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 / Coping / It’s time to focus on your own story

It’s time to focus on your own story

Last Updated: September 27, 2015

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.

I received an email from a friend recently about how she’d run across a great success story on Facebook. A woman who had been bed-bound from Fibro had found ways to improve her health (including exercise) and was ready to run a 5k. You go girl (the only time I’m running is if something is chasing me)! My friend was commenting on the huge amount of negative response this person’s story was receiving from those in the Fibro community. They were saying that she evidently never had Fibro, that exercise can’t help Fibro, and any other negative thing they could think of to discount this person’s success story.

Focus on your own story

Why do we we so often attack other people’s success?

Why do we feel the need to tear others down in order to feel better? That’s exactly what we are doing when we attack another person’s improvements. We feel so terrible living in chronic pain that when we see someone else find ways to improve their health, we tear them down rather than be happy for them and hopeful that one day we’ll find the treatment plan that will help us have that level of improvement. The reason is that we can’t imagine being successful in that way. We’ve lost hope.

I’ve been there. I was that woman. I could barely get out of bed, and when I did it was to go to the couch. During that time every time I read a story like this I had that same negative response. She didn’t really have Fibro, or that would work for her but not for me. I found some reason to discount something that should have given me hope. I hit rock bottom and thought about ending it, but I didn’t. Instead I decided that it was time to focus on my story and what I wanted that story to look like. I did have a choice and I chose to hope.

I believe that there is a way for all of us to feel better. The combination is likely a little different for each of us  but I believe that some combination of exercise, diet changes, and lifestyle changes can greatly improve the lives of those with Fibromyalgia to the point that they can live again. It may not be exactly the life they had before, but it can come really close, or at least it will feel like it after we’ve hit the bottom.

When I hit the point where I was willing to try anything I looked at all the advice I’d poo-pooed before. All that advice to eat differently -cut out processed foods, gluten, dairy, eggs- to exercise, to  try different supplements, that I’d ignored or discounted before I was finally willing to try it all. And not just a little bit but I went all-in. Because there was no point in just testing the waters only to find out that it wasn’t enough.

For me, taking action meant doing a week-long juice fast to clear out my body of the bad stuff and replace it with good. It meant finding better supplements, it meant exercising regularly, and it meant that when I did start eating whole food again it was whole healthy food minus the processed stuff, minus gluten, dairy, and eggs.

I chose to leave out those specific foods because part of my process included undergoing food sensitivity tests and while I showed a very low sensitivity to those foods, in my opinion any sensitivity could be enough to make me feel worse. Later on when I tried eating those foods again I found that I’d left them out for good reason – they did make me feel worse. In short, I stopped focusing on everyone else’s stories, and I started focusing on my own.

I think it’s important that we share our stories, that’s why I share the Fibro Warrior stories, but I think it’s more important that we support each other and encourage each other to make positive changes. To not give up.

Too often I see posts where people are complaining about getting certain advice (often related to diet, lifestyle, and exercise) and how they are aware of these things and “don’t you think if they worked I’d do them.” Or they say they’ve tried it but it didn’t work, when the reality was they tried it for a week, or a few days. Or, they gave up bread but never considered that gluten (or even wheat) is in so many things.

These attitudes and responses frustrate me because I want to see them succeed. I want to see them feel better. I want us all to be able to share our success stories and get support from each other. I want us to be able to focus on our own personal journey without tearing down others for their journey.

It’s time to write your story. How do you want it to end? You get to choose as this life we have is the greatest choose your own adventure story there is. You can continue to follow the easy path and continue to feel terrible all the while tearing others down that have chosen a different path, or you can choose the difficult path (it is difficult) in hopes of writing a happy ending. Whichever adventure you choose make it your own, and be happy for others as they choose theirs.

So to my friend, who is now afraid to share her own triumphs for fear of a negative response, and to anyone else who has found a way to improve your symptoms and change the direction of your story, please don’t be afraid to share your successes.

I don’t spend a lot of time these days focusing on what I’ve done to turn my symptoms around. I shared that when it happened. I think that we all should. These days I do continue to focus on my story, and continue to try to improve my life and my symptoms. I continue to share where I am on my journey. Current chapters of my story are not focused on changing to feel better, but on maintaining and continuing to do what I’ve learned helps. These days I stay focused on living a positive and happy life. I continue to focus on having a happy ending to my story, and happiness along the way. That’s all any of us can do.

9 Comments Filed Under: Coping, Extra Spoons

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. Tobi Dannemiller says

    October 7, 2015 at 3:13 pm

    I love your articles. You are a true friend to a lot of us. I have to admit this; because it may help me and other’s like me. I can’t concentrate long enough to read a full article. I’m lost after the first paragraph. Have you had this problem? I want to read so bad, but my cognitive skills are hedging on breakdown. I commend you for being able to write such beautiful articles. I do wish I could do the same. Thank you and blessings!

    Reply
    • Julie says

      October 8, 2015 at 12:24 pm

      I totally understand. These days I do ok most of the time with reading but I still have times when I try to read something and I can’t get past a single line. Others have said the same. I try to keep things as short and simple as I can when I write, but I know sometimes I ramble.

      Reply
  2. Melissa says

    September 28, 2015 at 12:36 pm

    I think a reason for negativity regarding others’ success might have to do with the way far too many in society and the medical community view Fibromyalgia – as a bs diagnosis. We’re often left to defend the existence of Fibro and our inability to do what we used to do. For that reason, we become very defensive when a success story comes out. Rather than being happy for that person, we fear that it’ll further erode belief that Fibromyalgia is real and/or that our friends and family will doubt the severity of and impact of it on us.

    I’m willing to bet this happens with other illnesses fighting to gain respect from society and some ignorant doctors. I bet that it very rarely happens with illnesses for which diagnostic tests are available.

    I hope what I wrote makes sense. I’m in the midst of a flare and my brain decided it’s going on vacation.

    Reply
    • Julie says

      September 28, 2015 at 12:39 pm

      I think you are probably right Melissa. Another aspect I thought of earlier today is that those articles don’t really share the struggle that that person went to have their success, they gloss over it. so all we get is this sudden success without balance.

      Reply
  3. Sean says

    September 28, 2015 at 9:01 am

    Love the story! And I am GLAD that people post their sucess stories. I find it odd that we (because I sometimes do it too) acknowledge that Fibromyalgia is different for everyone, but then cast doubt when someone has success. We are all individuals, struggling with a syndrome that has no singular cause, effect, or treatment plan. It makes sense that what works for one person, will not necessarily work for another. I have found it necessary to even vary what I do, what has given me some success, because the symptoms I suffer from change depending upon stress, weather, sleep, etc. The only thing I don’t appreciate is when someone touts their own path to relief as ‘this is what YOU should do if you suffer from Fibromyalgia’, and I typically don’t read those stories. As long as someone shares what is working for THEM, I am happy for them and inspired, and it keeps me going back to trying to find a way to get better. (The ‘right’ level of exercise, stretching, and pacing still eludes me smile emoticon ).

    Reply
    • Julie says

      September 28, 2015 at 12:04 pm

      I’m with you. My symptoms change with everything going on around me. What worked well at one time, may not work as well now because of other things going on. But, we just have to keep trying. Thanks much for sharing.

      Reply
  4. Sue says

    September 27, 2015 at 5:21 pm

    I agree with you 100%. You have to be willing to try anything, within reason of course. And you have to keep trying until you find what works for you. It’s not easy. I was so sick of being in bed all the time. Some people for whatever reason aren’t willing to try. Some are angry and hurt so they lash out at others, with or without chronic pain. Happy people encourage others. I think you have to have an inner strength in order to truly have a life with chronic illness because as you know, it’s a battle. You have to fight to win.

    Reply
    • Julie says

      September 28, 2015 at 12:04 pm

      Truth! Thanks Sue!

      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