Binkie4
Senior Member (Voting Rights)
This thread includes some moved posts
Newsnight today 28th Feb- approx 10.45-55pm, introduced by Victoria Derbyshire
Study on cognitive impairment/ brain fog and IQ after long covid. A scientist from the study ( sorry I didn't catch the name of the author or his institution) and a ?scientist with long covid suffering from brain fog who had been unemployed for 4 years, were interviewed by Victoria Derbyshire.
From a very brain fogged memory that was not initially properly listening, a statement was made that IQ drops by 3 points in those who have had covid for less than 12 weeks rising to 9 in those who had been hospitalised with covid. This was particularly noticeable in those who had had covid early.
I kept longing for there to be a reference to ME and the study scientist was asked by Victoria if this effect was found in other illnesses but ME was not mentioned at all. The patient did say she had PEM as well as brain fog - it seemed that she might fit criteria for ME. Very frustrated that there was no reference to ME. How did they not know that these symptoms were not new? I couldn't help but think that she would be doing GET if it hadn't been for ME advocates.
It then moved on to the need for clinics, treatments etc.
edit:Study was by a neuro scientist at Imperial with over 100,000 participants.
Newsnight today 28th Feb- approx 10.45-55pm, introduced by Victoria Derbyshire
Study on cognitive impairment/ brain fog and IQ after long covid. A scientist from the study ( sorry I didn't catch the name of the author or his institution) and a ?scientist with long covid suffering from brain fog who had been unemployed for 4 years, were interviewed by Victoria Derbyshire.
From a very brain fogged memory that was not initially properly listening, a statement was made that IQ drops by 3 points in those who have had covid for less than 12 weeks rising to 9 in those who had been hospitalised with covid. This was particularly noticeable in those who had had covid early.
I kept longing for there to be a reference to ME and the study scientist was asked by Victoria if this effect was found in other illnesses but ME was not mentioned at all. The patient did say she had PEM as well as brain fog - it seemed that she might fit criteria for ME. Very frustrated that there was no reference to ME. How did they not know that these symptoms were not new? I couldn't help but think that she would be doing GET if it hadn't been for ME advocates.
It then moved on to the need for clinics, treatments etc.
edit:Study was by a neuro scientist at Imperial with over 100,000 participants.
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