The Martin Family and Mito

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We have busted the $20K mark!! THANK YOU! THANK YOU!! THANK YOU!

The latest contributors:

Robert Barkley

Kathy Burt

Lydia L. Gumm

Kristen Janssen

Laura Jirele-Borleske

Trey Lynn

Erik Olson

Pete Winckler

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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