The Multiple Sclerosis International Federation (MSIF) was established in 1967 as an international body linking the work of national MS Societies worldwide.

Together we share the global vision of a world without MS. That’s why we also work with the international scientific community to stimulate international collaborative research. In the meantime however, MSIF continues to support people affected by MS in a variety of ways.

We communicate best practice knowledge, experience and information on all aspects of MS and in a variety of languages. This helps people affected by MS make their own choices and decisions.

We also aim to improve the services offered worldwide, so we actively encourage and support the development of effective and efficient national MS societies wherever there is a prevalence of MS. Another worldwide initiative is our support for advocacy campaigns to influence public policy in favor of people with MS.

Our various activities are underpinned by good governance and leadership, transparent financial and administrative structures, and a healthy fundraising capacity.

As a person with MS myself I have first-hand experience of the impact MS can have on quality of life, not only for the individual with MS but also for family and friends. By producing the Principles to Promote the Quality of Life of People with MS, MSIF leads the global MS movement, and I am honoured to be a part of it.


Sarah Phillips
Chairman & President
Multiple Sclerosis
International Federation