A fellow mito mom from North Carolina put together the following video in an effort to raise more awareness for mito. The more awareness that is brought to this disease, the more funding scientists will have for potential treatments and hopefully a cure. Thanks to Amber Greenawalt for all her work on making the video.
To help us find a cure for Ethan and the many others suffering from Mitochondrial Disease please support the United Mitochondrial Disease Foundation, www.umdf.org.
I'm a child of God, a daughter to wonderful parents, wife to an amazing husband, Mother to 4 little Hams and a friend to many. Our youngest son was born 6 weeks premature with multiple birth defects. He is Globally Developmentally Delayed, Intellectually Disabled and has a diagnosis of a Defect in Complex I of his Mitochondria. Follow us while we learn our new "typical". We are living and learning everyday and praising God every moment for our blessings!
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