As a charity we are dedicated to supporting all patient groups in our treatment and research programme. These include those most often denied involvement in research initiatives, such as the chronically bed-bound and those sufferers from ethnic minorities.
We are focused on channelling our resources to innovative scientists working in biomedical research for the treatment of M.E.
By developing our special access to both the scientific and the business communities, we are able to support research initiatives most likely to make a direct and meaningful difference to M.E. patients.
We are committed to a philosophy of making every pound count. Our research programme is orchestrated to minimise duplication and waste in research.
Our approach is patient-centered
We take the patient, their specific symptomatology and distinctive illness experience as a starting point.
We then work outward by using this real-life knowledge as a basis for scientific hypotheses. By taking this ‘bottom-up’ approach, we can ensure that the research we fund is tailored for ME.
This process is key to M.E. Solutions. It enables us to give the patient a voice and actual influence, not only over their care, but also in future biomedical research projects.
Hence we are committed to bringing together eminent scientific minds and the lived experience of ME sufferers.


