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You are here: Home / Coping / “But You Don’t Look Sick!” – Understanding Invisible Illness

“But You Don’t Look Sick!” – Understanding Invisible Illness

Last Updated: August 15, 2016

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.

Living with a condition such as Lupus, Fibromyalgia or Rheumatoid Arthritis is horrible enough without also having to cope with the cynicism of people who cannot detect these illnesses and take the stance that you’re exaggerating the level of your suffering.

This doesn’t just stem from the general public, either – many invisible illness sufferers will tell you that they had to consult a number of doctors before finally being diagnosed, with even medical professionals being so dismissive as to make accusations like ‘it’s all in your head’.

The infographic featured below was written by Victoria Abbott-Fleming from chronic pain charity, Burning Nights, and, as an invisible illness sufferer, she knows all too well just how much of an uphill battle it can be.

For people like Victoria, daily tasks which come easy to many people are quite difficult, tasks like getting dressed, taking a shower or cooking a meal. There are only so many of these tasks that we can do in a single day before our energy levels have totally diminished, and if we overstretch ourselves in one day, we will pay for it the next.

For sufferers of invisible illnesses, the words of others can make a significant impact on our mood. If a person shows empathy and says something along the lines of ‘What can I do to help?’ or ‘I don’t know how bad it feels, but I imagine it must be very hard, their words are usually appreciated massively, as the sufferer can see that they are being considerate and understanding.

What You Should Say to Someone With Chronic Illness

On the other hand, comments such as ‘Oh, you don’t look sick’ or ‘Get a bit of exercise and you’ll be fine’ can be hugely damaging to a sufferer’s self-esteem. This type of behavior smacks of ignorance and is the last thing an invisible illness sufferer needs to hear.

Things You Should NEVER Say to Someone with Chronic Illness

Please take a few minutes to read through the infographic and get a flavor of the daily life of what it is like to have an illness such as Fibromyalgia or arthritis.

Understanding Invisible Illness

 

Related Posts:

  • 10 Things You Should Know About Fibromyalgia
  • 10 Things People with Fibromyalgia Need to Know
  • What you should say to a friend with chronic illness
  • I didn’t write the spoon theory, I just live it

3 Comments Filed Under: Coping, Extra Spoons, Fibromyalgia, Tips and Tricks Tagged With: invisible illness, lupus

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. Dione says

    August 17, 2016 at 2:12 pm

    This is great. Thanks so much for taking the time and effort to write your articles and share helpful things. It means alot.

    Reply
  2. Valerie says

    August 16, 2016 at 5:30 pm

    I love this! The infographics are perfect. Sharing! Thank you!

    Reply
  3. Genevieve says

    August 16, 2016 at 9:47 am

    This is FANTASTIC. Thank you!!!

    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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