Energising Research into ME
The long standing issues with regard to myalgic encephalomyelitis that still exist across Europe
and continue to affect people with ME and their families -
lack of consistent and accurate diagnosis, lack of standardised up-to-date education about the disease,
the lack of high quality biomedical research into ME andclinical trials, caused by lack of any adequate Funding for research.
These all help feed misinformation about the disease and subsequent stigmas that permeates societies.
As principled advocates, we stand firm for patient rights without compromise by funding rigorous biomedical
research and facilitating targeted science and education for professionals and policymakers.
We therefore concentrate on three main areas -
Research
- Education
- Advocacy Strategy