Conference Video: Medical Aspects of Raynaud’s

After years of thinking I was just sensitive, I’ve found the truth!  So much great info on your site.  Thanks!!! by S.B. (Twitter Follower)

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)

As a fairly new Raynaud’s sufferer, it’s great to see this organization spreading the word and providing support. by Anonymous

I just discovered this page and am greatly encouraged by knowing that I’m not alone. by R.J. (Facebook Fan)

When I was diagnosed with Raynaud’s, my Doctor provided very little information about the disease, or how to live with it. Upon searching online, I found the Raynaud’s Association to be the best source for information and support. by J.W.

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

You’re a star.  Thank you so much for the information. by L. W. (UK)

I have it in my hands and feet and find it very painful. I felt very alone till I came upon your group THANK YOU SO MUCH. by S.H. (Facebook)

Incredibly helpful and useful resource for an underfunded cause.  So many sufferers and even more who remain undiagnosed. Thanks. by Anonymous

I really appreciate all you’re doing to help those suffering from Raynauds syndrome! M.B. (VA)