Quote:
Originally Posted by Lynn
Wow - my feet go like that too - well similar anyhow. No fun at all!
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No, not fun, especially when the blood flow starts to get back into those areas. Oh the ache.
My friend recommended these slippers she swears by (she has fibromyalgia and is constantly cold). They're down-filled and so light, as light as socks. They don't make my feet feel as though they're sweating, but when I take them off my feet are toasty warm.
Great investment for sure, as I understand with Raynaud's, keeping extremities warm is a big part of dealing with episodes. Now, to find something similar for my hands.