• Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Kate the (Almost) Great

Chronic illness blog

  • Home
  • Start Here
    • About
    • As Seen On
    • Tags & Topics
    • Popular Posts
  • Blogging Resources
  • Freebie
  • Shop the Blog
    • Products for the Chronically Ill
  • Contact & Work with Me
    • Ads and Sponsoring
  • Follow
  • Holiday
    • Gift Guides

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.

Share this with your family and friends:

  • Share on X (Opens in new window) X
  • Share on Facebook (Opens in new window) Facebook
  • Share on Pinterest (Opens in new window) Pinterest
  • Email a link to a friend (Opens in new window) Email
  • Share on LinkedIn (Opens in new window) LinkedIn
  • Print (Opens in new window) Print
  • Share on Tumblr (Opens in new window) Tumblr

Related

Previous Post: « July Blog Traffic Report
Next Post: Why You Should Just Write Your Damn Book »

Reader Interactions

Comments

  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.

    Loading...
    Reply
    • 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.)

      Loading...
      Reply
      • 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.

        Loading...
        Reply
  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.

    Loading...
    Reply
    • 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.

      Loading...
      Reply
  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.

    Loading...
    Reply
  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

    Loading...
    Reply

Trackbacks

  1. Kate the (Almost) Great | Boston Lifestyle Blog - Dating with Chronic Conditions | Kate the (Almost) Great, Boston Lifestyle says:
    August 14, 2017 at 8:02 am

    […] you’re concerned about continuing ableism, you can send them these posts: Everyday Ableism, Examples of Ableist Language in Everyday Life, and We Need To Talk about […]

    Loading...
    Reply
  2. Kate the (Almost) Great | Boston Lifestyle Blog - What You Should Know about Disability | Kate the (Almost) Great says:
    October 6, 2017 at 8:01 am

    […] I’ll leave these pieces here for you to read instead of repeating myself: Everyday Ableism, Examples of Ableist Language in Everyday Life, and On Inspiration […]

    Loading...
    Reply
  3. Kate the (Almost) Great | Boston Lifestyle Blog - How Is Chronic Pain Differerent from Acute Pain? | Kate the (Almost) Great says:
    January 18, 2019 at 9:23 am

    […] for Rheumatoid Arthritis Patients, Tools for Pain Management That Aren’t Medications, Examples of Ableist Language in Everyday Life, Why the Traditional Pain Scale Needs To […]

    Loading...
    Reply
  4. How Arthritis Affects the Body | Kate the (Almost) Great, Boston Blogger says:
    June 22, 2021 at 3:31 pm

    […] Beginner’s Guide: Infusion for Arthritis, Arthritis Glossary: Frequently-Used Words, The Lifestyle Changes I Made for My Rheumatoid Arthritis, Examples of Ableist Language in Everyday Life […]

    Loading...
    Reply
  5. 9 Ways To Advocate for Disability Rights says:
    September 3, 2022 at 10:30 am

    […] language we use affects other people, even if we think that it’s harmless. Learn more about everyday ableism in this post, which goes into more details about, well, everyday […]

    Loading...
    Reply
  6. Do I Have a Chronic Illness? Tips for New Patients says:
    January 21, 2024 at 8:55 am

    […] use affects other people, even if we think that it’s harmless. Learn more about everyday ableism in this post, which goes into more details about, well, everyday […]

    Loading...
    Reply
  7. The Art of Managing Anxiety | Kate the (Almost) Great, Boston Lifestyle says:
    February 9, 2024 at 6:34 pm

    […] The 3 Natural Anxiety Treatments I Use, Questions Not To Ask Someone with a Chronic Illness, Dating with a Chronic Illness, Examples of Ableist Language in Everyday Life […]

    Loading...
    Reply

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Primary Sidebar

Kate the (Almost) Great® is a chronic illness lifestyle blog. It is a resource for chronic illness patients and their loved ones.

  • Bluesky
  • Email
  • Facebook
  • Instagram
  • Pinterest
  • Threads
  • TikTok
  • Twitter

Categories

Health
Lifestyle
Writing & Blogging

Pages To Start With

  • About Kate the (Almost) Great®: Meet the Health Blogger
  • As Seen On
  • Contact & Work with Me
  • Follow
  • Health Blog Resources I Actually Use + Recommend
  • Newsletter
  • Popular Posts
  • Privacy Policy & Disclaimer Policy
  • Products for the Chronically Ill: My Recommendations
  • Shop
  • Start Here
  • Tags & Topics

Search

As an Amazon Associate I earn from qualifying purchases.

This blog uses affiliate links. Thank you for supporting Kate the (Almost) Great!

Sign Up for the Newsletter

Please wait...

Thank you for sign up!

Most Popular Posts

  • What Every POTS Syndrome Patient Needs for the Summer
  • 9 Arthritis Products That Help My Rheumatoid Arthritis
  • The Lifestyle Changes I Made for My Rheumatoid Arthritis
  • Beginner’s Guide: Rheumatoid Arthritis Flare Up
  • The Products I Loved (And Wanted) in Grad School
  • Seronegative Rheumatoid Arthritis Diagnosis: What I’ve Learned
  • What Is the Difference between Osteoarthritis and Rheumatoid Arthritis?
  • What Sjögren’s Syndrome Is: A Beginner’s Guide
  • What Does Arthritis Pain Actually Feel Like?


Bluehost.com Web Hosting $3.95

Health Union Patient Leader Certification

Support KTAG

If you like what I do, please support me on Ko-fi.




Footer

Sign Up for FREE Instagram Challenge

Get 25 FREE Instagram prompts for chronic health creators!

You can unsubscribe anytime. For more details, review our Privacy Policy.

Thank you!

You have successfully joined our subscriber list.

Get your FREE Instagram challenge here 

and 

For just $5 get your copy of my ebook Take Your Blog (And Income!) to the Next Level with code "greatest".

.

Kate the (Almost) Great

Chronic health lifestyle blog

Lets Go!
  • Facebook
  • Instagram
  • Pinterest
  • Twitter
Week 19 of #2026Weekly I’m not going to lie - my Week 19 of #2026Weekly 

I’m not going to lie - my life now focuses even more on maintaining my body. Trying to avoid foot surgery + keep my bone density up so I don’t break another bone for a while on top of all the other things I do to manage my 10+ illnesses … it’s a lot of work. I did go to actual work this week lol but my camera roll is all chronic illness stuff this week. 

1️⃣ The machine that will hopefully prevent surgery!!! Every day, I do 40 minutes of this ultrasound machine (20 min on 1 fracture, 20 min on the other) and it will speed up healing 🤞🏻🤞🏻🤞🏻 
2️⃣ Continuing my exercise routine per my endocrinologist. Up to 30 minutes of Pilates 4 days a week … and since I don’t do exercises requiring pressure on my feet, the cast comes off. 

◾ 

IDs:
1️⃣ Looking at an at-home ultrasound treatment machine 
2️⃣ Kate’s cast next to her yoga mat 

#Osteoporosis #RheumatoidArthritis #ChronicIllness #ChronicPain
I personally have rheumatoid arthritis, fibromyalg I personally have rheumatoid arthritis, fibromyalgia, and Sjögren's syndrome, which makes 3 forms of arthritis.⁣
⁣
May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
⁣
Like, comment, and share to spread awareness 💖 ⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⬛⁣
⁣
ID: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis means only 1 thing.⁣
Fact⁣
There are over 100 kinds of arthritis, including osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and more!⁣
katethealmostgreat⁣
⁣
#ArthritisAwareness #RheumatoidArthritis #Fibromyalgia #SjogrensSyndrome #Arthritis
SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
⁣
I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
⁣
If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
⁣
That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
⁣
For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
⁣
And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⬛⁣
⁣
IDs: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
⁣
#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

⬛⁣⁣⁣⁣⁣⁣

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⁣⁣.

⬛ 

IDs: 
1️⃣ Looking down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
⁣
Like, comment, and share to spread awareness 💖⁣
⁣
⬛⁣
⁣
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⁣⁣.⁣
⁣
⬛⁣
⁣
ID: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis only affects people as they age.⁣
Fact⁣
Arthritis can affect anyone at any age, including kids as young as 3.⁣
katethealmostgreat⁣
⁣
#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
⁣
*This is all just for me and my case!*⁣
⁣
1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⬛⁣
⁣
ID: A bunch of IVIG supplies, including a pump. ⁣
⁣
#ChronicallyIll #ChronicIllness #ChronicPain #AutoimmuneDisease #Autoimmune
Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

⬛⁣⁣⁣⁣⁣⁣

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⁣⁣.

⬛

IDs:
1️⃣ An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
⁣
Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
⁣
It's a lot. ⁣⁣⁣⁣
⁣
It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
⁣
This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
⁣
⬛⁣⁣⁣
⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
⬛⁣⁣
⁣
ID: Kate takes a selfie. She's a redheaded white woman wearing a gray sweater and pink glasses.⁣
⁣
#ChronicallyIll #RheumatoidArthritis #Fibromyalgia #Endometriosis #POTS
Follow on Instagram

Copyright © 2026 · Kate the (Almost) Great · Design by Studio Mommy

%d