THANKS TO EVERYONE WHO MADE THE KICKOFF PARTY A SUCCESS ON 2/27/20
Join the Fight Against MPS IIIa (Sanfilippo Syndrome)
Join the Fight Against MPS IIIa (Sanfilippo Syndrome)
Join the Fight Against MPS IIIa (Sanfilippo Syndrome)Join the Fight Against MPS IIIa (Sanfilippo Syndrome)Join the Fight Against MPS IIIa (Sanfilippo Syndrome)Learn about our mission and how you can help!
Join the Fight Against MPS IIIa (Sanfilippo Syndrome)
Join the Fight Against MPS IIIa (Sanfilippo Syndrome)
Join the Fight Against MPS IIIa (Sanfilippo Syndrome)Join the Fight Against MPS IIIa (Sanfilippo Syndrome)Join the Fight Against MPS IIIa (Sanfilippo Syndrome)Learn about our mission and how you can help!
About Us
Our Team
Our History
Our History
Our team is made up of the family, friends, and community members that love Cameron. Together, we take that love and turn it into energy toward finding a cure for Sanfilippo Syndrome.
Our History
Our History
Our History
Cameron Hyman was diagnosed with Sanfilippo Syndrome in July of 2018. Immediately, her friends and family reached out and offered anything and everything that they could. When the dust settled, Rob and Christina (parents) vowed to work with the team to give back to this often-underfunded cause.
Our Goals
Our History
Our Goals
We formed The CAM (Cameron Against MPS) Foundation to:
- Help fund ongoing research
- Support families with Sanfilippo Syndrome
- Spread the word about Sanfilippo Syndrome
Help Our Cause
Your generous donation will fund our mission. We are a 501(c)(3) tax exempt organization. EIN: 83-2153782
Stay in Touch
Sign up to hear from us regarding upcoming events and Sanfilippo updates
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