IMPDWF is a volunteer-driven foundation supporting children with inherited metabolic disorders in Pakistan. We raise awareness, provide nutrition, and guide families through their toughest battles
Children’s Journey of Hope & Healing
Meet the brave children fighting metabolic disorders and see how your support changes their lives.
Specialized care for a child
Family support gives us love, strength, and confidence. It helps us face problems and makes life happier and easier.
Adapting to their unique dietary needs
It means adjusting meals to match a person’s health, age, or condition, helping them stay healthy and strong.
Specialized care for a child
Specialized care means giving extra attention, medical help, or therapy to meet a child’s special health or developmental needs.
Every Child Deserves a Chance at Survival, Dignity, and Hope
Every year, thousands of children in Pakistan are born with rare metabolic conditions. Without proper treatment, these children face seizures, delayed growth, and life-threatening complications. At IMPDWF, we believe every child deserves a chance at survival, dignity, and hope. Through awareness, specialized nutrition, and family support, we are filling urgent gaps where systems fall short.
Our Aims & Objectives
We are dedicated to improving the lives of individuals affected by Inherited Metabolic Disorders (IMDs) through early diagnosis, awareness, and lifelong medical and emotional support.
Awareness & Education
Spreading awareness about metabolic disorders through community programs, workshops, and online campaigns.
Access to Treatment
Supporting patients with affordable diagnosis, therapies, and nutritional management for a better quality of life.
Research & Collaboration
Encouraging research and partnerships with healthcare professionals and global organizations to find better cures.
Understanding Inborn Errors of Metabolism
Discover real stories and trusted information about rare inherited metabolic disorders. Learn how early diagnosis, awareness, and medical care can transform lives and bring hope to families.
Alkaptonuria (AKU)
Also known as “black bone disease,” AKU prevents the body from breaking down homogentisic acid, causing cartilage and bones to darken and become fragile. Early treatment with Nitisinone can reduce progression and improve mobility.
“With early care, I found new strength and hope in daily movement.”
Maple Syrup Urine Disease (MSUD)
MSUD is a rare genetic disorder that affects the body’s ability to process amino acids, giving urine a sweet smell. With a special diet and medical monitoring, children can live full, active lives.
“Our baby’s journey began with fear but turned into hope through careful nutrition.”
Phenylketonuria (PKU)
PKU is a lifelong condition that prevents the breakdown of phenylalanine, an amino acid found in protein. Early screening and diet control help children reach their full potential without complications.
“Newborn screening saved our daughter’s health — awareness truly matters.”
We are a Trusted Charity Foundation
We work to make invisible disorders visible, pushing for early screening and diagnosis.
We source and provide vital medical foods that are otherwise unavailable, a direct lifeline for children.
We walk alongside families, offering counseling and practical support from diagnosis onward.
Act of an individual or group freely giving time and labor, often for community service
Stories of Courage — Metabolic Disorders
Emma’s Journey with PKU
Emma’s courage in managing Phenylketonuria (PKU) shows that awareness and hope can lead to strength.
Noah’s Victory Over MCADD
Diagnosed early with MCADD, Noah proves that proper care and support can make all the difference.
Sophia’s Resilience with MSUD
Sophia’s journey through Maple Syrup Urine Disease inspires families to keep believing in brighter days.
WE DELIVER ALL OVER PAKISTAN
What Our People’s Say About IMPDWF









