Limb Care Foundation: Advancing Limb Health Through Education, Advocacy & Outreach

In this episode of the We’re not Stumped podcast, I have the honor of speaking with all four executive members of the Limb Care Foundation. The mission of Limb Care Foundation is to promote multidisciplinary approaches to limb salvage, function, and patient quality of life through relevant & meaningful education, advocacy, and outreach. The Limb Care Foundation and their executive members are driven by a desire to provide preventive limb care to those in need and educate the future generation of health care providers on the importance of limb health.

They are a DMEPOS (Durable Medical Equipment, Prosthetics/Orthotics & Supplies) donation center. They will collect your unused or gently used medical equipment and get it in the hands of someone in desperate need. See their website linked below for more information. They also aid the homeless. The Limb Care Foundation is dedicated to reaching out to homeless communities and providing them with much needed medical equipment and supplies that help to promote limb health and awareness. This population is very susceptible to amputations that could largely be avoided with proper care and preventative measures.

Executive Board:
Laduan Smedley, Jr., CPO – President, Co-Founder
Aarron Flowers DPM, AACFAS – Vice President, Co-Founder
Brandon U. Edenedo, PT, DPT – Treasurer, Co-Founder
Quincy Amarikwa, 13 Year MLS/USL Pro – Secretary, Co-Founder

Limb Care Website: https://limbcarefoundation.org
Facebook: https://www.facebook.com/LimbCareFoundation
Instagram: https://www.instagram.com/limbcarefoundation/

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 |2025-04-09T20:56:13-07:00December 12th, 2022|General Disability Related Resources and News, Podcast|0 Comments

Share This Story, Choose Your Platform!

Go to Top