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You are here: Home / Conditions / Fibromyalgia / Do you use your illness as an excuse?

Do you use your illness as an excuse?

Last Updated: September 7, 2014

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.

uncomfortable situations

I have a confession, I’ve used my illness as an excuse a time or two. I’ve said I had a migraine to get out of something or to leave something early. We’ve had an event or two that neither of us really wanted to attend, so I developed a migraine after we got there to give us an early out. On the other hand, there’s been a time or two that we agreed that would occur only to have a real migraine make an appearance. I’ve about decided that using an illness as an excuse is a sure way to jinx myself into feeling bad.

So, now that I’ve gotten my confession out-of-the-way, I want to share my inspiration for this post. A few weeks back, The Daily Headache shared an article from an advice column where the columnist actually suggested saying you have a migraine (instead of cramps) to get yourself out of work. Basically, male bosses may not feel comfortable with (or empathy for) PMS symptoms, but they may be more understanding of the idea of a migraine (it’s not just a girl thing). The columnist went so far as to say that migraines are seen as mysterious and even… glamorous? WTF!

As TDH points out, there’s nothing glamorous about migraines, or any chronic illness, for that matter. It’s bad enough that Fibromyalgia (especially) gets thrown around as an excuse on television and media in such a way that it exacerbates the feelings that many have that Fibromyalgia isn’t real. Chronic illness is not an excuse, and it should never be used as one. We deal with our symptoms enough, they poke their way into our reality on a constant basis, so why on earth would we want to throw them around when they aren’t really there?

I know the thought has crossed my mind a few times that my symptoms are there so much that it’s no big deal to call on them when needed to get out of a situation. The truth may even be that symptoms are there, but they aren’t really bad enough to make me leave an event (the truth is that if they were that bad – except for migraine – I probably wouldn’t have attended whatever it was in the first place). Yes, there are times when the environment of an event increases my symptoms to the point where I really do have to leave. And, maybe if I didn’t use my illness as an excuse when I did, staying would have increased my stress/symptoms to a point where I really did need to leave.

Then there’s the “What do I say to get out of it if I don’t use an illness?” The truth maybe? “I’m not up to being here tonight.” (Which is true, even if it’s that I’m mentally not up to being there). Isn’t it interesting that we would fake being well constantly, saying “I’m fine” when we don’t mean it. Yet, when we actually feel ok but just want out of a situation we will evoke our symptoms? Our illnesses are not there to be used as needed. How often are we really honest about our symptoms?

[Tweet “#Spoonie Do you ever use your illness as an excuse to get out of a situation?”]

2 Comments Filed Under: Fibromyalgia, inspiration, migraine Tagged With: chronic illness, chronic pain

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. ChronicMom says

    September 7, 2014 at 2:45 pm

    Your post was timely, I just used my illness as an excuse for the first time this weekend. I figured there were very few benefits to being sick, so I should let it work for me for once! I do generally go for telling the truth though, I usually just say I want to have family time so I can’t make it.

    Reply
    • Julie says

      September 7, 2014 at 4:26 pm

      Just re-reading my post I felt guilty for having used it that way. It’s kinda scary to break down and admit that I’ve done that (and the truth is I’ll probably do it again). I do think it’s one thing to use it as an excuse occasionally, it’s another thing to make it our excuse for life. It does get in the way of enough things without.

      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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