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SRF LT Webinar, MDBR, Therapies, Learning at Conferences. #S10e141

SRF LT Webinar, MDBR, Therapies, Learning at Conferences. #S10e141

FromSynGAP10 weekly 10 minute updates on SYNGAP1


SRF LT Webinar, MDBR, Therapies, Learning at Conferences. #S10e141

FromSynGAP10 weekly 10 minute updates on SYNGAP1

ratings:
Length:
24 minutes
Released:
May 20, 2024
Format:
Podcast episode

Description

JOIN SRF LT on Thursday:
Volunteer Info session with Leadership Team is this week: 
https://syngap.fund/LT Thursday 5/23 at 5:30 Pacific.
 
MDBR is 3 weeks away! https://Syngap.Fund/Unite  
$5k match https://x.com/phalliburton/status/1792288377049415835
 
It’s all about therapies.  Precision Genetic and Repurposed.
 
Conferences are where we engage professional communities around SYNGAP1 & SRF.
 - Last week I was at Milken Global.  All diseases are talking about biomarkers & endpoints. https://milkeninstitute.org/events/global-conference-2024/program
 - This week I was at the #Ultragenyx Bootcamp with our CSO
https://www.ultragenyx.com/video-this-bootcamp-helps-parents-advance-rare-disease-research/ So good to see Kathryn energized by this role.
 - ASGCT was last week and that means announcements…
 - Kathryn and I are off to BIO in June in San Diego.
 
Ionis for Angelman
https://www.linkedin.com/posts/cureangelman_exciting-news-for-the-angelman-syndrome-community-activity-7196872264976322563-_rvX 
Capsida for STX https://www.linkedin.com/posts/graglia_capsida-biotherapeutics-presents-new-preclinical-activity-7194004214635716608-M01Y 
Encoded for STX https://www.linkedin.com/posts/stxbp1-foundation_encoded-therapeutics-provides-pipeline-updates-activity-7196942568859787265-leKO 
Nasha at FOXG1 https://www.youtube.com/watch?v=ELKijSx0uwQ
 
Repurposed therapies are just as important.
 
Cost effective.  Globally available.
They are here now.  We must act, the suffering is immense.
They show us what is improvable and therefore inform clinical trial design.
They are not compromising other trials.  And to even suggest that is unethical if it suggests people should hold off on helping patients.  How about we just diagnose more kids?  Or think harder about which kids go to which trials?
Precision Genetic Therapies are going to be more effective than repurposed drugs, people will happily participate in trials.
 
Review of repurposed drugs:
RAVICTI Rx- 10+ patients with Dr. Grinspan, not all but a few have had significant seizure reduction.  I remain worried about cost and look to STXBP1 and SLC6A1 for guidance here.
NORTRIPTYLINE Rx - Has helped me, a handful of families are getting a Rx.  I am hopeful that some researcher does an investigator led trial.  But until then, ask your Neuro.
ACETYL-LEUCINE is a Nutraceutical - Update 1 has really been noticed and Update 2 will share a few potential mechanisms of action.  Many are trying this drug from https://bit.ly/tanganil24 Encouraging… no, updating.  Please share data with us if you are trying.  We are collecting case studies for Update 3.  Thank you to the team here.
 
NEWLY DIAGNOSED?
New families have resources here! https://syngap.fund/Resources

SOCIAL MATTERS - AMPLIFY SRF TO MAKE SURE FAMILIES FIND US
 - 1,010 YouTube.  https://www.youtube.com/@CureSYNGAP1 
 - 9,900 Twitter https://twitter.com/cureSYNGAP1
 - 3,560 LinkedIn.  https://www.linkedin.com/company/curesyngap1/
- 49k TikTok https://www.instagram.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 141 of #Syngap10 - May 20, 2024
#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1 #CureSYNGAP1
Released:
May 20, 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/