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You are here: Home / Coping / The Delicate Balance of Being Enough

The Delicate Balance of Being Enough

Last Updated: August 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.

delicatebalance

This guest post on Turning Straw Into Gold, along with the post from Toni Bernhard, that she referred to, really got me thinking about the balance beam that we walk with chronic illness. We play a constant game that I’m going to call – The Delicate Balance of Being Enough.

When you live with a chronic illness, like Fibromyalgia, there is a constant worry that you aren’t doing enough to pull your own weight. We often end up over-doing it to feel like we’ve done enough. Am I good enough spouse? A good enough parent? Am I working hard enough? Am I taking enough classes? Am I doing enough? Those are constant questions that I know I ask myself (except for the parent part, since I don’t have kids). Once upon a time I brought in the higher portion of income to our household, however as I got sick and as my husband worked his way up the ladder, that changed. And, now I barely bring home anything. It’s more than I’d make on disability and I’m not even close to the point of considering that option yet. I’m also back in school and it’s a constant balance with that. I want to finish school, but I know that I have limits. So, I’m trying to go slow. But, at the same time I feel like I have to prove that I’m putting forth this effort. I have to balance trying to finish school with feeling like I’m adding enough to the household.

On the other hand, there’s the looks I get when people find out I’m sick. I don’t look sick. I’m doing all these normal things that normal people do, going to school, trying to create an income. Going in and asking for disability services at school was difficult. I worry that I’m going to get instructors that don’t believe I’m sick. That question my need for accommodations. Of course, the fact that I rarely tell anyone I don’t feel well doesn’t help. If someone asks me how I am the answer is always “I’m ok.” there are a handful of people who I give that answer to, only to stop and think about it and change my answer to the truth. However, even then I don’t go into details. I don’t want to be a whiner. Lately, I’ve been on a vicious roller coaster. The 8am class through July really wore me out and I’m still not quite recovered. I worry that I won’t be recovered before classes start again in  two weeks.

She talks about this in the post I linked at the top. This need to prove that we are sick. For some of us, who have already started the process to receive disability, it’s about proving you are really sick enough to deserve disability. Getting not just the disability services, but those around you to realize that just because there’s a day here and there where you feel decent. Or, just because you decide to stretch beyond your comfort level and do something that you probably shouldn’t be doing physically, because it will make you feel better mentally, that doesn’t mean that you aren’t sick. Just because we show up and we’ve made an effort to look good, and we put a smile on our face, doesn’t mean we suddenly feel good, or that we are better. Are we doing the healthy a disservice by now looking sick enough? On the other hand, if we look too sick then that offends too. Just another tightrope walk down the delicate balance of being enough – sick enough, healthy enough, wife enough, giving enough, accepting enough, providing enough. Enough.

[Tweet “Do you struggle with the delicate balance of being enough?”]

Where do you encounter this balance the most in your life? How do you deal with it when it comes up?

5 Comments Filed Under: Coping, Extra Spoons, inspiration Tagged With: disability accommodations, 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. Trisha says

    August 11, 2014 at 8:31 pm

    I struggle with all of this too. I’m not sure what area of my life I struggle with it the most. Maybe not bringing in any income for the past fifteen years. I have to keep reminding myself of all the things I actually do. In a different era, it would have been enough in the eyes of the world. Not so today.

    Reply
    • Julie says

      August 12, 2014 at 10:08 am

      You are doing what you can, and that’s what you have to remember. You are enough.

      Reply
  2. Di says

    August 11, 2014 at 5:12 am

    “Love”

    Reply
    • Julie says

      August 11, 2014 at 10:55 am

      I knew what you meant 🙂 Glad to have you here, and thank you for commenting.

      Reply
  3. Di says

    August 11, 2014 at 5:12 am

    Thanks for that post-I could relate to it totally ….and it got me thinking! Live your blog x

    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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