The Express: Coronavirus sufferers may be experiencing a “post-Covid syndrome” according to expert Dr Charles Shepherd.
Tag: Chronic Illness
ME, Myself and I: Caution and Controversy
“Too often we see fractures within the ME/CFS Community that are causing incredible damage to the very people who are on our ‘team’.”
ME Awareness: “What you need,” he said, “is a job harvesting cabbages,” by Ruth Rookledge | 25 May 2020
“For about the next year or so I thought I must just be imagining an illness, that it was my fault, it wasn’t real…”
ME Awareness: The Lost Years and Rediscovery by Kate Stanforth | 12 May 2020
“I’d like to say once I got the diagnosis, things got easier, but they didn’t. I ended up bedbound then ultimately paralysed in some of the darkest days I’ve experienced.”
News: Could the coronavirus trigger post-viral fatigue syndromes? | 16 April 2020
Evidence is mounting that Covid-19 infection might lead to instances of PVFS meaning we may see an increase in cases of Myalgic Encephalomyelitis.
Introducing The ME Association’s Champion Bloggers! | 15 April 2020
We have some incredible ‘champion bloggers’ who produce valuable content and insights. We’re looking for more writers to join the team.
Jenny’s ready and waiting – for when business comes knocking on her door! | 19 March 2020
Jenny McGibbon – hit by M.E. in her late teens – has proved she has what it takes to be a freelance graphic designer.
Debut Survival Guide from York ME sufferer, Pippa Stacey | 05 February 2020
Pippa Stacey has released her non-fiction book titled ‘University and Chronic Illness: A Survival Guide’.
Buy a Box of Stationery Treats by our Graphic Design Star | 28 January 2020
Jenny McGibbon has given a compassionate disability twist to the latest Papergang box of stationery treats.
“Get Well Soon” – Guest Blog by Louise Shepherd | 22 November 2019
Such small but powerful words – for right and wrong reasons… When there’s no chance of becoming 100% better, hearing or reading them can really drag you down to the dark places of your mind.
Make ME Visible Campaign – Mummying and ME | 16 October 2019
The term “invisible illness” suggests there is nothing to show for it. No clear symptom that Joe Bloggs on the street would see as such.