FAST What to Know
Now available: Check out the 2024 Global Science Summit schedule!

We are pleased to announce that the schedule for our 2024 Global Science Summit Schedule is now available. We are looking forward to the impressive lineup of speakers who will provide updates on Angelman syndrome research, clinical trials, and more! Be sure to also check out the community events sprinkled throughout the weekend.


Check out the schedule now:

View the schedule
FAST's Roadmap to a Cure 2.0: Learn more about Pillar 1

As we gear up for the upcoming FAST Global Science Summit, we would like to take a moment to revisit the four Pillars that form the foundation of FAST’s Roadmap to a Cure 2.0. We will review each Pillar, the progress shared during last year’s Summit, and the exciting new developments to look forward to at this year’s event. 


Learn more about Pillar 1:

Learn more
Niki Armstrong, VP of Genetic Services & Education, now offering Full genetic counseling services in all 50 US States

Niki Armstrong, VP of Genetic Services & Education, is now a “coast-to-coast" genetic counselor, able to provide genetic counseling services to the Angelman syndrome community in all 50 US states. 

 

Niki can help you understand your loved one’s genetic report, offer insight on clinical trials and studies, and answer questions you have around AS genetics and all its complexities.


Schedule a 1:1 today:

Schedule a 1:1
CAN Spotlight: CAN Spotlight: Charlie's Angels Chari-Tee Golf Tournament

The 4th Annual Charlie's Angels Chari-Tee Golf Tournament, benefiting the Foundation for Angelman Syndrome Therapeutics, was another hole in one! This impressive community raised more than $45,000 in support of FAST's mission to cure AS. Thank you!


Learn more and check out photos:

Learn more
The inaugural Angelman Syndrome Congress in Bogotá, Colombia, organized by FAST Latam

We are thrilled to share the resounding success of the inaugural Angelman Syndrome Congress in Bogotá, Colombia, organized by FAST Latam. This historic event marks a significant step forward for the Angelman syndrome community in Latin America and FAST HQ was proud to be part of it.  


Read the event recap:

Read more
Submit your family photo

We’re now taking photo submissions to feature on our social media! Submit a photo of your family today for a chance to be featured in the coming weeks and months.


Submit a family photo today:

Submit a photo

By providing the information requested, you grant the Foundation for Angelman Syndrome Therapeutics (FAST), its agents, and/or representatives the irrevocable, perpetual, royalty-free, and worldwide right and permission to use, reproduce, publish, distribute and display the information you shared about yourself and/or your child including any photographs, videos, recordings, writings or other media (Media) on FAST’s website and other marketing platforms, including but not limited to blogs, social media accounts, press releases, and related sites. If you have shared any Media of your child(ren), you confirm that you are the parent or legal guardian of mentioned child(ren) and that you are providing your consent to use said Media as described herein. You acknowledge that you are not receiving any compensation for the use of the Media you have provided. You also consent to being emailed by FAST via the contact information you provide.


For a full disclosure of how your information is used, please visit our Privacy Policy.



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