🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

We are gearing up for year 10! Mark those calendars & we will see you real soon! #PennMedMDBR2023 #raredisease #cycling #philadelphia

SPEAKER ANNOUNCEMENT: We are pleased to share that the ODC's Deborah V. Requesens will be a speaker at the 1st Latin American Congress on Rare Diseases on March 16–17 in Bogotá, Colombia. congresoercal.com #latinamerica #rarediseases #RSVP #rarediseaseawareness #healthcarepolicy

In honor of #RareDiseaseDay2023, the ODC created this video to help educate young people about what it means to have a rare disease. Are you an educator or school administrator? Please share in your classrooms this week! Press play and pass it on! youtube.com/watch?v=9GcQ9m…

REMINDER! Don't forget about the upcoming case presentations by our JumpStart partner, Rare Epilepsy Network (REN), together with the Epilepsy Foundation of America and the American Academy of Pediatrics (AAP). Register today! surveymonkey.com/r/CCXDDGY

I had a wonderful first day of talks, workshops, networking and meeting the experts Global Genes #RDDS symposium. Ready for day 2!

"Just published our latest study in Nature Communications! 🎉 We've used #SpatialMetabolomics to study in pulmonary fibrosis . Excited about the possibilities this opens up for the future of #PulmonaryFibrosis research! 🧪🔬 #ScienceTwitter rdcu.be/dcgM9

Not riding in the MDBR but still want to participate? Join us for our inaugural Million Dollar Mile! Registration is required for the Million Dollar Mile; register here: bit.ly/MDBR2023 #pennmedmdbr2023 #mdbr #raredisease #mdbr2023

Maintenance of pig brain function under extracorporeal pulsatile circulatory control (EPCC) biorxiv.org/cgi/content/sh… #biorxiv_neursci

The @chowlab is looking for multiple postdocs to work on Precision Medicine for rare disease! Opportunities to work with industry, patient foundations and physicians. Starting pay will be substantially higher than NIH minimum. DM or email me! static1.squarespace.com/static/5586048…

There are only three days left to register for our first Research Ready Series session in Indianapolis on August 26th! We hope to see you there! Find more information and register here: g1dfoundation.org/research-ready…

🚨🚨🚨The 2023 #MDBR Pilot Grant Program is now open and accepting Letters of Interest (LOIs)! Apply here today: bit.ly/MDBR2023RFA LOIs are due Sept. 15th. Grants are open to the international research community. 🔬🔬🔬 #raredisease #rfa #pennmedmdbr2023 #rarediseasegrants

Thrilled to share the $61,901 grant available for Glut1 Deficiency research through the MDBR. LOI's are due September 15th. We can't wait to see where this road leads and thank all who put their hope in motion and supported our efforts! Learn more: static1.squarespace.com/static/5fbd2cd…

We're proud to be part of the 8th Global Symposium on Ketogenic Therapies right around the corner! Hotel discounts end today...make your plans and learn more at the links below: web.cvent.com/event/cc711566…

Key point: Even if exome sequencing is negative in patients with epilepsy there are additional diagnostic options in the pipeline doi.org/10.1111/epi.17… #epilepsy #epilepsygenetics #reanalysis #DNAmethylation #transcriptomics #ILAE International League Against Epilepsy @epilepsiajourn Wiley Neuro

Honoring Dr. Darryl De Vivo's move to Professor Emeritus. Read: g1dfoundation.org/dr-darryl-de-v… Watch: vimeo.com/858390018

Speech and language impairments are a hallmark symptom of Glut1 Deficiency. A new international study is enrolling now to learn more. More details on our Glut1 Glimpses blog: g1dfoundation.org/speech-and-lan…

Our 2024 Love Some1 With Glut1 campaign video is out now and we’re so excited to share it with you! The annual fundraising campaign is just two weeks away! youtu.be/8EHptVSNb6w?si…

Contrary to popular belief, rare diseases aren't that rare. Shockingly, over 400 million people worldwide are living with one. That’s larger than the population of the US. Reshare this post to help spread awareness that #RareIsCommon. #RareDisease #CareAboutRare #RareDiseaseDay

Today is International Epilepsy Day. Check out our Glut1 Glimpses blog to read about some of the special advocacy efforts today aimed at focusing more attention and funding on the epilepsies. g1dfoundation.org/international-…

Now online! Infant microbes and metabolites point to childhood neurodevelopmental disorders dlvr.it/T53w3p