2024 Cincinnati Walk

pAuL'S pals

As most of you know,  I was diagnosed with ALS in May of 2022.  Prior to that, I knew nothing about ALS, except that it was also known as Lou Gehrig's disease.  I did not know anyone that had ALS or anyone that had passed from ALS.  Since that time, I have learned quite a bit about the 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 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. 


  


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. 



To join my team and/or donate, please click on the links on this page.



Thank you,


Paul Tepe


Team: pAuL'S pals

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