First day of school. Stronger together for SLC6A1 💪 Wear your SLC6A1 shirt, show you care 💟 #StrongerTogether #SiempreLuchandoContigo #SLC6A1 Siempre Luchando Contigo

Congrats to Rachel June Smith, Ph.D., and Scott Cruikshank, Ph.D., winners of the 2025 FCIDD McNulty Civitan Scientist Award! Their research will study SLC6A1 neurodevelopmental disorders using cutting-edge neuroscience tools. 🧠🔬 UAB Heersink School of Medicine Read more: buff.ly/sx4SwzY

✨ Ricerca, famiglie e speranza per il futuro 🧠💚 #Uninsubria al 1° Simposio europeo #SLC6A1Europe: la prof.ssa Elena Bossi e la ricercatrice Tiziana Romanazzi hanno presentato studi innovativi sulla rara patologia #SLC6A1-NDD 🔬🤝 🔗 uninsubria.it/simposio-SLC6A… #MalattieRare

💜 "Entre consultas y urgencias, la incertidumbre ahoga a las familias ante una enfermedad grave". El testimonio de Ana, madre de Luis con Hiperplasia Suprarrenal Congénita, refleja la urgencia de un cribado neonatal universal y equitativo en España. 👉enfermedades-raras.org/actualidad/not…

We invite you to participate in a study assessing #EEG competence.🧠⚡️The task is to review 15 routine EEGs. No personally identifiable info will be collected. You will receive a personalized performance summary benchmarked against expert consensus. #ILAE ilae.org/news-and-media…

Siempre Luchando Contigo celebró en Lisboa su primera conferencia internacional sobre esta enfermedad neurológica rara 💜. Familias 👨‍👩‍👧 y más de 30 expertos unieron fuerzas para dar visibilidad, impulsar la investigación 🔬 y sembrar esperanza. 👉Más información: enfermedades-raras.org/movimiento-aso…

📣 Applications are OPEN for the 2026 EURORDIS Open Academy in Barcelona! 📣 Be part of the next wave of patient advocates shaping research, regulation & policy. 🗓️ Apply by 17 Oct 2025 🔗 Info: openacademy.eurordis.org #EURORDIS #ERDERA #OpenAcademy #RareDiseases

Congratulations #RachelJuneSmith, #ScottCruikshank and grateful from the #slc6a1 community! 🎉

🧠 WHAT is #SLC6A1? 🔎 HOW does it originate? 🔬 WHEN will be therapies? ℹ️ WHERE to get information? 🤖🎙️ AI explains it to you youtu.be/2TJsJmDFG94?si… 🇬🇧🇪🇸🇩🇪🇵🇹 A very usefull "artificial" podcast by Dennis Lal for the needs of a 🤏#raredisease and with ⚠️high #underdiagnosis

🔤🧬 LET'S LEARN about #genetics to understand the #SLC6A1 mutation, 👨‍🔬🧠 and its ROLE with #GABA, the main #BRAIN inhibitory #neurotransmitter. 💡 Explained simply, visually, and for families. The more we understand, the closer we will be to a cure. #NoFutureWithoutScience

Ya estamos por aquí!!! A darlo todo! 💪 Todo por mi Isabel y los niños como ella. #SiempreLuchandoContigo #SLC6A1 Siempre Luchando Contigo Fedeepilepsia SLC6A1 Europe

Today we are attending in Madrid, Spain, the 3rd meeting of the Spanish Federation of Epilepsy (FEDE) #SLC6A1 #SIEMPRELUCHANDOCONTIGO Fedeepilepsia

🚨 Called rare but 30M people in 🇪🇺 live with a #raredisease. 🐣 1/20 births are affected. 🌱 On #RareDiseaseDay, we raise awareness for #SLC6A1. 👂 Until Feb28th hear from doctors, scientists & families fighting for progress. 🌈 Rare is the condition. Inaction shouldn’t be.

SLC6A1 Europe Siempre Luchando Contigo SLC6A1 Connect Todo por Isabel. SLC6A1 🌍 Rare Disease Day Rare Disease Advocates EURORDIS-Rare Diseases Europe Fundación Poco Frecuente Rare Diseases Soy mamá de Hugo, un niño con #SLC6A1. Su vida está llena de retos invisibles, pero también de una fuerza que me enseña cada día lo que es el amor de verdad. Nos dicen que es raro. Para mí, raro sería no luchar por él. #RareDiseaseDay #EnfermedadesRaras