From what I have read in other articles, families are told not to support the patient in what are described as maladaptive beliefs and behaviours....
Her name is trending on Twitter
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Not that I know of, but when researchers publish, they tend to look back on existing research data.
People who have got a genetic analysis done can submit their results to the Nancy Klimas team who are collecting them from around the world.
I know that Newport Pharmaceuticals had planned to do a multicentre trial of Imunovir in the 2000s. Then it was dropped. I read somebody who had...
Additional points I’ve remembered: The Arthritis charity in my country had a very insulting rheumatologist give talks about Fibromyalgia. He’s now...
An issue in the ME world is I think it is important that people with the illness along with family members (who live with them) are involved in a...
Thanks. Could somebody download the file and attach it here or post it somewhere e.g. dropbox. I don't want to give my credit card details to Scribd.
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We have this data for adults from English clinics at five year follow-up. It suggests non-recovery is very common. My guess is the recovery rate...
Maybe there is a value in sometimes thinking about these issues. But it's also important to give patients factual information or allow them have...
Not a particularly pessimistic group.
Not a full selection of theories there.
So they weren't unduly pessimistic.
The normal English clinics where these people work offer something closer to the usual care group in the FITNET trial (rather than online CBT)....
If more than one letter is submitted, it should increase the chances one will be published.
I’d say there is a good chance she didn’t suggest the title, “chronic fatigue”, and instead it was someone in the paper.
Even though this looks short, from what I recall most published letters are shorter. How about also sending a shorter version. I previously did...
Separate names with a comma.
