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You are here: Home / Coping / Learn to Control Your Pain and Flares

Learn to Control Your Pain and Flares

Last Updated: August 17, 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.

Control Your Stress, Control Your Flares

At this point anyone with a chronic illness knows that stress increases their flares (or likelihood of a flare). But, are you creating your own flares, and the stress that creates them? You could be controlling both the stress and the flares. I know it’s hard to imagine that we actually have any control over this pain that our bodies give us. But, the truth is that you can control your pain.

Not long ago I wrote a post on how our perceptions of stress impact our pain. Then recently I read this post on Forget Fibromyalgia and it triggered the thought again. How often do we create the perception of pain when it’s not really there. I say this because I know that for me early on in Fibromyalgia storms were my worst trigger. Almost everyone with Fibro carries the belief that weather changes make them feel worse. We all have something that “know” makes us feel worse. But, does it really? Does it really make us feel worse all the time? Or, is possible that maybe it did once (or many times) but now it’s not the trigger that makes you feel worse but the stress that is created by simply thinking about how that trigger has made you feel in the past.

I think of it a bit like Pavlov’s dog. The trigger is our bell, but the pain may or may not really be there anymore. We are just so used to feeling that pain when we “hear the bell” (or encounter the trigger) that we automatically stress out and that stress is what creates the pain. I know that for me, storms don’t impact me nearly the way that they used to. Occasionally, a bad one will still set my nerves on fire. But, overall they don’t really bother me as much. Sex is another area that I’ve had a lot of pain and I know that at times the pain is created simply by the stress that I create in my brain at the knowledge that it COULD hurt. My brain knows it could hurt, so I stress at the thought of the potential pain, tightening my muscles, and then creating the very pain I was worried might occur.

Can you think of times that you might be creating the pain you are trying to avoid? Does thinking about the potential of pain stress you out to the point that you might be creating the pain you wish to avoid?

So, what’s the answer? Check out this quote from Forget Fibromyalgia’s post:

“Our perception is based on our beliefs and values. Generally people think that when an event occurs, it triggers an emotion such as stress, but that is not actually the case. It is the emotion that leads to thoughts that in turn result in the emotion.”

“Your current mood changes your perception, which some days makes you feel like everything is wrong and intensifies the pain you feel.”

The answer goes back to my earlier post. We have to change our perceptions to take control of our pain. When we can feel that we have more control over the situation (something we all crave with our Type A personalities), and we can say to ourselves: “That thing it doesn’t really affect me all that much. I’ll be alright”, instead of saying “I hate storms, they really mess with my body and leave me in a lot of pain”, then we don’t feel as much pain. Over time, the more you do this the less pain you feel. The more positive your outlook is, and the more positive your outlook is, the fewer symptoms you will experience.

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2 Comments Filed Under: Coping, Extra Spoons, Symptoms Tagged With: decreasing pain, decreasing stress, sunday inspiration

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. Harriet says

    August 17, 2014 at 9:44 am

    I have both Fibro and ME so not sure which one gets triggered but find meat makes me exhausted. I’m now slowly reintroducing it and trying to work out which, if any is the trigger. I don’t want to shut anything out on chance! I think it will turn out to be the lovely processed stuff like bacon *sob*

    Reply
    • Julie says

      August 18, 2014 at 12:15 pm

      That would be sad. I do love bacon. Of course, it could be not the bacon but the nitrates/nitrates in it (and you can find some nitrate/nitrite free bacon/sausage), so don’t feel like you have to write it off completely. I agree, take it one meat at a time to figure out what bothers you. I know a lot of people find that red meat really slows them down. I’ve not found a meat link for myself, but gluten is terrible for me. I’m still seeking more trigger foods, and I know they have expanded. Things that I know didn’t bother me 2 years ago do bother me now (but these days it’s more about headaches and IBS issues, than the pain and fatigue).

      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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