- Provides support via 24 hour telephone support line
- Updated information on AS
- Regional meetings are held in different locations throughout the year
- Maintains links with similar AS organisations overseas
- Provides an information pack for doctors to give families of those newly diagnosed with AS
- Produces a national register of families indicating those willing to be a point of contact for families of those newly diagnosed with AS
- Funds research into Angleman syndrome.
PO Box 4962