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On the first Synovial Sarcoma Day, hear from families, patients and specialists about why we urgently need more research into this rare cancer. Each year in England, 79 people are diagnosed with synovial sarcoma. Behind this number are countless stories of delayed diagnoses, challenging treatments, and families facing difficult journeys. In this video, Kate shares her daughter Amber's story of being misdiagnosed for 12 months, James talks about mistaking his symptoms for a sports injury, and other families speak openly about their experiences. The Synovial Sarcoma Fund aims to change the future for people affected by this rare cancer. With only 50% of people surviving five years or more after diagnosis, we need better treatments and earlier diagnoses. As Kate Quillen, Research Manager at Sarcoma UK explains, there are promising developments worldwide - but funding remains a barrier. Join us in supporting vital research into synovial sarcoma. To donate or learn more about the Synovial Sarcoma Fund: sarcoma.org.uk/ssf