Pediatric Arachnoid Cyst Foundation

Posted on March 31, 2014 by - Entry

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I created this foundation in honor of my son who was diagnosed with an Arachnoid Cyst. The Arachnoid Cyst had grown by 30% from the age of 3 when we first found out about it and Ethan had brain surgery within 2 weeks. PACF was founded through the frustration of the lack of research, funding, and connection for families with children who have this diagnosis. PACF is now impacting families and connecting them on Facebook and Twitter. Our board has many goals to impact through research.