FAST Global: Cure Angelman Now Fundraising Efforts
From a 1,100km run across Australia to festivals in Paris and golf in Canada, FAST families worldwide raised hundreds of thousands for Angelman syndrome research this season.
FAST Speaks at the 2025 MENA Congress for Rare Diseases
FAST representatives Amelia Beatty and Ellen Koekoeckx presented at the MENA Congress for Rare Diseases in Abu Dhabi, highlighting the Angelman syndrome therapeutic pipeline and connecting with regional families and researchers.