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You are here: Home / Medical Studies / Relationship Between a Positive Attitude and Fibromyalgia Symptoms

Relationship Between a Positive Attitude and Fibromyalgia Symptoms

Last Updated: October 10, 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.

A study of 735 Fibromyalgia patients, examined their affect (mood), breaking them into four sub-groups and examining the correlation between affect and symptoms.

The four groups were

  • Healthy (low negative affect/ high positive affect)
  • Depressive (high negative affect / low positive affect)
  • Reactive (high negative affect / high positive affect)
  • Low (low negative affect / low positive affect)

Definitions:

Negative Affect = negative emotions (sadness, anger, and fear, tension, nervousness, irritability, etc)
Positive Affect = positive emotions (happiness, hopefulness, enthusiasm, determination, etc)

Multiple studies have shown a relationship between affect and pain. Increased negative affect typically results in an increase in pain. Increased positive affect conversely is associated with a decrease in pain. Basically, those who display a more positive affect report fewer symptoms, and lower levels of symptoms.

51% had Depressive Affect Balance Style
12% had Healthy Affect Balance Style

Those with Depressive Affect Balance style had significantly worse Fibro symptoms (including pain, sleep issues, brain fog, etc). Patients with Healthy Affect Balance Style had the least symptoms, followed by those with Low Affect Style.

Overall, it would seem that reducing our negative affect, and working towards being more positive could have an impact on our physical Fibromyalgia symptoms, reducing not only our pain, but also other symptoms.

I know it’s difficult, but it’s something that I’ve really been working on this year. It’s so much easier to be negative, and it’s easy to fall into a negativity trap (it’s a circle of sorts, the more negative you are, the more negative things happen, and the more negative you become). The same circle works for positivity. My focus this year has been on catching myself when I have a negative thought and just stopping. I stop and tell myself that whatever the negative thought was is not true, then I restate the thought in a positive way. Sometimes I have to do this multiple times for the same thought. When I catch myself saying “This is a sucky day.” I stop, I breathe, then I say to myself “This is going to be a great day.” Instead of thinking of school as “hard” I use the word “challenging”, because I can handle a challenge, a challenge can even be fun. But, when I think of something as being hard, then I focus on the negative of the stress that will be created by doing something that is difficult.

Source:
A comparison of fibromyalgia symptoms in patients with Healthy versus Depressive, Low and Reactive affect balance styles. Toussaint, Loren L. et al.Scandinavian Journal of Pain , Volume 5 , Issue 3 , 161 – 166

4 Comments Filed Under: Medical Studies, Symptoms

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. Trisha says

    October 18, 2014 at 11:31 pm

    Very interesting! I’ll have to remind myself of this the next time I find myself spiraling into negativity.

    Reply
    • Julie says

      October 19, 2014 at 11:20 am

      It’s something I’ve had to work really hard to fight (the negativity) but I’ve found it to be worth the effort.

      Reply
  2. Donna Grant says

    October 10, 2014 at 10:21 am

    It’s so true and I know myself that if I am having a bad day mentally, then I will also have a bad day physically. I know it’s horrible to hear ‘it’s in your head’ but there is some truth to it with regards to the intensity of symptoms. I try not be symptoms focused either because the moment I draw my full attention to my pain is the moment when I feel it most intensely. Instead I stop, close my eyes and focus on breathing slowly and deeply and it’s amazing the difference that simple act makes.

    Reply
    • Julie says

      October 15, 2014 at 9:05 am

      I hate to think of it as being “in your head” but more as learning to distract ourselves from the pain rather than focusing on it. It’s too easy to go down the worst case scenario route, like lately when my shoulder has been giving me issues again, I will find myself thinking “oh great there it goes again, now what? Is it going to lock up on me again? Do I have what my brother has? Am I going to need surgery too?…..” And, I have to stop myself and just breath and tell myself that it’s ok, and then think about other unrelated things. It doesn’t mean it doesn’t hurt, it just keeps me from giving it control of my thoughts and my day. Focusing on the pain really does make it hurt worse.

      I’m happy to find that others have found that focusing on the positive helps.

      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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