A lot has changed in the five years since I first created Diary of a Disabled Person, so I decided to take a look back at content…… Read more “Revisited: GETting Nowhere.”
Tag: GET
Out With the Old, In With the Same.
Towards the end of October 2021, after months of back and forth, the National Institute for Health and Care Excellence (NICE) finally published the Myalgic Encephalomyelitis (M.E)…… Read more “Out With the Old, In With the Same.”
Falling at the Final Hurdle.
Earlier in the month I wrote about the National Institute for Health and Care Excellence’s review of M.E treatment guidelines, followed a few days later by a…… Read more “Falling at the Final Hurdle.”
Breakthrough.
Over the weekend I published my account of the recent NICE review of treatments offered to M.E patients in the UK. I expressed concern that either NICE…… Read more “Breakthrough.”
Naughty or NICE.
The National Institute for Health and Care Excellence is a government-funded body that oversees the NHS in the UK, monitoring research, informing public health policies, and ensuring…… Read more “Naughty or NICE.”
The Rise and Fall.
One of the most difficult things about having Myalgic Encephalomyelitis is the way it fluctuates more than a DNA strand by Chernobyl. I can go from feeling…… Read more “The Rise and Fall.”
GETting Nowhere.
Chronic Fatigue Syndrome (CFS) is one of those strange conditions that has no real treatment protocols assigned to the disease, mainly because so little is known about…… Read more “GETting Nowhere.”
Diary of a Disabled Person. 