advenplore:

Just Pen by Piotr Górski and Agata Zambrzycka

Independence is important for everyone. Unfortunately, for a person with such insignificant disability as the lack of thumb seams to be, life is not easy at all. We learn how to write in the earliest years of our life and it becomes an inherent element of our everyday life. When somebody is suddenly deprived of the opportunity to ordinarily use a writing tool, the disability starts to be inconvenient, it deprives of the independence.

gailsimone:

jayzsongwason:

mrgeef:

Disneyland and Walt Disney World now have guidebooks for guests with cognitive disabilities (such as autism). They include the above charts of what to expect at each attraction (strong smells, loud noises, restraint types used, duration, and more), lists of quiet areas for when you need down time, and answers to frequently asked questions, among other tips.

They are available to download in PDF format: Disneyland | Walt Disney World

If you don’t want to download a PDF (or prefer to click the download link on Disney’s site directly), here are their pages for Services for Guests with Cognitive Disabilities: Disneyland | Walt Disney World

This is awesome.

Lovely idea!

ieatbigtitss:

superwholockalypse:

dreamingofdoctorwho:

colorsofsocialjustice:

colorsofsocialjustice:

contra-indication:

spondylitis:

The nerve!….This goes out to all the spoonies.

Read this:

My name is Emelie Crecco, I’m 20 years old and I have cystic fibrosis. CF affects the lungs (as of many organs in the body) because of this I have a handicapped sticker. I’m not one to “abuse” the sticker, meaning I use it when I’m having a “bad day” (some days its a little harder to breathe). Today was HOT so I needed to use my sticker. I was running errands all day around my town, I pulled into a handicapped spot, placed the sticker in my mirror and continued into the store. Upon returning to my car I found a note written by someone, it said “Shame on you, you are NOT handicapped. You have taken a space that could have been used by an actually handicapped person. You are a selfish young lady.” I was LIVID. How can someone be so ignorant and cowardly? They clearly saw me walk out of my car, why not approach me? Not all handicaps are visible. I would love for you to share this story. It would help spread awareness for CF, but it would help open people’s minds to what handicapped really is.
Thank you for your time”
~Emelie Crecco

A friend of mine fell over 20 feet and basically broke half his ribs, punctured his lung, broke his arm in three places that required many surgeries to fix and messed up a nerve in his leg. He had to walk with a cane for a long time after it and some lady in a restaurant thought he was just walking with a cane for the hell of it and she ripped it from his hands and grabbed his messed up arm and shook him and told him he was an awful human being for pretending to be handicapped. What the fuck people?

This is what real ableism looks like.

I have ulcerative colitis, an autoimmune disorder which causes my body to attack my colon, and I qualify for one of those stickers. I’m scared to get one, though, because I look healthy and whole.
-Orange

A mutual friend of mine’s mother has severe fibromyalgia (that gives her a handicapped pass) and as she was walking to her car after buying her groceries, a man actually lunged at her and started yelling at her about her “not looking handicapped”. It left her mother shaking and crying, of course, and it just makes me so angry how awful and ignorant some people can be. 

Not all handicaps are visible

Can I just pin this sentence on every lamppost all over the planet please

Fucking assholes

Spoonies with dogs, talk to me.

deadly-voo:

chronic-illness-support:

perfectparamour:

Can you walk them? Are they overwhelming? Do you need to have help to keep up with the care? Is it doable?

spooniestrong, spooniepets, maybe you can help?

I think that really depends on 3 things – 1) if you have a fenced back yard, 2) how much exercise your dog needs, and 3) how much well-trained / well-behaved the dog is. 

Personally, I have a small, non-shedding dog who is low-energy / doesn’t need much exercise, and he isn’t hard for me to care for unless I’m having a pretty severe pain day. He wasn’t house-trained when I adopted him, and house-training a dog takes a lot of energy (at least it does for a person with already really limited energy). 

People won’t always let you do this, but you meet a pup & fall in love it’s worth asking if you can take it home with you on a trial basis to see how the dog meshes with your home / schedule / etc. 

My original plan was to train him to fetch things for me if I didn’t have the energy to get them myself. That hasn’t worked so well. He’s clever, though, so I have hope.

He does need to be walked every day but he doesn’t mind if I can only manage a short walk. It keeps me active and gets me out of the house and these are, most days, good things. His bags of food are heavy, so I need help with that often. If I’m not feeling well he lies with me and makes me feel better.

It’s basically a breed thing. A larger dog will be stronger, but giant breeds need less exercise. Little dogs can be energizer bunnies. Older dogs might be spoonies themselves, so if you’re looking at a shelter that’s a factor. Short walks for them, but still get them out often because they need the change of scenery. (Balance that with the fact that they will cost more at the vet and will die sooner.)

Puppies will take all your energy. They have to be trained, and their energy doesn’t dissipate for a couple of years. You’re better off with an adult dog who has calmed down a bit and knows all the basics. Puppies are cute and all but they don’t understand “no” and you’ll be running after them saving things from their chewing for a while.

It’s very important that they’re well-behaved on a lead. They’ll pull you off your feet otherwise and hurt your arms. If you can get an adult dog who is already well-behaved on a lead, great; if you’re getting a puppy, really focus early on on this so when he’s bigger he won’t be a pain.

chutzpadik:

if your disability activism doesn’t support belligerent disabled people, disabled people who refuse meds or therapy, disabled people who don’t trust the system that’s fucked them over too many times to count—if your disability activisim depends on disabled people being nice or respectable or willing to be made into inspiration porn—it is not good disability activism.

katharinisabelle:

sammit-janet:

smeagoled:

Daniel Radcliffe talking about his old stunt double, David Holmes, who was severely injured during a stunt on the HP films

i didn’t know about this…

David’s story is actually one I haven’t seen mentioned often and it really should be:

David Holmes was Daniel’s stunt double for the first six Harry Potter movies, and he was set to be his stunt double for the final two movies, but while testing out a flying stunt (famous for being a very dangerous stunt in itself) for Deathly Hallows Part I, he was thrown against a wall, and fractured his neck. The incident left him paralysed for life from the chest down, with only limited movement within his arms and hands. Basically, he never let his disability affect his life, and he’s become an Appeal Ambassador for RNOH, the largest orthopaedic hospital in the UK, and he launched Ripple Production company with two friends who are also tetraplegic, specifically releasing several podcasts aimed at people who have suffered similar injuries and allowing them to cope.

iasg:

wow the infantilization of disabled people really sucks bc when i think of all the accommodations that could make school (and possibly even work) livable, all I can think of is how childish they all sound, let alone the fact that I need accommodations at all. 

idk there’s this idea that as an adult yr supposed to be able to tough through things 100% of the time but that idea is very harmful and wrong, even to non-disabled and neurotypical people.

livesandliesofwizards:

Everyone would have agreed it was a shame that two weeks passed before Professor Flitwick realized why the child’s feather was failing to rise. “Louder, boy!” he instructed, when he finally reached the far left corner of the classroom to observe the student’s wandwork.

“Wingar——dium leviosa” the boy had said.

“Don’t pause in the middle, say it smoothly, like this.” Professor Flitwick demonstrated, the feather floating gracefully up a dozen inches then settling back to the desk. “Again!”

“W-w-w-ingar—-dium le-le-lev—-”

And that was when the professor had nodded in understanding and quickly ushered the child to the infirmary.

“No wonder he’s been so shy since he arrived, the poor thing’s ashamed to speak,” he explained to a bustling Madam Pomfrey. She shook three drops of Graphorn Gall onto the terrified boy’s tongue—expensive, but worth it for the permanent fix—flicked her wand twice and spoke the explicare charm. There was a quick red glow across his chin, and a loud pop that made him startle. The boy reached up tentatively to his lips.

“There, let’s hear you now.”

“Wingardium leviosa,” the boy said quietly.

“Ah ha! Very good,” exclaimed Madam Pomfrey. “Back to class, you’ll have those feathers flying in no time.” She escorted them out with a smile, placed her vial of Graphorn Gall back on the shelf, and proceeded to forget the incident entirely.

She wasn’t there to see the boy’s shy eyes when he greeted his parents at King’s Cross in December, his mother gasping at his free-flowing words, his father’s cheeks damp with pride. And many years later, when she noticed a former Head Boy return to Hogwarts with special permission to access the charms library, she could not have recalled their first meeting.

No one saw him alone in the guest quarters that night, pouring over ancient magical-reversal texts, muttering one incantation after another with wand pointed to his lips. “This is my voice,” he repeated quietly between each attempted spell. “This is my voice.” Another flick of his wand. “Th-th-this is my vvvvvoice.”

No, Madam Pomfrey was peacefully asleep after another day of mending the broken. She didn’t hear the man’s long, deep exhale, or see his bitter smile.

(Written and submitted by littleredspaces. This comes with the author’s note: “A look at non-consensual healing and the erasure of disabled identities in the wizarding world.

I’ll confess, I had to check in with littleredspaces before I understood this fully, not realizing that I had blinders on, so used to my way of looking at the world that I couldn’t understand the horror here. I’m extremely grateful to littleredspaces for taking the time to explain, and, even more so, I’m grateful that this was written. It uses the trappings of the magical world to tell us a story that is decidedly not magical in any way, that is real and all too painful.)

letterstothrive:

How can you be both fashion forward and inclusive?

How can we change the way beauty is represented?

What does celebrating our bodies and being comfortable in our own skin look like? 

Join our BEAUTY & FASHION Google Hangout discussion with special guests! Feb 7, 3:30 p.m. EST

Message us with questions you’d love to see discussed about this topic and we may include them. Please reblog and mark your calendars! 🙂