What is UNBS?
   


One family’s story of hope


When Matthew Chorey was born, a screening test for his disorder was not available in New York State. Unaware that he was born with a critical enzyme deficiency, Matthew was given protein dosages that unfortunately caused irreversible damage. Matthew will never sit
up on his own, or run around with his friends like most boys his age.

On December 9, 2006, Emma Joy Chorey was born. An expanded newborn screening
test revealed that she had the same disease as her older brother Matthew. Thanks to early
detection and a special low protein diet, Emma is now progressing normally.

 
 

Universal Newborn Screening is a state-based public health system that is essential for preventing the devastating consequences of a number of medical conditions not clinically recognizable at birth. All babies born in the U.S. receive newborn screening. 

Thousands and thousands of babies are born everyday in the United States. Most babies appear healthy at birth, full of life and possibility. Yet they could be hiding a rare or potentially devastating disease. By screening every baby at birth, we can prevent serious mental or physical disabilities, even death. And by making the requirement universal – in every state – we can ensure that no child will have to suffer unnecessarily.

Due to an inequity in each states newborn screening program, children are not being diagnosed for these many rare diseases.

Click here to see how many diseases your state screens for.
                        


 
   
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