Associations between long-term conditions and upper gastrointestinal cancer incidence: A prospective population-based cohort of UK Biobank participants
Abstract
Upper gastrointestinal cancers (oesophageal/stomach) have high mortality rates and are often diagnosed after the disease has...
Abstract
Background: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a long-term disabling illness accompanied by fatigue unsolved by rest. However, ME/CFS is a poorly understood illness that lacks a universally accepted pathophysiology and treatment. A lack of CFS-related...
"Main points
At 2 May 2021, an estimated 1.0 million people living in private households in the UK (1.6%) were experiencing self-reported long COVID (symptoms persisting for more than four weeks after the first suspected coronavirus (COVID-19) infection that were not explained by something...
Not new but thought it should be here.
"
Abstract
Background
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) or chronic fatigue syndrome (CFS) has been used to name a range of chronic conditions characterized by extreme fatigue and other disabling symptoms. Attempts to estimate the...
moved thread
Ok, but most of these studies are based on confirmed PCR tests which if I understand correctly require virus particles, not necessarily antibodies.
On Twitter someone pointed me to this Danish preprint which found that 16% of patients reported fatigue and 13% concentration...
Free full text:
http://www.sagpj.co.za/index.php/SAGPJ/article/view/41
South African General Practitioner 2020; 1(4):132-134
https://doi.org/10.36303/SAGP.2020.1.4.0041
Sick and tired of COVID-19: long haulers and post viral (fatigue) syndromes
Kim Outhoff
The full article is available at...
More interesting stuff from Goodelf, a two part article on MUS
https://opposingmega.wordpress.com/2020/08/19/so-what-if-23-get-worse-2/
Part 1: The PCPCS – a ‘One Door’ Approach to MUS
By Goodelf
https://opposingmega.wordpress.com/2020/08/19/so-what-if-23-get-worse/
Part 2: One Door, One...
Systematic Review of the Epidemiological Burden of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Across Europe: Current Evidence and EUROMENE Research Recommendations for Epidemiology
https://www.mdpi.com/2077-0383/9/5/1557
Leonard Jason research finds that many young people have ME/CFS
A new study finds that 0.75%, or 1 in 130 young people, have ME.CFS. That's a lot of people living with the illness. Only 5% of those diagnosed with the illness already had a diagnosis. Prevalence increased rapidly as children...
The team of Leonard Jason have performed a prevalence study in Chicago on children and adolescents with ME/CFS.
Because this was a community-based study with clinician confirmed diagnosis, this is probably one of the best studies on the prevalence of pediatric ME/CFS thus far...
Hello all,
I am very familiar with the ICC, CC, CDC vs Oxford criteria discussion, prevalence differences, Oxford obfuscation, etc. but I have a very specific question about what the Wessely crew mean by "CF" vs "CFS". This is not merely academic and is of consequence for important ongoing...
Moderator note: This post and the next two have been copied, and subsequent posts moved from this thread:
JAMA -"Advances in understanding the Pathophysiology of Chronic Fatigue Syndrome" by Anthony Komaroff
Posts about sex ratio have been moved to a new thread:
ME/CFS Epidemiology - sex...
charles shepherd
discussion thread
disease progression
epidemiology
gatekeeping
gender ratio
incidence
long covid
me association
me/cfs
prevalence
recovery rates
two age peaks
hi I’m sure I can get overall population for my city and region can anyone point me to what the % figure is that gives around 250k PWME in the UK. This could be useful on Sunday.
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