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You are here: Home / Coping / The Keys to Recovery

The Keys to Recovery

Last Updated: August 2, 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.

Julie Holiday (aka @MECFSSelfHelpGuru ) shared a great post on Prohealth recently about the Keys to Recovery. In sharing stories of those who have recovered she’s found a few simple ways these stories have overlapped. I go back and forth over whether I’m willing to say I’m “recovered” from Fibromyalgia. I’ve addressed that previously. Most of the time I do feel like I’ve recovered though and I can honestly say I attribute it completely to the first thing that Julie listed.

1. Commitment to doing whatever it takes

One common denominator is that most of the people who have recovered have exhibited an incredible commitment to doing whatever it takes to recover.

 

keep going

There are days now were I don’t have that commitment and I can feel the difference. It’s frustrating to see my symptoms morph. To find that I can’t eat the healthy way I’d like to eat because there’s a new batch of GI symptoms that come up because of eating healthy. Sometimes it feels like nothing works, but that doesn’t mean I quit trying. I don’t. I’m still willing to do anything and I continue to look for the answer.

As I said I’ve been having a new host of GI issues lately that are aggravated by eating healthy (fiber hates me, even my juice bloats me). So, I’ve been going round-robin with my GI doc trying to find a good solution and so far nothing is taking. I’m ready to go back to square one with or without his help. What is square one? Elimination diet. I think it’s that time again. I’m just not sure what it’s going to look like this time and that’s the one thing holding me back. Despite the fact that even juice bloats me I’m considering doing another juice cleanse just to see it if would help. The other alternative is a nutritionist. That’s one direction I’ve not gone before, so why not give it a try – in the name of trying anything. I plan to ask my GI doc for a referral at my next visit. I’m hoping that my insurance might cover it if I get a referral, but I’m at a point where I’m willing to give it a try even without help from the insurance.

Why am I willing to keep pushing for an answer? Because of the second thing on Julie’s list – I believe that recovery is possible. I believe that I can feel better. It helps that I have felt better than I currently do. I’m getting by with where I am but I’m not willing to settle for getting by, for being constantly bloated, for stomach aches, and all the other GI fun.

There are plenty of reasons why not to do things. We can always come up with those, and usually those “reasons” are really nothing more than excuses. I look through her list of things that prevent recovery and every one of them is within our control, or it’s just an excuse we are using. The one that popped out to me was “not being well enough to take the first steps”. I’ll give you that all of us at some point have been so sick that we can’t even think. But, the second you can think you should be thinking about what it’s going to take to recover and be willing to take those steps, no matter what.

Being willing to do whatever it takes to feel better is the first step to recovery. #chronicillness #fibro #cfs Share on X

4 Comments Filed Under: Coping, inspiration, Tips and Tricks, Treatment Tagged With: feeling better, recovery

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. Ewa says

    August 18, 2015 at 10:34 pm

    Have you ever heard about salicylates?

    Reply
    • Julie says

      August 19, 2015 at 9:50 am

      yes.

      Reply
  2. KD says

    August 6, 2015 at 7:37 pm

    Elimination was the only way I could really find out what was happening. Because I didnt test positive for the major GI stuff, we had no idea what was happening. There didnt seem to be a pattern. But I’m Gluten sensitive. For me, this means I stay sick all day, every day, if I eat regular foods with gluten. If I stay off of it completely, that part of my illness stays fairly okay, though I have to take miralax regularly at times. If I eat a little of it, it seems okay for a few days but then apparently builds up and I get very sick later for days on end. No one believes this stuff. Or can test for it. My numbers are not high enough to meet any criteria, but I have a bunch of numbers that are too high in a bunch of categories.

    Reply
    • Julie says

      August 7, 2015 at 11:44 am

      I’m the same way. Initially even a little gluten made me sick the next day. But, now i’ve been off it long enough that a little bit won’t hurt me, but if I eat a little bit too much it will build up. So, I just avoid it completely.

      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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