Article from Isle of Man Today published 28 May 2021
A man who has lived with ME since 2010 says that the current level of health care for the condition and other invisible illnesses is ’medieval’.
Craig Morris is from ME Support IoM, a charity set-up in 1988 to provide support and information for those with ME/chronic fatigue syndrome and fibromyalgia, their families or carers and anyone affected…
There have been major consequences to my health as a result [of a late diagnosis]. The reason why I’m bringing this up now is that it’s still happening – people are ringing me up for advice because they or their GP don’t know what to do and it’s really upsetting, especially young people, who are not being helpedCraig Morris
Isle of Man Minister savaged for delays in setting up specialist M.E service
We reported recently on a debate on local ME/CFS services in Tynwald, the Isle of Man Parliament. To read our our report, please click on the link below.