Action for ME
@actionforme.bsky.social
490 followers 11 following 360 posts
Providing support & holistic healthcare services to people of all ages affected by #MECFS Charity number: 1036419 / SC040452
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actionforme.bsky.social
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We're excited to announce that we've joined as an affiliate charity partner of Our Future Health, the UK's largest health research programme!

We'll support Our Future Health to ensure their programme serves the research needs of a range of health conditions & diseases, incl. ME

#pwME #MECFS
A graphic announcing that Action for ME has become the newest affiliate charity partner of Our Future Health. It shows two hands holding a card with the Action for ME logo, surrounded by a yellow and navy patterned border. A graphic featuring a quote from Dr Raghib Ali, CEO and Chief Medical Officer of Our Future Health, welcoming Action for ME as an affiliate charity partner and highlighting their shared aim to help people live longer, healthier lives.
actionforme.bsky.social
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Prof Chris Ponting of @decodemestudy.bsky.social flagged the need for the test to be fully validated by better-designed studies & said some claims made by the researchers were "premature"
actionforme.bsky.social
#MECFS #MyalgicE #MyalgicEncephaloymelitis
actionforme.bsky.social
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They examined blood samples from 47 patients with severe ME/CFS & 61 healthy adults, discovering "a unique pattern" that appeared consistently in #pwME & not the healthy controls

A test was developed & reported a 92% sensitivity (likelihood of a positive test if that patient has the condition)
actionforme.bsky.social
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🔬 Research news

Researchers at the University of East Anglia say they have developed the world's first blood test to diagnose ME

However, whilst acknowledging the research as an "interesting development", other researchers have offered cautionary responses to the results

#pwME #MEResearch

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A researcher wearing a mask, gloves, and a lab coat holds up a blood sample tube for examination. The image includes the Action for ME logo and a headline stating, “Researchers say they have developed the first accurate blood test to diagnose ME.
actionforme.bsky.social
We are delighted to welcome @catsmithmp.bsky.social as our newest Parliamentary Champion!

We would like to thank Cat and we look forward to working with her. Read more here: www.actionforme.org.uk/cat-smith-mp...
Headshot of Cat Smith MP, who has shoulder-length blonde hair and glasses, smiling against a grey background. The Action for M.E. logo appears in the top right corner. Below, a banner reads: “Policy news – Cat Smith joins our Parliamentary Champions network.” A statement from Cat Smith MP on joining Action for ME as a Parliamentary Champion. She speaks about hearing from constituents about the devastating impact of ME, recognising the overlap with other long-term illnesses, and the need for more awareness, research, and joined-up care.
actionforme.bsky.social
The recording from our 2025 AGM is now available to view on our YouTube channel!

🎬 youtu.be/N0mRuePXMgQ

And, in case you missed it, you can also find a copy of our most recent Annual Report & Accounts in the 'Resources' section of our website.

#pwME #MECF#pwMEa#MECFS##MyalgicEc#MyalgicEncephalomyelitis
Action for ME 2024/25 Annual General Meeting
Watch the recording from our 2024/25 Annual General Meeting.
youtu.be
actionforme.bsky.social
📢 2 weeks left to sign up for the Bath Half in aid of Action for ME!

Applications close on 12th October - don’t miss your spot at one of the UK’s most prestigious half marathons 👟

Find out more and apply for a place: GetPRO Bath Half Marathon - Action for ME
actionforme.bsky.social
📢 Invite your MP to the next APPG on ME meeting!

📆 Thurs 23 Oct, 11am–1pm

The session will follow the Severe ME Inquiry evidence session, with MPs drafting recommendations for a formal report.

✉️ Updated invite template via APPG site: appgme.co.uk/contact-your...
Poster for Action for ME, ME Association and APPG on ME. Background shows UK Parliament and Big Ben. Green icon of an envelope with text: “Invite your local MP!” Below: “APPG on ME – October meeting: Continuation of the Severe ME Inquiry.”
actionforme.bsky.social
This #FundraisingFriday, we are celebrating the brilliant Iara De Sousa and her partner who walked the Ultra Challenge Thames Bridge Trek in aid of Action for ME, surpassing her fundraising goal to raise £690!
Action for ME fundraising graphic featuring Iara De Sousa and her partner smiling during the Thames Bridges Trek, where they raised £690. Text highlights gratitude for their Ultra Challenge fundraising efforts.
actionforme.bsky.social
Good news! Learn about ME has been awarded £33,366 from the Scottish government to continue for another year.

Read the full response to Alex Cole-Hamilton's question 👇 tinyurl.com/4f66ub79
Action for ME policy news graphic showing the empty, modern wooden debating chamber of the Scottish Parliament with text announcing Learn about ME to receive funding for another year - helping more professionals understand ME
actionforme.bsky.social
📢 APPG on ME

The minutes from the 10 September APPG meeting are now available on the APPG’s website 👇 

appgme.co.uk/meetings/app...

Thank you to those with lived experience who used their valuable time and energy to provide evidence as part of the Severe ME Inquiry 🧡

#pwME #MECFS #MyalgicE
Graphic showing Big Ben and the Palace of Westminster with logos for Action for ME, the ME Association, and APPG on ME. An icon of documents is centred. Text reads: “APPG on ME - 10 September 2025 meeting minutes now available."
actionforme.bsky.social
We're pleased to share our 2024/25 Annual Report & Accounts!

The document outlines the progress we've made against our strategy, alongside demonstrating the impact our work has for #pwME

Available on our website 👇

www.actionforme.org.uk/resource/act...

#MECFS #MyalgicE #MyalgicEncephalomyelitis
Cover of Action for ME’s Annual report and accounts 2024/25. The design features bold orange and yellow waves at the top, the charity’s logo bottom right, and a photo of artist Alison Larkman with her artwork I would be here if I could by Sasha Snow.
actionforme.bsky.social
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Just 1 week to go until our 2025 Annual General Meeting (AGM)!

The Meeting will be held online (Zoom) & the recording will be shared soon after the meeting for those unable to attend.

📆 Wednesday 17 September

🕒 3pm - 4.15pm

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis

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Graphic announcing Action for ME’s 2025 AGM. Details: Wednesday 17 September, 3pm–4.15pm, online. Bold orange banner reads ‘1 week to go!’ with Action for ME logo at the bottom.
actionforme.bsky.social
Our ME Friends Online forum is a community for adults with ME, including carers, where you can connect with others who share your experiences.

Sign-up here 👇

www.actionforme.org.uk/sign-up/

All users must abide by our Terms of Use!

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #PeerSupport
Promotional graphic for Action for ME’s ME Friends Online Forum. Text in the upper half describes who the forum is for and what it offers. In the lower half is a photo of a man using a tablet. Action for ME logo in top right corner and QR code in bottom right corner.
actionforme.bsky.social
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A big thank you to Tom and his office for working with us to bring these concerns to the House’s attention 🤝

✍️ Please tag or contact your local MP, asking them to sign and show their support for the EDM!
actionforme.bsky.social
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▪️ Limited attention given to severe ME, with no guarantees on specialist care provision

▪️ Lack of robust accountability & resources to improve care, support & outcomes for #pwME

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actionforme.bsky.social
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▪️ The omission of a dedicated ME research hub & strategic funding

▪️ Lack of sufficient accountability for implementing services & updating medical education in line with NICE guidance

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actionforme.bsky.social
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The EDM references the need for the Plan and the work of everyone involved in its publication to be welcomed by the House, but also to recognise that the Plan falls short in a number of areas, including:

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actionforme.bsky.social
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📢 Early Day Motion (EDM) tabled on the Final Delivery Plan

We’re pleased to see this EDM tabled by @tommorrisonmp.bsky.social to discuss the Final Delivery Plan on ME/CFS.

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #EDM

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Graphic from Action for ME showing the Houses of Parliament with Big Ben. Text reads: ‘Policy news – Early Day Motion on the Final Delivery Plan on ME/CFS tabled by Tom Morrison MP’.
actionforme.bsky.social
Wishing our amazing Great North Run team the best of luck this weekend! 🙌

From all of us here, we'd also like to thank them for their dedication to raising funds to support our work & raising much-needed awareness of #MECFS 🧡

#pwME #MyalgicE #MyalgicEncephalomyelitis #GreatNorthRun
Smiling runner wearing an Action for ME vest and race bib number 27615 during the Great North Run, surrounded by other participants. Text overlay reads: “Wishing the best of luck to our Great North Run team today!” with a “Go Team” graphic.
actionforme.bsky.social
📢🏴󠁧󠁢󠁷󠁬󠁳󠁿

If you live in Wales, contact your MSs, asking them to support Adam Price's motion for a severe/very severe ME debate in the Senedd!

Details on how you can help below 👇

tinyurl.com/mxd3w28z

@severemecymru.bsky.social

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis
actionforme.bsky.social
Following @decodemestudy.bsky.social's success, it's vitally important that the Government commits to strategic research funding & we'll continue our calls for a national research platform

Thank you @johnmilnehorsham.bsky.social for leading on this call to the Secretary of State 🙏
johnmilnehorsham.bsky.social
Today I've joined Action for ME in writing to @rthonwesstreeting.bsky.social on the chronic underfunding of ME/CFS research. Despite their prevalence, these conditions are still poorly understood and are without effective treatment.