Raynauds

Raynauds

Philip Hayes2012-11-05T09:31:01-05:00November 5th, 2012|1 Comment

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About the Author: Philip Hayes

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What People are Saying About Us…

The Raynaud’s Association provides a lot of essential tips and resources to help me manage my day-to-day symptoms. I’m able to manage much better thanks to this association. by Anonymous

Able to Manage Much Better Thanks to This Association

Thank God I came to know what is my problem. You have an excellent page. by M.N. (Facebook Fan)

You Have an Excellent Page

I didn’t know that Raynauds can be secondary to another condition. I’ve learned this & much more from this site – thank you.

J. D. (Facebook)

I've Learned So Much From This Site

Thank you so much for making this page and having people donate to this. By M.J. (Facebook)

Thanks So Much for This Page

They (Raynaud’s Association) helped me in so many ways. First, that what I had been experiencing for so long had a name and I wasn’t alone. I had not come across anyone that experienced it in their nipples,” she said. By N. R. (AR)

Helped Me In So Many Ways

I am so happy I found this page. Having recently been diagnosed with RP, I’m trying to adjust to it and make sense of it all. by A. S. (Facebook Fan)

So Happy I Found This Page

Thanks for being a great Raynaud’s resource! by C.B.

Great Resource!

My 17 year old daughter has recently been diagnosed with Raynauds…I love this website and find it very helpful. Thank you. by L.B. (IL)

I Love This Website

The Raynaud’s Association has given me a platform to speak about my journey with Raynaud’s. I felt alone, but once I found this association I met thousands of other sufferers. by A.C. (NY)

Platform to Speak and Not Feel Alone

This Association has been so helpful for me – so supportive as I navigate this frustrating and under researched phenomenon. The information provided is always helpful. by Anonymous

Support Navigating this Frustrating Phenomenon