There are many misconceptions about chronic illness, things we hear and know that others think. The worst part is that often we think these same things about ourselves.
I have to say I’ve never seen a group of people talk so poorly about themselves, as those of us living with chronic illness often do. I don’t know what it is about chronic illness/ chronic pain that seems to have such a huge effect on our self-esteem, but I think that’s exactly what it is. We hurt so much that over time we begin to think that the misconceptions the outside world has about us are true.
Below are 11 misconceptions of chronic illness that I’ve noticed myself making (and have heard from others through social media); misconceptions that others make and misconceptions that we often make about ourselves.
1 – We are no longer the spouse, partner, parent that we should be. – We may no longer be exactly the spouse, partner, or parent that we were when we were healthy, but that’s ok. Even if we were healthy we would not be the same person we were years ago. We all change, chronic illness just leads to a different kind of change and it’s not all bad.
2 – We are unreliable flakes – I’ll be honest some of my friends thought I was an unreliable flake before I got sick, and I was. The truth is that being sick doesn’t make us flakes or unreliable. Yes, it makes it difficult to make plans, but that’s just the way it is, it doesn’t mean you are flaky. You just need to take precautions to not commit yourself to plans you may not be able to keep. Ask your friends to “pencil it in” and not agree outright.
3 – We have to apologize for our pain – we are not responsible for our pain. It’s that simple. You don’t owe anyone any apologies.
#Spoonie You are not responsible for your pain, you don't need to apologize for it. Share on X4 – We have to apologize for who we are – Again, stop apologizing. The funny thing is that I know healthy people who constantly feel the need to apologize, too. No one should feel they have to apologize for who they are. Own yourself, be yourself.
5 – We are responsible for our illness – I don’t know how many times I’ve felt this way and heard others express the same. It seems like every one of us goes through a stage at some point (or repeatedly) where we try to figure out what we did in our past that earned us this pain. We list out all the bad choices we’ve made in life and some how conclude that because of those bad choices we deserve the pain we now live with. No one deserves this pain and we are not responsible for our illness.
No one deserves this pain and we are not responsible for our illness. Share on X
6 – We Feel like no one cares – How many times have I said this to myself, that no one cares about me or about how I feel. It’s often my reason for not talking about how I feel openly and honestly. I open my mouth to share and I feel like whoever I’m talking to isn’t’ really listening or doesn’t really care what I have to say, so I shut my mouth. But, people do care. If nothing else the amazing online community of #spoonies cares, and what’s better is that they understand.
7 – We have to make others understand – Speaking of understanding, why do we have this unending need to make everyone understand our illness and how we feel? The truth is that not only doesn’t everyone need to understand, they can’t understand. Living with a chronic illness is one of those things that no one can really comprehend unless they live it.
You can't really ever understand chronic illness until you live it Share on X8 – We are failing at life – Chronic illness seems to make us all think we are failures when the reality is that we have just ended up on different paths than we originally planned. If there’s one thing I’ve learned in life it’s that the life you plan rarely occurs, things happen and I don’t necessarily mean bad things that change our course in life. You are not failing at life you are just on your way to discovering a new plan.
You are not failing at life you are just on your way to discovering a new plan. Share on X9 – We are lazy and unproductive – We hear others say it and eventually we start to believe it. We look around at the things we feel we ‘should’ be doing and we convince ourselves that because we aren’t doing those things it’s a choice and that we are lazy. We berate ourselves for not being as productive as we would like. The truth is that often if we really paid attention to what we do during the course of our day we’d be amazed at how much we do.
If we really paid attention to what we do we'd be amazed at how much we do. Share on X10 – We have to fake it – We convince ourselves that the only way we can get through life is to fake it. To pretend to be normal and not in pain, to pretend we have the energy that we are lacking. We present ourselves to the outside world as if all is well and we are feeling great, when the truth is we feel awful. All we want to do is go home and lay down. In faking it we are cheating ourselves and those we love out of the best parts of ourselves. We are present but we aren’t really there. We show up but we have nothing to give, because there is nothing left.
11 – We are on the outside looking in – We often feel like we are on the other side of a glass window to the world. We can see all that is going on, the lives our family and friends are living. As one reader put it to me she no longer visits Facebook because she felt that the happy and positive version of life that everyone presented there was a facade and it was just making her feel worse. There’s a lot of truth to that. The facade of social media – that everyone posts their best self only makes EVERYONE feel worse. Not just those of us with chronic illness, but everyone (there have been studies on this). The truth is that everyone feels like they are on the outside looking in at times.
Why do we allow ourselves to speak and think so poorly of the person we should love most?
I think one important thing to remember is that many of these misconceptions are not just held by those with chronic illness, but by everyone. If we only knew what others were thinking, we’d realize just how alike we all are. We are not alone.
I need to start looking at myself in the mirror and seeing the awesome person I still am. I should be my #1 ally, my wing-woman, selling myself as the awesome person I am. Despite my chronic illness, I still have many skills and many positive attributes, so I need to focus on those and remember that chronic illness has not taken away who I am. I am still an amazing person and so are you.
chronic illness has not taken away who I am. I am still an amazing person and so are you. #spoonie Share on X
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Caz / InvisiblyMe says
Yes to all of these! The one with being lazy & unproductive gets me the most at times, because the feelings of guilt already weigh so heavily. x
Rosa says
THANK YOU for this post! Followed you for a long time on IG but just got on your blog today and read a ton. But this post especially was needed today, as I fight crohns, fibro, hashimoto and other medical things. Been very down on myself so this post is one I need…going to memorize it! Lol. Thank you for all you do to help this community of warriors!
Julie says
So glad you found the blog and that you found this one helpful. 99% of what I share is something I write because I need to hear it. If I need it likely others do as well. Keep fighting!
Mare says
Thanks so much for spending your precious time trying to help others who are enduring similar, if not the same issues you are. I read your blog often, but don’t post much. I feel like you need some validation for all that you share that helps us to feel better about our struggles. Bravo!! Keep it up Girlfriend! We are all warriors, just trying to get thru each day.
Thanks again and God bless,
Mare
Julie says
Thank you Mare! It definitely helps to know that others are finding help in what I share.
angoe says
I am so sorry for not visiting this site as much as I’d like to. I am just wondering how do I get rid of all the apps that follow me down the page to the left. It’s hard enuf to read without my glasses but this is annoying. Not to mention I’ve found 2 other areas to access these apps on the same page.
Please help!
Angie
Julie says
Hi Angie, I’m guessing you are referring to the video that follows you down the page? You can close it by clicking the x on the top corner of the video. That said, it should stay to the side of the text you are trying to read. You might also want to wear your glasses to read, I know that if I try reading without mine I’ll end up with a migraine pretty quick.
Veronique says
I think I just deleted my comment… I wanted to say that I love this post and especially your image of the swan and how we need to look at a different reflection sometimes. My husband has been telling me this over the years – how to see myself through his love and his eyes – and I am slowly starting to learn to do that more. It is a learning process. I am also learning to look at my illness through different eyes – I have more and more appreciation for all that I am learning from it. learning to love myself, pace myself and slow down; have better boundaries; but also learning new perspectives about health and disease and how to not judge… it’s a life rich with learning!!
Julie says
That is amazing. It’s so hard to learn to love ourselves again when we feel like everything is lost. Just because our lives have changed doesn’t mean we don’t still have so much to give and so much to live for. Many hugs to you.
Veronique says
I loved this post (even though I’m a few weeks late in reading and commenting :-). I especially love the image… how to look at a different reflection. My husband has told me this many times – how can I shift the negative self-talk and see what he sees. It’s a slow process, but it’s changing and chronic illness is just a part of my life that is turning out to help me learn how to slow down, have better boundaries and learn to love myself more.
Julie says
It definitely takes work to shift away from the negative self talk and learn to look for the positive, but it’s possible. I was lucky had the help of a great therapist that really helped me make that shift.
Veronique says
I’ve done a lot of work in therapy too – and still ongoing (and retrained from a previous career to become a psychotherapist myself). It has helped tremendously, I couldn’t agree more. It’s a greatly underestimated resource! many hugs back!
Tara says
Thanks so much for posting this article! I have been struggling with several issues lately and your post really spoke to my heart.
Julie says
Thank you so much for commenting. It’s great to know that I’ve helped.
Sue says
Great post. I have thought or felt all of these at one time or another. The more pain you are in, the easier it is for negative thoughts to seep in. I think you are right, everyone feels like they are alone and not living up to their potential at times.
Julie says
Thank you for sharing Sue!
Lisa says
Great article here. Being a survivor of RSD/CRPS and Fibromyalgia, I understand and agree with everything said. I love that you shared this with the world!
Thanks so much!
Lisa
http://www.lifeshareuniversity.com
Julie says
Hopefully the world will see it. The thoughts are all things that have been shared with me by other warriors (and thoughts I’ve had myself plenty of times).
Donna says
Brilliant post Julie, agree with every point you make. We can be so unfair on ourselves sometimes. I recently deleted the fb app from my phone for exactly that reason. I still check fb as I am part of some groups on there but otherwise limit my exposure to it.
Julie says
I find Facebook through the eyes of my blog page much easier to deal with. I don’t really have any negative people on my feed towards my illness, but I also stopped sharing much about my illness on Facebook a long time ago.