Politics of toxicity. Politics of nutrition. Anti-ableism. Anti-stigma.
Me: PhD, humanities, Cantab; ME/CFS since 2017; chronic fatigue since 1998; any pronns.
I went back to work by avoiding toxins--sleeping outside on a plateau between the ocean and the national park for two yrs. No expensive detoxes, just clean air and lots of organic veg. I wasn't wrong, & now I pay taxes again. No thx to mainstream medicine https://t.co/BxswTvdFFc
This is what ableism looks like. The two groups do have something in common: experience of disabling chronic illness. Those with #MECFS have long been accused of being a cult for these kinds of reasons. This is not new analysis, just recycled prejudice.
And yes, of course we don't trust medicine. When (for example) you are disabled by a medical procedure, then told by every doc you see that "it doesn't happen, therefore it didn't happen," that kind of renews your perspective on medicine. Also when you are told you're not sick.
Note to #pwme: we are not welcome here!
Such useless fomenting of hate. Who knows what any illness is. This is some serious gatekeeping. Let's open the gate and help each other.
I am tired of people posing as Long Covid advocates when they don’t have Long Covid but rather, have other interests to promote. I don’t do that with other conditions.
to make a judgment. Here, we need to look in depth at the scientific claims being made. If we don't have info to decide, then we need to say, we don't know. These skills are ofc both humanities & science skills. But the humanities' attn to the case may be useful, here & elsewhere
One thing I'll miss about twitter is when science influencers inadvertently show just how crucial humanities-style skills could be to good critical reasoning, were that reasoning to take place... the whole concept of the specific case vs the general case is subsumed here 1/2
So GMK wants to say that @fitterhappierAJ is probably wrong bc that is statistically more likely. But that's the wrong way to go about answering the question of whether AJ is right or not. The general law doesn't determine the specific case, and the probabilities don't help us 2/
Your conference looks magical. But if you say you aim to "bring together people of all ... disabilities," and there are no masks and no Zoom option, then it is ok for me to write to you asking how I can attend.
@TimHuttonAu Yes, totally. I think supplements are often really key! If only they weren't so stereotyped! (The "expensive urine" stereotype for B vitamins is very ableist to my mind!) I hope you get some improvement.
@e_quinnIR @lelia_glass @matthewshaer If you have the electromagnetic hypersensitivity(EHS), the more research you read, the more you realise that "scientific consensus" is just what the mobile phone companies want you to think. I know my sensitivity is real. The researchers keep "proving" it isn't! And are believed!
@matthewshaer Maybe the CDC should look into ME/CFS and Long Covid, so that those of us who've been disabled for many years have to read more than a handful of papers to know more than the doctors treating us. I got better from my own research. I went back to work.
@loulou_mermaid @seraphrdm Electromagnetic radiation can cause tinnitus in people who are electromagnetically hypersensitive. That would be one way of explaining the "sound." People aren't necessarily wrong about their own bodies bc "physics."
@ABertheim @VirpiFlyg Those aren't harmless though! Gadolinium contrast has fairly recently been linked to fibromyalgia (sorry I don't have the ref to hand). Hope you feel better. Sometimes no one wants to do the research if it will make the companies look bad... sometimes we just don't know