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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!

SRF | Weekly Family Meeting

Wednesdays @ 5pm PT/ 8pm ET
Learn More
Dec 8

SRF | Families of Adult Syngapians Meeting

2nd Tuesday of every month | 1pm PST / 4pm EST / 9pm GMT
Dec 14
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Giving Tuesday is November 30th, but the time to start a fundraiser is now!

Discover our latest news & updates

Using Magnesium Supplements: A Syngap Community Discussion
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Fundraising: The Backbone of Research
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Join us for the 3rd Annual Roundtable
#SyngapCensus Q3 2021: +75 in #3Q21
883
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10 Reasons we chose #Ciitizen for the #SYNGAP1 Digital Natural History Study. #SRFdoCiitizen
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What you need to know about Augmentative and Alternative Communication (AAC)
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Another Study suggests Syngap1 Rescue is possible
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Meet SYNGAP1 Patients

Mya
Ontario, Canada
3 years old
Emilia
Georgetown, Texas
3.5 years old
Rafael
Concepión, Chile
4 years old
Read More Stories

Knowledge Center.

SynGAP

There are 3000+ papers available on Google if you search SynGAP, 2300+ for SYNGAP1. Where to begin?

Learn More →

Epilepsy

Our patients have some specific seizures which are well described in Sheffer’s paper, above as well as this paper from German researchers, see also the video attached.

Learn More →

Ketogenic Diet

Putting a child on the powerful drugs that are used to treat our kids is not easy. As a result many parents are turning to the oldest known treatment for Epilepsy, the Ketogenic Diet. Many have had great outcomes. We urge you to learn more about it.

Learn More →
Visit Knowledge Center

I was originally drawn to Syngap Research Fund after coming across their mantra: Collaboration. Transparency. Urgency. I knew that it was intentional and that the organization was true to their mission of accelerating the path to therapeutics for patients suffering from Syngap1. SRF has funded ~$1M in research to-date, and their founders cover all overheads, so 100% of all donations go directly to science. This team is really making a difference!

Peter Haliburton

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