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You are here: Home / Coping / The Storm After the Calm: Learning to tolerate pain

The Storm After the Calm: Learning to tolerate pain

Last Updated: November 2, 2011

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.

This flare is going on a week and it’s some of the worst pain I’ve had in over a year. But then I wonder… “Is it really?”. Is it really the worst pain I’ve had in a year? Or does it just feel that way because it followed such a nice period of (almost) pain-free calm?

I think the pain is getting better, no you're just getting used to it.

I’ve often felt like we are constantly adapting to pain; that we are learning to tolerate pain, more and more, the longer our illness continues. Studies have shown that those of us with Fibromyalgia actually have a higher pain tolerance (we can withstand higher levels of pain than normal people). This is how we can walk around with a pain level at 6 and no one is the wiser. This is how when we go to the Dr or PT and they ask “What is your pain level?” we actually have to stop and assess ourselves to figure it out, because after a while we just stop thinking about it. We know it’s there, but we do our best to ignore it and to just live through the pain.

However, when we’ve had a nice calm period where our pain levels lower and our energy levels are raised, we get used to not being in pain (or to being in a lot less pain). Even during my best days (which managed to last a little better than a month this time) my pain level was still between a 2 and a 4, but it was low enough that I didn’t even notice it. The first flare that started October was more of an absence of energy flare than a real pain flare. Yes, my pain increased but only back to a 5 or 6. And that flare only lasted a couple of days. This time the flare has hung around for a week and it’s been more of a pain flare than an energy flare (the energy isn’t there either, but mostly I just HURT). Today, I’d say the pain is a 7 or 8 but increases when I move certain ways or do certain things. Earlier I was trying to cut some coupons and just holding my arm up to cut the coupons cause the pain in my arms to increase to a 9.

Chances are the pain now isn’t any worse than it was in my last flare (which sadly lasted for several months) but it feels worse. I think, however, that it only feels worse because I’ve gotten used to a lower level of pain. When the pain is higher it can slowly increase without a great deal of notice on my part. However, when the pain has been low (2 to 4) and then suddenly jumps up to a 7 or 8, you can’t help but take notice and feel like it hurts more.

4 Comments Filed Under: Coping Tagged With: dealing with fibro, flares

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. carrie says

    May 7, 2014 at 9:25 am

    Hi. Think we have no memory for pain. If we did no one would have second child. When my pain comes on I always think its worse than ever, but is it ? We tolerate more and more. But after pain free period its a shock and we have to grieve for our well body all over again. ( I have M S) @ tangomango

    Reply
    • Julie says

      May 7, 2014 at 10:33 am

      I tend towards the opposite. All of my pain is compared to the worst pain I can remember (a month of TMJ migraines, combined with ulcers from said migraine meds and then my gallbladder went out) and very rarely has anything compared. Even when it comes close I can usually convince myself it’s not as bad as that was.

      Reply
  2. Julie says

    November 5, 2011 at 9:30 pm

    Becky, isn’t it amazing what we can ignore when we are distracted?

    Reply
  3. Becky says

    November 5, 2011 at 6:09 am

    Ya, I know. It’s crazy how our bodies get used to things. On the bright side…in a few more days you might get used to what you are feeling! j/k. I’ve been having more pain lately when I sleep. It’s like I’m not that bad all day then I go to lay down and can’t get comfortable. Just hurt. And I just realized maybe I’m feeling like that all day, but overlook it so I can get things done, and notice it when I can finally relax. I hope your flare goes down and you feel better soon.

    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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