Counting My Spoons

Inspired Living with Chronic Illness

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You are here: Home / Coping / Searching for Spoons

Searching for Spoons

Last Updated: March 23, 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.

Too often I hear things from other Fibro Warriors that just make me sad, they stop my heart a little, and make me wish there was something more that I could do for them. Earlier I took a look at my blog stats, specifically at the search terms that bring people to my blog. Seeing the terms that bring people here can sometimes make me really happy and other times make me really sad –today I was sad. Here’s a few examples of the things that made me wish I could do more for all of you. (I’ve provided what people were searching for and -where possible – what they found).

  • what to say to someone who does not believe your fibromyalgia pain – 10 Things You Should Never Say to Someone with Fibromyalgia
  • boss not empathetic to chronic illness – Do you use your illness as an excuse?
  • shes sick chronic, do i marry her – Fibro and Marriage
  • having fibromyalgia and having to cut ties with those who continually misunderstand you and put you down
  • what to do when you’ve had enough of life – Sunday Inspiration: I’ve Had Enough!
  • i have no sex because my girlfriend has fibromyalgia – Fibromyalgia and Sex: The Unspoken Reality
  • my wife has fibromyalgia sex is out – Fibromyalgia and Sex: The Unspoken Reality
  • he thinks i don’t do anything for my fibromyalgia
  • i hate my illness – Things to say to someone with chronic pain

And this just pissed me off:

  • ok we get it you’re chronically ill – The Slow Death of Compassion for the Chronically Ill
  • my wife uses chronic illness as excuses – Do you use your illness as an excuse?
  • husband says fibro fight not good enough – Fibromyalgia and Sex: The Unspoken Reality
  • chronic illness lazy – 11 Misconceptions of Chronic Illness

But, there have also been some that brought a smile to my face.

  • changes to a better you – 9 Changes to Make You Feel Better this Year
  • fibromyalgia – how to not let others ignorance effect you – 10 Things You Should Never Say to Someone with Fibromyalgia
  • deep encouragement for those suffering with chronic pain – Sunday Inspiration: We Make Room for Pain
  • helping someone in chronic pain – How you can help someone who has chronic pain
  • list if all things that make you feel better when you suffer with fibromyalgia – 10 Things You Should Never Say to Someone with Fibromyalgia
  • chronic pain inspirational blogs – Sunday Inspiration: Acute Pain vs Chronic Pain
  • list if all things that make you feel better when you suffer with fibromyalgia – 10 Things You Should Never Say to Someone with Fibromyalgia

And some that just make me say “huh?”

  • my guinea pig seems really weak he cant even eat his food without lying down

I hope that last one brought a giggle to you like it did to me. I have no idea how that search brought them here (I couldn’t track it down), but I thought it was quite funny that it would.

So, what have you been searching for? What answers are you looking for that you’ve not yet found?

 

1 Comment Filed Under: Coping, Fibromyalgia

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. Donna says

    March 23, 2015 at 8:07 am

    Oh some of them just made my heart sink! Especially the one questioning whether they should marry someone because they are chronically ill. I hope that the people who searched for the stuff that pissed you off (and most of us I imagine) changed their views after reading your posts

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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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