We are a volunteer-led charity based in the UK, our trustees are all parents or siblings of someone with Angelman Syndrome. We support people with AS and their families, as well as professionals and carers from the point of diagnosis and throughout their lives. We educate and raise awareness of Angelman Syndrome and the issues that surround it through delivering conferences and educational events to parents & professionals. We work with many organisations and researchers in the field of Angelman Syndrome to broaden our knowledge of the condition and improve our understanding of potential future therapeutics.