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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. 

 
Alex Grausnick
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Alex Grausnick

Hometown, state: Shoreview, Minn.

Age: 19

Hobbies/Interests: Golf, any sport, music.

Date of ALS diagnosis: May 2007

Tell us about your life before ALS: My life before ALS was no different than for all of the other teenagers around me. I loved sports, watching and playing any of them, and enjoyed school and time with my friends. I felt like I was no different than others, and certainly did not act any different than a teenager would.

Tell us about your life with ALS: To be honest, I do not think my life has changed one bit since I was diagnosed, except for having to swallow 30 supplements every day instead of just five. I still love sports, still play and watch them, and I am still going to school. No one really sees me as different, and that’s the way I would like to keep it.

Do you have a “life motto” or profound words to live by? I think I have matured well past my years since my diagnosis. The key is to keep it off your mind as much as possible.  The mind has as much if not more power than medicine in terms of healing powers. If you keep your mind state positive, you can achieve anything you want.

Has there been an “aha!” moment or a specific turn of events that has helped you live with ALS? My “aha” moment was the moment that my doctor told me I had ALS.  From that moment on, I decided that I was going to beat it by any means possible, and I have not stopped thinking that. You need to live your life with the sense that you may not have as much time as you wanted, but you need to achieve what you set out to achieve originally, in this shorter amount of time, because that is how it is.
 
Tell us how ALS has brought new significance to any aspect of your life — family, attitude, hobbies/passions, career, etc.: I think that the most important thing to me since my ALS diagnosis has been my family because I might not have as much time as I deserve with them, and I need them to know how much I care about and love them before it may be my time to go.  But I think I no longer fear death because now I feel like I can beat this and show everyone that death is nothing to be afraid of.

Is there anything else about you and/or ALS that you want to share with people who read your story? I would just say that life itself is more important than anything else, physical or otherwise. You need to realize that there is nothing besides your life and that nothing else matters…just live your life.

 
 
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