Kaitlyn Hatchard (Spinal Muscular Atrophy-Type 1)
Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway.
Tuesday, August 21, 2012
Monday, November 21, 2011
Monday, May 9, 2011
Thursday, March 24, 2011
Monday, March 14, 2011
Friday, January 7, 2011