Fellow Frostie Enrique Cubillo, innovator of a new endurance sport called SpikeBoarding, took to the road this month to help promote Raynaud’s Awareness Month. He’s spikeboarding for Raynaud’s!
Here’s a link to our press release announcing his team’s efforts, and you can see Dan Bowen from his group in action in the pictures below. For our earlier story on how Enrique’s need to keep his extremities warm led him to discover SpikeBoarding, here’s the blog post.
© 2017 SpikeBanner.com
© 2017 SpikeBanner.com
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What People are Saying About Us…
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.
Wealth of Information and Tips
Great website! Nice to read about people just like me! No one in my family understands how debilitating this can be-especially with winters in Iowa. by L.H. (IA)
Great Website!
I’m really glad I found your website, it has been a big help! I especially like the product reviews! by K.R. (WI)
Website Has Been a Big Help!
Thank you for your newsletter and for publishing these articles. They are helpful for those of us dealing with this illness. By M.S. (WA)
Your Newsletter and Articles Are Helpful
The site is great! by B.F. (IA)
The Site Is Great!
The Raynaud’s Association has helped me significantly providing info on warming products and medications, and most importantly making me feel less alone. Also helped me with explaining it to people who don’t experience the disease themselves. I am very appreciative of everything they have provided over the years. by K. M.
Helped Make Me Feel Less Alone
(Their) Facebook page helps me to better understand Raynaud’s. I have not found any other reliable source of information like this. It is very helpful to me. by Anonymous
Reliable Source of Information
The Raynaud’s Association has been a great source for information from other members as well as articles from magazines and health care professionals. Through the Association I have been able to better manage the disease, as well. by J.F.
Great Source for Information
Absolutely great to have a place to chat and learn about this difficult to manage hidden illness. Love the competitions, love the reviews & great to have so many links to Raynaud’s products! by L.A. (Facebook Fan)
Absolutely Great
This site is really helpful to those new with this rare condition like me. Health providers don’t really understandwhat Raynaud’s syndrome or the cause of it, again thank you for this Associatio n. by J.W. (Facebook Fan)
Site Is Really Helpful


