The Martin Family and Mito

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We are home! Will post more later.

The Martin Family: My name is Lori Martin and I started this blog to keep family and friends updated as we live with Mito AND more importantly to raise awareness of this deadly disease. Our son Will was diagnosed with a Mitochondrial Disorder specifically Leigh’s Syndrome on July 5, 2011. Thank you for your support as we embark on a journey towards the great unknown. To learn more about Mito disorders, please visit www.umdf.org, www.mitoaction.org or www.utmitocenter.org.

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