Explore every episode of the podcast Conquering Your Clownfish

n this powerful episode of Conquering Your Clownfish, Misty Coy Snyder sits down with therapist and author Amanda Griffith-Atkins, a mother navigating the complex realities of raising a child with Prader-Willi syndrome. Amanda opens up about the raw, unfiltered side of parenting a child with high support needs—the medical trauma that fuels hypervigilance, the guilt that creeps in with every “what if,” and the damaging weight of toxic positivity. She shares hard-earned wisdom from her new book, encouraging parents to allow space for grief and honest emotions while also carving out moments of joy beyond parenting. Through heartfelt stories and practical strategies like micro self-care and redefining success around love and safety (not milestones), Amanda offers a lifeline of hope and validation for families walking a similar path.

What happens when the picture-perfect plan of motherhood is shattered by an unexpected diagnosis? In this raw and revealing episode, Ashley Stringham opens up about the moment she learned her son Carter had Down syndrome — a moment that brought shock, grief, and an overwhelming sense of isolation. With brutal honesty, Ashley shares the emotional rollercoaster of denial, heartbreak, and eventual acceptance, inviting us into the messy, beautiful reality of parenting a child with special needs.

But this isn’t just a story about Carter. It’s a call to every mother who’s ever felt like she had to hold it all together. Ashley explores the often-unspoken truth that self-care isn’t selfish — it’s survival. That it’s okay to cry. That it’s okay to grieve. And that progress, not perfection, is what real motherhood looks like.

Through the power of community, Ashley found healing in the stories of other special needs moms. Her message is clear: advocacy begins at home, and joy can be found in the smallest victories — if we’re brave enough to stop comparing and start embracing the journey we didn’t expect.

This episode will challenge the narrative, crack open your heart, and remind you that sometimes the most unexpected detours lead to the most profound love.

In this episode of Conquering Your Clownfish, hosts Misty Coy Snyder, Ela, and Larry invite listeners into the raw and radiant journey of raising their daughter with Down syndrome—one that shattered their expectations, exposed the fear-based narratives still dominating the medical world, and ultimately gave rise to a global advocacy movement rooted in art.

What began as confusion and isolation quickly transformed into connection and purpose. Ela and Larry didn’t just find beauty in their daughter—they captured it, painted it, and put it on display for the world to see. Through their art, they’ve made it impossible to look away from the truth: children with Down syndrome are not a tragedy to grieve, but a light to follow.

They speak openly about the way limitations—imposed by doctors, systems, even well-meaning friends—can quietly crush potential. They spotlight the often-overlooked role of fathers, the fierce empathy that grows in siblings, and the community that every family deserves but so few actually find.

This episode doesn’t sugarcoat the journey. Instead, it flips the script: what if the “hard news” isn’t the diagnosis, but the lies we’re told about what that diagnosis means? What if the real disability is in how society chooses to see?

If you've ever been afraid of the unknown, or wondered how to turn pain into purpose—this one is for you.

What if the child you thought couldn’t understand you had been listening all along?

In this powerful episode of Conquering Your Clown Fish, Betsy Hicks-Russ—mother, advocate, and director of Autism Odyssey—opens up about her journey parenting Joey, a young man with non-speaking autism. For years, she was told Joey couldn’t comprehend the world around him. But everything changed when they discovered spelling to communicate—a method that unlocked Joey’s voice and transformed their entire relationship.

Betsy challenges the narrative that non-speaking means non-thinking. With fierce honesty and vulnerability, she shares how the vest Joey wears in public serves as more than a tool for safety—it’s a call for empathy in a world that too often makes assumptions. She dives into why society still underestimates people like Joey, and why it’s time we stop.

This conversation is a wake-up call to parents, educators, and anyone who’s ever judged what they didn’t understand. It’s also a love letter to the caregivers who keep showing up, even when Plan A fails—and who discover miracles in Plan B.

What if everything the world told you about disability was wrong?

In this powerful episode, Mitch Holeve shares the raw and transformative journey of raising his son Garrett, a trailblazer with Down syndrome who defied every limit—including stepping into the cage as a mixed martial artist. Mitch unpacks the emotional highs and societal hurdles of parenting a child with disabilities, exposing outdated perceptions and advocating for a world that expects more because our kids are capable of more.

From volunteering at Eunie's Buddies and mentoring new parents, Mitch challenges us to stop settling for sympathy and start building support systems that empower. This episode is a call to action—for positivity, for inclusion, and for a shift in how we define success, strength, and belonging.

To learn more about Eunie's Buddies, visit HERE.

What if the very thing you feared most became the source of your deepest joy?

In this raw and unfiltered episode, Amanda Ellard—mother, author, and fierce advocate—opens up about the life-altering journey of raising a child with Down syndrome. She doesn’t sugarcoat it. The grief is real. The trauma is real. But so is the joy—piercing, profound, and often found in the most unexpected places.

Amanda speaks to the quiet battles adoptive parents face: the emotional exhaustion, the fear of failure, the invisible weight of parenting children with trauma. She challenges the narrative that love is always easy—revealing how trust must be earned, how vulnerability is non-negotiable, and how therapy and self-care are not luxuries but lifelines.

This episode is a rallying cry: Every child—especially those the world too often overlooks—is worthy of celebration, belonging, and relentless advocacy. And perhaps the greatest transformation isn’t just in the child... but in us.

In this raw and riveting episode of Conquering Your Clown Fish, host Brady Murray sits down with Tim Ashcraft—Army aviator, father of four, and reluctant member of a club no parent asks to join: the parents of a child with a life-changing diagnosis. When Tim and his wife Ashley learned their youngest, Finley, would be born with Down syndrome, their world shifted in an instant. What followed wasn’t a tragedy—it was a transformation.

With unflinching honesty, Tim shares the emotional rollercoaster of receiving Finley’s diagnosis, the weight of uncertainty, and the unexpected beauty that emerged on the other side. He opens up about the sacred power of faith, the fierce importance of community, and the real, messy, miraculous moments of parenting a child with special needs. From celebrating milestones most overlook to grappling with the complexities of family dynamics and adoption, Tim’s story challenges cultural assumptions about what makes a life valuable.

This episode isn’t just about Down syndrome—it’s about what happens when you let go of the life you imagined and embrace the one you’ve been given. It’s about the kind of love that stretches you, surprises you, and ultimately saves you.

Prepare to be moved, challenged, and reminded that sometimes the greatest gifts come wrapped in uncertainty.

What if the stories the world needs most are the ones we rarely see on screen?

In this powerful episode, we sit down with David and Jackson Hughens—a father-son filmmaking team on a mission to challenge the status quo of storytelling. Their journey began not on a film set, but in the heart of a community too often overlooked: individuals with Down syndrome. What started as a personal connection evolved into a calling—to create films that don’t just include people with disabilities, but center them as heroes, artists, and changemakers.

From intimate mini-documentaries to the ambitious development of a feature film inspired by the magnetic and unforgettable Jay, the Hughens are flipping the script on what Hollywood thinks audiences want. They speak candidly about the uphill battle to secure funding, the emotional weight of telling stories that matter, and how their time in Armenia deepened their understanding of the global need for adoption and advocacy.

This episode isn’t just about filmmaking—it’s about demanding better from media, amplifying underrepresented voices, and proving that individuals with Down syndrome don’t need to be “fixed” or pitied. They need to be seen.

What if the world saw people with disabilities for who they really are—not as limitations to be pitied, but as leaders, change-makers, and warriors of hope?

In this powerful episode of See the Miracle, Brady Murray sits down with Katie Haynes, founder and CEO of Smiling While Sending Hope. Born from Katie’s own journey with chronic illness, this nonprofit is shaking up how we support and uplift individuals with disabilities. Katie opens up about her struggles, her triumphs, and the unshakable belief that every person—regardless of diagnosis—deserves dignity, purpose, and opportunity.

From the confidence she gained through 4-H to the bold vision she’s building today, Katie doesn’t just talk about advocacy—she lives it. With faith as her compass and community as her fuel, she’s challenging the status quo and calling out a world that too often overlooks the strength, intelligence, and value of people with disabilities.

Katie’s dream to become a motivational speaker is more than a goal—it’s a movement. One voice. One message. Thousands of lives waiting to be seen.

This episode is a wake-up call to rethink ability, reimagine leadership, and recognize the power of choosing purpose over pity.

In this powerful episode, Wendy Hooton opens up about the raw and real journey of raising her son Matt, who has Down syndrome. As a single mother, she faced overwhelming fears—not just about her son’s future, but about whether she could give him the life he deserved. From battling societal misconceptions to navigating the complexities of dating as a special needs parent, Wendy shares the deeply personal moments that shaped her into the fierce advocate she is today.

Her story is one of radical acceptance, unconditional love, and the transformative power of community. At the Dear Mom Conference, Wendy found not only healing but a tribe of mothers who reminded her that vulnerability is strength. She reflects on Matt’s incredible progress and the importance of celebrating each child’s path without comparison or shame.

Wendy doesn’t sugarcoat the hard stuff—divorce, isolation, the fear of adulthood—but she also doesn’t let it steal the joy. She urges other parents to stop apologizing for their children’s differences and instead, start building a life filled with laughter, connection, and bold hope. Because the truth is: the world is still catching up to what parents like Wendy have known all along—kids like Matt are not a burden; they’re the revolution.

What if everything the world assumes about disability is wrong? In this powerful episode, Pete Larkin invites us into the sacred, often overlooked bond between siblings—one shaped by unconditional love, grit, and a radical rethinking of what it means to live a meaningful life. Pete shares his journey growing up alongside his brother Brigham, who has Down syndrome, and how caregiving, once seen as a burden, became his greatest teacher.

Their story challenges the narrative that individuals with disabilities need to be "rescued" or "protected." Instead, Pete speaks to the strength, independence, and unapologetic joy Brigham embodies—reminding us that shielding people from struggle can rob them of growth. Through Brigham’s vibrant personality, infectious kindness, and the generational wisdom he unknowingly passes down, we’re forced to ask: are we underestimating the very people we should be learning from?

What happens when life throws you a plot twist that shifts your entire worldview? In this powerful episode, Devon Dowdell — a proud father, passionate ufologist, and deep thinker — shares the raw, beautiful, and deeply human journey of raising his son Jack, who was born with Down syndrome.

Devon opens up about receiving Jack’s diagnosis over the phone while away for work — a moment that shattered expectations but sparked an awakening. He speaks candidly about the emotional weight of that day, the fear of the unknown, and the transformation that came through love, acceptance, and presence. Devon doesn’t shy away from hard truths — about fatherhood, about societal pressure to "fix" what's different, and about the grief that often precedes joy.

But this isn't a story about sadness — it's a celebration. A reminder that the things we fear the most can become the greatest blessings. Devon’s perspective challenges conventional narratives around disability, masculinity, and what it means to show up — not with perfection, but with heart.

It’s honest. It’s bold. And it might just change how you see parenthood, purpose, and what truly matters.

What if the hardest thing you've ever faced as a parent turned out to be the most transformative?

In this powerful episode, Angela O’Brien—mother, Enneagram coach, and unapologetic truth-teller—opens up about raising a daughter with Down syndrome and how the experience shattered her expectations… and rebuilt her in the best way possible. Angela doesn’t sugarcoat the challenges of parenting a child with disabilities. From grief and isolation to identity loss and the pressure to “always be strong,” she dives deep into the emotional weight families carry—especially mothers.

But through that struggle comes beauty: unexpected friendships, deeply empathetic siblings, and the chance to rediscover who you are beyond caregiving. Angela reminds us that community isn’t optional—it’s oxygen. And that pretending everything’s fine helps no one.

If you’re ready to challenge the polished narratives of disability parenting and embrace the raw, beautiful, and often misunderstood reality—this conversation is for you.

What If Being a “Strong Dad” Is Actually Hurting Your Family?

In this raw and revealing episode of Conquering the Clown Fish, host Brady Murray sits down with Graham Andrews—a father of three and proud dad to Andy, his daughter with Down syndrome—for a conversation that challenges everything we think we know about fatherhood. Graham opens up about the gut-wrenching moment he received Andy’s diagnosis and the emotional rollercoaster that followed.

But this isn’t your typical “inspirational parent” story. Graham gets real about the pressure men face to be stoic providers, the myth of control in parenting, and how vulnerability—not strength—became his greatest asset. He credits his transformation to the everyday lessons Andy teaches him, the unwavering support of his own parents, and a journey that’s been as confusing as it’s been beautiful.

This episode dares to ask: what if the best thing a father can do is break down, ask for help, and stop pretending he’s got it all figured out?

What if the most heartbreaking diagnosis became your life’s greatest teacher?

In this powerful episode of Conquering Your Clown Fish, host Brady Murray sits down with Jillian Arnold—a mother, caregiver, and unapologetic warrior for the rare disease community. When her son Roman was diagnosed with ASMD, a rare and devastating genetic disorder, Jillian was already pregnant with her second child, Stella—who would later be diagnosed with the same condition.

Instead of surrendering to grief, Jillian chose a radical path: one of relentless advocacy, deep community connection, and fierce joy. She challenges the idea that parents of children with disabilities should only be pitied. Instead, she shows us they are the strongest experts in the room, forced to navigate complex systems, fight for treatment access, and still find laughter and light in the darkest places.

This episode isn’t just about rare disease. It’s about turning pain into power, about rejecting the pity narrative, and about redefining what it means to live a joyful life—on your own terms.

In this powerful and eye-opening conversation, Silvia Almond lays bare the raw, unfiltered reality of parenting a child with Down syndrome. She doesn’t sugarcoat the initial shock, the overwhelming panic, or the crippling anxiety that followed Jordan’s diagnosis. Instead, she boldly confronts the uncomfortable truths society often avoids: the fear of the unknown and the heavy responsibility of raising a child who defies expectations.

Silvia’s story is not just one of personal transformation but a call to challenge outdated narratives around disability and family. She reveals how Jordan shattered their preconceived notions, not by conforming to societal standards, but by thriving unapologetically in his own way. His infectious spirit and undeniable charisma have not only reshaped family dynamics but have also forced them to reconsider what success and happiness truly look like.

Silvia’s journey shows that the real struggle is not in raising a child with Down syndrome, but in breaking free from society’s pity-driven perspectives and embracing the pure, transformative love that only a child like Jordan can bring. Her story proves that children with Down syndrome are not just surviving—they are thriving, leading lives filled with friends, joy, and potential that the world too often underestimates.

This episode challenges listeners to rethink how they view children with disabilities, daring them to go beyond surface-level acceptance to a deeper understanding and admiration for their strengths and individuality. Silvia’s story is a battle cry for radical love, fierce advocacy, and the courage to reject limiting beliefs.

Breaking Barriers and Redefining Strength with Camille Robinson

On this unfiltered episode of Conquering Your Clownfish, we dive into the raw and powerful journey of Camille Robinson—a mother, podcast host, and relentless community force. Camille's story isn’t just about raising her son, Mason, who lives with congenital heart disease and autism—it’s about shattering expectations, defying the odds, and proving that adversity doesn’t define your destiny.

From surviving an abusive relationship as a young mother to reclaiming her power through faith and community, Camille refuses to let society dictate her story. She gets candid about the brutal realities of raising a child with disabilities—the toll on mental health, the impact on marriage, and the unspoken struggles that many families face but few dare to talk about.

This conversation isn’t just about parenting; it’s about dismantling outdated narratives and showing up fiercely for the ones we love. Camille shares the pivotal moments that transformed her into an unshakable advocate for special needs families and why she believes that waiting for support isn’t an option—you have to build it yourself.

She also gives us an inside look at Moments of Joy Fest, a groundbreaking event dedicated to uplifting families who often feel unseen, and her upcoming book, 100 Days of Encouragement for Families Raising Children with Special Needs—a must-read for anyone seeking hope, resilience, and unapologetic truth.

This episode will challenge your perspectives, ignite your determination, and remind you that real strength isn’t about having it all together—it’s about refusing to give up.

Breaking Barriers: The Unstoppable Journey of Caleb Prewitt

In this electrifying episode, Brady Murray sits down with Karen Prewitt, the fierce and determined momager behind Caleb Prewitt, a trailblazing athlete and entrepreneur who just happens to have Down syndrome. Karen shares the raw, unfiltered truth about raising a child society often underestimates—challenging outdated mindsets and proving that limitations exist only where we allow them.

Caleb has shattered expectations, from becoming the youngest person with Down syndrome to complete a half marathon to launching his own business, Caleb’s Cookies. But their story isn’t just about personal victories—it’s about rewriting the narrative for individuals with disabilities. Karen unapologetically calls out the lack of opportunities and systemic barriers, advocating for a world where people with disabilities are seen as capable, ambitious, and worthy of the same dreams as anyone else.

The conversation dives deep into the importance of community support, the power of mentorship, and the bold belief that no one—not doctors, not schools, not even well-meaning parents—should dictate the limits of a child’s potential. As Caleb transitions into adulthood, Karen envisions a future filled with independence, adventure, and possibilities that defy every outdated stereotype.

This episode will challenge you to rethink what you believe about ability, ambition, and what it truly means to live without limits.

Breaking Barriers in Faith, Disability, and Inclusion

In this powerful episode of Conquering Your Clownfish, host Brady Murray sits down with Monica Mangiacapra—an author, advocate, and mother who is reshaping the conversation around disability and faith. Inspired by her son Isaac, who has Down syndrome, Monica wrote Different by Design, a children’s book that challenges outdated narratives and educates young minds about disabilities in a way that fosters understanding rather than pity.

This episode doesn’t shy away from the hard truths: many families of children with disabilities feel excluded from church communities, often forced to leave due to a lack of accommodation. Monica calls for bold action—churches must stop seeing disability as a burden and start embracing it as an opportunity for radical inclusion. Her story of self-publishing Different by Design is proof that stepping into discomfort and breaking traditional molds can open unexpected doors of impact.

Monica’s journey is a wake-up call to parents, educators, and faith leaders: disabilities are not limitations; they are purposeful, designed differences that enrich our communities. She encourages all of us to ask tough questions, challenge the status quo, and create spaces where every child—regardless of ability—is seen, valued, and celebrated.

This episode will leave you inspired and maybe even a little uncomfortable—in the best way possible. Are we truly building inclusive spaces, or just offering performative support? It’s time for action, and Monica is leading the charge.

The Uncomfortable Truth About Purpose and Perseverance

In this powerful episode, Brady Murray sits down with Cathy Daub—a mother of eight, fierce advocate, and co-founder of Team Iron Will—to challenge society’s perception of value and purpose. Cathy shares the raw, unfiltered story of her son Will’s birth, a journey marked by both medical challenges and undeniable miracles. She refuses to see Down syndrome as a limitation, instead embracing it as a divine calling to disrupt the status quo.

This conversation forces us to ask: Do we truly believe that every life has value, or only the ones that fit our expectations? Cathy’s unwavering faith and relentless advocacy push back against a world that often measures worth in terms of productivity rather than purpose. Her story is a call to action—one that demands we rethink how we support, uplift, and fight for individuals with disabilities.

In this raw and unfiltered episode of Conquering Your Clown Fish, host Brady Murray sits down with Laurie Hellmann—author, podcaster, and fierce advocate for families with special needs children. Laurie doesn’t sugarcoat her journey. From the relentless battles of single motherhood to the emotional toll of raising a son with profound nonverbal autism and Crohn’s disease, she shares the hard truths that most people are too afraid to talk about.

Is society failing special needs families? Why are parents forced to fight for even the most basic support? And what happens when children with disabilities grow up and age out of the system?

Laurie's story is one of love, resilience, and defiance—a challenge to the world to do better. This conversation will inspire you, push you out of your comfort zone, and leave you questioning how we treat the most vulnerable in our communities.

In this gripping episode, Brady Murray interviews Sarah Stites, a fearless advocate challenging deeply ingrained societal biases in Armenia. Sarah left behind the comforts of her old life to reclaim her Armenian heritage and fight for one of the most overlooked communities—children with disabilities. She exposes the harsh realities these children face, from institutional neglect to the painful stigma that forces families to make unthinkable choices.

Sarah shares raw, emotional stories of resilience, proving that with the right support, these children aren’t just surviving—they're thriving. She highlights groundbreaking initiatives like the Emili Aregak Center, which dares to defy the system by keeping families together, and the Aregak Bakery, where inclusion isn’t just a concept but a revolution in action.

This conversation is a wake-up call for anyone who believes change is someone else's responsibility. Sarah makes it clear: the fight for dignity, inclusion, and equality starts now. Are you ready to be part of the solution?

Is the Toy Industry Failing Our Kids? In this episode of Conquering Your Clown Fish, host Brady Murray sits down with Amy Jandrisevits, the fearless founder of A Doll Like Me, a nonprofit that dares to challenge the status quo of the toy industry. Amy’s mission? To create custom dolls for children with disabilities and differences—because every child deserves to see themselves represented. She shares her unconventional journey from social work to doll-making and exposes the deep flaws in an industry that still marginalizes kids who don’t fit the “perfect” mold. From battling misconceptions to running a nonprofit on sheer passion, this conversation is a powerful reminder that one person can shake the world—and that representation in play isn’t just nice; it’s necessary.

In this eye-opening episode of Conquering Your Clown Fish, host Brady Murray dives into the raw reality of parenting a child on the autism spectrum with guest Courtney Mayorga. As a mother to Bennett, Courtney gets brutally honest about the emotional rollercoaster following his diagnosis, the uphill battle for proper education and resources, and the stigma that still plagues autism families. She challenges outdated societal norms, calls out the lack of real support, and reveals how embracing neurodiversity can change everything. Are we doing enough, or is the system built to fail these kids? Tune in and decide for yourself.

In this raw and riveting episode, Nicole Cowle invites us into her world, shattering societal expectations and offering a deeply personal perspective on parenting two children with disabilities—one with Down syndrome and another with a rare brain malformation. Nicole doesn’t hold back as she recounts the moments that broke her, the joys that reshaped her, and the resilience that keeps her moving forward.

She challenges the conventional narrative of what it means to parent children with special needs, speaking candidly about the unspoken grief, the triumphs in small victories, and the relentless strength required to navigate a world that often fails to understand or accommodate families like hers.

Chapters

00:00 Introduction to Nicole Kohl's Journey

01:22 The Birth of Peyton and Initial Challenges

04:53 Building a Community and Support System

06:51 Expectations and Fears of a Second Child

12:06 Ashton's Diagnosis and Its Impact

14:28 The Unique Love for Children with Disabilities

21:31 Looking Ahead: Hopes for the Future

In this eye-opening episode of the Conquering Your Clown Fish podcast, host Brady Murray sits down with Katie Rivera, a Texas mother of three whose journey through the world of parenting a child with Down syndrome shatters the glossed-over narrative of "perfect parenting." Katie pulls back the curtain on the raw, often controversial realities of fostering children with special needs, confronting the social stigma and system failures that make her family's story one of resistance, love, and gritty resilience.

From navigating the emotional minefield of raising a child with a disability to dismantling the exclusionary practices still rampant in education, Katie reveals the often-ignored challenges and hypocrisies that families like hers face every day. And while the world applauds her commitment, Katie doesn’t shy away from calling out the uncomfortable truths about community support, the pressures of social media, and the role of fathers in the disability space—issues rarely discussed but desperately needed in this conversation.

As Katie opens up about her plans to foster once again, this time with an even greater willingness to care for children with special needs, the question remains: Is society really ready for true inclusion, or are we just paying lip service to the idea of belonging? Tune in for an episode that will leave you questioning everything you thought you knew about disability, family, and the limits of love.

In this eye-opening episode of Conquering Your Clown Fish, host Brady sits down with Jennifer Allen, founder of Wonders Within Reach, for an unfiltered conversation about the unpredictable realities of adopting a child with spina bifida. Jennifer pulls no punches as she recounts her family's raw journey through the challenges of raising a child with special needs in a world that is often unprepared for them. From the overlooked obstacles of accessibility to the deeper, uncomfortable truths about inclusion, Jennifer argues that society is failing to meet the needs of families with disabilities—and it's time for that to change. But it’s not all doom and gloom. Jennifer shares how embracing adventure and travel has not only transformed her family’s experience but has also exposed the radical power of community support. Get ready for a conversation that will challenge your assumptions, spark your empathy, and leave you questioning what true inclusion really looks like.

In this eye-opening episode of Conquering Your Clown Fish, host Brady Murray sits down with Stefanie, the fierce and unapologetic president and co-founder of Lily's Voice, a nonprofit that’s challenging the broken system of assistive technology. Stefanie pulls no punches as she reveals the shocking obstacles families like hers face when trying to secure AAC devices for their non-speaking children, especially when these life-changing tools are often withheld due to financial or bureaucratic red tape.

Through the powerful lens of her daughter Lily’s journey—a vibrant, non-speaking autistic child who’s defying the odds and thriving—Stefanie passionately argues that the right to communicate is a fundamental human right, not a luxury. She exposes the uncomfortable truth about how society often fails to provide the necessary support for these children, and why organizations like Lily’s Voice are stepping in to fill a critical gap.

Stefanie doesn’t just talk about the struggle; she celebrates the victories, including the joy of watching Lily discover independence through customized AAC devices and her unexpected passion for ice skating. But it’s not all heartwarming stories—this conversation is an urgent call to action for better access to communication tools and a reminder that for too many families, the fight isn’t over.

Tune in to hear about the transformative power of AAC devices, the painful truth about accessibility, and the fight for equality that no one’s talking about.

In this heartfelt conversation, Rachel Vermeulen opens up about her journey as a mother to a child with Down syndrome, reflecting on both the challenges and the unexpected blessings that come with raising a child with disabilities. She underscores the vital role of faith, community, and inclusion in supporting families like hers. Alongside her husband, Kyle, Rachel co-leads *A Little Extra Love*, a ministry dedicated to offering faith-based support to families navigating disability. Together, they share the power of embracing differences, the profound impact of love, and the strength that comes from a supportive community in overcoming life's hurdles.

In this deeply moving and powerful conversation, Rachel Morris opens up about her extraordinary journey as a mother raising a child with Down syndrome while simultaneously battling pediatric cancer.

From the profound moments of receiving two life-altering diagnoses to the overwhelming power of love and the unwavering support of her community, Rachel’s story is one of unbreakable resilience and transformation. She takes us through the raw emotions of fear and uncertainty, the painful yet healing process of navigating these challenges, and the incredible joy of finding strength in her daughter, Rosie.

Rosie, in turn, has become not just a source of inspiration, but a beacon of hope, teaching Rachel the true meaning of courage, connection, and the boundless capacity for love.

This is a story of growth, of rising through adversity, and of the unshakeable bond between mother and daughter.

In this episode of the Conquering Your Clownfish podcast, host Brady Murray sits down with the incredible Carol Tingey, founder of the Hip Hop Homies—an awesome organization that’s all about helping individuals with Down syndrome live their best lives through dance, friendship, and community. Carol takes us on a journey from her early days in a special needs classroom to creating a vibrant space where everyone can bust a move, be themselves, and feel accepted. With tons of heart and soul, Carol talks about the magic of dance, the power of kindness, and the importance of building a supportive community. Plus, she shares her exciting vision for the future of the Hip Hop Homies. If you’re ready for some major inspiration and a whole lot of good vibes, this episode is a must-listen!

In this conversation, Michelle Fruhschien shares her journey as a mother and advocate for her daughter Haley, who has Jordan syndrome, a rare genetic condition. Michelle discusses the challenges of navigating the diagnosis, the importance of family support, and her advocacy work through her platform 'Mama Bear for Rare'. She emphasizes the need for true inclusion and understanding in society, and reflects on the emotional growth and resilience that comes from parenting a child with disabilities.

In this episode, Brady Murray interviews Monica Castro, a devoted mother and behavior analyst, who shares her journey raising her daughter Rio, who has Down syndrome and is completely blind. Monica discusses the challenges and triumphs of parenting a child with disabilities, the importance of inclusive toys, and her work in the ABA therapy space. She emphasizes the need for a positive mindset, understanding ableism, and providing compassionate care to families. Monica also shares her aspirations for the future, both for her daughter and her business, Rio's Place.

In this enlightening conversation, Amy Julia Becker shares her journey as a mother of a child with Down syndrome, exploring the profound concept of belovedness and its impact on her family dynamics. She discusses how Penny's presence has transformed their understanding of love, purpose, and the essence of being human. The dialogue delves into the importance of family support, the redefinition of perfection, and the vision for a future where everyone belongs and matters. Amy emphasizes the need to challenge societal assumptions about success and happiness, advocating for a more inclusive and loving world.

In this heartfelt conversation, Erin Eicher shares her journey as a homeschooling mother of four, including her experiences living on a seven-acre property, her time as a missionary in Southeast Asia, and the challenges and joys of raising a child with Down syndrome. Erin discusses her family's adoption journey, the miracles of parenthood, and the aspirations she holds for her son Maverick, emphasizing the importance of faith, trust, and the unique value each child brings to a family.

In this episode, Brady Murray and Jennie Dopp discuss their personal and professional journeys in the disability community, leading to the creation of CaringTide, a company dedicated to supporting families with loved ones who have disabilities. They share insights on the challenges faced by families, the importance of comprehensive planning, and the unique approach of CaringTide in guiding families through the complexities of disability planning. The conversation highlights real-life case studies and emphasizes the need for community and support in navigating the disability journey.

In this episode, Brady Murray interviews Mandy Breitenstein, a passionate advocate for adoption and special needs education. Mandy shares her personal journey of adopting a child with Down syndrome from Armenia and her efforts to create an inclusive school for children of all abilities. The conversation delves into the importance of faith in guiding life decisions, the beauty of Armenian culture, and the significance of loving children unconditionally. Mandy encourages potential adopters to embrace the journey, even when it feels daunting, and emphasizes that adoption is a brave act of love.

In this episode, Brady Murray shares the inspiring journey of creating a children's book titled 'Cooper is Super and So Are You,' which tells the story of his son Cooper, who has Down syndrome. The conversation explores the impact Cooper has had on his family and community, the motivation behind writing the book, and the launch of a Kickstarter campaign to fund its publication. Brady emphasizes the importance of sharing Cooper's story to inspire others and highlight the divine potential within everyone.

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In this heartfelt conversation, Mya-Lisa Ludwig shares her journey as a caregiver for her brother Adam, who has special needs. She reflects on their childhood, the challenges of caregiving, and the joy Adam brings to her life and family. The discussion touches on themes of love, protection, family dynamics, and the importance of understanding and acceptance in the community. Mya emphasizes the need for structure in Adam's life and the impact of their experiences on the next generation.

In this episode, Eileen Lamb shares her unique journey from France to the United States, her experiences as a mother of children with autism, and her work in raising awareness about the challenges faced by those with severe autism. She discusses the creation of the Autism Cafe, a platform aimed at connecting families and advocating for better resources and support. Eileen emphasizes the importance of community and understanding the diverse experiences within the autism spectrum.

In this heartfelt conversation, Abby Zachritz shares her journey as a mother of five, detailing the traumatic experience of her son Wyatt's near-drowning and miraculous recovery. Abby discusses the challenges her family faced and how they turned to community support and grants to navigate the financial burdens of Wyatt's care. She emphasizes the importance of hope and advocacy, leading to the creation of Connect, a platform that helps families find grant opportunities for disabilities. The conversation highlights the impact of Wyatt's journey on their family and community, showcasing the power of resilience and support.

In this episode of Conquering Your Clown Fish, host Brady Murray speaks with Reuben Mitchell, an entrepreneur and advocate for Down syndrome awareness. Reuben shares his emotional journey as a father to his son, Bam Bam, who was born with Down syndrome. The conversation delves into the challenges of receiving the diagnosis, the emotional rollercoaster of Bam's birth, and the transformative perspective that has emerged over the years. Reuben emphasizes the importance of support groups for fathers, the need for vulnerability, and the joy that Bam brings to their family. The episode concludes with reflections on the journey of acceptance and hope for the future.

On this episode of Conquering your Clownfish, we feature a heartfelt interview with Nicole Smith, a mother of three boys, one of whom, Abel, was born with Down syndrome. Nicole discusses her family life, her positive outlook on Abel’s diagnosis, and the overwhelming joy and blessing he brings to their lives. Her husband Josh’s prior experience working with people with disabilities prepared them for Abel’s arrival, fostering a strong, optimistic, and supportive family environment. Nicole shares insights into her other sons, Miller and Wyatt, and their interactions with Abel. She also touches on the importance of community connection, the value of everyone having a purpose, and her vision for Abel’s future. The conversational tone highlights both the challenges and the beautiful experiences that come with raising a child with Down syndrome.

Robin Knight, president of Just Breathe Adaptive Scuba, discusses the mission of her nonprofit organization to promote the health and well-being of individuals with disabilities through adaptive scuba diving. She shares stories of diving with people with various disabilities, including Down syndrome, spinal cord injuries, and ALS. Robin emphasizes the importance of adapting to the environment rather than the diver and creating a safe and inclusive space for everyone. She also highlights the personal growth and fulfillment she has experienced through her work.

Carla Mathis shares her journey as a mother of two sons on the autism spectrum, including the tragic loss of her 16-year-old son, Connor. She discusses how their family met and started, the different experiences of raising two sons on the spectrum, and the circumstances surrounding Connor's passing. Carla also talks about the challenges and lessons she has learned in the year since Connor's death, including starting the Connor Smiles Foundation and advocating for regulations in summer camps for children with special needs. She shares her experiences of feeling Connor's presence and finding peace in her daily life.

Abbey Benjamin, a mom, disability advocate, and nurse, shares her journey of raising a daughter with a genetic disorder and epilepsy. She discusses her experience working at a summer camp for children with disabilities, which opened her eyes to the abilities and potential of individuals with disabilities. Abbey emphasizes the importance of seeing the ability in every child and helping them flourish. She also talks about the challenges of attending her son's baseball games with Avery's seizures and how they decided to prioritize being together as a family. Abbey shares the exciting news that Avery has been chosen as an H&M kid hero, which will help raise awareness about her rare diagnosis. She reflects on how her journey has changed her perspective and given her a greater sense of purpose.

In this episode, I sat down with Courtney Morey, founder of the Annie Louise Foundation and mother to a child with Down syndrome. Courtney shares her experiences as an advocate for her children. Join us as she recounts the harrowing medical challenges Annie faced, and how those experiences inspired Courtney to create innovative support systems for other families. With a new baby on the way, Courtney offers a unique perspective that you won't want to miss.

In this episode of Conquering Your Clownfish, I sat down with Leah Crum, a young mom whose life took a sharp turn when her daughter Camilla was born and unexpectedly raced off to the NICU. Leah shares her thoughts on learning how to best care for her child despite the unique circumstances she had never assumed she would face. She discusses how God has prepared her for these challenges and ultimately strengthened and led her so she could embrace her new reality with confidence. Leah offers insights on navigating the healthcare system, dealing with public perception, and the importance of assuming competence in children with disabilities. Prepare to be impacted by Leah's mission to create a more inclusive environment for all children with special abilities.

In this episode, I sit down with Laney Wootten, who shared her family's story of raising a son with level three autism. Amidst the struggles, Lainey's faith and resilience shine through as she reveals how her son's disability has become a catalyst for hope and inspiration in their family as they had to make some very hard decisions. From praying for healing to finding purpose in pain, Laney's testimony is a beacon for families facing similar challenges. Even in life's darkest moments, nothing is wasted. This episode is a must-listen for anyone seeking strength, understanding, and a renewed perspective on the power of love and faith in the face of adversity.

Discover the inspiring journey of Amanda Owen, a lifelong disability advocate whose experiences as a special needs sibling shaped her mission to transform lives. From growing up with a brother with a rare chromosomal disorder to founding a groundbreaking nonprofit, Amanda shares intimate insights into the joys and challenges of disability advocacy. Learn how her childhood experiences and parents' tireless efforts fueled her passion for creating innovative support systems for individuals with disabilities and their families. Prepare to be moved and inspired by Amanda's unwavering dedication to ensuring every individual with a disability has a seat at the table and opportunities for happiness. You can follow Amanda and her journey on Instagram @puzzlepiecesky