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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!

Scramble for Syngap

October 8, 2022
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Oct 8

Caren Leib Gala

October 8, 2022
Oct 8
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SynGAP Siorée - Sparks of Hope

November 12, 2022
Nov 12
Learn More

🚴 Million Dollar Bike Ride is June 11! 🚴

Discover our latest news & updates

I Planned A Simple Garage Sale And Failed - In The Best Way!
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The Benefits of Ciitizen: One Mom’s Story
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Support New SYNGAP1 🐭 Models
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What you need to know about Augmentative and Alternative Communication (AAC)
#SYNGAPCENSUS 2022 Update: +70 in Q1 2022
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10 Reasons we chose #Ciitizen for the #SYNGAP1 Digital Natural History Study. #SRFdoCiitizen
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Stella Stays In School: Getting Educational Needs Met
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Sprint4Syngap Kicks off the 2022 Fundraising Season
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Meet SYNGAP1 Patients

Esme
Harrisonburg, VA, USA
3 years old
Rochon
Alabama, USA
6 years old
Cole
Ohio, USA
5 years old
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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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