Molly’s Fund Speaks Out on Raynaud’s

Thank you, Raynaud’s Association…I am glad that I’m not alone! by I.C. (Facebook Fan)

So nice to know there are fellow “frosties” out there – just found out what my white fingers were all about… by C. C. (Facebook Fan)

This is an awesome awareness video!…a great post to share with family and friends who are unaware of what Raynaud’s is…Thanks to the Raynaud’s Association for the great work! by J. W. (Canada)

Thank you so much! I have enjoyed reviewing your newsletters. It has helped me better understand what my mom is experiencing, and I think she will benefit from the information as well. Her doctors really don’t have much to offer her in terms of support.   by L.W. (OR)

Hi, I just joined today and I’m so happy to find this site. Only other sufferers can truly understand Raynauds. by Raynaud’s Forum Member

Raynaud’s plays a big role in my everyday life and feeling connected to others navigating it is reassuring.

S. L. (Canada)

It’s really nice to have come across this support page…most of my family just don’t understand…I appreciate this group so much! by H.B. (Facebook Fan)

I’m sure all who visit this page will agree that the Raynaud’s Association is the best source of information and support for all of us with Raynaud’s… by J.W. (Canada)

Lucky for me that I found your web site!  Keep up the phenomenal job. by M. H. (PA)

After years of thinking I was just sensitive, I’ve found the truth!  So much great info on your site.  Thanks!!! by S.B. (Twitter Follower)