28.6K
Downloads
158
Episodes
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 Aug 13, 2021
Friday Aug 13, 2021
Episode 22 of #Syngap10 - August 13th, 2021
- Webinars
-https://Syngap.fund/eduardo August 19 at 10 am PST
-https://Syngap.fund/ana Sept 2 at 10 am PST
- Mugs mugs mugs
-https://twitter.com/AAledo/status/1426207246149636099
- Blog: Genetics article is a must read for new families
- https://www.syngapresearchfund.org/post/what-should-i-ask-in-my-genetics-appointment-for-syngap1
- Genetic Counselors
- Tell me about your experience
- What do they need to know?
- Hug them
- Ciitizen
- Count 110 + 12, let's keep going, 28 spots left!
- Panel https://www.facebook.com/cureSYNGAP1/videos/221755526409431/
- Sign up https://ciitizen.com/syngap1
- Cure
- Rarebase article https://www.rarebase.org/post/what-does-it-mean-to-find-a-cure-for-a-disease
- See episode 19. Yes, we need to reach for this
- We may not know what is coming, but we need to work for it
- One Upon a Gene
- 94 https://effieparks.com/podcast/episode-094-mike-and-nasha
- 41 https://effieparks.com/podcast/episode-41-syngap-research-fund
- Cures go through clinical trials. Get ready: https://syngap.fund/ctr - $36k!
Comments (0)
To leave or reply to comments, please download free Podbean or
No Comments
To leave or reply to comments,
please download free Podbean App.