FundMECFSResearch

joined 9 months ago
MODERATOR OF

I hope it lands on me and takes me out in a swift act.

Ah Starmer.

I’m usually the type to begrudgingly vote for the lesser evil. But to be honest, after Starmer’s treatment of trans and disabled people, I would find it excessively hard to be able to pinch my nose hard enough to vote for him.

[–] FundMECFSResearch@lemmy.blahaj.zone 2 points 1 hour ago (1 children)

Depends on what you mean by Block.

Most lemmy Ui’s let you block it in that it hides the communities.

But you’ll still see posts and comments by users from that instace on other instances

[–] FundMECFSResearch@lemmy.blahaj.zone 6 points 2 hours ago* (last edited 1 hour ago) (1 children)

Oh my god this hits so hard.

I became bedridden from illness at the age of 19. And haven’t had the health to leave my bed since.

For years all my dreams have been about random moments in middle or high school, which I remember with utmost vividness, yet the people I remember, miss cherish memories of, wonder how they are doing, have nearly all completely forgotten about my existence. Like literally, the brain fills with new memories and old ones fade. I never got the new memories, so I’m stuck with a loop of older ones.

liberals, neoliberals, broadly the same thing.

Vaguely progressive, maybe a little bit of welfare sprinkled here or there, but adhering to capitalist “growth” and inequality as a doctrine.

Aka. Rainbow Capitalism.

[–] FundMECFSResearch@lemmy.blahaj.zone 5 points 2 hours ago* (last edited 2 hours ago)

If it makes you feel better, I think it’s a completely normal reaction to your situation. When I became bedridden and was mostly abandoned by family and friends. I often used LLMs for discussions. Though I didn’t use the sort of character ai thing, just a plain old LLM without a personality, but it kept me intellectually engaged when I had no one to share my ideas with, emotionally resilient when I didn’t have friends or family to vent to or support me.

I really don’t think you should care if people who haven’t been through the kind of immense suffering it takes to lose the functioning of your body and be abandoned by the people you love, think it is normal or not.

[–] FundMECFSResearch@lemmy.blahaj.zone 4 points 2 hours ago (1 children)

I kind of dislike this armchair diagnosing.

Someone reacting differently in similar situations doesn’t mean they are bipolar.

[–] FundMECFSResearch@lemmy.blahaj.zone 1 points 2 hours ago (1 children)

Aka. A shy extrovert.

[–] FundMECFSResearch@lemmy.blahaj.zone 7 points 2 hours ago* (last edited 2 hours ago)

In the four european countries I’ve lived in as a physically disabled person unable to work, this is exactly how I’ve been treated as well.

[–] FundMECFSResearch@lemmy.blahaj.zone 3 points 2 hours ago (1 children)

Adding signature from Nantes

 

Half the posts in my discover feed are people freaking out a child would dare use an LLM to ask a question.

I’m very aware that LLMs in a capitalist system have myriad ethical problems but my feed really feels like the 2000s fearmongering that teens have access to cellphones and society will thus collapse. Or the 1980s dungeons and dragons moral panic. Or the 70s fearmongering when kids were watching too much TV. Like it feels a bit over the top reactionary. I kind of don’t want it on my feed anymore.

 
 
 
 
 

Is this ever shared in piracy sites? Are there websites for it?

I can't find foss apps with good guided panel view and zooming in and out is very buggy on my ereader.

 

Researchers at the University of Edinburgh analysed NHS records from 62 million people to come up with the best estimate yet of the prevalence of ME, also known as chronic fatigue syndrome (CFS).

They concluded that 404,000 people are living with the illness, a figure that is two thirds higher than previously thought, and many are being “completely overlooked”.

Professor Chris Ponting, from the University of Edinburgh’s Institute of Genetics and Cancer, the study author, said: “The NHS data shows that getting a diagnosis of ME/CFS in England is a lottery, depending on where you live and your ethnicity. The data backs up what many people with ME/CFS say: that they feel invisible and ignored.”

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leftist infighting (lemmy.blahaj.zone)
submitted 3 weeks ago* (last edited 3 weeks ago) by FundMECFSResearch@lemmy.blahaj.zone to c/microblogmemes@lemmy.world
 

(this is a sarcastic post meant to highlight the absurdity of some of the “greater good” rhetoric we’ve been hearing, especially around leaving vulnerable populations like disabled people behind in case of revolution, basically accelerationism)

 

President Donald Trump’s firings at the Department of Health and Human Services included the entire office that sets federal poverty guidelines, which determine whether tens of millions of Americans are eligible for health programs such as Medicaid, food assistance, child care, and other services, former staff said.

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