Rachel Grow: Overcoming Symbrachydactyly and Success in Hollywood

In the first episode of season two of the We’re not Stumped podcast, I welcome television producer Rachel Grow. Rachel was born in Wiesbaden, Germany with a congenital condition called symbrachydactyly. Symbrachydactyly is a rare congenital hand condition in which a child is born with abnormally short fingers that may be webbed, misshaped or missing. It is often confused with other hand conditions but differs in that the underlying structure of the hand is affected — not just the fingers. The hand may not function well, and the bones, muscles, ligaments, and nerves of the hand are also often affected.

Even with her start in life, Rachel has continued to move forward with nothing but a positive attitude. She has worked in Hollywood both in front of and behind the camera, most notably as a producer on such shows as America’s Got Talent, American Idol and Shipping Wars. In this episode Rachel talks about her prosthetic designed by Arm Dynamics and created by Point Design, a great story on how she learned to tie her shoes…and much more!

To learn even more about Rachel, you can follow her on social:

YouTube: https://youtube.com/@BionicRachel

Instagram: https://www.instagram.com/bionic_rachel/

Her appearance on The Tex Factor: https://youtu.be/S2IBDkjZdJA?t=640

Prosthetic Links:

Arm Dynamics: https://www.armdynamics.com/

Point Design: https://www.pointdesignsllc.com/

#amputee #amputeelife #amputeestrong

Watch on YouTube

Listen on Spotify

  • Meegan Winters, CEO and founder of AbleVu

August 19th, 2025|

In this episode of We’re Not Stumped, Mike Bolland sits down with Meegan Winters, CEO and founder of AbleVu, the innovative accessibility search platform making the world easier to navigate for everyone. Meegan shares her inspiring journey—from special education teacher to tech entrepreneur—and how her friendship with Jessica, a power wheelchair user, sparked her mission to improve accessibility for all. Mike and Meegan explore AbleVu’s evolution from virtual tours to a “TripAdvisor for accessibility,” the business model that empowers contributors, and why accessible information benefits both consumers and businesses. Along the way, Meegan opens up about leaving a stable career, overcoming the challenges of building a startup, and the fulfillment that comes from creating real-world impact. Discover how technology and empathy intersect to make the world more inclusive.

  • individuals willing to share their experiences with prosthetists and prosthetic care

August 14th, 2025|

Podcast host Mike Bolland is looking to connect with individuals willing to share their experiences with prosthetists and prosthetic care. If you’ve ever faced challenges with a prosthetist, received a prosthetic that didn’t meet your needs, or discovered a provider who went above and beyond, your story can make a difference. On his show, We’re Not Stumped, Mike engages in open, honest conversations about life with limb loss, prosthetics, and advocacy. His mission is to give a voice to the limb loss community, spotlight real experiences — both the good and the bad — and work toward improving the system for everyone. Mike invites you to be part of this important dialogue, knowing that your insights could help others navigate their own prosthetic journeys with greater confidence and support. 📩 Interested in being a guest? Visit: https://werenotstumped.com/were-not-stumped-limb-loss-podcast-guest-guide/

  • Katie Thomas on Parenting, Advocacy, and Living One-Handed

August 12th, 2025|

In this heartfelt and uplifting episode of We’re Not Stumped, host Mike Bolland welcomes Katie Thomas for a conversation filled with honesty, humor, and hard-earned wisdom. Born without her right arm below the elbow, Katie began receiving care at Shriners Hospital in Tampa at age 3 and experimented with various prosthetics throughout her childhood. Over time, she discovered that prosthetics were a helpful tool—but not essential for her to live a full, capable life. Now a devoted parent, Katie opens up about raising her son, who has Witteveen Colk syndrome, a rare genetic disorder. She shares her journey through early intervention services, advocating for genetic testing, and ensuring her child receives the support he needs. Her advice to parents? Trust your instincts, push for answers, and never hesitate to speak up for your child.

By |2025-04-09T21:07:09-07:00February 22nd, 2023|Limb Difference Stories, Podcast, Upper Limb Amputees|0 Comments

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