In memory of my Richie and my dad, Louis Dimino, who passed in 1987 from this devastating disease.
This is an wonderful opportunity for us to work together to support those affected by Lou Gehrig's Disease and to spread awareness of the urgency to find treatments and a cure.
As I know first hand, the past few years have brought incredible advancements in ALS research, expanded access to care for ALS patients, and enabled legislation that impacts the quality of life of patients and their families.
Please consider walking with me. With your help, we will be able to make a difference in the lives of people affected by this disease and their caregivers.
Often referred to as Lou Gehrig's 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 an ALS patient averages 2 to 5 years from the time of diagnosis.
This crippling disease can strike anyone. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries. Presently there is no known cause of the disease though support is bringing researchers closer to an answer. In the mean time it costs an average of $200,000 a year to provide the care ALS patients need.
Help make a difference -- please donate and, if you can, I welcome you to join us for the walk to defeat this horrific disease in Long Branch, New Jersey on May 12th.
