Cold Feet

Cold Feet

Frostie2013-02-22T17:13:02-05:00February 22nd, 2013|0 Comments

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Love them for keeping us updated on products, and sharing stories of other people who live with Raynaud’s. by Anonymous

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Like seeing what other people are doing to treat and cope with Raynaud’s. Mine is pretty severe in my fingers so I’m always looking for advice. B. C. (IL)

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So happy that I found you, as I am newly-diagnosed with Raynaud’s and I need help! Thank you! L.C. (SD)

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Just wanna say I love your site because it helped me learn more about Raynaud’s…thought I was alone until I found you all…getting to read what others do for it helps a lot…thank you for your association :) by C.U. (KY)

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I’ve had Raynaud’s for years and was pleased to find this group. It’s a wealth of information about the disease & a great assistance in coping with its symptoms. by P.J.

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My Doctor provided very little information about the disease or how to live with it. I found the Raynaud’s Association to be the best source for information and support. by J.W.

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