My ALS journey started in March 2023 with my diagnosis. It has been 2 years since onset of symptoms which began with balance issues and then my legs not working well. It was many, many months of of therapy, testing and then a final unfortunate diagnosis. Please join me and my family in raising fund and/or joining us for the ALS walk on May 4th. 

Love, Shawnee 

Thank you for helping me reach my Walk ALS fundraising goal! The Walk ALS raises funds to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure.

Did you know?

 

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. 

 

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.