#TO RB

[its-arson-time]

this post is meant for mobile users

[fordp1nes]

funniest shit is going down on discord rn

[dopaminerjic]

credit: @stupid-twink-girl

(this was an accidental repost, do rb the original instead)

[butchfalin]

the funniest meltdown ive ever had was in college when i got so overstimulated that i could Not speak, including over text. one of my friends was trying to talk me through it but i was solely using emojis because they were easier than trying to come up with words so he started using primarily emojis as well just to make things feel balanced. this was not the Most effective strategy... until. he tried to ask me "you okay?" but the way he chose to do that was by sending "👉🏼👌🏼❓" and i was so shocked by suddenly being asked if i was dtf that i was like WHAT???? WHAT DID YOU JUST SAY TO ME?????????? and thus was verbal again

[jackalspine]

@schnuffel-danny hehehe

regarding this post: from schnuffle

[virtualplushy]

i want to be a sweet and friendly girl but there’s all this anxiety. and the horrors

[letmebegaytodd]

tragedy enjoyers when even good intentions lead to ruin

[zytes]

this manatee looks like it’s in a skyrim loading screen

[ghosthorse-tracks]

Lesser-known steps of the writing process:

Finding all the paragraphs where you used some hyper-specific word more than once

Rearranging paragraphs that you swear you wrote in the right order but turned out to be totally backwards

Going for a walk, coming up with the perfect line, and forgetting it as soon as you get home and open your laptop

Creating a separate document where you can dump all of those nice sentences that no longer fit in anywhere

Waking up in a cold sweat because so-and-so was supposed to be barefoot but never actually took his shoes off

[candieduranium]

rb to stare at a mutual like this:

[dreamsofrentboyandomoriandsnuuy]

[trinketbug]

"furry inflation" (2024)

[sidras-tak]

Accessibility takes too goddamn fucking long.

My brother was paralyzed in October 2023. We got him home from the hospital (in Texas, when we live in Iowa) in a clunky old hospital chair. He hated it. He was scared and angry and in pain and his life had just changed forever and he couldn’t do anything for himself in that wheelchair. His first goal (aside from learning how to transfer) was to get a wheelchair. My family was lucky enough to afford one so we thought it would be easy enough. Nope.

We couldn’t buy him a wheelchair. He needed a prescription. For a wheelchair. A doctor had to examine him and declare him in need of a wheelchair. It wasn’t good enough that he had scans and tests showing tumors cutting off his spinal cord. He needed his primary care doctor to examine him during a physical and write a prescription. He was making 2-4 transfers a day, tops. He had no energy to get to a doctor. Home health was in and out every day. He had no time to get to a doctor. He didn’t get a prescription for almost a month. Then it had to go through insurance.

We asked if we could skip insurance and just buy a wheelchair for him. Nope. They wouldn’t sell us one, not even at full sticker price. It needed to be approved by Medicare. We ordered a wheelchair, a nice one, a good shade of green, sporty, small. It would let him move around the house. He would be able to cook, to reach drawers and get stuff from the fridge and brush his teeth and put his contacts in at a sink. We were told it would take awhile, maybe two months. Silently we all hoped he would be around to see two more months.

He went on hospice care on a Saturday in March. On Monday, I was calling his friends to come see him before he died. I got a call on his phone. It was the wheelchair company. They were about to order his wheelchair, she said, but there was an issue with insurance— had he stopped being covered by Medicare? Well, yes. When he started hospice care, he got kicked off Medicare. The very nice woman I talked to told me to call her if he resumed Medicare coverage so she could order his wheelchair. He died less than 12 hours later.

We ordered that chair for him in early December. Medicare didn’t approve the order until March. He was dead before they got around to it. He wanted that fucking wheelchair so badly. The only reason he had any semblance of independence and any quality of life for the last five months of his life was because the wheelchair company lent him an old beater chair, a very used model of the chair he ordered. If I could go back and change one thing about his end-of-life, I would get him his dream wheelchair. He told me again and again he couldn’t wait to get it, so that he could feel like a person again. He made the best of what he had with that old beater chair, but it still makes me mad to this day. He was paralyzed. He needed a chair that afforded him dignity. We had the money for it. And yet, we were left waiting for five months, for a chair that wouldn’t even get ordered until the day he died.

[take-a-dip-in-the-deadpool]

THIS!!

THIS IS AN AMAZING WAY TO THINK OF CHRONIC PAIN

[ryan-sometimes]

I love the genre of picture “animal that clearly just woke up from a fat nap”