Upcoming Scleroderma Foundation Events

You all do an excellent job running this site and keeping everyone informed. by A.J. (TN)

The Raynaud’s Association’s support materials and blogs are helpful in finding solutions. By K. J.  (OR)

I find your info invaluable.  In fact I’m seeing my doc tomorrow based on the details you provided… by M. U. (Facebook Fan)

I am happy to finally come across a site like this…I really hope to learn more about this through other fellow members…and to try to help them with my experience. by H.R. (NY)

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

Always there for me when I need help.  Great advice, help and support and I thank you so much. by S. R.

This site is really helpful to those new with this rare condition like me.  Health providers don’t really understand what Raynaud’s syndrome or the cause of it, again thank you for this Association. by J.W. (Facebook Fan)

I have Raynaud’s Syndrome and I find the reports of great interest. I have forwarded info on to others who have this illness. by K.C. (AZ)

I am thankful to have the Raynaud’s Association as a very important source of information, without you guys many of us would never know of the useful tips and information you share! by J. W. (Canada)

I’m so glad to find this page because nobody understands how terrible this disease can be.  I’m so tired of being in pain! by M.B. (Facebook Fan)