Four years ago I was diagnosed with ALS, and despite such devastating news I have been inspired by my fellow patients and their families to remain strong in the face of adversity. As a scientist, I want to do whatever I can to support and advocate for the necessary research to determine what causes ALS and advance medical treatments that will someday lead to a cure. I have participated in a clinical trial on probiotics and I did Radicava infusion therapy for 18 months. Although the statistical probabilities for my survival of ALS are nonexistent, I am fully committed to the fight for a cure that will someday benefit others. The team "Dwyer's Hard Rockers" is a nod to the culture and music of my formative years and the field of geology that inspired my professional career.
The past four 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. WE CAN'T STOP NOW! Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.
WHY WE NEED YOUR HELP
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
That’s why we’re participating in the Walk to Defeat ALS. To bring hope. To raise awareness. To provide resources and services to families free of charge. To help unlock the mystery of ALS and find the key to treatments and a cure. Will you join us?
ABOUT ALS
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. Presently there is no known cause of the disease, yet it still costs loved ones an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to provide help and hope today!
