We have published a new leaflet to help people who want to claim early retirement on the grounds of ill-health because of ME/CFS.
The new leaflets explain what might be expected from a diagnosis of ME/CFS and how the illness is classed as a disability by the UK Government.
Ian Lazonby was a vet and a lawyer before glandular fever as an adult led to M.E. He talks about his experience with the condition, how he has recovered to an extent, and has accepted M.E.
The information in this new guide should be of help to people when managing post-Covid fatigue syndrome and post-Covid ME/CFS.
It is an authoritative publication representing the most comprehensive, evidence-based summary currently available.
“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.”
In this introduction you will find a discussion about the need for suitable healthcare. Also background about severe and very severe M.E. and the support that is available.
“I repeatedly pushed myself to return to work. Every time I ended up off sick again. I was bewildered by a situation where the will to be well failed every time.”
This free download provides information to help in the understanding of Myalgic Encephalopathy.
Post-viral fatigue is being reported following Covid-19 infection. We explain the issue and offer best management guidance.
In this month’s website survey we’re asking how your M.E. has affected your health over the last year.