Jordan

My story is a sad one. I am a parent of a PKU individual. My son was born June 17, 1985, diagnosed with PKU at 3 weeks of age. He was immediately started on a PKU formula and progressed to

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Declan

My son is currently ten years old. When he was first born, his father’s health insurance through work wouldn’t cover this low protein foods. Thankfully, the formula only was covered through a program. I met a young family of a

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Isabel

I have two daughters. Only the younger one has PKU. We struggle to find foods that Isabel can eat. Medical foods are incredibly expensive, and our insurance plan, which is otherwise good, is exempt from state mandates which should provide

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The Medical Nutrition Equity Act will provide key support for those Americans who rely on medical foods to survive and thrive.