In 2016 my Dad started complaining that his leg felt weak and that he couldn't move it.  Doctors couldn't figure out what could be the cause.  A year later in September of 2017, after numerous appointments he was diagnosed with 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. There is no known cause or cure.  

In the three years since his diagnosis,  my parents have had to do multiple remodels to their home in order to make it accessible and fit the medical equipment needed.  My family has made schedules to help my dad with every aspect of his life that you could imagine.  This disease has affected my family financially, physically and of course,  emotionally.

There are no words to explain the heartache of watching my dad fall as he tried to fight the fact he was losing his ability to walk. Hear the pain in his voice when he asked for help to get dressed for the first time. There is no explaining the anger and sadness I felt/feel watching him completely lose his independence. ALS is a terrible disease.

That’s why I’m walking. To try and change the statistics. To bring HELP and HOPE to those living with the disease. To try and ensure that no one ever hears the words: “You Have ALS” again. 

The past three 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 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.