This is a place-holding site for
Emily Hope Lee
Please visit our website: http://the-lee-family.us
Emily was born on July 15, 2005. Shortly after birth she was diagnosed with a terminal neuromuscular genetic disorder called Spinal Muscular Atrophy (SMA), Type I, or Werdnig-Hoffman Disease. (http://www.fsma.org/sma_facts.shtml)
Please visit our family website for updates on Emily's condition. Updates, Prayer Requests, Pictures, and information are a few of the things that you will find there. Please visit again soon!
Emily's older sister's site is: http://the-lee-family.us/index.php?linneagrace
The Lee Family site is http://the-lee-family.us
Supported by SMA Support