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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
Saturday Dec 04, 2021
Let’s make sure SYNGAP1 is cured in our lifetime. It’s up to us.
Saturday Dec 04, 2021
Saturday Dec 04, 2021
Let’s make sure SYNGAP1 is cured in our lifetime. It’s up to us.
Episode 38 of #Syngap10 - December 4th, 2021
Roundtable 3 #SRFRT3 was a great success, special thanks to all speakers.
The #FAST #Angleman meeting is incredible. https://cureangelman.org/events/gala2021
Sign up for #Ciitizen. https://Ciitizen.com/SYNGAP1
Raise funds for SYNGAP1
- Facebook Fundraisers: http://syngap.fund/FBFun
- Giving Tuesday Fundraiser: https://syngap.fund/gt21
- What is SYNGAP1? https://www.syngapresearchfund.org/home/what-is-syngap1
- Sign up for this 10 minute #podcast #SYNGAP10 here https://syngap.fund/10
#F78A1 #FAST #Angelman #SRFRT3 #SyngapaseRT #Syngap1 #syngap #epilepsy #autism #intellectualdisability #id #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #Genetics
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