Why? Personal choice. No one forced him.
Some free services (like buffer) let you post to threads twitter and mastodon at the same time. So no excuse here.
As far as I know if it is on the open web, no way to ensure.
Robots.txt can be configured but is not always followed.
More like suggesting there is no reliable evidence.
As the law of funding bias says, only research that corroborates powerful interests will get the funding necessary to create a reliable body of evidence.
Doesn’t help that the new parliament’s composition has a higher corporate bootlicker ratio
But “non-binary girl” was not included in your description. But I guess one could have searched the other words.
Anyways, new instance sound cool. Hope it goes well. Also, fuck threads, amen.
“I know there is lots of fear and anxiety”
This is classic psychologising. Branding others concerns as “anxiety” is not only medically false, but is used in order to belittle those criticising.
If you genuinely care about trans people then Streeting, how are you going to prevent the increased suicidality this decision will surely cause?
That’s not how it is here in switzerland.
High school is to be well rounded.
In uni 95% of your courses are in your subject matter. Also non-university jobs are well valued. To the point we are on of the only countries where the working class isn’t getting poorer year on year compared to the 1%
That’s what high school does (or should do).
That counter point is a classist view that id all too common in america. Not saying you are classist by having that view. But that a system based on that view, which america is, is classist.
++ disabled folks.
never heard of the source but url looks dodgy
This summary says “he” as if it’s her father but “he” is an ME expert who worked on the government guidelines who is criticising how the hospital is mistreating Carla.
repost unfortunately
I think one of the first things you’ll be interested to hear is modern definitions of ME/CFS don’t note fatigue as the most disabling symptom but a disease process called post-exertional malaise, wherein a person’s entire disease can worsen (sometimes permanently) based on the amount of energy they use.
It’s really fascinating, A recent study by Wust et al. found muscle clotting and abnormalities following exertion in people with ME/CFS.
Also people with ME are the only known disease group to preform markeldy worse in specific markers on a 2 day CPET. Which would serve as a biomarker if it were not for the fact doing the test can worsen people’s disease permanently.
I highly recommend this summarising article on the issue: https://www.nationalgeographic.com/premium/article/long-covid-patients-exercise-bad-medicine
If you are genuinely curious, I’d invite you to join a community of Long Covid and ME/CFS patients and researchers online, and ask any questions you have.
I understand.
For a while I had blindness and was partially paralysed because of a disease. The only thing we had at the time that I could really do was a CD of harry potter audiobooks so I listened to them on loop for months. It’s very engrained in me. Needless to say was very disappointed when I heard JK was a TERF.
I hate JK Rowling too but no need to be rude. I’m unable to read books anymore due to aquired physical disability.
Oh no. The tory party is like the Ministry of Magic, evil, but not crazy. Reform UK is like Voldemort. Teaming up is no good idea. (For anyone who wants a good future for the UK).
If you spend a long time scrounging through different polls and opinion surveys, you can find quite a bit to patchwork together.
I’d give my finger to be in the olympics. Already lost a finger in an accident and doesn’t change much 🤷