Episode 10: Kelsey

Episode 11: Des

Des is a patient living with diffuse TGCT of the knee who was originally from Singapore before relocating to the United Kingdom. In this episode, Des shares his personal journey navigating two very different healthcare systems and reflects on the lessons he learned along the way. He speaks candidly about the challenges of living with a rare disease, the importance of persistence, representation of all patients, and how self-advocacy became a powerful tool in shaping his care. Des’s story offers encouragement to others facing similar obstacles and reminding listeners that finding your voice can make a meaningful difference in your journey.

Episode 10: Kelsey

Meet Kelsey, a TGCT warrior from Canada who’s keeping it real about life with a localized TGCT of the knee diagnosis that didn’t go quite as expected. In this episode, she opens up about the shock of diagnosis, the anxiety that followed, and what it’s like when recovery takes longer than expected. Kelsey also shares the practical (and honest!) ways she navigated the ups and downs, including her go-to tips for protecting your mental health during recovery. Whether you’re newly diagnosed or somewhere along the journey, this episode is a mix of real talk, reassurance, and helpful takeaways you won’t want to miss.

Episode 9: Arthur

Meet Arthur, a patient living with diffuse TGCT of the knee and a passionate advocate as the Lead Representative of TGCT Support France. In this episode, he shares his journey and dives into the power of self-advocacy, showing how patients can take an active role in their care. From navigating the healthcare system in France to speaking up and being heard, Arthur offers insight, encouragement, and practical advice for anyone looking to feel more empowered in their own health journey.

Episode 8: Patrick

Meet Patrick, a patient living with diffuse TGCT of the elbow, who brings a thoughtful and honest perspective to this episode. He shares how he was diagnosed and how growing awareness around TGCT played a key role in his journey, even helping him choose the right doctor. Patrick has never had surgery which speaks to the evolution of treatment in TGCT. Patrick also opens up about navigating treatment decisions while building a growing family, including how he approached conversations around systemic therapies. It’s a candid discussion about balancing health, family, and the big decisions that come along the way.

Episode 7: RaSheeda

RaSheeda lives with diffuse TGCT of the knee and was diagnosed in the late 2000s, a time when treatment options were limited and the condition was often poorly understood. In 2021, she re-experienced symptoms and it was time to revisit this pesky disease. In this episode, she reflects on how the care landscape has evolved over the years, transforming what once felt like a life defined by recurrence and uncertainty into one with expanding possibilities. With access to newer therapies and more specialized care, RaSheeda was able to pursue higher education and reimagine her future. Her story highlights not only the personal impact of medical progress, but also how advances in awareness, research, and treatment can restore agency and long-term planning for people living with rare disease.