picophage.bsky.social
@picophage.bsky.social
Reposted
The NHS asked for support.
The public asked for transparency.
Nobody asked for PFI.

Yesterday's budget brought it back anyway.

So who did ask? 🧵

Read full investigation👉 everydoctor.org.uk/talking-poin...
November 28, 2025 at 8:02 AM
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Wow! The response to our Crowdfunder has been incredible 💙

Let’s keep the energy going — we need your help to fund our next round of NHS research before the autumn budget!

👉 If you can, please donate, share + tag 5 friends who care about the NHS: bit.ly/NHSandBudget
November 3, 2025 at 5:15 PM
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@cpeclse.bsky.social finds every tested AI model skews against women’s health - yet councils hide which models they use or how. If we don’t know the models, we can’t see the bias - and if we can’t see it, we can’t fix it. Bias must be found and corrected before AI shapes public services.
August 15, 2025 at 10:53 AM
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🔍Is there an issue where you think Parliament is not using reliable evidence to make #policy decisions
#EvidenceWeek is your chance to ask MPs

🗳️📢Vote for the policy issues that matter to you with our simple form

senseaboutscience.org/evidence-wee...

#EvidenceBasedPolicy #PolicyMaking
Ask Parliament
Ask Parliament Voters care about the evidence behind policy decisions. That’s why Evidence Week in Parliament opens with a Reverse Select Committee, where on Monday 3rd November 2025, the public will ...
senseaboutscience.org
June 26, 2025 at 12:14 PM
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From Brent's mom:

Brent worked with OMF. He is now severely ill and house-bound. He can’t read or write. He can barely communicate but wanted to share this message with other patients.
August 8, 2025 at 5:12 PM
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"Today we honor the sickest among us. The ones who have been least lucky among some of the least lucky people on earth..."

A Moment of Silence for Severe ME/CFS Patients by @DafoeWhitney: ow.ly/QrCt50WBCZZ

#MEmomentOfSilence #UnitedForME
A Moment of Silence for Severe ME/CFS Patients
To all those living in silence and darkness. Today we take a moment in silence and darkness to honor your courage, your bravery, your resilience, your strength, and we acknowledge your profound suffe...
ow.ly
August 8, 2025 at 2:18 PM
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On Aug. 8, we mark #SevereMEDay & raise awareness by elevating the experiences of those impacted. We also share free educational resources to help people understand the impact of #SevereME.

Learn more here:
ow.ly/KBjQ50WCcMh

#UnitedForME #LearnFromME
August 8, 2025 at 6:05 PM
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This #SevereME Awareness Month, we’re recognizing those living with the most severe and isolating form of #MECFS.

BHC + Solve M.E. co-hosted a 4-part series:
▶️ Caregiving
▶️ Legal Planning
▶️ Medical Panel
▶️ Removing Barriers

Watch Part 1: bit.ly/4o1gdUK
#UnitedForME @solveme.bsky.social
August 5, 2025 at 6:32 PM
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In honor of #SevereMEday, @meactnet.bsky.social @batemanhornecenter.bsky.social @solveme.bsky.social @openmedf.bsky.social would like to announce a new hashtag that we will be using to help amplify the voices of those with ME & educate about ME. We invite you to join us in using #UnitedForME!
August 7, 2025 at 1:21 PM
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What if your body couldn’t bear light, sound, movement — or even touch? Today, #SevereMEDay, we ask you to imagine living that way not just for a day… but for years. For people living with Very Severe ME, this isn’t a metaphor — it’s reality. 🧵
August 8, 2025 at 3:55 PM
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Today is #SevereMEDay - a day we come together to especially take time to honor the 25 percent living with the most severe form of this disease and remember those who have died from ME.

Myalgic encephalomyelitis is a complex chronic disease that presents with symptoms in multiple body systems.
August 8, 2025 at 2:55 PM
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Today is #SevereMEDay - a day to recognise and honour the people living with the most devastating forms of Myalgic Encephalomyelitis (ME).

We are deeply grateful to those with Severe ME who took part in the DecodeME study. Your contribution is vital.
August 8, 2025 at 11:18 AM
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In honor of #SevereMEday, #MEAction is honored to share the Severe ME Artists Project 2025! www.meartistsproject.com/severe-me-ar...

Over 100 of you submitted photos, drawings, writing, music and videos of your work for our 5th Severe ME Artists Project!

#SevereME #UnitedForME #pwME
August 8, 2025 at 4:01 PM
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Did you know PFI was first proposed in 1993 by a Tory frontbencher—in a pamphlet funded by private health insurer BUPA?

It didn’t take off then though... 👀

Find out more in Adam’s blog 👇

🔗https://everydoctor.org.uk/talking-points/pfi-the-buy-now-pay-triple-later-plan-returns-to-the-nhs/
July 31, 2025 at 7:42 AM
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🕵️‍♀️ EveryDoctor is digging into the backgrounds, financial ties, and public views of the people running NHS England + the Department of Health.

We want to know – do they reflect the values of the public?

We’ll be sharing our findings soon 👀
August 1, 2025 at 11:34 AM
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A reminder for Starmer: bold promises need honest answers.

Labour’s 10-Year Plan is full of ambition — but silent on funding.

We're demanding transparency 📢 Add your name to our open letter:

everydoctor.eaction.org.uk/show-us-the-...
August 2, 2025 at 9:48 AM
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BREAKING NEWS: #MEAction has just received a $25,000 fundraising match opportunity! Every donation will be doubled! www.meaction.net/donate

#MEAction is working hard to support and fight for this community on multiple fronts, but we CANNOT do this work without your financial support.

#pwME
June 25, 2025 at 7:23 PM
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Why has Bridget Phillipson taken a donation from a lobbying firm linked to private healthcare?🚨

EveryDoctor is very concerned about NHS privatisation, and we are investigating the links between MPs and the private healthcare sector.

Bridget Phillipson accepted a donation last year of £2,950 ...
June 18, 2025 at 1:23 PM