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
What happens when you survive COVID… but wake up to a completely different life? In this powerful episode of We’re Not Stumped, host Mike Bolland sits down with Brianna Heitzman, a certified employment specialist with Down Syndrome of Louisville, whose life was forever changed after a severe battle with COVID-19. After being placed on a ventilator and ECMO, Brianna faced an unimaginable outcome—the loss of her legs. But her story doesn’t end there. This is a conversation about resilience, identity, and rebuilding a life with purpose. Brianna’s journey is raw, real, and deeply inspiring—a reminder that even after life-changing trauma, there is still a path forward.
What happens when a story about limb loss hits the news—and suddenly everyone you know is texting you about it? If you’re part of the limb loss community, you already know. In this solo episode of We’re Not Stumped, host Mike Bolland dives into the experience of being “the limb loss friend”—the person others turn to when they don’t fully understand what they’re seeing but want to connect.
Stacy and Courtney Walker are proving that teamwork knows no limits. As the only known mother-daughter duo in wheelchair power soccer, they proudly represent Arizona Heat Power Soccer—competing, training, and pushing boundaries together on and off the court. Their journey is about more than just the game. It’s about resilience, family, and the power of adaptive sports to change lives. On this episode of We’re Not Stumped, host Mike Bolland sits down with Stacy and Courtney to share their story—how they got involved in power soccer, what it’s like competing side by side, and what being part of Arizona Heat Power Soccer truly means. Now, they’re working toward their next big goal: competing at Power Soccer Nationals.
Leave A Comment