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　　ALS Ice Bucket Challenge Takes U.S. by Storm

　　August 12, 2014

　　In the last two weeks, the Ice Bucket Challenge has quite literally

　　“soaked” the nation. Everyone from Ethel Kennedy to Justin Timberlake has poured

　　a bucket of ice water over his or her head and challenged others do the same or

　　make a donation to fight ALS within twenty-four hours.

　　Between July 29 and today, August 12, The ALS Association and its 38

　　chapters have received an astonishing $4 million in donations compared to $1.12

　　million during the same time period last year. The ALS Association is incredibly

　　grateful for the outpouring of support from those people who have been doused,

　　made a donation, or both. Contributions further The Association’s mission to

　　find a cure for ALS while funding the highest quality of care for people living

　　with the disease.

　　"We have never seen anything like this in the history of the disease,” said

　　Barbara Newhouse, President and CEO of The ALS Association. “We couldn’t be more

　　thrilled with the level of compassion, generosity and sense of humor that people

　　are exhibiting as they take part in this impactful viral initiative."

　　With only about half of the general public knowledgeable about amyotrophic

　　lateral sclerosis (ALS), also known as Lou Gehrig’s Disease, the Ice Bucket

　　Challenge is making a profound difference. Since July 29, The Association has

　　welcomed more than 70,000 new donors to the cause.

　　"While the monetary donations are absolutely incredible,” said Newhouse,

　　“the visibility that this disease is getting as a result of the challenge is

　　truly invaluable. People who have never before heard of ALS are now engaged in

　　the fight to find treatments and a cure for ALS."

　　(从这里开始不是真题内容Currently, there is only one drug approved by the U.S. Food and

　　Drug Administration (FDA) to treat ALS, which only modestly extends survival by

　　two to three months. Consequently, ALS is 100 percent fatal. In addition to

　　acclimating to the challenges that come with losing control of voluntary muscle

　　movement, people with the disease progressively lose their ability to eat,

　　speak, walk, and eventually breathe.

　　"With more people aware and more people engaged in the fight against ALS,

　　we are poised to work collaboratively with not only other ALS organizations, but

　　also with pharmaceutical companies and academia to expedite new treatments for

　　people impacted by the disease," Newhouse continued.)

　　Experience the #IceBucketChallenge phenomenon that's spreading ALS

　　Awareness across social media. Challenge your friends and family today.

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