COALITION TO CURE CHD2 INC
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Mission Statement
Coalition to Cure CHD2 is fueled by our desire to help children and adults with CHD2-related disorders. Our mission is to improve the lives of those affected by CHD2-related disorders by funding research necessary to uncover a cure.
About This Cause
CHD2 is a gene located on the 15th chromosome at 15.q26.1. A mutation in the CHD2 gene can cause epilepsy and/or autism. CHD2-related disorders are rare and likely affect only 1% of children with developmental and epileptic encephalopathy. The Coalition to Cure CHD2 (CCC) was founded in 2020 by parents of people with a CHD2-related disorder who joined forces to form the first patient-advocacy group focused on finding a cure for CHD2-related disorders. In addition to an Executive Director and active Board of Directors, we have a Scientific Advisory Board consisting of medical professionals working in the epilepsy field who advise our organization on how best to find safe and effective treatments that may cure CHD2-related disorders.