I decided to sort my wardrobe out today with help from my husband Paul, so we packed away the winter clothes and unpacked my summer clothes. Its getting too warm now for jeans and sweat shirts, although I do feel cold more than I ever did before. I never had any socks, but now I have a drawer full, from trainer socks to thick house socks, as my feet are usually freezing. But in summer I really feel the heat, so prefer vest tops and shorts to keep cool and comfortable. They say when you have Fibromylagia, your thermostat is broken, so I probably shouldn't be surprised.
Recently the skin on my hands has felt as though its burning all the time, hope it goes away soon as its an annoying feeling. The electric shock pains have flared up again, they hurt even though they don't last long, so not good in a different way. Imagine someone sticking a pin in you, it makes you jump and hurts as well, and you never know where or when it will happen next!
I felt beyond tired once we had finished, even though it took us all day, with breaks. I sat down for a rest and couldn't get up, as my muscles were so sore it felt like they had closed down. I felt about seventy five, not forty five when I slowly hobbled into the kitchen to help cook tea. Not that I was any help, as I could hardly move and when I did it hurt too much.
I really hope it will cool down a bit tonight, so I can sleep, pity we don't have A/C over here. I always dreaded going some where hot, but A/C makes so much difference and much easier to cope with the heat outdoors.
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