YOU ARE THE REASON
Today's Document
Kiana Khansmith
Sweet Seals For You, Always
todays bird
RMH
Three Goblin Art
Andulka
JBB: An Artblog!
❣ Chile in a Photography ❣
tumblr dot com
AnasAbdin
styofa doing anything
#extradirty
KIROKAZE
Xuebing Du
🪼
taylor price
dirt enthusiast
cherry valley forever
seen from United Kingdom
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seen from Malaysia
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@breaks-hetheon
hey gang i got popsicles pick one as pass the box to someone else
mint
lemon
orange
strawberry
cola
pineapple
dark cherry
anise
"i cant believe you dont have this or that flavor" listen they had these ones okay
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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READER BEWEADER YOU’RE IN FOR A SCEADER
You don't have to grieve alone.
Claiming he could eat the stuff every day and still not get tired of it, local yak Henry Cunningham expressed his sincere hope Tuesday that they never stop making grass. “Man, after a long day on the plateau, nothing hits the spot like a big mouthful of grass,” said Cunningham, adding that just thinking about grass’s unbeatable taste and satisfying texture was making his mouth water.
Full Story
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
before my egg cracked, i had noticed that trans people were often pro-accessibility and up-to-date on the needs of disabled people, but i hadn’t seen any inherent connection between the two (other than the obvious minority-looking-out-for-other-minority thing). but now that i’m trans and medically transitioning, and i have to constantly repeat myself while talking to doctors and nurses, and explain things about my own anatomy to medical staff who should already know this, and having every single problem i might have blamed on my “condition” so nothing i say is taken seriously, all of the sudden i have a little sneak peak into the life of someone who has to deal with this all the time. like shit bro, being disabled probably sucks ass, someone should do something about this
happy disability pride month, we all deserve autonomy and respect and access to medication
Fairytale
Rad photos of Skrunkle by @preston_yarger @neotropolisevent ! YOU WANT BUY BABIES???
Any chance we could get employee tackling Harley? Also I love your designs especially after they went in the goo
any attempt at tackling Sawyer just looks like this in my head
it’s going to be ok… here’s rodeo eating a piece of apple
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
new Into the Inkwell pages! four of them this time- and everyone say and extra big thank you to @celebi9 and @lizzybeanbutt for their enormous help with all the crowd shots!
updates might be slow as we enter yet another heat wave and survival is the priority, thanks for your patience!
read this whole dang comic from the beginning here
a week into artfight i would like to give out the following reminders: it is okay if you thought you were going to participate but ended up not having time. it is fine if you started out enthused and then lost steam. you do not owe anyone revenges. you are not 'behind' and you are not letting anybody down. it is a silly little game for fun. do not forget this.
If I ever don’t reblog this, you can assume I’m dead. It’s just pure, sound-design gold.
The cuts, the slow ramp-ups, how it matches his dance moves.
MWAH.
The last.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
call me the mountain goats the way im making no children
I don’t think healthy people every really get chronic illness.
I have a friend I know from when we were both 6. She is the only person living nearby and so she saw me go from walking through limping to wheelchair on a daily basis. I keep her updated on my health even tho we rarely hang out anymore. She was gonna come over yesterday and I had to cancel. She asked if I can’t hang out later that day. When I said i won’t feel better later, that if I feel that bad in the morning later will only get worse she got annoyed and “joked” that I’m just finding excuses. And I was surprised, she knows all about me being disabled after all? So, a bit taken aback, I told her it’s a normal thing for me.
“But you got the diagnosis now, aren’t you better?? I thought you’ll get better now”
She was honestly surprised and it made me realize a thing. They don’t get it. They don’t get that getting diagnosed only equals benefits like welfare or parking spot for us, and sometimes better pain meds but that is just like pushing luck. That it’s a forever thing. That that one day we felt good a week ago was just a bright spot and doesn’t mean we won’t need our aids anymore, cause chronic illness is not linear and will make a great comeback in next four hours, and the next good day is planned on when we’re 70. Cause when abled people are sick, they get better. And our illness is just an excuse for them. And when we say we will never get better they think we’re being dramatic and pessimistic. And I don’t think they’ll ever get it, cause to get it you need to live it. And I want my friends to stay healthy and not go through hell.
This is definitely okay to reblog and abled people are encouraged to reblog cause maybe it’ll help others understand
Hello it’s me Lexa and this post is relevant again as I just had the Legit Same Talk with someone and I exhausted my number of fucks to give
