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Over 1200 families are caring for a loved one with the rare disease ”SynGAP” resulting from a variant of the SYNGAP1 gene. This 10 minute weekly podcast is for them. A quick summary of the latest news in the space. The host is Mike Graglia, co-founder & managing director of the SynGAP Research Fund. SRF is a parent-led, all volunteer public charity in the US that strives to accelerate research into treatments for SYNGAP1 so that we can help our loved ones in a timeframe that matters. Learn more at https://www.syngapresearchfund.org/
Episodes

Monday Feb 03, 2025
Monday Feb 03, 2025
Tuesday, February 4, 2025 - Week 6
CONVO - Parent of 18 year old
- Travel now.
- Get meds under control fast
- Don’t do this alone
- Don’t give up on the adults
- Find doctors who want to learn and think, not dictate.
STUDIES OF THE WEEK - FRAZIER
Don’t underestimate this tool, please take part in this study.
Tracker page: https://docs.google.com/spreadsheets/d/1oQLNi85AUbISmcW0KbsgGn4cBK_4MNuvwGlKUUKLyIQ/edit?usp=sharing
ADVOCACY SHOUT OUT
REGULATORY UPDATE - Feb 4 at 4PM EST.
EF on EPILEPSY
Instagram - Facebook - LinkedIn - X
RESEARCH UPDATE
There are 317 papers on or related to SYNGAP1 since 1998, but 54 of those are in 2024! So far 7 (but really 8 if you count Coller) for 2025.
https://pubmed.ncbi.nlm.nih.gov/?term=syngap1&filter=years.1998-2025&sort=pubdate&timeline=expanded
- James Clements paper is exciting: https://pubmed.ncbi.nlm.nih.gov/39878322/
- JC LinkedIn: https://www.linkedin.com/posts/james-clement-chelliah_epigenetic-modulation-rescues-neurodevelopmental-activity-7290365551879569409-X_6G/
VOLUNTEER SPOTLIGHT
Aaron Harding is tireless
- Video - https://youtu.be/7LprhkhyU5I
CONFERENCE
Pre-register now: December 4 & 5 – https://cureSYNGAP1.org/Pre25
VOLUNTEER
Join us: https://curesyngap1.org/volunteer-with-srf/
SOCIAL MATTERS
- 3,922 LinkedIn. https://www.linkedin.com/company/curesyngap1/
- 1,270 YouTube. https://www.youtube.com/@CureSYNGAP1
- 11,550 Twitter https://twitter.com/cureSYNGAP1
- 47k Insta https://www.instagram.com/curesyngap1/
NEWLY DIAGNOSED?
New families have resources here! https://syngap.fund/Resources
Podcasts, give all of these a five star review!
https://podcasts.apple.com/us/channel/syngap1-podcasts-by-srf/id6464522917
Episode 160 of #Syngap10
#CureSYNGAP1 #epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1
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