The Multiple Sclerosis International Federation was established in 1967 as an international umbrella organization linking the activities of national MS societies around the world. MSIF's mission is to lead the global MS movement by stimulating research into the understanding and treatment of MS and by improving the quality of life of people affected by MS.
The MSIF Atlas of MS database provides information and data on the epidemiology of multiple sclerosis and the availability and accessibility of resources for people with MS at country, regional, and global levels.
The National Multiple Sclerosis Society is a non-profit organization which helps people affected by MS by funding cutting-edge research, driving change through advocacy, facilitating professional education, and providing programs and services that help people with MS and their families move their lives forward.
The Face of MS.org is an online community project sponsored by NMSS where people with MS and those in the fight against MS can share their experiences and hear the stories of others. It is where people who know little about MS can go to gain understanding from those closest to the disease.
The European Multiple Sclerosis Platform is a non-profit association whose purpose is to exchange and disseminate information relating to multiple sclerosis and deliberate upon and consider all questions, problems and measures, legislative or otherwise, connected therewith; to encourage research of all kinds that is appropriate to multiple sclerosis through medical and other associations; to promote the development of joint action programs with the participation of national MS societies in Europe, aimed at improving the quality of their activities and services; to act as a focal point for liaison with the institutions of the European Union (EU), the Council of Europe and other European organizations, in order to study and propose measures to improve the autonomy of persons with disability and their careers and promote their full participation in society; to engage in such other activity as may be necessary or appropriate to carry out the purposes described above.
The Multiple Sclerosis Association of America is a national nonprofit organization dedicated to enriching the quality of life for everyone affected by multiple sclerosis. MSAA provides ongoing support and direct services to these individuals with MS and the people close to them.
The Multiple Sclerosis Foundation is a service-based, non-profit organization whose primary mission is to ensure the best quality of life for those coping with MS by providing comprehensive support and educational programs. We strive to help make A Brighter Tomorrow by supporting research into its cause and cure as well as investigations of various medical and complementary treatment options.
The Multiple Sclerosis Society of Canada was founded in 1948 by a small group of dedicated volunteers in Montreal. Today it is the only national voluntary organization in Canada that supports both MS research and services for people with MS and their families.
The Multiple Sclerosis Trust is the definitive source of health information for people living and working with multiple sclerosis. The MS Trust provides information for anyone affected by multiple sclerosis, education programmes for health professionals working with people with MS, funding for practical research and campaigns for specialist multiple sclerosis services.
The Multiple Sclerosis Resource Center is a proactive and innovative charity, passionately committed to supporting anyone affected by Multiple Sclerosis through access to unbiased information and advice. Our approach is to encourage individuals to make choices that are appropriate to their daily lives, empowering them to maximise their potential.
OzMS - Australian Multiple Sclerosis Peer Support Our Mission - Peer Support - Information - Freedom
This site endeavours to help People with MS through online peer support, members helping each other, we have MS, we know what you're going through, we live it each day. We offer many ways for you to contribute to the information on this site, information that you can't get out of a text book, information that only people that suffer from this disease can honestly give you, for example, symptoms and how you feel, is this normal, is often asked.
The Rotarian Action Group for Multiple Sclerosis Awareness are Rotarians dedicated to promoting MS Awareness as an opportunity for Fellowship and Service. This Action Group acts in accordance with Rotary International policy but is not an agent of or controlled by Rotary International.
The Multiple Sclerosis Resource Network is an independent, not-for-profit organization in the Toronto area. The members of the Network are health care professionals in the Greater Toronto Area, and the organizations in which they practice are considered Network Partners.The MS Cooling Foundation (MSCF) is a nonprofit agency dedicated to providing information about temperature and its affects on individuals with multiple sclerosis.
The MS Mobility Foundation (MSMF) is a non-profit organization that is dedicated to making people disabled by MS mobile outside their home. There is currently very little to no funding for this. There is a desperate need for this kind of help. The Foundation is new, and we are in the process of submitting grants to be able to start making people mobile! For more information please click here.Job Accommodation Network - Welcome to JAN, a free consulting service designed to increase the employability of people with disabilities by: 1) providing individualized worksite accommodations solutions, 2) providing technical assistance regarding the ADA and other disability related legislation, and 3) educating callers about self-employment options.
