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Hello world!

August 15, 2022August 15, 2022 lifewithcentralpainsyndrome_7rzm45 1 Comment

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Why Join

If you have a rare disease, you know how lonely it can be to cope with symptoms and to seek out treatment. When you join a patient community, you realize that you're not alone in this.

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BLOGS

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The Impetus Behind Ben’s Friends Was a Rare Disease: Arteriovenous Malformation. Read and Learn
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TESTIMONIALS

Ben created this wonderful site. His Twitter feed is filled with many stories of hope over great challenges.

Ben’s Friends continues to expand this gift of love and support by creating more communities for folks sharing different great health challenges. Ben’s growing patient support sites continue to provide support with its members while new members share the challenges and share the joys. Thanks to Ben, Shalon and all the others who manage this site. It is a gift that keeps on giving.

--- Sharyn

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Your website then was my biggest support.

We met back in 2006, in Austin at St.Davids. I and my daughter, Britanny, who was then 16 years old were new to the site. Your website then was my biggest support and we came to know that so many others are struggling through very similar issues. Today Brittany is 21 and married almost a year ago. Britanny now lives here in Austin and had gone for a year in San Diego. After her gamma knife operation, we had to wait the two long years. I am so proud of YOU!!! You are such a wonderful example of turning the hurts and pains of this life into positive! May you be ever so BLESSED!!!

--- Pat