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PZ

@itsmepz.bsky.social
578 followers 323 following 399 posts

Music 🎶 Film 🎞️ Hot Chips 🍟 Happiest by the sea 🌊 Forever exhausted #pwME Living small with ME on unceded Whadjuk Noongar country ("Perth, Australia")

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PZ @itsmepz.bsky.social · 25/09/2026
From The Australian: "600,000 patients risk losing care over $220k grant". A bit on the current state of things for #pwME in Australia. #MyalgicEncephalomyelitis #MEcfs #GreatestMEdicalScandal
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PZ @itsmepz.bsky.social · 19/01/2026
It is as simple as that. There is no grey area or nuance needed. #GreatestMEdicalScandal #pwME #MyalgicEncephalomyelitis
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PZ @itsmepz.bsky.social · 19/01/2026
I have no grace for the author of that book. People are always happy for #pwME to be thrown under the bus and treating our harm as collateral damage. If you can't tell the raw factual story about #MyalgicEncephalomyelitis then you are burying the truth and hurting us. ##GreatestMEdicalScandal
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PZ @itsmepz.bsky.social · 21/12/2025
There's some "disruption" over on twitter about this. My take: 1. I understand why people resort to these protocols 2. I don't doubt some #pwME have responded well. I also know #pwME have had significant setbacks... #MyalgicEncephalomyelitis #MillionsMissing #GreatestMEdicalScandal
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PZ @itsmepz.bsky.social · 15/12/2025
Who wants to tell @slate.com #PACETrial #MyalgicEncephalomyelitis #MEcfs #pwME #MillionsMissing #GreatestMEdicalScandal
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PZ @itsmepz.bsky.social · 14/11/2025
I'm happy to see Emerge Australia work on improving access to care for Aboriginal & Torres Strait Islander #pwME There are surveys at this link and contact details for ATSI & CaLD community orgs. Please share! #MyalgicEncephalomyelitis #MEcfs #MillionsMissing emerge.org.au/news/strengt...
emerge.org.au
Strengthening culturally inclusive care for people with ME/CFS and long COVID   – Emerge Australia
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PZ @itsmepz.bsky.social · 13/11/2025
I appreciated this 😅 #pwME #MyalgicEncephalomyelitis #MillionsMissing
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emily fraser 🌿🐌✨ @emilyesfraser.bsky.social · 31/10/2025
People w/ severe ME are well practiced in the discipline of surviving for the sake of survival, of caring for bodies that may never “get better.” In a world of climate collapse & ecocide where *most* ecosystems are becoming sick & disabled, it’s a discipline we should all be practicing.
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The Real McCoy @rippermd41.bsky.social · 30/10/2025
This is the full quote. @medscape.com doesn’t mention ME/CFS once in the article. How this should read instead: Post-exertional malaise (PEM) is the hallmark of #MECFS, a condition found to affect at least 50% of those with #LongCovid. Why this matters🧵
Screenshot from article in quote post reads: According to Laura Malone, MD, PhD, the doctor who treated Lucas for long COVID, the most common symptoms pediatricians should watch for are profound fatigue and post-exertional malaise, also known as post-exertional symptom exacerbation. This is a debilitating and hallmark symptom of long COVID, where even minor physical or mental effort results in a severe crash, often delayed by hours or days, that can leave a patient bedridden.
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Yann (ME/LC) @me-cfs.bsky.social · 29/10/2025
Obvious cases of ME/CFS being labelled only as as Post-COVID is not only erasure, but also harmful. The people affected miss out on some crucial PEM and severity specific info. (Obviously, ME/CFS is rarely managed optimally by the medical system, but neither is long COVID!)
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PZ @itsmepz.bsky.social · 29/10/2025
Pediatricians should be acquainting themselves with #MEcfs, dysautonomia/POTS, and MCAS - some of the most common outcomes in Long Covid. PEM (and PENE) were coined for MEcfs/ME - an illness that extends back centuries under various names and iterations. (And a reminder that...
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Richard Vallée @richardvallee.bsky.social · 29/10/2025
Those are actually the hallmark features of ME/CFS. Medicine has completely botched everything dealing with ME/CFS for decades, has refused thousands of opportunities to do better about it. And yet again it has been botched so completely that the past doesn't even exist, erased from existence.
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PZ @itsmepz.bsky.social · 21/10/2025
I am so grateful for the honesty and vulnerability of #pwME who share their personal stories. It gives others the courage to speak and reminds us that we are not alone in this reduced and often painful experience of life. #MyalgicEncephalomyelitis #MillionsMissing
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PZ @itsmepz.bsky.social · 21/10/2025
When will people learn that a company won't love you?
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Isocomet @isocomet.bsky.social · 19/10/2025
People with ME/CFS are the antithesis of quitters. To keep showing up and choosing life and trying to find ways to be more alive in the face of immense physical and societal challenges is courageous, disciplined, and heroic.
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PZ @itsmepz.bsky.social · 19/10/2025
The school curriculum should include the teaching of *Genocide* under which the Holocaust is one event amongst other examples all across the world including Australia, America, Africa, Bosnia, Burma, India and so on and on and on and on...
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Béa Gonzalez @sophiacycles.bsky.social · 18/10/2025
This, then, is the human problem: there is a price to be paid for every increase in consciousness. We cannot be more sensitive to pleasure without being more sensitive to pain.~Alan Watts, 𝘛𝘩𝘦 𝘞𝘪𝘴𝘥𝘰𝘮 𝘰𝘧 𝘐𝘯𝘴𝘦𝘤𝘶𝘳𝘪𝘵𝘺
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PZ @itsmepz.bsky.social · 15/10/2025
How can we get people to become conscious of the fact that there is a disease that they don't know exists that will absolutely destroy your life, help is nonexistent and you'll be screaming into an abyss for the rest of your torturous life if it takes you down by a roll of the dice. #MEcfs
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PZ @itsmepz.bsky.social · 19/10/2025
- A school day should be 5 hours max and not start before 10am. - Essential food items (bread, milk, eggs, vegetables) and medicines should be govt subsidised. - All household appliances/electronics should be built to last 10 years min. If they fail within 10 yrs you get a free replacement.
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Scott Santens @scottsantens.com · 17/10/2025
It shouldn't be niche, but the moment private property was invented and land became owned by individuals and corporations, universal basic income became a human right, and every day since it has been unethical to not implement UBI.
scottsantens.com
The Spaceballs Argument for Unconditional Basic Income (UBI)
There is an argument frequently made against the concept of unconditional basic income (UBI) that essentially goes like this: "Life requires work. You can't just expect to live without work, and it's ...
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PZ @itsmepz.bsky.social · 18/10/2025
Remembering that Suzy Weiss wrote an awful piece "Hurts so good" about invisible chronic illnesses and " online spoonie-ism". Fucking awful person.
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Lauren Merry Vale (they/she) @pixielauren.bsky.social · 17/10/2025
3. There is NO ethical use of the planet-destroying, disinformation-spreading, fascist-enabling, billionaire-enriching plagiarism machine.
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PZ @itsmepz.bsky.social · 15/10/2025
How can we get people to become conscious of the fact that there is a disease that they don't know exists that will absolutely destroy your life, help is nonexistent and you'll be screaming into an abyss for the rest of your torturous life if it takes you down by a roll of the dice. #MEcfs
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Kate Violette @kateviolette.com · 08/10/2025
The truth of the matter is: anyone you know living with ME/CFS is one of the bravest mofos you know Abusive assholes don't have the strength of character and heart to be able to endure an illness like this; they'd crumble within their first week of having it.
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The Real McCoy @rippermd41.bsky.social · 04/10/2025
Honestly sometimes I get why people have a hard time believing people with #MECFS. The mechanics are so ridiculous. “What do you mean the vibrations from a car ride can crash you?!?”
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heather @heatherfeather.bsky.social · 30/09/2025
if you really knew what moderate--severe--very-severe ME/CFS was like, you would be screaming on our behalf. you would not stop screaming. there are no social supports and no medical treatments. the situation is so much more dire than you can possibly imagine
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PZ @itsmepz.bsky.social · 29/09/2025
A couple of years ago I was in touch with a journalist and I tried to pitch to her the story of Alem Matthees, the work he had contributed to uncovering the PACE trial fraud and how he had become more devastatingly ill in the process. I also said we needed someone asking the hard questions to...
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emily fraser 🌿🐌✨ @emilyesfraser.bsky.social · 27/09/2025
People with mild ME/Long Covid & people who have recovered, please start advocating for the most severe instead of mildwashing the disease & using your story to sell your personal projects while feeding the media narrative of “individual overcoming” 🙏
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Didier @medidier.bsky.social · 29/09/2025
Would there be actually any time at all deemed "right" to finally look at us? For media and medicine to say MYALGIC ENCEPHALOMYELITIS without bias, shame or minimisation? #pwME #GreatestMEdicalScandal
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PZ @itsmepz.bsky.social · 29/09/2025
It's 2025, 6 years into a pandemic that has caused an epidemic of new cases of #MECFS. There have never been so many advocacy orgs and quality resources available to inform on MECFS. And still, media pieces that mention #MyalgicEncephalomyelitis are misinformed and incorrect. #pwME
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PZ @itsmepz.bsky.social · 28/09/2025
I had taken a break from posting, and that Guardian article is a really good example of why. I can't handle that the main avenue to connect with other pwME & researchers, and keep up to date on current affairs is via this little anger box in my hand. Out of patience. 0 tolerance for ME misinfo.
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PZ @itsmepz.bsky.social · 28/09/2025
Very unfortunate that this article shares misinformation on ME/CFS. Additionally, "ME/CFS is a diagnosable sequela that develops at an increased rate following SARS-CoV-2 infection". link.springer.com/article/10.1... #pwME #MillionsMissing #LongCovid #MyalgicEncephalomyelitis
link.springer.com
Incidence and Prevalence of Post-COVID-19 Myalgic Encephalomyelitis: A Report from the Observational RECOVER-Adult Study - Journal of General Internal Medicine
Background Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) may occur after infection. How often people develop ME/CFS after SARS-CoV-2 infection is unknown. Objective To determine the incidence and prevalence of post-COVID-19 ME/CFS among adults enrolled in the Researching COVID to Enhance Recovery (RECOVER-Adult) study. Design, Setting, and Participants RECOVER-Adult is a longitudinal observational cohort study conducted across the U.S. We included participants who had a study visit at least 6 months after infection and had no pre-existing ME/CFS, grouped as (1) acute infected, enrolled within 30 days of infection or enrolled as uninfected who became infected (n=4515); (2) post-acute infected, enrolled greater than 30 days after infection (n=7270); and (3) uninfected (1439). Measurements Incidence rate and prevalence of post-COVID-19 ME/CFS based on the 2015 Institute of Medicine ME/CFS clinical diagnostic criteria. Results The incidence rate of ME/CFS in participants followed from time of SARS-CoV-2 infection was 2.66 (95% CI 2.63–2.70) per 100 person-years while the rate in matched uninfected participants was 0.93 (95% CI 0.91–10.95) per 100 person-years: a hazard ratio of 4.93 (95% CI 3.62–6.71). The proportion of all RECOVER-Adult participants that met criteria for ME/CFS following SARS-CoV-2 infection was 4.5% (531 of 11,785) compared to 0.6% (9 of 1439) in uninfected participants. Post-exertional malaise was the most common ME/CFS symptom in infected participants (24.0%, 2830 of 11,785). Most participants with post-COVID-19 ME/CFS also met RECOVER criteria for long COVID (88.7%, 471 of 531). Limitations The ME/CFS clinical diagnostic criteria uses self-reported symptoms. Symptoms can wax and wane. Conclusion ME/CFS is a diagnosable sequela that develops at an increased rate following SARS-CoV-2 infection. RECOVER provides an unprecedented opportunity to study post-COVID-19 ME/CFS.
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Lia Pas @liapas.bsky.social · 09/09/2025
#SciArtSeptember Day 9: vanishing • The term #MillionsMissing is used for #MECFS advocacy since most people with the disease—like myself—rarely have energy to leave their homes. My #Sciart #embroidery body map (2016) illustrates the invisible symptoms I experienced at the onset of ME/CFS.
Body Map (2016). An outline of a naked woman is embroidered on linen in the same bone white colour as the linen. She stands legs together, her right hand covering her groin, her left hand, palm up, extended slightly to her side. She looks to the right. Her entire body except for her belly is covered in intricate markings representing different neurological sensations. Her face is a mask of green lines, feathery grey lines cover her shoulders and chest. There is a thick band of intricate burgundy stitching around her waist. Her forearms and hands are covered in thick blue undulant lines. Her right leg has bands of burgundy along the muscles, with small dots around them. Her inner left leg has a thick line of blue running up it, with thin branches spreading towards her outer leg.
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PZ @itsmepz.bsky.social · 28/08/2025
Great thread. Some researchers and clinicians are *using* us - using the language, protocols, and our shared knowledge, without acknowledging #pwME or their peers that preceded them.
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Davey @historicaloracle.bsky.social · 26/08/2025
It's really fucked up the news media at large is searching so hard for humanity in machines, while systematically denying humanity to Palestinians, trans people, immigrants, and other persecuted people
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PZ @itsmepz.bsky.social · 26/08/2025
If you are joining the March for Australia on 31 August, you are walking with Nazis.
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PZ @itsmepz.bsky.social · 21/12/2024
Bateman Horne also have a great series on PEM, including information on studies showing the physiological process at work demonstrating how pwME respond to activity youtube.com/playlist?lis...
youtube.com
Post-Exertional Malaise Video Series - YouTube
Post-exertional malaise (PEM)/post-exertional symptom exacerbation (PESE) is an altered physiological state and pathognomonic finding unique to ME/CFS that i...
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emily fraser 🌿🐌✨ @emilyesfraser.bsky.social · 16/08/2025
It’s unspeakably demoralizing to lose your agency to a disease & then to have your voice/experience/energetic sacrifices devalued too. I’m so grateful to everyone who has fought so hard over the years & I also understand why people stop trying & go silent
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Fran H @franhaddock.bsky.social · 08/08/2025
Community video for Severe ME awareness day, please share and tag politicians and public figures who need to see this! All participants IG handles tagged at the end 💙💙 #SevereME #SevereMEAwarenessDay #MECFS #MillionsMissing #UnitedForME
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sarah boothby @swastrosarah.bsky.social · 31/07/2025
Isla's mother has been arrested under suspicion of causing her death from ME last year (heart failure). There was no inquest. Isla's younger sister (15), who also has ME, has been removed from the only people who understand how the disease must be managed. Imagine her fear. #MEKills #HumanRights
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PZ @itsmepz.bsky.social · 15/04/2025
⏰️⏰️⏰️ #pwME This survey closes in a couple of weeks!!!! Your input into the new 🇦🇺 guidelines is needed! It's open to everyone. #MillionsMissing #MyalgicEncephalomyelitis #MECFS #GreatestMEdicalScandal
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Niko Suvisto @nikosuvisto.com · 11/04/2025
Today it’s time to launch a big project I’ve had the privilege of working on: A Quiet Storm—an online art gallery showcasing the artwork of people living with severe ME/CFS. 1/7 www.aquietstorm.me #MECFS #pwME #OnlineArtGallery #AQuietStorm
aquietstorm.me
a quiet storm - an online gallery
An online art gallery showcasing the artwork of people living with severe ME/CFS
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PZ @itsmepz.bsky.social · 30/03/2025
Trying to stay connected to others - including other #pwME - to avoid falling further down a black hole of isolation... yet having nothing to say and no energy to say it anyway.
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PZ @itsmepz.bsky.social · 23/02/2025
⚠️Attention #pwME Scoping survey for Australian Clinical Practice Guidelines for ME/CFS consultations.nhmrc.gov.au/clinical-pra... Open to everyone so I encourage #pwME & carers outside 🇦🇺 to provide input if they are able! #MyalgicEncephalomyelitis #MECFS **Please repost**
consultations.nhmrc.gov.au
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PZ @itsmepz.bsky.social · 24/03/2025
I usually do quite well managing my emotions and grief, but today I've just been completely overcome by loss. I hate ME. It takes everything. (I'll probably delete this, I just needed to get it out).
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PZ @itsmepz.bsky.social · 26/02/2025
@nosuchthingshow.bsky.social Good pod on "Why are slurs making a comeback?" I feel it was a missed opportunity to not speak to the people currently on the receiving end of these slurs - like disabled people. Would definitely have brought a different perspective to the idea that...
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PZ @itsmepz.bsky.social · 23/02/2025
⚠️Attention #pwME Scoping survey for Australian Clinical Practice Guidelines for ME/CFS consultations.nhmrc.gov.au/clinical-pra... Open to everyone so I encourage #pwME & carers outside 🇦🇺 to provide input if they are able! #MyalgicEncephalomyelitis #MECFS **Please repost**
consultations.nhmrc.gov.au
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