PinnedSprint for Syngap 2021 a huge success!Thank you for making #Sprint4Syngap a success The first annual Sprint For Syngap is in the books, and it was a huge success! Thank you to everyone who participated, donated, or contributed in any way. You made it happen! What is Sprint For Syngap, or #Sprint4Syngap in social media-speak? On April 24, 2021, Syngap Research Fund (SRF)…Syngap13 min readSyngap13 min read
Mar 10, 2022SynGAP Research Fund Deploys #CouldItBeSYNGAP1 Screening Tool in Partnership with Probably GeneticPRESS RELEASES FEBRUARY 27, 2022 See official news release on EurekAlert here. For #RareDiseaseDay 2022, SynGAP Research Fund (SRF) announces a partnership with Probably Genetic to find more patients — the campaign is called #CouldItBeSYNGAP1. The partners have developed a pre-screening tool to provide undiagnosed patients and families a pathway…Rare Disease4 min readRare Disease4 min read
Mar 10, 2022SynGAP Research Fund announces $100,000 Exosome Grant to Professor Janos Zempleni of the University of Nebraska-LincolnPRESS RELEASES FEBRUARY 22, 2022 See official news release on EurekAlert here. What if milk could be used to deliver genetic therapies to the brain of SYNGAP1 patients? The first step is to see if natural nanoparticles (“exosomes”) in milk can improve SynGAP expression! The SynGAP Research Fund (SRF) announces…Rare Disease4 min readRare Disease4 min read
Mar 10, 2022SYNGAP1 Frequent de novo Missense Variant Alert — Study Opportunity for p.Gly344SCIENCE JANUARY 27, 2022 Aaron Harding is a scientist and director at Sharp HealthCare, member of SRF’s Board of Directors, and a SYNGAP1 dad. This article is based on information gathered through shared personal experiences in the SYNGAP1 community. …Rare Disease6 min readRare Disease6 min read
Mar 10, 2022Diapers & Pull Ups for Older Kids: A Mom’s ExperiencePARENT TIPS JANUARY 26, 2022 Lauren Perry is the Operations Manager at SRF and mom to two boys, including 11-year old Syngapian Will. Here, she shares valuable experience on a topic no one talks too much about, but one that many parents deal with on a daily basis. Parents look…Rare Disease5 min readRare Disease5 min read
Dec 31, 2021SRF | 2021 by the NumbersSRF NEWS DECEMBER 31, 2021 SRF 2021: The year in review by the numbers Listen to Mike’s latest podcast running down these numbers and view the numbers spreadsheet. $1.8M committed to SYNGAP1 Research via 13 different grants to 10 institutions. 75k+ following @cureSYNGAP1 on 6 social media channels. 985 Patients counted in 58 countries. 154 US patients enrolled in…Syngap2 min readSyngap2 min read
Dec 31, 2021#SYNGAPCENSUS 2021 Update: +102 in Q4 2021SYNGAP CENSUS DECEMBER 30, 2021 How many people in the world have SYNGAP1? #SYNGAPCENSUS 2021 Update: +102 in Q4 2021Syngap3 min readSyngap3 min read
Dec 17, 2021Brotherly Love: Dice stacking for a cure!PARENT TIPS DECEMBER 16, 2021 Ray is dad to Syngapian Miles, diagnosed at age 9. Ray, wife Charlotte, and two sons live in the UK. In November 2021, inspired by other fundraising events, 9 year old Theo decided it was his turn to help his big brother. Miles, aged 12…Syngap2 min readSyngap2 min read
Dec 10, 2021Third Annual Synapse Roundtable: Collaboration at Its FinestSCIENCE DECEMBER 10, 2021 Sandy is a volunteer with SRF and aunt to 5-year-old Syngapian Myla. …Syngap7 min readSyngap7 min read
Nov 30, 2021Using Magnesium Supplements: A Syngap Community DiscussionPARENT TIPS NOVEMBER 30, 2021 Barbara Gaillard is a retired engineering/IT professional and is the grandmother of Syngapian Naya. This article is based on anecdotal information, casually gathered through shared personal experiences in the SYNGAP1 community. Scientific information is alluded to via hyperlinks to other articles, but their accuracy is…Syngap15 min readSyngap15 min read