My MS and E - Byrne, Kevin
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Get a signed copy of the print book direct from the author at http://MyMSandE.com--There are two versions in this book. When the story was first written, Eleanor refused to read it with me unless there were pictures. The second version is the original picture board used to read this to my daughter at bedtime.--My MS and E is a children's picture book depicting a typical interaction between Kevin and his daughter, Eleanor. They share an unbreakable father-daughter bond, even in the face of his ongoing struggles with multiple sclerosis. This story is a heartwarming tale of how they grow, learn,…mehr

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Produktbeschreibung
Get a signed copy of the print book direct from the author at http://MyMSandE.com--There are two versions in this book. When the story was first written, Eleanor refused to read it with me unless there were pictures. The second version is the original picture board used to read this to my daughter at bedtime.--My MS and E is a children's picture book depicting a typical interaction between Kevin and his daughter, Eleanor. They share an unbreakable father-daughter bond, even in the face of his ongoing struggles with multiple sclerosis. This story is a heartwarming tale of how they grow, learn, struggle, and celebrate life in their mantra of Never Stop... Never Quit...--100% of the profits I earn from this book will be donated to the Oregon Chapter of the National Multiple Sclerosis Society, in support of their fight against MS.--Enjoy! ~Kevin
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Autorenporträt
Kevin was born and raised in the Bronx, New York. He was diagnosed with multiple sclerosis (MS) in 1999 while commanding a US Army Air Cavalry Troop overseas. Now medically retired, Kevin lives in Portland, Oregon, with his daughter, Rogue, devoting much of his time and energy towards overcoming the challenges of his own MS so that he may fight for others. Writing and blogging for the Department of Veterans Affairs, the National MS Society, and NEVER STOP NEVER QUIT expand his fundraising and advocacy in this fight. "...fantastic stories, where I'm limited only by my imagination, not by the confines of this stupid disease." NMSS Leadership Conference, Denver, CO, November 2016