Everand Logo

Welcome to Everand!

  • Discover this podcast and so much more

    Podcasts are free to enjoy without a subscription. We also offer ebooks, audiobooks, and so much more for just $11.99/month.

    Gather and connect. Learn from those who have come before. Keep hope alive!

    Gather and connect. Learn from those who have come before. Keep hope alive!

    FromSynGAP10 weekly 10 minute updates on SYNGAP1

    Start listeningView podcast show

    Gather and connect. Learn from those who have come before. Keep hope alive!

    FromSynGAP10 weekly 10 minute updates on SYNGAP1

    ratings:
    Length:
    10 minutes
    Released:
    Oct 29, 2021
    Format:
    Podcast episode

    Description

    Episode 33 of #Syngap10 - October 29th, 2021  
    -Caren Leib Gala was an epic success - #SRFGala - syngap.fund/gala 
    -Partnering with Dr. Danielle Andrade in Toronto who is including SYNGAP1 in gene study and is looking for at least 30 families with adult Syngapians. It’s a huge opportunity. https://www.uhnresearch.ca/researcher/danielle-andrade 
    - Be hopeful- there is a lot of progress happening below the surface and we have more coming! syngap.fund/grants 
    - Support SRF - syngap.fund/give 
    - 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 #ICD10  #Syngap #epilepsy #autism #intellectualdisability #id #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #Genetics #Pediatrics #SRFGala
    Released:
    Oct 29, 2021
    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/