Students and staff take the ALS Ice Bucket Challenge
The challenge has raised over $80 million so far
August 28, 2014
What do NBA star LeBron James, principal Tobie Waldeck, senior Kat White and junior Clayton Holmberg all have in common?
They are just a few of the millions of people to participate in the ALS Ice Bucket Challenge.
Pete Frates, a former Boston College baseball captain, was diagnosed with ALS (amyotrophic lateral sclerosis, or Lou Gehrig’s Disease) and started this challenge. He wanted to raise the awareness of ALS and how it is under-funded, and asked his friends to take videos of them dumping buckets of ice water on their heads and post the videos on social media sites. If they didn’t take on the challenge within 24 hours, they had to donate to the ALS Association. This, in turn, started the phenomenon that is the ALS Ice Bucket Challenge.
ALS affects nerve cells in the brain and spinal cord. It also causes motor neurons to progressively degenerate, and when these neurons die, it leads to total paralyzation, and ultimately, death.
While many people solely take part in the challenge to dump freezing water on their heads, others actually participate to help raise awareness and money. ALS raised $2.5 million all of last year, and as of Monday, Aug. 25, because of the challenge, the cause has raised over $80 million.
Mill Valley students, teachers and coaches were nominated to partake in the challenge, including robotics, Mill Valley News, girls golf and the administrative team.
“[The cheer team] got nominated by the dance team,” senior cheerleader Halie Breninger said. “We thought it was for a good cause and it was fun. I thought it was pretty cool how many people participate in it…It’s not very time-consuming, so it’s nice to see people supporting.”
Along with teammates doing the challenge, students also participated individually.
“[I did the ALS challenge] just to raise awareness. [I think] it’s important because it raises awareness for what ALS is, and it’s raised so much money,” Holmberg said. “I think [the challenge] can’t get more popular than it is now. I wouldn’t say it’s overdone, but everyone knows what it is now.”
While some teams and students were challenged by their friends, head football coach Joel Applebee said his players asked the football coaching staff to take on the challenge.
“Obviously it’s for a very good purpose, and once we got all the challenges…we [just did it] as a coaching staff. [We wanted] to have fun, you know, and at the same time put out the awareness of the whole thing,” Applebee said.
The coaching staff decided not only to do the challenge, but donate to the association as well. The staff’s total ended up at $110, but the players’ parents matched their donation, so the final donation was $220.
“How can [the challenge] be [a bad thing], you know, when it’s for a great cause? Even if, you know…there’s some people who don’t donate,” Applebee said. “It’s great that people are understanding and finding out what this disease is all about, and it can only be a good thing if people know about it.”
Veronica Mckall • Mar 5, 2023 at 12:52 am
My grandma has Lou Gehrig’s disease, she is about 75 years old it was diagnosed 2 years ago. Right now it’s getting more difficult to live for her, because of stiff muscles she can’t even move. Riluzole and Edaravone medicines are given, but won”t give much relief. She can”t eat food without choking. I thought this might be the last stage and the medications she was given did not help at all, so I started to do alot of research on natural treatments, I was introduced to Health Natural Centre and their ALS Herbal Protocol. She started on the ALS/MND Treatment last year, her symptoms gradually diminished including her vocal cord spasm, Body Weakness and Difficulty with swallowing. Reach them at healthnaturalcentre.org , She is getting active again since starting this treatment, she is able to walk again ( down the street and back )she have also resumed exercising to strengthen muscles!! God Bless all ALS Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you
Laurah Quayle • Jul 3, 2022 at 3:45 am
Hope this is allowed on here if not I understand. Around age 60 I noticed that my handwriting was getting smaller and I was writing faster. I also noticed twitches on my right hand. The doctor went over my different symptoms and he suspected I’d either had a small stroke or the beginnings of Parkinson’s. After finding a neurologist and some testing I was diagnosed with Early stages of Lou Gehrig’s disease. That was 2 years ago. I took Radicava four times a day to control my symptoms, which include drooling, muscle weakness, gait problems, swallowing difficulties, and my while body feeling faint, A year ago, I began to do a lot of research and came across Health Herbs Clinic (healthherbsclinic c om) and their ALS/MND HERBAL TREATMENT. After seeing positive reviews from other patients, I quickly decided to get started on the treatment, ( NOTE: Our family doctor was informing my family to prepare for my funeral as I had a year to live at that point ), After 2 months I experienced significant reduction/decline in major symptoms, including muscle weakness, speech problems, difficulty swallowing, fatigue and others, The truth is you can get off the drugs and help yourself by trying natural methods, i live symptoms free. I’m forever thankful to nature and Health Herbs Clinic
Marcia Stewart • Apr 4, 2022 at 8:54 am
With my amyotrophic lateral sclerosis (ALS), the first thing that happened almost 2 years ago now, was speaking as if I were drunk. I wasn’t. I initially did improve speech (articulating clearly but slow) but now I can no longer speak in an acceptable way. Then, a year later eating became problematic, I was biting my tongue and lips, and chewing became weak and less controlled. Soon after that some fingers started to fail me and things would drop out of my hands. Somewhere at that time bulbar ALS was diagnosed. The Rilutek (riluzole) did very little to help me. The medical team did even less. My decline was rapid and devastating.. We tried every shot available but nothing was working. There has been little if any progress in finding a reliable treatment, Our care provider introduced us to Kycuyu Health Clinic ALS/MND herbal treatment