We have produced a "words only" version of our 2022 - 2027 strategy with no images for those who struggle with visual stimulus. If you would prefer a printed copy, please get in touch.
What is M.E.? / Living with M.E. / Employers & teachers / Research / Children and young people with M.E./CFS / Health & care professionals / Make a difference
Read about our work supporting children and adults with M.E. and their families, alongside professionals working with them; and about how we are driving high-quality research.
What is M.E.? / Living with M.E. / Employers & teachers / Research / Children and young people with M.E./CFS / Health & care professionals / Make a difference
We set out four ambitious outcomes which we believe will help us end the decades of ignorance, injustice and neglect faced by people with M.E., including our call for a national strategy for M.E., led by the UK government and backed up by increased research investment leading to validated treatments and, one day, a cure.
What is M.E.? / Living with M.E. / Employers & teachers / Research / Children and young people with M.E./CFS / Health & care professionals / Make a difference
This process has been developed to provide clarity, transparency and a clear governance framework for our key stakeholders including researchers, universities, donors, Action for M.E. supporting members and other people affected by M.E. It sets out our five-stage process for assessing research funding applications.