Welcome to My Personal Page
Our Story
On March 17, 2020, while the whole country was preparing to shut down, my dad Robert received a life chaging diagnosis. He had ALS, Amyotrophic lateral sclerosis (ALS) a progressive, fatal neuromuscular disease that would slowly robs his body of its ability to walk, speak, swallow and breathe. Although this disease will work hard to take those things away, we will work harder to fight back. ALS cannot take away his determination, his sense of humor or his ability to always be the best looking guy in the room!
Whether you know him as Robert, Mr. Torres, Butchie, Chico, Dad or Grampie; you know how important this fight is. Please consider donating, please accept our invitation to join us Saturday September 30th and thank you for taking the time to read just a small part of his story. ALS will not be the final chapter.
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis. ALS can strike anyone, and presently there is no known cause or cure.
That’s why I’m walking. To change the statistics. To bring help and hope to those living with the disease. To support the caregivers who help their loved one fight this disease. To ensure that no one ever hears the words: “You Have ALS” again!
We can’t stop now! The key to a cure starts with all of US. Please consider walking with me or making a donation to my team. With your help, we will be able to make a difference in the lives of people affected by this disease.
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