Linkyn, 18 months

My daughter was born with PKU, a rare metabolic disorder. Right now, we are lucky to have insurance cover her formula and medical food, but I worry about the future. If we did not have this insurance, we would not be able to afford the cost of her needed formula and medical foods. She is an amazing little girl that is thriving and I hope nothing ever gets in the way of that.

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