Disabled people want to be included, but often we aren’t because not everything in life is accessible, and sometimes your disability prevents you from being able to participate in the same activities as your non-disabled friends. As a disabled person, I have accepted the fact that there are going to be some activities I can’t do, and that is okay because I am not bothered by every activity my disability limits. I am bothered when I am not invited to things that non-disabled people are. Most of the time I don’t think people are intentionally not including me and think a lot of the time people don’t think about it or know how to support their disabled friends. Disabled people often feel alone and isolated because their non-disabled friends will never fully understand what it’s like to be disabled and often when people see you have a disability you are treated like a charity case. Disabled people need more support than non-disabled people because we live with more challenges than most people and supporting your disabled friends is not as hard as people think. How do you support your disabled friends? In this post, I am sharing a few ways you can support your disabled friends.
Ask if we need help- As a disabled person with a physical disability, I need more help than most people because I can’t do a lot of things that require me to stand for long periods of time, and sometimes it’s easier to have other people do those things for me. I will ask for help if I need it, but I don’t always need it, and one of my biggest pet peeves is when people assume I need help and do a task for me without asking. There is nothing wrong with asking if a disabled person needs help, but don’t be that friend who assumes that I always need help and can’t do anything for myself, because disabled people hate that. Ask disabled people if they need help, and don’t go ahead and do it anyway after we have said we don’t want your help because it’s not helpful when you do things for me without permission and takes away the little independence I do have. I may struggle to get a glass of water, but I will never improve that skill if you always insist on doing it for me, because I learn how to work through barriers by doing things myself. Forcing help on a disabled person can be dangerous and can cause falls, and if we say we don’t need help, listen to us.
Before going somewhere check the accessibility- People sometimes think that checking the accessibility of a restaurant should always be the responsibility of the disabled person because we are the ones with the disability, but advocacy is not just for disabled people and non-disabled people should also be advocating for their loved ones. I am always thinking about accessibility and will advocate for myself, but I hate always being that person who has to disappoint everyone by telling them the restaurant they chose is not wheelchair accessible. Before you hang out with a disabled person check the accessibility because I love it when my non-disabled friends are proactive and check the accessibility of the movie theatre before I have gotten a chance to. It shouldn’t always be the responsibility of disabled people to advocate, and it shows you are a supportive friend when you check the accessibility without being asked.
Be mindful of your surroundings- When you have a physical disability, it is harder to move around than it is for non-disabled people, and there is nothing more frustrating than when someone dumps clothes in the middle of the floor that create even more barriers. As a disabled person, I do not think that non-disabled people are intentionally trying to create barriers when they spill water and leave it, but most of the time, I think people don’t think about how these things can be potential barriers for disabled people and cause falls. There are going to be times when things are going to be in the way, and there aren’t a lot of places to move them, but if you can eliminate obstacles, please do because it helps your disabled friend tremendously. Non-disabled people often aren’t as good at recognizing when something is a barrier for disabled people because disability doesn’t affect them, but if you know a disabled person and want to make their life easier, it’s important that you be more mindful of your surroundings.
Don’t try to relate to my disability- I have had many friends who have tried too hard to relate to my disability, because people often think that is what you should do but you can’t relate to something you have never experienced and that is okay. Be there for your friend and don’t try to relate to a disability you have never experienced, because I know you don’t understand my disability and will roll my eyes when you claim to be an expert. Disabled people don’t need their friends to relate to their disability, and you are actually being less supportive when you claim to be an expert because I know you are not. There are a lot of other things you can talk about with disabled people that we both can relate to, and my disability doesn’t have to be one of them.
Don’t talk to disabled people like children- Non-disabled people often talk to disabled people like they are children or are stupid. Some disabled people have more intellectual challenges and may struggle with having a conversation more than others and sometimes you have to talk slower, but a vast majority of disabled people can have a conversation without difficulty. Please stop talking to disabled people like they are children because most disabled people have average intelligence and can have a conversation just as easily as non-disabled people can. The only time you should talk to a disabled person like they are a child is if we are a child; otherwise, it’s probably unnecessary. When you talk to a full-grown adult who happens to be disabled like a child, it makes us feel stupid, and if you want to support your disabled loved ones, you have to treat us like we are actual people.
Do not touch my assistive devices without permission– There is absolutely no reason you need to be touching my assistive devices, and you should always ask disabled people before picking them up. Please do not touch my assistive devices without permission because my assistive devices are part of me, and it’s a violation of someone’s personal space. If I have given you permission, it’s okay to pick up my crutches, but don’t pick them up because you think they are cool.
Educate yourself on my disability- I love it when my friends take the time to learn about my disability because it tells me that you care about the challenges I face and want to help. People sometimes wait until disabled people tell them something about their disability, but you don’t have to wait because the Internet makes it easy to learn anything. I don’t expect my friends to be experts on Spina Bifida, but it does make me happy when people ask questions and take the time to educate themselves.
When you are disabled, it is harder to find friends because people often judge disabled people before meeting them, but it’s not as scary to be friends with a disabled person as people think it is, and we are just normal people that needs a little extra help sometimes. Supporting your disabled friends can be quite simple, and it can be as easy as checking the accessibility and asking if there is anything you can do to make my life easier, instead of assuming that I can’t do anything. As a disabled person, I don’t appreciate when people assume my abilities and go ahead and do things for me after I have said no, but I do appreciate it when people ask if I need help because sometimes, I can’t do something myself and need assistance. Listen to disabled people and try not to be ableist because ableism negatively affects disabled people, and it means so much to me when I see people educating themselves on ableism. How do you support your disabled friends? If you liked this post, please leave a comment below and share it with your friends.
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Dear Sarah, This is an important post …. a good reminder. The sentence that strikes me most is this:
”…advocacy is not just for disabled people …”
Thanks!💕
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You’ve got some great tips here! I would add a couple, from my perspective with a chronic immune disorder:
Excellent post –
Sue
<a href=http://livewithcfs.blogspot.com/>Live with ME/CFS</a>
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Great things to add! I don’t have a chronic immune disorder and didn’t think of those things.
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