#LongCovid. Imagine your car is damaged & only holds 1/4 tank of fuel. All the dashboard lights are on. Even a good garage can't diagnose or fix your car,they can only give you tips on driving more economically & wish you luck. That's treatment for most of us. #ResearchLongCovid
From ‘mental fog’ to post-acute COVID-19 syndrome's executive function alteration: Implications for clinical approach
Important recognition by specialists, sadly I only have an abstract…. Anybody full access?
➡️"Brain fog is experienced by 9–55% of people for months after having contracted SARS-CoV-2 virus"
➡️"Several theories have been proposed to explain PACS's brain fog, including a neuroinflammatory hypothesis, but the hypothesis remains to be proven"
➡️"Here, we examined inflammatory and immunological blood profile in a cohort of patients with PACS to investigate the association between executive functions and blood inflammatory markers"
➡️"Our findings demonstrate that PACS is characterized by the presence of an immuno-inflammatory process, which is associated with diminished executive functioning"
➡️"Here, we argue in favour of a shift from the non-descriptive definition of ‘mental fog’ to a characterization of a subtype of PACS(=LongCovid), associated with alteration in executive functioning.
https://t.co/nZMpOJC746
Have you read the @TheBMA report on the impact of Long Covid on medical staff yet? If not why not? Access it here: https://t.co/IJnPIPv32O
It sets out all the reasons we are working to set up a charity to support healthcare workers with Long Covid. @ProfEmer @rogerkline
BBCs @NickTriggle has just appeared on my TV screen presenting a graph for reasons for NHS staff sickness.
Are "flu" & "influenza" separate viruses or were you just desperate to not mention Covid?
What's going on in your dept. @BBCHughPym please?
No mention of #LongCovid?
A new report says Long Covid impacts patients' lives as much as Parkinson's disease or some cancers.
@Ruth5News has been speaking to someone who's affected.
#5News
Beware: the UK's @ONS long COVID survey shows that you still have a risk of developing long COVID after your second infection, even when you fully recovered from the first.
Prevent long COVID by preventing (re)infection.
Compared to non-LC, #LongCovid respondents displayed significantly higher scores on adaptive coping, use of instrumental support, planning, venting, and behavioral disengagement.
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The three gifts of Mild COVID brought to you by lying experts and politicians.
1) Vascular damage that can't be easier measured.
2) Brain damage marketed as brain fog.
3) Immune dysfunction making you susceptible to more infections.
Most people have at least one of these.
Today is #MEAwarenessDay with a focus on Post Exertional Malaise (PEM); new or exacerbation of current symptoms after exertion
PEM is relevant to all physios because our interventions can cause it
We now have a new page about PEM on our website
https://t.co/QnV3amXrYW
This week is #MEAwarenessWeek (9-15 May). It’s the 13th anniversary of the event and – with #LongCovid rampant round the world – the number of people being diagnosed with #MECFS is growing exponentially. HCPs can learn more about it here: https://t.co/H2Qyhtescc #MedTwitter
I don't know the alternative hypotheses or how to interpret this
Healthcare workers who likely caught covid from work in the hospital rather than the community had a 3x risk of Long Covid over 90 days
https://t.co/MfBlnmMlqo
Since September my best friend Chloé is bedridden with long Covid & ME/CFS.
Today marks almost a month of her biggest relapse to date. She went from being bedridden but awake, present, able to move around to eat, drink and shower, able to lie down on the balcony outside 🧵 1/n
The pandemic emergency may have been declared over by @WHO, but for people living with #LongCovid & the vast numbers still developing Long Covid from #Covid19 infections & reinfections, the emergency is very much ongoing.
#CovidIsNotOver#WearAMask@DrTedros@mvankerkhove
25% of #ME patients are bedbound, can’t walk and can’t take care of themselves. 75% are mostly housebound and can’t work. Most struggle with socialising. Scientists say #MECFS has been triggered in about half of #LongCovid cases. No treatment no cure.
#MyalgicEncephalomyelitis