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SARC’s mission is to connect individuals and organizations from around the world committed to discovering, developing, and delivering the latest and most promising treatments for sarcoma.
The sarcoma research, clinical, and patient communities are geographically scattered and under-resourced. It is essential to share scientific knowledge and advance research for improved treatments to defeat sarcoma.
Simply put, SARC drives high-impact, centrally-supported collaborations amongst the sarcoma research community.
Sarcomas are cancers of the bony skeleton (the skull, vertebrae, ribs, and extremities), and also the muscle and other tissues attached to, supporting, or joining those bones.
It is often thought that clinical trials are a last resort, but they may in fact be a good way to begin your treatment and receive excellent care from the very start.
“I got involved [in patient advocacy] because I’ve been passionate about cancer research ever since I was diagnosed with cancer when I was 11-years old. So now as a 12-year survivor the SARC Research Advocacy Council really allows me to do a few things. 1. It allows me to give back to a cause that is important; 2. It allows me to develop my skills as a psycho-oncology researcher; and 3. It allows me to fill a need for patient advocates.”
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