Amyotrophic lateral sclerosis (ALS) – also known as Lou Gehrig’s disease – is a rapidly progressive, neurodegenerative disease.1 Those living with ALS eventually lose their ability to walk, dress, write, speak, swallow and eat.1ALS can affect people of all races and ethnic backgrounds, but did you know that Veterans are twice as likely to develop ALS than those who haven’t served in the military?

This Veterans Day, we honor those who have served in the U.S. armed forces and thank them for the sacrifices they’ve made to protect our country.

I had the extreme honor of speaking with Juan Reyes, a U.S. Air Force Veteran living with ALS and a MTPA Patient Ambassador, to share his story of living with ALS, discuss how he’s helping to spread awareness of this devastating disease among Veterans, and how others living with the disease can help support the ALS community. Along with his wife of 33 years, Meg.