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A lack of funding has forced a Cardiff-based MS service to start a waiting list for patients who could benefit from beta interferon and copaxone.
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Anatole Otis, 67, has suffered from multiple sclerosis for more than a decade, but was diagnosed as demented when he first sought medical attention.
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he husband of a Nova Scotia woman who died at an assisted-suicide clinic in Switzerland this month said yesterday he doesn't fear a police investigation into the matter and doesn't expect charges to be laid against him.
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The neurologists called for new priorities in health care, saying billions could be saved through earlier diagnoses, stroke prevention programs and Alzheimer's research.
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IRELAND has some of the most inadequate provision for care of people with Multiple Sclerosis in Europe, a conference heard yesterday.
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Write your Representative today and ask them to support bio-generic drugs by including the Access to Life-Saving Medicine Act (H.R. 1038) with the re-authorization of PDUFA.
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House Speaker James A. Amann, D-Milford, has had second thoughts about shaking down lobbyists for his employer, the Greater Connecticut Chapter of the National Multiple Sclerosis Society.
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Candidate's wife discusses MS, stem cell research, abortion and debunks Mormonism myths
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The money quietly paid to 46 Newfoundland and Labrador legislators in 2004 could have provided drugs for seven multiple sclerosis patients, a national organization says
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The new rule proposed in the bill would allow cancer, glaucoma, multiple sclerosis, HIV positive, and AIDS patients to receive medicinal marijuana.
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Join the National Multiple Sclerosis Society-Greater Illinois Chapter as we urge Gov. Rod Blagojevich to sign into law SB 2917, which would secure insurance coverage of preventative physical therapy for people living with MS in Illinois.
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Doctors in Canada can start prescribing Tysabri on Nov. 15 and patients will begin receiving monthly infusions in January.
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The New Zealand Disability Strategy, published in 2001, aims to eliminate the barriers that prevent New Zealanders with disabilities from reaching their full potential or participating fully in the community.
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Multiple Sclerosis is unique to each patient, but for me it's kind of like a cat gone insane. When you wake up, it's right there in your face, looking all innocent, but you know that as soon as you set one foot on the floor you'll find it has left you
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National survey reveals bleak picture for people with Multiple Sclerosis NICE recommendations on MS care ‘not being implemented’
