ME/CFS patients in UK report being abandoned and dismissed by medical system
George Monbiot reported on experiences of people with myalgic encephalomyelitis/chronic fatigue syndrome in the UK who feel betrayed by the healthcare system.
Patient testimonies describe neglect
A journalist asked for accounts of recent treatment experiences on social media. Respondents shared stories of being told to give up seeking medical support. Many described feeling unheard and invalidated by their doctors.
Waiting lists remain long
One account mentioned a ten-year waiting list for necessary treatment. The condition affects an estimated 400,000 people in the UK alone. Women are diagnosed far more often than men at a ratio of about four to one.
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