iiinova — where your digital self keeps evolving

Reposted by Henrik Scheel

𝕊𝕦𝕟𝕕𝕒𝕖 𝔾𝕦𝕣𝕝 @sundaedivine.lol · 21/09/2026

“You didn’t tell me these were the same Persians who beat the Romans!”

Reposted by Henrik Scheel

European ME Alliance @europeanmealliance.bsky.social · 08/08/2026

"Turning a blind eye to #mecfs does not save money. It costs lives and drains public resources. Without early diagnosis and the correct support, ME can spiral into severe, lifelong disability - recovery becomes less likely, and care costs soar" www.europeanmealliance.org/severeMEday....

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Reposted by Henrik Scheel

Canadian Loyalist 🇨🇦 @shakespearesgal.bsky.social · 15/07/2026

Yup … technology is not all it’s cracked up to be … #cdnpoli

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#MEAction Network @meactnet.bsky.social · 26/05/2026

This is Severe ME. Lena is from Sweden and has Severe ME. She has been living in her parent’s home in a dark room since 2022. This photo was taken in 2024. Now she is too ill to take photos. Lena wanted to share and be part of this campaign. #SevereME #MillionsMissing #FrailAndFurious #MECFS

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Henrik Scheel @langemand.bsky.social · 20/05/2026

Earthquake in Denmark today. As always, nothing major (around 4 on the Richter scale), but still the largest I ever have experienced at home.

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Henrik Scheel @langemand.bsky.social · 31/03/2026

So, I seem to recollect that some files were supposed to be released, some time ago. Has anyone looked at them?

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Henrik Scheel @langemand.bsky.social · 31/01/2026

So, I was right, I guess. www.facebook.com/share/r/1Bqg...

facebook.com

Redirecting...

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Reposted by Henrik Scheel

Webanalyst @webanalyst.bsky.social · 24/01/2026

Dems need to go after Blanche who is clearly flouting the law requiring the release of the Epstein files! RELEASE THE FUCKING EPSTEIN FILES! ENOUGH STALLING! Repost if you agree.

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Henrik Scheel @langemand.bsky.social · 17/01/2026

Epstein provided "services" to people of wealth and power, thereby gaining leverage, by knowing their secrets. So, it is reasonable to assume, that ALL people of wealth and power were invited. And that all who visited, are in the files. Maybe this is the reason DOJ still haven't released them?

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Henrik Scheel @langemand.bsky.social · 17/01/2026

Have the files been released yet?

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Henrik Scheel @langemand.bsky.social · 15/01/2026

Have the files been released yet?

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Reposted by Henrik Scheel

jb592353.bsky.social @jb592353.bsky.social · 13/01/2026

Daily Reminder! Repost!

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Henrik Scheel @langemand.bsky.social · 13/01/2026

Have the files been released yet?

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Henrik Scheel @langemand.bsky.social · 12/01/2026

Have the files been released yet?

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Henrik Scheel @langemand.bsky.social · 10/01/2026

Have the files been released yet?

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Henrik Scheel @langemand.bsky.social · 08/01/2026

Have the files been released yet?

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Reposted by Henrik Scheel

Jon Cooper @joncooper-us.bsky.social · 07/01/2026

👇👇👇👇

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Henrik Scheel @langemand.bsky.social · 06/01/2026

Have the Epstein files been fully released yet?

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Didier @medidier.bsky.social · 21/10/2025

This is happening everyday, everywhere. Read the story of Rosie and Alice. Everyone who has been hospitalised with ME, knows it. "Hospitals should be places of healing – but for people with severe ME, they are often sources of harm". #GreatestMEdicalScandal www.thereforme.uk/p/sensory-he...

thereforme.uk

Sensory hell and medical harm

My sister’s experience of very severe ME in the NHS

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Henrik Scheel @langemand.bsky.social · 15/10/2025

While the danish health authorities have stopped diagnosing ME (G93.3A), and offers no effective treatments; Jesper Mehlsen, who privately has diagnosed and treated thousands with ME (incl. myself), is working on a European treatment plan, as well as assisting the US health authorities, about ME.

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Henrik Scheel @langemand.bsky.social · 15/10/2025

Har sundhedsministeren tillid til sundhedsstyrelsens direktør? ME-foreningen sender i dag den 4. bekymringsskrivelse, om sundhedsstyrelsens forældede opfattelse af hvad ME er, og manglende inddragelse af relevante somatiske læger der forsker / behandler ME (DG933A) me-foreningen.dk/me-og-politik/

me-foreningen.dk

test

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#MEAction Network @meactnet.bsky.social · 01/10/2025

We know there is a lot going on in the world right now! This is your reminder to stop and take at least 3 deep breaths. Feel the surface beneath you. Sink into it. Inhale for 4, exhale for 6. Repeat as often as needed. #pwME #pwLC #Spoonie #SelfCare

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Henrik Scheel @langemand.bsky.social · 27/09/2025

It would be nice if the danish politicians interested in health care would view this: More than 10% of the sick in Denmark are offered BPS-based "care" exclusively.

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Reposted by Henrik Scheel

ME/CFS Science @mecfsscience.org · 25/09/2025

1) There's a new review on the impact of ME/CFS. It concludes that "ME/CFS imposes a substantial health, social and economic burden of disease" but argues that its true burden may be even higher because many patients likely remain undiagnosed.

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ME/CFS Science @mecfsscience.org · 23/09/2025

1) 🇳🇴 A new Norwegian study looked at the health and economic impact on caregivers of people with ME/CFS. ME/CFS strengthening traditional gender roles: female caregivers worked less and males more. All caregiver groups experienced increased personal health problems.

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Reposted by Henrik Scheel

ME/CFS Science @mecfsscience.org · 02/09/2025

1) On May 12 2025, a group of researchers signed an International Declaration stating that "there is a moral, medical, economic and scientific imperative to invest robustly in international and collaborative research into the pathophysiology of ME/CFS and Long COVID."

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European ME Alliance @europeanmealliance.bsky.social · 19/08/2025

ME is a too often ignored humanitarian crisis in many European countries Today is #WorldHumanitarianDay – EMEA has called for EU to: -Use proven EU mechanisms -Fund & formalise existing efforts -Treat ME/CFS as a legitimate public health challenge www.europeanmealliance.org/documents/eu... #mecfs

European flags on a blue background for EMEA's call for action from EU

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ThereForME @thereforme.bsky.social · 30/06/2025

Thank you @tessamunt.bsky.social! 💪 👏👏👏👏

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Reposted by Henrik Scheel

Maggie Boxey Writes @maggieboxey.bsky.social · 27/06/2025

We’re up to 45k views!!! My big crazy dream is to have as many views as there are people living with MEcfs (FIVE to NINE MILLION!!!). Watch, comment & like on YouTube and share on social:https://youtu.be/JzKfi8LOMQU?si=1kP-zGDMtxsXIW8W @meactnet.bsky.social @solveme.bsky.social #momsky #mecfs

youtu.be

I Am One of the Millions Missing | Maggie Boxey | TEDxOjai

YouTube video by TEDx Talks

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Reposted by Henrik Scheel

#MEAction Network @meactnet.bsky.social · 21/05/2025

Check out this essay by Violet Affleck - "A Chronically Ill Earth: COVID Organizing as a Model Climate Response in Los Angeles." Impressed with the understanding of ME. yaleglobalhealthreview.com/2025/05/18/a... #PwME #MECFS #MyalgicEncephalomyelitis #LongCovid #PublicHealth

All text graphic with cream background and black writing. Text: “A Chronically Ill Earth: COVID Organizing as a Model Climate Response in Los Angeles” by Violet Affleck The hallmark symptom of ME is post-exertional malaise, or PEM, a kind of bodily overdraft fee that hits when people with ME expend energy beyond the slim “energy envelope” available to them. Minutes or hours after exertion, the body finds itself starved for energy, leading to a “crash” characterized by feelings of whole-body “poisoning,” “constant bouncing,” or even “suffocation.” The foundational nature of the illness – what bodily systems don’t rely on energy? – limit the possibilities of escape even into one’s own mind...The best way to avoid PEM is “pacing,” or carefully meting out one’s limited supply of energy in hopes that the body can put whatever remains toward improvement.

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ME/CFS Science @mecfsscience.org · 15/05/2025

1) This is an interesting economic report that will likely be very useful for advocacy. It estimates the costs of Long Covid and ME/CFS in Germany to be €63.1 billion (1.5% of GDP) in 2024.

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ThereForME @thereforme.bsky.social · 12/05/2025

On #WorldMEDay the UK ME community faces a twofold threat: the loss of critical welfare benefits, and a lack of meaningful treatments to pave their way back to work. This must change. We’re asking the government to back the new ME Delivery Plan with the resources it deserves.

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European ME Alliance @europeanmealliance.bsky.social · 11/05/2025

It is 𝗜𝗻𝘁𝗲𝗿𝗻𝗮𝘁𝗶𝗼𝗻𝗮𝗹 𝗠𝗘 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗗𝗮𝘆 𝗗𝗼 𝗻𝗼𝘁 𝗱𝗶𝘀𝗺𝗶𝘀𝘀 𝗺𝘆𝗮𝗹𝗴𝗶𝗰 𝗲𝗻𝗰𝗲𝗽𝗵𝗮𝗹𝗼𝗺𝘆𝗲𝗹𝗶𝘁𝗶𝘀 (𝗠𝗘) The science does not! Listen to the voices of patients Share the video #mecfs #InternationalMEawarenessDay #MedEd #MEAwareness #EndME youtube.com/shorts/16vBt...

youtube.com

European International ME Awareness 2025 Video 1

YouTube video by European ME Alliance

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#MEAction Network @meactnet.bsky.social · 09/05/2025

Most of our community are not well enough to protest on the street but we are making our voices heard from our beds about why cuts to ME/CFS research funding is so devastating to our community. Wilhelmina Jenkins is one of the #MillionsMissing showing up from home! youtube.com/shorts/ypEHp...

youtube.com

Wilhelmina shares why she joins with the #MillionsMissing this May 12th. #DisabilitySOS #pwME

YouTube video by The ME Action Network

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JD Random - RandomWhiteGuy @thereelrandom.bsky.social · 22/04/2025

Folks need to read this… we’ve forgotten Upton Sinclair and The Jungle.

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ME/CFS Science @mecfsscience.org · 19/04/2025

This looks like an interesting and much needed project. In Neunkirchen-Seelscheid in Germany, a housing project is being planned especially for severely ME/CFS sufferers with 24-hour assistance. sozialhummel.de/wohn...

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Tom Kindlon @tomkindlon.bsky.social · 08/03/2025

Remembering ME activist (& my friend) Robert "Bob" Courtney, who passed away on March 7, 2018. This is from the @meassociation.bsky.social magazine. One can read about some of the specifics of Bob's work here: me-pedia.org/wiki/Robert_... #MyalgicEncephalomyelitis #MEcfs #CFS #MyalgicE #PwME

Screenshot of ME Association article/obituary on Robert Courtney

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Henrik Scheel @langemand.bsky.social · 18/02/2025

Den røde bark på den tibetanske kirsebær pynter godt i vintersolen.

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Hilda Bastian @hildabast.bsky.social · 24/01/2025

I never thought a day would come when I would write a post this critical about the Cochrane Collaboration. But today was that day: absolutelymaybe.plos.org/2025/01/24/w... #mecfs

absolutelymaybe.plos.org

When Journal, Scientific Society, and Community Values Clash - Absolutely Maybe

A process I’ve been involved with at a journal recently exploded. It was meant to resolve a controversy about a publication, not…

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Henrik Scheel @langemand.bsky.social · 24/01/2025

Disturbing that Cochrane, the organization supposed to be a solid pillar of medical science, is re-dating an outdated low-quality and harmfull study, as if it was the latest knowledge! chng.it/GTfxRrrsFR

chng.it

Can you spare a minute to help this campaign?

Cochrane: Withdraw the harmful 2019/2024 Exercise therapy for CFS review

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Restless Sands @restlesssands.bsky.social · 22/01/2025

“Very Severe ME patient Line aged 26 from Denmark (@nebulow on IG) has appealed to the international ME and Long Covid community to help prevent her being involuntarily removed to a psychiatric hospital from the nursing home she has been living in for the past 10 months.”

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