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ALS: Anyone’s
  L
ife Story”
May 2007
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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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Roberto Rosado
Video Profile - 56k | 128k | 512k

Name: Roberto Rosado

City, State: New York, N.Y.

Age:  51

Family:
My 26-year-old daughter, Tashama, who is a nurse.

Hobbies/Interests: Fishing, softball, basketball, jogging, donating blood for charity, nature hikes, swimming and traveling.

Date of ALS diagnosis: December 10, 2001

Life before ALS: I was an Assistant Vice President at a Canadian banking firm. I was a captain on my softball and basketball teams, and I was also the main caregiver for my mother who had Parkinson’s.

Life with ALS: Initially, my life didn't change too much. My focus was on my mother. When she died in 2003, I lost some of my drive and strength - physically, emotionally and spiritually. At the same time, my disease progressed, so I lost my ability to work, play sports, do charity work and travel.

How has ALS brought new significance to your life: The love of my family, friends and my angel Clarisse has helped me to recapture my spirit, my laugh and my ability to smile.  The MDA has helped me to try and be an inspiration to others with my disease by airing my profile on TV and presenting me with a Personal Achievement Award.  I take part in clinical trials, not only to help myself, but to help everyone with ALS to have hope.

 
 
 
 
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