Would inclusivity to people with disabilities/medical safety be included in those regulations? These “seats” are extremely ableist and it’s not just exclusive to people with POTS, some people like wheelchair users also can’t stand/stand for long periods either.
Yeah I really can’t see how they could bring him back in a way that seems plausible. Really enjoyed Carrey’s performance though
I’m going to name a game I’m making “a game”
I’m skinny and I’ll pass out in less than an hour. Have severe POTS from EDS, heart went into asystole after 35 minutes into a tilt table test and they had to put me back down. I’ve passed out several times in other settings.
It can even be dangerous for some people to be in a standing position for too long. I have a severe case of POTS caused by a genetic disorder. My heart stopped during a tilt table test, which is where I was forced to remain in a standing position. If I’m expected to pay more for a normal seat just because I’m disabled, that’s ableism.
Why should I have to be forced to pay more for sitting seats just because I have a disability? What if all the sitting seats are fully booked or the plane has no sitting seats for passengers? It’s like intentionally designing a shop with several tall steps at the entrance that would make it impossible for wheelchair users to enter, and the wheelchair users have to pay each time they shop there to have a ramp extended at the entrance so they can enter. It’s an example of ablest design.
What about people like myself who have POTS and can’t be in a standing position for too long? My heart can legit stop causing me to pass out if I’m standing for too long.
I still need to play Link Between Worlds. Link To The Past is the best 2D Zelda imo
I can still hear that rabbit music
The original one?
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A virus that changes the font every time you go to a new page or hit refresh
Another reason I’ll never use Facebook. It’s been a hellsite for a long time
Was about to say this too. Can’t tell a difference between most games made in 2013 vs 2023.
I’ve had so many blood tests done when they were trying to figure out what was wrong with me pre POTS/EDS/CFS diagnosis
I have, but doctors don’t suspect it. I find my brain fog correlates to episodes of bad circulation/low blood volume, in that it gets worse whenever my blood volume or circulation is low/bad. How did they diagnose you with MCAS and is it easily treatable? Thanks
It really is. I’m aware of every mistake I’m making but it’s like trying to move my fingers rapidly when they’re too cold, I can’t stop it. Thanks for telling me about the ME community, I’ll check it out!
Yes. It’s worked very well in the recent Zelda games