Past Meetup

Walk To Defeat ALS Nashville

Hosted by The Atlanta Asterisk Users Group

Public group

This Meetup is past

5 people went

Location image of event venue


One of our friends and member of the AAUG has been diagnosed with amyotrophic lateral sclerosis (ALS). If you can participate in the ALS Walk in Nashville October 27th, 2012 (the weekend after Astricon 2012) please do. If you go to Nashville for the walk they are in the Central Time Zone. If you could make a donation to the ALS Association that would be wonderful. You can make a donation here:

About ALS

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually lead to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.

About The ALS Association

Established in 1985, The ALS Association is the only non-profit organization fighting Lou Gehrig’s Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure. As the preeminent ALS organization, The Association leads the way in research, patient and community services, public education, and advocacy — giving help and hope to those facing the disease. The Association’s nationwide network of chapters provides comprehensive patient services and support to the ALS community. The mission of The ALS Association is to lead the fight to cure and treat ALS through global cutting-edge research, and to empower people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.

Attendees (5)