SMA, or Spinal Muscular Atrophy, is a terminal genetic disorder for which there is no treatment or cure. A person with SMA develops the loss of nerves in the spinal cord and weakness of the muscles connected with those nerves. A darling little boy named Jonas Coleman was born with SMA 2 ½ years ago. Although he cannot walk, sit, eat, breathe, or even swallow, Jonas’ mind is untouched. His only means of communication is through sparkling blue eyes, which are filled with
expression and happiness! He has miraculously defied medical odds, and each day he has with his family is a blessing!
The Coleman family welcomed a new little baby girl, Margaret Rachel, to their family on August 27, 2010. While the chances were relatively low of having another child affected with SMA, Jonas’ parents recently learned that she, too has this rare illness. Now facing astronomical expenses, the Coleman family needs our help to maintain the life and comfort of these dear children.
We hope to generate funds and also awareness of SMA. As friends and neighbors we are requesting that you join our cause and run the Spread Magic Around 5k on October 30, 2010 at 8:00 a.m. All funds generated from the race will help make life easier for the Coleman family. Please help us make a difference in their lives.
On behalf of Jonas, his little sister, Margaret Rachel, and his parents, Whit and Lindsey Mathie Coleman, we thank you for your generosity! We live in a great community thanks to people like you!
