Category Archives: News
Welsh Government on NHS training for ME/CFS
How will health professionals learn about ME in Wales? Decades of stigma, misunderstanding and struggle have been experienced by people with ME/CFS when they have attempted to access healthcare in Wales. Knowing this, and realising that no local medical … Continue reading
World ME day: Ask UK to be a #GlobalVoiceForME
#World ME day, 12 May – Take action! Together, we are battling a global health crisis – help us let the WHO know A part of the World ME Alliance we are joining with nations all over the world, … Continue reading
No ME/CFS Delivery plan for Wales, say Welsh Government
No Welsh strategy to support ME/CFS service development Following a question in the Senedd and discussions with Welsh Government officials it is now clear that the Welsh Government have rejected WAMES’ request to develop an all-Wales strategy or Delivery … Continue reading
Research: ME/CFS & joint hypermobility – a disease subgroup?
Joint hypermobility & ME/CFS Solve ME’s analysis of its You + ME Registry-based population (now Solve Together) sheds light on the complex interplay between joint hypermobility, ME/CFS, and Ehlers Danlos Syndrome. “Our results showed distinctive clinical characteristics in ME/CFS … Continue reading
Rob’s #500miles4ME awareness raising with physio Karen Leslie
Physical Exertion in ME & the PEM/PESE effect, with Karen Leslie of Physios for ME Rob Messenger shared his motivations for raising funds and awareness for ME by walking 500 miles over 100 days and climbing a total of … Continue reading
In solidarity with International Long Covid Awareness Day
The Inextricable Link Between ME and Long Covid: Solidarity with International Long Covid Awareness Day As we observe International Long COVID Awareness Day on March 15th, WAMES and the World ME Alliance stands in solidarity with the millions worldwide … Continue reading
Research: Children & young people with severe ME/CFS get poor care
Better care needed for young people with severe ME/CFS A study of children and young people in the UK pre-pandemic found that investigation, referral and management of those with suspected severe ME/CFS do not always meet NICE recommendations. This … Continue reading
World ME Day 2024 campaign film – take part
Be part of the World ME Day 2024 campaign film As we approach World ME Day 2024, WAMES and the World ME Alliance (WMEA) invites you to be a part of a new short film that aims to shed light … Continue reading
DecodeME completion date extended to Aug 2025
DecodeME results now due August 2025 The DecodeME team posted an update on 7 March 2024 DecodeME was due to be completed by August of this year Extraction of the DNA from samples has taken far longer than anticipated. … Continue reading
NICE replies to criticism of ME/CFS guideline
ME/CFS NICE guideline based on a thorough review of the evidence Criticisms by 50+ international researchers and clinicians of the ME/CFS NICE guideline were published in July 2023 and available on open access. In February 2024 a response from … Continue reading