UK Gov CFS research funding – Q&A in parliament
UK Parliament Written Question & Answers: CFS 1. Question from Alex Norrie MP, Labour, Nottingham North To ask the Secretary of State for Health and Social Care, how much Government…

UK Parliament Written Question & Answers: CFS 1. Question from Alex Norrie MP, Labour, Nottingham North To ask the Secretary of State for Health and Social Care, how much Government…

Research on Covid-19 among ME/CFS patients The European ME Alliance (EMEA) invites people to take part in a study to find out whether: ME/CFS patients more often get infected…

Understanding the role of the GP in caring for patients with ME/CFS – volunteers needed Telephone interviews A 3rd year medical student at Cardiff University would like to interview…

Action for ME blog post, 10 Oct 2017: Call for biomedical PhD research proposals now open Action for M.E. is inviting PhD proposals for high-quality biomedical research pilot projects that will…

National ME/FM Action Network announcement: A senior Canadian researcher has been looking for genetic factors in people with ME/CFS for several years. His studies have already yielded promising results. The…

Phoenix rising forum post, by HIP, January 2016: Why so little ME/CFS research from France and Germany? There seems to be little ME/CFS research done in France and Germany, relative…