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It's useful to have a version that's not behind a pay wall. Thanks.

This reminded me of the recent New York Times article, and indeed it is, but this time it's not behind a pay wall

I hope there are enough researchers to make applications (which are deemed good quality) to ensure all the money is used. A lack of private money for research can mean there is a lack of researchers in a field to make applications.

Study points to vagus nerve dysfunction as a central pathophysiological feature of long COVID https://www.news-medical.net/news/20220212/Study-points-to-vagus-nerve-dysfunction-as-a-central-pathophysiological-feature-of-long-COVID.aspx

Pay-walled article in an Irish national newspaper: Tackling brain fog and other nasty legacies Covid-19 has left in its wake Luke O'Neill Insights gained into how to treat long Covid will be useful in dealing with other viral infections...

One can look at the references mentioned in it for free at the Lancet site: https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(22)00183-0/fulltext

First page can be read here: https://www.sciencedirect.com/science/article/abs/pii/S0140673622001830

The Hope for More Good Days (Bateman Horne Center) (Background to the ME/CFS Crash Survival Guidebook) https://batemanhornecenter.org/22542-2/

Bateman Horne Center During a crash, it can be incredibly difficult to communicate your needs to others. These communication cards aim to assist you and your support network by creating an unspoken dialogue to ensure your critical health and comfort needs are met. https://bit.ly/34nh5yX...

Irish article. No mention of ME/CFS or "post viral": Long Covid: Parents exposing kids to virus without knowing the risk, expert warns https://www.irishexaminer.com/news/arid-40801611.html Includes: "Model Care In June, the HSE published a draft ‘model of care’ for Long Covid, with a...

Moved post From the front page of the Sunday Times (Irish edition): I'm not sure whether these numbers hold up, given the numbers vaccinated.

Bateman Horne Center · RELEASED: "ME/CFS Crash Survival Guidebook: The Art of Living with ME/CFS" https://bit.ly/34nh5yX The guidebook is designed for the patient, their support network, and medical providers to: - Understand ME/CFS and its defining characteristic of post-exertional malaise...

https://pesquisa.bvsalud.org/global-literature-on-novel-coronavirus-2019-ncov/resource/pt/covidwho-1630932 Long COVID-19 and central sensitivity syndrome Cercas-Lobo, S.; Deniel-Rosanas, J.. Atencion Primaria Practica ; 3(3), 2021. Artigo em Inglês, Espanhol | Scopus | ID: covidwho-1630932...

Free full text: https://kinesiologybooks.org/index.php/stork/catalog/view/10/1/185-1 Chapter 18 Exercise and Chronic Fatigue James G. Wrightson1 and Rosemary Twomey2 1Department of Clinical Neurosciences, University of Calgary, Canada 2Cumming School of Medicine, University of Calgary...

https://www.surveymonkey.com/r/VNN5M2B ETA: I meant to ask did anyone think this was worth sharing around?

My position is a lot of people claiming to have chronic Lyme have ME/CFS while it’s them who don’t want to be associated with ME/CFS.

Somebody went to the trouble of sending me the following so I thought I should probably post it somewhere. I thought this place might be more sceptical than other places on average, so hopefully people will be cautious about any recommendations. The reviews on Amazon are mostly positive, but...

Studies that have followed adults after infection e.g. Dubbo (EBV/Ross River virus/Q-fever) and adolescents e.g. Chicago (Katz/Jason) have found that many who satisfied Fukuda criteria for CFS at 6 months didn’t at 24 months.