I lost my father too back in 2012, he really suffered a lot, he carried the disease for almost 18 years. He was one of the people who last for such a long time here in Mexico and is good to see that there are people that donate and gives support to this disease, cause is hard to handle, it's very difficult, not only for the person that has ALS but to all the family and loved ones around that person, we didn't have much support at the begining, but after a while, when people started to pay attention to details and what the disease causes, only then, family and close friends helped us. By seeing you Pete reminds me to my father, reminds me the strenght he got until the very end. God Bless You! and all the people that is close to this kind of situation. My heart is with all of you.
You are amazing! Yes, if you build it...they will come! Look at what your story has inspired in the Ice Bucket Challenge - together we can rewrite YOUR story! Thanks for sharing. Peace
Maybe a cure won't be found in time to reverse what's happening to Pete but what a difference you will make. To you, your wife, your brother and all of your family - well done on starting the #icebucketchallenge and raising so much money for ALS research. The awareness you have raised is going to make a difference. Amazing what you've done.
Dear Pete, I only want to thank you for the feelings that you are inspired in al the people, for the love that you share with all of us, I will always pray for you and your loving familiy. Remember that the miracles does exist, and you are part of it. God bless you.
God Bless you Pete!! Your attitude and courage are inspiration to a lot of people. I lost my father to ALS back in 2007 and he was one of the lucky ones who didn't have to suffer that long. You and your family will be in my prayers. Let's change the ending forever......
Pete and Julie- your story is quite inspirational. My whole family participated in the "ice bucket challenge" and that was how I learned of your story. Also we lived in Beverly for about10 years and my neice went to school with you. I can see that you are remaining strong which I am sure is not easy.
I've definitely heard of ALS, and am somewhat familiar with what it entails, but seeing someone my age, someone I actually knew and went to school with struggling with it is a huge eye opener. This was an amazing video.
Who the hell are the 2 maggots that had the audacity to vote this down? I mean, honestly, how can you? What didn't you like about it? The fact that it hits you right in your chest? Or how it turned an ordinary guy into a warrior? Either way I hope you never have a loved one affected by this horrible disease.
I am convinced that there are people who quite literally have nothing better to do with their time than to vote down every video they come across. I wish those people would either get a job or stop going on the internet.
They're called trolls. They spread negativity throughout the world with no other intention than to mess with good people. Their existence is pathetic and the best way to deal with them is to ignore them. "Don't feed the troll"
Custom Made Dude "ice bucket challenge" or "race for the cure" its the calling of folks coming together to help a cause. It may seem like a "money" thing but volunteering won't help this disease. If it doesn't help in time for Peter Frates, it may help for his grandchildren. Have faith, I mean God didn't say all your 10% needed to go to your church. Help out your fellow man is all its about. For the negative votes, no reason for it. Those folks are sad individuals and truly shouldn't affect anyone with their negative disease.
Custom Made My son died from ALS at 32. Don't tell me you have a cure and it's not time to give it! Do you really think it won't cost you any money to get "you cure" out there?
Pete and Julie, You are so articulate and your story is tremendously important for all to hear and learn. You are both so beautiful, so bright and so full of light. Your journey is very difficult but I believe the outcome of this terrible illness will be re-written. I know the system quite well (as I have a 42 year old son who suffers from Schizophrenia, a disabling brain disorder) I'm not an attorney...just a mother who is willing to offer answers in regards to Medicare and the frustrating bureaucracy. Julie, I requested you as a friend on FB...I'm a friend of Shane Sabine. Its an honor to hear your story from across the miles! May God watch over you and bless you, always! ~Gloria
So inspirational. Thank you for sharing and educating us. I am wishing you, Pete, the continued strength to meet the challenges you are facing. Your courage inspires me.
Too late for my brother and many others but HOPE for the future. Great job and I wish you and your family everything good. Keep living. Your life and your message are so incredibly important.
i feel for this young guy it brought a lump to my throat and tears in my eyes he is very courage's i done the icebucket challeng and would do it again god be with u pete x
This is the most inspiring video on #TH-cam today! This is the man who inspired millions to do the #alsicebucketchallenge to raise awareness and finding a cure for this diseases that has no origin or causes on where Lou Gehrig disease came from. I hope the charity money will help find the cure. Make this charity happen the battle against #ALS starts now! Greetings for the Philippines and stay strong #Pete!
Pete, I think you and your family are amazing in what you've all accomplished since your diagnosis. Always been a great guy man. All my best Pete, corey harrison :) lil blast from the past lol, no one forgets Pete Frates ;)
God bless you and your family! It brought tears into my eyes and at same time inspired. Please continue to fight with your disease you have lots of love from the people around you.
Pete you are a very strong and courageous person. I think the more exposure ALS gets the more people will do the research find the genetics that cause this disease and find a cure so you can watch your daughter grow up. P.S. I pray for you every day and that a cure is found in 2015.
se que es una enfermedad muy dificil actualmente lo vivo con mi tia tambien la sufre hay que tener muchas fuerzas y ganas de vivir es lo unico q detiene el avance violento de esta enfermedad que todavia no tiene cura
Querido valiente...Sorry...I no spike inglis...te escribo desde España...y conozco bien todo lo que dices y cuentas y sientes...Mi padre fue tan valiente como tú...Suerte...Congratuletions por tu fuerza...Bay!!!!
Kamal Abdelbaki they may hit the unlike button because they feel bad for him. Most likely if you think about it. I hesitated to hit the like button. Imo
I feel for this man. My former boss died from ALS a few years ago. It's a horrible disease. However I don't understand why he and his wife would conceive a child knowing full well that this disease is passed down genetically. That seems extremely selfish and foolish.
He has a wonderful brother,What selfless act.Quit his job to help take care of his brother.
Rip brother 🙏🏿 Heaven just received another angel. You will be missed and thank you for the awareness of others.
RIP Pete Frates, a true hero.
RIP.. A true hero that never wore a cape. Thank you for what you have inspired. Rest easy
Absolutely! Thanks for watching!
I lost my father too back in 2012, he really suffered a lot, he carried the disease for almost 18 years. He was one of the people who last for such a long time here in Mexico and is good to see that there are people that donate and gives support to this disease, cause is hard to handle, it's very difficult, not only for the person that has ALS but to all the family and loved ones around that person, we didn't have much support at the begining, but after a while, when people started to pay attention to details and what the disease causes, only then, family and close friends helped us. By seeing you Pete reminds me to my father, reminds me the strenght he got until the very end. God Bless You! and all the people that is close to this kind of situation. My heart is with all of you.
Damn. 18 years. Your father was a fighter.
Everyone who has taken the bucket challenge should listen to this story of Pete Frates
Rest in peace, young man. Thank you for your efforts in getting the word out about ALS.
My grandpa is suffering from this disease, he used to be a very active man, now he cant walk anymore. I wouldn't wish this disease to my worst enemy
Wow I pray that there is a cure for this disease. And why would anyone give this a thumbs down?
RIP my man, you fought the good fight.
God bless you, Pete, & all those suffering from this horrible disease!
Hes still very intelligent and can communicate extremely well
ALS does not affect your IQ
How could anyone dislike this video???
Rest in peace Pete.
You are amazing! Yes, if you build it...they will come! Look at what your story has inspired in the Ice Bucket Challenge - together we can rewrite YOUR story! Thanks for sharing. Peace
Maybe a cure won't be found in time to reverse what's happening to Pete but what a difference you will make. To you, your wife, your brother and all of your family - well done on starting the #icebucketchallenge and raising so much money for ALS research. The awareness you have raised is going to make a difference. Amazing what you've done.
Dear Pete, I only want to thank you for the feelings that you are inspired in al the people, for the love that you share with all of us, I will always pray for you and your loving familiy. Remember that the miracles does exist, and you are part of it. God bless you.
God Bless you Pete!! Your attitude and courage are inspiration to a lot of people. I lost my father to ALS back in 2007 and he was one of the lucky ones who didn't have to suffer that long. You and your family will be in my prayers. Let's change the ending forever......
Rest In Peace buddy, I hope one day I’ll have the honor of having a catch with you up there, and you telling me all about that Fenway game
You are a much better human and man than I will ever be, God Bless.
Wow... What an inspiration. Thank you for your boldness. God Bless You..
Pete and Julie- your story is quite inspirational. My whole family participated in the "ice bucket challenge" and that was how I learned of your story. Also we lived in Beverly for about10 years and my neice went to school with you. I can see that you are remaining strong which I am sure is not easy.
I've definitely heard of ALS, and am somewhat familiar with what it entails, but seeing someone my age, someone I actually knew and went to school with struggling with it is a huge eye opener. This was an amazing video.
Rest In Peace ❤️❤️
Bless his heart
Who the hell are the 2 maggots that had the audacity to vote this down? I mean, honestly, how can you? What didn't you like about it? The fact that it hits you right in your chest? Or how it turned an ordinary guy into a warrior? Either way I hope you never have a loved one affected by this horrible disease.
I am convinced that there are people who quite literally have nothing better to do with their time than to vote down every video they come across. I wish those people would either get a job or stop going on the internet.
They're called trolls. They spread negativity throughout the world with no other intention than to mess with good people. Their existence is pathetic and the best way to deal with them is to ignore them. "Don't feed the troll"
Custom Made
Dude "ice bucket challenge" or "race for the cure" its the calling of folks coming together to help a cause. It may seem like a "money" thing but volunteering won't help this disease. If it doesn't help in time for Peter Frates, it may help for his grandchildren. Have faith, I mean God didn't say all your 10% needed to go to your church. Help out your fellow man is all its about. For the negative votes, no reason for it. Those folks are sad individuals and truly shouldn't affect anyone with their negative disease.
Custom Made My son died from ALS at 32. Don't tell me you have a cure and it's not time to give it! Do you really think it won't cost you any money to get "you cure" out there?
You know how hard mentally and physically it is to do this video! Gosh dang people in this world
Pete and Julie,
You are so articulate and your story is tremendously important for all to hear and learn.
You are both so beautiful, so bright and so full of light. Your journey is very difficult but I believe the outcome of this terrible illness will be re-written.
I know the system quite well (as I have a 42 year old son who suffers from Schizophrenia, a disabling brain disorder) I'm not an attorney...just a mother who is willing to offer answers in regards to Medicare and the frustrating bureaucracy.
Julie, I requested you as a friend on FB...I'm a friend of Shane Sabine.
Its an honor to hear your story from across the miles!
May God watch over you and bless you, always!
~Gloria
So inspirational. Thank you for sharing and educating us. I am wishing you, Pete, the continued strength to meet the challenges you are facing. Your courage inspires me.
God bless you, and give you peace.
Too late for my brother and many others but HOPE for the future. Great job and I wish you and your family everything good. Keep living. Your life and your message are so incredibly important.
RIP Pete. 🙏🙏🙏
i feel for this young guy it brought a lump to my throat and tears in my eyes he is very courage's i done the icebucket challeng and would do it again god be with u pete x
This is the most inspiring video on #TH-cam today! This is the man who inspired millions to do the #alsicebucketchallenge to raise awareness and finding a cure for this diseases that has no origin or causes on where Lou Gehrig disease came from. I hope the charity money will help find the cure. Make this charity happen the battle against #ALS starts now! Greetings for the Philippines and stay strong #Pete!
Pete, I think you and your family are amazing in what you've all accomplished since your diagnosis. Always been a great guy man. All my best Pete, corey harrison :) lil blast from the past lol, no one forgets Pete Frates ;)
RIP Pete
Rest in peace
God bless you and your family!
It brought tears into my eyes and at same time inspired. Please continue to fight with your disease you have lots of love from the people around you.
Thanks for bringing this disease to my attention. Hang in there, Pete.
Pete you are a very strong and courageous person. I think the more exposure ALS gets the more people will do the research find the genetics that cause this disease and find a cure so you can watch your daughter grow up.
P.S. I pray for you every day and that a cure is found in 2015.
R.I.P Pete🙏🙏
se que es una enfermedad muy dificil actualmente lo vivo con mi tia tambien la sufre
hay que tener muchas fuerzas y ganas de vivir es lo unico q detiene el avance violento
de esta enfermedad que todavia no tiene cura
Querido valiente...Sorry...I no spike inglis...te escribo desde España...y conozco bien todo lo que dices y cuentas y sientes...Mi padre fue tan valiente como tú...Suerte...Congratuletions por tu fuerza...Bay!!!!
Brakes my heart this disease is mortal evil wish i can make a cured is not fair all the lives we have lost. ....
Amen!
keep fighting pete
Amazing. Speechless.
My brother in law was just diagnosed with ALS. I feel horrible!
How long can someone live with ALS? I hope he lives as long as he wishes to:-) bless him everyone!
The true horror of the disease. Your body deteriorating and your mind gets sharper. A very cruel disease. I’m so sorry.
R.I.P
RIP
Cried
#PETESTRONG #ALS GOD BLESS YOU PETE MAY ALL PRAYERS BE WITH YOU
che Dio ti benedica grande uomo.
How come cholinesterase inhibitors are not used for ALS ? If is helps in myesthenia gravis with muscle weakness shouldn't it also help in ALS?
TheLuckyOne there have been trials and it was unfortunately deemed to have no therapeutic effect.
What if he and others could be healed in 2-3 months? It's sad that people suffer when there is a cure..................
Do you think if I offered to pull him in an iron man hed accept?
💙💙💙
Pete...Looking at you I see our son Jon...wishing you more good days than tough ones...Mary Ann, Jon's mom
waronals.org
Who are the people who are unliking this??? You are the worst species in the universe
Kamal Abdelbaki they may hit the unlike button because they feel bad for him. Most likely if you think about it. I hesitated to hit the like button. Imo
:'(
I feel for this man. My former boss died from ALS a few years ago. It's a horrible disease.
However I don't understand why he and his wife would conceive a child knowing full well that this disease is passed down genetically. That seems extremely selfish and foolish.
You horrible, awful, terrible person. Who the FUCK are you to judge these people.
Pete's ALS was sporadic, meaning as far as science can tell, it's not genetic.
12 Evil human being proof of their existence on earth...
whats wrong with his voice