Join us on Tuesday Night to Address Care to Treat Chondrosarcoma

The Chondrosarcoma Foundation is developing a Patient / Family/ Caregiver Advisory Board in the effort to create a voice for chondrosarcoma patient’s and caretakers to address concerns and advocate for effective treatment and quality care.

The advisory board will serve to give those afflicted with this rare disease an opportunity to share their personal journeys, provide their point of view and insight into research, clinical trials; treatment and address related policies and procedures that effect their medical decisions and contribute to better care and solutions towards treatment. Bottom-line is we want to have CS Warriors, Family members and Caregivers have a seat at the table, provide their input and insight to decision makers where many decisions have been made about their care without them. This is an opportunity for the CS Community to come together and collectively share our views, include our voice in improving research, clinical trials and interventions / treatment of Chondrosarcoma.

Our first meeting will take place on this Tuesday night, March 7 at 7:30PM (EST / New York Time) via Zoom. If you would like to join us, please e-mail me at