Family Pushes for Universal Screening for Infant Disease

Shane Philipps is a happy, sweet 17-month-old baby. But he is also battling a rare genetic disorder that may mean he won't learn to walk on his own. Shane was diagnosed with spinal muscular atrophy (SMA) at 10 months old, when some of his motor nerve cells had already been damaged. Experts say the earlier the disease is diagnosed, the better chance the child will have at walking and learning to control other muscles.

Now, Shane's parents, Chris and Regina Philipps, are pushing to make a test for SMA part of universal newborn screenings because early intervention can help babies with the disease have better outcomes.

 

title

Content Goes Here