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Introduction As the title suggests, MS-ID is about information on MS and the benefit to be reaped from it. At present in Europe there is very little data gathered about MS, its incidence, who is affected by it, who is taking what drugs as treatment, how MS impacts on the lives of people who are diagnosed, what it results in for their participation in the labour market, what additional supports does the State provide and need to provide for people with MS. In order to better understand the impact of MS, we have to know the effects it brings to society at large. |
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