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in Health &middot August 4, 2017

Examples of Ableist Language in Everyday Life

Unfortunately, our world is filled with ableism, or discrimination based on disability. A lot of it is in how we speak, and many people don’t know that they’re being ableist. I went on a little rant on Twitter a few weeks ago about examples of ableism in everyday life, and I thought that I would turn it into a blog post so I could explore some of those examples in more detail. Most of these are examples of ableist language, and some are just ableism in general.

In the spirit of transparency, this post does contain ableist language. I am, of course, calling it out, but you should know before you read further that this post contains it. You should also know that I talk about weight a little bit, as well as food and medication.

Related: Everyday Ableism

Did you know that you're probably discriminating against people with disabilities in your regular conversation? Ableism is thoroughly embedded in our society, especially in how we talk. Here are a bunch of examples of this, as well as why it's a problem, so you can work on eliminating ableism from your vocabulary.

Accusing someone of being mentally ill because they’re wrong about something or acting unbelievable (crazy, stupid, insane, moron, etc.) – This is one of the most common examples of ableism and I’m pretty sure (or at least hopeful) that people don’t realize that what they’re doing is comparing someone with a mentally ill or intellectually disabled person. Crazy and insane described people who were ill and were used in a derogatory manner. Similarly, stupid, idiot, moron, etc. described people with intellectual disabilities. When you use these words, you are comparing the person or event you’re discussing with disabled people.

Being angry because someone who parks in a handicapped spot (and has a disabled placard) can walk. – I have talked a LOT about how there are invisible disabilities, so I won’t restate that here. One thing I will say is that I can walk and “look” fine (depending on how closely you look) but am very much not fine. See: Not All Disabilities Are Visible

Calling someone lazy because they need more rest than you – Many people with disabilities, like ones with chronic pain, have limited energy. They need to conserve that energy.

Saying that if someone doesn’t go vegan they’re selfish – There are so many people out there with medical issues that prevent them from going vegan. In my case, I have already had to cut out so many types of foods that if I cut out animal products I would have almost nothing left to eat. Don’t shame people because they can’t go vegan.

Claiming that people are only going gluten-free to lose weight – This is also one of the most annoying things about cutting out gluten; so many people have asked me if it’s because of trying to lose weight. First of all, if you cut out gluten but don’t cut out carbs, you’re not going to lose weight because gluten-free carbs are still carbs. Second of all, there are LOADS of people who don’t eat gluten because their bodies hate it. I don’t have Celiac, but my RA attacks my body if I eat gluten.

Making fun of someone who has a lot of food substitutions in their order – Similarly, I’ve had to cut out a lot of foods because my body doesn’t like them. I can’t eat them! I don’t have a traditional allergic reaction like hives or anaphylaxis, but my body does attack me. It’s not my fault that I have to change a lot of what I order!

Calling the weather (or someone) schizophrenic or bipolar when things keep changing – This is similar to the first item in this post. Schizophrenia and bipolar disorder are mental illnesses, not comparisons for you to use.

Calling someone who needs trigger warning entitled or a snowflake – Would you call a veteran with PTSD a snowflake because they can’t be around fireworks? Combat zones aren’t the only things that can cause PTSD, first of all, and there are plenty of other people who need trigger warnings for very real issues. Someone who has battled addiction, an eating disorder, or something similar does really need that trigger warning. Also, someone who has epilepsy could be triggered to have a seizure if they watch a video with flashing.

[bctt tweet=”Ways that you might be discriminating against disabled people without realizing it.” username=”kmitchellauthor”]

Saying you have PTSD from something when you very clearly don’t – You went to the mall on Black Friday and joke that it gave you PTSD? Shame on you. This is a medical condition and loads of people already don’t believe that people have it from something other than a combat zone. You don’t need to contribute to that by joking about it.

Faking a limp so you can use your grandparent’s handicapped placard (and just using it in general) – YOU ARE WHY PEOPLE DON’T BELIEVE THAT MY DISABLED PLACARD IS MINE.

Parking in the handicapped spot without a placard or license plate or in the spot with lines through it – There are loads of people who need that spot, and you’re taking it away from them. If I’m having a bad pain day, a handicapped spot can be the difference between going somewhere and not going, and parking in it instead of having to trek across the parking lot can be what prevents me from ending up in the ER. Also, the spot with the lines needs to be left open for vans that are wheelchair accessible, so you can’t park there. As a friendly reminder, it’s also illegal and wrong to park in that spot with your hazards flashing.

Saying you have ADD/ADHD when you’ve clearly just had a lot of coffee – I hope by this point in this post you get that comparing your life without illness to a real medical condition is wrong.

Saying you have OCD because you like things to be orderly or clean – See above.

Accusing someone of faking their disability or illness (especially if for attention) – Dude, my dude, why are you doing this? You also need to keep in mind the situation in which you’re accusing someone of faking. Is it someone who has evidence of medical appointments, infusions, medications, etc., and you’ve seen them, like on social media? Definitely not faking. Is it someone who looks fine but is parking in the handicapped spot? See above. I got accused of this in high school and it hurt so much – and that was years before I got diagnosed with a chronic illness.

Saying that someone with a mental illness is faking that their fidget spinner/object helps them – Do you have ADD/ADHD or anxiety? You don’t get a vote. Close your mouth.

Telling someone that your pet is a service animal because you want to take them into a restaurant, store, etc. – Similar to above: YOU ARE THE REASON WHY SOME PEOPLE WITH SERVICE ANIMALS AREN’T TREATED SERIOUSLY. You are taking advantage of a system that is supposed to help people with disabilities and making the people with disabilities (aka the people who are supposed to be helped by that system) believed less.

Our society is full of ableism, or the discrimination against disabled people. These are 23 ways you might be exhibiting ableism, with explanations of why it's a problem. You might be really hurting disabled people without realizing it!

Disregarding someone’s food allergy – Why on earth would you do that? This is dangerous and wrong. Yet there are people who still do this.

Saying that someone is only disabled if they’re in a wheelchair or use an assistive advice – As mentioned above (and loads of times on this site), there are so many people with invisible illnesses. Most people who are disabled do not use an assistive device. 90% of the time, I do not look disabled, but I am.

Saying people are weak for needing medication or trying to get someone to go off their medication and do all-natural treatments instead – Every now and then, I get a comment or email from someone telling me that the chemicals I’m putting in my body are terrible and I need to try XYZ random treatment and I’ll be healed. Sometimes those things work for some people, but it does not work for me. I have to take all of my chemicals in order to be a functional human being, and if I didn’t, my autoimmune disease would advance to my organs. Everyone is entitled to choose the course of treatment best for them, and saying that someone should take all-natural treatments or that they are less because they need medications is so beyond wrong. (PS – Don’t suggest a random treatment to someone who hasn’t asked for advice or help. But that’s an issue for another day.)

Calling someone or something tone-deaf or blind because of something or a comment that ignores an issue – This makes me super uncomfortable. Again, this goes back to comparing something or someone’s behavior with an actual medical condition. Stop it!

Saying that a big bad issue “cripples” something else, ie a storm cripples the coast (Side note: I personally hate the word cripple) – This is using language describing a disability as a metaphor. At this point in this post, I really hope I don’t need to explain to you why that’s wrong.

Asking your friend with a narcotic prescription for some of their meds or joking about how that person just uses them to get high – Do you have any idea how difficult it is for someone with chronic pain to get a narcotic prescription? Not only is it illegal for them to give you some of their medication, but it’s also incredibly insensitive of their medical needs. It’s also incredibly insensitive to suggest that they use their medication for recreation and not necessity. For me, my daily narcotics are not strong enough for me to get high, which I’m thankful for because that means I can still be a person. I don’t like how my emergency medication makes me feel, but if I need that medication, I’m probably not well enough to do things any way. You can learn more about alllll of this in my posts on How Chronic Pain Patients Use Opioids, Being a Chronic Pain Patient in the Opioid Epidemic, and Chronic Pain Patients Aren’t Automatically “Junkies.”

Saying that you had a panic/anxiety attack when you just felt anxious – This is something else that negates the experiences of people with a mental illness. Feeling anxious is something that everyone experiences; a full-on anxiety attack is a miserable feeling felt by people with an illness. If someone has an anxiety attack, it might not be considered a serious thing by others because they think that person just feels anxious.

What are some other examples of everyday ableism?

Like this post? Check out:

Everyday Ableism, Not All Disabilities Are Visible, At Letter to the Mom Who Yelled at Me on the Bus for My Disability, On Inspiration Porn

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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  1. Emily of Em Busy Living says

    August 4, 2017 at 8:00 am

    My MIL still uses the phrase “retarded” in a joking manner. Drives me insane. I’m still catching myself using “crazy” sometimes even though I’m trying my hardest to remind myself constantly why I shouldn’t use it. I think with continued awareness many of these ableist phrases and actions will go the way of the use of “retarded;” it will take time and practice, but one by one people can remove themselves from being one of the offenders.

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    • Kate Mitchell says

      August 9, 2017 at 11:42 am

      Ugh, that’s so frustrating. My hope is that things will change a lot over the next decade or so. Also, not getting mad at you or anything, but do you realize what word you used in this comment that you probably shouldn’t have? (I found it kinda of hilarious considering the post and your comment.)

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      • Emily of Em Busy Living says

        August 9, 2017 at 12:23 pm

        Insane! Ahhh see, it’s so hard when things are used so carelessly for so long.

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  2. Sarah @ Back to Carolina says

    August 6, 2017 at 12:32 pm

    These are all SO true. I think that the general public could really benefit from this list. You did a great job explaining the “whys,” too!
    I never noticed the handicapped parking abuse until I really needed it. I’ve sat on the phone and had it out with a Jimmy John’s manager over their delivery guy cutting me off to take the last handicapped spot at the doctor’s office to make a delivery. I blocked the delivery guy in while I waited to talk to him.
    That was just the tip of the iceberg after a weekend of seeing people in downtown Charlotte parking in the off loading zones/clearly parking in handicapped spots without a tag bc parking was so crowded.
    I also get very bothered with the OCD thing and people off handedly saying they have a mental illness that they clearly don’t have.
    But, all of the things you listed are super important.

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    • Kate Mitchell says

      August 9, 2017 at 11:43 am

      Thank you so much! I’m very impressed you blocked the delivery guy in – totally necessary.

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  3. Leigh Ann Stratakos says

    January 28, 2018 at 6:18 pm

    Thank you for this very thorough post. Cleaning up my ableist language has been an ongoing process for me the last year or two. There are a few here that I was not aware of and will now pay attention. Thank you again, I’m sure there was a lot of emotional labor involved in writing this post.

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  4. John says

    April 2, 2021 at 8:59 pm

    I understand the reason crazy, insane, moron, etc are ableist because their origins refer to mental illness or disability. Stupid was surprising to me because I did not relate the definition of stupid to a disability before I read this. A look of the definition of stupid does not indicate it’s use as a medical condition or disability. I agree it’s not a term that should be used because it is not nice to begin with but appears to be somewhat of a stretch to categorize it under ableist

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Weekj 26 of 2026 Weekly Scenes of a summer week Weekj 26 of 2026 Weekly 

Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣⁣⁣

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1️⃣ Harley the golden retriever on a deck as seen through some plants
2️⃣ Kate takes a selfie
3️⃣ A duck with little ducklings following on a lake
4️⃣ Harley coming up to Kate. Her legs are out on an ottoman, 1 foot in a walking cast, and an in-progress needlepoint project
5️⃣ Looking down at a Mahjong table with the game set up
6️⃣ A kayak on the shore of a lake 

#MaineTheWay #MaineSummer #Needlepoint #MaineLife
Living with chronic pain is really hard. You’re wi Living with chronic pain is really hard. You’re winning every day you’re still here.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
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#ChronicIllness #ChronicPain #RheumatoidArthritis #Fibromyalgia #Endometriosis
I've been spending a fair amount of time at my foo I've been spending a fair amount of time at my foot surgeon's office this year, and boy has it been messing with my head. ⁣
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I spent a lot of time from 2001-2010 dealing with my left foot. Long story short, it took until this foot surgeon saw me in 2010 after fixing this foot for me to be diagnosed with rheumatoid arthritis. But I spent those 9 years going from doctor to doctor, having surgery after surgery, trying to figure out what was causing my pain and to fix it. ⁣
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Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
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I spent from age 10 to 19 unsure what exactly was wrong with me and in huge amounts of pain. We thought we figured it out, and then something else happened. ⁣
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We know exactly what is wrong with this foot this time around: in 2024, I got 3 stress fractures, and no one put me in a boot. They almost fully healed before breaking in 2025, and then the same thing happened in 2026. ⁣
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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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PTSD is a bitch.⁣
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(PS - if you want to know why I'm going back to this guy when it messes with me, it's because I don't trust anyone else to fix my foot.)⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: Kate takes a selfie in a doctor's office. ⁣
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#PTSDAwareness #ChronicallyIll #TarsalCoalition #RheumatoidArthritis #Osteoporosis
Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣⁣⁣

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1️⃣ Looking at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
2️⃣ Birds arriving at a bird feeder as seen through a window

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What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and more. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Things I Do Every Day for My Chronic Illnesses⁣
Take pills at least 4 times a day⁣
Don’t eat gluten, dairy, corn, soy, or eggs⁣
Sleep 7+ hours a night⁣
Consume 80-100 grams of protein, 120 mg of calcium, 5-10 grams of sodium⁣
Wear a mask whenever I leave the house⁣
Do pilates 4+ days a week⁣
Work from home⁣
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#ChronicallyIll #InvisibleIllness #RheumatoidArthritis #Fibromyalgia
Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

Video: Kate talks to the camera while holding a purse. She holds up individual items mentioned in the video before putting them in the bag. There are captions. 

#ChronicallyIll #RheumatoidArthritis #Osteoporosis #ChronicPain
There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: A Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣

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1️⃣ Kate takes a selfie. Her new glasses are thin silver circles
2️⃣ An in-progress cross-stitched alphabet in a special hoop stand that Kate is sitting on.
3️⃣ Kate takes a selfie in an infusion chair.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
Week 22 of 2026 Weekly 1️⃣ Off to see my foot doc Week 22 of 2026 Weekly

1️⃣ Off to see my foot doc … and my foot is healing! Yay!
2️⃣ A very cool notification to get!
3️⃣ This is 35 🎂
4️⃣ Featuring Harley snuggles 
5️⃣ And then it was my mom’s birthday! 
6️⃣ With Harley again 

ID: 
1️⃣ Kate takes a mirror selfie 
2️⃣ a notification from WordPress saying “Receive views from 150+ counties. The United Nations has nothing on you!”
3️⃣ Kate smiles for the camera in a cafe 
4️⃣ Kate in the same outfit with Harley the golden retriever on her lap. 
5️⃣ Kate’s mom smiling in a restaurant 
6️⃣ Kate with Harley again 

#GoldenRetrieversOfInstagram #ChronicallyIll #ChronicPain #InvisibleIllness
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