Phoenix Sjögren’s Walkabout and Autoimmune Disease Health Awareness Fair

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 am a huge fan of (the RA) site. They continue to keep me up to date with research, potential methods to help reduce the frequency of a flare up, as well as new gadgets that can help! It is definitely my “go to” for the latest and greatest for trust worthy information…I highly recommend this site!!! by A.J. (TN)

Raynauds.org  has been an invaluable resource for my family…I’ve learned so much from your site and it has helped me to better care for my “frostie.”  by M.R.

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

So many doctors are unfamiliar (I send them here often). This community has been extremely helpful with info, support, and suggestions for a condition that impacts my life daily. Thank you to the page moderators! A.C. (Facebook)

I’ve learned a lot from this site, it’s such a great help – keep up the great work! by H. V. (PA)

This organization helped me with ways to explain what Raynaud’s is and how it affects me and my family. by Anonymous

After years of feeling alone. I am not.  Thank you. by B.D. (NY)

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. by Anonymous

Thank you!  The Association was THE resource after I was diagnosed!…enjoy your newsletters…always recommend your site to fellow sufferers and curious friends. by A. M. (Facebook Fan)