Donate
 
google
ALS: Anyone’s
  L
ife Story”
May 2007
S
M
T
W
T
F
S

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. 

Enter your zip code
 
 
    Home>Anyone's Life Story
Read other stories by clicking the date on the calendar.
Lynn Murray  

Name: Lynn Murray

City, State: Overland Park, Kansas

Age: 59

Family:
Husband – Steven
Son – Ryan
Daughter and Son-in-law – Andrea and Scott Dixon

Hobbies/Interests: Family photo albums, family history, visiting nature centers, gardens, parks and woods.  Picking fruit at local orchards and then making it into wonderful desserts.  Reading, visiting museums and traveling.

Date of ALS diagnosis: July, 1999

Life before ALS: Before and after ALS I have always found peace in nature.  Before and after ALS my family has always been the most important part of my life.  I loved gardening, and it was easy for me before I had ALS.  Before ALS affected my speech, I enjoyed volunteer work as a hospital visitor and delivering meals to the homebound.  Before ALS, I could more easily plan for my future.

Life with ALS: For more than seven years now I have fought ALS, but I have never felt alone.  There have been many difficulties to face such as problems with speaking, eating, sleeping, muscle loss and falling.  Yet I am fortunate to have the physical abilities that I still have.  I have been deeply saddened that this illness has stolen the lives of friends and acquaintances whom I admired so.

How has ALS brought new significance to your life: My faith in God strengthens me more than ever before.  I have spent years making photo albums: that is a part of my legacy to my family.  I realize that it is important for me not to procrastinate doing the things I’ve dreamed of doing, but especially important to communicate, while I am able, my love, respect and caring toward the people that mean the most to me.  It is my great privilege to think that in some way, however small, I may have helped others to cope with ALS.  Time well spent is an absolute treasure and I make the choice everyday to do at least one thing that I feel good about doing – that to me is significant.

 
 
 
 
All contents © copyright 2006 - 2008 MDA All rights reserved.
BBB logo