A new FREE 6-page leaflet that helps determine what is required to make an early and accurate diagnosis of ME/CFS.
This week we feature a new study that examines acute Epstein Barr as a trigger and another that reports on use of IV Saline as a potential treatment.
We highlight 3 studies from last week’s 6 ME/CFS research publications.
“Having M.E. robs us of just about everything, but not the ability to be supportive or kind. We are a community, and it should be us against the world not us against each other.”
We asked those who suffer with Severe M.E if they would like to submit their stories to be published on the ME Association website blog.
“I’ve tried so many different methods to manage my symptoms. Medication helps to a degree alongside self-management techniques.”
“The first big challenge was when I became wheelchair-bound 3 years ago. The next loss was when I could no longer read or watch a film.”
US FDA issue new safety concerns about the drugs and their use in people who have significant respiratory illnesses.
The number of people in Nottinghamshire suffering from fibromyalgia has soared in recent years, according to new NHS figures.
Physios 4 ME report on the results from the MEA website survey that took place in July.
Day after day this fragile hope is crushed, shattered, ground down like broken glass. Monotony, drudgery, despair! How can I escape?