The ALS Ice Bucket Challenge,Ā popularizedĀ by Pete Frates, BC ā07, went viral on the Internet soon after its conception in 2014. Videos of celebrities, students, and families pouring buckets of ice water over themselves cluttered Facebook, Instagram, and Twitter feeds.
On Thursday, the Undergraduate Government of Boston Collegeās Council for Students with Disabilities hosted Nancy Frates and her son, Pete, an ALS patient, and the former captain of the BC baseball team.
The Ice Bucket Challenge, which first gained prominence in August of 2014, was a social media phenomenon meant to raise awareness and funds for Amyotrophic Lateral Sclerosis (ALS), more commonly known as Lou Gehrigās disease, a debilitating and ultimately fatal condition. Frates and her family became involved in ALS advocacy in 2012 after Peteās diagnosis.
Speaking in front of a crowd of over 100 students at the Yawkey Center, Frates began her story by discussing her history at BC.
āThis is a story about family,ā she said, referring both to her immediate family, and the communities like BC that had given her family support as they tried to raise money and awareness about ALS. Frates and her husband were both graduates of BCās class of 1980.
āEvery day we wake up and choose to live in positivity.”
During his time at BC, Pete made a name for himself as the captain of the baseball team, and the MVP of the 2006 Beanpot. After he graduated, he moved to Germany to compete in the German Baseball League, but returned to Boston a few years later. It was during his time back in the U.S., while competing in Bostonās Intercity League, that Pete would be diagnosed with ALS at age 27.
After a check up for what seemed to be a routine wrist injury, Fratesā test results indicated he had ALS. Nancy Frates described the shock and terror she felt upon hearing the diagnoses, recalling her own diagnoses of cancer early in her life. She noted, however, that while she had been presented with two possible treatment options, her sonās doctors had no cure and no treatment, only the information that most ALS patients survived about 3 to 5 years after diagnosis.
āWeāre going to look forward,ā she recalled Pete saying after the diagnosis. āWhat a chance weāve been given to change the world.ā
Frates said the family immediately began thinking of ways to put ALS in front of a mainstream audience to raise money and awareness. As business majors, they began to think of ways of effectively branding and marketing ALS awareness. Shortly after Peteās diagnosis, they founded Team FrateTrain, a community dedicated to promoting ALS awareness and fundraising.
Frates said that the idea for the Ice Bucket Challenge first came about in August of 2014 from Peteās friend Pat Quinn. another ALS survivor from New York that had reached out to Pete after hearing his story. Quinn had seen an Ice Bucket Challenge video on the Internet, and thought this might be the way to bring ALS in front of a mainstream audience.
The challenge started locally, and Frates noted that BC was among the first communities to participate in the challenge. With the help of emails sent by Pete, the ALS Ice Bucket Challenge went viral, with celebrities like Bill Gates, Jack Black, Katy Perry, Drake, Mark Zuckerberg, Taylor Swift, and Lebron James participating. Atlanta Falcons quarterback Matt Ryan, a classmate and friend of Peteās, was among the first to take the challenge.
The popularity of the Ice Bucket Challenge spurred local, national, and eventually international media coverage. The response, Frates said, was enormous. In total, over 17 million videos were uploaded to Facebook, and these videos were viewed over 10 billion times by 440 million unique users. The Frates also said that the financial benefit to ALS charities was massive. In only six weeks time, over $220 million were raised for ALS research and treatment, including money from 2.4 million new donors.
The awareness raised was also significant, with Google reporting that āALSā was the number one searched topic in their āwhat isā category for 2014, and āALS IBCā was the sixth most popular search of 2014. ALS also reached a global audience that year, with Ice Bucket Challenge videos being uploaded from 150 different countries, according to statistics from YouTube.
Frates said the challenge also had a major impact on the progress toward a cure, citing higher rates of early diagnosis, increased interest in the field, and greater collaborations between professionals studying the disease.
Toward the end of the talk, Frates was joined onstage by Pete, who is currentlyĀ paralyzed, unable to speak, and confined to a wheelchair. With her son, she relayed some of the lessons she and her family had learned throughout out the course of Peteās battle with ALS, including the generous nature of people, the importance of being surrounded by a supporting community, and that great leaders are those that bring out the best in those around them. She stated, however, that the most important lesson had been her familyās commitment to keeping a good outlook.
āEvery day we wake up and choose to live in positivity,ā she said.
Featured Image by Josh Metzner / Heights Staff

Nancy Lavole • Nov 6, 2025 at 10:17 am
Last year, my 68-year-old partner was diagnosed with Lou Gehrig’s disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn’t given him attentive care and attention, as the hospital center didn’t provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested usingĀ ( UINE HEALTH CENTRE ) ALS/MND protocol, which my husband has been receiving for a few months now. and it has changed everything., he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best. We got the ALS/MND herba formula from Uinehealthcentre. n et