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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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Richard A. Quiroz
Richard A. Quiroz

Name: Richard A. Quiroz

Hometown, State: Los Angeles, CA

Age: 58

Family:
Wife: Laura Quiroz

Hobbies/Interests:
Drawing, modeling, reading, sword fighting, flying, attending theatre with my wife

Date of ALS diagnosis:
October 8, 2007

Tell us about your life before ALS:
I was in animation for 17 years and am a recipient of two Emmy certificates for my design work on “Pinky and the Brain” and “Animaniacs.” I then became a freelance artist. I enjoyed doing some acting and was learning stage fighting before this hit.

Tell us about your life with ALS:
Since being diagnosed with ALS I have begun to appreciate all the little things I used to be able to do that everyone else takes for granted. Everything is a struggle and I am not able to do the things I used to enjoy. I live with fear on a daily basis not knowing what’s ahead.

Tell us how ALS has brought new significance to any aspect of your life - family, attitude, hobbies/passions, career, etc.:
It has brought my wife and me closer than we have ever been. After learning of my diagnosis, my wife and I began living our lives to the fullest, renewing our wedding vows and making frequent trips to Disneyland. I also took the opportunity to fly a fighter plane. This is something that I have dreamt about since I was a young boy. Living with ALS has also shown me what human compassion and friendship are all about. I have had more people rally to help than I ever knew were there. I am living every day to its fullest and thank God for my wife, my friends and my family. I also thank Him every day I can get up and still walk and am alive – because that is a good day!

 
 
 
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