Pardar Willi Syndrome ( PWS) is a highly complex disability, where the genetic Chromosome 15 is deleted.  Chromosome 15 is where it signals the brain to send a signal down to your stomach to tell you your full, when this is deleted it causes a uncontrollable Hunger not just for food but hungry for a Cure, sadly there isn't a cure so people who have PWS can easliy become severely Obese, this leads to type 2 diabetes and even eventually eat themselves to death.  Babies who are born with Pardar Willi Syndrome appear very floppy because of weak muscle tone and poor with feeding, also they have small hands and feet.  There is 1 in 15,000 babies are born with this complex disability.

The History of PWS 

Pardar Willi Syndrome ( PWS ) was first discovered by Alexis Labhart  his studies show young children who have PWS appeared to be floppy due to poor muscle tone  and poor with feeding, they were also appeared to be very fat, so he discovered that the babies had a deleted chromosome 15.  Dr Alexis Labhart diagnosed 5 babies with PWS.  Two Swiss doctors named Dr Pardar and Dr practised under Dr Labhart,  together they discovered 5 more children with PWS and named the Syndrome Pardar Labhart Willi Syndrome (PWS).  When Alexis Labhart died Dr Pardar and Dr Willie used his studies, later discovered 10 children who were alot younger than toddlers born with the Syndrome , which they appeared to be more floppier and alot poorer with feeding, so Dr Pardar and Dr Willi renamed this complex Syndrome Pardar Willi Syndrome (PWS ) as it is known Today. Then an Irish Dr From Wexford General Hospital where he used Dr Pardar and Dr Willie Studies to Diagnosed the first baby in Ireland to be born with Pardar Willi Syndrome (PWS) through blood Tests, believe it or not I am that baby.