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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!!