Lisa_Cat (@AertbyLisa) header
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Artist and Designer - Sometimes a mess, mostly a work of art. #MEcfs #MEawarenesshour M.E. since "79

Belfast, planet Earth, mostly.
Joined July 2009
Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)Photo by Lisa_Cat (@AertbyLisa)
Many Thanks to @TheCanaryUK for publishing my piece and to @TheChronicColab for the media training that made it possible. #MedX #MECFS #MyalgicE #PwME #CFS #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
Grieving for loss of life: the untold #MEcfs - from silent, darkened rooms. As part of the Canary and @TheChronicColab Amplify media training programme, @AertbyLisa wrote this moving piece on living with ME & the side the media isn't showing. Please read: thecanary.co/opinion/2024/08…
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This from Beth Dobbin 👇 is why #ME patients avoid A&E, ringing the Dr, doing testimonial videos to raise awareness, talking to HCPs. We often can’t talk to our families or friends, our carers or helpers. Often a case of choosing between talking or eating. This is the reality 🤐
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Lisa_Cat retweeted
Replying to @BBCNews
youtu.be/RiwX9Y0NbiQ?si=oA3q… As a psychiatrist I would like to recommend that all my colleagues in medicine, nursing and allied health watch thus. I’m with @GeorgeMonbiot - this is the greatest scandal in modern medical history.
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"There is nothing out there. There is nowhere to go. You go to the GP and there's nowhere for them to send you to. It's really at the back of the queue as far as research, knowledge, expertise, funding." Thank you for talking so honestly about #ME Beth. I’m so sorry 🫂
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This is an extremely depressing, distressing, and very very important paper
Why do people with ME claim to know more about the medical aspects of their disease than their doctors? Bc the mechanisms that ensure doctors' knowledge fail in the case of ME, and sick people have created mechanisms of knowledge production and dissemination to pick up the slack
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Wow, this interview I did last week with Guardian columnist and social critic George Monbiot on the hpoor treatment of people with ME/CFS now has 23,000+ views! Here it is again: youtube.com/watch?v=MaaeQ7cr…
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Lisa_Cat retweeted
The ME (myalgic encephalomyelitis) deniers who’ve had to do rear guard action for 30 years as the science has evolved to discredit them won’t admit they are wrong precisely because of the damage they have done. That’s how human cliques work. The more damage, the harder to admit.
“The harm you have done is incalculable. It’s not me who has been spreading great harm around the world. It’s you, mate.” George Monbiot on being accused by Prof Michael Sharpe of “spreading” #LongCovid by writing about it and why he started writing about the #MECFS scandal.
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Newly knighted ME advocate Anil van der Zee (@AnilvanderZee) discusses his royal honor with David Tuller: thesicktimes.org/2026/10/02/…
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🌻 Share Like RT posts during #MEAwarenessHour in 12 hours time🌻 20:00 BST 21:00 Europe CEST Talking all things #MyalgicEncephalomyelitis Poster Credit: @AertbyLisa 🙏
If your doctor is pushing you to do graded exercise/any exercise treatment where you're told to ignore your #PEM, your clinician doesn't understand/care about the science & is giving you extremely dangerous advice that could cause permanent disability! This isn't hyperbole #pwME
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Lisa_Cat retweeted
“The harm you have done is incalculable. It’s not me who has been spreading great harm around the world. It’s you, mate.” George Monbiot on being accused by Prof Michael Sharpe of “spreading” #LongCovid by writing about it and why he started writing about the #MECFS scandal.
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May I remind new followers that there's now approximately three years' worth of tweets in this account. Many of the tweets feature rarely seen or forgotten bits of 'M.E.' history for you to study so do go through the archive if you have the time.
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This interview with George Monbiot about the plight of people with ME/CFS has had almost 5,000 views since I posted it yesterday...youtube.com/watch?v=MaaeQ7cr…
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"Abandoned, dismissed and gaslighted" #MEAwarenessHour Thanks to Adam you can hear the interview here, see below, with LBC's Natasha Devon talking with George Monbiot during her broadcast on Saturday evening. His article is linked as well...
Symptoms are “horrible” and severe cases are a “living nightmare.” George Monbiot speaks to Natasha Devon on LBC about ME/CFS, it’s long history of being dismissed and psychologised, and the role of governments and insurers.
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I wish I was free of M.E. and could walk for miles again in sunshine, mist or rain. #MEAWARENESSHOUR tonight at 8pm. All Welcome. #Justice4ME #MyalgicEncephalomyelitis #FreeMe
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Again enormous thanks to Adam for recording this for us all. And of course to George Monbiot for, once again, giving voice to the plight of all #ME sufferers. It’s two fold, being so ill and not being believed. Grim beyond belief.
Symptoms are “horrible” and severe cases are a “living nightmare.” George Monbiot speaks to Natasha Devon on LBC about ME/CFS, it’s long history of being dismissed and psychologised, and the role of governments and insurers.
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Thank you George Monbiot speaking with Natasha Devon at @LBC 26.9.26 Full interview (9 mins): youtu.be/H2rRf_f2hJs 2025 Final Delivery Plan on ME included public awareness raising, no Government actions seen yet @DHSCgovuk #MyalgicEncephalomyelitis #MEcfs
If you listen to this, & don't have M.E. you might think George Monbiot is exaggerating. Surely it can't be that bad? It is though. I lost everything - work, social life, husband, home & friends & have been housebound for 10 years, ill for 25 years with no medical help #pwME
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Excellent news. The coverage on the ME scandal is continuing! George Monbiot will be on Natasha Devon's LBC show this Saturday 6-9pm 📻 #pwME
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Replying to @BBCNewsnight
@BBCNewsnight Would it be possible for you to open up an #ME discussion based on this article. Many of us have been totally abandoned, often abused and belittled for decades. Friends have died or have taken their own lives as it’s unbearable.400,000 of us would be very grateful.
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Lisa_Cat retweeted
As many of you already know, George Monbiot has published another hard-hitting article on ME in the Guardian today. Great to see such coverage, especially as the Guardian published some rubbish by others before theguardian.com/commentisfre… #MEcfs #PwME
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George’s latest post. What an absolute treasure he is for all #pwME A highly respected journalist, he has supported us for years now and there is surely no better person to make our case so fearlessly and compassionately. I hope others follow his lead theguardian.com/commentisfre…
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