Patient and Family Resources

Every year, 15,000 individuals in the United States face the fear and uncertainty that comes with a new sarcoma diagnosis. For these patients and their loved ones, the Sarcoma Alliance is a crucial source of guidance, education, and support. We provide accurate, clear information during those difficult initial days following diagnosis, second opinion grants to help access quality care, and offer emotional support throughout the journey.

Patient care initiatives include: hosting in-person and online support groups; grants for second opinions from sarcoma specialists; providing the latest in sarcoma news through e-communications; sharing customized information about sarcoma subtypes, treatment guidelines, and clinical trials; engaging the sarcoma community in advocacy opportunities; and offering one-to-one healthcare navigation to help patients access social and financial services.