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in Health &middot October 21, 2016

Don’t Say “It Could Be Worse”

I’ve dealt with a lot of crap over the past 15 years of health issues. I got to the point where it annoys me when people don’t believe me but then I move on. But there are still a few things that really tick me off: doctors who talk down to patients, people who assume that because I still do things sometimes I’m not actually “sick,” and when someone says, “Well, it could be worse.” Oh goodness how I hate that phrase. So let’s talk about why you shouldn’t say that to someone who has a chronic illness and what to say instead.

Often, people don't know what to say to chronic illness patients so they tend to say, "Well at least it could be worse!" Here's why you shouldn't say that and what to say instead.

Why people say, “It could be worse.” – Generally, they’re trying to be comforting. They don’t know how to deal with the situation, and they don’t know what to say to someone who has a chronic 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 person about their illness/condition for the first time, mentions an increase in their symptoms, or discusses a large, negative event from their condition. In these moments, a healthy person who may not have ever had health problems like that before, is often at a loss of what to say. They don’t know how to relate to or improve the mood of who they’re talking to, so they say what they know: “Well at least it isn’t worse! It could always be worse!”

What it generally means (even if that’s not what is intended) – Unfortunately, the message that comes across is, “What you’re feeling right now is not that bad.” I understand that this is intended to be comforting. However, it puts down what the spoonie is feeling. It says, “Why are you complaining about this when it could be worse? Why aren’t you glad that it isn’t worse?” Obviously, this isn’t what is usually intended by the people who say it, but it doesn’t change that this is what many spoonies hear.

Last year, I asked spoonies to send me quotes of the ridiculous things people have said to them over the years. Several people (at least 5) told me variations of, “It could be worse.” Saying this to people is hurtful because what you’re saying is, “You don’t have anything to complain about. Why aren’t you grateful that it isn’t worse?”

Do you know how frustrating it is when people say, "It could be worse." Just because I'm not dying doesn't mean that my health isn't bad. So try saying something else instead.

What to say instead – There are so many things  you can stay instead. If you’re looking for a way to comfort someone, try asking, “Is there anything I can do?” or “How can I help?” If you don’t know what to say, you can tell them, “I don’t know how to respond to that.” That’s perfectly okay! Most people have no idea how to respond when I tell them about my health issues. You can also always say, “That sounds tough.” You are not obligated to comfort the person you are talking to. And if you’re talking to a friend who is upset about their health and you want to comfort them, you can ask them how to help or just give them a hug.

Saying, “It could be worse,” is not the required phrase for comforting someone with chronic illness. In fact, it you could stop saying it to spoonies overall, that would be great. We’re well aware that it could be worse, but that doesn’t change how tough our situation is.

[bctt tweet=”Don’t tell chronic illness patients, “It could be worse.” Here’s why.” username=”kmitchellauthor”]

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. Angela Tolsma says

    October 21, 2016 at 2:11 pm

    I’ve said things like I wish I knew how I could help better and usually left it at that, so that if they wanted help they knew I was open to it, but I don’t know if that’s a direct enough way to put it. I probably should be more blunt and say let me know if there’s anything I can do. Brushing it off though is something I never want to do.

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  2. Ariadne Shrubsole says

    August 24, 2017 at 7:18 pm

    Speaking from my own experience, and of people I’ve known with chronic illness, I would have to be at death’s door before I would call someone to say, “You said to let you know if there’s anything you can do..” I would recommend being specific. Examples, without all the quote marks because….
    How about I come over Thursday afternoon, if you’re up for company. I’d like to cook a meal or two for you, or vacuum the house, or give me a list and let me do some shopping. Things like that. Specific things that you know would be helpful if you had the flu or something. This presumes you know the person well enough and it’s not just a random ill person you’ve come across.
    The really angry part of me would want to say to the ‘it could be worse’ folks, ‘Yes. Things could be worse. For example, you could get in an accident and total your car and break your bones, your house could burn down, your spouse could run off with the mail delivery person. Things can always be worse. Does not mean what I am going through right now is not significant, because believe me, it really is.’ But then I am very angry at some people. 🙂

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  1. Round-up: Gilmore Girls, Chronic Pain, and Knitting - Second Breakfast says:
    November 15, 2016 at 10:24 am

    […] the thing. If you’ve never experienced chronic pain, and know someone who has, never, ever, ever say “it could be worse.” Or “just wait until you’re _____, everything will hurt more”, or anything like […]

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Dos and don'ts for when someone in your life is di Dos and don'ts for when someone in your life is diagnosed with autoimmune arthritis! What are some that you would add?⁣
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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: "So someone you know was diagnosed with Autoimmune Arthritis". Under the Do column (indicated with a green checkmark) is:⁣
"As how they feel about it⁣
Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
Under the don't don't column (indicated with an x in a red circle) is:⁣
"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
Assume nothing about their lives has changed⁣
Conflate autoimmune arthritis with osteoarthritis⁣
Pass your cold to an immunosuppressed person".⁣
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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 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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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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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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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 
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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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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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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 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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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.
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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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IDs: 
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