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You are here: Home / Coping / Things to Say to Someone with Chronic Illness

Things to Say to Someone with Chronic Illness

Last Updated: August 12, 2020

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

If you love someone with chronic illness, you want to show them you care. There are plenty of lists of things that you shouldn’t say, things that aren’t helpful to them or to your relationship. But, more important are the things that you should say to someone with chronic illness.

These are the phrases that help remind them that they are loved, that they matter, and that they are still important to you.

1 . I’m here for you – No matter what, we need to know that those who love us are there for us. We need to know that you aren’t walking away. Words are cheap, so we also need actions to show us that you aren’t going away, and believe me, we will do our best to push you away (thinking it’s for your own good). We hate being around ourselves when we feel bad, so we can’t imagine that anyone else would want to be around us.

 

2. How can I help? – Those of us with chronic illness suck at asking for help. But, that doesn’t mean we don’t want it and need it. We need it a lot, but we won’t ask for it, and we worry that no one wants to give it.

We need you to offer it, and keep offering it, and even offer specific help. Don’t stop offering until we take you up on it. Don’t just offer help, give it. If we keep saying we don’t need help, find ways to help anyway. If you live with us, make an effort to do things around the house, cook dinner, run errands. If you don’t live with us, give an ear. Pay attention to the things we complain about needing to do, and see if there’s some way you can help us with those things.

 

3. That must really hurt – On the rare occasion that we do talk about our pain, please let us know that you believe us, that you realize how much pain we must be in.

Just that we hurt enough to share it with you means we are hurting a lot. There’s so much pain and so many symptoms that we deal with from day to day to the point that we just stop talking about them. For us to speak up means we are really in pain (and probably means we could really use your help in some way).

4. You are so strong / brave – We don’t feel strong, we feel weak. We need those who love us to remind us how strong we are, that it takes a lot of strength and courage to keep fighting day after day when dealing with chronic pain and illness.

5. You don’t deserve this – No one deserves chronic pain, but that doesn’t keep us from feeling like we’ve done something to deserve it or didn’t in some way earn it through our bad choices. We need to be reminded that we don’t deserve it, that we deserve so much better. We deserve to be healthy and happy.

We know that no one deserves chronic pain, but that doesn't keep us from questioning it. Share on X

6. You are doing everything you can – We feel constantly feel guilty that we aren’t doing enough. And too often we get unsolicited advice about things we can do to feel better. We need to hear from those who love us that we are doing enough, that we are doing everything we can and that you know it.

 

7. Tell me how you feel – It’s difficult for anyone to know what to say in a situation they’ve never dealt with, but sometimes it’s not about what you say, but just that you sit and listen to us. It’s OK to say “I don’t know what to say, but I’m here for you”. Sometimes that’s all we need, we need to know that you are there and willing to listen.

8. I miss you – Those of us with chronic illness will avoid people (at least for a while) because we don’t think that you want to be around us when we are sick. We need to hear that we are missed, we need to hear that you want to be around us, and that you are there for us when we are ready to be with you. We need you to make that extra effort to remind us that you are there and that we should reach out, too.

9. How about we pencil these plans in? – When we do feel up to making plans with you, we need you to understand that those plans are always going to be tentative, that we may have to cancel at the last-minute. It helps so much that we know you understand that. When you say it first, it helps us relax and know that it’s not big deal.

10. Tell me about your illness… – We worry / feel that no one wants to hear about our illness. We don’t want to bog you down with it, but we do need to talk about it. The only way we will talk about it is if we know you really want to hear. Ask us about our illness, ask us how it feels, ask us how it affects our lives, ask us if we’ve found anything that helps.

10 things you NEED to say to someone with chronic illness Share on X

Related Posts:

  • 11 Things You Should Never Say to Someone With fibromyalgia
  • How to Help Your Chronically Ill Friend Feel Worse
  • Communicating Your Needs When You Have Chronic Illness
  • The importance of maintaining friendships in isolation

 

6 Comments Filed Under: Coping, Extra Spoons, Fibro and Marriage, Fibromyalgia, friendship, relationships Tagged With: chronic illness, communication

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. Melissa says

    September 30, 2014 at 7:54 am

    My best friend will tell me she doesn’t know how I do it (live, I guess?). Comments like that come from her as well as other friends and family when they’ve had a small sample of my daily symptoms.
    My brother told me he understood my pain while his wife was in labor. He said he recognized the look of being sheet white and far away, in intense pain.
    My ex recently started getting migraines. He said he doesn’t know how I function while I have daily migraines.
    The thing I HATE: advice from people who aren’t sick. Stuff like maybe a shower would help with the migraine (sure, the difference in barometric pressure and dizziness will make things better? ), have I tried the newest fad, etc.
    I’ve always done research; first in school, then on financial data during the decade I worked, then on my illnesses and newest research results and available treatments.
    I know people are well meaning but, I’ve made clear that I do my own research, am proficient at understanding medical jargon and that my doctor is at the top of his field. They don’t understand that their help comes across as both demeaning and underestimating of my illnesses.
    I’d rather just hear ‘how are you,’ ‘do you need anything from the store,’ and ‘I hope you’re well enough that we can get together soon.’

    Reply
    • Julie says

      September 30, 2014 at 7:58 am

      I get the same comments about the migraines. I agree about the comments from people who don’t deal with pain giving advice from some random thing they’ve read or heard, so frustrating. I did a post a while back on things not to say and felt like we needed to share the things that are helpful to hear, as well.

      Reply
  2. lee @ Fibro Blogger Directory says

    September 29, 2014 at 11:29 pm

    Love this positive approach, rather than what we don’t want to hear.

    Reply
  3. Heather says

    September 29, 2014 at 7:25 am

    All of these things are dead on!

    Reply
    • Julie says

      September 29, 2014 at 11:51 am

      Thanks Heather!

      Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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