Social care and the MS community

The MS Society has published Social care and the MS community in England.

This report presents the results of survey conducted in 2016 of people with MS to understand how they feel about their treatment, care and support.  The results are compared with a previous survey conducted in 2013.  Key findings include a smaller proportion of people are getting the care and support they need and demand for support has increased from 35% to 57% between 2013 and 2016.

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