Corey Baysden @CoreyBaysden
#RareDisease mom to Saylor w/ #Syngap1 🧬 Director of Community Activation @cureSYNGAP1 🧠Working 2 find a cure for #epilepsy #autism #hypotonia #nonverbal #ID linktr.ee/coreybaysden North Carolina, USA Joined July 2021-
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Today, on #RareDiseaseDay, we honor all affected by conditions like #Syngap1. Since Saylor's dx, our journey has been a mix of challenges & blessings. Let's also recognize the unsung heroes—teachers, caretakers, therapists—who play crucial roles in our journey 💜🧬🙏@cureSYNGAP1
Where is the best list of public drug repurposing wins for rare monogenic CNS disorders? @ClementYChow @rarebasepbc @omidkarkouti @eperlste @onnofaber @JMGraglia
So proud of this sweet girl! #syngap1 #AutismAwareness #intellectualdisability #Neurology @cureSYNGAP1
NEWS! @julietkknowles of @Stanford_Neuro awarded $1⃣3⃣0⃣,0⃣0⃣0⃣ to study maladaptive myelination 🧠 & epilepsy⚡️ in #SYNGAP1 🧬, testing in SRF supported 🐭 models from @rhuganir. #collaboration 🤝 👉 @cureSYNGAP1 Grant applications due in 15 days. eurekalert.org/news-releases/…
So great to hear from Suzanne 💜 Thankful to have her part of our team!
So great to hear from Suzanne 💜 Thankful to have her part of our team!
Saylor was able to participate in this study! Great work Dr. Frazier & team
There is no cure for #SYNGAP1, but SRF and its extensive team of volunteers are working daily toward that goal. Together, we can do great things! #SYNGAP1Conference2023 #Volunteer
Today, June 21, is SYNGAP1 Awareness Day! #SYNGAP1 families need family and friends to form a community of support. SRF needs similar support to help us achieve our ultimate goal of finding a cure. #strongertogether Syngap.Fund/Donate syngapresearchfund.org
Es un honor participar y representar a @cureSYNGAP1 como panelista compartiendo la historia de nuestra hija Amelia y la importancia de las organizaciones de pacientes que logran cambiar el rumbo de la enfermedad. @cureSYNGAP1 @SMNPediatrica @mexico #Chihuahua #Neurology
SYNGAP1 #WarriorWednesday🧬 Michael (age 2) from📍Vienna, Austria 🇦🇹“He likes slides and swings…” Read his story & see more photos at syngapresearchfund.org/syngap-warrior… #SRFWW no.186 #SYNGAP #epilepsyawareness #autismawareness #rarediseaseresearch #SYNGAPResearchFund #CareAboutRare…
Our legal director Kevin Frye and CEO @JMGraglia are @StJude PTNI to learn about Pediatric Translational Neuroscience alongside 3️⃣0️⃣ Patient Advocacy Groups. We are ensuring that #SYNGAP1 is part of the conversation & our patients will have every opportunity for new therapies.
Yesterday was our annual #Sprint4Syngap! Thankful for all the families that participated, researchers who are working hard & @cureSYNGAP1! Still time to donate! Syngap.Fund/Sprint
This is so great! Thank you @hanspschlecht!
This is so great! Thank you @hanspschlecht!
Effie Parks @OnceUponAGene
5K Followers 3K Following Nuclear Advocate | Award Winning Podcaster | Speaker | Captain Connection | #RareDisease #RareMama to my sweet, Ford, who lives with #CTNNB1 🦓Mike Graglia 🌻 @JMGraglia
7K Followers 3K Following CEO @cureSYNGAP1 🧬 Pod https://t.co/9jkDkMg5R8 🎧 Alum @GonzagaU @peacecorps @pdosoros @SAISHopkins @Columbia_Biz @IFC_org @bcg @gatesfoundation @newamericaBeacon for Rare Disea.. @RareBeacon
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26 Followers 367 Following 1° Congreso de Enfermedades Raras, Poco Frecuentes y Huérfanas que se realizará del 13 a 15 de noviembre próximo en 🇨🇱. Más información en: [email protected]lxjrj7dx2wgou3 @uq4othpktzh
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5K Followers 3K Following Nuclear Advocate | Award Winning Podcaster | Speaker | Captain Connection | #RareDisease #RareMama to my sweet, Ford, who lives with #CTNNB1 🦓SynGAP Research Fund .. @cureSYNGAP1
10K Followers 6K Following #SYNGAP1 🧬 = 🧠NDD DEE causing #Epilepsy #Autism #ID #Sleep #GI. Incidence = 6️⃣.1️⃣/💯k ICD10 https://t.co/4UJNF5bKTl https://t.co/pjCrzqlbV7 🎙Mike Graglia 🌻 @JMGraglia
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93 Followers 624 Following VC @food_labs | Interested in anything FoodTech & BioTechAbdulhadi Aman @abdulhadi_aman
111 Followers 304 Following Child Neurology Resident 🧠 at PSMMC, Medical University of Warsaw 🎓🇵🇱Commission for an epoxy piece to highlight SYNGAP1 protein localization in #neurons. Inspired by a cover from @SfNJournals (link in comments). Walnut, 19in tall. @cureSYNGAP1
@cureSYNGAP1 @ClementYChow @rarebasepbc @omidkarkouti @eperlste @onnofaber @JMGraglia Thanks for posting this @JMGraglia Response coming tomorrow. Sit tight.
@cureSYNGAP1 @ClementYChow @rarebasepbc @omidkarkouti @onnofaber @JMGraglia @mattmight @ssermone There could be an approved form of THC aka Jaden’s Juice for SYNGAP1 if someone actually picked up that ball and ran with it!
@cureSYNGAP1 @ClementYChow @rarebasepbc @omidkarkouti @eperlste @onnofaber This one by @ClementYChow on #NGLY1 feels like a win, journals.plos.org/plosgenetics/a…
@AleRossiNeuro @marlenerong @DrDaniAndrade @Quratulainzali @SyngapNetwork @Syngap1Fnd Thank you for this important work. There are so many #Syngap1 adults. Here is our movie about the oldest one syngap.fund/caren
NEWS! @julietkknowles of @Stanford_Neuro awarded $1⃣3⃣0⃣,0⃣0⃣0⃣ to study maladaptive myelination 🧠 & epilepsy⚡️ in #SYNGAP1 🧬, testing in SRF supported 🐭 models from @rhuganir. #collaboration 🤝 👉 @cureSYNGAP1 Grant applications due in 15 days. eurekalert.org/news-releases/…
ICYMI - #SYNGAP1Stories Episode 14 with SRF BOD Chair Suzanne Jones, featuring Jansen. Have you heard it? Have you subscribed? Syngap.Fund/Stories
There is no cure for #SYNGAP1, but SRF and its extensive team of volunteers are working daily toward that goal. Together, we can do great things! #SYNGAP1Conference2023 #Volunteer
I am absolutely honored to receive a McKnight Scholar award to help us tackle the critical challenge of how the brain encodes social isolation. Especially excited to be included in this incredible cohort of scientists!
📢Announcing the 2023 McKnight Scholar Awards🧠 These 10 scholars are committed to solving the most fundamental problems in neuroscience. Learn more about these incredible neuroscientists and the McKnight Endowment Fund for Neuroscience 👇 mcknight.org/news-ideas/202…
Es un honor participar y representar a @cureSYNGAP1 como panelista compartiendo la historia de nuestra hija Amelia y la importancia de las organizaciones de pacientes que logran cambiar el rumbo de la enfermedad. @cureSYNGAP1 @SMNPediatrica @mexico #Chihuahua #Neurology
Thank you @VickyAArteaga & Paulina for representing #SYNGAP1 🧠🧬at @SMNPediatrica. Our population is underdiagnosed everywhere and we need to raise awareness in Mexico 🇲🇽 and across Latin America. #FondoSyngap
Es un honor participar y representar a @cureSYNGAP1 como panelista compartiendo la historia de nuestra hija Amelia y la importancia de las organizaciones de pacientes que logran cambiar el rumbo de la enfermedad. @cureSYNGAP1 @SMNPediatrica @mexico #Chihuahua #Neurology
Who knew blueberries could teach us about healthy cells? 🫐😲. Today’s #IntroToPath, I use 'em to explain metaplasia (🖤 blackberries), hyperplasia, and hypertrophy 💪🏽. It's like a berry-licious journey through the world of pathology! 🌎#Path4People #BerriesForEducation 🍓🍒🔬
A nice write up at @KSLcom about our partnership with @cureSYNGAP1 to try to find a possible therapy for SYNGAP1. Flies to the rescue. ksl.com/article/506385…
Thank you @KSLcom & @loganstefanich for this writeup on @ClementYChow and @cureSYNGAP1! We are excited about this work and grateful for the partnership for patients with #SYNGAP1. 💊🪰🔬🧬🤞
A nice write up at @KSLcom about our partnership with @cureSYNGAP1 to try to find a possible therapy for SYNGAP1. Flies to the rescue. ksl.com/article/506385…
SYNGAP1 #WarriorWednesday🧬 Michael (age 2) from📍Vienna, Austria 🇦🇹“He likes slides and swings…” Read his story & see more photos at syngapresearchfund.org/syngap-warrior… #SRFWW no.186 #SYNGAP #epilepsyawareness #autismawareness #rarediseaseresearch #SYNGAPResearchFund #CareAboutRare…
Our legal director Kevin Frye and CEO @JMGraglia are @StJude PTNI to learn about Pediatric Translational Neuroscience alongside 3️⃣0️⃣ Patient Advocacy Groups. We are ensuring that #SYNGAP1 is part of the conversation & our patients will have every opportunity for new therapies.
@JMGraglia @curestxbp1 @PennMedicine @ChildrensPhila @Prosser_Lab @EAHellerPhD @IngoHelbig @JillianLMcKee @SydneyStel @charleneson @NolanJoeylynn @SarahRuggieroGC @JulieXXian @SyngapNetwork Can’t wait to see this progress! Also grateful we can go on this journey alongside @curestxbp1.
Another wonderful #Sprint4Syngap! Love connecting with other families while raising awareness and funds for Kai’s rare disease. @cureSYNGAP1
Yesterday was our annual #Sprint4Syngap! Thankful for all the families that participated, researchers who are working hard & @cureSYNGAP1! Still time to donate! Syngap.Fund/Sprint