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Published on Jan 7, 2012
This is part 1 of a story filmed on a boy who mysteriously became sick as a toddler and was found to have an extremely rare mitochondrial disorder named Pyruvate Dehydrogenase Complex Deficiency. He is inspirational to me in that not only does he have the same disorder as my son, Jonathan, but his story exhibits many of the same characteristics as him also. He is a symbol of hope for all children and parents of children that are diagnosed with this disorder.