1st Attempt was an epic failure

2nd Attempt went much better.

Ice Bucket Donations Continue to Rise: $94.3 Million Since July 29

Washington, D.C. (August  27, 2014) — As of Wednesday, August 27, The ALS Association has received $94.3 million in donations compared to $2.7 million during the same time period last year (July 29 to August 27). These donations have come from existing donors and 2.1 million new donors. The ALS Association is tremendously thankful for all of the generous support and awareness that this summer phenomenon has generated for the cause.

“The ALS Association has been given a great deal of money and with that comes tremendous responsibility,” said Barbara Newhouse, President and CEO of The ALS Association. “We are absolutely committed to transparency and will be communicating regularly with the ALS community, our donors, the media and the public about progress to invest these dollars wisely in areas that will have maximum impact on the fight against this devastating disease.”

The ALS Association’s mission includes providing care services to assist people with ALS and their families through a network of chapters working in communities across the nation and a global research program focused on the discovery of treatments and eventually a cure for the disease. In addition, The Association’s advocacy efforts empower people to advance public policies in our nation’s Capital that respond to the needs of people with ALS.

For inquiries regarding the use of these funds or other information about the Ice Bucket Challenge, please emailinquiries@alsa-national.org.

About The ALS Association
The ALS Association is the only national 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 Treatment Centers of Excellence, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.  For more information about The ALS Association, visit our website at www.alsa.org.