The FAP Gene Support Group

(Familial Adenomatous Polyposis)

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The Rosa Gallo Foundation

There are 3 pages for the Foundation on our Website

Page 1 Page 2 Page 3

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).

We also produced a presentation for their Annual Conference in Verona and also had an article published in a book entitled "Polyps and Polyposis, From Genetics to Treatment and Follow Up" that was published by Springer.