A Blueprint Within – Prader-Willi Syndrome (PWS)

Dini knew something was different with her second daughter, Ayoni, from the moment she was born.

Ayoni has Prader-Willi syndrome (PWS), a rare genetic disease that only affects about 20,000 newborns. One of the most difficult symptoms of the illness is hyperphagia, an intense hunger that never goes away.

Dini and her husband, Anju, share their journey in helping Ayoni thrive despite her diagnosis.

This episode also features in-depth commentary from renowned expert Jennifer Miller, MD, Professor of Pediatric Endocrinology at the University of Florida.