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We’re sharing a couple of videos recently discovered on the web with information and tips for fellow Frosties:
Raynaud’s Disease Video
Raynaud’s Disease of the Toes Video
Thank you for your newsletter and for publishing these articles. They are helpful for those of us dealing with this illness.
By M.S. (WA)
…relieved to know what it is…comforted to know there are other folks that have this condition…nice to have a place to share what works for us.
by J.J. (VA)
After years of feeling alone. I am not. Thank you.
by B.D. (NY)
I am thrilled to find this organization. I have suffered with Raynaud’s for probably 20 years and just dealt with it. Thank you for existing.
by S.W. (CA)
Has been a very informative group. Prior to them – there was no one that talked about it and ways to help. Thankful they are out there with tips and information needed!
Thank you for sharing all this info. I am trying to make people aware of this illness, too…
by J. F. (Facebook Fan)
I’m grateful for all the info you provide!!
by J. S. (MA)
I’m sure all who visit this page will agree that the Raynaud’s Association is the best source of information and support for all of us with Raynaud’s…
by J.W. (Canada)
Please keep up the great work. Your work touches so many unknown but eternally grateful people.
by M.W. (WA)
The Raynauds Association reminded me that I was not alone. It made me feel as if I was part of a community and for that I am thankful.