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 / Diet and Nutrition / Exercise / Journaling

Journaling

Last Updated: February 8, 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.

There was a while back when I felt the worst that I got pretty good at keeping a log of my symptoms. Isn’t it funny how that works? When you feel worse you will do anything to feel better but as you start feeling better you stop doing the things you should? At least I know that’s how it is for me. I was really great there for a while at exercising too; unless I felt so bad I couldn’t (or wouldn’t) get out of bed, I got on the treadmill. Lately, as I’ve felt better I’ve not been exercising as much. I have (on the other hand) been trying to work some other exercises into my routine when I do exercise. Lately, I’ve been getting back on the Wii Fit and the DDR (Dance Dance Revolution) to get a little more cardio and at the same time finally start to work my upper body a little more.

The pain from my TMJ has been a lot better lately too. I’ve been eating more normally. I’ll usually try to eat something if it’s in front of me and see how it’s going to affect me. I actually ate some salad a week or so ago. It wasn’t that it hurt it was just that some parts of it were impossible to chew and I knew after trying to eat it for a few minutes that if I kept it up it would hurt. But, I can chew again and I can do some crunchy foods again without them bothering me as much.

But to the journaling, I’ve been getting worse and worse. Often I think I should journal more just so I have a record of things. My memory still sucks. I still use Remember The Milk to help me track what I need to get done in a day, and I still can’t remember what stops I need to make when I’m out unless I write myself a sticky note and put it on the dashboard (and even then I’ll have to double back sometimes).

The thing is that it’s when I’m feeling better overall that I probably need to journal the most, or keep a log of my symptoms. Those are the days when I’m most likely to be able to find a link between what is bothering me and why it might be bothering me. Those are the days when I’m most likely to see that yes exercising in the morning does make me feel better and wakes me up. I know this and yet I still don’t do it enough. There’s no telling what other connections I might make if I started keeping track of what was going on.

Leave a Comment Filed Under: Exercise

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