Today we complete our major name change and rebrand, launching this new website. Formerly known as the International Alliance for ME, we are now the World ME Alliance. In order to modernise and promote our unique role, the World ME Alliance is launching this new website, with new logo, branding…
By Emily Taylor, Director of Advocacy and Community Relations Five years ago, the 21st Century Cures Act (Cures Act) was signed into law making national headlines, launching new health initiatives, and spearheading a new chapter in government scientific investment. With robust funding, multiple government agencies rolled out programs designed to…
It’s our one-year anniversary and we’re celebrating all month! Today, we announce our 2021 Ramsay Researchers! The Solve M.E. Ramsay Grant Program is designed to build a workforce, with a special focus on early-career investigators, and to allow researchers to generate data to support larger grant applications. The Ramsay network now includes…
This superb book by Dr. Neil Nathan is a must-read for anyone suffering from mold toxicity, Lyme disease, multiple chemical … News and Research – American ME and CFS Society Read More >>
September 23, 2021 Action for M.E. is saddened to learn of the death of M.E. campaigner Dr Richard Sykes, aged 89 years. Based in Bristol, Richard founded Westcare in 1990, offering counselling services,… This post first appeared on Action for M.E. Read more >>
September 23, 2021 Bringing people together to share learning, the ALLIANCE's Self-Management Week 2021 starts on Monday.Avril McLean, Action for M.E.'s Advocacy Senior Practitioner in Scotland, will… This post first appeared on Action for M.E. Read more >>
September 21, 2021 Special Educational Needs staff and other education professionals will hear about the impact of M.E., and how they can best support students, at nasen Live 2021 this week. Action for M.E. will co-host… This post first appeared on Action for M.E. Read more >>
Second year of Solve/UCLA partnership September 2021–Solve M.E. is again partnering with the University of California, Los Angeles (UCLA) Iris Cantor Women’s Health Center to fund ME/CFS research through their Annual Health Pilot Program. This round of funding follows last year’s, which supported a clinical study assessing the effects of repetitive transcranial magnetic…
NICE ME/CFS guideline publication delay drags on… Another delay in the revision process to the ME/CFS guideline was announced on 10th September: Updated: 10th September, to change the month of the meeting from September to October. A NICE spokesperson said: “In order for the meeting to be as effective as possible it…
September 17, 2021 On 16 September 2021, the Action for M.E. board approved a decision to merge with The ME Trust following a process of due diligence started in June, and after consulting with key stakeholders… This post first appeared on Action for M.E. Read more >>