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Evelien’s Journey to Meet the EU Parliament
Hi everyone!
First of all I would like to express my heartfelt thanks to all who contributed to the success of ...
NICE Called for Evidence: Read #MEAction UK’s Response
The National Institute for Health and Care Excellence (NICE) are re-writing their guidelines on ME. As part of this they ...
Are you Disabled? How does ME fit into the Disabled People’s Movement?
Values & Policy Initiative
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This article is part of our Values & Policy Initiative, a six-month long process for the community ...
Inside / Outside Activism: Why We Must Shout in the Streets and Sit at the Table.
Values & Policy Initiative
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This article is part of our Values & Policy Initiative, a six-month long process for the community ...
ME Activist Testifies before EU Parliament
Today Evelien Van Den Brink spoke powerfully and brilliantly to the Committee on Petitions in the European Parliament from her ...
Colorado Activist Introduces Rotary Club Resolution for ME
Colorado activist, Jim Lutey, has introduced a Rotary Club resolution to encourage research, education and funding for myalgic encephalomyelitis (ME!)
The ...
Why Civil Disagreement and Respect are Essential to the ME Movement
VALUES & POLICY INITIATIVE
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This article is part of our Values & Policy Initiative, a six-month long process for the community ...
Why We Must Build an Open, Grassroots Movement
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This article is part of our Values & Policy Initiative, a six-month long process ...
Brussels will Discuss EU Petition to Fund Biomedical Research for ME
Great news!
Remember the petition that asks the EU to fund biomedical research on ME? It will be discussed at the ...
NICE Call for Evidence on ME guidelines
The National Institute for Health and Care Excellence (NICE) have put out a call for evidence in relation to the ...