Molly’s Fund Speaks Out on Raynaud’s

Thank You for this site.  If it wasn’t for you, all with our disease would not get a better understanding… by D.J. (AR)

Thank you for maintaining this organization and for the newsletters. by M.L. (KS)

Thanks for all the info you guys provide. by J.L. (CA)

Never heard of this condition until I was diagnosed.  Came upon the Raynaud’s Association website where I was provided with a wealth of information and tips on how to deal with this disease. by S.S.

Raynaud’s Association website provided with a wealth of information and tips on how to deal with this disease. I enjoy reading about the stories, experiences, symptoms etc. that other people share through their Facebook page. by S.

Thank you so much for having your Facebook page. It’s comforting to know that people understand the pain. That we are not alone. by L.M. (Facebook Fan)

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

So glad I found this site…It’s great to know that support is out there…thought I would have to do this alone, but now I have hope to find some answers other than…it’s all in you head!!!! by Raynaud’s Forum Member

Found the information on products to help me cope with this disease very informative and helpful. The product reviews are exactly what I was looking for.  by E.M.

Raynaud’s sucks it’s nice to have support. by H.Y. (Ireland)