1,871 #SYNGAP1 Census, COMBINEDBrain RR-RGND, Conference Dinner/Drinks & $200K Unlock Match #S10e222 copertina

1,871 #SYNGAP1 Census, COMBINEDBrain RR-RGND, Conference Dinner/Drinks & $200K Unlock Match #S10e222

1,871 #SYNGAP1 Census, COMBINEDBrain RR-RGND, Conference Dinner/Drinks & $200K Unlock Match #S10e222

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Friday, October 2, 2026 — Week 40

CENSUS — 1,871 AND GROWING

  • 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

CURE SYNGAP1 CONFERENCE — DENVER

  • 9 Family Legacy Sponsors, up from 8 in 2025.
  • Thursday Rare Reception — free, register: https://cureSYNGAP1.org/RR26
  • Friday Family Dinner at Henry’s: https://cureSYNGAP1.org/Henrys
  • Conference registration ends OCT. 31. https://cureSYNGAP1.org/Reg26

UNLOCK THEIR TOMORROW

  • 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

USA - Use your ICD-10: F78.A1

SOCIAL MATTERS

5,301 LinkedIn. https://www.linkedin.com/company/cureSYNGAP1

1.63k YouTube. https://www.youtube.com/@CureSYNGAP1

11.0k X. https://twitter.com/cureSYNGAP1

43.4k Instagram. https://www.instagram.com/cureSYNGAP1

Like + subscribe wherever you listen. https://cureSYNGAP1.org/podcasts/syngap10

Episode 222 of #Syngap10 #SYNGAP1 #CureSYNGAP1 #Podcast #PatientAdvocacy

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