Human Rights Abuses of M.E/C.F.S Patients – Our Work So Far
Our vision is to improve the quality of life of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients. How do we do this? The experience of having the disease is bad enough but patients also have to deal with poor ‘treatment’ and support from those who have a duty of care over them. We are improving the quality …
