40 COMMENTS

The ALS Ice Bucket Challenge

Let me fill you in on a little scam that’s cruising the interwebs. It’s called the ALS Ice Bucket Challenge, and it’s a fund raising scheme concocted by a handful of us here in South Florida to dupe the rest of you into freezing your noggins off, knowing that when it cycled back around to us, we would be able to bask in our daily ritual of dunking our heads in a bucket of ice, and you all would think we were doing it for charity.

So far, the scheme is working brilliantly. The ALS Bucket Challenge has raised millions of dollars and tons of awareness for amyotrophic lateral sclerosis, a very nasty neurological degenerative disorder. The challenge goes like this: If you are called out by someone who took the challenge, you have 24 hours to take the challenge yourself and donate a little money to ALS, or you can skip the ice water and donate a lot to ALS. I mixed and matched and went with the ice water and a full donation. The point here is to raise money. And it’s super easy to give. Just go to this link to give over the web. You can use a credit card, Paypal, or your Amazon account. I went with Paypal, and it took five seconds.

It took longer to record and upload the video, which you can see after the break.

 

40 responses to “The ALS Ice Bucket Challenge”

  1. Scott Mulraney Avatar
    Scott Mulraney

    Haha… I told my brother in Phoenix that it didn’t count because it was 110 when he did it. He wrote back and said it wasn’t 110… it was 106. ;)

    Nice job, Hugh!

    Reply
    1. cory merlon Avatar
      cory merlon

      ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

      Reply
    2. Ruben Alvin Avatar
      Ruben Alvin

      I was diagnosed in March 2017, but was running around from doctor to doctor before I finally got a result that I was free from MND ALS. Mine started on top and progressed into the bottom. I could walk very little but need assistance as I have no balance. It is sad all the time that we thought this disease had no cure with all the technology we have, while some formulas at there can relieve all symptoms and get this of ALS. I’m passing this information to anyone who needs it, because www. madibaherbalcenter. com has the right cure and caregiver for this disease.I took various supplements, medicine prescribed by a neurologist, massage, and physiotherapy, still the disease was progressing very fast until the ALS formula from that company.

      Reply
    3. Barry K Avatar
      Barry K

      The absolute certainty of it all is the hardest to grasp. I wouldn’t want to see my father go down this road without the help of the natural organic formulas that were applied immediately. Some days are hard, and others are easy. All I’m saying is that there’s a cure at www .madibaherbalcenter. com God bless.They have given great relief to patients suffering from all types of diseases.

      Reply
  2. Nikki Avatar
    Nikki

    My favorite part of this was who you called out! I would love to see Mark Hamill do this. But I must say that the FanBoy in me is squealing at the fact you referenced two Star Wars actors :) (granted one is from the original awesome ones and one is from the new not so awesome ones).

    Reply
  3. Ernie Avatar
    Ernie

    Look at you getting your swolle on, flashing off the guns!

    Reply
  4. Simone Avatar
    Simone

    I love that you did this challenge. We lost a dear family member to ALS a couple years ago. It’s one of the most devastating ways to leave the earth. He was a masterful guitar player and when he lost the use of his fingers and couldn’t play any more, it was horrific. He became a prisoner in his body.

    Happier note: good to see you looking fit – nice guns (I mean this in a respectful non-creepy way).

    And I’m so glad you didn’t dump that ice on sweet, unsuspecting Bella.

    Here’s to raising awareness and money for ALS!

    Reply
  5. Hollis Avatar
    Hollis

    Your dog seems to know what you were saying!!! Also, this is an adorable video. And good on you!!

    Reply
  6. T. M. Bilderback Avatar
    T. M. Bilderback

    “You’re a better man than I am, Gunga Din!”
    –Rudyard Kipling

    Michael

    Reply
  7. Andrew Avatar
    Andrew

    Good for you, man. Yeah, here in Canberra it’d be a challenge right now, with temps down in the single digits. And all the t-shirts you wear, who knew such a BEAST lurked underneath? I guess you must type harder than other writers!

    Reply
  8. enabity Avatar
    enabity

    I commend Hugh calling out Obama, because that is definitely the right direction to be looking. The people who need to be called out are our representatives in the Federal Government. We spend about 2% of the federal budget on science in general, and somewhere around 1% on the NIH. Diseases like ALS and cancer that are a result of fundamental cellular failure aren’t going to be solved only by a direct effort, but by a strong effort to understand basic cellular mechanisms which will put us in the position to produce an effective treatment. If we value solutions to these problems, we need to make sure our government is aligned to help solve them.

    Reply
    1. Hugh C. Howey Avatar
      Hugh C. Howey

      All of this.

      Recent action in Iraq backs up something I’ve been saying for years: We don’t need troops on the ground in order to protect our interests. That’s where we lose wars, in fact. Air and sea support are plenty to protect our shores and to lend aid to our comrades. We could scale back our military by several factors and be just as effective as we are today, with far less loss of life and far less loss of prestige around the world.

      Every penny of those savings should go to infrastructure and research. Imagine what we could do if we spent those billions of dollars every year in these two areas. The effects would compound, and GDP growth would get back to 5%, year on year, rather than the anemic growth we see when we go around blowing shit up.

      Reply
      1. enabity Avatar
        enabity

        It is funny that you answered me anyway as I agonized over my silly response to myself below.

        Reply
      2. enabity Avatar
        enabity

        There is some limit to our capability to usefully direct research funding. More of the same from the NIH could quickly degenerate into even more of the incompetent researchers having an embarrassment of riches wasted on poorly designed studies that make erroneous conclusions. There are serious problems with the way research funding is distributed. However, big investments in research infrastructure like pushing genetic sequencing into higher volume and better economies of scale would be a worthy cause that would aid research immensely.

        Reply
        1. T. M. Bilderback Avatar
          T. M. Bilderback

          I agree with both of you. Wholeheartedly.

          If some of that military budget were spent on research for diseases like ALS, or for taking care of our own people’s hunger, or both, we could do so much more good than anything we might generate from having our troops on the ground in Iraq or Afghanistan.

          Just my two cents.

          And now, back to our program.

          Michael

          Reply
          1. T. M. Bilderback Avatar
            T. M. Bilderback

            Should have been “was” instead of “were”…where’s that edit button?

            Michael

    2. enabity Avatar
      enabity

      After posting this, it occurred to me that my post is not addressed to you, Hugh. Some small part of that is due to a realization that this is a one to the multitude relationship and it is unreasonable (and uncomfortable) to expect any of your attention. More of it is the understanding that there are other people reading the comments as I do. In retrospect, I’m bothered by what the construction of my comment says about me. To the degree which this was disrespectful of you and your blog, I’m sorry.

      When a friend shared a link to http://www.huffingtonpost.com/matthew-segal/the-ice-bucket-challenge_b_5688100.html , I lost all sense of restraint on the subject and felt compelled to share on Facebook and here a point of view that is more in line with the scientific community than the meme is. Hopefully, this point of view is also better aligned with the best interest of human health as well.

      The bottom line is that my personal experience in biological research has convinced me that the NIH is more important to progress against disease than these advocacy organizations that essentially serve a special interest and are focused on what amounts to improved palliative care (this can be seen by looking at their list of funded grants). The ALS Association is a perfectly fine cause from the perspective of making the disease more bearable for the families affected, and is money better spent than many other charities. Still, it is the NIH and organizations like it, not the ALS Association, that will “Create a world without ALS”.

      Reply
      1. Steve Avatar
        Steve

        The sequester cut $1.5 billion from the annual NIH budget, entirely to score political points.

        Reply
  9. J_Jammer Avatar
    J_Jammer

    Haha. I’m looking forward to this if ever I get called out. It’s that hot here in Houston. I would love to get cold water poured on me.

    Good job on passing on the info and great intro and of course donating.

    Reply
  10. T. M. Bilderback Avatar
    T. M. Bilderback

    On a totally different subject, look at the progress meter for “The Shell Collector”!

    Fantastic, Hugh! Keep it going!

    Michael

    Reply
  11. Johnmonk Avatar
    Johnmonk

    I will repeat my facebook comment, i think the big shots in Hachette and Amazon should be called out, maybe even together, maybe if those stuffed suits come together to dump ice water one each other, they might loosen up and start talking about other things?

    Reply
  12. Kathy czarnecki Avatar
    Kathy czarnecki

    First off, thanks for donating. I am doing the ALS walk in October and getting some donations for that. My Father-In-Law who died last year of ALS was determined to have gotten it as a service related disease. He was on a ship during the Viet Nam War where Agent Orange was housed. Seems there is a lot of connections between ALS and serving in the military (in certain circumstances).

    Reply
  13. Patrice Fitzgerald Avatar
    Patrice Fitzgerald

    Thanks for doing this, Hugh. My cousin is married to Pete Frates, who is now unable to walk, speak, or eat through his mouth. She’s due with their first child in about two weeks. The success of his viral campaign for support of ALS through the Ice Bucket Challenge is making his inevitable physical decline less painful for everyone in the family.

    And hey… awesome arms, man. Good for you for keeping in shape!

    Patrice

    Reply
  14. Kristy Avatar
    Kristy

    Yeah, I think you just wanted to show off the guns LOL.

    I think President Obama will do this, if he sees the challenge(s) or hears about them. I’m assuming you aren’t the only challenger.

    I’ll have to Google that in a few days, to see if it reached him. :)

    Reply
    1. Hugh C. Howey Avatar
      Hugh C. Howey

      I hear he’s already declined the challenge and just donated, which is awesome as far as I’m concerned. The giving money is the best part of this.

      And I thought I showed decorum by putting on any kind of shirt. These things have to dry, you know. :)

      Reply
  15. Quick Thoughts on the ALS Ice Bucket Challenge | Kelli Callahan Writes…

    […] Author, Hugh Howey […]

    Reply
  16. John Tayser Avatar
    John Tayser

    Gotta give a shout out to the person who invented this viral campaign for ALS – it’s brilliant.

    Unfortunately, almost half of our donations are going to ALS’ high-paid executive team and not to research or cures…

    Take a look this video:
    http://youtu.be/iGmnxisfPJQ

    Reply
  17. johnny Avatar
    johnny

    I would praise this program and challenge as well if more of the money went to research and less to suit salaries and admin fees.

    Reply
  18. Eagle Towing Avatar
    Eagle Towing

    Cheap towing Service

    Reply
  19. Violet Wholt Avatar
    Violet Wholt

    To me It is very bad what Big pharma are doing, why keep making humans suffer greatly just to get profits annually for medications that don’t work. I’m glad that herbal remedies are gaining so much awareness and many people are getting off medications and activating their entire body system with natural herbal remedies and they have become holistically healed totally, It’s also crucial to learn as much as you can about your diagnosis. Seek options: ( worldrehabilitateclinic.  com ).

    Reply
  20. Meyer Odette Avatar
    Meyer Odette

    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 using vine health centre com ALS/MND treatment, which my husband has been receiving for a few months now. I’m delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, 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.

    Reply
  21. Grace Nathan's Avatar
    Grace Nathan’s

    My husband was diagnosed with bulbar ALS. He started slurring his speech and clearing his throat constantly. He also started choking on food before we made the decision to try different medications, which significantly enhanced his condition. He received treatment for ALS/MND at uinehealthcentre . co m 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. Although it doesn’t cure his ALS, it has improved his quality of life.

    Reply
  22. Steven Westermann Avatar
    Steven Westermann

    I was diagnosed with bulbar ALS in May 2024. I live in Texas, and I’m 68 years old. I take Nudexta medication to help with the emotional outbursts of laughing and crying. The weakness, slurred speech, and muscle loss progressed quickly. Mobility has been an issue since Dec 26, when I fell and broke my hip, and although I made small strides at first, I felt like my life had been placed on a countdown, as there was no known cure other than the prescription of riluzole medications, vitamins, and therapies. As the disease progressed, my symptoms worsened. With my neurologist’s guidance we decided to try other approaches and started the ALS/MND treatment, and it changed everything. Within 5 months, I noticed more strength in my limbs, clearer speech, and I have stopped using feeding tubes. I’m starting to learn how to walk again & I now sleep better. This ALS/MND treatment program gave me back control and hope. we got the treatment from uine healthcentre. ne t This is a game changer for people with ALS.

    Reply
  23. Ruben Alvin Avatar
    Ruben Alvin

    I was diagnosed in March 2017, but was running around from doctor to doctor before I finally got a result that I was free from MND ALS. Mine started on top and progressed into the bottom. I could walk very little but need assistance as I have no balance. It is sad all the time that we thought this disease had no cure with all the technology we have, while some formulas at there can relieve all symptoms and get this of ALS. I’m passing this information to anyone who needs it, because www. madibaherbalcenter. com has the right cure and caregiver for this disease.I took various supplements, medicine prescribed by a neurologist, massage, and physiotherapy, still the disease was progressing very fast until the ALS formula from that company.

    Reply
  24. Robert Avatar
    Robert

    Living with ALS has been one of the hardest challenges of my life.The muscle weakness, fatigue, and gradual loss of mobility were heartbreaking. Conventional treatments offered little more than temporary comfort, and I was starting to lose hope.That’s when I discovered NaturePath Herbal Clinic.Skeptical but desperate for relief, I decided to try their herbal therapy. To my surprise, by the fourth month, I began noticing steady improvements less muscle twitching, better coordination, and renewed energy. It wasn’t an overnight miracle, but the progress felt real. For the first time in a long while, I felt a sense of control returning to my body.Today, I move more freely, sleep better, and most importantly I feel hopeful again. This journey with NaturePath has been life changing.If you or someone you love is battling ALS or any other neurodegenerative condition, I genuinely encourage you to explore natural alternatives. You might be surprised at what’s possible.I’m truly grateful I gave them a chance. www. naturepathherbalclinic. com

    Reply
    1. Eliza Avatar
      Eliza

      Robert, I really connect with your story. My mom has also been struggling, and we decided to try NaturePath Herbal Clinic for her too. The results have been so encouraging her energy improved, she’s moving with more ease, and we can see her confidence coming back. It’s given our whole family hope again.

      Reply
  25. Barry K Avatar
    Barry K

    My dad was diagnosed with ALS about 6 A months and a half ago, after 1.5 years of undiagnosed symptoms. We are just beginning this journey, and it’s very frightening. We started www .madibaherbalcenter. com immediately because they have the right medicine to cure this ALS disease permanently, to say the least. The absolute certainty of it all is the hardest to grasp. I wouldn’t want to see my father go down this road without the help of the natural organic formulas that were applied immediately. Some days are hard, and others are easy. All I’m saying is that there’s a cure at www .madibaherbalcenter. com God bless.They have given great relief to patients suffering from all types of diseases.

    Reply
  26. Cory Merlon Avatar
    Cory Merlon

    My first ALS  symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatiue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

    Reply
  27. Barbara Beimann Avatar
    Barbara Beimann

    I’ve been doing the ALS/MND Protocol from limitless health center . I was diagnosed with bulbar ALS in June 2024. I received the ALS/MND treatment for my ALS approximately four months ago; since then, i have stopped using a feeding tube, speech is getting better by the day, sleeps well, works out frequently. I’m surprised a lot of PALs, and their CALs haven’t heard of it.

    Reply
  28. Barbara Beimann Avatar
    Barbara Beimann

    My husband was diagnosed of Parkinson’s Disease a couple of years ago, he had severe fatigue, difficulty with mobility and sleeping. He was placed on Sinemet 3 times daily, which helped but only for a short while. So we decided to try alternative treatment and began on PD-5 protocol , It has made tremendous difference for my husband, he had improved walking balance, muscle strength and he is now very active. His Parkinson’s is totally under control, we got the treatment from Limitless healthcenter . c o m. This treatment is a breakthrough for PWP!

    Reply

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