This is a blog about my son Matthew's journey to get a diagnosis. The first year of my son's life he developed perfectly. At 14 months things started changing and haven't stopped. After 3 years of testing we don't know much more than when we started, many things have been ruled out and most of his current doctors agree it is metabolic. We are currently testing for mito.
Sunday, January 3, 2016
Today's task was find 10 jokes to text before the monsters inc laugh floor.