This thread has a Science for ME News in Brief post for each week in October 2020 written by @Trish, @Kalliope and others. Scroll down to see this week's news.
This thread has a Science for ME News in Brief post for each week in August 2020 written by @Trish, @Kalliope and others. Scroll down to see this week's news.
This thread has a Science for ME News in Brief post for each week in May 2020 written by @Trish, @Kalliope and others. Scroll down to see this week's news.
I thought it might be useful to have a thread on ME/CFS news for the Netherlands, similar to the threads we have on Scandinavian countries. If there's some really important news we could make a separate thread for it and link to it in this general thread that keeps an overview of all ME/CFS...
This thread has a Science for ME News in Brief post for each week in April 2020 written by @Trish, @Kalliope and others. Scroll down to see this week's news.
This thread has a Science for ME News in Brief post for each week in March 2020 written by @Trish, @Kalliope and others. Scroll down to see this week's news.
This thread has a Science for ME News in Brief post for each week in September 2019 written by @Trish and @Kalliope. Scroll down to see this week's news.
Open Medicine Foundation Canada:
https://www.omfcanada.ngo/?utm_source=email&utm_medium=news
I donate to the OMF - can now receive a Canadian tax receipt
ETA: It would be great to see some OMF funds going to Canadian ME researchers - there are collaborations, but I don't know if funds are...
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The following has come to my attention (thanks @Philipp):
http://dip21.bundestag.de/dip21/btd/19/126/1912632.pdf
It is a reply to a list of questions which a few German MPs put to the government:
The answers basically say that it's not the Government's concern, it's up to the scientists. The...
This thread has a Science for ME News In Brief post for each week in August 2019 written by @Trish and @Kalliope. Scroll down to find this week's news.
Some local news for once! A rare thing in Canada. Not much groundbreaking stuff in the article but it's a fair and generally accurate portrayal, centered on Dr Moreau's work on twin studies, with a personal account of one of the twins affected by ME.
Moreau's team is comparing the twins' mRNA...
I'm putting this in the members-only section because I was advised to keep it quiet until it's published (besides posting this here, of course).
I was informed by Sara Piccer, OMF volunteers relations manager, about an upcoming CNN coverage of May 12. The report is expected to be published on...
So there's some news from Belgium.
The government has extended its ME/CFS-convention until 2020. In parliament our Minister of Health said the assessment report of GET/CBT rehabilitation has shown to be highly successful. Patients however were not allowed to see the report...
The new...
The translation isn't all that great but not a bad article from Yahoo! news in Japan: https://translate.google.com/translate?hl=en&sl=auto&tl=en&u=https://news.yahoo.co.jp/feature/1117.
A lot has been written about the Hikikomori culture in Japan, recluse people who have withdrawn from society...
https://coach.nine.com.au/2018/07/03/18/52/chronic-fatigue-syndrome-myalgic-encephalomyelitis
The article is very good. Dr. Mark Guthridge is inerviewed about ME/CFS and the patient experience is well written. An accurate easy read.
The News from Scandinavia is such an interesting and useful thread, so I thought it could be worth seeing if we could sustain a similar one for New Zealand. We do have some good research being done, some active advocates and even a suggestion from David Tuller that he might get here in the next...
I have only just become aware of this and although I suspected that the SMC connection(ie SW) was at play with regards to Channel 4 News, Channel 5 News and ITN (who actually are in charge of all three) (for me)this confirms it.
"
The Royal Society of Medicine presents '21st Century Healthcare'...
Week beginning 1st January 2018
An unusual amount of positive media attention this week.
Independent: Time for Unrest: Why patients with ME are demanding justice
A new film sheds light on a condition that is largely ignored. Nathalie Wright reports on the struggles patients face to be taken...
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