Originally posted 4 December 2019
Beginning my 3rd summer with CRPS and I now know that the heat makes my symptoms much worse. The first summer I was still figuring everything out, the second I was mentally out of it, but I started this summer mostly sane so I recognise the pattern. Is the heat bad for everyone else? Or is winter worse for some of you?
Everything changes
I was actually surprised when I found this post. These days I love summer and dread winter. Warmth is everything for me, I have electric blankets in the lounge and bedroom and a foot warmer for the office. I guess this was before my left foot and leg turned into an ice block. It feels a bit unreal to me.
