Zoë and Stella

We are extremely lucky to have identical twins that can share the trials and tribulations that come along with having PKU, but the cost to provide both of them with adequate medical foods was so intense, especially during the picky

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Raelyn, Age 3

My daughter was born with PKU and our world was flipped upside down to say the least. I fought with our insurance company for months, we have “good” insurance, and yet they still they don’t see this as necessary. Having

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Sarina

I am no longer able to afford medical food coverage such as probiotics and none of my providers can ever get it approved.

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Leah, Age 12

We have an excellent private BCBS insurance policy, that we pay monthly for. As great as it is, it will not cover our daughters medical formula. This is a need, that comes accompanied by multiple letters of medical necessity from

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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.