Learning to Dance in the Rain Autoimmune Event

So glad there’s a place that I can turn to if I need help or questions. A.G. (Canada)

Your posts helped me to understand the condition and it was great to find helpful gadgets to deal with Raynaud’s.  N. D. (Facebook)

Thank you for your wonderful Association and grateful for your website.  It has guided me when there was nowhere to turn .

L. H. (CT)

It’s really helpful to know that you are not alone…For my family and friends it’s really hard to understand how uncomfortable it is to feel frozen even when the weather outside isn’t so cold. by C.T.

I’d like to take the opportunity to say that I really appreciate The Raynaud’s Association’s website and Facebook posts. by D.R. (OH)

This organization keeps me informed of ways to manage my Raynaud’s. From reviewing & testing warming products to keeping us up to date on the latest medical developments, I really appreciate it. by J.W.

I went to your website today for the first time and was very impressed…I’m anxious to learn how to control the symptoms and am anxious to receive your newsletter. by B.C. (NJ)

Glad I found a site that may offer a little more information for me about Raynaud’s and ways to manage this. by T.V. (Facebook Fan)

The Raynaud’s Association has been a great source for information from other members as well as articles from magazines and health care professionals. Through the Association I have been able to better manage the disease, as well. by J.F.

I was recently diagnosed with Raynaud’s, and I have found it to be a blessing to have found this Facebook page.  I now don’t feel as alone, and it has really helped me to understand the disease. by T.E. (Facebook Fan)