Rikke S. Møller EpiCARE Elena Gardella Epilepsihospitalet, Filadelfia Epilepsiforeningen Torie Robinson 🇺🇦 Madeleine Oudin Francesca Furia International SCN8A Alliance SCN2A Asia Pacific SCN2A Europe SCN2A Families UK @SCN2A Michelle Lewis SCN8A_EU Kris Pierce Katherine Howell I have a very rare type of epilepsy the neurologist said that there was no other epilepsy like the one that I suffer with

🙌A huge shout out to everyone who travelled in, woke at dawn and rode or walked with/for the #SCN2A Warriors! Another great year to fund research with the UPenn Million Dollar Bike Ride by ODC
Together, we will #cureSCN2A ! 💜💙💚

Amazing progress is being made! Excited for the developments in #PrecisionMedicine #actionforaccess #raregene
#curescn2a #scn2a #epilepsy

Taking a treatment from lab to clinical trials & then to becoming available for use is a complex and expensive process. We talk with Kiran Reddy , President/CEO of @PraxisMedicine, the RC-222 treatment program #SCN2A #cureSCN2A #SCN2A insights #podcast

4 months ago I began my journey to epilepsy with my son

#RareDisease #scn2a #epilepsy #geneticepilepsy #curescn2a

Calling all International #SCN2A Professionals...
The FamilieSCN2A Foundation provides International Travel Scholarships to both SRD families AND SRD professionals. Apply here: scn2a.org/conference-202…

Since 2018, we've awarded $1.7M in grants to advance & accelerate #SCN2A research. This has established a foundation of knowledge and resources that are rapidly propelling the entire field towards our Vision of a world with effective treatments and cures for all SRDs. #cureSCN2A

Jeff Lucht T in KC gofundme.com/f/nf36y-cover-…

It's #RareDisease Day2021 ! I've been so lucky to get to know so many #RareDisease champions through my line of work, like Leah, Amber Freed, Dr. Tracy Dixon-Salazar, Michelle Lewis, and Mary Anne Meskis just to name a few. They're amazing. 💜

FamilieSCN2A Michelle Lewis Praxis Medicines Proud of the progress the Praxis team has made

FamilieSCN2A CureCHD2.org Michelle Lewis Twinning!

Michelle Lewis 💙 Tahnk you!

The first half of 2023 has been very rewarding for us at OPKO Renal! We’ve enjoyed participating in events with the #CKD community and helping to push forward the progress of kidney care.  #OPKORenal

Thanks to the #SCN2A community of families, researchers, clinicians & industry groups, we now have two precision treatments approved for trials by the FDA. Many more are in pre-clinical stages & the work will continue until we can treat ALL SRDs. youtu.be/ygzh9zWKzMo

Beyond excited to announce our scientific team! Thank you to Shawn Egan
for leading the squad towards a #cureSCN2A
Big things to come!!!
#scn2a

📣Announcing the Team for Advancing Science and Clinical Outcomes (TASCO) Please join us in welcoming Shawn Egan, Brad Bryan, PhD, MBA Christina SanInocencio, PhD, CPH, CNP
and Dr. Karen Ho
Thank you to CZI Science
#RareAsOne for the support to plan boldly and create these positions to #cureSCN2A

Many thanks to Kris from SCN2A Asia Pacific who visited us at Oxford PharmaGenesis in Melbourne yesterday to talk to us about #SCN2A #cureSCN2A in recognition of #RareDiseaseDay . We really appreciated it!

Eliana had some visitors today from bigslickkc . Thanks Ginger Gonzaga ✨ , Aisling Bea , Taylor Williamson (IRVINE IMPROV JUNE 29!) , and Corbin for brightening our day and bringing your star power to Children's Mercy!

You don't have to wait. Augmented reality is here, now. People are already using Magic Leap 2 to change the way they work.

Rikke S. Møller EpiCARE Elena Gardella Epilepsihospitalet, Filadelfia Epilepsiforeningen Torie Robinson 🇺🇦 Madeleine Oudin Francesca Furia SCN2A Asia Pacific SCN2A Europe SCN2A Families UK @SCN2A Michelle Lewis SCN8A_EU Kris Pierce Katherine Howell See you there!

Today is #SCN2A AwarenessDay ! The more awareness and advocacy for #SCN2A Disorders and other Rare Disorders, the more we build our understanding and advance therapeutics. Our lab is grateful to be part of a very large group of collaborators with common goals to #CureSCN2A .

Michelle Lewis UCDavisMINDInstitute UC Davis Thank you!!!🥰

These really helped me!

Wonderful Meeting in OHIO #SCN2A#cureSCN2A#SCN2ASummerSeminar

Join us in July!

Attending the FamilieSCN2A conference today in Columbus, Ohio. $1 million in research in just a few years! Great start so far! #keeplearning #science #CureSCN2A

Jayne Spink Natasha Fox (Cotter) Genetic Alliance UK #geneticepilepsy #curescn2a #scn2auk