Talk:Primer for family, friends and care providers

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history

I have read that a biomarker has been found, so am challenging the statement that there is no biomarker. I am going to look for the article to present. In the meantime I wanted this documented as we all know the challenge of having to prove this is a physiological ailment.

You may find the following MEpedia article of interest: http://me-pedia.org/wiki/Diagnostic_biomarker
The problem is that there are no biomarkers ready for clinical use. All are still in the testing stage for accuracy and the ability to translate from bench-to-bedside. Kmdenmark (talk) 13:13, 1 June 2018 (PDT)