Molly’s Fund Speaks Out on Raynaud’s

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)

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

Everyone with Raynaud’s should Like and follow the Raynaud’s Association, it’s the best source for information, both from the association itself and fellow followers. by J.W. (Facebook Fan)

Thanks for all the very useful info and tips! by J.W. (Facebook Fan)

I was diagnosed with Raynaud’s in 2013. This website is very much appreciated. My doctor couldn’t really give me any tips on daily living, so your blog is invaluable. by Anonymous

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)

My daughter was just diagnosed with this. I am so upset for her. She is a photographer. I want to know how to help her cope. Thank You for this Association By R.S. (Facebook)

Thank you for the amazing work you do, year after year.  So many individuals’ lives are improved because of the work you do.  D. H. (AL)

Great to find you! Have very much appreciated reading your blog entry on Keeping Toes Warm! By P.M. (AR)