MS Int'l Federation
@MSIntFederation
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The MS International Federation is a unique global network of MS organisations. We have 50 member organisations from around the world, and links to many others.
Joined October 2011
MSIF’s vision is a world without MS. Our mission is to bring the world together with urgency, to improve the quality of life and wellbeing of everybody affected by MS, and to end MS forever. ✨ Read more in our 2023-2027 global strategy here. 📝👉
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On Feb 11, we celebrate the International Day of Women & Girls in Science. We spoke to Marie Kupjetz, researcher & cyclist, taking part in Cycle for MS. She shares her thoughts on being a #womaninscience and her expectations for #CycleforMS. 👉
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Join Cycle for MS: Conquer the Tour and push your limits on over 400km of breathtaking terrain, including Col d’Aubisque and Col d’Aspin. Time is running out to join the team. #CycleforMS
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Catch up with the latest #ProgressiveMSAlliance webcast with subtitles in Arabic, French, Italian, Spanish & English. Hear from researchers behind MS clinical trials as they discuss outcomes, learnings & how the findings are shaping future research. 🔬 👉
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Voting for the 2025 Smiley Charity Film Awards closes tomorrow! 🎬🏆Vote for the latest #WorldMSDay animation and help us shine a spotlight on MS diagnosis stories from around the world. 🌎 Every vote counts! #SmileyCharityFilmAwards #MyMSDiagnosis
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A new publication in @MSJ_Research shares recommendations for a group of treatments that the MS community believes should be available in low-resource settings. 💊💉 The MS community can use these recommendations to advocate for change. 📣 Learn more. 👉
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Policymakers, patient advocacy groups, healthcare workers, and people with MS can use these recommendations to advocate for change. 📣 Learn about the recommendations and how to use them. 👉
Recommendations for essential medicines for #MultipleSclerosis in low-resource settings. A @MSIntFederation initiative including @DeannaSaylor1 @JohnsHopkins @twpiggott @QueensKingston @Ptbohealth ▶️
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MSIF is delighted to announce Lydia Makaroff as its new CEO. 📣🎉 Lydia is public health leader, working to improve healthcare systems through the power of global collaboration. 👏 Read Lydia’s message to the global MS community. 👉
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Just one week left to vote for the ‘My MS Diagnosis Animation’ to be shortlisted for the Smiley Charity Film Awards. 🎞️📽️ Vote for the animation and help us amplify the voices of people with MS globally. 📣🌏 Vote here 👉 #WorldMSDay #MyMSDiagnosis
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LAST CHANCE TO RIDE! ⏰ #CycleforMS is one of Europe’s most unique and challenging charity cycling events and now is your final chance to join us in the #TourdeFrance mountains. We have very few places left. 🚴♂️ Find out more and sign up here:
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'The event is more than a cycling challenge; it’s a journey of resilience, community, and connection.' - Rouleur Magazine 👉 Sign up for Cycle for MS before the end of January to join the kick-off team meeting & secure your branded cycling jersey!
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In December last year, we reflected on our year and looked ahead to 2025. 2024 was a year of action towards our three strategic aims.🎯 Read our 2024 highlights to learn more about MSIF’s activities in 2024 and our plans for the year ahead. 👉
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New Year, New challenge! 💪 Join us at #CycleforMS 2025 which takes on the toughest mountains of the #TourdeFrance route, just weeks before the pros. 🚵♀️Take on the challenge, register for one of Europe's toughest charity cycling event now! 👉
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We would like to wish everyone from across the global MS movement a wonderful the New Year. 🎉 The global movement have achieved so much this year and will continue to work to improve the quality of life and wellbeing of everybody affected by MS, and to end MS forever. 💪📣
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📣 Calling all cyclists. 📣 Looking for a new year’s challenge for you and your friends? 👀 Try cycling the toughest mountains of the #TourdeFrance whilst raising vital funds for MS. 🚵♀️ Join #CycleforMS and take on the challenge in 2025. 👉
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Seasons greetings from the MS International Federation. 🥳
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It’s been a year of action at MSIF. As the year draws to a close, join us as we reflect on 2024 and look ahead to the future. Click the link to read about this year's highlights and more✨
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Don’t forget to vote for the ‘My MS Diagnosis Animation’ in the Smiley Charity Film Awards.📽️ 🌏 The awards celebrate and amplify cause-based films. We need your votes to get the video shortlisted. Vote now! 👉
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‘It was an experience that still feels like a dream’ – Tu D, 2024 Cyclist Do you dream of riding the #TourdeFrance? 🚵♀️ Join one of Europe’s toughest cycling events and #ConquertheTour in 2025. Read more here: #cycleforms #cycling
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‘We applied for support because it’s really expensive, but we were not successful.’ Tarrbinder, Malaysia The cost of MS treatments should be addressed to create fair and sustainable solutions. 💰📣 Read more: #InternationalUniversalHealthCoverageDay
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Cycle for MS: Conquer the Tour, our annual Tour de France cycling challenge has created a new Instagram page! Give them a 'Follow' to hear about all things to do with the event: #cycleforms #multiplesclerosis #tourdefrance #cycling #roadbike
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