The Isaac Foundation was formed in order to find a cure for a very rare and debilitating disease called MPS VI. My son, Isaac (2 1/2 years old) was diagnosed a year ago. This DVD details informtion about Isaac, his disease, and our quest for a cure. Please share it with friends and family
isaac is at my school we had a jump rope for isaac a week ago
dizzy123able 9 months ago
such a cute little boy
xoxbeauty1 1 year ago
I was in tears very moving emotional thing to go through, I cannot imagine bless Issac and his family <3
meeshellrene 1 year ago
Learning of your family today has blessed my heart and my soul.
HollBeth 3 years ago