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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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Eric Scoggins
Eric Scoggins

Name: Eric Scoggins

Hometown, State: Tracy, CA

Age: 49

Family (spouse/partner, children, grandchildren):
Wife, four children (three sons and one daughter)

Hobbies/Interests:
Golf

Date of ALS diagnosis:
January 12, 2007

Tell us about your life before ALS:
My dream as a child was to go to USC and play football and eventually progress to professional. Not one willing to have my dream deferred, I played football at USC and also had a professional football career. After football I had more dreams of transferring my ability into the corporate world and excelled there as well. Before ALS I was passionate about my work and thrived on success. I don’t believe in titles, only to work hard and help others reach their full potential.

Tell us about your life with ALS:
Being a dreamer from the start and my life with ALS now I have the dream of finding a cure and plan to attack the issue with the same passion that fueled my successful professional career. I live by the famous quote, “If you don’t stand for something, you’ll fall for anything.”

Tell us how ALS has brought new significance to any aspect of your life - family, attitude, hobbies/passions, career, etc. :
It has made me re-shift my focus and energy to help finding a cure. I have since met Augie Nieto who has inspired me to join forces in that quest for finding a cure. I have established “Eric’s Vision,” which supports Augie’s Quest.
One of my greatest rewards is seeing the people I have mentored and watching them grow successful.

List your favorite quote: “If I tell you a mouse can pull a mountain, then you better hitch him up!”

Do you have a “life motto” or “profound words to live by”: “If a man doesn’t stand for something, he’ll fall for anything.”

Has there been an “a-ha!” moment or a specific turn of events that has helped you live with ALS?
My ah-ha! moment was when I met Augie Nieto, who’s in the same situation as I, and he gave me some sound advice that I took to heart on how I should live my life from this point forward, not wasting any more time being upset about my situation and living my life to the fullest every day.

Is there anything else about you and/or ALS that you want to share with people who read your story?
First, having family support is extremely important. Second, having extended support from what I call my true friends Ronnie Lott and Keena Turner has been extremely beneficial throughout this journey. Third, educate yourself and others about the disease.

 
 
 
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