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You are here: Home / Coping / How to keep from growing bitter when you aren’t getting better

How to keep from growing bitter when you aren’t getting better

Last Updated: September 11, 2017

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.

How to Keep from Growing Bitter When You Aren’t Getting Better

guest post by Angie Glaser

On August 21, 2017, the moon, Earth, and sun lined up perfectly causing the morning sky to darken in a solar eclipse. Morning darkness is eerie. Everything is where it should be –  except the sunlight.

The absence of the sun, such an immensely powerful force, touches every corner with darkness in much the same way that the absence of health touches every corner of our lives.

Like the sudden darkness of a solar eclipse, illness darkens the world around us. The Earth still spins, leaves still flutter, but everything that we see and feel is touched by chronic illness.

Unlike an eclipse, chronic illness is not fleeting. It is with us every second of every day, intent on bringing darkness, but each of us has the power to bring light.

After living with Migraine symptoms every day for four years, my world is literally and figuratively darker than it was pre-chronic Migraine.

As a young woman in my early-20s, my health was like the sun: so pervasive to my daily experience that it never occurred to me that it would not always be there. Like so many of us living with chronic illness, my life was irreparably changed by disease.

It has been four years of specialists, pills, and treatments with little improvement in my symptoms and pain, but my life is not as dark as it once was. Every day I make a choice: I choose peace over despair. I refuse to let my world grow even darker – I refuse to grow bitter.

How do you add light to dark days when you’re sick? How do you deal with pain, stigma, disappointment, grief, and depression without letting it harden you? I would be lying if I said it was simple or straightforward. But bringing more light into your daily life, investing in your own peace of mind, is absolutely worth the effort.

 

7 Ways I remain strong in the face of chronic illnessHow to remain strong in the face of illness

Finding peace in the turbulent chronic life ultimately boils down to this: find what nourishes you and return to it as often as you can. Illness is constantly asking things of us, draining our patience and our energies. Activities that replenish you are necessary to keep your well of strength of up:

1 – TalkChronic illness changes your world, so your worldview must change if you want to thrive as best you can. Such a total shift in perception is really difficult on your own.

Working with a cognitive behavioral therapist, even for just a few short weeks, is immensely valuable. I personally owe a lot to my former therapist, and really value what I learned from her. [You can learn more about cognitive behavioral therapy and find a therapist here:  http://www.abct.org]

2 – ConnectFind a chronic illness buddy to vent to, to comfort, and to help the insane world of sickness feel a little less insane. The support on social media and in support groups among people with chronic illnesses is truly incredible.

If you don’t already have a network or a buddy who gets what you’re going through, please find one!

Related: The Importance of Support Groups for Fibromyalgia

3 – CuddleAn ancient, tried and true secret to peace and happiness is through pets. As a cat lady, I suggest adopting a kitten from a shelter in the spring and watching how much more you often you smile. Dogs, lizards, rabbits, even fish are soothing companions who will brighten even the ickiest of flare days.

4 – BreatheGet outside and breathe fresh air, as often as you can! Bonus points if you move your body while outside, but it isn’t necessary. I like to think of walking as a moving meditation. A way for me to cycle fresh air throughout my entire body and to give my spine and hips a break from lying in bed.

Walking, gentle yoga, or simple stretching all help our sore bodies release tension and benefit from pain-relieving endorphins.

5 – EatFalling in love with food again while sick is one of the most important things I have done for myself.

Dealing with Chronic Migraine means a lot of playing around with diet, and a lot of potential anxiety around food. To avoid that anxiety, I take to the internet. I research and pin tons and tons of recipes that work with my quirky diets and do everything I can to make food fun.

I put together shopping lists with pretty pens and listen to audiobooks while I cook. Any little thing to make nourishing my body more rewarding is worth it!

6 – LaughIt feels amazing and is necessary. Comedy shows, funny podcasts, your favorite funny movies from the 90s – anything that cracks a smile will bring more light into your day.

Related: The Importance of keeping a sense of humor

7 – CreateBeing creative evokes some of the best feelings of personal growth and love for the surrounding world.

Whether you’re coloring, gardening, listening to music, writing poems, drawing, cooking a meal, or singing in the shower, creativity is nourishment for your soul the way food is for your body.

Living with chronic illness means living with grief, and it is 100% okay to spend days in your PJ’s watching Netflix.

But after years of dealing with symptoms and fatigue, sometimes we have to make an effort to not become bitter – for our own sakes.

Spending time and energy on things that nourish you will help you live a full life, no matter what comes your way.

When you’ve been living with chronic illness for months, years, or even decades, your body seems intent on holding you back.

When you live with chronic illness, your body seems intent on holding you back. via @cmlifeblog Share on X
 

Related:

  • 10 ways to distract yourself from pain
  • Chronic Illness Does Not Make You a Failure
  • 11 Misconceptions of chronic illness
  • 15 ways Alexa makes life easier for those with chronic illness
 
 
Angie Glaser - How to keep from growing bitter when you aren't getting betterAuthor Bio:
Angie Glaser is a reader, sometimes-runner, health advocate, and author of the blog Chronic Migraine Life. She has dealt with Migraine since childhood but was truly submerged in Chronic Migraine in 2013 while working as a park ranger. Along with raising awareness on her personal blog, Angie is the Content Editor for Migraine Again. She currently lives in the mountains not far from Yosemite with her partner and blind kitty named Jupiter. 
Blog: http://chronicmigrainelife.com/
Twitter: https://twitter.com/cmlifeblog

 

 

 

4 Comments Filed Under: Coping, Extra Spoons Tagged With: acceptance, anxiety, chronic illness, mental health

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. Sharil says

    May 29, 2020 at 9:05 pm

    For the past 8 years I have tried so many ways to feel better and manage chronic pain due to Fibromyalgia and other conditions. While some have helped incrementally I still feel just as bad as ever a lot of the time. And it gets to be VERY discouraging. Especially having no one in my life who understands. I used to be in a support group, but got tired of all the generic memes…just be happy, etc and some other judgmental posts. Anyways, today I thought I really do need some kind of support and found your site. Your article gave me some motivation to try a couple things I gave up on. I’m inspired by your progress and hope to join your group. Thanks!

    Reply
    • Julie says

      June 1, 2020 at 2:23 pm

      Sharil, I’m glad to see you’ve joined our FB group. I hope you find it helpful. Please do reach out and ask any questions you have. I can’t promise we have answers, but overall I know people try and you won’t find any judgement there.

      Reply
  2. Paul says

    August 26, 2019 at 12:59 am

    Some good suggestions. However, I would query the last one. How can you create when your body is sending so many pain signals to your brain that you are simply unable to concentrate? I regularly have to cut short my harp practice because I am so overwhelmed with pain that a mental fog descends, leaving me unable to focus.

    Reply
    • Julie says

      August 26, 2019 at 1:38 pm

      There are so many ways to create. It may be a matter of finding new ways to allow your creative mind to work when it can.

      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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