Alpaca Sock Sale – Hurry Before May 11th!

It provides support & important information. by B.B. (LA)

Glad to find this page.  Newly diagnosed…any ideas or experience would be so welcomed at this point. by H.G. (Facebook Fan)

So glad I found this site…It’s great to know that support is out there…thought I would have to do this alone, but now I have hope to find some answers other than…it’s all in you head!!!! by Raynaud’s Forum Member

Just discovered your site, I found it very informative, thank you. by M.P. (Canada)

The Raynaud’s Association has helped me significantly providing info on warming products and medications, and most importantly making me feel less alone. Also helped me with explaining it to people who don’t experience the disease themselves.  I am very appreciative of everything they have provided over the years. by K. M.

This site is amazing, I’ve now met great other people that are in the same boat as myself and know that there are people out there that can help. by N.D.

Provided information and advice. Acknowledgement of the condition, as opposed to comments like, “yes, my hands go a bit pale when I’m cold, too….” J.A. (Facebook)

I wanted to take a moment to thank you for your efforts in creating an awareness program…People will normalize and dismiss any number of things in their lives, and creating awareness truly means a great deal in reaching these people…please continue the great work that you and your team are doing.  by V.K. (Canada)

Information is so important between patients.  Raynauds.org is a great resource!  Thanks. by N.E. (Canada)

I am so glad this organization exists. All I want is treatment that is helpful. By D.S. (MT)