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 / Fibro Warriors / Fibro Warrior Wednesday – DL Miller

Fibro Warrior Wednesday – DL Miller

Last Updated: October 2, 2013

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 sweet guy is D.L’s grand-dog.

A big welcome this week to my friend, D.L. Miller. Another of the wonderful women I consider myself lucky to have met through the local support group. We are really so lucky to have such a great active support group. So, let’s get to know D.L.

When were you diagnosed?
I was diagnosed in 1993, by Dr. Duelle our Family Practitioner. But there are memories in childhood that make me wonder if it was with me from a very early age.

What lead to your diagnoses?
Dr. Duelle noticed I was in his office every week for several months with flu like symptoms.

Were you working at the time?
Yes, I was part-time because of the fatigue and pain. I had worked full-time for several years but I was in the work, eat, sleep mode and life was depressing.

What was your family life like?
Stressful. I raised 3 kids and my husband’s job kept him away at lot. Most of the time we were not near family, but when we were the elder care began. The kid’s grew up, left home and only one boomeranged. Turns out he has mental health issues that need almost constant monitoring. It is truly like waiting for the other shoe to drop. Then my mom became ill and had to go into permanent care.

How did your family initially handle your illness?
At first, my oldest son accused me of being lazy! My daughter was too sweet, she would help any time she could. My youngest son was in a world of his own, we thought he was just an odd duck. My husband just wanted me to NOT have the pain and fatigue I was experiencing.

How has Your family/work situation changed since Fibromyalgia entered your life?
I had a hard time even accepting it would change my lifestyle because my doctor said it was NOT fatal and there was no treatment for it. He put me on Paxil and for 7 years that’s all I took besides Tylenol. In 2000 I could no longer work, so I put myself on a strict diet of only lean meats, fresh fruits and veggies. I slept a lot And I lost weight and in 3 months began to feel well enough to go back to work part-time.

My daughter went off to college, and my youngest son dropped out of high school. My husband was working out of state and I barely coped with life. In 2005 my husband had an epiphany and began to understand how limited I was. And that I was in a constant battle on a daily basis!

What do you feel is the most challenging aspect of Fibro?
All the time I was in and out of different dr. offices, taking any and all tests that were available, and no one could find anything wrong with me…physically ! Things are getting better slowly in the medical field but I can’t say I feel any better! I am back to a diet of ONLY fresh natural foods. The closer to the farm the better! That in itself is a lot Of WORK. Making good choices in all areas of my life are what allows me some health; My time, my emotions, my physical activities, my family’s needs and so forth.

Do you have any other co-existing conditions? If so, what are they and how do they impact your Fibro?
I have Hypo-thyroidism. I have weak muscles and back injuries, Asthma and food allergies. As a child I had pain often and I remember my parents medicated me with aspirin. As a teen I took lots of aspirin. At age 35 my thyroid slowed down and I started gaining weight. After that it seems I was a guinea pig. All different meds and exercises and so on. The side effects of most meds are horrible and not worth the stress and strain on the body for me! But I still take too many! Fibro has now become the number one factor to consider in everything I do in my life.

What have you found/done that has improved your symptoms?
Eating right, exercising appropriately for me, letting go of stress, finding ways to sleep better and reworking my self-care plan as often as it is needed! Because every day is different and meds only work so long.

What is the best advice you’ve received regarding Fibro?
My original doctor said “Don’t ever give up!” and I haven’t. My husband said “Honey take care of yourself and let us know what we can do to help.” And my friend Dawn said,” We are here for you!”

What is the worst advice that you followed?
Taking 3 anti-depressants at one time along with Lyrica.

That doesn’t sound good, what happened?
I was on Elavil, Buspar and Paxil. The goal was to relieve the muscle aching and spasms. Then Lyrica became available. I had mental and emotional issues caused by the meds that interfered with my daily activities and caused me to sleep through a lot of things. It felt like sleepwalking. I had to be slowly worked off the anti-depressants while starting Lyrica. I gained weight and became very depressed. I had good support from my husband and friends or I might have gone off the deep end! My oldest son had left home and joined the Army. He was doing well so that helped with my depression.

What is one thing you’ve learned about yourself since your diagnosis?
I am stronger than I ever imagined !
[Tweet “Fibro has taught me that I am stronger than I ever imagined !”]

Leave a Comment Filed Under: Fibro Warriors, friendship Tagged With: interviews, thyroid

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