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You are here: Home / Coping / Sunday Inspiration: Progress Amnesia

Sunday Inspiration: Progress Amnesia

Last Updated: January 11, 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 have hope that there are better days to comeMost of the time I write my Sunday Inspiration posts right when I first read a post. I read it and there’s just something I need to share based on what I’ve read. Sometimes, a post don’t quite inspire me right away but it lingers in the back of my mind, continually popping up until I realize I have to write about it. That’s what happened with this week’s post. I originally read this post from Sue Ingbretson a couple of weeks ago, and then shared it via social media. At the time it definitely spoke to me but I didn’t feel the need to really write about it. Then over the last week or so comments have been made or thoughts have just wandered through my brain that made me realize, there was more to this and I needed to write.

The thing that really struck me initially about Sue’s post was the idea of progress amnesia; how easy it is to forget how far we’ve come.

“When we learn new things and put them into practice, they become part of our everyday lives. That’s the whole idea, after all, but then something weird happens. We develop what I call, Progress Amnesia.” – The Flawed Fibromyalgia Success Map

She shares the story of a client she worked with who loved cereal. It was the hardest thing for her to give up (she even at it for dinner). Yet, years later when discussing her lifestyle changes with a friend she made a comment about how she didn’t even like cereal so it was no big deal to give up!

Now, that’s one example of progress amnesia. For me there are many foods that I’ve given up and I could see where I could easily forget just how attached I was to those foods before my diet/lifestyle change. But, the thought I have on progress amnesia isn’t about just some thing that we’ve changed and forget what a big change it is.

When talking with another Fibro friend over lunch recently she mentioned how about the time I got settled from making said lifestyle change and really started feeling better, something happened that messed it all up again. My response was “yes, but despite those issues that have cropped up, I’m still so far beyond what I was.”

It’s easy to forget how far we’ve come. It’s easy to focus on how bad today is. Most of the time these days the issues I’m dealing with aren’t even Fibro-related. Sure, those issues impact my Fibro and Fibro impacts those issues; but the main issue isn’t the Fibro like it was 3 or 4 years ago. I’ve come a long way and it’s so important that I don’t forget that. That I don’t let others forget that.
[Tweet “I’ve come a long way and it’s important that I don’t forget that.”]

There will always be challenges in life, even if they aren’t health-related. We all have struggles, and we all overcome. When we look back we need to remember just how far we’ve come, and what we’ve given up to get where we are. We need to remember that it was hard to give up that food and make that diet change, but then we need to focus on just how worth it that change was. For some of you, you haven’t reached a point where you can look back and see that things have improved, all you see is a life sliding downhill. I’ve been there, I lived for years thinking that I’d seen my best days and even reached a point where I seriously considered suicide because I didn’t see any hope of life improving. But, I held on and eventually I found a way to make things a bit better, so see a light at the end of the tunnel (even if it wasn’t as bright as I would have liked). I still have rough days, and rough times. I still have pain, but when the bad days show up instead of getting bogged down in them I try to remember that it has been worse, and that I have come so far. It helps me push through and have hope that there is more progress to come.
[Tweet “I have hope that there are better days to come.”]

6 Comments Filed Under: Coping, inspiration Tagged With: feeling better

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. Veronique says

    January 16, 2015 at 9:42 pm

    Hi Julie,
    I love this new term – I’m adding it to my list of favorites. I regularly forget what some things used to be like when my chronic fatigue was more severe – how hard it used to be to take a shower or make my meals; how grumpy I used to be when I went grocery shopping because the list of foods I could eat was so limiting. It’s still limited but now that I’ve made major dietary changes (akin to what you’ve done) and am sticking to them I actually look forward to it. My husband is the one who often reminds me of how things used to be compared to the (mostly less difficult) times now. Thanks for sharing this! I loved both your and Sue’s posts.

    Reply
    • Julie says

      January 17, 2015 at 4:58 pm

      Thank you Veronique! It’s so hard to think past where we are, whether it’s forward or backward. Most of the time we don’t want to look back, but sometimes it’s important so that we can remember where we’ve been.

      Reply
  2. Sue says

    January 11, 2015 at 12:00 pm

    Julie – what a lovely commentary on my original post. Thanks so much for sharing your personalized views and feelings on this journey that we both share 😉

    Reply
    • Julie says

      January 11, 2015 at 12:19 pm

      Thank you for sharing. Your posts are always inspiring!

      Reply
  3. Astrid says

    January 11, 2015 at 9:37 am

    I can totally relate to this. When I’m in a bad mental health state, I can’t seem to remember that it was a lot worse when I first entered this mental health journey. Same fo rmy physical health (I don’t have a diagnosis for that). Even when I feel relatively well, I downplay the progress I’ve made, or really, I don’t realize it.

    Reply
    • Julie says

      January 11, 2015 at 11:17 am

      I think a lot of times we get stuck in focusing only on today – how we feel today – and fail to think about it relative to where we’ve been.

      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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