Phenylketonuria, commonly known as PKU, is a metabolic disorder. It’s characterized by the body’s inability to properly process an amino acid called phenylalanine. When left untreated, this amino acid accumulates in the bloodstream, leading to potential health complications. Rooted in genetic mutations, PKU presents itself in roughly 1 in 10,000 newborns in the US each year.

Understanding PKU’s Genetic Origins

The genetic nature of PKU means it’s passed down through families. For a child to manifest the condition, they must inherit the mutated gene from both parents. However, inheriting just one mutated gene makes a child a carrier, where they won’t display the symptoms but can pass the gene to their offspring.

Our Comprehensive PKU Assistance

Children R Future has curated a robust assistance program for children grappling with PKU:

• We ensure they have access to special diet foods, even facilitating tools like electric ovens for preparation.
• Vital medications, such as Quan pills and daily powdered medication milk, form part of our medical aid.
• To address potential cognitive challenges, we offer speech and occupational therapies aimed at optimizing brain functions.
• Additionally, we provide essential equipment and products, like wheelchairs, and endorse PKU-friendly products, prominently featuring brands like Easy Life & Mbaby.

Our Pledge to PKU Children

Children with PKU face unique challenges every day, and at Children R Future, we’re committed to standing by their side every step of the way. Through comprehensive support, tailored interventions, and a deep understanding of their needs, we aim to enhance their quality of life and ensure they have every opportunity to thrive.