I'd still mention it to your doctor, just so they're aware.

They do have medications that you can take if it gets to be too much - for now, I'll deal with the kaleidoscope of colours I get with mine. Thank you for sharing the photo Lynn, that's a great photo (not great that you have the condition, but a fantastic example of it).

I wanted to post a photo of my feet from the pictures I took, but I will have to come back later with one, I seem to have "misplaced" them on my computer somewhere. ... we all know how that goes. lol.

Plus, I'm not entirely sure how to post a picture without a URL, but I'll figure it out.

Okay, I think I got them figured out. The first 2 are the same foot, you can see the progression of the white areas returning to 'normal' skin colour.

The 3rd was the other foot, which was harder for me to get a photo of for whatever reason, the markings on it were quite unique looking.

Attached Images

	Raynaud's1.jpg (81.0 KB, 87 views)
	Raynaud's2.jpg (84.8 KB, 77 views)
	Raynaud's3.jpg (98.3 KB, 76 views)

Wow - my feet go like that too - well similar anyhow. No fun at all!

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.