The MS International Federation is a unique global network of MS organisations. We have 48 member organisations from around the world, and links to many others.
Yesterday, the Scientific Steering Committee of the Global Patient-Reported Outcomes for Multiple Sclerosis (PROMS) Initiative met to review progress and discuss the next steps in advancing patient-centred research and care in MS.
#MultipleSclerosis#MS#PROMS
There are several hundred people living with MS in Yemen, and many struggle to access disease modifying therapies (DMTs) with no health insurance system or support programs providing sustained MS medication.
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Sign up for @ECTRIMS Patient Community Day 2026 – an online and onsite event hosted by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) https://t.co/rhnVEhmbXw
🎉 Final Total for The May 50K 2026
We are so happy to announce that globally The May 50K 2026 raised an incredible £1,609,836.58 (€1,869,060.52). Thank you so much for all your donations.
#themay50k@mssocietyuk@DMSG_BV@MS_Research@MSIRELAND
MSIF is proud to take over as the new host of the MS Brain Health Initiative. The transition creates new opportunities to connect the MS Brain Health Initiative with MSIF’s global network. Read more here: https://t.co/RdWBM7UR1x
🌍New research highlights global gaps in access to MS diagnostic testing
Advances in MS diagnostic criteria mean people can be diagnosed earlier than ever before. But access to the tests needed to make that diagnosis is not equal worldwide https://t.co/D0Zb3A6vUu
🌍 Join us at @ECTRIMS Patient Community Day on 23 Oct. Engage with global experts, ask your questions, and better understand what new discoveries mean for your care and daily living.
Sign up today ➡️ https://t.co/1E9pB0ziya
Celebrating the first AFRICTRIMS Conference 🌍
The first African Committee for Research and Treatment in MS (AFRICTRIMS) conference, held from 29–31 May 2026 in Ghana, marked a historic and inspiring milestone for the MS community across Africa. 👉https://t.co/kZYX8XbdHr
🧡 MS is often misunderstood, which can make life even harder for those affected by MS. Let's separate fact from fiction. This poster tackles the misconception that MS is the same for everyone. ➡️ https://t.co/z5HfxHYcZX
Apply now to run the London Marathon 2027 for MSIF 🏃 Join Team MSIF in the TCS London Marathon 2027 and turn every mile into meaningful impact. Apply now! 👉 https://t.co/ognlRz5DVH
📣 Registration now open! Patient Community Day is happening on 23 Oct, and we are excited to be supporting this event. Join us for this FREE online & onsite event sharing the latest research in MS, NMOSD, and MOGAD @ECTRIMS#ProudSupporter
➡️ https://t.co/nfZBghiVjj
MS fatigue is more than just feeling tired — it’s one of the most common and invisible symptoms of multiple sclerosis. It can feel like overwhelming exhaustion, heavy limbs, brain fog, or a complete lack of energy, even after rest.
➡️ https://t.co/n0d79myuLh
#multiplesclerosis
This time last year... 🚴♀️🏔️💛 Riders from around the world were taking on the challenge of a lifetime in the French Pyrenees as part of Cycle for MS.
Interested in joining the next adventure? Find out more: https://t.co/2tTJDdotIV
#cycleforms
🧠 Just one week left to join this free MS course!
Want to learn more about Multiple Sclerosis (MS)? There's still time to take the free online course "Multiple Sclerosis: Symptoms and Diagnosis" before it closes on 15 June. ⏳➡️ https://t.co/tXgM9jPUh4
🎉 £1.5 million raised by The May 50K (and counting...)
The May 50K is a virtual challenge to walk, run, or roll 50K throughout the month of May. This year, 14,000 participants all across the world have hit an incredible fundraising milestone of £1,500,000!
#TheMay50K
This free online course for World MS Day will deepen your understanding of MS symptoms, the diagnostic process, and the impact of an MS diagnosis. 🧠 Open to anyone with an interest in MS.
👉https://t.co/tXgM9jPUh4
@darwish_bassam Thank you for your comment. We need both awareness and advocacy to bring about positive change for people living with MS. Together with our members across the world we advocate for better access people-centred to healthcare, rehabilitation and care.
Hear from our CEO, Dr Lydia E Makaroff, about MSIF's recent global advocacy efforts at the World Health Organization. 📢From delivering a statement at the World Health Assembly to co-organising an official side event at #WHO Headquarters.🙌
#NeurologyAtWHA79#MultipleSclerosis
🌍🧡This World MS Day, we're calling for MS to be recognised as a global health priority.📢 Watch our CEO Dr Lydia E. Makaroff's message from Geneva as we continue to advocate for earlier diagnosis and better care worldwide. 🇺🇳
#WorldMSDay#MyMSDiagnosis
This #WorldMSDay, people with MS are invited to create a #MyMSDiagnosis poster and contribute to global research run by MSIF. 🔎Create a poster and share the link with your community. 📢
Poster Maker 👉https://t.co/a5QpeRNVU4