About The Cam foundation
The CAM Foundation was founded by the friends and family of Cameron Hyman soon after she was diagnosed with Sanfilippo Syndrome in July of 2018.
Sanfilippo Syndrome Facts:
- Sanfilippo Syndrome is also known as mucopolysaccharidosis type III.
- Sanfilippo is a rare genetic condition that affect several body systems.
- Symptoms begin in early childhood and worsen with time.
- Children often don't survive past their teen years.
- There is currently no approved cure or treatment for Sanfilippo Syndrome...that's where we all come in.
Cameron and Family Featured on NBC's "George to the Rescue"
Premiered April 5, 2020
"Cameron's Law"
Bi-Partisan legislation introduced by Congressman Gottheimer in support of rare disease research https://www.congress.gov/bill/118th-congress/house-bill/1350