I have been ill with fibromyalgia for about twenty years now. In that time, lots of things have changed, and one of them is my personal hygiene routine.
One would think that taking a bath or a shower would be an easy thing to accomplish, but if you suffer from chronic fatigue, fibromyalgia, back problems or angina problems like I do, you would realise that it consumes a lot of your spoons. So I had to do a bit of rethinking of my daily routines. I've discovered that one of the places that takes a lot of my spoons is the bathroom.
Because bathing and drying and dressing exhaust me, I varied my time in taking a bath depending on how well I feel. If I have enough energy, I would bathe in the morning, if not I would take a shower before bed as Chris is home and he helps me get dried and into my nightie. (When you are chronically ill, you quickly get over being humbled by needing assistance- you are grateful for any help available.)
I have found that if I take a bath or shower in the morning I am left with no energy for the rest of the day. If I take my shower at night, I have just enough energy afterwards to get myself to bed, which works out much better.
Hot baths or showers leave me too exhausted and give me angina pain, so I take showers with only warm or tepid water. While I would prefer to shower every day, showering is best done every other day for me to avoid flare-ups of pain, fatigue and soreness. I have decided on some new course of action to make time in my bathroom more fibro-friendly.
One of the first things I changed was how I take a shower, or rather, the position in which I shower: sitting. Here I find those telephone type showers are useful. When I get out of the shower, I sit down to dry off.
I can no longer blow dry my hair so by necessity my hairstyle has been wash and air dry for years now. Time in front of the sink brushing my teeth or washing my face has been modified by resting one foot on a stool while standing. Because of spinal problems and being a short person, I have a glass in my bathroom which I fill with water and use for rinsing and cleaning my toothbrush without straining to reach the tap.
I no longer wear makeup, the standing in front of the mirror and the use of my hands in holding the various tools of the task, is now limited to special occasions only; it is too painful a task to do on a daily basis. Also, my face is so sensitive that it breaks out in red welts at the slightest pressure... which includes smearing on foundation. This is called dermagraphia.
The bottom line is taking a shower is a real workout now. In addition to modifying how I take a shower, I am going to follow these 3 rules: I will only take a shower at night, I will only take warm water showers and I will only take a shower every other day. With the employment of a good deodorant after each shower and a fresh change of underwear each night and morning, I have found that I don't offend anyone and remain feminine and dainty.
Life with chronic illness is complicated, but at least I manage to stay clean while living it! No need to not enjoy staying dainty!
© Glenys Robyn Hicks
So teach [us] to number our days, that we may apply [our] hearts unto wisdom. Psalm 90:12
So teach [us] to number our days, that we may apply [our] hearts unto wisdom. Psalm 90:12
Sister this is all so true. Those who don't know how hard this is could never imagine what we go through just to stay fresh. I am so immobile now that I use special disposable wet washcloths for bathing. It does help me feel freshened up. I miss the water running over me but I don't miss the agony after the shower that would ruin a whole day. I do my washcloth bath at bedtime because then my arms are so sore then I go right to bed. Love Kelly
ReplyDeleteI hear you, Kelly! Those days may come to me as well... No one knows how agonising a shower or bath can be unless they suffer from fibromyalgia or some other chronic illness...
ReplyDeleteI am so sorry to hear that this is so challenging for you. Praying now.
ReplyDeleteThank you, Lauren!
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