“I hope that one day I will be able to use my lost years to help others by raising awareness of the plight of those living with M.E.”
“I’m struggling to come to terms with the fact I was not diagnosed for so long, and am angry that I suffered needlessly for 24 years.”
“To be a disabled person does not mean that you must solely be a wheelchair user or someone with a physical deformity.”
“I suspect that the losses faced by many people with M.E. are in some ways uniquely different to almost every other patient group.”
Is M.E. really an invisible illness? Which elements are visible and which parts remain hidden?
Dr Sarah Jarvis talks The Sun through the main signs your exhaustion could actually be a symptom of ME/CFS.