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   <subfield code="a">‘Too tired to go to the support group': a health needs assessment of myalgic encephalomyelitis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Graham C. Sutton]</subfield>
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   <subfield code="a">Background Myalgic encephalomyelitis (ME) is a mysterious and controversial condition. Debate has centred upon its causation, and the purchasing question - which services to commission for people with ME - has not been addressed. Methods A health needs assessment was made of people with ME in Wakefield, based upon published (including grey) literature, and local informants. Results Previous studies have mostly reflected institutional outbreaks; local needs will reflect community, sporadic cases but there is little information about these. The very wide estimates of prevalence (between zero and 57000 for a district the size of Wakefield) indicate a fundamental problem over the validity of the concept of ME. Four sets of health needs emerged from the literature and from local informants: a medical diagnosis, rest, specific treatments and social care. All four are highly debatable. Conclusion There are no proven services or interventions which the health authority should purchase for people with ME. Purchasing, being a blunt tool for service change, is unlikely to improve health care given the disagreements over the condition.</subfield>
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