Words shape how the world sees people with Angelman syndrome and how they see themselves. When we choose people-first language, we honor individuals for who they are, not a diagnosis. Behind every word is a person with personality, family, likes/dislikes, and a whole life being lived. ✨ Words matter. Choose them carefully. #angelmansyndrome #angelmansyndromefoundation #angelman #AngelmanStrong #StrengthInCommunity #WordsMatter #PeopleFirst #inclusionmatters | Angelman Syndrome Foundation

There’s something truly special about walking into a space where you don’t have to explain—because everyone just gets it. 💙 The ASF Family Conference is more than sessions and speakers. It’s hugs in the hallway, kids finding instant friends, siblings feeling seen, and families realizing they can relax and be their authentic selves. ✨ What to expect: • 1,300 attendees • 200 individuals with Angelman syndrome • 450 siblings • 250 researchers, clinicians & industry partners • 50 speakers over 30 s

Celebrate International Angelman Day with FAST! Around the world, families, researchers, advocates, and partners are raising awareness of Angelman syndrome and pushing research forward. This day reflects the strength of a global community united by progress, persistence, and shared purpose. Thank you to our global partners and affiliates for showing up and helping make Angelman syndrome visible today and every day. If you’re able, consider making a donation to support the research moving this fi