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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. 

 
Robert Murray
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Robert Murray

Hometown, state:  Bethel, Conn. 

Age: 40

Family (spouse/partner; child, grandchildren): Father, Bob, and two sisters, Kerry and Lee.

Hobbies/Interests: Books on tape; fantasy sports; poker online; Facebook; jokes; watching sports.

Favorite quote: “Fear keeps people in situations.” -- Unknown

Date of ALS diagnosis: January 2005

Tell us about your life before ALS: I had two passions: 1) working out; and 2) reading books. I was a sales rep for Red Bull energy drink. I am an enthusiastic Yankees fan.

Tell us about your life with ALS: My life with ALS is a challenge. The challenge is to stay ahead of the disease progression. It’s important to make other people aware of ALS through starting a support group and participating in clinical trials.

Do you have a “life motto” or profound words to live by? The fear I talked about above is mostly about death, and releasing that fear.

Has there been an “aha!” moment or a specific turn of events that has helped you live with ALS? A friend told me to honor God by not giving up.

Tell us how ALS has brought new significance to any aspect of your life — family, attitude, hobbies/passions, career, etc.: I am now part of something bigger than me. I participate in trials and started the support group to help other people with the disease and, through further education, to one day find a cure!

Is there anything else about you and/or ALS that you want to share with people who read your story?  I want to be part of the cure team and be part of any clinical trial that is available to me.

 
 
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