Q3 census: 1,871 known patients, +65 this quarter.
First patient in Rwanda. USA +11, China +16, Brazil +6, France +4.
Finding patients matters more than ever as trials approach. https://cureSYNGAP1.org/Census
COMBINEDBRAIN — RARE RESEARCH ROUNDTABLE
Wonderful Rare Research Roundtable on Genetic Neurodevelopmental Disorders. COMBINEDBrain is a gift to the rare neuro community — hug them when you see them. https://combinedbrain.org/RR-RGND
Dr. Emma James of Encoded, chair of our IAB, posted about the meeting. https://www.linkedin.com/posts/emma-james-71759a1a_the-combinedbrain-research-roundtable-on-ugcPost-7511223599165472768-jDkI
Q4 goal: $500,000 by Dec. 31, including a $200,000 match.
Families can start their own fundraiser; anyone can donate. https://cureSYNGAP1.org/Unlock
Your Idea. Your Fundraiser. Your SYNGAP1 Impact. https://curesyngap1.org/blog/your-idea-your-fundraiser-your-syngap1-impact
COMMUNITY ACTION
RARE Disease Week 2027, March 2-4, in DC. Travel reimbursement applications are open; deadline Nov. 6. https://bit.ly/4jo7fku
RARE Foundation travel reimbursement post: https://www.facebook.com/share/p/1EeF8jTWFi
• Sign up for ARI: https://cureSYNGAP1.org/Ari
WARRIORS — JACK
Jack is a 3-year-old from Berkeley who missed early milestones and was diagnosed with SYNGAP1 around age 3 after eyelid-fluttering episodes led to EEG, MRI and genetic testing. https://curesyngap1.org/syngap-warriors/jack-w
NEWSLETTER #52
All the latest news and links in one place: https://cureSYNGAP1.org/NL52
Subscribe: https://cureSYNGAP1.org/Newsletter
PUBMED + SCIENCE
PubMed 2026: 54. +14 vs Week 40. https://pubmed.ncbi.nlm.nih.gov/?term=syngap1&filter=years.2026-2026&sort=date
Podden och tillhörande omslagsbild på den här sidan tillhör
Syngap Research Fund, 501(c)(3). Innehållet i podden är skapat av Syngap Research Fund, 501(c)(3) och inte av,
eller tillsammans med, Poddtoppen.