Neil Alexander spoke recently at The Pittsburgh Foundation December 2011 Board Meeting introducing the LiveLikeLou.org Foundation and its mission to continue the fight for people with ALS. Neil and Suzanne Alexander established LiveLikeLou.org in 2011 when Neil was diagnosed with Amyotrophic Lateral Sclerosis (ALS), the devastating condition known as Lou Gehrig's disease. Through this fund they hope to raise awareness of ALS, provide care and comfort to ALS families in Western Pennsylvania, and support scientific research targeted at finding a cure. The fund is named for baseball legend Lou Gehrig to honor the example that he set for all people living with ALS. Thank you for your support!