on a cure for IA, and that the hosts will cover in this in a future episode, but please do send in your most bizarre/obscure comments you have received as the hosts would love to hear them. 

They end with a few humorous questions one about T-shirts, and the other what their dream jobs were. Tracy Island is a clue for Katy and how did Kylie Minogue inspire Debbie?

Please do leave a review and rating from where you listen to the podcast.

Follow us on Social media: 

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Bluesky 

LinkedIn

Sign up to our newsletter to be first to know about any upcoming episodes, research opportunities and any IA news/events at https://inflammatoryarthritis.org/ 

If you enjoy this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to www.inflammatoryarthritis.org

A Boutique Broadcast production for Inflammatory Arthritis UK

Hosted on Acast. See acast.com/privacy for more information.

In this episode, Debbie and Katy dive into the realities of aging with inflammatory arthritis during Autoimmune Awareness Month. Reflecting on their March birthdays, they ask—are they any wiser? Katy shares her experience with a steroid injection in her wrist, detailing the unexpected pain and unique circumstances, while Debbie talks about a mishap with her microphone, sparking a conversation on clumsiness, strength loss, and how arthritis affects daily life.

The discussion expands to aging with chronic illness, including shifting perspectives on midlife, family longevity, and balancing activity with fatigue. They also share how they’ve adapted to physical limitations, from car choices to planning for future living arrangements.

Despite these challenges, they emphasize the importance of staying positive, active, and finding new passions, with a metaphor about old furniture symbolizing resilience.

They also explore the emotional impact of inflammatory arthritis, how to distinguish disease-related symptoms from natural aging, and the need for better support from healthcare professionals in managing aging and stress.

The episode concludes with a hopeful message about ongoing research, new treatments, and the importance of open communication with medical teams. They preview their next discussion on parenting a child with JIA, reminding listeners to embrace life despite its challenges.

Key Topics Discussed:

• Ageing with autoimmune disease and inflammatory arthritis
• Autoimmune Awareness Month and World Young Rheumatic Diseases Day
• Katy's steroid injection experience
• Daily life challenges: clumsiness, strength loss, and adaptations
• Shifting perspectives on midlife and family longevity
• Balancing activity and fatigue
• Psychological impact of inflammatory arthritis
• The need for better healthcare support and communication
• Encouragement to stay positive and embrace life’s opportunities

Resources & Links:

• Follow us on social media: Instagram, Facebook, Blue Sky, and LinkedIn
• Sign up for our newsletter at inflammatoryarthritis.org
• Don’t forget to rate and review the podcast on your favourite platform!

Next Episode Preview:

Next week, we’ll be discussing parenting a child with juvenile idiopathic arthritis and the unique challenges families face. Be sure to tune in!

Thank you for listening!

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

A Boutique Broadcast production for Inflammatory Arthritis UK

Hosted on Acast. See acast.com/privacy for more information.

In this episode, Debbie and Katy start by sharing light-hearted moments, including stories about Pancake Day and how Debbie met her husband. Katy talks about her recent experiences with tennis and netball while managing ongoing foot pain despite using orthotics.

The conversation explores who inspires them, a common theme is those who are living with long term diseases anddrawing inspiration from athletes like Caroline Wozniackiand actor Kathleen Turner. They go on to compare chronic illness management to the mental and physical strength required in professional sports. They also explore how the 1% trend, by doing 1% more to make yourself better each day, can be helpful for people living with IA, but recognise that sometimes you can feel like going backwards.

They discuss the pressures of the “perfect body” shown through social media, and they encourage realistic expectations. They highlight the value of self-acceptance and learning to appreciate your body, especially as having inflammatory arthritis has already put your body through a lot. The episode concludes with reflections on parenting with inflammatory arthritis and fostering resilience in the next generation.

Key Topics Discussed:

✅ Managing Inflammatory Arthritis – The impact on mobility, ongoing pain, and frustrations with medical assessments.

✅ Finding Inspiration in Athletes – Lessons from sports stars like , Andre Agassi, Rafael Nadal and Caroline Wozniacki on perseverance.

✅ The Power of Small Changes: 1% – How making incremental improvements can lead to long-term benefits.

✅ Balancing Life & Chronic Illness – Navigating social expectations, personal goals, and physical limitations.

✅ Parenting & Support Networks – The importance of community and encouraging resilience in children.

Resources & Links:

🔗 Join Our Community: InflammatoryArthritis.org

📩 Sign Up for Our Newsletter – Stay updated on new episodes and resources.

📱 Follow Us on Social Media: Instagram | Facebook | LinkedIn

🎧 Listen Now & Subscribe! If you enjoyed this episode, don’t forget to rate and review us on your favourite podcast platform!

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

A Boutique Broadcast production for Inflammatory Arthritis UK

Hosted on Acast. See acast.com/privacy for more information.

In this heartfelt episode, in recognition of World Young Rheumatic Diseases Day, Katy interviews Debbie on the realities of parenting a child with juvenile idiopathic arthritis (a type of inflammatory arthritis), offering personal insights and reflections. 

The conversation begins with personal updates, including Katy’s reflections on imposter syndrome and the differences between shame and guilt. Debbie shares her recent fibromyalgia diagnosis and the challenges of managing medications, fatigue, and brain fog.

As the discussion unfolds, Debbie speaks candidly aboutthe reason she didn’t want to have children when she was younger, but how the conversation with her rheumatologist at university changed her mind. Then sharing the guilt andthe emotional weight of her daughter’s JIA diagnosis, the overwhelming medical appointments, and the impact on family dynamics. She shares the strategies she has developed to stay organised, create a strong support system, and foster resilience within her family.

Despite the challenges, Debbie highlights the importance of open communication, honesty, and allowing others, especially her husband, to be more involved. The value of a support network that get what you are going through. The episode concludes with an uplifting message of hope, encouragement, and practical advice for other parents navigating similar experiences.

Key Takeaways:

• Managing a Parent’s & Child’s Health: Debbie opens up about her own struggles with IA andfibromyalgia while supporting her daughter’s JIA journey.

• The Power of Organisation: Keeping track of appointments, treatments, and paperwork is essential for managing a child’s chronic illness.

• The Emotional Impact of Diagnosis: Feelings of guilt and worry are common, but building a strong support network helps ease the burden.

• Resilience & Positivity: Open communication and embracing support from loved ones can make a difference in managing long-term conditions.

Resources & Links:

• NHS link for Fibromyalgia

• Sign up for our newsletter at inflammatoryarthritis.org

• Follow us on social media: LinkedIn, Instagram, Facebook, and BlueSky

• Stay tuned for next week’s Q&A session—submit your questions now!

If you enjoyed this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

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In this episode, Debbie and Katy answer questions in their third monthly Q&A session. They start by discussing Katy’s recent 10K race experience, discussing the impact of overexertion and fatigue. They explore the difference between general tiredness and inflammatory arthritis (IA)-related exhaustion, as well as Debbie’s experience with new fibromyalgia painkillers causing drowsiness and vivid dreams.

The discussion moves to eye health and the importance of regular checkups for those on IA medications. They answer the first question on the proposed upcoming changes to the UK’s Personal Independence Payment (PIP) and how it might affect people with IA. They also highlight the significance of workplace support, early diagnosis, and improved rheumatology services.

They also explore foot health and rheumatoid arthritis assessment with expert insights from Professor Adam Croft. They discuss the limitations of the DAS 28 score, which doesn’t include foot involvement, and share personal experiences with tracking disease activity and accessing biologic treatment.

Parenting with IA is another key topic with two questions, with practical advice for parents of children with juvenile idiopathic arthritis (JIA), covering clinic visits, self-care, and preparing kids for independence. 

The episode wraps up with a fun discussion on irrational phobias—ranging from bees to polystyrene—and a humorous anecdote about a painful bee sting.

Resources & Links:

• What is PIP Government Link

• Our response to proposed changes in PIP

• Learn more about inflammatory arthritis at inflammatoryarthritis.org

• Foot Health and IA

Follow us on social media:

• BlueSky, LinkedIn, Instagram, Facebook: Search for Inflammatory Arthritis UK

• Sign up for our weekly newsletter for updates and resources

• Leave a review & rating on your favorite podcast platform!

Next Episode:

Next week, we’re back with a deep dive into parenting with inflammatory arthritis—how it affects our daily lives and our children’s experiences. Stay tuned!

🎧 Listen & Subscribe: Available on all major podcast platforms.

Resources & Links:

If you enjoyed this episode, please do follow the series. And please do leave us a rating or a review, if you have a few minutes to do so, thank you.

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

Hosted on Acast. See acast.com/privacy for more information.

In this episode of Inflammatory, Debbie and Katy get real about how even a simple cold can wreak havoc when you're living with inflammatory arthritis (IA). Debbie opens up about a recent bout of illness that hit her hard and amplified her joint pain (especially in her jaw), flaring up her fibromyalgia, and throwing her reactive hypoglycaemia into chaos. Katy, on the other hand, shares her experience of rarely getting sick despite being on medication, and reflects on the fear and uncertainty she felt early in the COVID pandemic.

Together, they explore how illness can throw off everything—energy levels, medication schedules, even mental health. They talk about the tricky balance between rest and movement, how stress (even over little things) can spark flares, and the lingering emotional impact of being extra cautious during COVID. There’s also a candid discussion around how isolating chronic illness can be, especially when others don’t see or understand what you’re going through and how you can feel like a prisoner in your own body. 

Throughout the conversation, Debbie and Katy emphasize that no two journeys with IA are the same—but community, honesty, and listening to your own body can make all the difference.

🎙️ In this episode:

• How minor illnesses can trigger major flares

• The toll of managing multiple conditions at once

• Reactive hypoglycaemia + IA = a tough combo

• Pandemic stress and long-term mental health impacts

• Why self-awareness and a holistic mindset matter

👉 Subscribe to our newsletter at inflammatoryarthritis.org, and follow us on Instagram, Facebook, LinkedIn, and Blue Sky (search for Inflammatory Arthritis). We’ll be back after a short Easter break—see you then!

Leave a review & rating on your favourite podcast platform!

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

Hosted on Acast. See acast.com/privacy for more information.

In this powerful and heartfelt episode, hosts Debbie and Katie, both parents living with inflammatory arthritis (IA), share their experiences balancing parenthood with chronic illness. They discuss the challenges of raising children while managing IA, the importance of awareness, support networks, and resilience.

Firstly, they share their recent experience attending an event at the House of Parliament with the National Axial Spondyloarthritis Society (NASS), advocating for faster diagnosis times. The event was a great success, and they were thrilled to receive recognition for their podcast and charity work. They also discussed their charity Board Awayday, how they are developing the charity to help improve the lives of anyone living with IA. Along with the importance of fundraising to continue their work. They share moving listener stories about how the podcast has helped them feel less alone and where you can donate, at our website Inflammatoryarthritis.org

The hosts go on to explore how their children knew about their inflammatory arthritis and has IA enabled them to be better parents? They discuss the use of age-appropriate language being key to help foster compassion and resilience, and Debbie shares the TikTok she watched from a rheumatologist explain the immune system like a sound system, and for auto-immune diseases the volume is turned up and the medications help to turn it down again. 

The also explore balancing honesty with protecting childhood innocence, the role of young carers programs and support systems and how amongst all the hard times of IA this can create a kinder more empathic child.

Please do continue to:

💜 Support Their Work – Donate or take part in fundraising efforts.

📢 Raise Awareness – Share this episode to help educate and support those affected by IA.

🎧 Stay Connected – Subscribe to the podcast for more stories, insights, and advocacy updates.

📧Sign up to our newsletter at Inflamamtoryarthritis.org

This episode is a must-listen for anyone navigating chronic illness, parenting, or wanting to support those living with IA. Tune in for insight, encouragement, and inspiration! 🎙️

Follow us on social media:

• BlueSky, LinkedIn, Instagram, Facebook: Search for Inflammatory Arthritis UK

• Sign up for our weekly newsletter for updates and resources

• Leave a review & rating on your favorrite podcast platform!

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

Hosted on Acast. See acast.com/privacy for more information.

Inflammatory Arthritis UK are hosting their first ever online event on the 20 May at 6-7pm to raise awareness of World Autoimmune and Autoinflammatory Arthritis Day. Please do join us and a chance to meet Debbie and Katy online to hear more about the charity and be part of our community. More information and full agenda will follow. Please do join us and to sign up email us at: info@inflammatoryarthritis.org 

In this lively and heartfelt episode, Debbie and Katy reflect on a busy week and preview next week's exciting guest — acclaimed photographer Rachell Smith, who lives with axial spondyloarthritis. Please make sure you don’t miss it.

Debbie covers how she did a Katy, and went to the wrong hospital for an Xray, and they kick off their fourth Q&A session by answering a question about traveling while taking biologic medications. The hosts share their own travel tips, stress the importance of medical guidance, and offer reassurance for those navigating similar journeys.

Next, the conversation turns to sleep and inflammatory arthritis. From bedtime routines and positioning to gadgets and frustrations, Debbie and Katy talk openly about what helps — and what doesn’t — when it comes to getting quality rest with a chronic condition.

They also tackle the question of whether inflammatory arthritis is more common in females, exploring key differences between RA, axial SpA, PsA, and juvenile arthritis. They address what frustrates them most about living with IA and they cover widespread misconceptions, including the confusion between inflammatory and osteoarthritis, and highlight the need for more male representation in arthritis narratives.

The episode wraps up on a fun note with each host sharing their go-to feel-good songs and how music brings moments of joy amid daily challenges.

💬 Topics Covered:

• Traveling with biologic medications
• Sleep challenges and hacks
• Gender and arthritis prevalence
• Inflammatory vs. osteoarthritis
• Personal reflections and musical cheer

Join us next week for our special guest, Rachell Smith!

Follow us on social media:

• BlueSky, LinkedIn, Instagram, Facebook:Search for Inflammatory Arthritis UK
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•  Leave a review & rating on your favourite podcast platform!

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

Hosted on Acast. See acast.com/privacy for more information.

In this episode of Inflammatory!, Debbie and Katy kick things off with a light-hearted chat about springtime chaos, parenting, and the never-ending battle with household cleaning, offering a humorous but relatable peek into how daily life intersects with chronic illness. The conversation then dives into a powerful and personal discussion about exercise and inflammatory arthritis, challenging outdated fitness ideology of "no pain, no gain."

Katy opens up about her journey training for marathons post-diagnosis, including a dramatic fall at mile 20 of the Edinburgh Marathon and her later attempt at the Brighton Marathon, complete with new injuries and mid-race regrets (sausage roll, anyone?). Through these stories, she highlights the emotional highs and lows of pushing her limits and adapting workouts to suit her body.

The hosts reflect on how chronic illness shape how they move, underscoring that exercise doesn't have to be extreme to be effective. Whether it’s swimming, strength training, or simply taking a short walk, finding what works for you is key. They also touch on the mental and emotional benefits of movement, the value of physiotherapy, and how changing the narrative from "can't" to "can" empowers people living with inflammatory arthritis.

Key Topics:

• Redefining exercise with chronic illness

• Katy’s marathon stories: Edinburgh disaster & Brighton comeback

• How age and parenting shift fitness goals

• Mental health benefits of movement

• Making peace with low-impact, feel-good movement

• Physiotherapy: importance and asking how it can fit it into your daily routine

• Encouragement to focus on what you can do

Follow us on social media:

• BlueSky, LinkedIn, Instagram, Facebook: Search for Inflammatory Arthritis UK

• Sign up for our weekly newsletter for updates and resources

• Leave a review & rating on your favourite podcast platform!

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

Hosted on Acast. See acast.com/privacy for more information.

In this week’s episode, hosts Debbie and Katy welcome their first guest, Rachell Smith, a leading portrait and fashion photographer who lives with axial spondyloarthritis (axial SpA) and is behind the new national campaign “Faces of Axial SpA”. Rachell opens up about her deeply personal journey, from experiencing symptoms as a teenager to finally being diagnosed over a decade later.

She discusses the vital role of family support, including her sister who also lives with axial SpA, and how the condition has brought her even closer to her husband. Rachell also shares how she navigates motherhood with a young daughter, emphasising the power of honest communication and emotional connection.

Rachell speaks candidly about how her diagnosis has increased her empathy, for others and for herself, and how this has come across in her photography. She also explains she is open with her clients about living with inflammatory arthritis and unashamed of her condition.

Most importantly, she talks about her impactful collaboration with NASS (National Axial Spondyloarthritis Society) on a national awareness campaign. Her mission: to empower others, shorten diagnostic delays, and break the silence around axial SpA.

Rachell’s story is one of resilience, creativity, and advocacy. Tune in for a moving conversation that highlights strength, vulnerability, and the importance of raising awareness.

🔗 Resources & Mentions:

·       For more information about “Faces of Axial SpA” please visit: Faces of Axial SpA

·       NASS website NASS.co.uk

• Learn more about axial SpA and access the symptom checker: symptom checker
• Follow Rachell on Instagram: @rachell_photo

This podcast is in collaboration with National Axial Spondyloarthritis Society

Disclaimer: The podcast is for informational purposes only and is not intended to replace professional medical advice. We talk about our personal health journeys and the podcast is not intended to provide professional medical advice, diagnosis, or treatment. We are not medical professionals and in no way claim to be medically trained. The podcast does not take responsibility for any losses, damages, or liabilities that may arise from the use of the podcast. The podcast does not assume responsibility for the accuracy of third-party content.

For more information, head to https://inflammatoryarthritis.org/

Hosted on Acast. See acast.com/privacy for more information.