The Rosa Gallo Foundation

Website in Italian

We have tried without success to provide an English translation to their website and instead provided a translation on our own pages.

The Rosa Gallo Foundation contacted John in April 2008 with an invitation to speak at their 3rd Annual Conference. The Foundation was born to continue the long and courageous journey undertaken by Rosa Gallo, a girl of Salerno, which ended prematurely after 21 years following a multi organ transplant (intestine, liver and pancreas) for a disease called familial adenomatous polyposis (FAP).

John is now in the process of providing a written account of our work for the conference and also, hopefully for inclusion in a book titled "Polyps and Polyposis, From Genetics to Treatment and Follow Up" that will be published by Springer.