• 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
  • Work with Me
    • Ads and Sponsoring
  • Follow
  • Holiday
    • Gift Guides

in Health, Uncategorized · June 19, 2014

How Many Spoons Do You Have?

No, I’m not asking you to go count your silverware drawer, although you’re more than welcome to if that’s your thing. I’m talking about spoon theory.

spoon theory

What is spoon theory?

For those of you who aren’t familiar with it, spoon theory is a way to help explain/understand living with chronic illness. Feel free to go right ahead and click that there link for the full story. If you don’t have the time or aren’t interested enough, here’s the long and short of it: the difference between being sick and healthy is that people who are sick “have to make choices or consciously think about things when the rest of the world doesn’t have to.” In essence, people who are sick have a certain number of spoons to use in a day. It takes a certain number of spoons to get out of bed, shower, walk downstairs … basically all the normal parts of a day. It takes even more spoons to go walk around the block or run errands. (Seriously, go read Christine Miserandino’s explanation of spoon theory, since she came up with it. Do it.)

spoon theory
Source

Spoon theory came into existence because Christine has lupus. It has helped countless numbers of people with illnesses/conditions/disabilities explain what their life is like to other people. For example, you may see me eating breakfast and wonder why I’m already so sluggish and hurting. But I know that I had to give up a spoon to get out of bed, another to walk down the stairs, a handful to do yoga, and another one to make my breakfast.

Contrary to what you might be thinking, though, explaining spoon theory is not the main focus on this post. So now those of you who haven’t heard of it before have it explained, and those of you who have should be ready for the next portion of this post.

Who gets to use spoon theory?

spoon theory meme
Source

There has been some debate in the chronic illness community over who gets to use spoon theory. Since it was developed by someone who has lupus, it has always applied to those who have autoimmune diseases. It also applies to anyone who claims the umbrella term “sick,” as Christine uses that term in her explanation.

The real debate comes from whether or not people with mental illness get to use spoon theory. Some people who have a physical illness are deeply offended when someone with mental illness uses it.

I can understand both sides of the argument, but I am inclined to lean towards one. Many people from the physical illness side don’t see how spoon theory can apply to mental illness. (For the sake of my typing and your reading, I’m going to abbreviate. PI = physical illness and MI = mental illness, cool?) Some people with PI also see those with MI claiming spoon theory as encroaching on their space.

Because let me make this extremely clear – it is not okay to use spoon theory if you are a normal person not dealing with a chronic health concern that affects your day-to-day abilities. The entire point of it is to explain to people who don’t deal with it what life is like. It does not apply to you if you do not fall under that category. Do not use it. Do not claim it. Even if you are joking, please do not use it. It may not seem like much to you, but we take it very seriously.

It might seem silly that people with PI (including myself) feel so strongly about it. That is because spoon theory is something that has united people with chronic illness – we call ourselves spoonies. You may have seen me use #spoonie on some of my tweets. That’s because this is an identifier used across the world for people living with chronic pain/illness.

I can understand why some people are really against those with MI using spoon theory. In fact, when I first heard that people with no PI whatsoever were using it, I felt pretty upset. And then I thought about it.

I don’t know a lot about many different MI, but I do know about anxiety and depression, and I can see how spoon theory can apply there. It is incredibly impressive for someone with severe depression to get out of bed, have a shower, and walk down the street to get a cup of coffee. I know that if my anxiety is bad, there’s only so much I can take. I have a whole lot more spoons for anxiety than I do for pain, but I can see that the theory can apply there.

Like I said, I don’t know a lot of a lot of different mental illnesses. But in my opinion, if the theory can apply to two of them, it can apply to others.

So. What’s your take? Do you think that spoon theory can apply to mental illness? Do you think that it should? 

My most recent video | Send me questions about self-publishing | Self-Publishing Sunday posts

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:

  • Click to share on X (Opens in new window) X
  • Click to share on Facebook (Opens in new window) Facebook
  • Click to share on Pinterest (Opens in new window) Pinterest
  • Click to email a link to a friend (Opens in new window) Email
  • Click to share on LinkedIn (Opens in new window) LinkedIn
  • Click to print (Opens in new window) Print
  • Click to share on Tumblr (Opens in new window) Tumblr

Related

Previous Post: « Maine Weekend Recap
Next Post: Self-Publishing Sunday {Week 11}: Q&A 2 »

Reader Interactions

Comments

  1. Kendra Loisel says

    June 19, 2014 at 8:34 pm

    I never really understood how the spoon theory could apply to MI but I was watching a show and it was about someone with extreme anxiety and depression. I found myself crying along side her because she was explaining what I would go through. Maybe not exactly, but there were days she couldn't get out of bed for hours, or even leave her house. While I don't think the Spoon Theory applies to everyone with MI, I think it does in a small way. Where we use it in reference to physically not being able to do things due to pain and it wearing us thin, they feel their pain in a different way. I think at the end of the day it's so hard for all of us to accurately describe what we are going through to those without PI or MI, that the Spoon theory in a way works for them too. Anything to help them express what thy are feeling works for me.

    Loading...
    Reply
  2. Marla Rogers says

    July 1, 2014 at 5:42 pm

    I don't have PI or MI, but some of the people in my life who I'm closest to suffer from MI and it really really upsets me that there is so much stigma in society about it. Illness is illness…mental or physical, it doesn't matter. The point is that the person is suffering in a way that "normal" people don't. MI is debilitating just as PI is…I've seen my dear ones unable to get out of bed for hours or even find a purpose in being alive anymore and I know it's really a struggle for them to see through their black clouds. I don't think there's a need to be on two different teams…PI/MI should be there to support one another in any way possible.

    Loading...
    Reply
  3. Natalie B. says

    July 2, 2014 at 4:19 am

    I was so excited when I saw this post. I have definitely heard and read about spoon theory. I suffer with two chronic physical illnesses but also severe depressive episodes. I believe it could apply to MI only if it's in a severe category. People with mild depression and mild anxiety can still function. They can still work and be productive. From my personal experience with MI, when I'm in these episodes, I have even fewer spoons than I do with my PI. Does that make sense? I would certainly be personally offended if someone joked about it or was a working functioning person with a mild mental illness and claimed to be a spoonie. Thank-you for this wonderful post!

    Loading...
    Reply
  4. Nisha says

    May 9, 2016 at 12:28 pm

    This is a pretty old post now, but I have PI and MI. Both feel like torture and the PI makes the MI so much worse. But for me personally, I have way more spoons for the PI than the MI. The PI is so awful but with MI, I don’t even have a will to live, so the spoons are one or less a day. I would be more insulted by people saying that people with mental illness cannot use the spoon theory. They can – and should. There’s nothing made up or less valid about a mental illness it is still a medical illness and not any less real than a chronic illness, nor less serious, nor more curable. I find myself often trying to figure out if I’m more depressed about my chronic pain or my mental pain. My spoon supply is almost nil. I actually remember when I first noticed there was something wrong with me physically, I wanted to get up and walk about 8 feet to the kitchen and couldn’t really do it. Before that I used to exercise six hours a day with no problem. I’ll never understand why it happened so suddenly, my doctors don’t understand it either. I have 3 sources of chronic pain and 5 mental illnesses, 3 of which decrease energy. With the pain, somethimes I can literally barely walk. With the mental illness, most times I cannot bring myself to move a single part of my body. They are both terrible and I wouldn’t wish either on my worst enemy, but there is no way that chronic pain is worse. Mental illness is chronic illness and shouldn’t be seen any different.

    By the way, I love this post and this blog overall is immensely helpful. Thank you. 🙂

    Loading...
    Reply
  5. CM says

    July 19, 2016 at 11:34 pm

    Honestly as a mental health professional, and someone who learned of spoon theory through a book written by someone suffering with MI, it makes me upset to think that those suffering with PI would not want those suffering with MI identifying with this theory. It’s a statement about our society and their value of physical health over mental health (both of which I think are very important please don’t get me wrong!!). I think that working with people with serious mental illness (SMI) it’s clear to me that people with mental illness have a limited number of spoons. For someone with anxiety they hoard their spoons for fear that giving too many will leave them with nothing. And so maybe they don’t leave their house. And maybe they’re unable to care for themselves. Or maybe their anxiety is more low level and they have enough spoons to go to work or care for their children. But not both. For those with depression leaving their bed is sometimes an insurmountable feat with the same issues as anxiety. For someone with Bipolar disorder they have this abundance of spoons during their mania and they throw these spoons into things like wrenches in a machine until they hit a wall of depression and they’re left with no spoons and sometimes a ruin of a life. Those with schizophrenia may give their spoons to delusions and hallucinations and are unable to give them to their loved ones and their activities of daily living. In some ways I think that people suffering with PI have it easier because people are much more understanding of physical pain even if it is invisible. When someone is suffering with MI it is much more difficult for their loved ones to understand because they should be able to just do the things they need to do. But sometimes they don’t have the spoons. By letting those with MI into the ‘club’, by letting them explain their struggle the way that you do yours, maybe it would help break that stigma and help people understand MI more. Pain is pain whether it is physical or mental.

    Loading...
    Reply
  6. SA says

    September 6, 2016 at 4:34 pm

    I suffer from both PI (tumoeffective MS) and MI (severe depression). I feel like the depression requires as many, if not more on some days, spoons as my PI. if I’m having a bad pain day but feeling lucid, I’m almost always better off than the other way around.

    Loading...
    Reply
  7. SweetPea says

    September 24, 2016 at 12:13 pm

    Honestly, I don’t think this theory is about being in a club. Support is important, yes. And people who use this term to get sympathy from others when they have no reason to, is just wrong on so many levels. But the whole point of it was to try to explain to loved ones, in an effective manner, what you are going through with a crippling health issue (be it physically or mentally) that may not be physically evident from your outside appearance. Most often a mental issue fits this bill better then one involving say, pain. (Not trying to discredit pain sufferers, at all.) I’m just making the point that someone with pain is still going through a physical symptom. Doctor’s are gong ho about treating pain. But try finding a doctor to treat PMDD. It’s near impossible. And I fear my PMDD more then I do my pain. Mental illness is all but invisible in the body, however crippling it is. And it is crippling. It can destroy all kinds of relationships, motivation for living, and joy in life. The over all point is that the spoon theory is an easy to digest conversational tool that can help to build bridges in our relationships with those around us. When you have a severe health problem those relationships can be few and far between and anything that can help you keep those bonds strong in a positive manner is worth being invested in. The visual cues of spoon jewelry for instance are a fantastic way to lead into these conversations and can be a positive reminder for us to know our limitations. Work with them and still achieve our goals. Our goals only being the most important aspects of our lives because we don’t have spoons to spare!

    Loading...
    Reply
  8. Joanne Fletcher says

    October 12, 2019 at 10:39 pm

    Usually chronic illnesses come hand in hand with mental illnesses. They are so closely linked there’s no way to compare. Having had both, I’d say mental illness requires FAR more spoons.

    Loading...
    Reply
  9. Lilac Giraffe says

    July 25, 2020 at 5:57 pm

    One thing that hasn’t been mentioned is that chronic, unexplained pain is often a symptom of depression. So, just like PI often goes hand in hand with MI, the opposite is true as well. I feel anyone with a debilitating disease can and should use spoon theory, if it helps. Great article!

    Loading...
    Reply

Trackbacks

  1. Living with Chronic Illness and Accepting Your Body says:
    January 14, 2016 at 8:00 am

    […] point in spend a large amount of time angry with my body. If I only have a certain number of “spoons” per day, I would rather spend them in physical therapy than by hating my […]

    Loading...
    Reply
  2. Kate the (Almost) Great | Boston Lifestyle Blog - Don't Say "It Could Be Worse" - Kate the (Almost) Great | Boston Lifestyle Blog says:
    October 21, 2016 at 8:00 am

    […] illness. It’s often said when a chronically ill person – who I’ll refer to as a spoonie here, and you can click that link to learn more about what that means – tells a healthy […]

    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
  • Twitter

Categories

Health
Lifestyle
Writing & Blogging

Pages To Start With

  • About Kate the (Almost) Great®: Meet the Health Blogger
  • As Seen On
  • 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
  • Work with Me

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!


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
Having decades-long health problems sometimes mean Having decades-long health problems sometimes means coming across something in your health history that you completely forgot about⁣
⁣
◾ ⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣◾ ⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣ID: Screenshot of a thread post written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat. ⁣⁣The background is dark teal. All text is what’s above the first black square.⁣⁣⁣
⁣
#AlmostGreatHealth #rheumatoidarthritis #arthritis #spoonielife #healthblogger #autoimmune #autoimmunedisease #chronicallyill #healthblog #dysautonomia #fibro #fibromyalgia #endo #chronicallyill #disability #disabled #invisibleillness #spoonielife #healthblogger
Here are some ways I practice self care, aka talki Here are some ways I practice self care, aka talking care of myself AND who I am as a person separate from illness⁣
⁣
This is my Wonderful Things jar. Every day, I write down something wonderful or good that happened that day. ⁣
⁣
I know it looks like I'm forcing Harley to sit like this, but he was making this face before I put my arm around him. Dog snuggle time is the best!⁣
⁣
I got a Kindle this year and it has been amazing. It's so much easier on my body than lugging around books and it makes borrowing from the library a lot easier.⁣
⁣
Yes, I share this all the time, but filling my pill boxes every 3 weeks make it so I stick with all of my medications. But the self-care part of this is that I don't have to take the time to refill a box every single week.⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
IDs: ⁣
1️⃣ A glass jar on a desk with a lot of multi-color post-its inside⁣
2️⃣ Kate has her face in a golden retriever who is slumped onto her. They're in a teal room with a red rug. Kate is a brunette white woman wearing red pants and a gray sweater.⁣
3️⃣ A Kindle on dark mode in Kate's lap⁣
4️⃣ 3 open pill cases on a yellow bedspread ⁣
⁣
#AlmostGreatHealth #AlmostGreatLife #SelfCare #ChronicallyIll #ChronicallyAwesome #SpoonieLife #Spoonie #ChronicLife #ButYouDontLookSick #InvisibleIllness #MentalHealthMatters #RetrieversOfInstagram #Readers #Kindle #WonderfulThings #GratitudePractice
What I Bring To the Doctor _______ Video: a pa What I Bring To the Doctor 

_______ 

Video: a pan of an exam room. White text reads “What I Bring To the Doctor ” and the “1. Planner/notebook
2. List of current medications 
3. Notes on my biggest concerns and questions 
4. My kindle for wait time” 
The intro to Maroon 5’s Priceless plays. 

#AlmostGreatHealth #ChronicIllness #ChronicPain #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #Endometriosis
💃🏼 Week 17 of #2025Weekly 💃🏼⁣
⁣
1️⃣ She’s married!! ⁣
2️⃣ She married the best person in the world for her!!!!!⁣
3️⃣ I got dressed up! ⁣
4️⃣ The reality of doing fun things with chronic illness and pain is that then you have to recover from the fun things. It took … a while. One million percent worth it, but this is why I don’t do big events on a regular basis. ⁣
5️⃣ And then I had to be a person again for an appointment!⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
IDs: ⁣
1️⃣ Kate stands hugging Emmie. They're both white woman. Emmie is in a wedding dress and Kate is in a red dress and wearing round tortiseshell glasses.⁣
2️⃣ Kate and Emmie stand next to Matt, Emmie's husband. He is a white man.⁣
3️⃣ Kate takes a mirror selfie. she's in the same red dress but now also wears a jean jacket and holds a cane and mask.⁣
4️⃣ Kate takes a selfie while giving a thumbs up. She looks tired. She's now wearing a pink flowery dress. ⁣
5️⃣ Kate takes a mirror selfie. She's wearing black shorts, a gray shirt, a jean jacket, a blue mask, and black aviator sunglasses. She has a bag over her shoulder and holds a cane.⁣
⁣
#AlmostGreatHealth #AlmostGreatLife #ChronicallyIll #InvisibleIllness #SpoonieLife #RheumatoidArthritis #RheumatoidDisease #Autoimmune #ButYouDontLookSick #AutoimmuneDisease #SpoonieLife #InvisibleIllness #DisabledAndCute
On the one hand, you should always believe what pe On the one hand, you should always believe what people tell you about their bodies.⁣
⁣
On the other hand, I’ve had so much ridiculous and unconnected health things happen that I do understand why people might not believe me.⁣
⁣
◾ ⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
◾ ⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣ID: Screenshots of a thread posts written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat. ⁣⁣The background is dark teal. All text is what’s above the first black square.⁣⁣
⁣
#AlmostGreatHealth #ChronicallyIll #ChronicPain #Autoimmune #AutoimmuneDisease #RheumatoidArthritis #RheumatoidDisease #SpoonieLife #InvisibleIllness
Last week, I talked about how it surprised me how Last week, I talked about how it surprised me how systemic autoimmune arthritis can be. But something else that surprised me was how much pain can be caused by small things.⁣
⁣
In this picture, I was getting ready to have an MRI on my knee. It has been bothering me a fair amount the last 6+ months, so I'm trying to do something about that. ⁣
⁣
Unsurprisingly, some of the tissue is damaged, but it's not bad. What's probably causing it to bother me so much is a teeny tiny cyst. ⁣
⁣
Baker's cysts are a type of cyst in the knee that are generally caused by arthritis. But having a cyst in my knee means that it's causing pressure on that damaged tissue. ⁣
⁣
The body is a weird thing, and one of these weird things is developing tiny cysts that cause a lot of pain. ⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣
⁣
◾⁣⁣⁣⁣
⁣
ID: Kate takes a mirror selfie. She's a brunette white woman wearing a hospital gown, scrub bottoms, black mask, round tortoiseshell glasses, and round tortoiseshell glasses. ⁣
🌸 Week 16 of #2025Weekly 🌸 ⁣ ⁣ 1️⃣ S 🌸 Week 16 of #2025Weekly 🌸 ⁣
⁣
1️⃣ Spring has sprung … ⁣
2️⃣ … Which means I am overheating! ⁣
3️⃣ A quick view of NYC on my travels ⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
IDs: ⁣
1️⃣ A flowering tree on a street ⁣
2️⃣ Kate takes a mirror selfie. She's a brunette white woman wearing a blue t-shirt saying "The Future Is Accessible," a black mask, a green hat reading "Facilities Management), black shorts, a black knee sleeve, and a black knee brace. She holds a pink cane.⁣
3️⃣ A picture of the New York City skyline behind a bridge.⁣
⁣
#AlmostGreatHealth #AlmostGreatLife #ChronicallyIll #RheumatoidArthritis #SpoonieLife #Autoimmune #AutoimmuneDisease #ChronicPain #Arthritis #RheumatoidDisease #Dysautonomia #PosturalOrthostaticTachycardiaSyndrome #POTS #InvisibleIllness
If I met my newly diagnosed self for coffee ... ⁣
⁣
I tell her how things would get worse before they got better. ⁣
⁣
I'd tell her to stop eating gluten, dairy, corn, soy, and eggs immediately (although that would have been a lot harder in 2010, more than it even is now). ⁣
⁣
I'd tell her that she still needs to keep advocating for herself. ⁣
⁣
I'd tell her that having a diagnosis unfortunately doesn't mean everything automatically falls into place. ⁣
⁣
I'd tell her that she'll develop many more illnesses but her quality of life will actually get significantly better. ⁣
⁣
I'd tell her that she would eventually have to get her right foot fixed, although she does expect that.⁣
⁣
I'd tell her that using a cane is not a sign of failure, but a tool to make life better.⁣
⁣
(I did a sort of tongue-in-cheek post about this a while ago and thought I'd post a more serious one).⁣
⁣
◾ ⁣
⁣
⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
◾⁣
⁣
ID: Kate poses for the camera holding a mug with the letter M on it. Kate is a brunette white woman wearing a blue sweater and round tortoiseshell glasses. A white text box reads "If I met my newly diagnosed self for coffee ...". ⁣
⁣
#AlmostGreatHealth #RheumatoidArthritis #RheumatoidDisease #ChronicallyIll #Autoimmune #AutoimmuneDisease #AutoimmuneArthritis #Rheum #InvisibleIllness #Arthritis #ButYouDontLookSick #ArthritisWarrior #CureArthritis
The thing that surprised me the most about autoimm The thing that surprised me the most about autoimmune arthritis is how systemic it is. ⁣
⁣
Like with most things, it's one thing to know the fact and it's something else to experience it. ⁣
⁣
Yes, my joints are affected (a lot). ⁣
⁣
But I've had enough serious infections thats I have to see an immunologist because we need to be aware of my antibodies and I sometimes need help recovering from illnesses. ⁣
⁣
And, yes, I see pulmonology because of my asthma, but we also have to keep an eye out on developing rheumatoid nodules in my lungs. (So far so good!)⁣
⁣
Not to mention that, when I developed POTS, the hospital admitted me to run every heart test to make sure that, at 26, I wasn't experiencing heart failure. ⁣
⁣
Plus, when I developed endometriosis, I also went through a number of GI tests because one theory was that I had ulcerative colitis. ⁣
⁣
Anyway, RA is so much more than "just" joints. If it wasn't, I wouldn't have to kill my immune system every 3 months like I am in this picture.⁣
⁣
◾⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣
⁣
◾⁣⁣⁣⁣
⁣
ID: Kate takes a selfie in an infusion chair. She is a brunette white woman wearing a Boston Red Sox shirt, blue mask, and round tortoiseshell glasses.⁣⁣
⁣
#AlmostGreatHealth #RheumatoidArthritis #RheumatoidDisease #Rheum #Autoimmune #AutoimmuneDisease #InvisibleIllness #ButYouDontLookSick #Sjogrens #SjogrensSyndrome #POTS #PosturalOrthostaticTachycardiaSyndrome #Dysautonomia
Follow on Instagram

Copyright © 2025 · Kate the (Almost) Great · Design by Studio Mommy

%d