Conquering Your Clownfish Brady Murray

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

In this episode of Conquering Your Clownfish, I sat down with Marci Dunning, a medical mom and parent to her daughter Freya, who has the rare Cornelia de Lange Syndrome. Marci shares the impact this has had on her family, and the challenges of raising a child with a life-altering condition. She discusses the weight of anticipatory grief, the struggle to plan for an uncertain future, and the power of living in the present. Offering invaluable insights for families facing similar challenges and those seeking to understand the complex world of rare disabilities, this episode is a must-listen for anyone grappling with simply wanting to expand their perspective on disability and parenthood.

In this week’s episode, I was joined by Anna Owen, a Montessori mom and an advocate for a more natural way of life. Ana shares her family's experiences after her daughter Josephine was born with a rare musculoskeletal disorder called Antley Bixler syndrome, greatly affecting her physical development. Anna and her family have felt so much joy with Josephine in their lives, and through their faith, patience, and willingness to learn as they go in the face of the unknown, they have come closer together because of it. Join us as we dive deeper into what contributes to the joy of seeing your child sing the song they were meant to sing in this episode of Conquering Your Clownfish!

For more from Anna Owens and her experiences with Antley Bixler syndrome find her on Instagram @annaowen.

In this powerful episode of Conquering Your Clownfish, Amanda Griffith Atkins opens up about her journey as the mother of Asher, who was born with the rare condition Prader-Willi syndrome. Amanda shares the challenges of living in a world that often feels inaccessible, adapting to new perspectives, and the hard parts of raising a child as a part of the rare disease community. Amanda is on a mission to give parents permission to acknowledge their struggles while still loving and supporting their kids. She offers advice for planning for the future as a caregiver and the importance of guilt-free self-care. Any parent or caregiver feeling alone in their journey will not want to miss this episode, offering validation, compassion, and the reminder that the special abilities community is in this together.

If you would like to learn more about Amanda and her experiences with Prader-Willi Syndrome, you can learn more about her on Instagram @amanda.griffith.atkins

In this episode, Brady shares the incredible journey of his adopted son Cooper. From being abandoned on a street corner in China to throwing out the first pitch at iconic Major League Baseball stadiums across North America, Cooper's story is all about conquering limitations. For Brady, it’s about finding the courage to let his son spread his wings in the face of the unknown, pushing past his own worries to let his son truly shine. Cooper's infectious joy and determination help him enrich the lives of those around him as he and his special abilities help connect communities across America. Join us this week to hear Cooper’s story from China to the Major Leagues!