Counting My Spoons

Inspired Living with Chronic Illness

  • About Julie
    • What’s Helped Me Most
      • ToolKit
      • Vital Plan
      • Oska Pulse
    • Contact Me
    • Work With Me
    • Terms of Service
  • Warriors
  • Coping
    • Tips & Tricks
    • inspiration
  • relationships
    • Fibro and Marriage
    • friendship
  • Conditions
    • Fibromyalgia
      • Fibro Warriors
    • migraine
    • endometriosis
    • Medical Studies
    • Treatment
      • Diet and Nutrition
  • Reading List
  • Toolkit
You are here: Home / Conditions / Fibromyalgia / Surviving Fibromyalgia: How I #defypain

Surviving Fibromyalgia: How I #defypain

Last Updated: May 12, 2015

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.

#defypain Surviving Fibromyalgia

Today is Fibromyalgia Awareness Day (May 12, in case you are coming to this post later), and I thought it was an appropriate day to share a post on how I #defypain and how I’m Surviving Fibromyalgia.

Fibromyalgia is characterized by widespread chronic pain, and while I may look healthy, and perky, and not the least bit in pain most days, the truth is that I’m in pain almost every day. I just refuse to let it win. When I first got sick, I had no choice. I had no tools with which to cope with the chronic pain and fatigue of Fibromyalgia. I dropped my classes, I barely worked, and I suffered. But, over the last five years I’ve learned a few things, and now I survive and some days I even thrive.

How do you #defypain when you live with #fibromyalgia ? Share on X
  • Diet – Diet was the first tool that I really found that assisted in decreasing my pain. By choosing what I eat wisely and eliminating certain foods from my diet altogether, I was able to drastically decrease my pain. I still have bad days, and sometimes I still have a craving for bad food. But, I’ve seen the effects of making good decisions and I know that it’s worth passing on the gluten and dairy. It’s just not worth it.

 

  • Pacing – Pacing should have been the first tool I found. I’d heard the instructions enough time as my support group leader lead us through “Do it, Delegate it, or Dump it” at least once a year. But, I didn’t listen. I either did nothing or I tried to do everything. I remember one month in the early years when I was feeling a bit better and decided I was going to clean my house from top to bottom. In my defense I did try to “pace” myself creating a list of what I would do each day, but what I didn’t consider was that there would be days when I could do nothing. It took me a long time to be ok with what. These days, I don’t worry so much about how clean the house is, or if someone else will be upset if I don’t get to something. If I don’t get to it I don’t get to it. These days I make sure that instead of scheduling my task list, I expect downtime and accept it.

 

  • Positive Attitude – This is one that a lot of people hate to hear as much as they hate to hear “diet choices”, but I really have found that doing my best to keep up a positive outlook makes a huge difference. Getting bogged down in negativity, only makes me feel worse. It adds depression to the chronic pain, it makes me want to curl up in a little ball and cry. And, quite honestly, when I get hit with negativity it adds stress, and stress increases my pain. So, I do my best to avoid stress and one of the best ways I’ve found to do that is to focus on the positive. Whether it’s the positive of what someone meant when they said something that may have hurt my feelings, or the positive of the day when I don’t want to get out of bed. Little things really do make a big difference.

Chronic pain sucks, and while we can’t necessarily make it go away, we can find ways to decrease it, and ways to focus on other things, beautiful things, around us. We can #defypain.

1 Comment Filed Under: Fibromyalgia, inspiration Tagged With: acceptance, chronic illness, chronic pain, decreasing pain, decreasing stress

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.

Leave a Reply Cancel reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.

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).

Common Tags

abdominal pain acceptance alternative therapies anxiety asking for help book review books brain fog cbd oil chronic fatigue chronic illness chronic pain communication dairy-free dealing with doctors decreasing pain decreasing stress depression diagnosis diet doctors documentary family feeling better flares food sensitivities gifts health holidays ibs interviews mental health oska pacing pain relief product review review self-compassion sensitivities sleep sleep aids stress sunday inspiration support travel

Copyright

All content copyright CountingMySpoons Any content reblogged from this site must adhere to the terms of © Copyright and TOS
That page states in part: "A brief excerpt of content that does not exceed 75 words may be quoted as long as a link is provided back to the source page on this blog and authorship is properly attributed."

Proudly Hosted By:

Wordpress Hosting Done Right

Proud To Be Included

 

Chronic Illness Bloggers
 

Privacy Policy

Counting My Spoons respects your privacy. Your information will never be provided to any third party unless you provide explicit permission to do so (something I'm not likely to ever ask you to do).

Read full privacy policy

Content Copyright © 2025 - Webz Plus Inc