MPs Fight for House of Commons debate on ME in UK

MPs across the parties in the U.K. came together today to argue the case for scheduling a debate about Myalgic Encephalomyelitis (ME) in the main chamber of the House of Commons. Watch the video below.

Carol Monaghan MP joined five other MPs on June 5th to argue the merits of holding a debate on ME in the House of Commons in her application before the Backbench Business Committee. The MPs spoke about the need for greater biomedical research, medical education and public awareness for ME.

We will likely hear whether or not the application was successful by the end of the week – stay tuned. There’s also the possibility that the committee might grant a 90-minute Westminster Hall debate on ME, instead, depending on what other parliamentary business arises. 

Supporting MPs include:

Nicky Morgan MP (Cons)

Stephen Pound (Lab)

Alex Chalk (Cons)

Ben Lake (Plaid)

Kerry McCarthy (Lab)

Watch the MPs argue for the debate on ME before the Backbench Business Committee: 

Monaghan led the parliamentary debate on the PACE trial last February in which the Minister acknowledged a wider debate would be warranted.

If you haven’t contacted your MP about supporting the Early Day Motion for ME, now is the chance. Encouraging your MP to sign EDM 1247, not only gives weight to an application for a debate but helps us to know where our supportive MP’s are. The EDM currently has 111 signatures (as of publishing); it will likely attract press attention if it achieves more than 150 signatures. 

Contact your MP

We need your help to keep the momentum going. Help us hire a full-time, on-the-ground #MEAction team member in the UK to support more work like this by donating to our UK crowdfunding campaign today.

Facebook
Twitter
WhatsApp
Email

Latest News

redish square image with the US Capitol photo with a red overlay on top of it. The words Congress is hearing from us. Then the MEAction logo in the center bottom.

#MEAction: Congress Is Hearing from Us

#MEAction has been hard at work connecting individuals to their elected officials to talk about the ME/CFS Research Roadmap, Medicaid, and telehealth.  We’ve been partnering with #NotJustFatigue on setting up congressional meetings in order to ask our elected officials for their support in making funding of the ME/CFS Research Roadmap a reality. #MEAction State Chapter

Read More »
blackish rectangle with the words, MEAction Georgia Volunteer - Maggie Boxey- at TEDxOjia with the meaction logo in the bottom right corner.

#MEAction Georgia Volunteer, Maggie Boxey, Speaks at TEDxOjai

#MEAction Georgia recently had a huge accomplishment. Maggie Boxey, who is a member of the Georgia State Chapter, a Navy veteran, and a published author, recently gave a Tedx talk about her experience as a person with ME. Maggie was diagnosed a year ago but has been sick since 2020. Before becoming sick Maggie and

Read More »

SOS: Save our Science

People disabled by ME and Long Covid across the UK send out an SOS.  It’s time to send out our SOS signal, if we want to have funded research. May 12th is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing with myalgic encephalomyelitis (ME) gather to demand an increase in research and care for

Read More »