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SynGAP Research Fund (SRF) is a global group of families committed to accelerating the science to cure SynGAP & to supporting each other.

Our mission is to support the research and development of treatments, therapies and support systems for SynGAP1 patients worldwide.

Learn More about SYNGAP1
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Upcoming events!

SYNGAP1 Splice Forms: Implications for understanding the disorder and development of therapies

Thursday, June 2 @ 10am PT / 1pm ET / 6pm BST
Learn More
Jun 2

Finding more SYNGAP1 patients with Probably Genetic

Thursday, June 9, 2022 @ 9am PT / 12pm ET / 5pm BST
Jun 9
Learn More

Scramble for Syngap

October 8, 2022
Oct 8
Learn More

🚴 Million Dollar Bike Ride is June 11! 🚴

Discover our latest news & updates

Stella Stays In School: Getting Educational Needs Met
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Sprint4Syngap Kicks off the 2022 Fundraising Season
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Support New SYNGAP1 🐭 Models
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What you need to know about Augmentative and Alternative Communication (AAC)
#SyngapCensus Q4 2021: +102 in #3Q21
985
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10 Reasons we chose #Ciitizen for the #SYNGAP1 Digital Natural History Study. #SRFdoCiitizen
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The Arc Financial Planning Video Series
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SRF Fundraising Status Update, April 2022
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Meet SYNGAP1 Patients

Cole
Ohio, USA
5 years old
Ethan
Charlotte, North Carolina
4 years old
Aidan
Sydney, Australia
3 years old
Read More Stories

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SRF is phenomenal! I love how devoted they are to finding a treatment/cure for our favorite syngapians! I am blown away with this nonprofit organization and everything that they stand for. So thankful to have amazing individuals who have made it their life mission to helping our loved ones and their own!

Brittney

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