The Guilt of Being Sick

The Guilt of Being Sick

Guilt. It’s a feeling I’ve had to process a lot lately. It’s something we all deal with from time to time. Maybe it’s due to a forgotten meeting, the dirty dishes piled up in the sink, or stumbling to bed without a kiss goodnight. Things happen, we are human. The guilt caused by being sick reaches an entirely new level of emotion, in a completely different ballpark. This is guilt without something to fix or to control.

The guilt for me increased more and more when I stopped being able to live up to my responsibilities. It’s not that people don’t understand. I know that the people in my life get that I’m sick. What makes me feel guilty is that I ask for — or more realistically, just receive — this understanding from people time after time. It’s not once in a while or an isolated incident — it’s several times a year, for weeks at a time.

My partner understood when a past bout of sickness caused me to cancel plans for our anniversary and his birthday. We were supposed to go on a lovely weekend trip, something we had been looking forward to for a while. Our lives have been full of paperwork, major life planning, job hunting, and other nitty-gritty adult life tasks. We needed a short break. Instead, we spent the weekend in separate beds, as my poor partner tried to get some sleep between middle-of-the-night IV changes and coughing fits. Much of my time was spent in a zombie-like gaze, incapable of any meaningful conversation or romantic cuddling. “In sickness and in health” it goes, but “in health” is so much easier.

My employers had to acknowledge and understand yet again after I failed to complete my work. I am lucky to work for people who are incredibly kind and understanding, but it doesn’t negate the fact that I am behind in my work. People are counting on me.

My family and friends understand when they have to change plans last-minute, assuming they even get a plan out of me in the first place. My poor service dog, who needs constant upkeep in his training and loves to play, had to be understanding. Heck, even the general public has to be understanding when I’m coughing up a storm or stopped in an aisle at a store.

It’s not that I think anyone blames me, although I can’t say the thought has never crossed my mind. It’s the constant feeling of asking too much and not being able to do anything about it. The phrase goes: “It takes a village.” I would be lost without all of the help and understanding I receive from friends and family, and even strangers. It doesn’t mean that I don’t wish things were different.

I think there will always be a piece of me that feels guilty for not being physically capable of living up to my own expectations. The guilt of being sick isn’t always bad, though. I’d say it keeps me pretty grounded and pushes me to do as much as possible before throwing in the towel. But, man, does it suck.

» Follow my journey at The Living, Breathing Wendy «

***

Note: Cystic Fibrosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Cystic Fibrosis News Today, or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to cystic fibrosis.

2 comments

  1. Gisele Lapointe says:

    How I understand your feelings and how I sympathize with you. I remember my daughter how guilty she felt, postponing using oxygen so her children would not have to deal with it, how guilty she felt to leave them behind when she had to go for a tune-up at the hospital, to rely on family and friends to take them to and back from school, to see that their lives were not too much disturbed by her absences, how difficult it was for her husband to cope with it all although he never complained.

    As her parents, how guilty we both felt (and still do) about giving her this awful disease (we did not even know we were carriers of the CF gene then). How, in our old age, we feel for not having her around. Yes, guilt can affect a whole lot of people. Yes, CF sucks!

    • Wendy Caroline says:

      Thank you for sharing those sweet memories of your daughter and your experience with guilt as a CF parent. I’m glad that you could relate to my writing, as much as I wish it wasn’t so relatable.

Leave a Comment

Your email address will not be published. Required fields are marked *