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. 

This is a new foundation and website that will be going through a lot of changes during the upcoming year.   Please be patient as we get our Foundation up and running.

Some of the information you will find on our web site includes:
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.

Brenda U. Bostic, Founder & CEO