Wasn’t aware of this thread before now. But it clearly puts science editor N. Kristiansen (forskning.no) unjust claims to rest, the one that ME-patients didn’t oppose this study, ref her latest piece regarding NICE on pause and the usual patient blaming (news from Scandinavia).
I find this alarming. Seems to be in line with Remes previous study some years ago on adolescents and ME, 12-13 persons and a qualitative study of very limited value.
What psychologists and psychiatrists may do without any limits, doesn’t surprise anyone. But it is scary that they “seduce”
trained oncologists. The latter probably understand that these young patients bodies has taken a big hit, and they know a lot of what’s coming afterwards, but still you want patients to go into ignore-modus and just push through it. Cause your nervous system is wired the wrong way and that’s cause....?
Is that really a sound thing to do? I understand the frustration of not having a a remedy or cure for what is called chronic fatigue, that some “professionals” unfortunately gets desperate and very creative, but does that mean that you should try everything, turn it to the person and persona, not be careful and cautious and consider completely different options?
I have very limited knowledge of cancer, but I wonder what may happen if you do LP and ignore symptoms. I assume that it is beyond doubt that your immune system is whacked, and who knows what going to happen in just a little more time, beyond the one to two months and some questionares when continuing LP, telling yourself that you are “doing fatigue”. Is that what a cancer-whacked body needs? Who will take the risk and responsibility for gambling with these young patients health? How did they get the approval?
Just saying, for a fact, many patients developed ME after pushing through an ongoing infection and a compromised immune system. The risk of doing harm must be exponential in this case.