15 Things Not to Say to Someone with a Chronic or Invisible Illness


Invisible illnesses are illnesses that you can’t see just by looking at someone. Things like Type 1 diabetes, Chronic Migraines, Lupus, Postural Orthostatic Tachycardia Syndrome, which I live with, and Fibromyalgia, may not affect your appearance, but they affect how your body functions and feels. Every day. Probably for the rest of your life.

When you say the following things to someone with a chronic illness, you probably don’t mean to hurt their feelings. A lot of the time you are just trying to understand or sympathize. Well, from the perspective of someone who lives with a chronic illness, here are 15 things you should never say to someone with a chronic illness:

1. You don’t look sick

Not everyone “looks like” what is happening to them. You would never say “you don’t look like someone who is going through a terrible divorce” if your stressed out friends still manage to put on a brave face and pull themselves together. Not all illnesses are manifested outwardly.


But you don't look sick - Invisible Illness

2. You’re too young to be sick

I get this one more than #1. You can get ill or go through any kind of stressful situation no matter your age. Age is completely irrelevant here. Young, unfortunately, does not always equal disease-free. When you tell someone they’re too young to be sick, it just makes them feel even more guilty or embarrassed for having an illness they have no control over when society expects them to be healthy.  And, moreover, just because you have an illness, doesn’t mean you want to be called “sick.”

3. Everyone gets tired

That may be true. And most people are not getting enough sleep and rest. But the difference between someone with chronic illness associated fatigue and an otherwise healthy person is the level of fatigue. If I go out drinking with friends and stay up late, it could take me a week to recover. I have to carefully plan every activity of the day so that I can save energy to do all of them. The best line I’ve heard for this one is: you don’t know what fatigue is until you’ve had to rest after taking a shower. Unless you literally think to yourself “how much energy will that take?” for every single action you take during the day (including brushing teeth, combing hair, standing to do dishes, putting on makeup, cleaning, driving, etc.) then you experience a completely different kind of tired than people with certain chronic illnesses. I’m not saying you aren’t tired. Everyone does get tired. But my kind of tired is not the same as a healthy person’s kind of tired. If I push myself past the amount of energy I have in a given day, the consequences are pretty bad. See the spoon theory for more about this one.

4. You’re just having a bad day

I know you are trying to motivate someone and make them feel better when you say this, but it doesn’t come off like that. Personally, only about 10 people in my life see me on my bad days. If I am outside, dressed, and active, that is a good day. So instead of making someone with a chronic illness feel supported and motivated when you say this, it feels like you are brushing off their symptoms. Chronic illnesses are with you for life. You can change your lifestyle and find treatments to help them, and some of them can be “managed,” but for the most part, that person will have to deal with a lot of bad days for many years to come.

5. It must be nice not having to go to work/school

This one. Oh man. If you only knew. Sure, it can feel that way when you take a day to play hooky or a long vacation. But when you are forced not to go to work or school, even when you want to be there, it is a different story. People with chronic illnesses don’t want to fall behind in school and fight with the school district to get the accommodations they need. People with chronic illnesses don’t want to miss work and not be able to generate an income. Everyone wants independence.

Personally, I loved school and hated every day I wasn’t there. It is way more stressful not being in school and knowing all the work you will have to do to make up for it than being there on any given day. And I have loved the jobs I’ve had and been sad about every day I have missed. Believe me, it is not nice having to stay home instead of being productive, just trying to find ways to distract yourself from pain or exhaustion. It’s fun to watch TV for a day or two, but after that, I feel trapped. I guarantee anyone with a chronic illness would gladly trade in their symptoms for a full time job.

6. You need to get more exercise

Exercise is really important and no one is denying that. It helps pretty much any health condition. But it isn’t a cure-all. For someone like me, whose heart rate regularly reaches 120 bpm just from standing still, exercise isn’t always doable. I do “exercise” but it is more like physical therapy exercises than what most people would consider a good work out. But remember, everyone has limitations. For people with chronic illnesses, their physical limitations may make it harder for them to do traditional exercises. And even if they do, it will probably not be a cure for a condition that is caused by something totally different like an immune system that attacks itself or a nervous system that doesn’t regulate itself correctly.

7. I wish I had time to take a nap

See numbers 3 and 5, which relate to this one. To someone with a chronic illness, to whom napping is not a luxury but in fact a necessity, hearing someone say this is as much a slap in the face as hearing someone say they wish they could take a break from work or school too. Hearing anyone “wish” they could have a part of a chronic illness just shows how misinformed they are when they say this. Wishing you had more time is pretty much a universal wish. But wishing you had the time that a person with a chronic illness has is not the same. If your wish is granted, you can get more time, but you also have to get the pain, the exhaustion, and the difficulty figuring out how to be productive in society. Remember that next time you have the desire to say this.

8. The power of positive thinking

Positivity is really important and having a negative outlook can negatively affect an illness. But having a positive outlook will probably not cure it. I’ve gone through all the stages of positive thinking and denying my illness. I have thought, if I just put my mind to it, I can do that. And then I’ve suffered the consequences of pushing myself beyond my limits.

Positive thinking that is productive for chronic illness sufferers is not telling someone that thinking positively will help them with their symptoms. Instead, productive positive thinking is finding the positivity that comes with their illness. For me, if I hadn’t had POTS, I wouldn’t have gone to Lake Forest College to stay close to home and my doctors. It was there that I learned and discovered my passion for environmental studies and met the love of my life. I wouldn’t have found an inner strength in myself and learned to value the time I have in the same way I do. That is productive positive thinking. But it’s not a cure.

9. Just push through it

Hearing this makes me want to hit my head against a wall. This goes along with #3 “Everyone gets tired/ headaches/ back pain/ insert symptom, just push through it.” The problem with this statement is the underlying assumption that a person with a chronic illness is not already pushing themselves. Every day I push myself. I push through my symptoms all the time. If I didn’t, on my bad days I would not eat, walk, or shower. And the same is true of anyone with a chronic illness. Remember: there is a difference between pushing and pushing past your limits. Pushing yourself is good and necessary. But pushing past your limits can set someone with a chronic illness back for a while as they recover from overextending themselves. Suggesting to someone to just push through it may not feel insulting, but it is like telling a marathon runner to just go faster on their last mile.

10. It will get better, just be patient

I’m sure everyone who says this truly means well. And it is true of a lot of things that patience is important. But not all chronic illnesses will get better. Patience is a virtue, and an important one. But please don’t say this to someone who has an illness that they will have for their entire life. It could get better, but it also may not. So figuring out how to live within the confines of your illness and make the most of it is more productive than expecting to get better. This is not to say that you shouldn’t hope to get better- just that you shouldn’t count on it. That’s denial.

11. Have you tried ____

… the paleo diet, acupuncture, super magic moon crystals, this weird new therapy that I heard about one time but know nothing about? Unless you are a medical professional and/or a person with a chronic illness has asked for your advice, please keep it to yourself. I haven’t tried super magic moon crystals, but I have tried just about everything else including alternative and new treatments. I’m actually trying a new one now. And I probably won’t stop trying because science makes advances. But someone with a chronic illness doesn’t want to defend themselves to you on how they have already tried or don’t trust the efficacy of a certain treatment, especially if your evidence is only anecdotal. I know you probably mean well and are trying to help, but just assume that someone with a chronic illness has tried every option available to them. Everyone wants to feel good.


12. You should stop ____

See number 11. I know you mean well and you want to help. Everyone has bad habits they should probably stop. Did you know that one of the parts of my treatment is to increase sodium in my diet? So if you want to tell me how you or someone you know of feels so good because they cut out salt, it will go in one ear and out the other. What works for one person does not always work for another. Please keep your unsolicited unprofessional anecdotal medical advice to yourself, because you are wasting your time and possibly insulting or discouraging someone with a chronic illness.

13. It’s all in your head/ you’re just stressed/ depressed/ anxious

If I had a nickel for every person (including doctors) who told me this before I was diagnosed with POTS (and some afterwards) I would have really heavy pockets. I guess when we don’t understand something and don’t look physically sick we assume it is mental. It must be cultural or part of human nature based on how often this is said to people with chronic illnesses. Stress, depression, and anxiety can all make symptoms of chronic illnesses worse. But they do not usually cause them.  Chances are when you say this to someone you are only contributing to their stress, not helping them see something they never saw before.

14. You need to get out more

A change of scenery can do some good. And I believe that spending time outdoors is good for your health. But when you say this to someone with a chronic illness, it doesn’t sound encouraging. Someone with a chronic illness wants to get out more (see number 5). All it does is make them feel guilty for not being able to do something they already want to and are probably trying to do. So before you say this, remember that they probably agree with you and they don’t need the guilt on top of it.

15. You take too many medications

People differ on their opinions of whether medications help or are bad for you. In some cases they are medically necessary. This is one of those things where you should probably keep your judgement to yourself. If I take a medication, I have researched the side effects and I have tried every other lifestyle change and vitamin that I can before I get to that point. Not everyone wants to just pop a pill to solve a problem. If someone is having a symptom that is controlling their life medication is sometimes the best way to manage it. People with chronic illnesses do many things to try to live as normal life as possible, and medication is one small piece of that puzzle. It is part of a lifetime of adaptations, treatments, and figuring out how to live with a chronic illness.

So now that you know better than to say these things, you can relate better to the people in your life with chronic or invisible illnesses.

And remember: the absolute best and most powerful thing you can ever say to someone with a chronic or invisible illness:

I believe you.

 You would be surprised just how much that will mean to them.

*A version of this article originally appeared on Pins and Procrastination.

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Never tell a type1 a cure is 5 years away.


Hi thank you for this post.I have chronic vertigo and I have also had chronic fatigue before.
I’ve had vertigo for 29 years, the chronic fatigue started about 18 years ago and that comes and goes. I’ve been free of chronic fatigue now for a couple of years. I have come across many of these comments over the years, even from doctors or specialists. It does get very frustrating when people say this stuff. This post was insightful and makes me realize I am not alone x


I have lupus. I have to say FAMILY IS THE WORST. I hear the most condescending comments from one in particular, my own mother. If I dare mention a symptom I hear ” OH THAT’S NOTHING..I HAVE THIS..THIS ..AND THISSSSSS”. OMG you know.She has narcisstic tendencies to say the least, mildly… I am NOT looking for sympathy. I am NOT looking for validation. I am looking for UNDERSTANDING.. It’s not that hard people who are not ill and have no idea…Just be there and listen sometimes. We aren’t looking for the sympathy vote, we are just looking for compassion and… Read more »


Thank you. You just described my mother. I have Sjogrens syndrome, and rheumatoid arthritis. I have maybe one day a week to decide what to do. Go grocery shopping. Do laundry. Clean my house. Everytime she calls to ask why I haven’t been over, and I tell her what symptom, of the many I have has kept me from doing anything. She says, oh yeah, my ” fill in the blank” has been bothering me. From there, I get to listen to what her week has been like. And this is why I don’t leave my house,or call anyone. Recently… Read more »


If I go out drinking with friends and stay up late, it could take me a week to recover. If you have a chronic illness why would you do this to yourself? Looks like you have prioirities to get straight.


?? Where does it say the person went out drinking with friends? That’s what you got from reading this? Too bad there wasn’t a pill for being an ass…


So because someone has a chronic illness, they should not be allowed to go to a birthday party for the rest of their lives? Sometimes, prioritizing important life events of people you care about IS a victory for those of us with a chronic illness. Most of them manifest as pain and fatigue. If your spouse wanted to have their 30th birthday party at a bar, would you feel good saying “honey I can’t?” Or your best friend? Or a sibling? She’s not saying let’s all go out and get shitfaced. She’s saying that even an occasional stay up later… Read more »


Yep.. When I was younger (20’s and early 30’s) if I went out with friends for a few drinks or a concert, ” YOU CAN’T BE THAT SICK BECAUSE YOU ARE GOING UT PARTYING ALL THE TIME!!!”.Going out occasionally isnot partying all the time and socializing is key for mental health… On the flip side, if people invited me places and I DIDN’T go, I was accused of suffering severe depression and needed to see ” a shrink” as my family put it. It was a no win situation.


Oh, my friend’s son had M.E. He got better after two months and now he runs marathons. Well, then he didn’t have it, did he, MORON. ARRRRRGGGHHHHHHH.




Ok, I when I got to the statement, “You don’t know fatigue until you’ve had to rest after taken a shower,” I cried. I said this very thing to someone just yesterday. Excellent article.

Timothy Velting
Timothy Velting

I have been sick for just over ten years, and have heard all 15. I always hear, ” Well you have had one small, and one large stroke but that should not be causing your shaking, left side pain and weakness. It has nothing to do with you having problems talking or no short term memory. I went to the ER with a lot of pain in my mid right side of my back only to have the ER doctor call me a street bum just there for pain med’s. It was a 4mm kidney stone. No, he didn’t say… Read more »


One of the reasons that people with chronic hidden illnesses are often isolated from others is that most people don’t know how to truly express compassion and to merely start by being present to the person who is suffering. I’ve heard most of these and their variations. Another reason for isolation is that if your illness is bordering on a terminal issue or the stress could be injurious then you must eliminate certain people from your personal circle of friends and associates. Healthy people can often be obstinate because they are afraid of dealing with mortality issues so diminishing the… Read more »


I suffer from endometriosis and I have heard every single one of these said to me. Also the ‘You just need to relax, then you’ll get pregnant’ or ‘If you get pregnant then the endometriosis goes away’. I just don’t understand how people think you care about their personal opinions about your illness….

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