Angelman Syndrome Foundation
Chloe G. Knouff serves as a Community Engagement Coordinator at the Angelman Syndrome Foundation. In addition, Chloe is a Content Curator at Rare Sibling Stories and the Owner of Wild Angles Creative. With experience as a Subcontractor in Philanthropic Fundraising and as a Board Member at the Foundation for Angelman Syndrome Therapeutics, Chloe brings a diverse background in marketing, fundraising, and community engagement. Graduating with a Bachelor's Degree in Marketing and Human Resources from the University of South Carolina, Chloe has a strong foundation in both business and social impact initiatives.
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Angelman Syndrome Foundation
Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births. AS is often misdiagnosed as cerebral palsy or autism due to lack of awareness. Characteristics of the disorder include developmental delay, lack of speech, seizures, and walking and balance disorders. Individuals with Angelman syndrome will require life-long care. Because of its genetic relationship to autism and other disorders, many researchers believe that curing Angelman syndrome will lead to cures for similar disorders. Angelman syndrome research is on the cusp of potential treatments to reverse the debilitating symptoms of Angelman syndrome. The Angelman Syndrome Foundation raises funds for Angelman syndrome research and supports families. Use this website to keep abreast of current information regarding research, education, general information and therapies for Angelman syndrome. If you have any questions or would like additional information please email the ASF at info@angelman.org.