In 2015 we went out with F.A.S.T to create a series of filming highlighting the complex diagnosis of Angelman Syndrome. You can view the project here. Five years on we revisited the families plus a whole lot more to understand what changes have happened, what new support there is and how far the science has […]
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Raising awareness of a rare disease
The Foundation was founded by parents of Angels, a term for to people with Angelman Syndrome, a condition discovered by Dr. Harry Angelman. They have been on a quest to find therapeutics to help support families with Angels. Angelman Syndrome (often abbreviated AS) is a severe neurological disorder characterized by profound developmental delays, problems with […]
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