This past summer (2023) my Mom, Ann Lynch, was diagnosed with PLS (primary lateral sclerosis). PLS is in the same family as ALS and we pray that the diagnosis stays PLS and does not change to ALS. However, we are now involved with generous support from many people and families who are dealing with PLS or ALS. I am raising money to help with research as this one hits close to home. This has been life changing for all of us as we learn this new way of life. 

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 ensure that no one ever hears the words: "You have ALS" again. 

 

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. 

 

But we can't stop now. The key to a cure begins with you. 

 

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.