The parents of a Bay Ridge boy suffering from a rare form of muscular dystrophy are bringing their fight to save his life to Washington D.C. next month.

Manni and Dayna Scarso said they will speak at a Food and Drug Administration (FDA) meeting in the nation’s capital on Jan. 22 to urge the agency to fast-track approval of a promising new drug called Eteplirsen to fight Duchenne Muscular Dystrophy, the disease…read full article >>