Friday, June 6, 2014

LUPUS: Day 21, no medication

Day 21, no medication. For days now I felt like things were leveling out and then two days ago they started to rear their ugly heads. Loopy Lou (my pet name for Lupus) has decimated my appetite. I’ll eat once a day because I force myself, twice if I’m lucky. I’m exhausted but can’t sleep. Joint pain all over my body. Headaches. Neurologically I’m still having muscle weakness and pain. Sharp shooting pain with no warning. Burning or tingling sensations in my feet and hands. Sensation of being lightly brushed by fingers across the tops of my feet. Tremors, blurred vision, choking. All when I thought we leveled out. In their true nature…they did a sneak attack. Like when you turn your back on the ocean…

Needless to say, I’ve developed more coping skills over the past three weeks but some of that may be a sort of “immunity” to the difficulties. Lol. I can tell you this, DO NOT EVER UNDERESTIMATE your brain. Talk about being made painfully aware of how much it does and controls. Jeez. If you have deal with any type of health or physical limitations…laugh. Laugh a lot. It does so much for me. Don’t get me wrong, it’s not always easy to crack a smile between the pains, but if you can you will see its worth. Hell, I even laugh at the pain sometimes, for I can’t help myself. Damn shooting pains catch me so off guard that I need to laugh in order to  mask the crazy shouts that come from my mouth with no warning. Lol. One of the new frustrations: Doc is prescribing a wheelchair to have for the times when the neuropathy is preventing me from being mobile on my own. I finally wrap my head around the idea of it and I call to make an appointment to be fitted for it and so far 6 dealers in my area will sell me a chair but do not do any type of measurements. Can I get a break here. SHIAT!


Have a blessed weekend. MUAH

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