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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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David L. Emmert  
David L. Emmert

Name: David L. Emmert

Hometown, State: Moline, IL

Age: 70

Family:
Wife: Judie
Sons: Greg and Brad
Daughter: Beth
6 wonderful grandchildren

Hobbies/Interests:
I like to oil paint pictures and be outdoors.

Date of ALS diagnosis:
November 1996

Tell us about your life before ALS:
I was a teacher (art) for 17 years. After teaching, I was in sales, then when I got ALS, I was a landscape designer.

Tell us about your life with ALS:
Having ALS has given me the opportunity to pursue my interests in oil painting. Thankfully, I can use my hands to so even though I can’t speak.

Tell us how ALS has brought new significance to any aspect of your life - family, attitude, hobbies/passions, career, etc.:
I found I have a wonderful family, who have been wonderful helping me through this disease. You have to keep a sense of humor above all! Since having ALS, I am able to pursue my interest in oil painting, where I never had time before. I am strong-willed and independent and continue to “keep going” as long as I can. Believe in tomorrow! MDA and ALS support groups help me a lot!

List your favorite quote:
If life deals you lemons – you make apple cider.

Do you have a “life motto” or “profound words to live by”: I think the first thing is to have a good sense of humor. Second, when I look around there is always someone worse off than you.

Has there been an “a-ha!” moment or a specific turn of events that has helped you live with ALS?
No one wants to be a disabled or crippled. We all go through denial, frustration, learning how to cope, each day. The a-ha part is “Hey, I can do more than I thought. It may not be much, but it is something.”

Is there anything else about you and/or ALS that you want to share with people who read your story?
I have been very busy so far – as a retired art teacher, I am starting my 12th year of ALS. I’ve lost my voice, but my hands can still hold a paint brush. I paint many hours each week. With God’s help and family support, I try to enjoy each day as it comes. Last of all, the MDA family has been 110% support. They are always there if you need anything. I go to both MDA and ALS support groups. Coffee is pretty good there, too!!

 
 
 
 
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