The Rosa Gallo Foundation
are 3 pages for the Foundation on our Website
1 Page 2 Page
have tried without success to provide an English translation
to their website and instead provided a translation
on our own pages.
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
a book entitled "Polyps and Polyposis, From Genetics
to Treatment and Follow Up" that was published