European Parliament adopts ME 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 “European Parliament adopts ME resolution”

Research into the long-term consequences of the COVID-19 pandemic

In an open letter published on ME Awareness Day 2020, Evelien Van Den Brink asks the European parliament to make sufficient funds available for scientific research into the long-term consequences of COVID-19. COVID-19 has an enormous impact on European countries. The great number of people who have become infected, the severity of the infection, andContinue reading “Research into the long-term consequences of the COVID-19 pandemic”

EU Committee adopts motion for resolution on ME

On Thursday, April 30th 2020 the Committee on Petitions of the European Parliament (PETI) adopted the Motion for a Resolution on additional funding for biomedical research on Myalgic Encephalomyelitis (ME). All 30 votes were in favour of the resolution, there were no abstentions. A press release about the vote was published on the website of the European Parliament.Continue reading “EU Committee adopts motion for resolution on ME”