Global #SYNGAP1 @cureSYNGAP1 🇺🇸🇬🇧🇪🇺 @Syngap1A 🇦🇷 @SyngapAus 🇦🇺 @OSyngap1 🇨🇦🇫🇷 @syngap1Germany 🇩🇪🇦🇹@syngap1italia 🇮🇹 & 🇪🇸🇮🇳🇯🇵🇸🇪🇨🇭

Planet Earth
Joined April 2020
#NDD #Epilepsy Clinicians & Researchers! Help secure a 🌍 global #ICD11 for #SYNGAP1 Log into the WHO portal & support the proposal for #LD90point5 Full instructions here: syngap.fund/icd11 cc: @ingridscheffer @DrDaniAndrade @hanspschlecht @Syngap1Germany @SyngapAus
Listen to the latest #SYNGAP10 episode with @jmgraglia! What is #SynGAPResearchFund doing to help SYNGAP1 families this week? Subscribe to the #podcast at youtu.be/C3L9psuaMOg #SYNGAP1
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6/21 is #SplashForSyngap - Listen to this important segment from the latest episode of 𝘚𝘠𝘕𝘎𝘈𝘗𝟣 Stories - then share with your world! Spread awareness of #SYNGAP1 and the place in this world for our loved ones suffering from this terrible disease! Listen to all episodes at cureSYNGAP1.org/Stories or wherever you listen to podcasts. #CureSYNGAP1 #SYNGAP1 #Epilepsy💜 #Autism💙 #IntellectualDisability💚 #RareDisease #SYNGAP1StoriesAndrew
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🇪🇺 Webinar for our friends in 𝙀𝙪𝙧𝙤𝙥𝙚: 🎤💻 New SYNGAP1 #SRFWebinar with @camp4tx 🧬 SRF EU | What you need to know about ASOs before clinical trials — CAMP4 Case Study 🗓 Wednesday, June 11 🕘 2:30pm ET 🕔 8:30pm CEST 👉cureSYNGAP1.org/CAMP4EU
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RT @cureSYNGAP1: 🎤💻 New SYNGAP1 #SRFWebinar with Virginie McNamar & Mike Graglia 🧬 SRF | SRF’s 2024 Impact Report 🗓 Thursday, March 27 🕘…
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Listen to the latest #SYNGAP10 episode with special guest host Monica Meyer! What is #SynGAPResearchFund doing to help SYNGAP1 families this week? Subscribe to the #podcast at youtu.be/bK2z0xPQGWQ #SYNGAP1
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Listen to the latest #SYNGAP10 episode with @jmgraglia! What is #SynGAPResearchFund doing to help SYNGAP1 families this week? Subscribe to the #podcast at youtu.be/iDvW7HfzSGA #SYNGAP1
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SYNGAP1 Global Network (SGN) retweeted
Hope for ULD is celebrating Rare Disease Day by raising awareness for our fight against the ultra rare EPM1, Unverricht-Lundborg Disease. We are working to end the suffering of ULD! #rarediseaseday #epm1 #unverrichtlundborgdisease #genetherapy #RareEpilepsy
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Listen to the latest #SYNGAP10 episode with @jmgraglia! What is #SynGAPResearchFund doing to help SYNGAP1 families this week? Subscribe to the #podcast at youtu.be/-6XnYok6EnY #SYNGAP1
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Listen to the latest #SYNGAP10 episode with @jmgraglia! What is #SynGAPResearchFund doing to help SYNGAP1 families this week? Subscribe to the #podcast at youtu.be/ymCUn9YGMYQ #SYNGAP1
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How many people have SYNGAP1? 4Q24 #SYNGAPcensus = 🌏1,530 Details: cureSYNGAP1.org/Census 🇺🇸432 🇬🇧128 🇩🇪126 🇨🇳113 🇫🇷99 🇳🇱55 🇪🇸53 🇮🇹52 🇦🇺45 🇵🇱44 🇨🇦41 🇷🇺33 🇧🇷32 🇰🇷22 🇦🇷16 🇨🇭15 🇳🇴🇸🇪🇨🇴13 🇩🇰🇧🇪12 🇮🇪11 🇮🇱10 🇵🇹🇯🇵🇨🇱9 🇹🇷8 🇸🇮7 🇫🇮🇮🇳6 🇷🇸🇲🇽5 🇪🇪🇧🇾🇦🇹🇪🇬🇺🇦🇨🇿🇬🇷🇷🇴4 🇩🇴🇭🇺🇦🇪3 🇭🇰🇸🇷🇲🇦🇲🇾🇧🇦🇸🇰🇸🇬🇭🇷2 🇹🇹🇩🇿🇻🇪🇽🇰🇸🇦🇲🇨🇶🇦🇳🇿🇦🇲🇮🇷🇵🇪🇮🇸🇹🇭🇹🇼🇰🇿🇹🇳🇦🇱🇮🇶🇬🇹1 If we missed you, let us know! #SYNGAP1 #SYNGAPCensus #CureSYNGAP1 @SyngapAus @SyngapGlobal @SRFEurope @SyngapAmericaLatina
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The SYNGAP1 community is at a loss as we share the passing of Annie. Please keep her family in your thoughts during this difficult time. As a community, we promise to always fight in your honor, Annie.
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