Participants in a ceremony on the 10th anniversary of the Ice Bucket Challenge, from left, Boston Red Sox president and CEO Sam Kennedy, Massachusetts Gov. Maura Healey, John Frates, former Atlanta Falcons quarterback Matt Ryan and former Boston Bruins' Ray Borque pour water over their heads at Fenway Park, Thursday, Aug. 1, 2024, in Boston. (AP Photo/Michael Dwyer) Credit: AP

By MICHAEL CASEY Associated Press

BOSTON (AP) — Dozens of people, including the Massachusetts governor and several sports stars, dumped cold water on themselves at Fenway Park Thursday to mark the 10th anniversary of the ALS ice bucket challenge.

The event is part of an effort to renew interest in the viral social media campaign that has raised money to find a cure for Lou Gehrig’s disease. Organizers said the campaign has raised $250 million thus far and led to an additional $1 billion in research funding.

“Our son’s life was one of grace, determination and purpose, that through his resilience, diligence and courage, he created a movement that is still being celebrated today for all those that have been affected by this horrific disease,” said Nancy Frates, the mother of Pete Frates, who helped popularize the challenge along with Pat Quinn. Both were diagnosed with ALS and have since died.

“Even though his human body is no longer with us, his powerful spirit is still being celebrated along with the historic movement,” she said. “You brought results. But as Pete would say, ‘We can have fun today but the job isn’t done. Let’s get back to work tomorrow.’”

Dr. Merit Cudkowicz, the director of the Sean M. Healey & AMG Center for ALS at Mass General Hospital who was also Pete Frates’ doctor, recalled her first meeting with him and how he vowed to raise $1 billion for ALS research. Among the benefits there have been more drugs to treat the disease.

“It’s hard to believe that dumping a bucket of ice over your head was going to change how we think about ALS, but that simple act did more to raise awareness for ALS than any other effort, and it catalyzed amazing research advances,” she told the crowed of several hundred including ALS patients and their families. “It brought so many new scientists to the field all over the world and that’s making the difference today for people living with ALS.”

After the speakers finished, about 75 people, including several families with small children, lined up on the baseball field in front of tiny buckets. All at once, they dumped ice-cold water from tiny buckets onto their heads, a relief to many on the day when temperatures reached into the 90s.

In the stands, Mike Cunningham, 54, of Canton, Massachusetts, was watching the event from his wheelchair.

Diagnosed with ALS last year, he admitted it can sometimes be hard to get out of his house. But he said he wasn’t going to miss Thursday’s event, which gave him a sense of pride, hope, courage and “thankfulness for all the kindness that people show.”

“People are good. People are kind and they step up when people need help,” he said. “It’s easy to forget that with all the news you hear every day. You see it. You feel it, the kindness. Friends, neighbors, strangers that come out and try to help fight this awful disease.”

In 2014, Quinn saw the ice bucket challenge on the social media feed of professional golfer Chris Kennedy, who first dared his wife’s cousin Jeanette Senerchia to take a bucket of ice water, dump it over her head, post a video on social media and ask others to do the same or to make a donation to charity. Senerchia’s husband had ALS.

Quinn and Frates helped popularize the challenge. When the two picked it up, the phenomenon exploded. Thousands of people participated in the viral trend, including celebrities, sports stars and politicians. Online videos were viewed millions of times.

Lou Gehrig’s disease, named after the New York Yankees great who suffered from it — is also known as ALS or motor neuron disease. It is a progressive neurodegenerative disease that leads to paralysis due to the death of motor neurons in the spinal cord and brain. There is no known cure.

The Associated Press (AP) is an independent global news organization dedicated to factual reporting.

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4 Comments

  1. One of the toughest things for my husband, diagnosed four years ago, is the frustration with the loss of function and communication. He recently told me “you don’t understand”. I responded, “you are right,I do not….But I am trying with everything I have”. It is that gap between being a Caretaker and significant other. we started ALS/MND programme from vine health centre . c o m 5 months ago, he has regain some functionalities, we noticed his speaking has gotten better since we started on this treatment programme, it didn’t make the ALS go away but it gave him a better quality of life. I also understand that God does not give us more than we can handle…

  2. Thanks to Dr Ofua Ofure of The Great Herbal Healing Home for helping us with Als herbal formula for my father, he is now cured from ALS after using this herbal formula, he fully regain control of itself totally, no sluggishness while talking and his hands and feet are normal now, he can now walk by himself and can use his hands by himself as well,… if you are out there having someone with this disease i recommend you get ALS herbal formula from Dr Ofua Ofure it works perfectly his contacts are +2347055955394 or thegreatherbalhealinghome gmail com ___Rex Clarkson

  3. I am a CALS. My husband is PALS. It’s was hard and I cry daily but not in front of him unless we cry together. He couldn’t find anything to give him happiness or hope. We have been focusing on our faith. He was only loosing his voice before we made the decision to try different medications, which significantly enhanced his condition. He received treatment for ALS/MND at uine health centre from Canada approximately four months ago; since then, he has stopped using a feeding tube, speech is getting better by the day, sleeps well, works out frequently, and has become very active.

  4. One of the toughest things for my husband, diagnosed four years ago, is the frustration with the loss of function and communication. He recently told me “you don’t understand”. I responded, “you are right,I do not….But I am trying with everything I have”. It is that gap between being a Caretaker and significant other. we started ALS/MND programme from uinehealth centre . c om 5 months ago, he has regain some functionalities, we noticed his speaking has gotten better since we started on this treatment programme, it didn’t make the ALS go away but it gave him a better quality of life. I also understand that God does not give us more than we can handle…

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