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I think all the BPS and FND stuff has these beliefs at the root of it, as do all the roadblocks put in the way of people getting benefits.

The BPS stuff sometimes comes across as a system that is primarily concerned with acting as moral police when in reality medicine has nothing to do with policing people to be good diligent citizens.

The explanations they give for illness tend to involve moral failure, and the solutions they propose tend to involve patients overcoming their flaws and becoming a better person.
 
An Irish doctor on the journey from Aids to long Covid: ‘The suffering was monumental’
Pulmonary physician Mario Kinsella expects coronavirus effects to linger for 30-40 years
about 19 hours ago

https://www.irishtimes.com/life-and...-covid-the-suffering-was-monumental-1.4502178

What he is seeing, however, is a “greatly increasing number of patients with residual disease secondary to Covid”. This is now one of the most common reasons for referral to a pulmonary physician in Erie, he says. He has seen a dramatic increase in this patient group since the beginning of the year. Kinsella believes this will be the most common reason patients are referred to his practice by this summer.

Although the number of acute Covid-19 cases is declining in northwest Pennsylvania, he says, the number of chronic Covid-19 patients – those with so-called long Covid – is increasing dramatically. Not much long-term data is available, as the disease is only a year old, but Kinsella knows five physicians who have contracted Covid-19. One, who is in his 40s, received a double lung transplant last week, he says. Another, a heart surgeon who is originally from Limerick, made a full recovery. An ICU physician has persistent shortness of breath several months in, and two hospitalists have recovered fully.
More of the article discusses long Covid but I'm not sure it's that interesting from our point of view, e.g. other symptoms aren't discussed.

 
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Google translation of a Japanese article.

Symptoms of suspected corona sequelae "myalgic encephalomyelitis / chronic fatigue syndrome"
"Myalgic encephalomyelitis / chronic fatigue syndrome (ME / CFS)" is attracting attention as a sequela of the new coronavirus. We spoke with Dr. Takashi Yamamura, director of the Immunology Research Department, National Center of Neurology and Psychiatry, National Center of Neurology and Psychiatry, who is a leading expert in ME / CFS treatment and research.
Original, https://hc.nikkan-gendai.com/articles/275994
Translation, https://translate.google.com/translate?sl=auto&tl=en&u=https://hc.nikkan-gendai.com/articles/275994
 
Long Covid: Warning over combining ME treatment
Charities that support people with ME have warned against combining new specialist treatment for the condition with proposed services for long Covid.

The Health and Social Care Board [in Northern Ireland] is developing plans to help those still experiencing long-term health issues months after being unwell with Covid.

Some of the debilitating symptoms are similar to those reported by people with ME.
https://www.bbc.co.uk/news/uk-northern-ireland-56341431
 
Long Covid: Warning over combining ME treatment

https://www.bbc.co.uk/news/uk-northern-ireland-56341431
Why segregate ME and long-COVID? I totally disagree with the ideas put forward in this article.

Long-COVID must be assessed and treated side by side with ME. It will bring new doctors to the field, the same ones who are seeing from their own eyes what happens when a person does not recover. New doctors materialized for Long-COVID programs, some of which who got COVID I presume.

And wait times? We currently have a 28 months wait time over here for ME. As for Long Covid, patients get seen at 3 months and 6 months, to start with. There will be research and clinical trials, much faster than ME.

It would be a grave mistake to keep both segregated.
 
Seems to be a New Scientist article published in full via ScienceDirect.

Children with long covid

Almost half of children who contract covid-19 may have lasting symptoms, which should factor into decisions on reopening schools, reports Helen Thomson

A SERIOUS picture is emerging about the long-term health effects of covid-19 in some children, with UK politicians calling the lack of acknowledgment of the problem a “national scandal”.

Children seem to be fairly well-protected from the most severe symptoms of covid-19. According to the European Centre for Disease Prevention and Control, the majority of children don't develop symptoms when infected with the coronavirus, or their symptoms are very mild.

However, it is becoming increasingly apparent that a large number of children with symptomatic and asymptomatic covid-19 are experiencing long-term effects, many months after the initial infection.

https://www.sciencedirect.com/science/article/pii/S0262407921003031
 
The Norwegian Institute of Public Health has published a report:
COVID-19-Epidemic: Covid-19: Long-Term Effects of COVID-19 - a rapid review

It has a summary in Norwegian, the rest is in English. Not able to read it, but noticed that one of the authors was Brurberg, who also was co author on the Cochrane review on ME/CFS and Graded Exercise Therapy. I doubt this Covid-19 report mentions ME, but worry there will be a "biopsychosocial" approach also towards Long Covid from the Norwegian Institute of Public Health.
 
Is there any opinion on a maximum when something unexplainable can not be psychogenic?

Serious question, where does medicine draw the line?

I get how you can sweep a couple of people under the rug.

But depending on the definition of LC we're talking about 10-30% of all infected. Maybe more since even asymptomatic patients seem to develop LC.

Even as an enthusiastic PBSer, how likely is a psychogenic explanation at this point?
 
Even as an enthusiastic PBSer, how likely is a psychogenic explanation at this point?

It's a very good question.

Unfortunately, as caffeine withdrawal, bereavement that lasts more than two weeks over the loss of a loved one and someone else deciding that you're focusing too much on any symptom of a recognised and diagnosed physical ailment can now all be classed as mental health complaints I'd say fairly likely.

They've gotten away with it so far. They've made huge amounts of money and had glittering careers off the back of gaslighting prey patients. No reason why they'll stop now with all that fresh meat.

If anything it will only encourage them.
 
Long-haul Covid patients can experience 'waves of symptoms,' early research suggests

https://www.nbcnews.com/health/heal...rience-waves-symptoms-early-research-n1259281

Long-term symptoms may emerge in a distinct pattern over weeks and months.

...

Natalie Lambert, an associate research professor at Indiana University School of Medicine, surveyed thousands of "long-hauler" Covid-19 patients, finding that specific symptoms tend to emerge at regular intervals — usually a week or 10 days — resulting in what she calls "waves of symptoms."

...

"The first wave is clearly the more flu-like symptoms," such as fatigue, headache, fever and chills, she said. "Then it seems like diarrhea, nausea and vomiting are five days later, typically."

The new waves don't mean the previous symptoms disappear; those symptoms can linger, or they may fade and re-emerge later.

Ten days into illness, another wave crashes. This time, the new symptoms tend to be more neurologic, including confusion, dizziness and difficulty concentrating. Patients may also develop joint pain and low back pain. Some report pressure in the brain that is so intense that it feels like their heads might explode.

Fifteen days into illness, yet another wave of new symptoms: high or low blood pressure, heart palpitations, a tendency to faint.

A week later — about 21 days in — patients start experiencing issues like mouth sores, muscle twitching, eye infections and a skin condition that has been referred to as "Covid toes."

Medicine starting to notice things that were obvious to many as early as last May. I'm not sure about this slow-learning approach thing, it's not very impressive.
 
Long Covid patients 'told to go away by GPs'

https://www.bbc.com/news/uk-wales-56346444.amp

Aka standard medical practice for chronic illness.

Some patients who suffered ongoing health problems after contracting Covid-19 "were told to go away and get on with things" by their family doctors, a Senedd committee has heard.

...

"There are some people who were told to go away and get on with things, and they may not have come back. And that does concern me. If we have got people who weren't listened to in the beginning, they need to be listened to now."

Yikes, though:

Dr Elaine Maxwell, from the National Institute for Health Research Centre for Engagement and Dissemination, said it was important patients' concerns were not ignored in the way that those with ME had felt overlooked in the past.

She told the committee: "I think it is about believing people and taking medically unexplained symptoms seriously. That is the main problem for people with ME, they had something people didn't understand and were told it was all psychological.

"It is important we don't do that again, whilst recognising that we don't understand it. And we need to keep our minds open to a whole range of possible explanatory hypotheses, and not narrow it down too quickly. "

Saying this past tense is both massively annoying and incompetent. Especially as this reinforces the very problem, by insisting on the nonsense of MUS. This is exactly why this keeps happening, because people keep pretending that what is an ongoing human rights disaster used to happen. WTH? The sheer laziness of these people is insufferable.
 
Is there any opinion on a maximum when something unexplainable can not be psychogenic?

Serious question, where does medicine draw the line?

I don't think it has anything to do with medicine per se. Just the aspects of it that are tied up in academic empire building, financial self-interest, and small-state politics.

People who're interested in medicine as a scientific discipline are probably able to spot the gaping voids in the arguments fairly quickly.
 
Guardian: People with long Covid urgently need help. Why can't we access it?

I have just finished a remote rehab class with a physiotherapist at my local teaching hospital. It’s the first time I’ve attempted an hour of exercise since getting Covid nearly a year ago, and I managed a paltry 20 minutes of marching on the spot and strengthening exercises before I had to lie down. I used to be strong, fit and healthy, teaching yoga when I wasn’t working as a consultant in infectious diseases. Since developing long Covid, my ability to manage daily activities is unpredictable. On good days I can manage a 45-minute walk, but on bad days I will struggle to make dinner.
....
When fit to work, Joanna Herman is a consultant in infectious diseases in London, and teaches at the London School of Hygiene and Tropical Medicine

https://www.theguardian.com/commentisfree/2021/mar/10/people-long-covid-need-help-boris-johnson-
 
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