Times Square Photo for Raynaud’s Awareness Month

Helped me feel ‘normal’, and not alone. Raynaud’s should be recognized as a disability…to accommodate and enhance the wellbeing of people who experience symptoms. C.C. (Facebook)

It helps me realize that I’m not alone and also can get good advice. by A.E. (Facebook)

Thank you for the information…my daughter is suffering quite a bit but I think she is relieved that she is not alone and her pain is not in her head…We are both thankful for the support given and information. by B.N. (Australia)

Great video – I’ve recently been diagnosed…mine is secondary to another autoimmune disorder.  Raynaud’s is what sent me to the doctor.  Thanks for this clear explanation! by M. F. (Facebook Fan)

Thank you for all your support.  I used to feel so alone in my suffering!!! by M.D. (NH)

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

I’ve just found this page with great relief. by J.A. (UK)

Thanks to The Raynaud’s Association for making people aware of this disease and for all those that have shared their story making those of us who suffer from the disease to know we are not alone. by L. L. (NH)

Thank you! This newsletter is SO comforting and helpful. by A.C. (NE)

It is a great website to go for products that have been tested by Raynaud’s sufferers, instead of having to Google…and be overwhelmed by so many search results. by Anonymous