The ALS Ice Bucket Challenge

3 min read
Summary

Join the Ice Bucket Challenge by filming yourself, sharing on social media, and nominating others to amplify ALS awareness and funding for research and patient services. Your participation connects you to a compassionate community providing free equipment, financial grants, and support that transforms lives.

Participating in the Ice Bucket Challenge: How to Get Nominated and Make Your Impact Count

Tag your regional ALS affiliate in your video to boost visibility of local services and connect newly aware people directly into supported communities.

The Official Rules: Nomination, Timing, and Video Documentation

The ALS Ice Bucket Challenge follows a three-step process: film yourself pouring a bucket of ice water over your head, post the video publicly on social media using #alsicebucketchallenge, and tag two to five people you're nominating to participate. [1] Once nominated, participants have 24 hours to complete the challenge -- either by taking the ice bucket and donating $10, or by skipping the water and donating $100 instead. [13] Tagging your nominees directly in the video is what drives participation forward, since the public call-out creates social accountability rather than leaving acceptance as an optional choice. [1] If you want to extend your impact beyond a single video, our [create a fundraiser](https://alsunited.org/blog/create-a-fundraiser/) page has tools to build a personal campaign around your challenge.

Amplifying Your Challenge: Directing Donations to ALS United and Local Support Programs

When you take the challenge, directing your donation to a local ALS United member organization keeps funds close to the families who need them most. The impact of the challenge continues to ripple at the regional level -- funding local programs, patient services, and advocacy efforts that serve people directly in their communities. [15] Tagging your regional ALS affiliate in your video, beyond the general hashtag, increases the visibility of local services for people in your area who may not know help is available. [1] For anyone newly connected to the cause, [ALS support groups](https://alsunited.org/blog/als-support-groups-connecting-with-others-facing-the-disease/) through local member organizations are a direct path from awareness into an active, supported community. [14]

Creative Variations That Keep the Movement Alive in 2025 and Beyond

The challenge has proven adaptable beyond its original format. In spring 2025, a University of South Carolina student group called MIND launched the "Speak Your Mind Ice Bucket Challenge," directing donations to a nonprofit focused on youth mental health -- a cause that directly intersects with ALS, since caregivers and people living with ALS commonly face depression, anxiety, and grief.[16] The ALS Association publicly praised MIND's efforts, noting that mental health "affects the ALS community in profound ways" and that the original challenge's spirit of collective action continues to inspire new forms of activism.[16] Influencers including James Charles and Haley Kalil participated in the mental health variation, confirming the format still draws public engagement more than a decade after Pete Frates helped connect it to ALS research -- and that each new version has the potential to bring fresh audiences back to the original cause.[16]

From Viral Moment to Sustained Action: What Happens After You Take the Challenge

From your first challenge donation to sustained involvement, ALS United connects you to free medical equipment, financial grants, and a community ready to support families at every step.

Connecting Challenge Participants to ALS United's Comprehensive Support Network

Taking the Ice Bucket Challenge is often a person's first direct encounter with the ALS community -- and ALS United member organizations are built to meet people at that moment. [1] Each member organization offers coordinated services including free medical equipment loans, financial grants, caregiver guidance, and direct referrals to multidisciplinary ALS clinics, all built to support families from diagnosis forward. [1] Caregivers and family members can find region-specific resources and next steps through our [caregivers and families](https://alsunited.org/blog/for-caregivers-families) page, which connects people to social work consultations, equipment specialists, and financial assistance programs. [17] We are here for you -- whether you came to the ALS community through a viral video or a diagnosis, the support network built by challenge donations is ready to walk with you.

Turning Awareness Into Advocacy: Next Steps for Newly Engaged Community Members

The most durable contribution a newly engaged person can make is moving from a single challenge into sustained action -- through advocacy, regular giving, or volunteer work. Research on viral campaigns shows donations typically return to pre-challenge levels within weeks when social pressure is the only motivator; people who build personal connections to a cause through recurring involvement sustain their impact far longer. [4] Practical next steps include creating a fundraiser tied to a local ALS event, joining advocacy campaigns for increased research funding, or attending community walks throughout the year. [1] Local ALS organizations have clear pathways into each of these roles, and we are here for you at every step of the way.

Resource Guide: Where Your Donation Goes and How to Stay Involved

Knowing where donations go makes it easier to decide how to stay involved. Challenge funds supported 130 active research projects across 12 countries and 40 treatments in development, including $2.2 million toward AMX0035 -- a drug the FDA approved to slow ALS progression and the most direct proof that the challenge produced clinical results. [18] Local member organizations used their portion to expand free equipment loans, financial grants, and ALS clinic partnerships -- services that remain available to families today regardless of when they first connected with the cause. [1] For families navigating the financial complexity that comes with an ALS diagnosis, our [insurance and coverage guide](https://alsunited.org/blog/medicare-medicaid-and-private-employer-insurance) outlines the options available at each stage of care.

References

  1. Take a photo or video of yourself pouring a bucket of ice water over your head. Share the photo/video on social media... and challenge others to do the same. Make a donation to the ALS Network!
  2. MLB star Derek Jeter, actor Dwayne 'The Rock' Johnson and beloved Muppet Kermit the Frog were among the celebrities who got soaked after Pete Frates got the ball rolling on social media in August 2014. Vital in kicking off the challenge was the late Pete Frates, who was 27 when he was diagnosed with the rare illness in 2012.
  3. Chris Kennedy, a golfer in Sarasota, Fla., was nominated by a friend to participate in the Ice Bucket Challenge, which at the time, had nothing to do with ALS... Kennedy nominated his wife's cousin Jeanette Senerchia, whose husband Anthony is the one suffering from ALS. Kennedy posted this video on July 15--what appears to be the first instance in which the Ice Bucket Challenge and ALS were linked... The ALS Association says it started seeing an unexplained uptick in donations on July 29, and on Aug. 4, it was clear something was really taking off.
  4. The ALS Association received $115 million from the challenge, about half of the funds raised worldwide, and a huge jump from the $2.8 million raised by the organization in the same period the previous year.
  5. Van der Linden has set out his recipe for viral altruism using the acronym SMART: Social influences; Moral imperatives; Affective Reactions; Translational impact. Those who mentioned the ALS charity in their Ice Bucket Challenge video were five times more likely to donate money than those who did not.
  6. Over 17 million people participated in the Challenge and raised $115 million for The ALS Association.
  7. On 20 August, ALSA received more than $11.5m overnight... the challenge had raised more than $115m for ALSA, and millions more around the world, including £7m for the Motor Neurone Disease (MND) Association in the UK... a windfall amounting to almost five times the charity's typical annual revenue
  8. around 70% of the money is being spent on research, and 20% on patient and community service. The remainder is split between fundraising, publicity and administration costs.
  9. Scientists have identified a new gene contributing to the disease, NEK1. Although only 10% of ALS patients have the inherited form, researchers believe that genetics contribute to a much larger percentage of cases.
  10. 'Global collaboration among scientists, which was really made possible by ALS Ice Bucket Challenge donations, led to this important discovery,' said John Landers of the University of Massachusetts Medical School.
  11. $77 million of that went directly toward promising research. That led to the discovery of a new gene for ALS, called NEK1. The research project was called Project MinE, and was made up of 80 scientists from across the globe.
  12. Pete Frates Home Health Initiative, named in honor of one of the IBC co-founders, has recently been receiving national media attention. Working with private donors and our Massachusetts chapter, we will be covering the home health care costs for some individuals living with ALS in that chapter.
  13. Participants can either dump a bucket of ice water over their head and donate $10 to the ALS Association or skip the water and donate $100. They have 24 hours to complete the challenge and, if they choose the ice bucket, they have to upload a video as proof.
  14. Still, there is much to be done! Advances in research continue, policy reforms are improving, and our local programs continue to have an amazing impact on those we serve.
  15. its impact continues to ripple locally, including right here in New Mexico. The funds raised helped unlock new research pathways, expand patient services, and fuel advocacy efforts that endure today.
  16. A University of South Carolina student-run organization called MIND launched the 'Speak Your Mind Ice Bucket Challenge' at the end of March, encouraging donations to Active Minds. The ALS Association stated they are 'thrilled' that the ALS Ice Bucket Challenge lives on in 'new forms of activism,' applauding efforts to raise awareness for mental health -- an issue that also affects the ALS community in profound ways. Influencers like James Charles and Haley Kalil participated.
  17. the clinic helps with equipment and support to coordinate insurance. Caregivers also receive help from consultation with social workers to relief stress.
  18. $2.2 million of funds that were raised from the Ice Bucket Challenge went into funding the development and trial of the new drug...the ALS Association said it is funding 130 research projects in 12 different countries, as well as 40 potential treatments that are in development.