Welcome to FAP International Information Foundation website. As founder of FAPIIF, I wanted to create a place where anyone could access information on the heredity disease of Familial Adenomatous Polyposis, contact others with FAP and be kept up-to-date on research and treatment of FAP.
Some of the information you will find on our web
Guidelines for Clinical Management; genetic testing, duodenal polyps and cancer, surgical options (J-pouch, BCIR, Brooke ileostomy), the APC gene, MYH-associated polyposis and member stories.
My desire is to have a reader-friendly website and forum. The Forum only works with your participation. We can all learn and live a better quality of life by being proactive and learning from each other.
May God Bless you and keep you healthy.
Brenda U. Bostic, Founder & CEO
Larry T. Ulmer, Co-Founder & Webmaster
The information and advice contained in or made available though this Web site is not intended to replace the services of a trained health professional or to be a substitute for medical advice of physicians. The user should regularly consult a physician in all matters related to his or her health, particularly in respect to any symptoms that may require diagnosis or medical attention. The FAP International Information Foundation, Inc. makes no representations or warranties with respect to any treatment, action, or application of medication or preparation by any person following the information offered or provided within or through this Web site. The FAP International Information Foundation, Inc, will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising there from.
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