Top Tweets for #FSHDAwareness
Chris Carrino, The Voice of the Nets, and long-time advocate for #FSHDAwareness, #FSHDResearch, and fundraising was featured in a recent Coaches Corner segment.
Catch one of our favorite commentators below:
When it comes to telling the story of the game, few do it better than Chris Carrino 🎙️
The Voice of the Nets has turned his childhood dream into a 30-year career. Learn more about the behind-the-scenes heroes in Coaches Corner presented by @evernorth.
Watch the Full Episode on the NBA APP! https://t.co/1uMWjyfX8k
📢 The CDC released an update to their website w/ new pages covering the various types of #MuscularDystrophy including #FSHD! Take a peek at the pages which include helpful links and the Kevin's story.
#CureFSHD #FSHDAwareness #FSHMuscularDystrophy #MDAwarenessMonth #MDAwareness
¡Hoy, 20 de junio, conmemoramos el Día Mundial de la Distrofia Muscular Facioescapulohumeral (FSHD)! 💪
¡Ayúdanos a crear conciencia sobre la FSHD! 🧡
#DiaMundialFSHD #FSHD #DistrofiaMuscular #FSHDAwareness #DimusChile
Today on #RareDiseaseDay, we stand with the 870,000 people living with FSHD. 💜 Awareness fuels research, and research leads to a cure. Share and support! 💪 #CureFSHD #FSHDawareness
Happy World FSHD Day from TREAT-NMD! 🧡 Let's unite globally for FSHD awareness. Read more and join us in making a lasting impact > https://t.co/DGcbJskJtb #WorldFSHDDay #FSHDAwareness
#NewsAlert. Fulcrum has entered into a collaboration and licenses agreement with Sanofi for the development and commercialization of Losmapimod, for the treatment of FSHD. Read here: https://t.co/hTEWZNpEVj
#FSHD #FSHDawareness #Biotech #FulcrumTherapeutics #healthinnovations
We recently had the opportunity to interview Michele, a dedicated FSHD advocacy member. When asked about advice for newly diagnosed people with FSHD, Michele emphasized the importance of connecting with an advocacy group. #voicesofrare #projectmercury #fshdawareness #fshd
In several recent posts, we have mentioned the new Project Mercury initiative. We thought it would be helpful to elaborate more on how Fulcrum is joining forces with the @fshdsociety and many other partners. #fulcrumtherapeutics #fshdsociety #projectmercury #fshdawareness
Today is #WorldFSHDDay!
La Jolla Labs is happy to share our Orange Slice Selfie to express our support for all FSHD patients and their families.
#WorldFSHDDay #CureFSHD #FSHDAwareness #LaJollaLabs #RareDiseaseAwareness #RareDiseaseResearch #OrangeSliceSelfie @FSHDSociety
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Today is #WorldFSHDDay – a day to raise awareness of facioscapulohumeral muscular dystrophy (FSHD). In an effort to do just that, here are some interesting #FastFacts. Please share with friends and family!
#FSHD #FacioscapulohumeralMuscularDystrophy #FSHDAwareness
![MD_Canada's tweet photo. [1/2]
Today is #WorldFSHDDay – a day to raise awareness of facioscapulohumeral muscular dystrophy (FSHD). In an effort to do just that, here are some interesting #FastFacts. Please share with friends and family!
#FSHD #FacioscapulohumeralMuscularDystrophy #FSHDAwareness https://t.co/wDlL2PzYqW](https://pbs.twimg.com/media/FVtMrCUWAAEn1TL.jpg)
![MD_Canada's tweet photo. [1/2]
Today is #WorldFSHDDay – a day to raise awareness of facioscapulohumeral muscular dystrophy (FSHD). In an effort to do just that, here are some interesting #FastFacts. Please share with friends and family!
#FSHD #FacioscapulohumeralMuscularDystrophy #FSHDAwareness https://t.co/wDlL2PzYqW](https://pbs.twimg.com/media/FVtMrCTXEAAOSuy.jpg)
![MD_Canada's tweet photo. [1/2]
Today is #WorldFSHDDay – a day to raise awareness of facioscapulohumeral muscular dystrophy (FSHD). In an effort to do just that, here are some interesting #FastFacts. Please share with friends and family!
#FSHD #FacioscapulohumeralMuscularDystrophy #FSHDAwareness https://t.co/wDlL2PzYqW](https://pbs.twimg.com/media/FVtMrCSXsAUzN1M.jpg)
![MD_Canada's tweet photo. [1/2]
Today is #WorldFSHDDay – a day to raise awareness of facioscapulohumeral muscular dystrophy (FSHD). In an effort to do just that, here are some interesting #FastFacts. Please share with friends and family!
#FSHD #FacioscapulohumeralMuscularDystrophy #FSHDAwareness https://t.co/wDlL2PzYqW](https://pbs.twimg.com/media/FVtMrCSWIAEnHT6.jpg)
#TBT to the @FSHDSociety's Virtual Walk and Roll! Our team was proud to walk over 400,000 steps during this year's event! #FSHDAwareness #RareDisease #FSHD
A hearty congratulations to our friends @SchittsCreek on their MANY Emmy nominations! Special thanks to @danjlevy & @sarahlevy_ for your support of those living with FSH Muscular Dystrophy! Good Luck!
#danlevy #sarahlevy #fshd #cureFSHD #fshdawareness #schittscreek #Emmys2020
Our SVP and Head of Clinical Development, Dr. Diego Cadavid recently discussed the genetic factors behind #FSHD and the progression of its symptoms in an interview with @CheckRare See the full interview here: https://t.co/5oqtT0SJQJ
#raredisease #FSHDAwareness
Facioscapulohumeral #musculardystrophy (FSHD) is a genetic muscle disorder in which the muscles of the face, shoulder blades and upper arms are damaged. Pogo is very active in the @FSHSociety. FSHD hasn’t taken away his smile. #fshdawareness #neuromuscular #travelerschampionship
Ik heb weer gedoneerd https://t.co/rUKJ2nv3Ya #FSHDawareness #FSHDhebjenietalleen #geefFSHDeengeicht #donerenblijftnodig
Please follow @dougngracie and help Doug spread the word about his planned Xcountry scooter ride to raise #FSHDawareness!
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