On April 19, 2006 we learned our little Gracey developed a rare autoimmune disorder known as Juvenile Dermatomyositis (JDM) - she was 5 1/2 years old. At that time Gracey had become very weak and absolutely unable to get up from the floor. The diagnosis was the beginning of a long road to remission as there is no cure for JDM. This site is meant to track Gracey's progress as she works hard every day to conquer JDM. Thank you for your support and please check back often.
Our sweet little Gracey was diagnosed with a rare autoimmune disorder called Juvenile Dermatomyositis. We've created this site as a way to keep everyone informed as to Gracey's current status as well as all the fun things she comes up with. Thank you for your support and please keep checking back often.
posted by Wes (Gracey's Dad) at
11/26/2006 07:34:00 PM
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