© 2017 Hereditary Colon Cancer Foundation

 

www.HereditaryColonCancerFoundation.org and www.HCCTakesGuts.org are informational and support websites for those affected by hereditary colon cancer syndromes. The website does not provide medical advice, recommend or endorse health care products or services, or control the information found on external websites.

 

Hereditary Colon Cancer Foundation and the Familial Adenomatous Polyposis Foundation are registered charitable organizations in Illinois and Utah, and tax-exempt under Internal Revenue Code Section 501(c)(3). Mailing address: 3519 NE 15th Avenue, Unit 518, Portland, OR 97212  |  info@HCCTakesGuts.org

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Hereditary Colon Cancer Takes Guts

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    Attenuated FAP, Cowden Syndrome, Familial Adenomatous Polyposis, Gardner Syndrome, 

    Hereditary Mixed Polyposis, Juvenile Polyposis Syndrome, Lynch Syndrome, Muir-Torre Syndrome, MYH-Associated Polyposis, Peutz-Jeghers Syndrome, Turcot Syndrome

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    April 14, 2015

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    Travis H. Bray, PhD; Executive Director

    "Whenever you grow up in a family of people who think they’re going to die young, childhood ends pretty early. When I was a kid, they would do colonoscopies and not give you anything to put you to sleep like they do today. You were stone cold sober. One time when I was around 13 years old, I was undergoing a colonoscopy and told the doctor to give me the camera. “Dude, if you can see, I want to see.” So there I was…looking in my own camera. That was the stuff I was doing when I was 13 years...

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