Hi, I am Trout Daddy, a.k.a. Bryan Peters and I am the PALS (Person living with ALS) on our team. This is an insidious disease,  often leading to a much delayed diagnosis and is progressively disabling and ultimately fatal.  The psychological and physical toll that it takes on the families of its victims is immense.

ALS has taken the life of my wife's uncle and two of my personal heroes (surfer Mike Doyle and flyfisherman/author Gary Lafontaine). It has stricken the wives of two of my business associates.  In my search to learn more about this condition I have seen it afflict teenagers, new mothers, newlyweds, parents of teenagers, teachers, community leaders and military veterans. It affects virtually all parts of our society.

And please read below to learn more about this disease and why team Trout Daddy is invested in this worthy cause.  

 

Amyotrophic lateral sclerosis (ALS) is a progressive, fatal disease that slowly robs the body of its ability to walk, talk, 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, at any age and there is still no known cause or cure.

 

That's why I'm walking. To build a future without ALS.  To bring help and hope to patients and families affected by this terrible disease, in the hopes that one day ALS is a disease of the past. 

 

Over the past few years, there have been advancements in ALS research, as well as expanded resources and access to care for people living with ALS.  

 

But now, more than ever, we need to keep the momentum going.  We need to continue to push for more treatments and find a cure for ALS.

 

 

Please consider joining me at the walk - we will walk and roll together, united with wheelchairs and scooters, families, neighbors and friends, strollers and pets – all are welcome!  If you can't make it to the walk, please consider making a donation. With your support, we can make a difference in the lives of people affected by this disease right here in North Carolina.