It's M.E. Linda
Senior Member (Voting Rights)
Actually - just had an update - we offered them a call and they have yet to come back to us!
But they are on on your radar, and that’s good!
Actually - just had an update - we offered them a call and they have yet to come back to us!
She told newsGP ‘mild’ cases of the virus should be renamed ‘non-hospitalised’ cases, given the longer-term damage to heart, lungs and brain seen in a minority of survivors, as well as the more common issues such as fatigue, breathlessness, brain fog, difficulty undertaking exercise, and even psychological symptoms resembling PTSD in those who were in intensive care.
‘It’s very hard to know how to go about preventing long COVID. It’s really very disconcerting,’ Professor McLaws said.
While there is limited evidence on symptoms and treatments specifically for long COVID, clinicians have drawn on the experience of survivors of the closely related SARS-CoV-1 coronavirus which also triggered post-viral fatigue and other issues.
‘Everyone is pushing for more collaboration between primary and secondary care and this is a great chance for us to do that,’ Dr Miller said. ‘This will be a very interprofessional space.
‘GPs are well placed to provide psychological support and to refer off for formal support if necessary.
‘We based this pathway on the first SARS, which also had [post-viral] breathlessness, fatigue and psychological distress,’ he said.
‘What we have found is that symptoms are often out of proportion to physiological abnormalities,’ he said.
I love that post-viral illness is both successfully handled but also completely data-free.‘At the moment, it’s a data-free zone as to whether interventions make any difference to long-term outcomes. No one can say,’ he said.
But, is it? The very thing that has been a total catastrophic failure in decades of practice? That's "terrific"? According to who?‘It’s terrific the PHNs are going to provide a GP-centric holistic model to assess these patients as individuals,’ he said.
He recently treated patients with severe fatigue, sleep and mood disturbances and heart palpitations, a combination suggesting both PTSD and chronic fatigue. Such patients represent the extreme end of the spectrum, he said, having often come out of intensive care with lung scarring and/or cardiac abnormalities as well as deconditioning.
‘Some seem to simply not have fully recovered from a virus, with their main problem being a lack of energy. They just don’t have as much petrol in the tank,’ Associate Professor Irving said.
‘For these patients, we can reassure them they don’t have lung scarring or cardiomyopathy or a neurological syndrome, and to suggest it is likely that time will heal them.’
You don't want to do what you've already done and continue to do in regular practice? Why? Would it be bad? Because it clearly is. You are doing this right now, though. And think it's bad. But also you have this under control. You've known about "post-viral fatigue" for a long time and have effective treatments but also this is brand-new and you have nothing useful, except for the decades of failure in practice, which exist when asked but also have never existed.‘Young people aged 20–39 now represent 40% of cases in Australia. That’s a very large group. We don’t want them going into middle age with chronic ill health.
From his past ramblings, I think this is the implication he means here. That attitude and belief in recovery is literally the main determinant and making it something to fear would create more cases of severe psychological distress, that if no one talked about it there would hardly be any cases.Should we make allowances for the fact that English is not his first language, and he may not understand the implications of "risk factor"?
Should we make allowances for the fact that English is not his first language, and he may not understand the implications of "risk factor"?
Over time, the use of BPS approaches at practice, organisational and national levels could reduce the reliance of communities and individuals on state services, but this will take a significant investment. With public attitude in favour of equitable solutions and re-investment in education, health and social care, this could be the moment to achieve significant improvements in social justice, enabling all to feel and function better than before the pandemic.
I skimmed through and this is basically someone liking the sound of their voice and sprinkling biopsychosocial! way too many times.
Certainly hasn't worked with the BPS approach to ME/CFS.The conclusion about "reduce the reliance of communities and individuals on state services" is not justified based on their study.
There is no distinction between "physical" and "mental".
Wait, why do we spend billions on basic research when Henrik knows? All we need to do is ask him. Since he knows. He knows whether research is necessary or not. I'm sure he has an impressive track record of that. With arguments like that, who wouldn't be convinced?Can research show that organic damage can explain all the symptoms in people who have had covid-19? No.
There are, in fact, many differences. They are, in fact, completely different things.
Literally don't even have a hypothesis. When asked, they just pretend it's not a valid question. And these people are taken seriously. Absurd.The GET manual used in the PACE trial says otherwise.
But I get that they are making it up as they go along. So this time it's about fitness, then it's about cognitions. In reality they don't have a viable theory.
Well either they don't know any better because they haven't done their homework, or they're deliberately lying.
McLaren’s recurrent theme is that some psychiatrists repeatedly invoke Engel’s biopsychosocial “model” and that they accept without demur (or references) that it is a reality, when nothing could be further from the truth.
McLaren asks: “Why do these intelligent people (ie. psychiatrists), their reviewers, their editors and, above all, their readers, continue to pay homage to something that does not exist?”
Wessely School psychiatrists, however, are certain that their own beliefs and their reliance upon the biopsychosocial model are right.They have built their careers upon it, so they must be right.
They are deliberately lying. These people don't believe in anything other than the advancement of their own careers. I can still remember the details of exams I had 15 years ago, there's no way they don't remember the details of their 5 million pound study which was based on the idea that patients were suffering from deconditioning or false beliefs about their own illness. There's also no way they wouldn't remember that 'pacing' was included in the study as a sort of control group? With the puprose of showing that the patients preferred strategy of 'pacing' did not lead to recovery unlike their bogus treatments.
At this point I am also absolutely certain that the only reason they really engage with patients online is an attempt to bait poor mistreated patients into behaviour that can be characterized as harassment or threats. This is done to further advance their career, by having a narrative of being poor victims, or to attempt to convince people like Paul that these ME/CFS patients are crazies and not to be listened to, regardless of their arguments.
Honestly, we're really lucky to have people like Robert who are able to engage in a civil and convincing manner with these hacks, which reflects well upon our community.
Because he is not as smart as he thinks he is, has nothing solid to back his case, and is getting desperate as reality closes in.Why does he bother to make such a fool of himself?
Yep. Sharpe's Twittering is exactly that.At this point I am also absolutely certain that the only reason they really engage with patients online is an attempt to bait poor mistreated patients into behaviour that can be characterized as harassment or threats.