Open Letters to Healthcare Professionals from people with ME/CFS – Part 2 Nicola and Jules
Against the background of a new NICE Clinical Guideline for […]
Against the background of a new NICE Clinical Guideline for […]
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
Personal Relationships: Intimacy and ME/CFS Read More »
Warning: Contains adult content. Intimacy among those who are disabled
People are asked to watch their language when faced by things they don’t understand
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.
Four young women talk to ‘Cosmopolitan’ about their Long Covid (and Dr Charles joins in) Read More »
Our medical adviser, Dr Charles Shepherd, contributed heavily to this piece in this week’s ‘Cosmopolitan’.
Medscape: Small-Fiber Polyneuropathy May Underlie Dysautonomia in ME/CFS Read More »
These potentially important findings were presented by Ryan Whelan from the Simmaron Research Institute at the recent IACFS/ME virtual conference.
Severe ME Week 2020: Sophia’s Story Read More »
The 8th August is Understanding & Remembrance Day for Severe
Severe ME: Why is improvement subject to such harsh judgement and not celebrated? Read More »
“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.”
ME Association Monthly Poll: Your Confidence in the NHS During Covid-19 Lockdown Read More »
During the covid-19 lockdown, have you felt confident in the NHS’s ability to provide appropriate care and support as a person with ME/CFS?