Grateful and grieving. SRF is growing with our community, all 1,400 of us! #S10e138 SynGAP10 weekly 10 minute updates on SYNGAP1

TOGETHER WE ARE STRONGER
 - 1,400 strong, thank you Jess & team. https://curesyngap1.org/blog/syngap1-census-2024-update-61-in-q1-2024-total-1400/
 - Stoke webinar: one of the most important considerations for deciding which disease to work on was, “…how strong is the patient advocacy group?” 
 - Stoke CMO Barry Ticho, MD, PhD, FACC during webinar 4/2/24 to discuss findings of STK-001
 
WELCOME AND CONNECT
 - New parents are coming fast, reach out to them, tell them how much hope to have.
 - Connect, connect, connect.
  - San Diego next week: https://curesyngap1.org/resources/movies/jaxon/
  - Hope https://curesyngap1.org/blog/my-syngap1-drive-a-thon-hope4thecure/
- TU to Emily Barnes who is at FasterCures meeting today in Boston, see #S10e98 to see my thoughts about this workshop https://www.youtube.com/watch?v=iOLjUdVUtqo
 
TEAM IS GROWING
 BOARD - https://www.eurekalert.org/news-releases/1038978
 CSO - https://www.eurekalert.org/news-releases/1040061
 COO - You?
 
PRESS
 - UK https://www.channel4.com/news/govt-send-funding-boost-still-billions-short-says-tory-mp-with-affected-family/
 - GA https://www.gpb.org/news/2024/04/03/80-of-rare-diseases-are-genetic-thats-why-whole-genome-sequencing-can-help/ 
 
What does my genetic report mean? 
We wrote a blog, but as I’ve had this conversation a few dozen times, my answer is simpler now.  Is it missense or is it truncating?  If missense, do more research, if truncating, it is in the first 4 exons (p. Address of 129 or lower).
Who else has it?  Look on ClinVar and call SRF.
Blog: https://curesyngap1.org/blog/understanding-your-genetic-report-with-syngap1-a-rare-disease/
 
STUDIES
https://curesyngap1.org/blog/my-syngap1-drive-a-thon-hope4thecure/ 
CHOP: ENDD@chop.edu 
Adults:
 - Press Release: https://www.eurekalert.org/news-releases/1040062
 - Study Info:  https://drive.google.com/file/d/1tOdodcV7E5ROOHWyLn8a48x1WNBOr-U2/view 
QOL: https://Syngap.Fund/QOL24 39 and counting.
 
#Sprint4Syngap 2024
Total: $168,572 from 347 people
Tavilla: $126,385 from 62
Big thanks to them and all teams especially those already over $1k, Phoebe, Kaia, Louie, Kiera, Theo, Hadley & Gracyn.
https://curesyngap1.org/events/featured/sprint4syngap-2024/
https://givebutter.com/ALjJXJ
 
REPURPOSING
 - NAL, blog coming.
 - Ravicti, enrolled, and blog on Butyrate coming.
 - Nortriptyline, has been game changing, discussing a larger trial.
 
REFLECTIONS
 - Family Medical Leave Act #FMLA https://www.dol.gov/general/topic/benefits-leave/fmla
 - Homeschooling… again, avoid the kneejerk.  See #S10e64 https://www.youtube.com/watch?v=01uhSjxGgGE  
 - Tony update.  Grateful and grieving.
 
SOCIAL MATTERS
967 Subscribers on YouTube.  https://www.youtube.com/@CureSYNGAP1 
3,483 Subscribers on LinkedIn.  https://www.linkedin.com/company/18940628/admin/feed/posts/
Socials matters so we can find more people, like this: https://curesyngap1.org/blog/an-emotional-journey-begins-after-a-syngap1-diagnosis/ 
 
Podcasts, give all of these a five star review!
SRF Channel - https://podcasts.apple.com/us/channel/syngap1-podcasts-by-srf/id6464522917
 
Episode 138 of #Syngap10 - April 4, 2024
#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1 #CureSYNGAP1