ANGELMAN SYNDROME FOUNDATION INC

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Angelman Syndrome Foundation advances the awareness and treatment of Angelman Syndrome through education, information, research and support. The Angelman Syndrome Foundation works to advance the awareness and treatment of Angelman Syndrome t Our mission is to advance the awareness and treatment of Angelman Syndrome through education and information, research, advocacy, Β and support for individuals with Angelman Syndrome, their families, and other concerned parties.

Founded

1992

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Address: 3015 E New York St #A2-285, AuroraWeb: Sign in to see organisation websiteFacebook: AngelmanSyndromeFoundationX (Twitter): angelmanEmployees: 6Volunteers: 2500Revenue: 3638325ICO: 593092842

Angelman Syndrome Foundation – With you for the journey With you for the journey Families. Research. Clinics. Communities.

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Deborah

🌟 Can't wait for the community event on May 17th! It's such a wonderful opportunity to connect with others and celebrate the amazing individuals living with Angelman Syndrome. Let's make a difference together! #ASFCommunity

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ANGELMAN SYNDROME FOUNDATION INC

May is Mental Health Awareness Month 🌿 For some families, behavior and anxiety challenges can be an everyday part of life with Angelman syndrome. Check our website to find resources that can help you navigate these struggles. πŸ‘‰ www.

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Matthew

2. What are some emerging research areas that hold promise for potential treatments for Angelman Syndrome, and how can the Angelman Syndrome Foundation facilitate these advancements?

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Benjamin

1. How can community events, like the Angelman Strong walks, help increase awareness and support for families affected by Angelman Syndrome?

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Margaret

❀️ So grateful for the Angelman Syndrome Foundation and everything they do to support families like mine. Together, we can raise awareness and bring hope! #AngelmanStrong

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ANGELMAN SYNDROME FOUNDATION INC

πŸ’₯ Thanks to the Pritzker family and their generous match, every dollar you give in May for Angelman Strong, will be matched for Angelman syndrome research up to $150,000. We're already at $135,000. Let’s keep the momentum going.

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