We’re Not Stumped Amputee Podcast Season 2 Episode 7 Hillary Sussman, Author of Adventures of Roxy

Hillary has been a physical therapist for over 24 years in the Philadelphia area, working primarily in the home care setting with the geriatric population. She was inspired to write a story to help young children overcome their fears and insecurities surrounding differences; and to live life with confidence. That story became a series of books, The Adventures of Roxy.

Her first book, Roxy and Maliboo, It’s Okay to Be Different, is a story about two lovable dogs with unique features who teach the important lessons of limb difference awareness, inclusion, kindness, and acceptance. In her newest book, Roxy and Tully, Words Matter, Roxy teaches new lessons and raises awareness about prosthetics, how to handle bullying, the importance of word choices, and how they impact others.

Hillary plans to continue writing additional books in the Adventures of Roxy series where Roxy learns something new in each book, meets new friends, and teaches life lessons as she faces new challenges. She also providing programs to schools and organizations to help spread Roxy’s important messages.

Links:

Website: https://www.adventuresofroxy.com/

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

Facebook: https://www.facebook.com/adventuresofroxyroo

Linkedin: https://www.linkedin.com/in/hillary-sussman-65056b101/

Palmetto Publishing: https://www.palmettopublishing.com/

#limbloss #limbdifference #amputee #antibully #antibullying

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  • 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 |2023-09-12T18:03:25-07:00April 22nd, 2023|Podcast|0 Comments

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