#MEAction Network UK (@MEActNetUK) header
#MEAction Network UK (@MEActNetUK) profile picture

#MEAction UK focuses on campaigning and advocacy in the UK a part of the charity MEAction UK.

United Kingdom
Joined June 2016
Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)Photo by #MEAction Network UK (@MEActNetUK)
It was a busy day on Thursday at the @rcgp conference. Volunteers such as Pam, joined by Avril from Action for ME, engaged with more than 130 doctors from all over the UK, handed out many more leaflets & quite a few chocolates! #MyalgicEncephalomyelitis #pwME #RCGPAC26
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We had a busy day on Thursday at the @rcgp conference. Volunteers such as Pam, joined by Avril from Action for ME, engaged with more than 130 doctors from all over the UK, handed out many more leaflets & quite a few chocolates! #MyalgicEncephalomyelitis #pwME #RCGPAC26
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MEAction UK were pleased to meet a representative of the Lyme Resource Centre - Scotland at the #RCGPAC26 The MEAction UK & Action for ME stand has been busy with our volunteers working hard to answer questions & hand out information. #MyalgicEncephalomyelitis
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MEAction UK are attending the #RCGP conference in Glasgow with Action for ME. We’re here to tell delegates about #LearnAboutME & how to support #pwme. We’ve already engaged with GPs, registrars, medical students & pharmacists with positive reactions. #MyalgicEncephalomyelitis
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Did you know that MEAction UK has its own mailing list? Sign up for a closer look at our work in England, Scotland and Wales, including campaigns, updates and information. meaction.org.uk/sign-up #MECFS #LongCovid #MillionsMissing
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Our thanks go out to @BethDobbin for speaking about her illness to raise awareness, even at the cost of her own health and for describing the impact of ME so vividly. Beth is bed bound for 22 hours a day.
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Through an online video interview, people answer questions about their lives and experiences in their own words, from home. Clips from these interviews are woven into the documentary to show what living with these illnesses is really like.
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If you are interesting in taking part follow the ink below. Please bear in mind that the film trailer contains upsetting content and be mindful of your energy limits while watching or contributing your story. #VerySevereME #pwME #SevereME
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Clips from these interviews are woven into the documentary to show what living with these illnesses is really like. If you are interesting in taking part follow the ink below.
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Please bear in mind that the film trailer contains upsetting content and be mindful of your energy limits while watching or contributing your story. #VerySevereME #pwME #SevereME
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Watch David Tuller's interview with George Monbiot using the link below. youtu.be/MaaeQ7crLz4?si=8R-f… #SevereME #pwME
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George Monbiot has sent out a call asking 'Are any of you still being offered inappropriate (psych/GET etc) "treatments"? Please email [email protected] #pwME #VerySevereME
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We have heard that he has received more emails than he can read and has asked for no more.
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Please read this petition update about Karen Gordon and sign if you haven't already. Be aware that Karen is still very ill and having a hard time in hospital, so read with caution. change.org/p/save-karen-gord… #VerySevereME
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The #MEAction Network Severe ME Artists Project has many wonderful pieces of art to share with you. Please share some love with the artists. nitter.cf/MEActNet/status/208607… #SevereMEWeek2026
In honor of #SevereMEday, #MEAction is honored to share the Severe ME Artists Project 2026! Over 100 of you submitted photos, drawings, writing, and videos of your work! We are thrilled to share so many amazing and powerful pieces of artwork. meaction.net/post/honoring-s… #SevereME
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The most severely ill people with ME have nowhere to go, no treatment, no ward, no NHS service. They need a specialised service and virtual wards to be commissioned now! Your MP can help by lobbying Yvette Cooper, the new Secretary of State for Health and Social Care.
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