https://www.theatlantic.com/ideas/archive/2022/10/long-post-covid-symptoms-mild-cases/670469/
The Atlantic hedging it's bets after the brilliant Ed Yong article from the other day...
Yes I worry about that. I could not tell the difference when mild and undiagnosed and jogged/worked myself into a moderate and largely housebound state, which declined to severe after Covid months later. I had had ME for over three years at that point so it concerns me when pwLC think they can...
I completed the study today and wasn't chosen to take part. It is quite disappointing on an emotional level even if intellectually I entirely agree with all that's been said.
I guess it's just a consequence of years of uncertainty and gaslighting by docs.
But other than that I am hopeful about...
My only concern is that by excluding people with common co morbidities (if that is indeed what is occuring), is there not a chance that Decode will end up not studying a significant cohort of ME patients and therefore exclude them from future biomarkers/treatments?
I agree with a lot of what you're saying here, but just to clarify I meant that we as ME patients might do better to counter the 'whiny negative attitude' narrative and use it to raise awareness of how awful ME can be, as opposed to getting sucked into the argument around this other character...
I wonder if this might not be approached as a teachable moment in regards to why people with ME tend to have a more bleak outlook than suffers of MS or amputees or what have you.
Maybe explaining how ME takes away the ability to do basic things/hobbies, see family and friends and the low...
I found this article a little upsetting, as someone who had a similar quality of life to Khan Harris for nearly four years. I then became bedbound after being convinced my fatigue was partly psychological and trying to exercise my way out of it, then catching Covid a couple of months later.
I...
https://www.bbc.co.uk/programmes/articles/3gxJbg6f1FDv4tzrbtfp1Y3/how-your-expectations-can-transform-your-life
Steam came out of my ears when I read this. Literally magical thinking, as far as I can tell.
This happened to me after worsening to severe following Covid. Cardio recommended intense physio... The rehab team called me and said no way are we putting someone with LC through this.
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