Foundation for Angelman Syndrome Therapeutics

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FAST is the premier patient advocacy organization working to cure Angelman syndrome. As the largest funder of Angelman syndrome research in the world, our goal is to drive forward transformative research and development programs as quickly as possible for those living with Angelman syndrome regardless of age or genotype.

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2008

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Address: PO BOX 40307, AUSTINWeb: Sign in to see organisation websiteEmployees: 9Volunteers: 291Revenue: 6525815ICO: 263160079

Angelman Syndrome Research and Advocacy For Researchers For Industry For Families Caregivers For Donors Welcome to the Foundation for Angelman Syndrome Therapeutics We have one goal to cure Angelman syndrome. Register Today. Angelman Syndrome Congressional Advocacy Day March 45th in Washington DC For Families Caregivers Learn More For Researchers Learn More For Industry Learn More For Donors Learn More Not sure where to go. Start Here What is Angelman Syndrome.

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Catherine

1. How can families and caregivers effectively advocate for increased funding and research into treatments for Angelman syndrome at events like the Congressional Advocacy Day?

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Veronica

2. What role do biotech companies play in the advancement of gene-targeted therapies for Angelman syndrome, and how can we foster collaboration between researchers and industry partners?

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Ray

So inspired by the incredible work FAST is doing to raise awareness for Angelman Syndrome! Together, we can make a difference and pave the way for a cure! πŸ’™βœ¨

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Daniel

I can't wait for the Angelman Syndrome Congressional Advocacy Day! It's so important to advocate for our loved ones and push for advancements in research! Let’s come together! πŸ’ͺ #HopeForAS

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AUSTIN

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