[WATCH]: Journey- Blaise & Prader Willi Syndrome-The Diagnosis Until Now

Pictures September 2009 through April 2011. I wanted to share this video to remind everybody never to give up hope. With a little hard work anything is possible. Blaise is living proof of this . These are pictures of Blaise from the time of his late diagnosis around age 3; after which, he traveled to see the amazing Dr. Jennifer Miller in Florida, started growth hormone, his food intake, type and quantity changed , became carefully monitored and he started many therapies . He turned 4 January 2011. Blaise does not get to indulge in the same foods that other children do as his body does not process calories like you or I, as well as other medical concerns the food could cause. Please follow the link below to find out more regarding

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