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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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James E. Wallace
James E. Wallace

Name: James E. Wallace

Hometown, State: Worcester, MA

Age: 64

Family:
Wife: Jane Wallace
Children: Jane, Christopher, Allison

Hobbies/Interests: Family, law, golf, basketball

Date of ALS diagnosis: 2004

Tell us about your life before ALS:
I had an active life playing basketball and golf regularly; practicing law as a trial lawyer and advising college and university clients; traveling to visit family in San Francisco and Santa Fe.

Tell us about your life with ALS:
As ALS has progressed, I am now in a power wheelchair; unable to do many of the activities I used to do.

Tell us how ALS has brought new significance to any aspect of your life - family, attitude, hobbies/passions, career, etc.:
I continue to work as a lawyer but have accepted other limitations. Needless to say, I take nothing for granted and have profound respect for those living with more disabling conditions than I have and for those caring for them. Each day is an opportunity.

List your favorite quote:
"Wisdom too often never comes, and so one ought not to reject it merely because it comes late." --Felix Frankfurter

Do you have a “life motto” or “profound words to live by”:
"Illegitimati non carborundum." (Don't let the bastards grind you down.)

Has there been an “a-ha!” moment or a specific turn of events that has helped you live with ALS?
When I realized that my (much appreciated) appointments with the ALS Center were not to cure me but to care for me.

Is there anything else about you and/or ALS that you want to share with people who read your story?
Never give up.

 
 
 
 
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