Medical Nutrition Equity Act (MNEA) Video

PKU is diagnosed through Newborn Screening, and although all babies in the United States have been screened at birth for over 50 years, coverage for medically necessary treatment is often denied and unreliable.  Without early and lifelong treatment, PKU causes irreversible intellectual and physical disability.  Congress has an opportunity to prevent these devastating results by passing the Medical Nutrition Equity Act, a bi-partisan bill waiting for action in the U.S. Senate and House of Representatives. 

For additional information and advocacy guides visit the MNEA home page. 

 

PHENYLKETONURIA (PKU): CLOSING THE GAP IN TREATMENT COVERAGE (SHORT VERSION 5.08 MINUTES)

Please share PKU: Closing the Gap in Treatment Coverage with Members of Congress and all of your contacts. This version is great for social mediahttps://youtu.be/K3ETf7OJ8tY



PHENYLKETONURIA (PKU): CLOSING THE GAP IN TREATMENT COVERAGE (FULL VERSION 7.35 MINUTES)

This version has additional details about why passage of the Medical Nutrition Equity Act is critical to preventing disability from untreated PKU.  Please share the full length version with anyone willing to watch https://youtu.be/5hW1z1mZOtc



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