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🩵 avery cochrane 🩵
2025 on Tumblr: Trends That Defined the Year
YOU ARE THE REASON

Kiana Khansmith
Keni
cherry valley forever
todays bird


#extradirty
taylor price
h
Aqua Utopia|海の底で記憶を紡ぐ

izzy's playlists!
macklin celebrini has autism
noise dept.

Game Changer & Make Some Noise

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@glassbonespaprskin

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fucking goldfish tiktok made me cry bro
humans be like “is anyone going to nurse this animal back to health?” and not wait for an answer
I somehow just realized I have never in my entire life seen a panda this clearly? Any image or video I can recall was usually lit starker so you couldn’t easily make out the eyes and the panda was kind of facing down or off to the side. This is the first time I’ve really been aware of them like, having a real face like a real animal and not a cartoonish abstract mass of sad fur.

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Friendly reminder that:
Young people can have arthritis too.
There are hundreds of life long conditions and diseases out there that are typically diagnosed between 12 and 30.
There is a vast difference between being tired and having chronic fatigue.
Just because you can’t tell that someone is unwell from looking at them, doesn’t mean that you should assume that they are ok.
Many chronic illnesses are life long, and incurable. Many of them are potentially fatal.
If you have a disease like Lupus, on good days you still feel like you have a bad flu, 24/7.
Many of the medications used to treat chronic conditions have side effects that can really affect someone’s self esteem - like extreme weight gain, skin changes and hair loss.
Most chronic illnesses have very little awareness - its unlikely that you’ve heard of Sjogren’s Syndrome, Scleroderma, Ehlers-Danlos Syndrome or Fibromyalgia.
However these diseases can cause symptoms as varied as joint pain, fatigue, constant nausea, kidney failure, pneumonia, photo sensitivity, full body rashes, paralysis, strokes etc.
So please remember that invisible illnesses exist too :)
josh?
where’s the body of christ?
Every year I diagnose at least one cat with renal failure due to lily poisoning. If you have cats please don’t have lilies.
We’ve had 4 this year already, not really looking forward to Easter

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Oh oh oh here it COME—
that swing had more screen time than tenten
yesterday at the mall i decided to borrow a “complimentary wheelchair”, because standing upright had become considerably hard, and if i wanted to keep up with my friends, i needed mobility. this post could become an essay about internalized ableism or a complaint about how the woman at customer service treated us, but then the post would be way too long, an i want to make a specific point.
once i got the wheelchair, i got into it, collapsed my cane, and began a combo of wheeling and scooting myself with my feet to the elevator, so we could go to the food court. the wheelchair was manual, and a shitty one at that, and i have horrible upper body strength, so this was how i could keep up.
my god, the amount of high and mighty people that stared at me as i made my way with my friends. i could practically see them staring intently at my legs, waiting for any sign that i was undeserving of a wheelchair. they would look at my legs, i would stare them in the eyes, they would meet my eyes, and bashfully look away. i began to get embarassed, and exclusively used my arms to wheel myself, not using my legs. so that judging people would not frown at my moving legs. this was painful, and i was painfully slow.
we eventually made it to the food court, and split up. (with a little help from my girlfriend, who, god bless her, wheeled me with my consent over to the burger joint.) i wheeled myself into line, and the amount of people who asked me, looking at my phone, if i needed help, was insane. no! i’m waiting for a burger! and then, inevitably, when i got my meal, no one at the counter was willing to help me assemble all of the things onto a tray to carry back to my friends. i slowly wheeled back to my friends, precariously balancing my burger and shake, while people stepped in front of me to ask if i needed help. no! just move! i got it!
eventually, we travelled back to the help desk to hand back in the wheelchair, and i began the cane walk of shame back to my car. people who had seen my scoot/wheel past, saw me with my cane and gave me dirty looks, and i could feel my cheeks heat up. it was embarrassing and infuriating. i wanted to yell at them and tell them all the gory details of my medical history. i was so mad. but i was in public with my friends, so i kept walking.
the only positive thing that happened, was when i got into the up elevator, a middle aged wheelchair user using the same technique as me in her custom chair scooted out of the elevator, and gave me a thumbs up as i got in, and smiled at me. thinking back on it, it makes me think about how the people who really get it, are the people who are living it. it sounds mean and alienating, but it’s true. i find talking to disabled people about these things so much better than talking to abled people, because i feel like i can be a person, rather than an encyclopedia.
if you read all the way through, thank you, and please give this a reblog.
i’m being serious if you’re not disabled don’t speak over disabled people in the notes FFS
You guys are Jeff the killing me
help girl im ben drowning
gunmazoo on twitter
A panda sitting in a pool twiddling its legs
(Source)

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Watching this dude match paint swatches is so relaxing...
happy holiday