
SLC6A1 Connect
@slc6a1_connect
SLC6A1 Connect is a non-profit dedicated to curing the rare neurological disease SLC6A1.
ID: 1024378045874954240
http://www.SLC6A1Connect.org 31-07-2018 19:35:32
164 Tweet
442 Followers
201 Following

Clement Chow
@clementychow
henfluencer - geriatric millennial - #stopasianhate - don’t call me Clem - emotional eater™️- he/him- @chowlab
Prof Ingrid Scheffer
@ingridscheffer
Laureate Professor of Paediatric Neurology at @unimelb, @theflorey, @austin_health, @RCHMelbourne. Research epilepsy, classn, genetics, speech & mentorship
Andres Jimenez-Gomez MD
@dretico
🇨🇴 Developmental neurologist in TX. I like #DEEs, mind-body integration, #neurogenetics. opinions strictly my own and do not reflect those of my employer
Ricardo Morcos
@richmrc4
Complex Epilepsy @UCLIoN @UCLH⚡️🧠 🌎Geopolitics. Economy. Social Justice
Coalition to Cure CHD2
@curechd2
Fighting for our kiddos, and others, with CHD2-related neurodevelopmental disorders. Contact us: info@curechd2org
Rocio Rodriguez
@rociormiralles
The more I know, the less I want to know
Ethan Perlstein bio/acc
@eperlste
ceo @PerlaraPBC (@ycombinator W16), ceo @epalrestat, ceo @endrarediseases, solo vc @AngelList, evo pharmacologist, mTOR worshipper, cofounder of K&L, $CURES
Terry Theologes
@terryicu

Agustina Fernandez G
@agusferg
Partner @FernandezSecco. Rare Mum VP & Patient Care Lead @CureGABAA
Ana Mingorance
@cnsdrughunter
🧠 🧬 Neuroscientist. Looking for new medicines for CDKL5, SCN1A, SHANK3, DHPS and a few others. @cnsdrughunter.bsky.social
Becky Sansbury
@aftrtheshock
Emotional Support Specialist | Rare Disease | Palliative Care | Author of "After the Shock" | former hospice chaplain | always a mom
Stephanie Fischer
@rarepov
#Raredisease patient advocate & #stroke survivor.🦓 Member of @PARareDisease. Opinions are my own.
Ɱìʂʂ Ɱąçąɾróղ 🌍🌎
@macarron_i
Hispanista Crítica
Tracy Dixon-Salazar
@tracydixonsalaz
Mom. Rare Disease & LGS Advocate. Neuroscientist. The largest most neglected healthcare resource, worldwide, is the patient. Executive Director @LGS_Foundation
Jillian Hastings Ward
@hastingsj123
'that mother' - #R4Today🎙Patient advocate, mum and wife. Genomics fan. Write a bit, talk a lot. MBE!
Dennis Lal
@laldennis
Director of the Center for Neurogenetics; Associate Professor at UTH - Neurogenetics & Informatics - My opinions are my own & do not reflect my employer.
FamilieSCN2A
@familiescn2a
Our vision is to find effective treatments and a cure for SCN2A disorders.
Laura DC
@laudika12

Dr. Lidia Sabater
@lidiasabater1
Neurobiologa-Científica. Catalana y del mundo.
CReyes-Housholder
@reyeshousholder
Associate Professor, ICP-Universidad Católica. Author: How Women Win Presidential Elections in Latin America (Forthcoming. Temple University Press)
Leah
@leahedscn2a
Founder, Executive Director and Former President of the FamilieSCN2A Foundation. Mom and rare disease advocate of epilepsy and autism, SCN2A-related disorders.
ResearchNet ERI
@researchneteri
Researcher Network of @EpilepsyInst. Radically advancing research into epilepsy. For #epilepsyresearch funding and capacity building opportunities join The Hub
Effie Parks
@onceuponagene
Rare Disease Advocate | Award Winning Podcaster | Speaker | Captain Connection | RareMama to my sweet, Ford, who lives with #CTNNB1 🦓
Long-Cheng Li
@rnaa_biologist
President & CEO, Ractigen Therapeutics
Erica Enneking
@ennekingerica

Brain Ablaze
@brainablaze
As people with Epilepsy, we raise awareness for Epilepsy and support anyone having seizures. | The Brain Ablaze Epilepsy Podcast | Blog | Support
CACNA1A Foundation
@cacna1a
Nonprofit dedicated to a brighter future for those with CACNA1A variants. On a mission to fund life changing research while supporting families along the way.
n-Lorem Foundation
@n_lorem
Discovering, developing, and providing personalized experimental ASO medicines to treat nano-rare patients — for free, for life
Luzsolidaria_oficial
@luzsolidariao
La única eléctrica 100 % renovable que destina su beneficio a proyectos solidarios y a crecer para seguir ayudando a las personas. #AhorroSolidarioYSostenible
Katrien
@katriendeckers
Rare disease Mum working to find a cure for her son, Bear @cureSYNGAP1 #Syngap1 #epilepsy #autism #ID
Isabel de Hungría
@isabelhungary
Vamos a dar visibilidad a la enfermedad de Isabel, de 8 años, la mutación del gen #SLC6A1.
Adrigal
@adrigal6
Pediatric neurologist with special interest in epilepsy
Alejandra Vasquez, MD
@alejavasquezmd
Epilepsy Fellow @MayoClinic| Proud wife @felipejonesMD | Tweets are my own
Fundación Energía Responsable
@energiarespons
Organización sin ánimo de lucro que lucha contra la pobreza energética, impulsa la inclusión laboral de personas con discapacidad y los 17 ODS del Pacto Mundial
Hanan Atwan
@hananatwan12
Pediatric neurologist
Abby Turnwald (she/her)
@pedsgcabby
Pediatric genetic counselor, neurogenetics, advocate for the rare disease community, let’s talk about sibling health
AYER PACIENTE HOY DOLIENTE 🧬🦋
@linarg17
DIOS 🇻🇦 FAMILIA👨👩👧👦👼🏻🤱🏻 (Madre de 4) 🧬 Madre de niña con mutación SLC6A1 (Buscando respuestas) Patria 🇨🇴 LIBERTAD y ORDEN👮🏻♂️ DIOS Y PATRIA
Mahesh Kumar
@mkumartweets
Materials Sci, Computer Science, - dad to GNAO1 warrior princess. bassist, guitarist, curiosity may have killed the cat, it keeps me going. love rule breakers
Priyanka Kakkar
@pkakkar98

Black
@lisatedasm76761

Teautis
@teautis111727
Undiluted joy.
Seauteasm
@seauteasm95375
digital Art
McSmeme
@smememc85802

Tesanee
@tesanee193083

The Med13L Foundation
@med13l_fdn
Supporting MED13L families through awareness, research, and community. Connecting hearts and minds to overcome challenges. #NDD #Epilepsy #Autism #ID 🧬💙🧠
Siempre Luchando Contigo
@slc6a1_spain
Ass. de familias con hij@s con #EnfermedadRara (1/38.000): “#EncefalopatíaEpiléptica y del Desarrollo por la mutación del gen #SLC6A1”
WitWinslet
@winsletwit94286

CERPOHCHI
@cerpohchi
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]
Melinda Hughie Blalock
@mmhblalock
mom • wife • medical mom {epilepsy⚡️ASD} advocate 🧠epilepsy parent support navigator🫀#TAAD aneurysm & #THYCA🦋 survivor 🏥St. Jude fundraiser
Ben Forred
@zebrasites
I make and manage awesome websites for #raredisease advocacy organizations. Husband, father, rare disease patient/researcher, web designer 🤓
@AutismHopeX
@autismhopex
#autism #asd #autismawareness #saveourchildren #autismismedical #autismepidemic #MAHA #autismhope #vaccinescauseautism #autisticlivesmatter
Kim D
@kimd7572

Bobby
@bobby1471144

Geartsoa
@geartsoax2cdi

Tiziana Romanazzi
@romanazzi1994

Tiopairs
@tiopairs18z

Daniel Destine
@danieldestines
I Help BizOwner Scale Online & ppl 9-5 💳 Build Your Cardit To 750+🏦 Account $500k Funding 💸😴🛌🏿 📱 DM Me Mentor for Access 👇🏾 FREE MASTERCLASS
FOXG1 Research Center
@foxg1center

Kira Durgan
@kiradurgan97910

Theechest
@theechestw888r
To be human is not just to be sorry, but to be human, please work hard
Dr. Heather Mefford @hcmefford.bsky.social
@hcmefford
Physician, scientist, mom, wife #genetics #epilepsy #pediatrics #raredisease @StJude @StJudeResearch formerly @UWMedicine
Helen Chen, PhD
@helenc327
#iPSC scientist & #organoids engineer for #RareDisease working on disease modeling & precision medicine. @StJudeResearch, @ubc alumnus🇨🇦
Heidi Grabenstatter
@patientintv
RDCA-DAP Scientific Director @CPathInstitute, patient advocate, neuroscientist, and proud mom. Opinions are my own.
Erin Hackett
@erinhackett84

The Notorious EEG (M. Scott Perry MD)
@thenotoriouseeg
Epileptologist/Head of Neurosciences @cookchildrens, I 💜 #HailState, buffalo wings, art, music & foremost Becky & my daughters. Views are mine, not my employer
Brian Wallach
@bsw5020
Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.
Barbara Vona
@drbarbaravona
Group leader | UMG (Göttingen) | @AuditoryNeuros | #Genetics of #HearingLoss | 🇨🇦➡️🇺🇸➡️🇩🇪| Here to tweet about science and #Genes 🧬
Ella Mercer (she/her)
@ella_mercer1
Research Involvement and Comms Officer @UKTSA. Passionate about amplifying patients and carers voices. All views are my own, retweets are not endorsements.