Top Tweets for #Musculardystrophy
Thanks to @RHPFFA for raising funds for Muscular Dystrophy Canada @MSCanOfficial at Boot Drive in Richmond Hill today. @YorkRegion #RichmondHill @1059TheRegion #firefighters #musculardystrophy #MS #boots #fundraiser #ONPoli #ONMuni
📢 Big news!
@SecretomeTx has raised $30 million to advance its neonatal cardiac progenitor cell-derived therapy toward late-stage clinical development for Duchenne #MuscularDystrophy-associated #cardiomyopathy.
Learn more: https://t.co/d4QqiIiDyG
Delhi | Mumbai
📞 +91-9820850187 | +91-9820800187
🌐 https://t.co/PH9RUbf9ne
Free DMD Treatment, Jharkhand CM Relief Fund, Bone Marrow Cellular Transplant, Neuromuscular Disorder Treatment, DMD Awareness, Cellular Therapy
#DMDTreatment #MuscularDystrophy #DrBSRajput
Latest Editor’s Choice article in #TheJournalOfPathology (July 26 issue): https://t.co/oEjf2sq37W
#Duchenne #Becker #MuscularDystrophy #Pathology #PathSoc #PathTwitter #OpenAccess
https://t.co/RWnHSr1Maj
Myths & Facts About Muscular Dystrophy.
Clearing up misconceptions and sharing the truth from my lived experience.
#MuscularDystrophy #DisabilityAwareness #MythsAndFacts
Join us TONIGHT to see the impact your support is making for individuals and families affected by #Duchenne #musculardystrophy across Canada.
📍 2026 Community Annual General Meeting
🕡 6:30-7:30 p.m. ET
💻 Online open to all: https://t.co/JqvS83iTHR
⌛ We hope to see you tomorrow for our virtual Annual General Meeting!
Together, we’ll reflect, look ahead, and continue building a stronger, more connected community for everyone living with #Duchenne #musculardystrophy: https://t.co/JqvS83iTHR
New work from the lab of Dr. Atsushi Asakura at @umnmedschool has shown that pathogenic JAG2 mutations disrupt #Notch signaling in muscle stem cells and their niche, impairing muscle regeneration and causing #MuscularDystrophy.
📖 Read the @jclinicalinvest study: https://t.co/Pn41xbUKll
Researchers led by Dr. @DJSiegwart at @UTSWMedCenter have identified a #LipidNanoparticle capable of efficiently delivering RNA and gene-editing therapies to heart cells, enabling correction of a duchenne #MuscularDystrophy mutation and restoration of dystrophin expression.
📑 Read the @PNASNews study: https://t.co/gX9biNUXvZ
தசைகள் தேய்ந்தாலும் கனவுகள் தேய்வதில்லை! | நட்சத்திரக் குழந்தைகள் 22
| #MuscularDystrophy | #Muscles |
https://t.co/mkslgcFxNK
During #Pride Month it is important to acknowledge our intersecting identities. I am gay and I have Becker #MuscularDystrophy. #BMD @MD_Canada
If you're going to the @Cardinals game tonight, look for our son, Liam, who will be representing the @MDAorg in a pre-game ceremony on the field. The game starts at 6:45, so it'll be shortly before game time. #STLCards #DuchenneMD #MuscularDystrophy #MDA
Pro-Palestine prisoner Umer Khalid, a 22-year-old with muscular dystrophy, has been dragging himself across his prison cell floor because he has been denied a wheelchair.
He hasn't had access to a shower for over 20 weeks.
He has been waiting for a neurology appointment for over 12 weeks while experiencing chest pain and breathlessness.
This is happening in a British prison right now.
I've written to David Lammy to demand answers:
“ Lo más pesado de la silla no son las ruedas es la mirada de la gente” cuando existe una rampa que no va a ningún lado o que está mal hecha ♿️
#distrophiemusculaire #silladeruedas #03Dic #wheelchair #discapacidad #distrofiamuscular #musculardystrophy #Duchenne #fauteuilroulant
A final decision from the FDA is expected by Nov. 27, and if approved, BBP-418 would become the first FDA-approved therapy for LGMD2i. https://t.co/6fgekFeUO0
#musculardystrophynews #musculardystrophy #musculardystrophycommunity #livingwithMD
Dyne launched a global clinical trial, FORZETTO, to test its exon-skipping therapy z-rostudirsen in boys with Duchenne muscular dystrophy. https://t.co/ZXGmYoawOd
#musculardystrophynews #musculardystrophy #musculardystrophycommunity #livingwithMD
Columnist Patrick Moeschen invites readers to join the newly relaunched Muscular Dystrophy News Today Forums, where a community is growing. https://t.co/tuJRY3VHKJ
#musculardystrophynews #musculardystrophy #musculardystrophycommunity #livingwithMD
Day #3. #MuscularDystrophy has taken away certainty about what my body will be able to do tomorrow. It hasn’t taken away my ability to #hope.
Hope that accessibility will improve.
Hope that people with disabilities will be valued.
Hope that the next generation won’t have to fight the same barriers.
Hope keeps people going. It keeps me going, too. ♿️
#WalkRollMDC #WalkRoll2026
Final Walk & Roll fundraising week. Help me reach my goal.
https://t.co/k7LOVhFsm3
Day #2. #MuscularDystrophy has made many things harder and slower for me. It hasn’t taken my appreciation for the people who continue to care about me and help me. Your support matters more than you probably realize. ♿️
#WalkRollMDC #WalkRoll2026
Final Walk & Roll fundraising week. Help me reach my goal.
https://t.co/k7LOVhFsm3
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