Neuro Voices Wales – Support Groups The Wales Neurological Alliance invites anyone with a neurological condition, including ME & FM, to attend one of the new neuro support groups... News | WAMES (Working for ME in Wales) | Welsh Association of ME & CFS Support Read More
Last year was, by all accounts, a doozy. The nation endured a spate of tornadoes, fires, floods and, of course… News and Research – American ME and CFS Society Read More
In survey, 19% of people with ME/CFS said health worsened after vaccination compared to 4% reported by controls. A recent survey conducted by our You + ME Registry found that the health... This post first appeared on Solve M.E. Read More
ME/Research priority workshops The ME/CFS Priority Setting Partnership (PSP) is holding 3 final workshops to decide the top 10 ME/CFS research priorities. Apply to take part by January 11 2022. When and where? The workshops will take place on Zoom: Saturday 5th March 1.00pm – 2.30pmThursday 10th March 5.30pm -7.00pmFriday…
Dear friend, With an onslaught of Covid-19 cases from the Omicron variant looming, identifying treatments for Long Covid has become even more imperative. Since the beginning of the pandemic,... This post appeared first on Solve ME. Read More
In survey, 30% of people with Long Covid said health improved after vaccination and 28% said health worsened, compared to 4% and 7%, respectively, reported by controls. With an onslaught from the Omicron variant looming,... This post appeared first on Solve ME/CFS Initiative. Read More
WAMES helpline hours The WAMES helpline is run by volunteers and will be closed over the festive period. helpline@wames.org.uk 0290 2051 5061 24 December – 2 January closed we will reopen on the 3rd Feel free to email queries and we will reply as soon as possible. For emotional support, the…
December 17, 2021 Over the past few weeks, we have been collecting design entries for our Christmas e-card competition. We are delighted to announce that Jen was voted the winner for the competition,… This post first appeared on Action for M.E. Read more >>
As we enter the holidays we have a positive development to report coming out of yesterday’s ME/CFS stakeholder call with the U.S. Centers for Disease Control and Prevention (CDC). CDC has announced that it will not publish a systematic evidence review of ME/CFS treatments by the Oregon Health Science University…
As every year, we turn to you to wish you a happy holiday season and a very happy new year 2022. When taking stock of how the year has gone, let me tell you that unfortunately - one more year - we cannot be satisfied with the progress made in…