My Nonprofit Reviews

When I was first diagnosed with Raynaud’s, and looking for information, I found Raynaud’s association ‘s website, where a I discovered lots of information all in one place. This is a great organization that provides information, tips on products to help make suffers lead a more comfortable life, and are always there to answer questions. They are definitely the best source of information.

When I was diagnosed with Raynaud's, my Doctor provided very little information about the disease, or how to live with it. Upon searching for information online, I found the Raynaud's Association to be the best source for information and support.

The Raynaud's Association is, without a doubt, the best source of information for anyone with Raynaud's. They are always sharing the latest medical information, information about products and tips to help Raynaud's sufferers. So many people have Raynaud's but are undiagnosed because of the lack of awareness for this condition. The Raynaud's Association are working very hard at providing that awareness. I have found out more helpful information from them, than I have from my doctor.

I was diagnosed with Raynaud's 3 years ago and with little information from my Doctor I went to the Internet, and there I found the Raynaud's association Inc website. This group of dedicated individuals provide many fellow Raynaud's sufferers with a great resource for information, support, and awareness that I have found nowhere else. They provide information that helps living with Raynaud's more bearable!

When I was diagnosed with Raynaud's six months ago, I knew nothing about this disease but needed information. My online research led me to the Raynaud's Association website which provided information on the numerous symptoms, medical research, tips and information of products that help protect a Raynaud's sufferer. I have since purchased some of these products and they truly help me deal with this disease on a daily basis. I am also very thankful for their Facebook page and website forum that provides advice and information from others and reminds me that I am not the only one with this condition. Without the Raynaud's Association I would not have a useful resource for information nor would I know of the great products like my Volt Heated slippers. I appreciate all that this Association does, they are awesome!

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