Rare Disease Day
February 28People around the world work to advocate and raise awareness for those living with rare diseases, like Angelman syndrome.
More infoThroughout the year, the Angelman Syndrome Foundation hosts, participates in and receives support from events across the country. Below find a list of upcoming events.
See Fundraising for ASF for information on hosting an event in your area.
People around the world work to advocate and raise awareness for those living with rare diseases, like Angelman syndrome.
More infoThe Angelman Syndrome Foundation and 50 Angelman organizations around the globe work to spread the word about what AS is and how it affects our children! Find out how to get involved.
More infoEvery other year the ASF holds the Family Conference to gather families, care providers, therapists, teachers, scientists, researchers and doctors under one roof to learn and discuss the latest information on Angelman syndrome.
More infoWith cash prizes, raffle items, food and fun for all, it's an event you won't want to miss.
More infoJoin the Windy City Angels running in the Bank of America Chicago Marathon!
More infoEvery other year the ASF holds the Family Conference to gather families, care providers, therapists, teachers, scientists, researchers and doctors under one roof to learn and discuss the latest information on Angelman syndrome.
More infoThe annual research symposium is a chance for leading researchers, scientists and doctors to discuss the latest research in the world of AS. The first day is focused on a specific topic with 5-8 presenters. This day is a unique opportunity for researchers to present their latest findings of their works and compare notes with colleagues from around the globe. The second day includes short presentations on all areas of AS.
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