Full title: Barriers and facilitators of healthcare access for long COVID-19 patients in a universal healthcare system: qualitative evidence from...
From the #MEAction website: Questions to Ask Prospective MPs About ME/CFS...
In communities of color, long-covid patients are tired of being sick and neglected Regular link:...
“They seemed to be like cogs working in different directions”: a longitudinal qualitative study on Long COVID healthcare services in the United...
Abstract Background: Myalgic encephalomyelitis (ME, also known as chronic fatigue syndrome or ME/CFS) is a debilitating, complex, multi-system...
This: The gathering storm: The transformative impact of inflation on the healthcare sector is one of a series of reports by management consultants...
Britons now have the worst access to healthcare in Europe, and it shows "For the past few months, a fierce debate has been raging over the...
I haven't fill this in myself so far. https://www.surveymonkey.com/r/8NWFDC2 COVID-19 impact on healthcare management of people with chronic...
Dear All, I am very happy to say that i successfully filed for a US patent for a methodology that uses Artificial Intelligence, Network Analysis...
Abstract Many people with severe Myalgic Encephalopathy/Chronic Fatigue Syndrome (ME/CFS) commonly receive no care from healthcare professionals,...
Submissions are now sought for a special journal edition, "ME/CFS - The Severely & Very Severely Affected" Guest Editors: Dr. Kenneth Friedman...
The Guardian have a series of perspectives from healthcare professionals. https://www.theguardian.com/society/series/blood-sweat-and-tears
Speech she gave on May 12, 2018, at the Washington, DC Millions Missing Rally, with a few details added. ".......Prior to my ME diagnosis, I...
https://www.nrshealthcare.co.uk/articles/condition/chronic-fatigue-syndrome The most in-depth guide to Chronic Fatigue Syndrome. Learn all about...
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