The variety of care is very substantial. In fact the word ‘care’ is used in such a range of ways that, to a degree, it has lost much of its original and particular meaning. In this chapter we focus on ‘care’ in the sense of the formal provision of services by mainly statutory health or social care bodies for people with Multiple Sclerosis and their families. The degree to which such services constitute individual ‘care’ as considered for people with MS and their families is a matter of (their) judgement. Indeed the perennial issue for people with MS is the degree to which health care and social care services can meet both the diversity and scale of their care needs.