Matthew is the youngest of our three boys. He has been diagnosed with Mitochondrial Disorder Complex I and III, Chronic Intestinal Pseudo Obstruction, FTT and Glucose Intolerance. He has been through countless tests and procedures in the past 8 years . We do not know what the future holds for him, but we are going to do our best to cherish every day with him. Stay strong little man.

Monday, September 28, 2009

Matthew's week went well. He still is enjoying school. His class invited Grandparents in on Friday for a special grandparent get together. They sang a few songs, and ate some special treats together
Matthew was shy during the performance and didn't sing much, but he was very happy to have his Gramma, Grandpa and Nana there to visit.
We went to our friends Friday night for dinner and Matthew had a blast playing with his friend Ava. He insisted on wearing her pink vest and her old Baby pants(size 0-3 mos) home that night. He is just so cute.
We heard from Boston this morning. They are still working out a time for Matthew to have the Botox injection done. It should be sometime soon. Matthew's new AFO's are ready . We are going down to Saratoga this Thursday afternoon to pick them up.
Medical wise, everything is the same. Nothing more, nothing less. We are just enjoying every good day he has been having.

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