We’re Not Stumped Podcast – Kara Skrubis, Osteosarcoma Cancer Survivor & Above Knee Amputee S3 E10

Since the age of three, Kara Skrubis has practiced ballet. Throughout her youth, she traveled the nation, showcasing her ballet prowess. Alongside her performances, she commenced teaching ballet and started her studies as a dance major at University at Buffalo.

However, her trajectory took an unforeseen twist during her inaugural semester at UB. In October 2019, Skrubis awoke to excruciating pain in her left knee, soon accompanied by a concerning “warm lump.” Despite a visit to a local urgent care facility, the ailment remained undiagnosed. It wasn’t until three months later, under the care of an orthopedic specialist, that a tumor was discovered in her left tibia.

At 18 years old, Skrubis received the diagnosis of osteosarcoma, a rare form of bone cancer predominantly affecting teenagers and young adults. While receiving treatment, Skrubis was compelled to take a time off from her studies for a year. Her journey started with chemotherapy in February 2020, followed by the amputation of her left leg in April 2020 to eradicate the cancer. Subsequently, she underwent immunotherapy until June 2021, concluding her treatment regimen with chemotherapy in September 2021.

During her stay in the hospital, Skrubis says her mother, Lisa, 54, found and connected with MIB Agents, a pediatric osteosarcoma nonprofit that provides resources, information and support to patients and families.

Skrubis still practices ballet, but she changed her majors from dance and psychology to psychology and health and human sciences so she can work with other youth diagnosed with cancer.

Links:

MIB Agents: https://www.mibagents.org

People Magazine Article: https://people.com/health/kara-skrubis-talks-continuing-ballet-following-bone-cancer-leg-amputation-i-never-gave-up/

#amputee #amputeelife #amputeestrong #prosthetics #prostheticleg #amputeegirl #amplife #amputation #limbloss #amputees #adaptiveathlete #amputeefitness #prosthetic #motivation #prosthesis #adaptive #oneleg #amputados #amputeewoman #inspiration #osteosarcoma #cancer #sarcoma #bonecancer #cancersucks #childhoodcancer #cancersurvivor #osteosarcomaawareness #childhoodcancerawareness #cancerawareness #cancerfighter #pediatriccancer #bonetumor

Listen on Apple Podcasts

Watch on YouTube

Listen on Spotify

  • Stephanie W. Cawthon Disability is Human

May 27th, 2025|

What does it truly mean to be seen as fully human in a world that often overlooks disability? In this thought-provoking episode of We’re Not Stumped, host Mike Bolland welcomes back Dr. Stephanie W. Cawthon—an acclaimed deaf author, speaker, and researcher—for an honest and insightful conversation about identity, accessibility, and belonging. With ASL interpreters Amanda Ford and Steven Nugent joining, Dr. Cawthon shares the personal and cultural impact of her book Disability is Human, a work that has deeply influenced Mike’s own journey.

  • limb loss differences congenital and adult amputation

May 22nd, 2025|

What’s the difference between being born with a limb difference and losing a limb later in life? In this episode of We’re Not Stumped, host Mike Bolland (born without a right hand) breaks down the emotional, physical, and social differences between congenital limb loss and adult amputation—two very different starting points that often lead to the same powerful resilience. Mike shares personal experiences, insights from recent guest interviews like Stevia Walker (who became an amputee in 2023), and stories from others who’ve learned to adapt and thrive no matter how their journey began. Whether you’ve lived with a limb difference your whole life, recently became an amputee, or support someone who has—this episode is for you.

  • Jessica Frew Speaks Out: Fashion, Film, and Fighting for Disability Rights

May 20th, 2025|

What does it mean to truly be heard when you can’t speak? Jessica Frew, a nonverbal actress, model, and passionate disability advocate, joins We’re Not Stumped to share her powerful story of living with cerebral palsy and using an eye gaze device to communicate—a technology she began using at just nine years old. While Jess initially limited the device to school and close friends, she opens up about the emotional weight of using it publicly and the deeply personal regret of not speaking to her father through it before he passed away. Over time, Jess found strength in her voice and now uses it to educate, advocate, and challenge misconceptions about nonverbal individuals. She speaks with host Mike Bolland about the common experience of being talked down to or ignored—and how she responds with patience, courage, and relentless advocacy.

Share This Story, Choose Your Platform!

Leave A Comment

Go to Top