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Posted: Published on May 9th, 2014

This post was added by Dr Simmons

Originally published May 8, 2014 at 7:03 PM | Page modified May 8, 2014 at 7:25 PM

Every kid has a dream. This was mine.

Standing on the pitchers mound in a major-league ballpark going with a full count, two outs and the bases loaded in the top of the ninth with a 2-1 lead. The adrenaline rushing through my veins. My heart beating faster than it ever has.

Baseball was my life. It was a part of me. I lived and breathed the sport that America calls the National Pastime. I played Little League growing up and practiced with my Mom and Dad whenever I got the chance. I made sure I did each drill right every time. I remember spending hours and hours at the ballpark doing drills again and again. Practice makes perfect, right?

As I got older, my body began to change, along with my friends bodies. Yet somehow, I was getting worse at baseball while my friends were excelling at it. During my freshman year at Nathan Hale High School, I got cut from the baseball team. I didnt even make the freshman squad and didnt play high-school baseball that spring. I would never play organized baseball ever again.

In the summer of 2006, my family and I learned that I have Friedreichs Ataxia, called FA for short. Through many doctors visits, we were told that FA is a genetic, progressive, life-shortening neuromuscular disease that causes loss of coordination from the toes to the fingertips. Symptoms include scoliosis, diabetes and, worst of all, heart disease. FA will eventually cause me to use a wheelchair full time. Daily tasks will become nearly impossible. There is no treatment and no cure.

At first, my world was shattered. My dream of standing on that pitchers mound and playing for a Major League Baseball team was obliterated. I didnt know what to do. I did not want to lose the game I loved. So I made a choice.

I became student manager for the Nathan Hale High School baseball team the next spring. It did not feel like I was just the student manager, however. I went to every practice, wore a uniform on game days and was treated as if I was one of the players. All the while, I was losing the ability to do things like tie my shoes .

During my freshman year at the University of Portland, I was forced into a wheelchair part time. A year later, I had to use one full time. I now switch between a power and manual chair and do not stand unless I am holding onto something.

This progressive disease has taken away my ability to play the sport I love, but I have not let baseball leave my life. I strive to live every day to the fullest! No matter the challenge, I keep moving forward! With the help of friends and family, anything is possible!

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