A small organisation that regularly punches above its weight, Action for M.E. is leading, with others, a growing community working to create real change on the scale so urgently needed at a local, national and international level. Our 2016 – 2021 strategy sets out how we meet need now to improve the lives of people with M.E. while taking action to secure change for the future.
Much of the work we do is made possible by our fantastic volunteers. Some have been with us for many years, while others gain valuable work experience over shorter periods. Supporting our administrative, communications, marketing, fundraising and support work, some of our volunteers work with us in our Bristol office, while others make their essential contribution from home.
If you have skills and experience you think we could make the most of, please get in touch.
Some key services for our children and young people’s community are led by young volunteers living with M.E. Some contribute to our community forum, helping users feel less isolated and more confident about making connections. Others write to those children and young people severely affected by M.E., without the expectation of a reply.
A range of medical, research and professional advisors also provide an invaluable network of support on a pro bono basis.
All have one thing in common: they are hugely valued not just by our staff and Trustees, but also the people with M.E. they help us support. We are immeasurably grateful value for the time and energy they spend enriching our work, and helping us reach even more people affected by M.E.
Action for M.E.’s Mentor M.E. peer-support network is a five-year project to develop a network of volunteer peer mentors supporting people living with M.E. in Scotland. If you have direct experience of M.E. (this can include caring for a friend or family member), are aged 18 or over, and live in Scotland, we'd love to hear from you. Find out more.
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