The story of Vanesa
Hi, Im Vanesa and Im 5 years girl from Slovakia living with rare disease called Phenylketonuria, in short PKU.
PKU is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine.
The main treatment for PKU patients is a low-protein diet that completely avoids high-protein foods (e.g. Fish, meat, eggs, standard wheat flour, dairy products, legumes) and control a daily protein intake. PKU patients also have to drink PKU formula after each meal. The formula is a special blend of amino acids that provides protein without the amino acid phenylalanine. The formula contains important vitamins, fat, minerals that help meet nutritional needs.
Untreated, PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders.
Vanesa is our sunshine full of energy and smile every day. She loves music and good movies, sport as well as cooking & baking with mom.