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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

Join us for the Science & Family Conference on Dec 1 & 2

Discover our latest news & updates

Probably Genetic Three Month Program Update
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#SYNGAPCENSUS 2022 Update: +43 in Q2 2022
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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: +43 in Q2 2022
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10 Reasons we chose #Ciitizen for the #SYNGAP1 Digital Natural History Study. #SRFdoCiitizen
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We Were Searching for Syngap; We Just Didn't Know It
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I Planned A Simple Garage Sale And Failed - In The Best Way!
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Meet SYNGAP1 Patients

Meryem
Trabzon, Turkey
4 years old
Esme
Harrisonburg, VA, USA
3 years old
Rochon
Alabama, USA
6 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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