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Branford mother continues push for ALD screening with patience and passion

BRANFORD – When we first met Jean Kelley, she was pushing for a new law to require newborn screening for adrenoleukodystrophy (ALD), the devastating genet...
BRANFORD - When we first met Jean Kelley, she was pushing for a new law to require newborn screening for adrenoleukodystrophy (ALD), the devastating genetic disease that took away her young son's ability to talk, move or feed himself.
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"If one is able to intervene at the point where the first neurological symptoms appear, either with bone marrow transplant or with … stem cell therapy, it's very likely that you will arrest further deterioration," says Dr. Myron Genel of the Yale Child Health Research Center.

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Click here for the entire column from The Hartford Courant.

Click here to learn more about Brian's Hope.

 

 

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