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NHS in Colorado! Real talk about new therapies. Planning for RAA & the Conf! #S10e142

NHS in Colorado! Real talk about new therapies. Planning for RAA & the Conf! #S10e142

FromSynGAP10 weekly 10 minute updates on SYNGAP1


NHS in Colorado! Real talk about new therapies. Planning for RAA & the Conf! #S10e142

FromSynGAP10 weekly 10 minute updates on SYNGAP1

ratings:
Length:
15 minutes
Released:
May 31, 2024
Format:
Podcast episode

Description

Full show notes: https://syngap.fund/n142 
 
BIG NHS UPDATE
66 Kids evaluated, 11 have had follow-ups, ~20 new kids scheduled.
Colorado should start seeing patients in August!

WHERE TO DONATE
MONEY: MDBR is next week, donate now! https://charity.pledgeit.org/t/jY577u7uMc Thanks to the team. https://Syngap.Fund/Unite  

BLOOD: June 7 & 8, Loews Coronado Bay Resort, email CSO@cureSYNGAP1.org

TIME TO JOIN #TEAMSRF
 - Volunteer Webinar: https://syngap.fund/LT
- Fifty families lent their good names to SRF in this wonderful blog: https://syngap.fund/Community 
 - https://curesyngap1.org/volunteer-with-srf/ 
 
CHATS WITH INDUSTRY
 - Is IT delivery a blocker for precision therapies, NO!
 - 2026 is feeling like the earliest we see trials.
 - BIO with Kathryn next week!


CALENDAR MANAGEMENT
Rare Across America is 66 days away, register now:
https://everylifefoundation.org/rare-advocates/rare-across-america/ 
 
Conference is 188 days away:
https://curesyngap1.org/events/conferences/syngap1-conference-2024/
 
PUBLICATION ALERT
https://x.com/cureSYNGAP1/status/1795837761678962799 
 
NEWLY DIAGNOSED?
New families have resources here! https://syngap.fund/Resources

SOCIAL MATTERS - AMPLIFY SRF TO MAKE SURE FAMILIES FIND US
 - 1,020 YouTube.  https://www.youtube.com/@CureSYNGAP1 
 - 10,000 Twitter https://twitter.com/cureSYNGAP1
 - 3,591 LinkedIn.  https://www.linkedin.com/company/curesyngap1/
- 49k Insta https://www.instagram.com/curesyngap1/
- 392 TikTok https://www.tiktok.com/@curesyngap1


Podcasts, give all of these a five star review!
SRF Channel - https://podcasts.apple.com/us/channel/syngap1-podcasts-by-srf/id6464522917

Episode 142 of #Syngap10 - May 31, 2024
#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1 #CureSYNGAP1
Released:
May 31, 2024
Format:
Podcast episode

Titles in the series (100)

Over 900 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/