LAST CHANCE TO RIDE! 🚵♂️ Cykelnerven is Europe’s most unique and challenging charity cycling event and now is your final chance to join us in the Alps. We have very few places left. ⏰ Find out more and sign up here: cykelnerveninternational.orgpic.twitter.com/N9MGBwZCEK
Dr Mariano Marrodan from Argentina is one of the 2022 MSIF Du Pré Grant winners🏅 Dr Marrodan will be studying the treatment response of previously untreated MS patients given high-efficacy treatment. Learn more & meet our other awardees 👉 msintfederation.org/fellowshipsand… 🔬 #MSResearchpic.twitter.com/fy23WWhEOO
An international panel of MS experts has published a paper that proposes a new approach to how different types of MS are typically described. 📰
Watch this video to hear more from Tim Coetzee, from the @mssociety (USA), and read more here: bit.ly/3hCN58Ztwitter.com/mssociety/stat…
Neural stem cell therapy is a type of treatment that has potential benefits for slowing down or even reversing the effects of MS. Learn about the results from the first clinical trial using neural stem cells to treat people with MS. 📣 👉 msintfederation.org/3R7yKPt
Do you have what it takes to tackle the toughest climbs of the Tour de France? 🚴♂️
If you think you do, then why not join the Cykelnerven 2023 International team and take on Europe’s most challenging charity cycling event. Find out more here: cykelnerveninternational.orgpic.twitter.com/wHCY0491jr
Public consultation for MSIF’s recommendations of essential DMT's for MS for low-resource settings closes Friday 27 January. ⏰ MSIF has been working with an international panel, @cochrane and @GRADE_Center. Read the recommendations and comment here. 📣👉 msintfederation.org/consultation
Meet Dr Agustin Pappolla from Argentina who is the the 2022 MSIF-ARSEP McDonald Fellow 🏅 Dr Pappolla aims to link blood biomarkers to the treatment response in highly aggressive MS. Thank you to @FondationARSEP for funding this Fellowship. 👉 msintfederation.org/fellowshipsand… 🔬 pic.twitter.com/p7wWBVuqPj
Join us this June as we tackle the toughest climbs of the Tour de France, just weeks before the pro riders at Cykelnerven 2023. Time to join is running out, join the Cykelnerven International team today!
For more information and to sign up visit: cykelnerveninternational.orgpic.twitter.com/riqAQTsDKI
A new Australian study, led by Prof Tomas Kalincik and Dr Izanne Roos (recipient of the 2017 ARSEP-MSIF McDonald Fellowship), investigated the return of MS activity after people stop a range of disease modifying therapies. Read more here. 👉 msintfederation.org/3D0Gug5twitter.com/MS_Australia/s…
This is the moment you have been waiting for, the Cykelnerven 2023 routes are finally here! 📣 This year, the route is based on Stages 14, 15, 16 and 17 of the Tour de France. 🚵
See the whole route here. 👉cykelnerveninternational.org/the-routes
We are proud to announce the winners of the 2022 McDonald Fellowship and Du Pré Grants!📢 The awards promote international collaboration in #MSResearch and support young MS researchers. Meet our awardees from Argentina, Brazil, India, and Mongolia. msintfederation.org/fellowshipsand…pic.twitter.com/BvkQtwxReR
'The most important thing is that you and others around you know that cog fog can be a symptom of this condition, and you aren’t stupid!’
In this blog from the @mssocietyuk, Craig talks about his experience of cog fog in MS and shares his top three coping strategies. 👇 twitter.com/mssocietyuk/st…
There are many ways to protect your independence, whilst ensuring you get the support you need as you age with MS. Find tips on protecting your independence & identity in the graphic below and read more in 'Living well with MS as you grow older'. msintfederation.org/ageingbookletpic.twitter.com/016h8O0kUB
Over the years the inspirational Cyckelnerven team have taken on over 400km of the toughest climbs from the Tour de France and raised thousands of euros. This year it could be you… Don’t miss your chance to join this once in a lifetime event: cykelnerveninternational.orgpic.twitter.com/YZTlOcIuxJ
Public consultation is now open for MSIF’s recommendations of essential disease-modifying therapies for MS for low-resource settings. MSIF has been working with an international panel, @cochrane and @GRADE_Center. You can read and comment here. 📄👉 msintfederation.org/consultation