Librarian
If Trump cuts social security, it’s euthanasia for me. I’m too disabled to care for myself and prefer killing myself than starving in the streets.
Preferred to the original.
But real thing should be. Vote, it won’t change much, but it’s a start. If you truly believe in change, you should be doing much more, but never let go of the right to vote.
I was liking you until I saw this meme. I was about to subscribe to anaval.
I’m an anarchist and think we should seek to destroy the state. I also think it matters that while the state exists we should make it so that the least people possible suffer. By not voting, you are contributing to immense suffering.
Due to my memory problems I don’t remember most of what I read for long. But I really enjoyed a deep dive into learning about purpoises the other day. If you’re ever bored, or want to get through a commute, reading random wikipedia pages and seeing where the links take you is quite enjoyable in my opinion.
I’m deaf and mute. I was focusing on Manifold Learning but due to neurocognitive deficits I’m unable to continue with math. I’m able to use my phone and communicate sometimes but most of the time I’m only able to be alone with my thoughts. But I do enjoy watching some repetitive shows when my condition permits (animated sitcoms tend to be the easiest to follow with my cognitive problems).
Though what I spend most of the time I’m able to go on my phone is endlessly scrolling through wikipedia and learning new things, it’s what really excites me.
Aquired. I was actually a math student at one of the top 5 universuties in the world before I got struck down. I was engaged too. I had everything, and then nothing… I’ve been pretty good at adapting to the new life. After a couple months of feeling sad I was able to make the best of it. But sometimes the physical pain and fact that there is almost no chance I ever get better hits hard.
I did go to public school though but skipped a couple years ahah.
As someone with an aquired disability, The thing that hurt the most about others is them being overly positive. Like them saying I’ll get better when I’m almost certain not too, or them acting like my disability is a phase that will pass. I imagine they did it of good faith. But to me it’s denying who I am as a person, my struggles, and my pain, acting like it doesn’t really exist. It almost felt like a coping mechanism more for them than for me.
Thanks for your answer by the way.