There has been good news in recent days about potential vaccines for Covid-19 that could see an end to restrictions for people in the UK by Easter 2021…
We hear from someone with severe ME who describes what Post-Exertional Malaise feels like and the measures that can help when in this situation…
The information in this new guide should be of help to people when managing post-Covid fatigue syndrome and post-Covid ME/CFS.
Paul Garner continues his BMJ Blog, explaining his experiences with Long-Covid and calls for appropriate guidance and support.
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 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.”
“The GP’s I have seen treat everyone based on symptoms rather than the whole illness itself…”
“I’ve got steadily worse, less and less able to work, missing out on all social outings, not able to take holidays due mainly to lack of finances…”
ME Carers Connected can help put carers in touch with one another for mutual support and to share experiences.
Dr Shepherd provides another update and comprehensive guidance for people with ME/CFS.
We review the shopping situation in light of the restrictions and have written to supermarkets asking for more help.
It is Severe ME Day on Thursday, but we think people severely affected deserve to have a full week dedicated to raising awareness.