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Multiple Sclerosis Registries: Value, current efforts, and glimpse from Greece
25.04.2023
Are you curious about how Multiple Sclerosis (MS) registries can benefit the MS community? Discover the efforts of EMSP and…
People with NMOSD and MOGAD in Italy raise their voice
25.04.2023
We will work to support people, and promote scientific research & the development of new treatments for a better quality…
Romanian Youth with MS National Conference 2022
21.12.2022
During November 18-20, 2022, the Romanian Association of Patients with Neurodegenerative Diseases (APAN) organized the fifth edition of the Youth…
Tyrolean MS Society takes a new approach to exchanging information with „look and listen“
21.12.2022
The COVID-19 pandemic heralded a time in which the Tyrolean MS society had to and was allowed to deal with…
UK MS Society launches Neurology Now campaign
29.11.2021
The UK MS Society launched a campaign calling for prioritisation and investment in neurology services. As part of the campaign…
“MS has a thousand faces. I am one of them.”
29.11.2021
Carina, 31, has been living with multiple sclerosis for 13 years. At the age of 18, Carina was diagnosed with…
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