I am one of the 250,000 people in the UK suffering with CFS/ME.
The 2007 NICE guidelines need a full revision. Suggestions from these guidelines have reported to worsen the condition.
On top of this many parts of the UK do not even have a local hospital-based specialist in which GPs can refer them to.
A lot more funding for biomedical research is desperately needed from the government and shouldn’t be left largely to the charity sector.
Please help us to get the help that we so desperately need.
![a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.](https://www.meaction.net/wp-content/uploads/2024/06/Severe-ME-Artists-Project-2024-1200-x-630-px-1-300x158.png)
Severe ME Artists Project 2024
Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by