UK Parliament

#MEAction UK’s parliamentary work involves a team of dedicated volunteers and thousands of constituents who have been engaging in campaigning since the organisation’s launch.

#MEAction UK works to educate MPs about the injustice and neglect faced by people with ME, galvanising them to take action with and on behalf of their constituents. 

Our Aims

Awareness

To raise the profile of people with ME with MPs and call on them to support their constituents with ME.

Action

Encouraging MPs to support our campaigns and bring pressure to bear on the government to make meaningful change. 

To persuade Parliament and funding bodies to ring-fence funding for ME research in line with disease prevalence and burden. 

How to set up a meeting with your MP

Meeting  your MP, virtually or personally, can help gain valuable support for you and for the ME community.  To make it as easy as possible we have put together a step-by-step guide.

Link to Parliamentary Advocacy Guide

Send us any feedback from your MP

If you have received a response from your MP please email us admin@meaction.org.uk and tell us about it. The information you provide will help us improve our overall strategy so that we can better target our campaigns.  




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September 2017

EARLY DAY MOTION 271

On the 6th September, Early Day Motion (EDM) 271 is tabled calling on NICE to overturn their original decision and agree  to review and update the guidelines on ME.





September 2017

UNREST SHOWN IN PARLIAMENT

Our Parliamentary presentation and showing  of the film Unrest, directed by the co-founder  of #MEAction, Jennifer Brea, helped 40 MPs understand the devastating nature of ME, focused attention on how NICE guidelines  had let individuals down and the need for more research funding.



February 2018

FIRST WESTMINSTER HALL DEBATE ON PACE TRIAL

#MEAction UK ran a campaign to urge MPs to attend the first Westminster Hall debate on the PACE trial and its effects on people with ME Carol Monaghan MP, who secured the debate, raised many valid and important concerns, as did several MPs who intervened during her speech. However, there was a disappointing response from the Minister for Care.





May 2018

EARLY DAY MOTION 1247 TURNS UP POLITICAL VOLUME

#MEAction UK created tools to to help people encourage their MPs to sign EDM 1247. The motion turned up the heat by acknowledging the detrimental effect of the PACE trial and recognising the work being done by organisations such as #MEAction UK o highlight ME as a physical condition.



June 2018

SECOND WESTMINSTER HALL DEBATE ON PACE TRIAL

#MEAction worked with other charities  to prepare a parliamentary briefing forthis debate. MPs then called for the immediate removal of Graded Exercise Therapy (GET)  from the NICE guidelines, as patients consistently reported being harmed from attempting to undergo this treatment.



January 2019

HOUSE OF COMMONS MAIN CHAMBER DEBATE

#MEAction UK coordinates the community in  sending almost 3000 messages to MPs, imploring them to speak up on their behalf and ensuring the human cost of this devastating disease is heard in the corridors of power during this historic debate on the treatment and funding of patients with ME led by Carol Monaghan MP.

The motion was passed unanimously.




January 2020

ALL-PARTY PARLIAMENTARY GROUP (APPG) ON M.E. REVIVED

Disbanded in June 2017, Carol Monaghan MP led the revival of the group to work on behalf of  the 750,000+ people in the UK with ME.  Please encourage your MP to attend future meetings of the APPG.



October 2023

We respond to the DHSC Interim Delivery Plan on ME/CFS

We send a full response to the DHSC's Interim Delivery Plan on ME/CFS outlining the lack of funding and health services for the very severe.

September 2024

We lobby Andrew Gwynne MP

We lobby Andrew Gwynne MP committing to ensuring publication of the DHSC ME/CFS Delivery Plan without more delay

May 2025

We send SOS messages to government ministers

We ask people to send SOS messages to government ministers and funding organisations urging them to include funding for research in the ME/CFS Delivery Plan as part of #MillionsMissing.