His Ice Bucket Challenge Did Not End Like All The Rest, You Gotta See This

The ice bucket challenge is making waves across the world and for a good reason. The donations from these individuals go toward the research of ALS. These seemingly silly antics have raised over $22 million to fight this disease.

However most people do not know the reality of it. After taking the ice bucket challenge, Anthony shows you a bit more of how it feels to live with this every day.

Videos starts right after his challenge. Rewind if you want to see it.

I saw this and felt like it needed to be shared, if this touched you in any way please share it with your friends to help spread the word. Maybe together, we can find a cure.

Hat Tip to / Upworthy for finding this beautiful video.

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3,058 Comments

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    For all of you "Non-Conformists" that refuse to do the challenge because you don't want to "become a slave to the whims social media". Check this out and tell me you feel the same way after you watch it. I've made my donation and I have never been happier to do something as stupid as dumping 5 gallons of ice and water on my own head. Thanks for nominating me Owen Winkler!!

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      I’ll immediately seize your rss feed as I can’t to find your email subscription link or newsletter service. Do you’ve any? Please let me understand in order that I may just subscribe. Thanks.

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    Hugs to you!! I know a family that had 7 generation of family members who have passed.. They were all in their 40's.. Now the last person has a son and daughter who are in 6th and 4th grade.. We sooooo desperately need a cure..please play or donate.

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    I really never knew what ALS was until I seen this video and I am sure there is more to the video than what was shown on how to cope and care for someone you love or know with this disease taking over the body. This video really touched my heart and brought me to tears no one should ever have to go through this. I am praying for you and your mom and all that are effected by ALS. We have to find a CURE for this life taking Disease so please do the challenge because for the people who have ALS it is a challenge for them everyday. Lets all work together and find the cure. God Bless the people who are fighting for there lives I am sorry life is so hard for the. Thanks for sharing this video now I am going to share it..

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    I am truly sorry that you have this horrible disease. I lived with a family for 2 years and helped take care of their older son that had the disease. He was one of the longer living ones and he actually lived for 15 plus years before passing away. I don't know what will help, but would like to suggest juicing fruits and vegetables as one option. I know that our diet of nutrition-less over processed food causes most disease in America. I would start there instead of waiting for a magic pill from companies that profits from disease and sickness. A good place to start would be: https://gerson.org/gerpress/ I know they have helped people heal themselves from food and proper nutrition. God bless you on your journey! Another good resource would be: http://www.forksoverknives.com/

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    May they find a cure. Thank you for sharing I can only imagine how hard this was for you.

    I hope all the people that are refusing to do this challenge are donating and those who are doing it are donating also.

    Blessed be.

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    Heartbreaking but happy he sees positivity in the challenges and the awareness they bring. I can't imagine how strong his emotions are when mine ran high just watching him.

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    Heartbreaking but happy he sees positivity in the challenges and the awareness they bring. I can't imagine how strong his emotions are when mine ran high just watching him.

  23. 41

    I'm not sure what to say, I'm 52 yrs old have had several back surgeries starting in my early 20's and have done my share of complaining. After watching this video I'm so blessed to have the health I have & I'am truly sorry for all of you suffering with ALS, I don't have $ but if I did I would donate has much as I could to help find a cure, in the mean time I will post videos and share with others what I now know about ALS! My heart & prayers go out to all of you, I'm in tear's writing this and I don't cry much but this has touch me in a very special way. God bless all of you!

  24. 42

    I'm not sure what to say, I'm 52 yrs old have had several back surgeries starting in my early 20's and have done my share of complaining. After watching this video I'm so blessed to have the health I have & I'am truly sorry for all of you suffering with ALS, I don't have $ but if I did I would donate has much as I could to help find a cure, in the mean time I will post videos and share with others what I now know about ALS! My heart & prayers go out to all of you, I'm in tear's writing this and I don't cry much but this has touch me in a very special way. God bless all of you!

  25. 43

    I have something that is helping ALS people, we were just on channel 5 news. Three months ago w/someone sharing their ALS story on how they got their life back. Would you be interested in watching the TV segment and learning more?

  26. 44

    I have something that is helping ALS people, we were just on channel 5 news. Three months ago w/someone sharing their ALS story on how they got their life back. Would you be interested in watching the TV segment and learning more?

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    thank you for your donation. The Ice Challenge brings it to the surface, and thats is fine with me, but donations are certainly helpful. Perhaps if a movie star was diagnosed with it then more people would be prone to help as they did with Michael Fox and Parkinson

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    thank you for your donation. The Ice Challenge brings it to the surface, and thats is fine with me, but donations are certainly helpful. Perhaps if a movie star was diagnosed with it then more people would be prone to help as they did with Michael Fox and Parkinson

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    It is not a food group disease. It is ALS> Nutrition is not always the answer and stop!!!! I can't stand it. How about all the people who have been on a healthy diet as my brother and still get it.

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    It is not a food group disease. It is ALS> Nutrition is not always the answer and stop!!!! I can't stand it. How about all the people who have been on a healthy diet as my brother and still get it.

  31. 49

    I was very grateful to hear your words. As I listened to you, I could see my son, who lives every day worrying about inheriting Huntington's Disease which his father has, his aunt and uncle have and his grandmother and another aunt died from. At times, he is terrified and it is never far from his thoughts. He is 20 and shouldn't have to be worrying about dying before he's even had a chance to live! Like ALS, HD has no cure and since it is only hereditary, it stays within families and doesn't affect the general population. I, too, get frustrated at the slowness with which research progresses and pray that pharmaceutical companies will place saving lives ahead of profits. I do believe that many of these neuro degenerative diseases will share success from each other and hope that the research accelerates for both of these diseases! I pray that God bless you abundantly and that your sense of humor holds you in the days to come!

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    I will donate but can't do the challenge due to severe chronic cold urticaria….. This could kill me believe it or not…… so I hop it helps and remember others are dealing iwth things too.. no cure or med. for me but at least I have a chance to be careful but this is a dreadful disease… hugs and prayers to all…

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    May god bless you and your family. No words of comfort we send you today can compare to what your family endures on a day basis, but please know there are a lot of good people is this world who got your back. Love your friends we care

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    I am so sorry that you and your family are going through this. I have lost my Mom after her battle with ALS. She only lived for 2.5 yrs after her diagnosis. It is so horrifying watching a loved one go through this. I live in fear of getting ALS at some point. I wish you the best and hope that you have someone to take care of you, as you have been taking such good care of your mom. I bet she is so proud of you.

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    Son, I am so, so sorry for you and your mom. My father was diagnosed at 68 and died at 70 fifteen years ago. Watching you take care of her feeding tube was so sadly familiar. There's nothing to say but how deeply, deeply sorry I am that you and your family are dealing with this. I fervently hope there is meaningful progress in time to help you. My family works with The ALS Association- Jim "Catfish" Hunter Chapter in Raleigh, my brother in law runs a fundraising golf tournament, and we get annual updates from the fine dedicated researchers at Duke. He–we–are walking on air to see this out of the blue viral bump in awareness and funding. Progress is being made, but it's too slow. We need to use this unexpected exposure, and your incredibly brave and honest video is so important to that end, to kick some ass and also redirect some of our collective tax dollars on something worthwhile like pumping up our search efforts for a cure, for some understanding of why, and do it now. Thank you again for your bravery and transparency. You are making a huge difference, and I hope something promising is discovered which can help you soon.

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    My family suffers from Huntington's Disease, which is similar to ALS in some ways. It is a rare inherited neurodegenerative disease that really can tear a family apart. I am so happy to see ALS doing so well and getting so much recognition. ALS is an awful disease and I hope and pray for a cure. As I also hope and pray for a cure for Huntington's. Hang in there.

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    My family suffers from Huntington's Disease, which is similar to ALS in some ways. It is a rare inherited neurodegenerative disease that really can tear a family apart. I am so happy to see ALS doing so well and getting so much recognition. ALS is an awful disease and I hope and pray for a cure. As I also hope and pray for a cure for Huntington's. Hang in there.

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    Good bless you and your family. Thanks for opening up and showing the world what all ALS patients deal with….hopefully this will soften their hearts and opn their wallets and send even more donations to find a cure.

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    Juicing? You're absolutely ridiculous. Open a book or maybe do even the slightest bit of research into what you are talking about before plugging some stupid diet as a cure for one of the most terrifying diseases on the planet.

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    Carol Coughlin – i realize this is a sensitive subject to you… but try to cut Britt some slack. She simply wanted to help…. A simple thanks or no comment at all would suffice. Negativity and stress also fuel disease…but you don't want to hear that either, right?
    How about lets all be more positive and loving creatures towards everyone….

    "Who's to say" is a great way of approaching life… who's to say Britt's post won't save a life or help someone with or without ALS….

    Britt, thanks for caring about people enough to take time to write your experiences and resources. While it may not be applicable to certain diseases… it is applicable to everyone.

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    This challenge is a smart thing to do other than I have seen many, many people doing the challenge but not donating a thing. I have also seen posts of people doing the challenge and mentioning nothin about donating a cent to this charity unless the refuse to do the challenge they have to donate $100.

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    My heart goes out to you and your family. I pray to God that they will find a cure very very soon. I am so glad there is awareness of ALS. Honestly, I didn't know what is was until the challenges began. My prayers and faith in God are with you. Keep your head up and have faith.

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    I can't even begin to imagine how this guy's life is. It breaks my heart to people go thru any type of illness knowing that right at this time all you can is pray. I believe this guy is a hero in my book. I give him all the props cause he is strong enough to handle what may come his way. God bless you and your family.

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    I can't even begin to imagine how this guy's life is. It breaks my heart to people go thru any type of illness knowing that right at this time all you can is pray. I believe this guy is a hero in my book. I give him all the props cause he is strong enough to handle what may come his way. God bless you and your family.

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    Ok what about families suffering also with Ohhhhh I don't know Cancer, depression, parents and grand parents that have had strokes, hearth attacks or even soldiers that come home broken and torn apart from war. Everyone and everything is struggling, I am glad to see everyone with a heart do something for these people suffering but this is nothing but a drop in the bucket compared to what many others are suffering from and get no relief and no help from anyone. I don't want to piss in anyone's cheerios, but can we stop pretending that because we throw some money at something and say look I helped. do half of you know that these same charities take 60-90% of all proceeds and donate only a portion of what was donated. if you really want to help try going for the root of the problem, the corrupt government that is allowing these diseases to run free and corporations profit off them and the sick people we should stop ignoring it and actually make a difference by ending that shit and getting these hospitals and scientists the money they need for research to end horrible diseases like posted so people don't have to suffer.

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    Ok what about families suffering also with Ohhhhh I don't know Cancer, depression, parents and grand parents that have had strokes, hearth attacks or even soldiers that come home broken and torn apart from war. Everyone and everything is struggling, I am glad to see everyone with a heart do something for these people suffering but this is nothing but a drop in the bucket compared to what many others are suffering from and get no relief and no help from anyone. I don't want to piss in anyone's cheerios, but can we stop pretending that because we throw some money at something and say look I helped. do half of you know that these same charities take 60-90% of all proceeds and donate only a portion of what was donated. if you really want to help try going for the root of the problem, the corrupt government that is allowing these diseases to run free and corporations profit off them and the sick people we should stop ignoring it and actually make a difference by ending that shit and getting these hospitals and scientists the money they need for research to end horrible diseases like posted so people don't have to suffer.

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    My grandfather had als & passed several years ago. It was talked about even less then. A Dr said he had a slipped disc in his back & opened him up. That exposure sped up his process of als & he passed a little over a year after he was diagnosed. It was so sad to see him going through that.

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    My grandfather had als & passed several years ago. It was talked about even less then. A Dr said he had a slipped disc in his back & opened him up. That exposure sped up his process of als & he passed a little over a year after he was diagnosed. It was so sad to see him going through that.

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    "Let's put this another way: A month-long viral social media campaign consisting of billionaires, media moguls, and celebrities alike has raised $13 million, while a seemingly trivial percent cut in NIH funding means billions of dollars. "

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    Thank you to this young man for sharing his heart-felt story. He will certainly be in my thoughts & prayers as will the thousands of individuals who suffer from ALS. Recently, I lost my only brother from complications of Primary Progressive Multiple Sclerosis (PPMS). PPMS is an aggressive form of MS & unfortunately, unlike other forms of MS, this type never goes into remission. I was told the progression & prognosis of PPMS are very similar to that of ALS. Sadly, I watched my brother's health deteriorate right before my eyes from once being a very independent, healthy, active & athletic man to someone who became 100% reliant on others for his care. During the last 5 years of his life he was confined to a hospital bed paralyzed by the disease, tube-fed, on oxygen, & could no longer talk- yet, his mind was completely alert, a prisoner in his own body. These neurological diseases have NO place on this Earth… It's time to stomp them out once & for all! With that said, I accept the Ice water challenge Angel Smith-Gonzalez!!!

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    This video makes me so sad because I understand what he means about the pharmaceutical companies. My T1 child was lucky enough to have Charles Banting to develop insulin. Or T1 would be a death sentence. I wish/hope/ pray with all my heart right now that someone somewhere could find a way to help them. Find their for Freddward Banting.

  85. 103

    Dear Young Man, first I want to say, you are a very brave and honorable man as you take care of your mother like you do. Everyone who sees your video couldn't help but have empathy towards those who have this condition and hope for that day a cure will surface as we join together in support. I just want to extend my caring and prayers to you. Remember the 'Footprints in the Sand', God bless you and your mother.

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    I caught myself staring into the most painful of eyes as I saw this man and I wish to god I could do more than a donation or challenge to get a cure started. I wish that I was able to be a guinea pig to help find a drug or something to save the 30,000+ that are affected.

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    This video was extremely touching, started crying once he did. This video definitely makes you appreciate the things you have. And to also reach out to others and help them in times of need. This video educated me more on the actual disease and not just the ice bucket challenge although I do believe it has helped raise awareness .. my heart goes out to everyone suffering. You learn something new everyday. And In today's world, as a young person I'm glad I could learn about something that actually has a real affect on people's lives instead of something irrelevant in the media.

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    I am sharing your video with my 841 friends and had my daughter post it on her social networking of 10,000. I am praying for you and everyone with ALS. I personally have done the ice challenge 3 times and donated also. I wish I could give you a gigantic hug

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    Love this! ! I just posted a status saying…look at the awareness and convos this has started…look at the joy & smiles shared by so many!! Keeo the challenge going!! Lets ice out ALS!! ?? AND PRAYERS TO SURVIVORS & CARRIER'S MAY YOUR JOURNEY PEACEFUL AND MAY YOU FEEL THE LOVE AND SUPPORT! ! Appleton WI

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    Julie- you're a person who doesn't care about other people are you? You take the coward way out by saying we all have issues. We do. That's exactly why we need to come together and help out each other so when we need help with our own issues we know itl be there. You have never witnessed this before much less anything traumatic because you wouldn't be a bitch if you had. Enjoy living your Care free life now because we all get sick and we all die. And when you're diagnosed with a disease that will ruin your body and kill you, youl know exactly what these people went through and how wrong you were. And youl have no one there to help you. But I hope that doesn't happen to you. Because things like this make those who go through it stronger and you deserve to be a weak bitch

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    You really wanna help. First show me you doin the bucket! Then give me an address where I can send funding? I've seen a lot of vids with the ice. I've done it myself. But all that's happening is only a fad if no one knows where to send the money!

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    You really wanna help. First show me you doin the bucket! Then give me an address where I can send funding? I've seen a lot of vids with the ice. I've done it myself. But all that's happening is only a fad if no one knows where to send the money!

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    Sending big love to you. Thank you for being so vulnerable and showing the world why this challenge is so important. As the mom of a pediatric cancer survivor I want to tell you you are not alone in your frustration. Our kid's cancers are considered RARE so we are not profitable to the pharmaceutical companies either. We basically spend much of our time advocating and fundraising to support research that the government will not pay for. Kudos to the ALS community for finding a way to grab so much national attention. If I could figure out a way to do it for the kids, I would.

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    Thank you for posting your very personal video… a very sweet neighbor and friend of many in our little town was recently diagnosed it is very hard to watch the swift decline that ALS serves up.. Hug your Mom tight, she is still in there…. Hugs to you.

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    Being a caregiver for those with ALS, I may not know your struggles from a first hand basis, but I Know them….
    I'm so thankful that the word has spread out about this devastating disease and the money going into the funding of research is incredible.
    Bless all of you with ALS, and those families and caregivers going through it. You are all angels <3

  123. 141

    I do my ice bucket challenge for you, and I sure as hell will donate and say my prayers for you. This isn't just all fun and games. We do this for a reason. If something as dumping cold water on your head can spread over the Internet why can't we do something to make a difference? Dumping water on your head is only the first part! Don't forget you're doing this for a reason.

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    You have just listed about twenty different issues and sub issues within themselves. Yes, there are all these other awful things out there. But why the fuck should we rely on them if we can do it ourselves. The fight against disease is fought with baby steps. And this is actually contributing to awareness and raising the money. No amount of pessimism can undo that. If everyone always worried about everything all at the same time, nothing would ever get accomplished.

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    Christopher Malamet Maybe juicing is silly to you, but I know for a fact that nutrition is but one aspect of an ALS patient that needs to be addressed…… my stepdad has ALS and his diet is of the greatest importance to help insure the best health he can be in at this time in his life……….. no judgements……..

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    Jake M Leisher Dear Mr. Leisher, Oh My God……. thanks so much for your response to Carol Coughlin regarding ALS……. as a retired RN, and a person who lives with her stepdad with ALS, your comments are so appropriate and so on target……. thank you thank you, could not have said it better…………. so much love and respect to you and yours……….

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    I am glad you did this video as many people are unaware. It takes courage to do this. I hope they can fine a cure or some relief so you & your Mom so you can have a somewhat normal life. I have MS so I kind of know how you feel. Smooches

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    I don't think anyone else in the world could have helped me understand this terrible disease and it's affects but watching this video, I saw the fear, stress, pain, agony, and sincerity all negatives a side he still has the courage and determination to fight. I nominate #kissmyALS to be the, for lack of better words poster child. While his body and health is strong and raise awareness for a cure. I'm No one just an average guy with a wife and 2 kids in this big world, I could not imagine the pain and suffering. Put the faith back in humanity and work together. Corny analogy but Gees are considered to be the best in the world when it comes to teamwork because they communicate and fly in uniform each bird shifting to the lead position while others rest Back. we are stronger together than we are individually. sorry for the rant that video touched my heart and opened my eyes. Thanks

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    I just want the man who made this video to know that I'm praying for him and his family <3 this video has broken my heart and I want him to know that I will fight for him and every other ALS patient all around the world for a cure for this horrible disease!

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    God bless you and best wishes your way. A good friend of mine was just diagnosed and I didn't know what to say to comfort him. He doesn't believe in God so,prayers didn't offer him comfort, but they have for me.

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    if they solve the problem, they'd have to find j*bs…

    if you're not part of the problem, there's lots of money to be made in prolonging the search for a solution.

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    As a nurse I have seen how devastating this disease is to patients and their families. This challenge has brought awareness about this disease to so many people. We as a society spend money on game apps and other things that may not have purpose. Donations for ALS research has so much of a purpose because this disease is so awful to those affectected by it. Whether or not you choose to take the ice bucket challenge, choose to atleast make a donation

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    Laura Funseth Man I wish I could do anything to help you out, I pray to God that the disease does not effect you and you remain in good health. I would hope that you look into alternative medicines. http://www.ericiswinning.com/ ——- http://dherbs.com/…/4669/Lou-Gehrig-s-Disease/d,ai.html… ——–http://www.itmonline.org/arts/als.htm—————— http://www.naturalnews.com/028734_ALS_remedies.html It may intrest to you to know that in Islam, in the Quran it says that Allah/God said "there is a cure for every disease except death". Some of the top foods in the Quran are Dates, Pomegranate, Lemon and Lemon Grass (LG is better boiled andwater reduced and then drink), Figs, Honey, Vinegar, Squash and many others. If your interested you can Google 'Foods in the Quran, but also look into mixing foods, some foods are hot and some are cold so they should be balanced so as to keep the stomach alkaline. This is probably easier to find in Chinese Medicine. Anyway, from the bottom of my heart I wish you excellent health and a long and happy life.

    Eric Is Winning
    http://www.ericiswinning.com
    This web site contains information primarily for ALS patients who have read our …See More

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    I'm hurt and very speechless about this it breaks my heart and tears me up too that ppl in this world can be heartless to find a cure for these ppl with ASL my love out to u all and I did the challenge for u scared out of my mind I lose my breath from trying to take cold showers in summer and no clue about ALS but I did it because I felt in my heart there's a good reason to do this and I did hang in there best u can love u all

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    some people, well most anymore just don't care, but i was challenged yesterday i will be doing it today.I really wish that people could have hearts. I just want to say God bless you in your struggle and all my prayers go out to you.

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    Your words touched my heart. After watching your video I went and looked up what ALS really is. I did not want to do the ice bucket challenge for a cause that I didn't fully understand. I was shocked. Thank you for opening my eyes and I hope others to what living with this disease is all about. My prayers are with you and your mom. Your a wonderful son.

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    My eyes have never seen and my heart has never felt such an emotionally moving video. I thank you for sharing and like many here…we felt each tear and had tears streaming down our faces. I lost a very dear friend to ALS. A disease i hate with every ounce of my being. Keeping you, your family and many others who face this disease each day in prayer. Let's find a cure!!

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    Hi
    I have a suggestion that will get you further coverage to very wide communities. This is my https://www.XeeMe.com/cve4me Social Media Profile. Go there through that link and make a social media profile. It is free. Takes some doing though. The community behind the profiles is world wide. They will share your story rapidly in many different ways. Which is where I am going now to post this link as well as share it.

    Thank you for taking the time to cry. That was a raw version of the truth.

    Susan

    : cve4me

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    Anthony, I'm not sure if you'll read this but you should know that you are worth MORE than anything in this world and in heaven to God. It says in Gods love letter, aka The Bible, that our bodies wither and die but in heaven we will be made anew with a body unlike ours here on earth, you will never experience pain or disease. My prayers go out to you and your family. You have an unbreakable soul and a new unwithering body in heaven through Jesus. God Bless.

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    I SOO SORRY MY BROTHER,HEALING IS ON THEWAY FOR YO AND YOUR FAMILY,THAT TEARS FROM YOUR EYES IS A FOUNTAIN OF HEALING FROM HEAVEN FOR YOU AND AS MANY THAT ARE IN SUCH CONDITIONS,GOD HELP YOU AND SAVE YOU

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    i read your story and its very heart felt, very happy to see the ALS ice bucket challenge has went viral on facebk and everyone is doing an donating., (even me) I hope the find a cure and prayers go out to you and your family.

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    I had no idea the ice challenge was for ALS. I had seen video'a of people dumping water on their heads to "not donate to a charity" and they were all saying it was a "charity of choice" so in my confusion I did dish the whole ice bucket challenge only because I was confused why someone would dump ice on their head so they didn't have to help somebody. I feel so bad for being that guy. Like I said, I didn't know. I'm not that in touch with my social media I guess.

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    Wow very touching video. I suffer from fasiculations and some other weird neuro stuff, have a family history of MS (my dad and his sister). So my condition is benign, which means it won't get any worse, but either way, I still have to live with it every day with no help and no advice from any doctor. So i just don't talk about it but it;s tough. I try to do as much as possible and just enjoy every minute of life. After living with this nearly 2 years, I wholeheartedly believe I will not get worse, and I never did not believe that, but the curiousity is what kills me. Finally, I have kind of just accepted I will just have to live with this forever, there just isn't any answers, and there never will be, because pharmaceutical companies and researchers will never invest in a benign condition, even though i suffer every day. There is just no money to be made. So i know where this guy that did this video is coming from. People don't understand how frustrating it is. My body constantly does weird things every single day and i just have to keep plugging along. Can't talk about it because people don't understand, and people don't know what to say. WIth that being said, i won't get worse, but the reality is that people with ALS and MS do get worse. I really really hope this icebucket challenge continues to get to at least 1 billion dollars raised, and while i don't think a cure is going to happen, at least a medication to help stop the progression of the muscle atrophy would be so awesome. There has to be a cure, like injecting maybe a toxin through the blood brain barrier or maybe some type of protein injection that could hijack an autoantibody and redirect it or kill it so it never goes to attack the tissue. It's as easy as that, but it takes billions of dollars to get to that point. Keep hope alive!

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    Wow very touching video. I suffer from fasiculations and some other weird neuro stuff, have a family history of MS (my dad and his sister). So my condition is benign, which means it won't get any worse, but either way, I still have to live with it every day with no help and no advice from any doctor. So i just don't talk about it but it;s tough. I try to do as much as possible and just enjoy every minute of life. After living with this nearly 2 years, I wholeheartedly believe I will not get worse, and I never did not believe that, but the curiousity is what kills me. Finally, I have kind of just accepted I will just have to live with this forever, there just isn't any answers, and there never will be, because pharmaceutical companies and researchers will never invest in a benign condition, even though i suffer every day. There is just no money to be made. So i know where this guy that did this video is coming from. People don't understand how frustrating it is. My body constantly does weird things every single day and i just have to keep plugging along. Can't talk about it because people don't understand, and people don't know what to say. WIth that being said, i won't get worse, but the reality is that people with ALS and MS do get worse. I really really hope this icebucket challenge continues to get to at least 1 billion dollars raised, and while i don't think a cure is going to happen, at least a medication to help stop the progression of the muscle atrophy would be so awesome. There has to be a cure, like injecting maybe a toxin through the blood brain barrier or maybe some type of protein injection that could hijack an autoantibody and redirect it or kill it so it never goes to attack the tissue. It's as easy as that, but it takes billions of dollars to get to that point. Keep hope alive!

  176. 194

    Wow very touching video. I suffer from fasiculations and some other weird neuro stuff, have a family history of MS (my dad and his sister). So my condition is benign, which means it won't get any worse, but either way, I still have to live with it every day with no help and no advice from any doctor. So i just don't talk about it but it;s tough. I try to do as much as possible and just enjoy every minute of life. After living with this nearly 2 years, I wholeheartedly believe I will not get worse, and I never did not believe that, but the curiousity is what kills me. Finally, I have kind of just accepted I will just have to live with this forever, there just isn't any answers, and there never will be, because pharmaceutical companies and researchers will never invest in a benign condition, even though i suffer every day. There is just no money to be made. So i know where this guy that did this video is coming from. People don't understand how frustrating it is. My body constantly does weird things every single day and i just have to keep plugging along. Can't talk about it because people don't understand, and people don't know what to say. WIth that being said, i won't get worse, but the reality is that people with ALS and MS do get worse. I really really hope this icebucket challenge continues to get to at least 1 billion dollars raised, and while i don't think a cure is going to happen, at least a medication to help stop the progression of the muscle atrophy would be so awesome. There has to be a cure, like injecting maybe a toxin through the blood brain barrier or maybe some type of protein injection that could hijack an autoantibody and redirect it or kill it so it never goes to attack the tissue. It's as easy as that, but it takes billions of dollars to get to that point. Keep hope alive!

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    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  178. 196

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  179. 197

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  180. 198

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  181. 199

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  182. 200

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  183. 201

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

  184. 202

    Thank you for sharing your beautiful touching video we are doing an ice bucket challenge here but it's for Macmillan Nurses to help those who have cancer my beautiful son has cancer in his brain they can't cure him but these wonderful people make a difference

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    Bless your heart for posting this video and giving people a glimpse into this horrible disease. I know the frustration felt when there seems to be lack of progress toward treatment for a disease that is deemed a death sentence…pancreatic cancer killed my sister.

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    Bless your heart for posting this video and giving people a glimpse into this horrible disease. I know the frustration felt when there seems to be lack of progress toward treatment for a disease that is deemed a death sentence…pancreatic cancer killed my sister.

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    Bless your heart for posting this video and giving people a glimpse into this horrible disease. I know the frustration felt when there seems to be lack of progress toward treatment for a disease that is deemed a death sentence…pancreatic cancer killed my sister.

  188. 206

    Bless your heart for posting this video and giving people a glimpse into this horrible disease. I know the frustration felt when there seems to be lack of progress toward treatment for a disease that is deemed a death sentence…pancreatic cancer killed my sister.

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    Bless your heart for posting this video and giving people a glimpse into this horrible disease. I know the frustration felt when there seems to be lack of progress toward treatment for a disease that is deemed a death sentence…pancreatic cancer killed my sister.

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    What a truly incredible man. This video made me cry. Seeing how ALS affects an individual…feeling it slowly creep through their body is one of the most terrifying things I have heard. My heart goes out to him.

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    What a truly incredible man. This video made me cry. Seeing how ALS affects an individual…feeling it slowly creep through their body is one of the most terrifying things I have heard. My heart goes out to him.

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    What a truly incredible man. This video made me cry. Seeing how ALS affects an individual…feeling it slowly creep through their body is one of the most terrifying things I have heard. My heart goes out to him.

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    I think the Ice Bucket Challenge is an amazing effort. I have a friend in NC that does a therapy module that helps slow down the process. Wish more people with ALS knew about it.

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    I think the Ice Bucket Challenge is an amazing effort. I have a friend in NC that does a therapy module that helps slow down the process. Wish more people with ALS knew about it.

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    I think the Ice Bucket Challenge is an amazing effort. I have a friend in NC that does a therapy module that helps slow down the process. Wish more people with ALS knew about it.

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    Christopher Malamet I'm sorry, I didn't know that you were the expert on ALS. So what is the cure you have come up with? So many people are depending on you. Do share all your vast knowledge and understanding on this subject as we are waiting with baited breath to hear. Thanks for all your breakthroughs. your awesome… no really, you are!

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    Christopher Malamet I'm sorry, I didn't know that you were the expert on ALS. So what is the cure you have come up with? So many people are depending on you. Do share all your vast knowledge and understanding on this subject as we are waiting with baited breath to hear. Thanks for all your breakthroughs. your awesome… no really, you are!

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    Christopher Malamet I'm sorry, I didn't know that you were the expert on ALS. So what is the cure you have come up with? So many people are depending on you. Do share all your vast knowledge and understanding on this subject as we are waiting with baited breath to hear. Thanks for all your breakthroughs. your awesome… no really, you are!

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    Christopher Malamet I'm sorry, I didn't know that you were the expert on ALS. So what is the cure you have come up with? So many people are depending on you. Do share all your vast knowledge and understanding on this subject as we are waiting with baited breath to hear. Thanks for all your breakthroughs. your awesome… no really, you are!

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    it was so touching and u really changed my view Anthony! when we hear something it is different from what it may look in reality or when we see it for real !! I hope they find a cure for this disease and be strong! I'm so sorry to see your mom like that , so so sad, it brought tears to my eyes! just keep hoping ….

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    When there seems to be no way, there is God who always finds a way. Have enough faith brother, He shall heal the disease you and your loved ones are suffering. As always, in Jesus' name…..

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    I know how you feel mJD runs in my family i lost almostll of them believe me i know what it feels like i have mJD now it sucks to its just like m S stay strong God Bless you

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    I've been seeing people dump ice water over themselves, notreally understanding what Iits all about. This video is so touching and has inspired me to look up what ALS is and learn what you and others are going through, and more importantly, to help :) A very memorable clip indeed xxx

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    God Bless You and the lives of all that this touches. Thank you ever so much for taking the time, and enduring so much pain during the filming of this..Prayers. If we can just donate in a small way, maybe we can save a life! .

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    Amyotrophic Lateral Sclerosis is on of many Neuro Muscular Diseases (ALS is also known as Lou Gherig's disease since he was the most famous person who developed it while playing baseball for The New York Yankees) . This & other diseases like it are being researched by MDA (The Muscular Dystrophy Association) which holds telethons every year on Labor Day in September. The Telethons have been reduced to a few hours since Jerry Lewis has passed away…they used to last a lot longer while he was alive (i guess support has dwindled). For anyone suffering from this or any of the other forms of neuro muscular diseases you have my sympathy and admirationin in dealing with your very difficult struggle.

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    He hit the nail on the head: not enough for the pharmaceutical companies to care about. We are having the same fight for Pediatric Cancer. (& I'm sure Huntingtons). It all comes down to how the Pharmaceutical companies can make a profit. :(

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    Thank you Keith for sharing this video. My brother and three cousins have died of this disease. It is more commonly known here as Motor Neurone Disease (ALS) It is the worst possible disease to be diagnosed with, as you can see in this excellent video. Age is not a factor. In order to find a cure it is vitally important that we share this video to raise awareness and much needed cash for clinical trials and research. Thanks to all who have taken the challenge. I am eternally grateful.

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    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  221. 239

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  222. 240

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  223. 241

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  224. 242

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  225. 243

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  226. 244

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  227. 245

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  228. 246

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

  229. 247

    I know two families who have lost loved ones to ALS. One at age 40, one a few years older. It's a horrible disease–to have your mind sharp and your body deteriorate. If there was something to be thankful for, one only lived 7 months after diagnosis, the other just a few weeks. I know that is very uncommon. I have a website for a product for which I have recently become a distributor. There are about 30 double-blind, placebo-controlled studies listed. I'm only giving you the one with my name so you can go read about it. It is http://smcintyre.juiceplus.com. Please just look–and if you are interested in finding out more, you can contact me thru the website. I don't even know your name–but I am right now lifting you and your family in prayer. This isn't even about trying to get business for myself. I just want to help if I can. God bless you, young man.

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    According to their website it says only 7% of what they raised last year went to research. ..Most of it went to pay their salaries….look it up its Public records!!!! Donate for nothing…just because it's a non profit organization doesn't mean they don't make a profit. ..it means they don't pay federal tax

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    According to their website it says only 7% of what they raised last year went to research. ..Most of it went to pay their salaries….look it up its Public records!!!! Donate for nothing…just because it's a non profit organization doesn't mean they don't make a profit. ..it means they don't pay federal tax

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    According to their website it says only 7% of what they raised last year went to research. ..Most of it went to pay their salaries….look it up its Public records!!!! Donate for nothing…just because it's a non profit organization doesn't mean they don't make a profit. ..it means they don't pay federal tax

  233. 251

    According to their website it says only 7% of what they raised last year went to research. ..Most of it went to pay their salaries….look it up its Public records!!!! Donate for nothing…just because it's a non profit organization doesn't mean they don't make a profit. ..it means they don't pay federal tax

  234. 252

    According to their website it says only 7% of what they raised last year went to research. ..Most of it went to pay their salaries….look it up its Public records!!!! Donate for nothing…just because it's a non profit organization doesn't mean they don't make a profit. ..it means they don't pay federal tax

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    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  274. 292

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  275. 293

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  276. 294

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  277. 295

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  278. 296

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  279. 297

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  280. 298

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  281. 299

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  282. 300

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

  283. 301

    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

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    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

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    Here's the thing… it IS wonderful that these videos are raising money and awareness. However, only a small percentage of the donations go to research UNLESS you, the donor, specify that you want your entire donation to go to research. Apparently, from one of the videos / postings that was on my wall, this can be done according to a local chapter board person. SO, we should not only challenge everyone to do this and to donate, BUT to challenge the organization to take ALL of the money that they have "made" during this campaign AND use it for research — no board meetings to discuss WHAT to do with all of this money …. RESEARCH!! It's a no brainer.

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    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  327. 345

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  328. 346

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  329. 347

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  330. 348

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  331. 349

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  332. 350

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  333. 351

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  334. 352

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  335. 353

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  336. 354

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  337. 355

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  338. 356

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  339. 357

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  340. 358

    This video… The feels… Dat ass thO!!! All kidding aside… I haven't officially been challenged BUT after watching this video I'll be donating regardless. You're strength is an inspiration. Keep on keeping on man the whole world is with you!

  341. 359

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  342. 360

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  343. 361

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  344. 362

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  345. 363

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  346. 364

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  347. 365

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  348. 366

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  349. 367

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  350. 368

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  351. 369

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  352. 370

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  353. 371

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  354. 372

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  355. 373

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  356. 374

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  357. 375

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  358. 376

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  359. 377

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  360. 378

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  361. 379

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

  362. 380

    It's da fricking drugs that this govt pumps into pregnant mums thru prenatal pills and all those effin shots your children are subjected to before they even reach 3 yrz old.. Shit is killing ya'll.. Never seen so many ailments and diseases until i came to this country.. Govt has been using its population as guinea pigs for many a years.. Infect ya then give you free or low cost meds.. Really?? IJS…. Feel very sorry that you or anyone has to basically become a prisoner in their own body…

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    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  402. 420

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  403. 421

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  404. 422

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  405. 423

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  406. 424

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  407. 425

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  408. 426

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  409. 427

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

  410. 428

    I'm praying for you and your family and I hope enough money is raised to help the causeand thanks for sharing your video I understand more what ALS is never really understood it till now your video I will be proud to share

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    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  435. 453

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  436. 454

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  437. 455

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  438. 456

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  439. 457

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  440. 458

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  441. 459

    Chris Jones No one made me an expert Chris. I simply offered a suggestion and was devoured by negative people such as yourself. How do you know that nutrition will not heal all disease? Instead of criticizing, people should be sympathetic and offer solutions. It might seem crazy to people but nutrition can cure a lot of things, maybe not this, but it couldn't hurt.

  442. 460

    The really sad thing is of that 22 million raised, half probably will go to the top 1 percent of the company doing the research, and another 45 percent will go to pay the inflated salaries of the doctors, and after that runs out research halts or slows down until they can find a band-aid, or market a drug that causes other diseases. I haven't seen a pill cure anything but balance sheets.

  443. 461

    The really sad thing is of that 22 million raised, half probably will go to the top 1 percent of the company doing the research, and another 45 percent will go to pay the inflated salaries of the doctors, and after that runs out research halts or slows down until they can find a band-aid, or market a drug that causes other diseases. I haven't seen a pill cure anything but balance sheets.

  444. 462

    The really sad thing is of that 22 million raised, half probably will go to the top 1 percent of the company doing the research, and another 45 percent will go to pay the inflated salaries of the doctors, and after that runs out research halts or slows down until they can find a band-aid, or market a drug that causes other diseases. I haven't seen a pill cure anything but balance sheets.

  445. 463

    The really sad thing is of that 22 million raised, half probably will go to the top 1 percent of the company doing the research, and another 45 percent will go to pay the inflated salaries of the doctors, and after that runs out research halts or slows down until they can find a band-aid, or market a drug that causes other diseases. I haven't seen a pill cure anything but balance sheets.

  446. 464

    The really sad thing is of that 22 million raised, half probably will go to the top 1 percent of the company doing the research, and another 45 percent will go to pay the inflated salaries of the doctors, and after that runs out research halts or slows down until they can find a band-aid, or market a drug that causes other diseases. I haven't seen a pill cure anything but balance sheets.

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    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  464. 482

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  465. 483

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  466. 484

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  467. 485

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  468. 486

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  469. 487

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

  470. 488

    Did you try juicing… I would consider going on an all plant diet learning what each vegetable and grit dies and coming up with a combination that can either slow the progression of stop it all together

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    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  481. 499

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  482. 500

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  483. 501

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  484. 502

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  485. 503

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  486. 504

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  487. 505

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  488. 506

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  489. 507

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

  490. 508

    To all my therapy friends, this is a great video. When WE walk in the room they are usually by now hospice and we are fine tuning the swallow, the communication board, their secretions. Wee never have the privilege of meeting and enjoying the family at the beginning. This takes us all to the beginning. I will send my $$$$$ today.

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    Just a thought. Approaching it in a holistic way. We all don't have the answers and I'm not here to be put down for a thought just as everybody else has. If people would just try and come together not only during a time of need but anytime.. You will see just how powerful together we are.. Rather than always arguing and thinking one point if view is better than the others..

  511. 529

    Just a thought. Approaching it in a holistic way. We all don't have the answers and I'm not here to be put down for a thought just as everybody else has. If people would just try and come together not only during a time of need but anytime.. You will see just how powerful together we are.. Rather than always arguing and thinking one point if view is better than the others..

  512. 530

    Just a thought. Approaching it in a holistic way. We all don't have the answers and I'm not here to be put down for a thought just as everybody else has. If people would just try and come together not only during a time of need but anytime.. You will see just how powerful together we are.. Rather than always arguing and thinking one point if view is better than the others..

  513. 531

    Julie I live with a horrible disease that no one does a thing for called Trigrminal Neuralgia but I live everyday praying and helping others hoping that they may have a better day or life than I do. I will pray for you because my dear Karma has a way of making you fall on your face, and I hope you don't reach rock bottom and honor is there to pick you up because the world is a cold place when you are sick. I hope you realize your words are hurtful and ill in you need help because yes we all gave things but try facing every day without a dr without a job with no one nothing and soon you will see that you need something and you will change your tune. Yes we all face things I have something that kills people too but I help others to help myself so get off your power trip and do something to become a better person and pray for yourself

  514. 532

    Oh ye have little faith. I know my god can heal all diseases and sickness. I'll be praying, that The Lord takes it away. If he can make a stage 4 cancer go down to 2 then to nothing and that person healed, I know he can heal.

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    Hi, maybe if you had watched the video, you would know that there is NO CURE for ALS. Everything you listed has some type of medication. The man in the video stated that this disease is not a money maker for the pharmaceutical companies because these people die within two to five years of diagnoses. You would have known that if you watched it. You're welcome.

  517. 535

    I agree with Brittany. I have seen juicing improve or cure several diseases. Closed minded people. Everyone will pop 20 prescription drugs with no problem but bottom line is if you build up your immune system, your body had a better chance at healing itself than if you pump it full of drugs. If you have no knowledge pic juicing and it benefits, educate yourself and try it before maKing a judgment. It works wonders and I have seen it first hand. Thank you Brittany for trying to help people. Dont let uneducated loud mouth know it alls bring you down. These type of negative people.Are what is wrong with our society today.

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    My father was diagnosed in December. It's been a steady downhill battle, but as with most patients, he has started to stagnate. Hopefully this will last for a bit before the hell that is ALS continues. When I first read your post Brit, I was definitely one of those that had some negative thoughts. However, once I calmed down a bit, I realized that nutrition does play a huge part in this disease. Juicing would probably not help, but those that are diagnosed do need to watch what they eat. Certain foods might hirt more than help. My dad has to eat over three times the amount of protein that normal people eat just to try to keep his muscle mass. Thank you for your help and I hope one day everything will turn out in such a way that nutrition will fix everything.

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    Hello, I am dismayed about the fact that there is such an illness. Certainly there are or will give even other ones which are up to now uninvestigated one. Nevertheless, I wish a lot of strength all affected persons and in particular the members endlessly. Greetings from Germany Eve

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    I lost a dear Aunt to this insidious, devastating disease in 8 months after she had a fall & was diagnosed. I wish you nothing but the best. You are amazing. May God bless you & keep you. You are in my prayers. I just want to give you an enormous hug xx

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    Never apologize for this. What you have done with this video was so greatly needed. We all need educated on this disease and I appreciate your candidness immensely! Wishing you the very best and remember, never give up hope <3

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    My gram fought a good fight but lost her life fighting ALS. It is a very scary disease and I no my gram hated having no control of her muscles and couldn't do anything for herself and was just like this guys mother she too ended up with feeding tubes cuz the muscles in her throat went and she could no longer chew or swallow food. It's a scary disease and I recommend everybody watch this video on how serious the disease really is. It's not about the stupid Ice water people r soaking themselves with and they should all have awareness of ALS.

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    My grandma passed away in 1991 bc of ALS. I was there everyday with her. It is very hard for anyone but for a 10 year old to sit there and watch their grandma fade away was horrible. She was diagnosed and 13 months later she passed. I miss her greatly every day. She was only 51 and missed her other kids get married and was not able to be there for 5 more grandkids and 5 great grandkids.

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    Worthy cause , stupid challenge y would anyone that has als want anyone else to know what thats like , and y would u poor ice cold water over ur head instead of reaching in ur pocket and just givin money ,really u dont go and get cancer so u know how a cancer paient feels, u know it sux and u do what u can to help. Just wait till someone has a heartattck it wont be so cool then

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    God Bless you!! I am one of the many who dont get frustrated by my news feed with all the ALS challenges. I think it is wonderful that this disease if finally starting to make people aware of its effects. I had a friend whose father passed away from ALS and it was heartbreaking to watch his life fade away from this disease..I say keep those posts coming!!

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    Just be careful who you donate to. The alsa.org uses embryonic stem cell research….. for my fellow pro lifers…. babies, think abortion donated embryos….. babies! Be diligent in finding sound research sites like gleason

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    Truly an amazing video and before being challenged, I didn't know to much about ALS. I did the challenge, I donated and I have been made aware…..And that my friends is what the "challenge" is all about! Thank you for sharing your video. Stay strong, you truly are an inspiration.

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    We are currently helpless, the power is controlled by the pharmaceutical companies and the White House. Donations are necessary but research is where the cure will be found. I encourage the Ice Challenge but a donation is critical. Center Valley Automotive will continue the fight around the holidays.

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    This video touch my heart I had cried I want to donate the100.00 instead of doing the ice challenge where do I send it ? I cried so much it reminded me of my mother they couldn't out rule what was wrong with her and when I seen this video that's how exactly the way she went I couldn't stop crying when I seen this video my heart goes out to all so please send me the info so I can donate the 100.00 thank you god bless you

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    I'm so great full for my health, my heart pains for those who suffer this disease. I have watched a loved one suffer this dreadful horrific disease. Count your blessings people!!!!

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    Need a bit of education here.
    Do we want people to take the challenge?
    Not take it and donate
    Take and donate
    Or Raise awareness and donate.
    Is taking the challenge then not profitable.
    I want to help but not sure the best way.

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    Very touched by this video and what you go thru. I am doing this challenge tonight I was challenged yesterday and I will be donating. I pray for a cure for you and all others affected by this. Prayers go out to you and ur family..stay strong and continue to fight

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    I am just like this guy it's unreal I'm 28 over the last ten I've lost all the family on my mums side no one left, I have no courage to do what this man is doing, I know if I had the money I'd travel to china to prolong my life as I'm not ready to die I suffer with cerrabella ataxia type unknown by uk doctors, I
    Have tears in my eyes as I want a chance in life I don't know how but please help. I'm alone n in bits xxxxx

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    A DEAR FRIEND OF MINE'S SON DIED OF ALS,…SHE LEARNED TOO LATE IN HIS ILLNESS THAT INJECTIONS OF PURE VITAMIN "C" WILL ARREST OR "RETARD" THE SPEED OF DABILITATION FROM THIS MONSTER DISEASE,…BUT WE LIVE IN CANADA, AND SHE COULD NOT FIND A DOCTOR WHO WOULD PROVIDE OR ADMINISTER THIS TREATMENT FOR HIM,..SO SHE GOT THE PURE VITAMIN C FROM AN (ANONYMOUS) DOCTOR IN THE U.S.A……TOO LATE

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    Beautiful, real, and touching but maybe ppl would rather help other ways but don't know where to send a check. …. that onto would be helpful if added to the end of the video… thanks for the awareness….Anthony, I lifted you in prayer, may you be lifted with them….

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    To know and watch someone over the four yrs or so it takes to die with ALS is about the most horrible thing ,I lost a good friend to this disease,she was always the life of the party,and to hear her sing was a pleasure,she was a wonderful mother,wife,friend,we can't have her back,but we can sure help others.her family and friends do a walk to raise money for ALS and it certainly helps to raise awareness and a little money.and for the gentleman who made this video,go and read about Phoenix tears ,"the Rick Simpson storey" and try this it might work.

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    God Bless You, and your family, I will send up prayers from here in England. my father-in-law had MND which is also affecting the motor neurones as is ALS. Heartbreakingly progressive.
    Much love xxx

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    This was the best and most heart-warming IBC video I've seen! We have witnessed what this terrifying disease has done to our incredibly gregarious and athletic friend. Miraculously, he has far outlived his life expectancy after his diagnosis. But it is not much of a life being that same smart, funny, outgoing, athletic man who is now trapped inside a dying shell. He was diagnosed as a very young man as well. We pray for you and your family, and for everyone facing ALS on any level that there is a cure in your lifetime.

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    Some parts of this video may be offensive to some, but you must see it all the way through to appreciate this young mans story efforts and suffering. This tells so much more than just a bucket of ice water ever could! Please watch it all! He needs our help and support!! I may not do the ice bucket, but I will certainly donate!

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