Ian tells how he had to lower his sporting horizons after being struck down with M.E. Read More »
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.
ME Association New Free Leaflet – The Importance of Early & Accurate Diagnosis in ME/CFS Read More »
A new FREE 6-page leaflet that helps determine what is required to make an early and accurate diagnosis of ME/CFS.
The ME Association Research Round-up Read More »
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.
Coronavirus warning as victims staying sick for MONTHS with ‘post-Covid syndrome’ Read More »
The Express: Coronavirus sufferers may be experiencing a “post-Covid syndrome” according to expert Dr Charles Shepherd.
The Sun: NHS faces ‘post coronavirus tsunami’ as survivors are struck by ME, docs warn Read More »
The ME Association said many people are asking whether or not their post-Covid fatigue could be developing into ME.
Paul Garner, Professor at the Liverpool School of Tropical Medicine, talks about those who have not recovered from Covid-19.
“My husband has taken on housework, shopping, cooking and the garden so is effectively my carer.”
“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.”
ME Awareness: Why Chronic Fatigue is not M.E. by Joanne Hunt | 15 May 2020 Read More »
“What I am suggesting is that, however people refer to M.E., however people experience it, chronic fatigue is not the same thing.”
Dr Charles Shepherd contributes to a new article about Covid-19 and possible Post-Viral Fatigue Syndrome.
“It is incredible how strong she has been. I don’t think I would have coped with what Dee has experienced. She is my inspiration to keep on going and to support her on this journey.”
ME Awareness: The Lost Years by Rachel Hill | 10 May 2020 Read More »
“I continue to be confined to the house. Sitting or standing up for more than 2 minutes makes me very lightheaded, so I spend 23 hours each day lying down.”
New ME Association Leaflet: Is ME a neurological disease? | 19 February 2020 Read More »
We summarise all the key clinical, research and political evidence supporting a neurological classification for M.E.
