My mother is a caring, kind, and generous person who has spent years of her life caring for others. She is the heart and soul of our enormous family and deserves only the best in this world.
Earlier this year, my mother was diagnosed with ALS. It has been a difficult few months coming to terms with this diagnosis and helping her navigate the challenges of this terrible disease.
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, like my mom, living with the disease.
The past two years have brought incredible advancements in ALS research, expanded access to care for people living with ALS, and enabled legislation that impacts the quality of life of people with ALS and their families.
Please consider joining me or making a donation. With your help, we will be able to make a difference in the lives of people affected by this disease.
