1.6K views · 31 reactions | If you recently received a diagnosis of Angelman syndrome, the ASF and our network of Angelman families are here for you at every step of your journey. Complete the ASF Contact Registry to receive information and get connected. More info here: www.angelman.org/for-parents/newly-diagnosed | Angelman Syndrome Foundation | Facebook

332 reactions · 128 shares | The Angelman Syndrome Foundation is committed to supporting every individual, every step of the way. Introducing AS Grows Up: a movement dedicated to ensuring adults with Angelman syndrome have the resources they need to thrive. Growing up doesn’t mean growing out of support. It’s time to talk about what comes next. #angelmansyndrome #angelmansyndromefoundation #angelmanresources #angelman | Angelman Syndrome Foundation | Facebook

24K views · 654 reactions | The first few steps for individuals with Angelman syndrome are a significant milestone in life. Today, take YOUR symbolic first step for people with AS by registering for the 2017 ASF Walk today at www.angelman.org/walk. | Angelman Syndrome Foundation | Facebook

11K views · 110 reactions | Angelman syndrome is a rare disorder that affects chromosome 15, resulting in intellectual and developmental delay. Common signs and symptoms usually appear in early childhood but despite these symptoms, people with Angelman syndrome have an overall happy and excitable demeanor. #InternationalAngelmanDay #angelmanday2024 | Angelman Syndrome Foundation | Facebook