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You are here: Home / relationships / Fibro and Marriage / We just want a little empathy and understanding

We just want a little empathy and understanding

Last Updated: July 30, 2020

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.

There are three things those of us living with chronic pain need more than anything else – acknowledgement, empathy, and understanding. Yet, too often these are the things are lacking most. 

“The worst thing about having an invisible illness is that people have a very hard time believing you are sick because you look good on the outside… People with chronic pain only want their loved ones to acknowledge their pain and give them encouragement and support. Most of all people with chronic pain just want to have people believe their illness even if it is no longer visible. “
– No One Gets Flowers for Chronic Pain

“I don’t seek sympathy; it’s empathy and understanding that I want. Just some understanding goes a long way toward feeling a part of something and not feeling so all alone with the burdens that I bear.”
– FibroDirtDigger

 

We all want to be acknowledged and understood. Empathy is really just sympathy with understanding. Most of the time people can’t understand what we are experiencing unless they’ve lived through it (or something very similar). 

The best any of us can do is compare what another is experiencing to a situation we’ve experienced (or are experiencing that is similar). We can’t imagine worse pain than the worst pain we’ve felt. So, when we hear someone else complain about something we do the only thing we can, we try to empathize by comparing what they are describing to our own experience. Unless we’ve felt the exact pain that the person is experiencing we can never have true understanding, but we can still be empathetic, and most importantly we can do our best to acknowledge that pain.

I had a discussion with several friends about migraines. All of us experience them to some degree. Someone commented about how people can say they have a migraine while continuing to sit upright and look completely normal. I replied that I do that all the time, and it doesn’t mean it doesn’t hurt. It just means that comparatively (to other migraines I’ve experienced) I can push through. Perhaps it’s an element of having chronic pain or chronic migraines that you learn to just push through. While others who only experience that level of pain on occasion haven’t had the need to do so.

 

There's no way you can be hurting that much AND sitting up! You must be lying!

Pushing through as much as we can is something that we learn when we live with chronic pain (of any kind). That doesn’t mean that it can’t get worse or reach a point where pushing through isn’t possible. I spent 3 months with excruciating migraines to the point that I didn’t leave the couch except to go to the doctor or chiropractor, hoping for release.  Every pain experience is different. It’s difficult enough living with chronic pain without the worry that even those closest to you may be questioning the reality of your pain.

I admit that often I am not empathetic enough of the pain others who are generally healthy feel. Knowing that I live with pain every day and push through, it’s difficult to look at someone with a pain that will pass relatively quickly and understand what they are going through. Not comparing their pain to my own chronic pain is difficult.

Unfortunately, many with chronic pain look at others who also suffer from chronic pain and think that the other person can’t possibly be hurting as much as they say they do, all the time. We judge those around us, and their experiences based on our own experiences. We also judge our own experiences based on our own experiences, because really what else can we judge them on?

Too often, even those who live with chronic pain may question whether someone else's pain is real. #thepainisreal Share on X

Ken over at Don’t Punish Pain shared his wisdom on how you can honor someone and acknowledge their pain without downplaying it. We all want to be respected. We all have to remember that just because we have our own pain to deal with doesn’t mean that someone else is hurting any less.

Just because someone wears their pain differently, is able to smile through it, walk through it, work through it, doesn’t mean that they aren’t in pain. They may be hurting just as much or more than we are. All it takes is a moment to simply acknowledge that their pain is real. You may never understand what their specific pain is, but simply acknowledging goes a long way.

The next time a friend tells you that they are in pain, just take a moment and let them know that you get it. Simply saying “I can’t compare my pain to yours, but I know you must really be hurting.” goes a long way.

Related Posts:

  • Chronic Pain: No one Gets chronic pain until they get it
  • Who are we to judge another’s illness?
  • When Chronic Pain Causes Shame, Practice Self-Compassion

4 Comments Filed Under: Fibro and Marriage, inspiration, relationships Tagged With: chronic pain

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. Lori says

    August 11, 2020 at 1:30 am

    I have been living with severe chronic pain for 15 yrs. there isn’t a moment in all those years my pain hasn’t been there. Even with all my arsenal of antipain weapons, I never get below a 4 my husband of 31 years said to me today I could work if I wanted to. That made me so sad. Sometimes I think he gets it but that’s not possible. If it were, he would have got it by now.

    Reply
    • Julie says

      August 11, 2020 at 1:42 pm

      I feel for you. Only those of us who live it understand what it’s like. That four may mean we can stand up and dance, but it doesn’t mean we aren’t hurting or that we don’t have limits or that we can work. Unfortunately, for those around us who have seen us at a 10, a 4 can seem like we are pain free. Your husband’s comment reminded me of something one of my psych professors (who also happened to be the staff counselor at a pain clinic) said. It pissed me off then, and it still pisses me off just re-reading it.

      Reply
  2. Jaydubblah says

    March 27, 2015 at 2:33 am

    I would go one step further and not even mention my pain in that moment. If someone tells me they are in pain they don’t need to know that I am too, at least not straight away

    Reply
    • Julie says

      March 27, 2015 at 9:36 am

      True. Often when we think we are identifying with someone by sharing our similarities we are really just diminishing their share and pulling the spotlight onto ourselves.

      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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