Maine

Brittany

My daughter, Brittany, was born with PKU and we were able to provide her with the nutritional products that she needed to avoid significant brain development problems. Unfortunately, that is not the case for all children and adults in the US.

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Kathleen

I am disabled so we are a one-income family (I am unable to work outside the home). I have several diseases and syndromes that cause multiple issues: I am unable to digest gluten, I need a special diet for my

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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.