Welcome to FAP International Information Foundation website. As founder of FAPIIF, I wanted to create a place were 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.
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.
Take charge of your disease — do not let it take charge of your life. By being proactive you can LIVE LIFE TO THE FULLEST.
May God Bless you and keep you healthy.
Founder & CEO, Brenda Bostic