Join our Facebook group

EMEC works in collaboration with ME Action, a Los Angeles-based organization that supports ME/CFS advocacy projects around the world. ME Action has created a strong online network for ME/CFS patients and their loves ones including several popular Facebook groups. The #MEAction European Union (EU) Facebook group has been an important meeting place for ME/CFS advocatesContinue reading “Join our Facebook group”

Petition

EMEC co-founder Evelien Van Den Brink has submitted petition No 0204/2019 on a request for funding for biomedical research on Myalgic Encephalomyelitis. The petition has received strong support from the ME/CFS community and has been signed 14.000 times In March 2019 Dutch ME/CFS patient Evelien Van Den Brink submitted petition No 0204/2019 to the EuropeanContinue reading “Petition”

Resolution

On 17 June 2020, the European Parliament adopted a resolution on additional funding for biomedical research on Myalgic Encephalomyelitis (ME). 676 members of parliament voted in favour, 4 against with 8 abstentions. This is the first-ever resolution on ME adopted by the European Parliament and it could mean a historic breakthrough for scientific research intoContinue reading “Resolution”

Open letter

More than one hundred scientists have signed an open letter calling for more European research into the illness Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). The open letter and a full list of signees is available below. Open letter on funding for biomedical research into Myalgic Encephalomyelitisin the European Union Myalgic Encephalomyelitis (ME), sometimes referred to asContinue reading “Open letter”