someone commented on my video yesterday to tell me a brand told them that they don’t use disabled models because disability distracts from their products,
another made me aware that a brand told them that disability didn’t ‘fit their aesthetics’
(Cont in thread)
Ig @ luuudaw
I remembered being told that booking disabled models would be ‘too risky’.
There have definitely been increases in the use of disabled people in the media over the years,
but to know that this is still the attitude held by individuals at the top of some of the biggest companies and brands is honestly so disheartening and just plain horrible.
If your product is so forgettable that it would be unnoticeable on 15% of the population, if your ‘aesthetic’ doesn’t include the largest minority in the world, if it’s too much of a ‘risk’ to represent disabled people… then I’m not interested anyway.
Brands like these forget the huge spending power of disabled people, and how great the value of the Purple Pound is.
I think that this shows that it’s super important for disabled people to be seated around every table, not just in front of the cameras and on screens, but also in high up positions in businesses in order for disabled voices to truly be heard.
Disabled people deserve representation, and this representation should include disabled people from all intersections of society.
I’d be interested to know any brands or companies that you’ve seen work really well to support disabled people, and equally if you’ve had any particularly bad experiences that echo any of the statements at the beginning of this post, so I will know where not to put my 💜£ -
& one more photo for luck
• • •
Missing some Tweet in this thread? You can try to
force a refresh
Hi buds. London coffee festival messaged me apologising on Instagram
I’ll text back in 3 days I think I’m tired atm lol no offence and only a bit bitter and all that but feeling the damage is done currently. Always room for progress and time for improvement but I am a bit drained with it now
It’s great that when we speak up together and unite as disabled people stuff does get done but it’s just still shit that in those situations in public when you don’t have the #NEISvoid besties who understand you to help out, people don’t care. Sigh. Love u all thank you
Cropped the name cos it was very quickly deleted but. My parents ‘ALLOWED’ me to be sectioned for 3 months because neither one of them is a doctor. And they trusted what the doctors told them, why wouldn’t they? Isn’t that a doctors job? Don’t ever question my family’s actions.
My parents drove an hour every day to visit me and stayed in that psychiatric ward waiting room in despair for days in a row when I refused to see them and didn’t know who they were. They watched me dying in front of their eyes completely helpless. My parents did nothing wrong
You think my mum wasn’t awake every single night trying to find some sort of answers and make some sort of sense of it? She was told BY PROFESSIONALS to go and work out why I’d had a mental breakdown and so she put all of her energy into that. Sorry but this has made me so cross.
Ok talk time. I went to London coffee festival today. The brochure said ‘all levels are wheelchair accessible’. I was sent up stairs to enter (I have a paralysed lower leg and use mobility aids - I can just about manage stairs). Once inside I was in pain and needed to
use a lift - I couldn’t manage any more stairs. I am DISABLED and require accessibility. I asked 4 different people where the lift was. All of them passed me on to the next person. The final security guard laughed at me, pointed to the stairs and said
‘here you go, much quicker’. He could clearly see I had a walking stick and a leg brace but just laughed in my face and mocked me. I stood with a disgusted look on my face and spoke back to him - and all the others. For them to just legit offer me no solution at all
Today is the most important day of my year, #WorldEncephalitisDay 2021. #Red4WED
Encephalitis is the rare brain disease I had age 20, which was misdiagnosed as being a mental breakdown, left to worsen for 3 months in a psychiatric ward and ultimately led to me becoming (1/9)
permanently disabled, both visibly and invisibly.
It may be hard to imagine if you are a newer follower that there was a time just a few years ago that I couldn’t walk, talk, read or write – and by just looking at my pictures on Instagram, you’d probably have no idea that(2/9)
I am living with an acquired brain injury which has completely altered the direction and path of my life. I choose to speak about Encephalitis wherever I can, because I know that despite the fact that there are hundreds of thousands of cases of the disease worldwide per year(3/9)
lol someone just replied to the pic of my burn scar on my bum with this and I oopidoopidooooo. Why do some men?
Hey by the way. Scars aren’t ugly at all. They just aren’t. And also, if you think my scar is ugly then I am so sorry for having a brain disease and a big seizure and burning my bum on a radiator pipe I WAS CATATONIC SORRY silly ME
I’m so bored of all the nasty comments about my disability and body etc online atm. I’m replying to everything from now on with sorry for having a brain disease SILLY ME LOL