ALS is very personal for me as my dad was diagnosed with ALS in 2014. After his diagnosis the disease progressed extremely fast and sadly by the end of 2017 we had to say goodbye to him entirely too soon. Military service members are twice as likely to develop ALS and there is still no answer as to why, and that is part of the reason I walk as well, to help raise funds to find the reason and hopefully a cure.

 

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Thank you for helping me reach my Walk ALS Greensboro fundraising goal! The Walk ALS Greensboro raises funds to support the ALS community in North Carolina and to build ALS awareness to find treatments and a cure.

 

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.