RT @eurordis: Read a new #livingwith story-...
RT @eurordis: Read a new #livingwith story- #PraderWilliSyndrome: A Story of a Rare and Unique Life: http://t.co/u9Z9Et1KdR
October 07, 2015
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Prader-Willi Syndrome: A Story of a Rare and Unique Life
My name is Pia. My husband John and I have a rare and unique daughter, Olivia, who is 15 years old. Olivia was diagnosed with Prader-Willi syndrome (p-ter-q 11.1) and also partial monosomy of chromosome 10 (p-ter-p14). Olivia was diagnosed a week after birth because I demanded a chromosome test as I knew something was wrong.