Home - Cure Angelman Syndrome
1167984
2016
SW6 6NS
cureangelman.org.uk
fastunitedkingdom
Foundation for Angelman Syndrome Therapeutics UK
The Foundation for Angelman Syndrome Therapeutics UK (FAST UK) is a registered UK charity (charity number 1167984) dedicated to advancing research and raising awareness for Angelman syndrome, a rare genetic neurological disorder characterized by severe developmental delay, speech impairment, and problems with movement and balance. The foundation's primary goal is to find a cure for Angelman syndrome by supporting scientific research and fostering collaboration among experts.
Mission and Activities
FAST UK focuses on funding and promoting research aimed at understanding Angelman syndrome and developing effective therapies. The charity has established a clear research agenda and assembled a multidisciplinary team of over two dozen scientists from leading universities and pharmaceutical companies to work toward a cure. The organization operates exclusively within the UK but collaborates closely with international counterparts in the United States, Australia, Canada, Italy, and France to maximize research impact.
Fundraising and Financial Information
The foundation raises funds primarily through donations and fundraising activities. For the financial year ending 31 December 2023, FAST UK reported a total income of £267,648, with expenditures amounting to £13,076. All trustee roles are voluntary, with no remuneration or benefits paid to any trustees.
Governance
FAST UK is governed by a board of six trustees who oversee the charity's operations, ensuring transparency and alignment with its mission. The charity does not have subsidiaries and employs no staff earning over £60,000, reflecting its focused and lean organizational structure.
Collaboration and Impact
By uniting researchers, healthcare professionals, families, and advocates, FAST UK plays a crucial role in driving progress toward innovative treatments for Angelman syndrome. The foundation's commitment to collaboration and scientific excellence contributes significantly to the global effort to improve the lives of individuals affected by this condition.
This article summarizes publicly available information on the Foundation for Angelman Syndrome Therapeutics UK as of 2025.
[1] https://cureangelman.org.uk [2] https://register-of-charities.charitycommission.gov.uk/charity-details/?regid=1167984&subid=0 [3] https://www.angelmanuk.org [4] https://cureangelman.org [5] https://www.angelmanuk.org/fundraising-events/
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Novinky
📢 Webinar Reminder: Navigating Angelman Syndrome in Clinical Practice Join us this evening with a session organised by FAST in collaboration with ERN-ITHACA at 4:00–5:30 PM BST. This free webinar will explore the genotype-phenotype correlation in Angelman syndrome and related medical conditions, providing valuable insights for both professionals and families. Featuring expert speakers: Dr. Karen Bindels-de Heus (Erasmus MC, Rotterdam) Dr. Ana Roche (Parc Taulí, Barcelona) Register and find the full programme here: https://events.teams.microsoft.com/event/6ada80bc-997b-49b0-b196-835ee16db8f5@2461c129-d44f-406d-a778-d1a3c4c1527c We’re pleased to share this with our UK community 💙 #AngelmanSyndrome #fastuk #ERNITHACA #RareDisease #AngelmanAwareness #FASTGlobal #CureAngelman (fb)
MavriX Bio, a clinical-stage biotechnology company focused on the development of transformative genetic therapies for Angelman syndrome (AS), today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for MVX-220, an investigational adeno-associated virus (AAV) gene therapy for the treatment of AS. Read the press release & FAQs: https://buff.ly/lXTh19C MavriX Bio will host a webinar in the coming months to provide additional details regarding the clinical trial design, eligibility criteria, and expected timelines. (fb)
Poslední komentáře
What a wonderful initiative! 💙 It's so inspiring to see everyone working together towards finding a cure for Angelman Syndrome. Keeping Bella and all those affected in my thoughts! 🙏 #CureAngelmandetail |
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Thank you for raising awareness about Angelman Syndrome! Every little contribution counts and together, we can make a difference for those who need our support the most. Let’s keep fighting for a brighter future! 🌟 #FASTUK #AngelmanAwarenessdetail |
Poslední diskuze
What are some innovative therapies or research breakthroughs that could potentially lead to a cure for Angelman Syndrome?Odpovědí: 3, Naposledy před 1 den detail |
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How can caregivers of individuals with Angelman Syndrome collaborate to share their experiences and support one another in their journeys?Odpovědí: 3, Naposledy před 1 den detail |
V okolí
4.5
SW6 6NS
O společnosti
- B80, H99, G30 -
Home Help us Find a Cure for Angelman Syndrome Welcome to the Foundation for Angelman Syndrome Therapeutics. We have one goal to cure Angelman Syndrome. Are you a caregiver for someone with Angelman syndrome. Your experiences are invaluable and we want to hear from you.
Služby a organizace pro studenty Ostatní lékařský výzkum j. n. (jiné než specifikované) Rakovina