MS Int'l Federation @MSIntFederation
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. msif.org Joined October 2011-
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The MS Clinical & Imaging Data Resource is a new tool that gives scientists access to anonymised and harmonised MRI scans and clinical data from thousands of people with MS who participated in clinical trials.🧠 Learn more: msintfederation.org/3K1xwp9
Dr Agustín Pappolla is an MS researcher from Argentina who recently completed a two-year MSIF-FRANCESEP McDonald Fellowship. We reached out to find out more about his research and why it matters to people with MS. Step into the lab with Dr Pappolla ➡️ msintfederation.org/Agustín
The National MS Society in the UAE has developed the country’s first national MS treatment guidelines to support healthcare professionals, align clinical decision-making, and improve access to evidence-based MS care. 📃👨⚕️ Learn more: msintfederation.org/UAEguidelines
Applications for the 2026 MSIF McDonald Fellowships are now open! 📣 These awards provide an exciting opportunity for MS researchers and clinicians in low- and middle-income countries, to work in a research institution abroad gaining expertise. 🔬 msintfederation.org/3H3fGBe
Don’t forget to register for Patient Community Day at #ECTRIMS2025! Designed for anyone living with MS, attendees will learn and share throughout the event. 🔍💡 The lived experience panel will highlight the importance of connecting to research. Sign up: buff.ly/078P8v6
‘Understanding MS’ is an award-winning free online course that aims to improve understanding and awareness of MS. Open to anyone across the world including people living with MS, their families, carers and healthcare professionals. Sign up. 👉 msintfederation.org/understandingMS
The Charcot Lecture titled ‘Developing MS therapeutics - success factors and call for innovation’, will be presented by Professor Ludwig Kappos, recipient of the 2025 Charcot Award, during the closing session of @ECTRIMS in Barcelona. #ECTRIMS2025 #MSResearch #CharcotAward
The International #ProgressiveMSAlliance has launched a ground breaking collaboration - the MS Clinical & Imaging Data Resource. This tool provides access to anonymized MRI and clinical data from more than 13,500 people with MS. Learn more: msintfederation.org/45HvT7w
ECTRIMS Patient community day is coming up! Join people from across the globe to hear from experts, sharing updates on the latest research and answering your questions. Don’t miss your chance to connect and learn. 👉 Register here: ectrimspatientcommunity.eu #ECTRIMS4me
In the latest webcast from the #ProgressiveMSAlliance, researchers, experts and people with MS discussed insights into digital tools and their potential to improve care and speed life-changing solutions for those living with progressive MS. 💻 Catch-up! msintfederation.org/40A5oiu
The next understanding MS course opens soon. This is a free online course all about MS. 🎓 Learn more and register now: ms.mooc.utas.edu.au/i/mssm Understanding MS was developed by Menzies in partnership with MS Australia and MS Plus.
Run the London Marathon 2026 for MSIF and raise funds to support research, vital support, and strong advocacy for the MS community. Apply for a charity place with MSIF and help us get closer to our vision of a world without MS. msintfederation.org/4iD7KDx #LondonMarathon2026
The National Association for MS has been working to improve access to MS treatment across the country and secured a major fund increase this World MS Day. 👏 Find out how the Association advocated for change. 👉 msintfederation.org/44NL9R5
Register for the ECTRIMS Patient Community Day! On 26 September, join people affected by MS worldwide. ✅ Online or in Barcelona — free and accessible to all with AI translation 50+ languages. Learn more and register here ➡️ ectrimspatientcommunity.eu #ECTRIMS4me
Young people living with MS face unique challenges. The Associazione Italiana Sclerosi Multipla created an animated series to shine a spotlight on the experiences of young people living with MS. Find out more: msintfederation.org/3lNNZzl #InternationalYouthDay
Over 10,000 people worldwide came together to take on The May 50K 2025. MSIF and its members are delighted to announce that £905,500 has been raised in the fifth year of the global challenge. 🏅 🌎 Read more: msintfederation.org/4lP7HXE
Want run one of the world’s most iconic races? Join Team MSIF in the TCS London Marathon 2026 and turn every mile into meaningful impact. 🏃🏅 ❗ Apply now – spots are limited! msintfederation.org/456lAcO
MSIF co-designed a training course with the American University in Cairo to support MS organisations in the Middle East & North Africa. The course brought MS leaders together and strengthen their skills & prepare to apply for project grants on access. 📔👉 msintfederation.org/3UBryxf
Digital tools are rapidly evolving, with the potential to improve care and speed life-changing solutions for those living with progressive MS. In this webcast experts discuss how they view digital tools in the future of MS research. 💻 Watch now: msintfederation.org/40A5oiu
A recent MSIF visit to MS South Africa and MS Namibia offered insights into the lived experiences of people with MS in the region. The trip showcased the incredible impact of community-driven action and highlighted the need for better MS awareness. 👉 msintfederation.org/4kT8xkD
Rachel Horne @RachelHorne19
7K Followers 4K Following Journalist with MS, Honorary Research Fellow @QMUL, set up Rachel Horne Prize for Women's Research in MS, Co-chair @DeNPRU-QM’s patient/public engagement group
theMSguide.com 🧠 @themsguide
6K Followers 5K Following I have had MS since ‘93. in May ‘25 I will ride 8000km across Canada to raise $1m for MS Brain Health. Follow it all on https://t.co/aHXj0R1KWe 🇬🇧+🇨🇦
ECTRIMS @ECTRIMS
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ECTRIMS @ECTRIMS
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12K Followers 3K Following We are dedicated to sharing the latest news, research, and multiple sclerosis patient perspectives.
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67K Followers 372 Following We will cure multiple sclerosis while empowering people affected by MS to live their best lives.
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790 Followers 267 Following On the 29-31 August 2015 the African Academy of Neurology (AFAN) was created as the sole representative body of the African region within the WFN
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American Academy of N... @AANmember
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