Help us Find a Cure for
Angelman Syndrome
Welcome to the Foundation for Angelman Syndrome Therapeutics UK.
We have one goal: to cure Angelman Syndrome.
What is Angelman Syndrome?
Drug Development Pipline
It’s our job to push forward all promising Angelman syndrome (AS) programs, and to ensure that the community has a birds-eye view of the entire landscape.
Meet Bella...
Has your loved one been newly diagnosed with Angelman Syndrome?
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The Latest at FAST UK
Alton Towers IAD Weekend 2026 – Celebrating 13 Years!
The 2026 Alton Towers event for International Angelman Day marked an incredible 13 years of bringing families together for a weekend of fun, connection, and celebration!
Supporting FAST UK and raising awareness of Angelman Syndrome – our journey so far… by Sarah Washbrook
So where did it all begin? I knew very early on that something was unique about Ivor. I waved my hands, but people said I was fussing; he’s just a boy. I suppose this is when the grieving started for me, the fear, the worries.
A Working Mum and Carer, one year in…
My life took an unexpected turn when my 4-year-old son, Ivor, was diagnosed with Angelman Syndrome just after his third birthday.
International Angelman Day 2026 – Alton Towers Weekend
To everyone who helped make this year’s International Angelman Day Alton Towers weekend possible, thank you.
FAST Global Search & Rescue Initiative Joins the Global Angelman Syndrome Registry
A Unified Effort to Connect Families, Accelerate Research, and Find a Cure for Angelman Syndrome
International Angelman Day @ Alton Towers
February 15th 2023, marks the 10 year anniversary of International Angelman Day, It is also the tenth year that an Angelman group, created by an Angelman mum, Linda Holmes, took place at their usual venue Alton Towers.
Supporting FAST UK and raising awareness of Angelman Syndrome – our journey so far… by Sarah Washbrook
So where did it all begin? I knew very early on that something was unique about Ivor. I waved my hands, but people said I was fussing; he’s just a boy. I suppose this is when the grieving started for me, the fear, the worries.
Fundraising News
Ivor’s Splashathon raises £1,926 for FAST UK
Paul completes the Sydney Marathon for FAST UK
Team FAST UK conquers Tough Mudder Yorkshire for Angelman Syndrome research
Scientific Updates
Ionis shares update on CHAMPION Phase 3 clinical trial
Oak Hill Bio has shared a community letter to the Angelman syndrome community
Ionis shares update on CHAMPION Phase 3 clinical trial
Oak Hill Bio has shared a community letter to the Angelman syndrome community
FAST Global
This website is operated by FAST UK, an independent entity organised and existing under the laws of (England and Wales). While FAST UK uses the branding of the Foundation for Angelman Syndrome Therapeutics, FAST UK is a separate and distinct entity, operating under its own governance.
At FAST UK, we’re dedicated to keeping our community informed about advancements in Angelman syndrome treatments. We’ve provided a link to the global FAST site, where you can explore an up to date overview of the drug development pipeline. This resource highlights the progress of various programs, some of which are supported by FAST and others disclosed by external organisations.
Click below to gain insight into the promising developments bringing us closer to effective treatments and, ultimately, a cure.
Prof Art Beaudet
There are many disorders that will not be cured or treated in our lifetime, but Angelman Syndrome will not be one of them.