This treatment modality says much more about Dr Fam and nothing at all about ME also known as cfs.
It goes beyond patronising the patient to IMO a level of dislike for the people he wants so much to 'help' (by bullying them).
Just wanted to add that there was some good coverage in national news via the Canadian broadcasting Corp (CBC):
https://www.cbc.ca/news/canada/montreal/myalgic-encephalomyelitis-canada-icancme-1.5257415
Ah, I see @rvallee Thanks for the attempt. And you're right of course and I believe the point was even made at the big big reveal speech yesterday patient input should be valued as well informed on some of the issues around any illness.
Are there any Canadian MD's among us?
Yes, if nothing has come out I'm now thinking the future may never come (so to speak). Although it was less optimism on my part and more a passing whim to guess. :bored:
Hilariously I just had the thought (if we were all financially better off) that we could start betting pools on this sort of...
An aside from the actual paper abstract:
I've always loved the name psychNET. It feels like there should be a 1-800 phone number attached.
Perhaps they can prognosticate if I will have further morbidities in the future so I can book an appointment now and avoid the wait.
Though they could...
Would there be info here that you're looking for: https://www.s4me.info/threads/updates-on-status-of-icd-11-and-changes-to-other-classification-and-terminology-systems.3912/page-14#post-180508
Sorry, running out of steam so will just post a link to new pain definition as devised by this group: https://www.iasp-pain.org/PublicationsNews/NewsDetail.aspx?ItemNumber=9218&navItemNumber=643
Two Canadians involved and they are inviting comments.
Here is the official announcement on the GoC website:
https://www.canada.ca/en/institutes-health-research/news/2019/08/government-of-canada-invests-14m-in-biomedical-research-to-improve-the-quality-of-life-of-people-living-with-myalgic-encephalomyelitis.html
I forget who said it (maybe Alain Moreau) but there was specific mention of Stanford and Cornell and one other (can't remember) centre based in another country that this group would collaborate with. IIRC.
The moving personal account of living with ME came from Christiane Garcia of @Action CIND
I am immensely grateful to all who worked toward this moment. I hope that this momentum continues with more initiatives.
I'm not sure what's going on here but I think in general there are different links for different locations and being locked out geographically could simply reflect something to do with their revenue stream from whoever is viewing a particular link.
I have a hankering to turn this concept and organisation into a comedy tv show.
Only thing is while the patients are variously diagnosed with these ailments week after week the comedy would be that the fearless/peerless medics would be the ones who exhibit all of the symptoms without any...
I have a solution for that. It's called cut funding at the source so we have vastly fewer psych programs and therefore PhD students and profs who need to fill the universe with trivia.
I don't know but expect that the only reason there are so many out there now has to do with the university...
Not sure how much of interest this will be:
https://www.cbc.ca/news/canada/edmonton/gadolinium-concerns-1.5239055
From the article:
Gadolinium alone is toxic to humans, but in GBCAs, the element is bonded with other substances, which the body expels within 24 to 36 hours after the injection...
I just wish there was some way (and by extension some able people) who could be proactive on this. For some people who will be given IAPT they will believe what they are told at first and will be willing to explore all manner of personal traumas or failings when that has nothing to do with...
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