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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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Deborah Christensen
Deborah Christensen

Name: Deborah Christensen

Hometown, State: LaGrange, NY

Age: 43

Family:
Husband: Keith Christensen
Daughters: Rylee, 12, and Skylar, 9

Hobbies/Interests:
Skiing, swimming, biking, Jazzercise, shopping, making jewelry, cake decorating, going to see movies, out for dinner, computer design

Date of ALS diagnosis:
March 2006. My grandfather and my dad passed away from ALS. My only sibling also has ALS. We do not have the SOD I gene.

Tell us about your life before ALS:
I was extremely active and involved. I volunteered to help out with school and after school activities and loved to be with people. I was a room mom for six years and a Girl Scout leader for three years. I was active on PTA also. I was always on the go between work and activities.

Tell us about your life with ALS:
I am still active and involved – just not as much as I would like. I still help out in things I am capable of, such as doing design work on the computer. I still love to be with people however with my very limited speech I don’t say nearly as much as I used to. My on the go lifestyle takes a little longer and I don’t do as much as I used to.

Tell us how ALS has brought new significance to any aspect of your life - family, attitude, hobbies/passions, career, etc. :
I find increasing enjoyment in the moment. Friends and family have been extremely supportive, and I thank God for them. I love to sit and watch my girls in their events and I am thankful for each new day. I take each day as it comes with a smile on my face.

List your favorite quote:
Live every day like it was your last.

Do you have a “life motto” or “profound words to live by”:
Smile … and the world smiles with you!!

Has there been an “a-ha!” moment or a specific turn of events that has helped you live with ALS?
I have the inherited gene. There’s not anything that can be done. It is what is. Hopefully God has a plan with me.

Is there anything else about you and/or ALS that you want to share with people who read your story?
Make some noise. Let’s find a cure.

 
 
 
 
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