Multiple Sclerosis International Federation

The Multiple Sclerosis International Federation stands in London as an international body founded in 1967. It links 48 national MS societies and works with the World Health Organization to share global data. The federation’s annual budget of around £2 million comes from member societies, charities and health care firms. It publishes the Atlas of MS, which shows 2.8 million people worldwide live with the condition. MSIF also supports the International Pediatric MS Study Group, uniting doctors to improve care for children with MS. During the COVID-19 pandemic, MSIF gathered experts to create global advice for people with MS. The organisation set up the COVID-19 and MS Global Data Sharing Initiative with the MS Data Alliance. This collected data on how the virus affected people with MS and shaped updated guidance. MSIF’s work includes research, advocacy and helping new societies grow. Its priorities cover international studies, information exchange and support for those living with MS. Visitors find MSIF’s London office a hub for global cooperation on multiple sclerosis. The federation’s campaigns, such as World MS Day on 30 May, draw support from nearly 100 countries. The ‘MS Connections’ theme focuses on community links, self-care and better care services. Events and awareness-raising take place throughout May each year. The organisation’s efforts aim to reduce isolation and improve lives across the world.