Top Tweets for #WDAD20
Continuing our efforts to spread awareness of #Duchenne Muscular Dystrophy (DMD) this week, Parexel experts explain how making progress in treating DMD patients benefits the broader #raredisease community and how Parexel is making a difference. https://t.co/db5AEIUjy5 #WDAD20
We are proud to sponsor the Jett Foundation and World Duchenne Awareness Day to help raise awareness for the Duchenne community and focus attention on the need for research and therapies. #TogetherWeAreSolid #StrongerThanDuchenne #WDAD20
La #DistrofiaMuscularDeDuchenne es una #EnfermedadRara de origen genético que afecta el funcionamiento del tejido muscular
La invitación es a publicar en #RedesSociales fotos con escaleras y etiquetarlas con #DMDday
¡Contamos contigo!
#JuntosSomosMásFuertes #WDAD20 #Duchenne
🎈🎈TODAY is World Duchenne Awareness Day!🎈 Duchenne is the #1 genetic killer of boys, yet many people have never heard of it. 1 in 3,600 boys and 1 in 50 million girls are born with Duchenne. ...
#WDAD20 #DuchenneAwareness #stopDUCHENNE
🎈🎈TODAY is World Duchenne Awareness Day!🎈 Duchenne is the #1 genetic killer of boys, yet many people have never heard of it. 1 in 3,600 boys and 1 in 50 million girls are born with Duchenne.
#WDAD20 #DuchenneAwareness #stopDUCHENNE
Hoy 7 de septiembre es el día mundial de la concienciación de Duchenne. Con este día se intenta dar visibilidad a la enfermedad. Conseguir q se conozca más, q haya + investigación y mejorar la asistencia sanitaria y el diagnóstico. #desafioduchenne #duchenneawarenessday #WDAD20
Thank you @vijaychandru for joining us at the #WDAD20 virtual conference and opening our eyes to the Future of Genomic Medicine.
We sincerely believe we are at the cutting edge of technology to personalized medicine as potential therapy for #RareDiseases.
Thank you sir!
It's World Duchenne Day! @US_FDA has accepted a New Drug Application from @Sarepta, seeking accelerated approval for casimersen, created by our own Prof Steve Wilton & Prof Sue Fletcher. Let's wait for the Feb 2021 announcement to see if it's approved. #WDAD20 #neuroscience
Today is World Duchenne Awareness Day. If you have, know or love someone with Duchenne or Becker Muscular Dystrophy, show your involvement by posting on social media to increase awareness around the world! #WDAD20
Imorgon 7/9 uppmärksammar vi den obotliga allvarliga sällsynta diagnosen Duchennes muskeldystrofi över hela världen 🎈 #wdad20 https://t.co/CE6eHFXzcp
#wdad20 tommorow please help us raise awareness by sharing the red balloon 🎈🎈🎈
Join us tomorrow at the #WDAD20 Virtual Conference and you can get to meet our DMD warriors!
Say hello to Master Muscle Karanveer Singh!
#DMDWarrior #RareDiseases
Register here! - https://t.co/iMrFedUmGj
Join us at the #WDAD20 Virtual Conference and you can get to meet our DMD warriors!
Say hello to Amogh Petkar!
#DMDWarrior #RareDiseases
Register here! - https://t.co/iMrFedUmGj
Join us at the #WDAD20 Virtual Conference and you can get to meet our DMD warriors!
Say hello to Ameya Karpur!
#DMDWarrior #RareDiseases
Register here! - https://t.co/iMrFedUmGj
If you'd like to be part of our Virtual Conference on #WDAD20 - September 7, and listen to global experts and families do register here ASAP as only limited seats remain - https://t.co/iMrFedUmGj
Join us at the #WDAD20 Virtual Conference and you can get to meet our DMD warriors!
Say hello to Rishi Chowhan!
#DMDWarrior #RareDiseases
Here is the complete list of speakers for the #WDAD20 Virtual Conference
1/4
From the world of Research
Here is the complete list of speakers for the #WDAD20 Virtual Conference
1/4
From the world of Research
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