Scientific Reports is a Springer Nature journal, but it is a tier or two down from the big Nature journals. It is usually where papers rejected from the leading Nature lines end up. Still, a respected journal.
this is the original paper: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680051/
Could problems with storage and sample time really account for the original results, which show clear demarcation between HC and PWME, and also strong correlation between degree of disfunction and illness severity?
Exactly. She's making a killing down at Myhill farm. The tests provided are extremely expensive, and the results looked so convinving in the paper she published. it seems this was all due to sampling time and storage?
If Chalder and co didn't have enough rubbish papers based around that damned questionnaire, they can now add another to the list about how to complete the god damn thing. How very meta.
this is essentially what I was getting at. there are so many who are marginalised from mainstream society and they can become very bitter, defensive, and genuinely unable to have a normal conversation. This really isn't helpful to anyone. Perhaps we just see the worst sides on social media.
https://www.thecut.com/2019/07/what-happens-when-lyme-disease-becomes-an-identity.html
This is a very long read and I've only skimmed through, but this is a topic I hoped someone would write about. From the comments it seems the article could be somewhat dismissive to patients.
This doesn't...
I'm back going through these horrible brain symptoms that come about for a few days every few weeks or so. I just hate it. Another thing I forgot to mention was 'brain surges' lasting a few seconds and coming about periodically when in bed trying to fall asleep. I think I've seen these elsewhere...
I knew when I saw this link that Mark Fisher would be mentioned somewhere in the article.
For those who want to read more about this from a cultural and politico-economic standpoint, I recommend Mark's essay 'The Privatisation of Stress'...
https://www.sciencedirect.com/science/article/pii/S2452231719300077?via=ihub&fbclid=IwAR3xQzNGvlwamXbx_F9ZKohGcOiIMGOIbXnz4WgVwZqScW3c-CoS9zTRx64
Note that this is a study written by the owners of the clinic where the FMT is done. I'd take with a pinch of salt.
This is the same as all that herx stuff everyone always puts a worsening of symptoms down to. probability is the person is just going through a rough patch!
oh no. sorry to hear this. do you think the neuro symptoms were from Symprove or could they be from other factors? this doesn't fill me with much hope!
Have recently started a course of Symprove. I have a three-month supply. I'm on day 6 and I have felt very washed out this week - the fatigue has been quite brutal and has been present throughout most days.
I need to stick with it because I have no firm evidence that I'm not just going through...
I may do this. I did talk to someone before starting my claim. I can manage the system pretty well. I'm intelligent and well enough to understand the system. I just wondered if anyone had been in this, or a similar, position.
I do however regret not making it specifically clear that I could not...
Thanks Adam. Perhaps I wasn't clear in my original post because I didn't want to go into too much detail. As I have just started to claim UC I am in the self-employed start up year where the minimum income level doesn't count. So it's not so much what I'm expected to work (I could get round that...
Hi all,
I am looking for advice RE: Universal Credit and limited capability for work.
A few months ago I started claiming UC. I work freelance and despite suggesting that the maximum I work in a given week was around 10 hours, the option of limited capability for work did not come up, and I am...
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.