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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.
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