So sample is not likely fully representative of the population. Whether this should matter in comparisons between the two countries, I'm not sure.
This is how stigma was measured:
This is the question they used:
2017 Canadian Pain Society: Is sex worth the pain? Willingness to engage in sexual activity among partnered women with fibromyalgia....
I'm not sure whether we have seen the PDF layout of this before: Editor's note on correction to Crawley et al. (2018)...
Free full text: https://translational-medicine.biomedcentral.com/articles/10.1186/s12967-019-02155-4 Research Open Access Published: 03...
Not all supposedly prospective research in ME/CFS is really for prospective. People can wait a long time to be diagnosed so people can be ill in...
Well, it certainly provided relief for me. Without a diagnosis, I was expected to have the workload of someone who was fully healthy, which caused...
Cook (one of the authors) did this study on ME/CFS in 2017. —- Neural consequences of post-exertion malaise in Myalgic Encephalomyelitis/Chronic...
https://onlinelibrary.wiley.com/doi/pdf/10.1002/psb.1797
https://www.sciencedirect.com/science/article/abs/pii/S0167876019305495 International Journal of Psychophysiology Available online 28 November...
Not sure I understand. Anytime I have donated to a US charity, I have donated in US dollars despite not being in the US. Dollar donations are...
I presume that minimum only applies if people want to donate and ensure the extra credit is claimed through their national tax system. The text...
Kathleen McCall, the chairperson, is in Hampshire but the Simpsons are in Norwich. I, too, presume a big reason they are looking at things...
Some others that have done long, valuable service to the ME community in the UK: Simon Lawrence (25% ME Group); Charles Shepherd (ME Association...
Separate names with a comma.
