Illustrator Interrupted
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franceyme.bsky.social
Illustrator Interrupted
@franceyme.bsky.social
https://amandafrancey.com/ Australian illustrator, graphic designer, photographer. Advocating for myalgic encephalomyelitis #MECFS #LongCovid #ClimateAction
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ME is not “chronic fatigue.”

It’s a devastating neuroimmune disease that destroys lives, and far too many people are still being dismissed, neglected, and left without hope or proper care.

I wrote this after another tragic loss in the ME community. 💔

amandafrancey.medium.com/the-me-you-d...
The ME You Don’t See
I was motivated to create the below graphic after hearing the heartbreaking news that another beautiful person from the ME community passed…
amandafrancey.medium.com
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'Recovery' was always a big problem for the PACE trial, to the extent that they didn't actually mention it at all in the main trial paper in 2011.

Discussion of it was relegated to a later paper in 2013, which also contained a metric tonne of fudge, because they knew they were in trouble over it.
The #PACEtrial recovery song by the late Graham McPhee uploaded to Youtube around 2014, which along with his more serious videos on the same channel, was used to argue that he was part of an organised campaign of harassment when he submitted a FOIA request for the fitness data from the PACE trial.
6: ME Recovery Song
YouTube video by MEAnalysis
www.youtube.com
October 7, 2026 at 9:49 AM
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Artist: oblyvian on Tumblr
October 7, 2026 at 6:33 PM
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October 5, 2026 at 7:30 PM
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People with #ME/CFS have been misunderstood for decades: reputable researcher offers surprising advice to those struggling with the illness

Myalgic Encephalomyelitis aka ME/CFS has often been overlooked by doctors and researchers. Geneticist Chris Ponting has revolutionised our understanding
People with chronic fatigue have been misunderstood for decades: reputable researcher offers surprising advice to those struggling with the illness
Chronic fatigue syndrome has often been overlooked by doctors and researchers. Geneticist Chris Ponting has revolutionised our understanding of the disease – and he has a remarkable message for those ...
scienceillustrated.com
October 4, 2026 at 6:53 PM
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This interview with @georgemonbiot.bsky.social has had almost 5,000 views since I posted it yesterday: www.youtube.com/watch?v=Maae...
Interview with George Monbiot about Guardian column on ME/CFS
YouTube video by David M Tuller
www.youtube.com
October 2, 2026 at 6:09 PM
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ME/CFS Care Crisis: @georgemonbiot.bsky.social examines patients’ reports of abandonment, inappropriate treatment and outdated approaches despite updated guidance. www.theguardian.com/commentisfre...
Abandoned, dismissed and gaslighted: there is no excuse for the way ME sufferers have been betrayed | George Monbiot
Changes in guidance and science seem to have little impact on millions of devastated lives. It’s a social crisis playing out behind closed doors, says Guardian columnist George Monbiot
www.theguardian.com
September 24, 2026 at 8:15 PM
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A blog about the response of many denialist dismissive cognitive dissonance comments on social media whenever they are confronted with very severe ME in the media.

anilvanderzee.com/the-rush-to-...

#pwme #myalgicE #millionsmissing
The rush to dismiss severe ME or Long Covid in the media may harm you or your loved ones in the future. - Anil van der Zee
The last couple of weeks my social media has had a lot more traffic. Partly due to my own story in the media, but also because other people with (very) severe ME or infectious associated chronic illne...
anilvanderzee.com
September 20, 2026 at 4:06 PM
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This is accurate science
September 20, 2026 at 6:01 PM
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May I remind everyone that there is currently NO cure for rabies.

May I also remind everyone there is absolutely NO scientific proof connecting ANY vaccine that we produce today with autism.

This is true regarding vaccination in both humans AND in dogs.

Vaccinate your pets please.
September 14, 2026 at 4:00 PM
I just lost one of my wireless earbuds, and as I was searching for it, I could smell a burning chemical smell coming from the microwave that was heating my wheat bag 🤦🏻‍♀️
August 31, 2026 at 10:02 PM
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August 26, 2026 at 8:46 PM
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Sick Times: “Hope to outlast the storm”: How severe ME impacts two brothers ** Trigger Warning: Upsetting Content **

thesicktimes.org/2026/08/21/h...

#MECFS #pwME @thesicktimes.org
August 26, 2026 at 8:56 PM
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"Post-exertional malaise I think sounds quite benign as compared to the actual reality of experiencing that. It feels like there is actual poison flowing through my veins"
www.meresearch.org.uk/post-exertio...
PLEASE, pay attention to how #MEKills @england.nhs.uk
Thanks @meresearchuk.bsky.social
Post-exertional malaise (PEM) in ME/CFS
Post-exertional malaise (PEM), the cardinal feature of ME/CFS, is particularly debilitating as it involves the amplification of existing symptoms, alongside the potential appearance of new ones, follo...
www.meresearch.org.uk
August 23, 2026 at 7:13 PM
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🧵
ME Research UK:

Careers, relationships, family life, hobbies, basic tasks – PEM can tear through it all.

The sheer symptom burden and ripple effects can impact mental health. We urge anyone in distress to consider reaching out to appropriate organisations e.g. Mind (mind.org.uk)
#MEcfs #PwME
1/
August 23, 2026 at 4:34 PM
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And now here's a trial of the Lightning Process for Long Covid from Canada's McMaster University. This stuff never ends...
virology.ws/2026/08/22/t...
Trial By Error: Canada's McMaster University Launches Trial of Lightning Process for Long Covid | Virology Blog
By David Tuller, DrPH McMaster University in Hamilton, Ontario, has launched a clinical trial of the Lightning Process (LP), a well-known “mind-body” interv ...
virology.ws
August 22, 2026 at 5:48 PM
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#Research #ME #LongCovidME
Essential viewing for everyone working on international standardisation in study design.
Especially interesting on 'brain fog' as a meaningless descriptor.
Thank you @investinmeresearch.bsky.social
youtu.be/_Qcu40jtE7k?...
IIMEC18 Dr Vicky Whittemore
YouTube video by InvestinME Research
youtu.be
August 17, 2026 at 6:30 PM
Scooby-Doo: The Mystery of the Reflecting Pool
youtu.be/GU_ID0asQ3M?...
Scooby-Doo: The Mystery of the Reflecting Pool | Donald Trump Parody #ScoobyDoo #Satire #DonaldTrump
YouTube video by Midnight Oil Productions (Jason Moore)
youtu.be
August 16, 2026 at 8:46 PM
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“On BPS [BioPsychoSocial] & disease causation: George Davey Smith’s cautionary tale” by Prof Chris Ponting @cgatist.bsky.social

mecfsresearchreview.me/2026/08/11/o...

#MEcfs #PwME #CFS
August 15, 2026 at 8:52 PM
Graphic Design 101
August 11, 2026 at 8:45 PM
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#pwME #pwLC

In case you were wondering, David Strain has now taken over a position at DWP

www.disabilitynewsservice.com/dwp-faces-qu...
August 9, 2026 at 7:19 PM
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This photography print by Whitney Dafoe sits on my bookshelves in the room in which I spend most of my time. For me it evokes grief & time, the gloom & haze of illness, hope of sun peeking through, the power of nature in a world that continually goes on, a pathway into the unknown. #SevereMEDay
August 8, 2026 at 6:43 PM
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Digestion is, IMO, the most important focus of improving care for people with severe ME. Without proper digestion, nutrients are not utilized and medications are not metabolized. There are multiple mechanisms by which digestion potentially fails/slows. 🧪

#SevereMEDay 🧪
August 8, 2024 at 3:11 PM
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View from the Trenches of #MyalgicEncephalomyelitis latest article covers #SevereME day for 2026.

Includes news and resources.

open.substack.com/pub/colleens...
Recognizing Severe Myalgic Encephalomyelitis
August 8, 2026
open.substack.com
August 8, 2026 at 7:54 PM
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The Star: "Sheffield woman calls for urgent change in care and support for people with severe ME"

www.thestar.co.uk/your-world/s...
Sheffield woman calls for urgent change in care and support for people with severe ME
Sheffield woman calls for urgent change in care and support for people with severe ME
www.thestar.co.uk
August 6, 2026 at 7:08 PM
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