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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
Friday Sep 02, 2022
Leon #S10e73
Friday Sep 02, 2022
Friday Sep 02, 2022
SRF Page on Leon - https://www.syngapresearchfund.org/leon
SRF Grant with Leon & Friends - https://www.eurekalert.org/news-releases/957967
Light a candle for Leon - https://www.bestattung-huettner.at/sterbefall/52048/
SRF on Social for Leon
-https://www.facebook.com/cureSYNGAP1/posts/pfbid0RqALzmaTh8zGeT1KMUbfiXgv9o7PPR2JJPcZNPpR91ce7tYz5foWmb47652r8c2Ml
- https://twitter.com/cureSYNGAP1/status/1564626096640901121
- https://www.linkedin.com/feed/update/urn:li:activity:6970394298483630080
This is a podcast: subscribe to and rate this 10 minute #podcast #SYNGAP10 here https://www.syngapresearchfund.org/syngap10-podcast
Apple podcasts: https://syngap.fund/10a
Episode 73 of #Syngap10 - September 2, 2022
#CareAboutRare #Syngap #epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GlobalCollaboration
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