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 / Close to My Heart / Sunday Inspiration: Be True To Yourself

Sunday Inspiration: Be True To Yourself

Last Updated: May 25, 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.

The Importance of Being True to Yourself

Sue Ingbretson, author of FibroWhyAlgia, posted something on her blog this week that hit me pretty hard. Her post, Do Any of These 10 Regrets Look Familiar referred to a post on the MarcandAngel blog, about 10 Choices You Will Regret in 10 Years. I didn’t have to read far to see one I am guilty of.

 

Stop Hiding: The importance of being true to yourselfWearing a mask to impress others.

It’s not so much that I wear a mask to impress anyone, I’ve never cared much what people think of me. However, as someone with chronic pain I often hide behind a mask that allows me to look a lot happier and healthier than I am. I pretend A LOT.

My feeling is often that no one wants to see the dark side. We all have enough negative in our own world we don’t want to deal with another’s darkness, too. I hide the true me so that I don’t make others uncomfortable.

[socialpug_tweet tweet=”I often hide the true me so that I don’t make others uncomfortable. But, in the end I make myself uncomfortable. #nomoremask” display_tweet=”I often hide the true me so that I don’t make others uncomfortable. ” style=”2″]

I am extremely guilty of this here on my blog. I do my best to avoid sharing/ writing negative things. You can usually tell when I feel my worst because my blogging becomes more sporadic.

When I do write a post that starts to sound negative I think to myself – What a whiner! stop that. No one wants to read it.

On the other hand, I recently wrote about The Importance of Being Vulnerable, and I need to apply that to myself as well. I need to be more honest, more vulnerable with everyone.

Funny-ish story. A few months ago I began seeing a Psychologist. After several months of dealing with the impact the pain in my shoulder was having on my life, and the negativity it was creating in my marriage, I was depressed.

I knew I had to get help ASAP and head it off before things got to the point where they did a few years back. I was already to the point where I was willing to verbally admit (at least to my husband) that I would eventually commit suicide to get away from chronic pain. It wouldn’t likely be anytime soon, but that’s how I’d likely go out.

So, I saw this counselor the first time and he had me do the usual personality tests and Beck Depression test. When I went for my second appointment he had to admit that he was quite shocked at how depressed I actually was, and more so at the fact that I was suicidal.

 

[socialpug_tweet tweet=”We wear our masks too well. Be True to Yourself. Stop hiding your reality, and let others see the real you.” display_tweet=”We wear our masks too well.” style=”1″]

 

Related Posts:

  • Acting healthy takes talent
  • What those with Chronic Illness Wish Healthy People Understood
  • Study Shows: You look too good to be sick
  • Are these seven habits increasing your pain and fatigue?

 

Nikki at BrainlessBlogger.com also shared a great post about this whole idea of masking our pain.

 

We wear our masks too well: The importance of being true to yourself

6 Comments Filed Under: Close to My Heart, inspiration Tagged With: self-compassion

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. Tracy Lee Karner says

    July 9, 2014 at 8:14 am

    I SO get it! (you saw my recent post….) Pain is, frankly, depressing. I reached the point, about 5 years ago, where I felt like, “I just can’t do this anymore. I simply can’t deal with this for one more day.”

    We all need to reach out sometimes, and ask for help. It’s very, very dangerous if we can’t tell anyone when we feel like giving up. Cheers to you, for being brave enough to ask for help.

    It’s a tricky business, trying to decide with whom to be vulnerable, when. Because vulnerability makes us, well, vulnerable! And it’s not really smart to make ourselves vulnerable to certain people. Some people are cruel, self-absorbed, or judgmental and I don’t believe in exposing myself to them (I have enough pain to deal with….)

    For me, as long as I know why I’m wearing a mask, and for what purpose (to protect myself from unsolicited advice, or meanness, or nosy questions), and as long as I’m not wearing a mask to PLEASE people or to deny to myself what I’m thinking/feeling, and if, at home and with my true friends, I’m not wearing a mask–there are times when masking can be appropriate. Because honestly, acting as if I feel better than I do, makes me feel better. And that’s important, too.

    But in order to get to this place, where wearing a mask, some of the time with some of the people, isn’t harmful–I first had to take off the mask I wore ALL the time, and leave it off for a good while.

    There are no easy answers. Which is why it’s an important discussion. Thanks for initiating it!

    Reply
    • Julie says

      July 10, 2014 at 1:19 pm

      Thank you for the feedback. It is scary to never know how people will react. Especially, when dealing with something that has the stigma of Fibromyalgia. Some people are just cruel, but I have to remind myself that that’s their problem, not mine, and do my best to not take it personal.

      Reply
  2. Trisha Pearson says

    May 28, 2014 at 12:01 pm

    I’m so guilty of hiding, both the good and the bad. Your post is a reminder to me that I need to stop it! I’m glad you were able to open up about the desperation you sometimes feel about the pain and I hope the psychologist can help you work through that. Sometimes it’s really overwhelming and scary to look at all the pain waiting for us in the days to come.

    Reply
    • Julie says

      May 28, 2014 at 12:36 pm

      Thanks Trisha. You are so correct at how over-whelming and scary it can be to think about the future. I imagine my grandmother and all the pain she was in in her last decade or so and think “I don’t want that”.

      Reply
      • Trisha Pearson says

        May 28, 2014 at 12:44 pm

        I know what you mean. I see my mom in so much pain that she just sits and watches TV all day. I definitely don’t want that! I guess all we can do for now is take it one day at a time. Maybe ten years down the road someone will figure this fibro thing out and we won’t bear the burden of pain that we have now. You never know!

        Reply
        • Julie says

          May 28, 2014 at 1:00 pm

          We have to hold onto that hope.

          Reply

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