An excellent letter-to-the-editor by physiotherapist and mother of a severe ME patient. It is written for a health political journal and directed towards the Danish Minister of Health Magnus Heunicke. As many of you will remember, the Danish Parliament overruled the medical establishment this year by deciding that ME should be defined as a physiological illness and that international consensus criteria must be followed. Since then nothing has happened besides objections from doctors on the Parliament's decision. Vibeke Ilsøe Gustavussen: Trods politikernes indgriben svigtes ME-patienter stadig google translation: Despite the intervention of politicians, ME patients are still being failed In March, the Parliament agreed that the conditions for Denmark's 14,000 ME patients must be improved and the approach to the disease be changed. ME was thereby recognized in Denmark as a somatic disease, as it is also classified by WHO. It no longer hovers in psychosomatics and is no longer categorized under the term 'functional disorders'. Completely in line with international developments in understanding the disease. However, since the Danish Parliament's decision in March, Danish doctors have raged over the politicians' interference in a matter that they believe is theirs alone, rather than accepting that it is now recognized from the Parliament that the efforts for the patient group are far from sufficient. Ignorance and lack of interest in ME in Denmark have left the patients and their relatives in a void for years. Many of the sick have no contact with the health care system and receive no medical help. The hospitals believe that the task of monitoring and treating these seriously ill and bedridden patients lies with the general practitioners, while the general practitioners believe that it's a task for the specialized hospital departments. Nobody takes responsibility for these very sick people.
That was just plain bizarre. So many false claims. When you have to resort to this much nonsense to promote an ignorant opinion it's clearly indefensible. It's religious dogma at this point, it's not supposed to make sense.
The logic behind defending this is incredible. The status quo is so clearly a complete and total disaster for the very reason of this obstinate belief in a psychogenic thing with zero evidence, and the response is angry, aggressive even, ranting that, yes, this is what we deserve and in fact more of this is needed. The privileges of a profession, even medicine, cannot trample on the rights of individuals. It's insane that there is such strong insistence in maintaining that the rights of ME sufferers should not only be denied but done so by forcefully rejecting the very idea of informed consent. When the lives of so many people are threatened, authorities have a legal obligation to act, even if those responsible are medical professionals themselves. Nobody is taking responsibility and yet everyone wants it to remain the same even though it doesn't affect them, with a result that is nothing short of catastrophic. I don't see any arguments in favor of it, just petulant insistence that the lives of ME sufferers should remain null and void. Out of mere beliefs. What insanity. The banality of evil may be unimpressive but it is no less grotesque than the direct use of violence, which this adds up to. It's simple criminal negligence to allow this.
Two informative articles today about ME and PEM from the Norwegian news site ABCNyheter. The first article interviews doctors and researchers Kristian Sommerfelt and Katarina Lien. They explain the basics and warn against GET as treatment approach. Sommerfelt doesn't believe the knowledge about PEM among health professional is sufficient. - I think there has been a good increase in the knowledge of PEM among those who have been in contact with ME sufferers over time, such as teachers, GPs, physical therapists and occupational therapists. - But many find it difficult to acknowledge that PEM is there and how it behaves, and that it means one cannot advice that the patient to just "go for it". He explains that the usual advice for ME is to try to find a constant level of activity that works, and then slowly increase steadily. It's called graded exercise treatment. - There, in my opinion, the research does not support that it provides improvement in strictly defined ME, where PEM is present. On the contrary, I have repeatedly met patients who have had severe deterioration of the disease, which can last for many months. But I believe that most ME patients have come to the conclusion that this is a bad idea and that few people are now increasing the level of activity in this way, whether or not they are recommended. Katarina Lien talks a bit about her research on exercise and ME and says: - Exercise is important in almost all diseases, but ME patients appear to be get worse by activity beyond their tolerance limits. It fits with what the patients are saying. So it might also mean that exercise is not the right medicine for these patients, rather it can lead to deterioration. ABCNyheter: Anstrengelsesutløst sykdomsforverring (PEM) ved ME: - Som en reservetank som gir straff etterpå ved bruk google translation: Post Exertional Malaise (PEM) in ME: As a reserve tank that gives penalties after use Two ME patients are also interviewed and talk about living with ME. She believes the most important thing you can do as health and professional professionals is to take patients seriously, listen to them and understand the symptom PEM. - Then you will be able to achieve better facilitation, avoid unnecessary worsening of symptoms and the patient may experience increased quality of life. If you don't understand this symptom, you may be fooled when meeting an ME patient who manages to do something one day, but not necessarily the next. - There is no medicine yet that can make us healthy, but understanding PEM is something which can be done for ME patients, it will give us an easier path in the system and better quality of life. ABCNyheter: ME-symptomet PEM: - Man blir så glad fordi man føler seg friskere, men BANG! google translation: The ME symptom PEM: - You're so happy because you're feeling better, then BANG!
This is rare and needs to be said. Whenever people are saying that "ME is real", what it means is that what patients have consistently reported and has been researched as a flu-like type of illness for decades is the real description of this disease. It doesn't mean anything else and it is in sharp contrast with the made-up BPS nonsense that has nothing to do with reality and what patients report, essentially built on the assumption that what patients report is incorrect, because reasons. It's not a difference of opinions, there is only one set of opinions that is completely at odds with what is reported by patients and has been studied through careful observation. I have no opinions, I only ever reported the symptoms and their presentation. In isolation they are puzzling, in aggregation between millions of patients they do make sense. Opinions have no place in this. To say that being psychological does or does not mean that it's real or not is completely besides the point, it is making a completely different point, a distortion of what is said. What we mean is that we report one thing, factual, and a completely different set of opinions are believed and used in standard practice. What we mean by "ME is real" is that what patients report represents reality, not the distorted and self-inconsistent narrative invented to kick this disease out of medicine.
Interview with Ragnhild Holmås, who has ME and is battling prejudice towards invisible illnesses with humour as tool. Until now she's used Instagram as a platform, but next year she will be publishing a book titled "But you don't look sick". I really enjoy her sense of humour. The article begins with: Sometimes Ragnhild (31) wishes she had a frying pan. Mostly in order to strike people asking her "have you tried yoga?". I hope some of her writing will get translated to English in time. From the interview: - We have a language for the acute and the temporary. The things you can send flowers to and say feel better. But what if the improvement doesn't come? A few second passes. - And why do people have this intense urge to advice me to drink smoothies? ... - Now there are, somewhat simplified, two sick roles to choose from: the sad, suffering, or the jubilant "thank-you-for-the-cancer" type... I think we need to expand the repertoire. NRK: "Men du ser ikke syk ut" google translation: "But you don't look sick"
Opinion piece in Tidningen Ångermanland, written by a pwME: Hjälp att dö – eller hjälp att leva för ME-patienter? ("Help to die - or help to live for ME patients?") https://etidning.allehanda.se/369/T...-att-do-eller-hjalp-att-leva-for-ME-patienter
What good is that if it's disputed in practice and not covered in medical school? That knowledge has been available for decades, hasn't made any difference because it was rejected, contradicted even. It's impossible to move ahead without explicitly acknowledging that the last 30 years have been a complete, and avoidable, failure. Ultimately it's that it's not taught properly in medical school that makes any progress impossible. Physicians receive very little updates to their education during their career, relative to what they cover in training. There are thousands of diseases and various health problems, that's not the right way to do things, it just gets lost in the mix because "fatigue". In truth it would take years and years for a whole generation of properly trained physicians to make any difference, to change the balance. That's the typical thing: people keep saying change is coming and/or happening, but it never does. 50% failure, and I very much doubt that, is atrocious, especially when talking about giving harmful advice. About 90% of the relevant information we have today was already known before the BPS sabotage. It actually has to be disseminated, otherwise that's just as good as the IOM report, which some jackasses still pretend to read and claim it somehow supports their prior beliefs (referring to a recent twitter thing if anyone remembers), sitting there, being now available, but not having any impact.
More about Nordingrå, this time an interview with the man himself (who was recently sentenced to 1,5 years in prison for helping his severely ill wife end her own life). Tidningen Ångermanland: Jag kunde inte ha agerat annorlunda ("I couldn't have done anything differently") https://etidning.allehanda.se/369/Tidningen-Angermanland/265545/2019-11-30/r/3/
Oh? Sorry, it was open access when I posted the link. Maybe they will reopen it later? ETA: It's still open access for me. I printed the article to pdf, would be happy to send a copy through PM, just let me know.
Probably geoblocked. Oh well, I'm sure there will be more coverage. I'm good, thanks, I probably wouldn't remember much anyway, I usually just skim articles.
#MEvårdsaknas: När vården gör de sjuka ännu sjukare… ("When healthcare makes the sick even sicker…") https://mevardsaknas.wordpress.com/2019/12/01/nar-varden-gor-de-sjuka-annu-sjukare/
This speaks to me. I am foregoing a GP visit this year because what's the point? Nothing has changed much (including unrelated problems that still haven't been fixed years later and apparently won't until I can take charge because no one else will), it's too far away, the clinic is noisy, brightly lit, chaotic, demands .5-2h wait on uncomfortable plastic chairs with periodic blaring on overhead speakers and the pediatric waiting room from which constant wails and crying escape because the door is never closed. And for what? A standard blood test and a shrug. Which is a good preventative measure but it's just not worth it. I generally forget half the stuff I should be mentioning anyway because I am utterly drained by the time I get to the consult room and anyway there's always the damn 1 symptom per consult so why bother? And that's with my father doing most of the work to make it happen in the first place. And I'm not even bedbound, it's way worse than that for many patients. The myth is that we are heavy utilizers of medical resources. It's probably true early on, but the experience of interacting with health care services is so incredibly unpleasant and ultimately useless that I think that most of us simply don't bother after a few years. An issue well worth studying because, as is tradition, the different between perception and reality is pretty much, well, reality.
Betsy Keller Speaks in Norway November 2019 As part of the Norwegian ME Association’s Knowledge Campaign 2019, Dr. Betsy Keller traveled to Norway to present on post-exertional malaise. The Norwegian ME Association has uploaded her talk to YouTube and can be watched using the embedded video below. https://www.youtube.com/watch?v=kyVPonB6p28 Source: https://neuroimmune.cornell.edu/news/
Betsy Keller's talk is discussed here: https://www.s4me.info/threads/norwa...e-nov-25th-26th-2019.11827/page-2#post-223642
Region Västra Götaland, Sweden, are currently reviewing their healthcare for patients with ME. They ended their contract with the Gottfries Clinic (biomed) a few years ago. They currently have a contract with Smärthjälpen (BPS), a private pain clinic, which also includes pain and fibromyalgia patients. https://opengov.360online.com/Meetings/vgregion/Meetings/Details/1655808?agendaItemId=255836 Excerpts from the report:
This can be summarized as: just do your damn job, everything is still yet to be done, begin at step 0 and stop doing harm then work from there based on actual patient needs, not on what you personally prefer. Bit implicit but as an evaluation of current practices, it's yet again a simple grade of zero. Complete and total failure. Refusing to do your job only works for so long, problems don't magically disappear this way. Now if only there were accountability, any at all.
