Support group for people with Angelman syndrome and their families

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Services provided:

  • 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
CV11 9FD

Helpline number: 0300 999 0102

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