TV2 has a good report today of Erika 16 with long covid, no minimizers from NIPH this time. Though the researchers who talk about the consequences...
I would think "scam". I havent had the energy to read it, but based on how people in Norway think pwME are trying to scam others for the...
She was admitted to Røysumtunet centre for severe ME in autumn last year (is still is admitted?) which may explain some of it. Story in local...
There's also that small study on increased translocation of LPS in pwME following exertion.
There's a story on social media of a potential patient with severe ME that has been placed in a psychiatric institution in Norway :( I say...
Posts on the IQWIG report have been moved to the thread "Germany: IQWIG Report to government on ME/CFS - report out now May 2023"
Posts have been moved here from the "News from Germany" thread.
A nice article on cognitive impairment following covid Trodde hun var frisk etter korona. Så sviktet hukommelsen totalt. Thought she was healthy...
Should have said health record researchERS ;) The problems are known, but still it just keeps on being done... I do love forskning.no's headline...
Cool. Some research at University of Oslo have also found impaired cholesterol metabolism in hospital admitted patients. Focus primarily on LDL....
My faith in health record research has plumetted.
Agree. It makes me so frustrated and sad. There has been more students who have taken zero ECTSs/credits as well, but there were also record high...
[ATTACH] The table on absenteeismen is sobering if that shows that about 1/4 of participants is absent from school/work/extracuricular activities...
I was thinking about adding a caveat about the numbers :rofl:
Just a note for those of you not in Norway, the second opinion piece in the above post is written by a known pro low-carb doctor team that run...
I missed this, but a "young voices" opinion from a young doctor in Norway (who is a phd student at the same hospital as Wyller) concluded that...
Sigh..
Thanks for adding Kalliope! This image from the article at FaFo's own page of what experience pwME have with various treatments they have to do...
I'm happy to see this published, the results have been mentioned in various talks by the researchers already. I don't have the energy to read it...
Full title: Do diagnostic criteria for ME matter to patient experience with services and interventions? Key results from an online RDS survey...
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