ocd stands for “oh CMON dude” which is what you say to your brain when you catch it spinning a complex web of the stupidest shit imaginable that it has never the less managed to completely entrap you within

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@wolfdaeva
ocd stands for “oh CMON dude” which is what you say to your brain when you catch it spinning a complex web of the stupidest shit imaginable that it has never the less managed to completely entrap you within

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
"reblog if __, who wouldn't?"
"if you don't reblog this unfollow me"
"reblog for__ ignore for --"
"who wouldn't reblog this?"
"you have to reblog this"
"no __ will reblog this"
No. Shut up. These statements are not safe for those with moral ocd. Reblogging something or not does not change opinions and actions. It does not define a person. It does not represent beliefs. You can share your beliefs without harming others.
I have had two sword fights. Both were wonderful.
Part 1 Part 2 Part 3
reblog if you need a hug
Reblog to give the person you reblogged this from a much needed hug

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
Reblog if you'll PUBLICLY answer anything in your ask right now.
Im game
ANYTHING.
there’s nothing shameful about making things easier or more accessible for yourself btw.
if your disability means you can rarely/never cook so you have to order out a lot, or buy precut ingredients, or if you need other people to help you cook even “simple” meals.
if your disability means you struggle with personal hygiene so you don’t shower standing up, or don’t brush & floss “correctly” or long enough, or put up your hair when you can’t handle brushing it.
if your disability means you’re not able to engage in your hobbies in a “normal” or “correct” way. if you have to watch movies multiple times because your brain fog is making it hard to follow the plot. if you need accessibility tools to be able to draw or paint. if you have to do everything from bed.
you’re not doing anything bad or wrong. you’re being kind to yourself and caring for yourself in the ways that you’re able to. it’s nothing to be ashamed of.
Chronic pain pisses me off cause I'm not even incapacitated for like a cool or badass reason instead my body is throwing the world's biggest temper tantrum because it's raining outside
Sometimes yes, people with meltdowns do need to be retrained. Sometimes yes, they can seriously hurt themselves. Yes, there is nuance. Restraint can be seriously harmful, but restraint can mean the difference between injuring yourself severely, and someone else hurting you from the restraint.
I’m an autistic person that has violent meltdowns with self injurious behaviors. And yes, this does mean that sometimes I need to be restrained.
I think that in the autism community, there’s a lot of people saying “never restrain!! Never do that!!” And they forget about people like me, who WILL hurt themselves severely if they are not restrained. Does this mean that I allow random people to restrain me during meltdowns? Absolutely fucking not. My caregiver is the ONLY person I trust to restrain me during meltdowns. Why? Because they know how to do it in a way that won’t hurt me, or lead to me hurting them.
I feel like within the autism community, there’s so many people telling us what we can and cannot do. And what our caregivers can and cannot do. YES! Restraint can be life threatening and harmful, but I am prone to hurting myself. To giving myself a head injury, to self harming. It is far more safer for me to be restrained correctly from my caregiver.
Please remember that those of us with higher support needs and more violent meltdowns, do sometimes need to be restrained. However, it’s important to remember anatomy. When my caregiver became my caregiver, that’s one of the first things we talked about, and we came to an agreement and I talked to them about the CORRECT way to restrain me during meltdowns.
Please remember those of us who do need restrained, and please remember those of us that this is the safest option for us.
Feeling extra disabled, gonna start saying that abled people doing normal amount of stuff is them “having the zoomies”

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
floor time save me. floor time. save me floor time
Remember that it is officially disability pride month now. it is just as important as lgbtq+ pride month. we exist. we are being hurt by the system as it is now. we will not be silenced or placated. disabled is not a bad word.
Take a reassurance and pass this on to your followers:
Making a mistake doesn't make you a bad person
You're allowed to have boundaries even when they upset people
They shouldn't have treated you like that; you didn't deserve it
People would miss you if you weren't here anymore
It's okay to take a break and rest
You've made so much progress already even if it doesn't seem like it
Your unique contributions are worthwhile; no one else does it like you
You can have more than one feeling at the same time; that's normal
A little treat does make it better for a little while
People will love you even when you're not perfect
It's really hard to unlearn bad coping methods but you're doing a great job
Where you are right now is not your final destination: keep going
It can be really hard to learn to engage in positive self talk, but sometimes it's easier to start by pretending it's coming from a friend, first 💜
Reblog to hug the person you reblogged this from and tell them that everything's going to be okay
tumblr is great bc I feel a little less alone in my experiences as a disabled person

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
It's tough being used to feeling incredible amounts of pain that when it becomes worse or more frequent you don't even mention it
And bc it's been going on for so long, when you finally do figure out it's not normal or start actually trying to talk about it the people around you get Very confused about why 'all of a sudden' you're being impacted so heavily and are now actively disabled. Like, actually this isn't new I've just spent years teetering on the edge without realizing how abnormal it is due to a variety of reasons I won't get into on tumblr dot com :')
I don't know how to describe the experience other than I feel a lot like a cat in pain, like you can read it in my body language, but my face says little to nothing and I'm not saying much at all about it until it is too much to bear.
ah yes, daydreaming of owning a good quality manual wheelchair so i dont have to worry about my legs giving out from under me. A normal, ablebodied daily activity