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ALS: Anyone’s
  L
ife Story”
May 2008
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MDA’s ALS Division introduces you to 31 people  - one each day for the month of May - who are living with ALS (amyotrophic lateral sclerosis or Lou Gehrig’s disease). 

This series was inspired by Augie Nieto, ALS Division Co-Chairperson, who says that since his ALS diagnosis, instead of striving for success, his goal each day is to be significant.

In their own words, otherwise “ordinary” people describe the impact of living with a progressive, incurable and deadly disease. But their stories also tell how ALS has brought new significance to their lives in ways that you might not expect. 

ALS can become anyone’s life story. Please join MDA’s world-leading effort to stop it. 

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Matt Williams
Matt Williams

Name: Matt Williams

Hometown, State: Osage, IA

Age: 36

Family:
Wife: Val
Children: Emma (8), Zach (6), Nolan (2)

Hobbies/Interests:
Camping, turkey hunting, college football, high school athletics

Date of ALS diagnosis:
January 2006

Tell us about your life before ALS:
I had a career working as a sales professional. I was an avid golfer and enjoyed boating on the weekends. I spent many hours on “do it yourself” projects at home.

Tell us about your life with ALS:
Even with the physical difficulties, I still enjoy doing things with my family, like camping, going to sporting events and coaching Emma’s ball team. With some minor adaptive equipment, I still hunt turkeys in the spring. I just make sure to conserve energy so I can do the things I like.

Tell us how ALS has brought new significance to any aspect of your life - family, attitude, hobbies/passions, career, etc.:
ALS does bring a new perspective. For me, I make changes in my life that allow me to be as active as possible. If there was something I couldn’t do, like golf, I replaced it with camping. The disease brought a sense of urgency, also, so I decided early on that I didn’t have time to sulk and feel sorry for myself.

List your favorite quote:
“Don’t give up, don’t ever give up…” by Jim Valvano, former N.C. State basketball coach.

Do you have a “life motto” or “profound words to live by”:
I am a firm believer that no matter how bad things may seem, they can always be worse.

Has there been an “a-ha!” moment or a specific turn of events that has helped you live with ALS?
One day, shortly after my diagnosis, I was watching my kids play in the yard and it hit me… No way was I going to let this disease define our lives.

Is there anything else about you and/or ALS that you want to share with people who read your story?
I think everyone with ALS should be able to maintain a high quality of life. We have made some adjustments, but for the most part, we still participate in most of the activities that we enjoyed before ALS.

 
 
 
 
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