Please Join Us for the 2023 Cocktail Party on 2/16/23
Currently, there are no approved cures or treatments for Sanfilippo Syndrome. With that said, clinical trials are underway and are closer than ever to a viable solution. These trials, and trials that will occur in the future, have been and will be funded on the heels of groups like The CAM Foundation. We are committed to supporting these efforts.
The day a family learns of a Sanfilippo diagnosis is devastating. The challenges that lie ahead are countless. Among those often come unexpected expenses (travel, medical, home remediation, etc). The CAM Foundation is committed to providing financial support to families battling Sanfilippo Syndrome.
Like many rare diseases, Sanfilippo Syndrome is far from many peoples' radar. The CAM Foundation is committed to educating others about the realities of Sanfilippo Syndrome and inspiring them to get involved in the fight.