…to be research misconduct by posting a 3,000-word correction/clarification rather than retracting the paper. In retrospect, those in the ME/CFS patient and advocacy community who challenged Professor Crawley’s decision to…
…was posted in early October of last year. The article’s second reference is to a 2007 NICE guidance on what the agency then called CFS/ME. The link for the 2007…
…success. So The Times‘ linguistic position on this matter seems notable to me. (Government agencies in the UK and the US now routinely use the term ME/CFS.) What’s also interesting…
…That’s not always easy, given the volume of material now being produced about ME/CFS, long Covid, so-called “medically unexplained symptoms,” and related issues. But here are a few more. **********…
…Virology Blog posted my very, very, very long investigation of the PACE trial two weeks ago, I hoped that the information would gradually leak out beyond the ME/CFS world. So…
…‘pacing.’” Added the article: “If a CFS patient does not gradually increase their activity, supported by an appropriate therapist, then their recovery will be slower. This seems a simple message…
