Please Join Us for the 2024 Cocktail Party on 2/15/24
Learn about our mission and how you can help!
Learn about our mission and how you can help!
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.
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.
We formed The CAM (Cameron Against MPS) Foundation to:
Your generous donation will fund our mission. We are a 501(c)(3) tax exempt organization. EIN: 83-2153782
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