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.

Joined October 2011
MS Int'l Federation retweeted
🌸 International Women’s Day is this Sunday, 8 March. MS affects three times as many women as men. Today we begin sharing stories from the incredible women in our community. In this video, Ava Battles, CEO of MS Ireland, reflects on the strength of women living with MS. #IWD
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🔺¡Nueva guía de bienestar para la #EsclerosisMúltiple! 🌿La @MSIntFederation ha publicado un manual con prácticas de bienestar y terapias complementarias. Meditación 🧘‍♂️ Acupuntura 💆‍♀️ Alimentación 🥗 Ejercicio 🏋️‍♀️ 📥 Descárgala en español desde la web: aedem.org/nueva-guia-sobre-b…
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MS Int'l Federation retweeted
🟠Ana Torredemer, presidenta de Esclerosis Múltiple España (EME), será la nueva vicepresidenta de la Federación Internacional de #EsclerosisMúltiple (@MSIntFederation) 🙌 Su compromiso con la enfermedad de su hija, diagnosticada hace 19 años, le lleva ahora a un compromiso mucho mayor con las personas con EM de todo el mundo. 👏Una gran noticia para EME, extensiva al mundo hispanoparlante vinculado al movimiento asociativo. 🗣️“Soy consciente de la responsabilidad que esto supone en mi vida, y agradezco la confianza que líderes de otros países han depositado en mí”, expresa Torredemer. ➡️esclerosismultiple.com/ana-t…
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MS Int'l Federation retweeted
Some 3bn people worldwide (7m in Australia) have a neurological condition, many not getting the care & treatment needed. That’s why I have signed the open letter to all gvts to take action during Global Week for Action on #NCDs. actonncds.org/take-action/ca… actonncds.org
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MS Int'l Federation retweeted
🟠El movimiento global de la @MSIntFederation (Plataforma Internacional de #EsclerosisMúltiple), del que forma parte Esclerosis Múltiple España, celebró su encuentro anual en Londres la semana pasada, con los responsables del asociacionismo de EM de todo el mundo. En él tuvimos la oportunidad de compartir aprendizajes, experiencias y temas claves en el abordaje de la EM para aunar esfuerzos en el movimiento asociativo a nivel mundial.
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MS Int'l Federation retweeted
Il prof. #MarioAlbertoBattaglia, ordinario di Igiene al dipartimento di Scienze della Vita dell'#Università di #Siena, eletto presidente della Federazione internazionale sclerosi multipla: un prestigioso riconoscimento per il suo instancabile impegno. 👉 unisi.it/unisilife/notizie/i…
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MS Int'l Federation retweeted
📣 Exciting news! The 2024 MSIF-ECTRIMS McDonald Fellowship has been awarded to Dr @YGadama, who will collaborate with Prof Flanclo Henning at @StellenboschUni on vital research into the impact of HIV on MS. Learn about our fellowships 👉 bit.ly/3ZBesDZ @MSIntFederation
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Mario Alberto Battaglia, da 50 anni volontario nella nostra associazione, è il nuovo presidente della @MSIntFederation: "Lavoreremo per un mondo in cui ogni persona con #sclerosimultipla possa vivere la propria vita al massimo delle possibilità": 👉 aism.it/mario-alberto-battag…
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MS Int'l Federation retweeted
Last week, the global MSIF (Multiple Sclerosis International Federation) movement gathered in London and online, for their Global Networking Meetings. Our CEO Ava Battles had the privilege of Chairing the CEO Advisory Group of the @MSIntFederation
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MS Int'l Federation retweeted
🟠De las 2.800.000 personas que viven con #EsclerosisMúltiple en todo el mundo🌍, aproximadamente 1 de cada 10 tiene al menos 65 años. 'Cómo vivir bien con Esclerosis Múltiple en la tercera edad' es una publicación elaborada por la @MSIntFederation para #PersonasMayores con EM sobre el manejo de la enfermedad junto con los efectos de la edad. 👉Explica cómo sacar el mayor provecho posible de la salud física y cognitiva mientras van pasando los años.  A medida que envejecemos, nuestros cuerpos cambian, lo que puede traer nuevos desafíos para vivir con EM. También somos más propensos a desarrollar nuevas condiciones de #salud adicionales y los síntomas de la EM tienden a progresar con los años. Por estas y otras razones, es importante que las personas con EM puedan acceder a información fiable sobre cómo pueden maximizar sus capacidades físicas y cognitivas, gestionar su EM y aprovechar al máximo la vida a medida que envejecen. 🔗 Accede a la guía completa ➡️esclerosismultiple.com/wp-co… #DíaInternacionaldelasPersonasMayores #DíaMundialdelasPersonasMayores #DíadelasPersonasMayores
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MS Int'l Federation retweeted
Live at #ECTRIMS2024: Prof. Kerstin Hellwig (@KerstinHellwig) from @ruhrunibochum, has been awarded the 2024 Rachel Horne Prize for Women’s Research in MS. Join us in congratulating Prof. Hellwig for her invaluable contributions to women's health!
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MS Int'l Federation retweeted
Patient Community Day @ECTRIMS discussing hot research topics with people with #MS and their caregivers! 🤝 great attendance and even greater interest linking researchers and the MS community!
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MS Int'l Federation retweeted
#ECTRIMS2024 | Welcome to the 1st day of the 40th Congress of ECTRIMS! Thank YOU for being a vital part of this journey. 📽️ Watch MS experts Prof. Tobias Sejbæk, Prof. Jette Frederiksen, and Prof. Melinda Magyari (@melindamagyari), present today’s Daily Highlights. 👇 👇 👇
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Da segnare in agenda: il #20settembre, online, nell'ambito di @ECTRIMS, le persone con sclerosi multipla e patologie correlate di tutto il mondo possono confrontarsi con i massimi esperti della ricerca scientifica e fare loro domande. Info: 👉 aism.it/speciale-ectrims-202…
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MS Int'l Federation retweeted
🌏 Patients & caregivers: Join us at Patient Community Day, where we prioritise the voices of those living with #MS & neurological disorders. 📅 20 Sep | 15:00 - 18:00 CEST 📍 Copenhagen, DK & ONLINE 🗣️ Translations into 50+ languages FREE registration: bit.ly/3SQkJYR
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MS Int'l Federation retweeted
It's World MS Day tomorrow! The MS community is gearing up for 30 May across the globe. 🙌 Support the My MS Diagnosis campaign and stand in solidarity with everyone affected by MS: worldmsday.org/about/ #WorldMSDay #MyMSDiagnosis
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MS Int'l Federation retweeted
"At that moment I had the impression that this was happening to someone else, and I was an observer from the outside." Lidija reflects back on the moment she was diagnosed and what she has learnt since. Read her story: msintfederation.org/44ISKyq #MyMSDiagnosis #WorldMSDay
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MS Int'l Federation retweeted
Take part in the MS Heart Challenge this #WorldMSDay and share a MS Heart somewhere special! This could be next to a national landmark, a favourite local spot or a significant event. The best submissions will receive a World MS Day Certificate. 🏆 worldmsday.org/ms-heart-chal…
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MS Int'l Federation retweeted
Watch the new #MyMSDiagnosis animation for #WorldMSDay. All about navigating an MS diagnosis, the animation features the real voices of people living with MS. It explores the challenges people face in search of answers and why the right diagnosis matters so much.
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MS Int'l Federation retweeted
We are delighted to launch the May 50K fitness challenge today at the MS Care Centre, Ireland’s only national respite centre for people with MS. We'd LOVE for you to join The May 50K community once again to leave MS behind. Register now👉themay50k.ie #TheMay50k
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