"How Are You Doing?": The Question That Drives Me Crazy!

Having a chronic illness like psoriatic arthritis means that we’re stuck with this disease until we die or a cure is found. If the physical part wasn’t bad enough, we also must endure a lifetime of being asked the same questions over and over. “How are you doing?” is one question that either makes me scream or cry.

Testing, testing, 1-2-3

This question often feels like a test. Is she really in pain? How much pain could she really be in if she managed to leave the house? Whether someone is testing me or not, I must examine myself in order to answer. Sometimes I don’t want to acknowledge my pain. I distract myself when my pain is elevated; not focusing on my pain is how I cope when it is at its worst. When I am experiencing a “good” day or am in remission I don’t want to think about my bad days. However that is just what has to be done anytime someone asks me how I am doing. What hurts and how intense is the pain? The problem with this is that the pain or pains I was successfully distracting myself from take center stage and once there those drama queens refuse to exit the stage.

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Open the flood gates

Sometimes just hearing those words from someone brings me to tears. Not because I am annoyed or don’t want to talk about my conditions, but because I am worn down and it feels so absolutely wonderful to have someone express concern. I keep a pretty darn strong lock on my flood gates, but every once in a while the lock falls off and the doors fly open. When this occurs, the person asking won’t have a clue to my physical state as all I am able to express are emotions. Forget putting sentences together, I am lucky to toss a few words out between my sobbing cries.

No win situation

I honestly don’t know which is worse. Both scenarios are exhausting and neither gives a full picture. Just sharing my physical pains doesn’t express where I am at emotionally. It took me long enough, but I have learned to be happy and content while living a life filled with physical pain. Yet only sharing my emotional status doesn’t give insight to where I am struggling physically. The problem with trying to convey both aspects is that there isn’t enough time in the day to do it. For the most part I stick with my standard response of “could be worse/could be better”, because it is easy and it’s true.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Psoriatic-Arthritis.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

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