Brain fog plagues COVID-19 survivors

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kitesandtrainsandcats
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12 Oct 2020, 7:24 am

Hmm, interesting; wonder what of any help might eventually come out of it for those of us who have had ME/CFS with its brain fog for a little while to a couple decades or longer?
https://www.baltimoresun.com/coronaviru ... ed-content

Quote:
‘I feel like I have dementia’: Brain fog plagues COVID-19 survivors
By Pam Belluck
The New York Times |
Oct 11, 2020 at 7:28 PM

... Scientists aren’t sure what causes brain fog, which varies widely and affects even people who became only mildly physically ill from COVID-19 and had no previous medical conditions. Leading theories are that it arises when the body’s immune response to the virus doesn’t shut down or from inflammation in blood vessels leading to the brain.

Confusion, delirium and other types of altered mental function, called encephalopathy, have occurred during hospitalization for COVID-19 respiratory problems, and a study found such patients needed longer hospitalizations, had higher mortality rates and often couldn’t manage daily activities right after hospitalization.

But research on long-lasting brain fog is just beginning. A French report in August on 120 patients who had been hospitalized found that 34% had memory loss and 27% had concentration problems months later.
...


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Sylkat
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12 Oct 2020, 11:25 am

This needs to be more widely known.


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kitesandtrainsandcats
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12 Oct 2020, 1:03 pm

Sylkat wrote:
This needs to be more widely known.


There are publications, news services, and medical professionals, trying to do that; a few samples,

Long-Haulers Are Redefining COVID-19
Without understanding the lingering illness that some patients experience, we can’t understand the pandemic.
The Atlantic Story by Ed Yong August 19, 2020
https://www.theatlantic.com/health/arch ... ms/615382/


As post-COVID heart and brain problems linger, some coronavirus survivors find it's a long haul to recovery
Suzanne Smalley Reporter, Yahoo News•July 22, 2020
https://news.yahoo.com/as-post-covid-he ... 34453.html


Published online 2020 Jun 27.
Into the looking glass: Post-viral syndrome post COVID-19
Ray Perrin, Lisa Riste, and Mark Hann
The School of Medicine and Manchester Academic Health Sciences Centre, Manchester University, UK
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320866/
Quote:
Letter to the Editor

We are writing to highlight the potential for a post-viral syndrome to manifest following COVID-19 infection as previously reported following Severe Acute Respiratory Syndrome (SARS) infection, also a coronavirus [1]. After the acute SARS episode some patients, many of whom were healthcare workers went on to develop a Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) – like illness which nearly 20 months on prevented them returning to work [2]. We propose that once an acute COVID-19 infection has been overcome, a subgroup of remitted patients are likely to experience long-term adverse effects resembling CFS/ME symptomatology such as persistent fatigue, diffuse myalgia, depressive symptoms, and non-restorative sleep.

Post-mortem SARS research indicated the virus had crossed the blood brain barrier into the hypothalamus via the olfactory pathway [2]. The pathway of the virus seemed to follow that previously suggested in CFS/ME patients, involving disturbance of lymphatic drainage from the microglia in the brain [3].One of the main pathways of the lymphatic drainage of the brain is via the perivascular spaces along the olfactory nerves through the cribriform plate into the nasal mucosa [4]. If the pathogenesis of coronavirus affects a similar pathway, it could explain the anosmia observed in a proportion of COVID-19 patients.


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ASPartOfMe
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12 Oct 2020, 3:10 pm

These after-effects scare more than dying from COVID-19.

I am at high risk from tongue replacement surgery that left me with speech and swallow issues.

That said my risk of becoming a long hauler is greater than my risk of dying. I don't want any more physical disabilities nor am I keen on adding COVID-19 brain fog to my executive functioning issues.

I am glad I do not live in an area where mask-wearing and social distancing get you bullied.


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kitesandtrainsandcats
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12 Oct 2020, 3:22 pm

ASPartOfMe wrote:
I don't want any more physical disabilities nor am I keen on adding COVID-19 brain fog to my executive functioning issues.

I totally get that concept. Brain fog even as mildly as I have it compared to a couple people in those articles, is not fun at all and seriously messes with living life in this world.


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12 Oct 2020, 4:47 pm

Imagine trying to get through just the next four years with a coronavirus-induced "Brain Fog"...

... while trying to run the country.


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