La Force DMD
@laforcedmd
La Force se donne pour mission de rassembler la communauté de la DMD, autour d’un objectif commun : accéder aux nouveaux traitements le + rapidement possible
ID: 2588028470
http://laforcedmd.com/ 25-06-2014 18:53:45
2,2K Tweet
441 Followers
757 Following
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Meta
@meta
Connect with what you love to make things happen. It’s Your World.
The Daily Beast
@thedailybeast
Independent. Intelligent. Influential. Send tips to [email protected] Check out @beastobsessed, our new hub for pop-culture's moments, movies and shows!
Doc Vadeboncoeur
@vadeboncoeur_al
@docvadeboncoeur.bsky.social
Novartis
@novartis
An innovative medicines company working to reimagine medicine. See our community guidelines: go.novartis.social/4bqbjuA
Muscular Dystrophy UK
@mduk_news
We connect a community of over 110,000 people living with muscle wasting and weakening conditions. Together we are stronger. Join us. Our #MusclesMatter.
Rare Disease Day
@rarediseaseday
29 February 2024 is Rare Disease Day. Raising awareness for patients, families and carers around the world that are affected by rare diseases. #RareDiseaseDay
Donald J. Trump
@realdonaldtrump
45th & 47th President of the United States of America🇺🇸
SpaceX
@spacex
SpaceX designs, manufactures and launches the world’s most advanced rockets and spacecraft
CureDuchenne
@cureduchenne
We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community.
Sanofi
@sanofi
We chase the miracles of science to improve people’s lives. Interactions with this account must comply with the Terms: bit.ly/sanofi-terms
The Economic Club of Canada
@economicclubca
THE Podium of Record. We are a national non-partisan organization hosting events with the world's influencers and decision makers across the country.
Elon Musk
@elonmusk
Pharmaceutical Market Europe
@pmlivecom
News & analysis of healthcare, pharma and biotech. Magazines, directories, profiles, jobs & awards.
Parent Project Muscular Dystrophy (PPMD)
@parentprojectmd
Let's advance the research evolution. #EndDuchenne
Pfizer Inc.
@pfizer
We’re celebrating over 175 years of daring scientific innovation and we’re not done yet. Protect your health at PfizerForAll.com on.pfizer.com/CGs
Santhera
@santhera
#Santhera is passionate about improving the lives of patients suffering from a rare disease. #Duchenne #DMD #neuromuscular #theirfutureourfocus #raredisease
Muscular Dystrophy Canada
@md_canada
MDC's mission is to help people with neuromuscular disorders live life on their own terms. #WalkRollMDC #MuscularDystrophy FR: @Action_Musclee
AstraZeneca
@astrazeneca
We're transforming the future of healthcare by unlocking the power of what science can do. Community Guidelines: bit.ly/2MgAcio
Dystrophie musculaire Canada
@action_musclee
DMC soutient l’autonomie des personnes atteintes de maladies neuromusculaires et leur participation à la vie collective. #MarcherRoulerDMC EN: @MD_Canada
Perry Esler
@4kidsforever
Husband, proud father of 4 (one heavenly), die hard Leaf's fan, love travel and craft beer.
Lesley - FPL ⚽️
@weggster
Managed to offend Fess Hole. My laugh triggers fire alarm systems. Music junkie. Gig addict. Incompetent Fantasy Football Manager. Potty mouth. #FPL
TREAT-NMD®
@treat_nmd
Advancing diagnosis, care and treatment for those living with neuromuscular diseases around the world
Safehaven
@safehavento
Safehaven supports individuals with complex care needs by providing high quality, family-centered and community-based residential, respite and transitional care
Sanofi Canada
@sanoficanada
We chase the miracles of science to improve people’s lives. Nous poursuivons les miracles de la science pour améliorer la vie des gens.
Defeat Duchenne Canada
@defeatduchenne
Defeat Duchenne Canada is the country’s only national charity dedicated to ending Duchenne muscular dystrophy.
Who Really Cares?
@theparentcarer
Shelley | SEND Mum | Parent Carer | Disability Rights Advocate & Activist | Accessibility & Inclusion Campaigner | Healthcare Equality & Ethics Enthusiast
Duchenne UK
@duchenneuk
Duchenne UK has one clear aim – to end Duchenne, a devastating muscle-wasting disease. We are the leading Duchenne muscular dystrophy charity in the UK.
Terri Ellsworth
@terriellsworth
Duchenne Advocate/Rare Disease Activist Mom, Designing Mom-Creating awareness & advocating for approval of safe & effective drugs. Words are always my own.
SCDAC
@sicklecellca
Sickle Cell Disease Association of Canada. Advocating for those with SCD in Canada. Like us on Facebook m.facebook.com/SickleCellDise…
Le Pharmachien
@lepharmachien
Mon vrai profil, mais j'ai quitté X.
ADMO A.C.
@admoac
Asociación de Distrofia Muscular de Occidente A.C. somos una institución comunitaria en pro de las personas que viven con esta y otras discapacidades.
Little Steps - Association for DBMD
@tali_steps
עמותת צעדים קטנים למען ילדים חולי ניוון שרירים דושן ובקר. Israeli association for Duchenne/Becker MD
Jett Foundation
@jettfoundation
Empowering families. Fighting Duchenne muscular dystrophy.
mdahellas
@mdahellas
MDA Hellas was established in January 2000, as a non-profit association in order to improve the quality of life of people with neuromuscular diseases in Greece.
Pfizer Canada
@pfizerca
Impacting the health of Canadians / Avoir un impact sur la santé des Canadiens. Commenting Policy / Politique sur les commentaires spr.ly/6009DMpRL
Ilan Ganot
@ilanganot
Sarepta Therapeutics
@sarepta
Commercial-stage biopharma company focused on the discovery & development of precision genetic medicine to treat rare neuromuscular diseases. bit.ly/3XgXshH
Pathfinders Neuromuscular Alliance
@pathfindersnma
User-led organisation, campaigning for choice, control & quality of life for adults with #MuscularDystrophy and related conditions. We offer peer support & info
WuXi AppTec
@wuxi_apptec
WuXi AppTec provides a broad portfolio of R&D and manufacturing services to advance discoveries and deliver groundbreaking treatments to patients.
Bruce Babington
@bruceb39
Dad, Clinical director of Babington Clinic, Mont Tremblant, Québec. Canada. Consultant Sports Osteopath. MD4 medical student SJSM
End Duchenne z.s.
@duchenneend
END DUCHENNE is a patient organization for DMD and BMD in the Czech Republic. We have been working for patients since 2001.
Médecine de Spécialités Sanofi en France
@sanofigenzymefr
Nous poursuivons les miracles de la science pour améliorer la vie des gens.
Scholar Rock
@scholarrock
Biopharma leader in the biology of the #TGFbeta superfamily of protein growth factors. Community Guidelines: bit.ly/3oTuh4a
GENETHON France
@genethonfr
With 200+ experts, Genethon is pursuing its mission to bring life-changing gene therapy products to patients suffering from rare genetic diseases
Journal of Neuromuscular Diseases
@journal_nd
JND | Dedicated to expediting our understanding & improving treatments of neuromuscular diseases | Editors: Carsten G. Bönnemann & Hanns Lochmüller
Lochmüller Lab
@lochmullerlab
Hanns Lochmüller's research lab in Ottawa, Canada. Clinical and basic research in neuromuscular and rare disease. Tweets by Hanns and team.
PERFECT LIFT
@liftperfect
Welcome to perfect lift. Created to make those with disabilities to live life to the fullest again. follow us on Facebook
United Brain Association
@unitedbrainassn
The United Brain Association, Inc. is a 501(c)3 nonprofit organization working to find cures for over 600 Brain and Mental Health-related issues and disorders.
Duchenne Data Foundation
@duchennedf
Bringing data to life to improve the world of dystrophinopathies
Muscular Dystrophy News Today
@mdnewstoday_
We are dedicated to sharing the latest news, research, and muscular dystrophy patient perspectives.
Parent Project Duchenne Russia
@parentrussia
ПЕРВЫЙ РОДИТЕЛЬСКИЙ ПРОЕКТ был создан для улучшения качества жизни пациентов с мышечной дистрофией Дюшенна в Российской Федерации.
Neuromuscular Disease Network for Canada (NMD4C)
@nmd4canada
Canadian network connecting clinicians, scientists, patients, and industry to improve neuromuscular disease outcomes.
BINDproject
@eu_bind
EU funded project to assess and address learning and behavioural challenges in Duchenne and Becker muscular dystrophy
DMD Awareness
@dmdaware
Information on symptoms and statistics about DMD. See instagram.com/dmdaware?igshi… for information on diagnosis and medical research.
NS Pharma
@nspharmainc
Dedicated to improving patient outcomes in #Duchenne muscular dystrophy, eosinophilic granulomatosis with polyangiitis (#EGPA) and other #rarediseases.
Bonjour Menu
@bonjourmenu
Une initiative solidaire pour aider les restaurateurs à mettre gratuitement leurs menus en ligne, accessibles par QR code. #menusanscontact
Duchenne Australia
@duchenneaus
Duchenne Australia
AnnemiekeAartsma-Rus
@oligogirl
Translating science from bench to bedside and from jargon to lay language
Suzie-Ann Bakker
@suzieannbakker
Comms & Events @worldduchenne, @DuchenneDF, soup aficionado, runner 🌱
Sickle Cell Anemia
@sickleacell
Solid Biosciences
@solid_bio
Solid’s mandate is to improve the lives of patients living with devastating neuromuscular and cardiac diseases. #TogetherWeAreSolid
Idorsia
@idorsia
The purpose of Idorsia is to discover, develop and bring more, innovative medicines to patients. See our community guidelines: bit.ly/3gtrhr7
Trump Posts on 𝕏
@trump_repost
Recreating your favorite president Donald J. Trump's Truth Social feed using 𝕏 users & posts when possible.
World Duchenne Organization
@worldduchenne
Global organization to find a cure and viable treatment for those lives affected by dystrophinopathies: Duchenne and Becker Muscular Dystrophy. RT ≠ endorsement
Share4Rare
@share4rare
💻🌍 Collective platform dedicated to promote research in #RareDiseases 🚀 | Tweets en español: @Share4Rare_es | Coordination: @IRSJD_info