We have kicked off GETA 2024!

Join us live via this link geneticepilepsy.5stream.net

Presentations will also be available via this link after the conference.

#GETA2024

2Q23 #SYNGAPcensus =🌏1,238
Details: syngapresearchfund.org/post/syngapcen…
🇺🇸351
🇬🇧120
🇩🇪107
🇫🇷🇨🇳81
🇳🇱47
🇪🇸39
🇨🇦38
🇦🇺36
🇮🇹35
🇵🇱31
🇷🇺25
🇧🇷22
🇰🇷21
🇦🇷13
🇸🇪🇳🇴🇨🇭🇩🇰12
🇧🇪11
🇵🇹🇨🇴9
🇮🇪8
🇹🇷7
🇨🇱🇫🇮🇸🇮6
🇮🇱🇲🇽5
🇪🇪🇧🇾🇦🇹🇷🇸🇮🇳🇪🇬🇺🇦4
🇯🇵🇨🇿🇩🇴🇭🇺🇬🇷3
🇭🇰🇷🇴🇸🇷🇲🇦🇲🇾🇧🇦🇸🇰🇸🇬🇦🇪2
🇹🇹🇩🇿🇻🇪🇭🇷🇽🇰🇸🇦🇲🇨🇶🇦🇳🇿🇦🇲1
If we missed you, let us know!

NEW EPISODE! SYNGAP1 Stories comes from 'down under' as Ashley talks with Danielle Williams, Mom to two daughters, each with SYNGAP1. Syngap.Fund/Stories

#SYNGAP1

1Q23 #SYNGAPcensus = 🌏1,215
Details: syngapresearchfund.org/post/142-synga…

🇺🇸343
🇬🇧119
🇩🇪99
🇫🇷95
🇨🇳75
🇳🇱46
🇪🇸39
🇨🇦38
🇦🇺35
🇮🇹33
🇵🇱31
🇧🇷🇷🇺22
🇰🇷21
🇸🇪🇨🇭🇩🇰12
🇧🇪🇳🇴🇦🇷11
🇨🇴10
🇵🇹9
🇮🇪8
🇹🇷7
🇨🇱🇫🇮6
🇮🇱🇸🇮🇲🇽5
🇪🇪🇦🇹🇮🇳🇪🇬4
🇧🇾🇯🇵🇨🇿🇷🇸🇩🇴🇭🇺🇬🇷3
🇭🇰🇷🇴🇸🇷🇲🇦🇺🇦🇲🇾🇧🇦🇸🇰🇸🇬🇦🇪2
🇹🇹🇩🇿🇻🇪🇭🇷🇽🇰🇸🇦🇲🇨🇶🇦🇳🇿🇦🇲1
If we missed you, let us…

Read & share this Newsweek story profiling SRF, our founders (@SYNGAP1mom & Mike Graglia 🌻) and Tony's diagnostic journey.

newsweek.com/my-son-syngap1…

FYI Stanford Children's Elli Brimble Invitae Labcorp (MNG)

Here is my summary from #AES2022 , focused on the development of therapies for the rare epilepsy syndromes, and more specifically on treatments for the *cause* of the disease.

I reviewed 8 syndromes, there is so much going on!

draccon.com/dracaena-repor…

#syngapconf22 brilliant science and collegiality - so good to see the hope for new precision therapies! Thanks Mike Graglia 🌻 SynGAP Research Fund (SRF) Epilepsy Genetics Program GETA

3Q22 #SYNGAPcensus = 🌏 1,135
Details: syngapresearchfund.org/post/123-synga…

🇺🇸336
🇬🇧116
🇫🇷91
🇩🇪92
🇨🇳66
🇳🇱41
🇪🇸36
🇨🇦35
🇦🇺33
🇮🇹🇵🇱30
🇰🇷20
🇧🇷19
🇷🇺18
🇸🇪12
🇩🇰🇨🇭11
🇳🇴🇧🇪10
🇮🇪🇵🇹8
🇨🇴🇦🇷🇹🇷7
🇨🇱🇫🇮5
🇮🇱🇪🇪🇸🇮🇲🇽🇪🇬4
🇧🇾🇦🇹🇯🇵🇨🇿🇭🇺🇮🇳3
🇺🇦🇭🇰🇷🇴🇷🇸🇸🇷🇲🇦🇲🇾🇦🇪🇬🇷🇸🇬2
🇧🇦🇸🇰🇹🇹🇩🇿🇻🇪🇭🇷🇽🇰🇸🇦🇲🇨🇶🇦🇩🇴🇳🇿🇦🇲1

If we missed you, let us know!

Clinicians and patients’ parents working together for SYNGAP1 to answer one of the most important questions: Which are the best medications for SYNGAP1 syndrome? Here are the results if 170 patients for seizures, sleep, behavior and development. #epilepsy #syngap1 #research

📢 overcome syngap1🇨🇦, Wandoan Campdraft Syngap Research Fund Australia🇦🇺 & SynGAP Research Fund (SRF) 🇺🇸 grant CAD$150,000 to Derek Bowie at McGill University for Small Molecule Translational Research for #SYNGAP1 🧬 #intellectualdisability . #Collaboration eurekalert.org/news-releases/… via EurekAlert!

Today is Splash4Syngap, Syngap1 Awareness Day.
We're thinking of all syngapian families today in Australia 🇦🇺 and around the world! Together we will find a treatment for our syngapians.

Thank you to everyone for your support.
#SYNGAP #SYNGAP 1

#GETA2022 is less than 2 weeks away. Looking forward to this! Join us in person or livestream facebook.com/genetic.epilep…

We are 2 weeks away from GETA - schedule below. There is still time to get your tickets here:
eventbrite.com.au/e/geta-2022-sy…

#GETA #raredisease #DEE #epilepsy #genetics #family #conference #neurotwitter

Massive fundraiser for Syngap research in Qld this weekend. Over $220k raised for Syngap. facebook.com/16835174219617…

This is the 6th year we will bring hope to families impacted by genetic epilepsy. Hope delivered by researchers, updating us on the latest precision medicine therapies and hope through connecting with other families.

Now this gives us hope, a great example of gene therapy working

DEE Survey (Australia Only). Please share with your communities and families.
We’re working with The Royal Children's Hospital, Melbourne Epilepsy Foundation of Australia , Murdoch Children's Research Institute (MCRI) & Australian Genomics to understand caring for a child with complex needs. Link to do survey - redcap.mcri.edu.au/surveys/?s=JER…
#DEE #raredisease

We are gearing up for rare disease day. Are you aware of how many genetic causes of epilepsy? #raredisease #epilepsy