I have completed the ice bucket challenge and sent the challenge out to other people. I think it is a worthy cause that people need to be made aware of. I hope that people that are challenged either complete it or donate to the cause.
The ice bucket challenge is a good cause and I’ve seen people with this disease and it attacks the carrier. The people with the disease don’t have a chance but not many people know about this disease so the ice bucket challenge is a great way to spread awareness for the cause. Peter Frates accomplished many things he wanted to do and I think he deserved that happiness through being in his situation.
The ice bucket challenge has shown significance influence on social media which has brought up ALS and debates regarding how I would live if diagnosed. I believe that Peter has lived his life as full as possible with his current condition. I respect him for not letting his disease control his life.
If I were in Peter Frates shoes, I would like to think that I could accomplish as much as he did. By getting married and having a child, he didn’t let ALS stop him.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. healthcareherbalcentre .com I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
Great comments everyone! I took am astonished at what he has done with his time left on earth. It would have been easy to turn on ESPN and lie in bed. He chose other options, despite the lousy prognosis. It makes me wonder if I would be that courageous! Still waiting for the challenge!
This was really insightful, it not only connected to teens in a way of social media but it also threw in bits of information of the disease. It made me want to read to the end.
It’s amazing how just one person that wants to raise awareness for something. How he came up with the ice bucket challenge to raise money for ALS and now millions of dollars has been donated for ALS. I’ve seen so many people on social media doing the ice bucket challenge. Everybody has their own opinion to the ice bucket challenge, but the fact that ONE person decided to do this, and has raised so much money for it recently, is pretty cool.
this challenge is phenomonal and its amazing how someone did this and how this ice bucket challenge even became a thing. it even looks kind of fun to do way better then walking or jogging a mile.
I have particpated in the ALS ice bukcet challenge and to me it proved that leadership is a key role in society. I never knew that so many people looked up to me, until we actually sat down and talked about it. To be leader you should motivate yourself and push yourself past your comfort zome and past what you think you are capable of into the extremties.
The idea behind the ice bucket challenge is geinus and fun. i enjoyed watching everyone do this on Facebook. I feel like in this generation to raise money you have to make it fun.
I have done the ice bucket challenge and have also donated. The whole thing is just amazing. How one man can start a national phenomena. I never even knew ALS was a thing until I saw people on Facebook doing it. It is a great way to raise awareness and money.
I’ll be honest, I have been nominated to do the ice bucket challenge but never did it. I think it’s because it never really struck home about what the disease was. Now I’ve learned that in any awareness it’s extremely important to do your research on what the disease is and how it effects the lives of the people dealing with it and their family. Since I didn’t end up doing the ice bucket challenge I will be donating money to the cause because I now know how crucial that money is to finding a cure. Something I have taken from this is to be informed. Don’t be a person who just pushes things off to the side. Create personal ties to these people because with every moment they are struggling. Inform others on information like this. Give them details on where to donate money to. Be the change.
The ice bucket challenge is a good way to help people realize about the seriousness of this disease. Even though there is no treatment for this disease, it’s at least a good thing to help others prepare for the consequences of having this disease. It’s important to be aware of what will happen to you.
i think ALS ice bucket challenge is amazing . all these people out there helping raising money and putting time in to do the ice bucket challenge are great people .
Reading about ALS made me put into perspective my problems and realize life isn’t that hard, many people have real problems and we take our lives for granted. If you were diagnosed with ALS no doubt it would not be easy to come to the reality. The fact is no one has found a cure for ALS which is very saddening but enjoying your life to the full with loved ones is very rewarding. Even though Pete Frates and few others are diagnosed with ALS they do not let the disease be them. Someone or anyone can be diagnosed with ALS so wouldn’t you want to to live your life to the full. I believe everyone should spend as much time with loved ones friends and family don’t take any moment for granted.
I believe that this challenge is a good way to spread awareness, but it does kind of suck because we waste so much water. Also, many people used this as a trend and didn’t really donate any money, the thing that really mattered. The result in raising awareness was a great success raising over 100 million dollars for patients.
If I were to spread awareness for a disease, I would do it by challenging people to do something that involved fitness, or acrobatics
If i was diagnosed with this disease I would take the last days of my life to spread the knowledge of this disease and make people aware so they can donate money to help make a cure for others. I would also nominate my friends to do the ALS ice bucket challenge.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit http://www.treeoflifeherbalclinic.com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
I stopped the ALS medications due to severe side effects. My care provider Dr Miller introduced me to Kykuyu Health Clinic and their amazing ALS/MND treatment. The herbal treatment is a miracle. The ALS natural formula immensely helped my condition, it reversed my ALS. my slurred speech. And then the inability to eat without getting choked, breathing, and coughing. gradually disappeared. DON’T GIVE UP HOPE!!!
After my Lou Gehrig’s disease diagnosis, my primary care provider introduced me to Kycuyu Health Clinic and their ALS/MND Formula protocol, the herbal treatment has made a tremendous difference for me. My symptoms including numbness and muscle weakness all disappeared after the treatment plan!
With my amyotrophic lateral sclerosis (ALS), the first thing that happened almost 2 years ago now, was speaking as if I were drunk. I wasn’t. I initially did improve speech (articulating clearly but slow) but now I can no longer speak in an acceptable way. Then, a year later eating became problematic, I was biting my tongue and lips, and chewing became weak and less controlled. Soon after that some fingers started to fail me and things would drop out of my hands. Somewhere at that time bulbar ALS was diagnosed. The Rilutek (riluzole) did very little to help me. The medical team did even less. My decline was rapid and devastating.. We tried every shot available but nothing was working. There has been little if any progress in finding a reliable treatment, Our care provider introduced us to Kycuyu Health Clinic ALS/MND herbal treatment. The treatment is a miracle.i recovered significantly
Marcia, I am very sad this is happening to you. After reading so much about this disease, I don’t want anyone to have to go through it. It’s sad and cruel. I hope scientists can find a cure to save thousands of people from further suffering.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. treeoflifeherbalclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me ((Visit www.healthcareherbalcentre.com) ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit www.healthcareherbalcentre.com) I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
I have completed the ice bucket challenge and sent the challenge out to other people. I think it is a worthy cause that people need to be made aware of. I hope that people that are challenged either complete it or donate to the cause.
The ice bucket challenge is a good cause and I’ve seen people with this disease and it attacks the carrier. The people with the disease don’t have a chance but not many people know about this disease so the ice bucket challenge is a great way to spread awareness for the cause. Peter Frates accomplished many things he wanted to do and I think he deserved that happiness through being in his situation.
I believe that his wife is very brave especially when she’s bringing a new child into the world.
I would cry yo :'(
The ice bucket challenge has shown significance influence on social media which has brought up ALS and debates regarding how I would live if diagnosed.
I believe that Peter has lived his life as full as possible with his current condition. I respect him for not letting his disease control his life.
If I were in Peter Frates shoes, I would like to think that I could accomplish as much as he did. By getting married and having a child, he didn’t let ALS stop him.
I’ve never heard of the ALS challenge and I love how the Ice Bucket brought this to my awareness.
This is a vary inspirational story and to think that we complain about running a mile.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. healthcareherbalcentre .com I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
Great comments everyone! I took am astonished at what he has done with his time left on earth. It would have been easy to turn on ESPN and lie in bed. He chose other options, despite the lousy prognosis. It makes me wonder if I would be that courageous! Still waiting for the challenge!
This was really insightful, it not only connected to teens in a way of social media but it also threw in bits of information of the disease. It made me want to read to the end.
I feel that much leadership is shown here. He gave hope to the people who are down and needed to be picked back up.
It’s amazing how just one person that wants to raise awareness for something. How he came up with the ice bucket challenge to raise money for ALS and now millions of dollars has been donated for ALS. I’ve seen so many people on social media doing the ice bucket challenge. Everybody has their own opinion to the ice bucket challenge, but the fact that ONE person decided to do this, and has raised so much money for it recently, is pretty cool.
this challenge is phenomonal and its amazing how someone did this and how this ice bucket challenge even became a thing.
it even looks kind of fun to do
way better then walking or jogging a mile.
I have particpated in the ALS ice bukcet challenge and to me it proved that leadership is a key role in society. I never knew that so many people looked up to me, until we actually sat down and talked about it. To be leader you should motivate yourself and push yourself past your comfort zome and past what you think you are capable of into the extremties.
The idea behind the ice bucket challenge is geinus and fun. i enjoyed watching everyone do this on Facebook. I feel like in this generation to raise money you have to make it fun.
I have done the ice bucket challenge and have also donated. The whole thing is just amazing. How one man can start a national phenomena. I never even knew ALS was a thing until I saw people on Facebook doing it. It is a great way to raise awareness and money.
I’ll be honest, I have been nominated to do the ice bucket challenge but never did it. I think it’s because it never really struck home about what the disease was. Now I’ve learned that in any awareness it’s extremely important to do your research on what the disease is and how it effects the lives of the people dealing with it and their family. Since I didn’t end up doing the ice bucket challenge I will be donating money to the cause because I now know how crucial that money is to finding a cure. Something I have taken from this is to be informed. Don’t be a person who just pushes things off to the side. Create personal ties to these people because with every moment they are struggling. Inform others on information like this. Give them details on where to donate money to. Be the change.
The ice bucket challenge is a good way to help people realize about the seriousness of this disease. Even though there is no treatment for this disease, it’s at least a good thing to help others prepare for the consequences of having this disease. It’s important to be aware of what will happen to you.
I have taken the ice bucket challenge and really made me think about how those diagnosed feel 24/7.
i think ALS ice bucket challenge is amazing . all these people out there helping raising money and putting time in to do the ice bucket challenge are great people .
thay were saying that you should still donation money to charidey
i think he was very brave
Reading about ALS made me put into perspective my problems and realize life isn’t that hard, many people have real problems and we take our lives for granted. If you were diagnosed with ALS no doubt it would not be easy to come to the reality. The fact is no one has found a cure for ALS which is very saddening but enjoying your life to the full with loved ones is very rewarding. Even though Pete Frates and few others are diagnosed with ALS they do not let the disease be them. Someone or anyone can be diagnosed with ALS so wouldn’t you want to to live your life to the full. I believe everyone should spend as much time with loved ones friends and family don’t take any moment for granted.
I believe that this challenge is a good way to spread awareness, but it does kind of suck because we waste so much water. Also, many people used this as a trend and didn’t really donate any money, the thing that really mattered. The result in raising awareness was a great success raising over 100 million dollars for patients.
If I were to spread awareness for a disease, I would do it by challenging people to do something that involved fitness, or acrobatics
If i was diagnosed with this disease I would take the last days of my life to spread the knowledge of this disease and make people aware so they can donate money to help make a cure for others. I would also nominate my friends to do the ALS ice bucket challenge.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit http://www.treeoflifeherbalclinic.com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
I stopped the ALS medications due to severe side effects. My care provider Dr Miller introduced me to Kykuyu Health Clinic and their amazing ALS/MND treatment. The herbal treatment is a miracle. The ALS natural formula immensely helped my condition, it reversed my ALS. my slurred speech. And then the inability to eat without getting choked, breathing, and coughing. gradually disappeared. DON’T GIVE UP HOPE!!!
Nice try. Everyone, this is a South African scammer that stole the picture from an American couple. Piece of trash scammer!
After my Lou Gehrig’s disease diagnosis, my primary care provider introduced me to Kycuyu Health Clinic and their ALS/MND Formula protocol, the herbal treatment has made a tremendous difference for me. My symptoms including numbness and muscle weakness all disappeared after the treatment plan!
Google Kycuyu Health Clinic I had improved walking balance, increased appetite, muscle strength, just amazing how effective this treatment helped me
With my amyotrophic lateral sclerosis (ALS), the first thing that happened almost 2 years ago now, was speaking as if I were drunk. I wasn’t. I initially did improve speech (articulating clearly but slow) but now I can no longer speak in an acceptable way. Then, a year later eating became problematic, I was biting my tongue and lips, and chewing became weak and less controlled. Soon after that some fingers started to fail me and things would drop out of my hands. Somewhere at that time bulbar ALS was diagnosed. The Rilutek (riluzole) did very little to help me. The medical team did even less. My decline was rapid and devastating.. We tried every shot available but nothing was working. There has been little if any progress in finding a reliable treatment, Our care provider introduced us to Kycuyu Health Clinic ALS/MND herbal treatment. The treatment is a miracle.i recovered significantly
Author
Marcia, I am very sad this is happening to you. After reading so much about this disease, I don’t want anyone to have to go through it. It’s sad and cruel. I hope scientists can find a cure to save thousands of people from further suffering.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. treeoflifeherbalclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me ((Visit www.healthcareherbalcentre.com) ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit www.healthcareherbalcentre.com) I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]