I was the same Tony as i am like Burrow i have this dreadful illness and i am lucky i am able to have called Rob as my patron in his short life may he RIP now and thy ever more
Every single person in this video are absolute legends! So sad, Rob is a great, his family are amazing too. Wow, so sad, and inspirational at the same time. If that even make sense. And Sinfield, what a machine he has been !!
Just watched the Amazing Rob Burrows documentary and 😢emotional is not the word. This man is a true legend of Rugby league. I’m from Perth Australia and a huge West Tigers fan. The NRL family have raised loads of money for MND and I hope more people if possible can donate to this charity. From all the NRL family we send our love to the whole Burrows family and our hearts are with you ..!
Lost dad with this recently and only had it for a few months. Wouldn't wish this on anyone. Total respect for Rob and his family and the way they're fighting it. Keep going Rob..... ynwa
The bravery shown by Rob, his family and his friends have shown in producing this film to raise awareness of and garner support for those suffering from MND is so admirable. What lovely children he has also to carry on his legacy. He will be remembered not only as a great sportsman but as a great man. I can't imagine why anyone would have disliked this video
Lost my father to this disease 4 years ago - his death I could handle - watching the disease take a grip I couldn’t. When he eventually died as horrible as it sounds it was a huge relief knowing he wasn’t suffering no more. As harsh as it seems Rob has the hardest days to come - it broke my heart knowing what lies ahead for him and his family
I couldn’t stop crying as I watched. Rob you’re a strong man and Lindsey, love you for sticking with him and still loving him through this cruel disease.
What a legend on the field and off it. You left an incredible legacy and touched the lives of so many. Thanks for all you have done to bring a spotlight to this cruel disease. Rest in peace Champion
I dont mean to cause any offence to anybody but watching this makes me appreciate loosing my Dad when I did. On the 12th of February this year my dad was diagnosed with MND, on the 14th of February he suffered an MND related seizure, never regained consciousness and died on 16th of February. Now I dont want to sound disrespectful when I say this but after watching this and seeing what it has done to Rob in such a short space of time makes me feel a little relieved that I never had to see my Dad deteriorate to such a state. As I say I don't mean to cause any offence to anybody nor do I mean to be disrespectful. Here's hoping that one day soon we can find a cure for this horrible disease🤞🏼
Steve, you spoke from your heart, rob has stayed with us longer than my wfe, diagnose in July 2018 with MND, in the 6 months we had left together, there was no time for anything, my head was buzzing at 90mph, i looked after my wife as best as i could, changes everyday, harder to eat, losing her voice, losing her strengh until i had to pick her up to get her into a wheel chair, to all those people commenting good or bad, they haven't a clue what its like for the sufferer or family, my wife passed away in her sleep 6 months from diagnoses.
RIP Rob. You shone through with your amazing personality and with Lindsay and the whole family. I think I have watched this programme many times. Night God Bless ❤xx
This film shows Rob's true greatness even in such heart-breaking circumstances. I hope they find a cure as soon as possible because this disease is beyond cruel. Love to all his family x
What Dr Jung says at 9:15 is exactly my reason for going into medicine. I'm a second year medical student now and feel so privileged to be entering this profession
Y5 medical student. I'm with you. We do it for others. And thanks for watching the documentary. My father has MND and I wish more people knew about it and how devastating it can be
@@samyakjain727 I’m sorry to hear that, that must be very hard for you and your family. I agree that too few people know enough about MMD and it’s impact on people’s lives. Good luck with your final (?) year 🙂
@@abbyhuntley3171 Physiology at Bristol. Don't do it. Such a hard year and I didn't gain much long-term. Mate in the year below is with the same struggle currently. Enjoyed living out in a new city though
I speak for every rugby league fan out there. We have lost one of the greatest ever players to play rugby league. He fought on the pitch and he fought till the end and never give up. If we could all be like this man life would be a better place. My thoughts go out to all his family. Rip 🙏 Rob. Warrington.
Rob transcended Rugby. I’m a football man but it matters not a jot what sport he played, he touched everyone in the country. He was an incredibly special and inspirational man. I have two young kids myself and just cannot bare to think about what Rob had to face. 10 times the man I am.
This was truly incredible my heart goes out to you and family rob and to every single person and. There families fighting this truly awful disease stay strong everyone x
I don't know what to say really. I cannot comprehend the courage, selflessness, and love that Rob and his family have. I played rugby league for a year as a scrawny teenager, but couldn't take the pain and head knocks so gave up. Rob, who is much smaller than me, not only played for many years but did so magnificently at the highest level. Now, he is taking on, while putting himself aside for his love of others, the cruellest of diseases. An inspiration to all. 💪💙💛
Never been the biggest Rugby League fan and used to think why do these doughballs at Leeds call Sinfield, Sir Kev? He's been unreal. What an absolute colossal of a man and leader.
I'm 60 n this story has got me gripped it's soso sad to see a lovely decent man with lovely wife n kids n loving parents with this illness but also on other hand it's inspiring how rob n others are trying to help others it's certainly helped me see life in a different light + when I'm out running n feel tired I think of rob n his truly great friend Kevin sinfield n I keep going god bless all these lovely genuine decent people
“A heart is not judged by how much you love; but by how much you are loved by others”. L. Frank Baum, The Wonderful Wizard of Oz. My word this man was loved. He was clearly a very, very special person. RIP Rob.
A teacher of mine died of mnd some years ago. It was painful to visit him. To pick him off the floor when all he wanted to do was go over a style to walk in the countryside. For Rob .... To be loved and to have family & friends around him at this time, is the greatest gift of all. It is an honour to stand by anyone who has a journey like this to endure .. to help & to watch! Just to be there!
Have only watch Rob Burrow documentary now oh sad it is but what an incredible man family and friends he has my husband is very sick with a lot of illness but you would ask at times why but my god the day you get up is a good day terrible in 2024 and not a significant indication of any break through yet please god in the coming years somewhere the will find it 🙏🙏🙏
Wigan fan in peace...... Just watching this again now. I only booed you because you were a pain. You kept scoring and creating tries. A real great in my eyes. Keep scoring tries against the stronger team and running through the biggest guys.
Anyone arguing the toss about whether they should comply with social distancing rules and wear masks should just think about people like Rob, who have missed out on important therapy needed to help them live the best lives possible
My great uncle died of MND. He was a much older man at that time and his children were grown up with children of their own. It is so awful to see this happening to such a young man, how devastating - we must find a cure for this disease. Or at least some treatment to slow or halt its progression so people can enjoy more time.
My late husbands twin sister died of this age 60. It took many years to be diagnosed . She was 60 . Also very brave as was Rob and the other brave people ❤
As a life long St Helens supporter I watched rob a few times playing against us , and wished he wasn’t going to play because he was that good , that all I can say a one off.
From Leeds, live abroad, just watched it now, makes me so pissed off, at the end the BBC taking the credit.... Billions spent on the "CONVID" fucking discrace.... God bless YOU Rob and family.
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I was in tears all way through, but when it got 7.25 I just burst.
I was the same Tony as i am like Burrow i have this dreadful illness and i am lucky i am able to have called Rob as my patron in his short life may he RIP now and thy ever more
Every single person in this video are absolute legends! So sad, Rob is a great, his family are amazing too. Wow, so sad, and inspirational at the same time. If that even make sense. And Sinfield, what a machine he has been !!
Rob u are amazing and so are your family keep going u are an inspiration
Just watched the Amazing Rob Burrows documentary and 😢emotional is not the word. This man is a true legend of Rugby league. I’m from Perth Australia and a huge West Tigers fan. The NRL family have raised loads of money for MND and I hope more people if possible can donate to this charity.
From all the NRL family we send our love to the whole Burrows family and our hearts are with you ..!
I knew this guy when i stuied in leeds，hes a legend，respect
This really choked me up when watching... stay strong Rob
I've got too many reasons to live and i'm not giving in til my last breath''. That's the spirit Rob
Lindsay and Rob this is true love I respect you both unbelievable team 👍👊🏼
Oh my god…I cried so much watching this. INSPIRATIONAL.
Lost dad with this recently and only had it for a few months. Wouldn't wish this on anyone. Total respect for Rob and his family and the way they're fighting it. Keep going Rob..... ynwa
His kids are amazing with him. What a lovely family ❤️
What a great Man Rob is and the support from his wife, children and parents is incredible - Bless you all
Legend as a player, even greater as a man!!!!!
Little man, big ❤!! not a dry eye when I watched this, Keep fighting Rob!
The bravery shown by Rob, his family and his friends have shown in producing this film to raise awareness of and garner support for those suffering from MND is so admirable. What lovely children he has also to carry on his legacy. He will be remembered not only as a great sportsman but as a great man. I can't imagine why anyone would have disliked this video
Lost my father to this disease 4 years ago - his death I could handle - watching the disease take a grip I couldn’t. When he eventually died as horrible as it sounds it was a huge relief knowing he wasn’t suffering no more. As harsh as it seems Rob has the hardest days to come - it broke my heart knowing what lies ahead for him and his family
I’m very sorry for your loss 🕊
Same I lost my father 4 years ago aged 59, this is terrible disease , hope soon medicine find the cure🙏
An ex work colleague of mine lost his Mother to MND, absolutely heartbreaking to see people deteriorate so quickly.
I couldn’t stop crying as I watched. Rob you’re a strong man and Lindsey, love you for sticking with him and still loving him through this cruel disease.
God bless him tears in my eyes watching this what an amazing man
THIS…..Documentary! I cried more than I have to anything in my life…! I really felt this.
In bits watching this. What a man, what a family!
What a legend on the field and off it. You left an incredible legacy and touched the lives of so many. Thanks for all you have done to bring a spotlight to this cruel disease. Rest in peace Champion
One of the most real life documentaries I’ve ever watched
Rest easy rob, you’ve inspired so many people at how brave you’ve been, what a legacy you’ve left behind for your kids and family ❤
Absolute Legend. A lionhearted warrior Feel so sorry for him and family. From a Bulls fan. Good luck mate
Big strong heart Rob
God bless u and your family and friends .
Tears in the morning watching this 😢😢
Rob Burrow, you're a legend. 🙏🏾❤
I dont mean to cause any offence to anybody but watching this makes me appreciate loosing my Dad when I did. On the 12th of February this year my dad was diagnosed with MND, on the 14th of February he suffered an MND related seizure, never regained consciousness and died on 16th of February. Now I dont want to sound disrespectful when I say this but after watching this and seeing what it has done to Rob in such a short space of time makes me feel a little relieved that I never had to see my Dad deteriorate to such a state. As I say I don't mean to cause any offence to anybody nor do I mean to be disrespectful. Here's hoping that one day soon we can find a cure for this horrible disease🤞🏼
Sorry for your loss.
You could have kept this in your head ....it is utterly inappropriate shame on you
I'm so sorry for you're loss, my sister has just been diagnosed and I'm not really sure how to feel about it
@@drewlaventure9735 Show some empathy.
Steve, you spoke from your heart, rob has stayed with us longer than my wfe, diagnose in July 2018 with MND, in the 6 months we had left together, there was no time for anything, my head was buzzing at 90mph, i looked after my wife as best as i could, changes everyday, harder to eat, losing her voice, losing her strengh until i had to pick her up to get her into a wheel chair, to all those people commenting good or bad, they haven't a clue what its like for the sufferer or family, my wife passed away in her sleep 6 months from diagnoses.
Sally you are a true darling thanks so much, God bless you, xxx
Keep fighting rob the whole of the rugby community are behind you
I came here after the passing of Rob please rest in peace xx
Me too ..godblesz rob
Same
RIP Rob. You shone through with your amazing personality and with Lindsay and the whole family. I think I have watched this programme many times. Night God Bless ❤xx
RIP Rob, what an incredible person both in sport and determination through your illness. Rugby league has lost one of its greats ❤
Respect to Sally Nugent as well. She seems like a really sincere, lovely person. I'm sure Rob appreciated her kindness.
Well said ,she shows so much respect and love. Lovely woman
She’s so lovely im robs niece and she offered to buy us all an ice cream x
What an inspirational family. They’re all a credit to each other. Wishing for a miracle and hoping for peaceful days together if there is no cure!
Awestruck at the dignity and bravery of the Burrows family and their friends.
Incredibly strong man.
This film shows Rob's true greatness even in such heart-breaking circumstances. I hope they find a cure as soon as possible because this disease is beyond cruel. Love to all his family x
You are an exceptional guy. Every strength to you Rob. Best wishes to you and your family.👍
Please let me meet whoever thumbed this down. Rob you and everyone going through MND is a hero in my view. Good luck pal
Thank you for caring
What Dr Jung says at 9:15 is exactly my reason for going into medicine. I'm a second year medical student now and feel so privileged to be entering this profession
Y5 medical student. I'm with you. We do it for others. And thanks for watching the documentary. My father has MND and I wish more people knew about it and how devastating it can be
@@samyakjain727 I’m sorry to hear that, that must be very hard for you and your family. I agree that too few people know enough about MMD and it’s impact on people’s lives. Good luck with your final (?) year 🙂
@@abbyhuntley3171 Thank you. Y5 out of 6 (I intercalated). Current at Southampton. Where are you studying?
@@samyakjain727 oh cool, what did you intercalated in? I’m at Newcastle 🙂
@@abbyhuntley3171 Physiology at Bristol. Don't do it. Such a hard year and I didn't gain much long-term. Mate in the year below is with the same struggle currently. Enjoyed living out in a new city though
I speak for every rugby league fan out there. We have lost one of the greatest ever players to play rugby league. He fought on the pitch and he fought till the end and never give up. If we could all be like this man life would be a better place. My thoughts go out to all his family. Rip 🙏 Rob. Warrington.
So true xxx
Rob transcended Rugby. I’m a football man but it matters not a jot what sport he played, he touched everyone in the country. He was an incredibly special and inspirational man. I have two young kids myself and just cannot bare to think about what Rob had to face.
10 times the man I am.
I like this guy😢😢❤❤❤/Kevin Sinfield Respect
This was truly incredible my heart goes out to you and family rob and to every single person and. There families fighting this truly awful disease stay strong everyone x
Thank you for posting this. With living abroad this is the first time I’ve been able to watch it. Keep fighting Rob you’re an inspiration to us all ❤️
"My MIND IS SO STRONG AND POSITIVE!!!"
Feel so sorry for Rob nobody should go though this keep fighting Rob we are all behind you from a hull fc fan
What an inspirational man , and such a wonderful family , I certainly make a contribution to mind foundation , loved watching you play wee man
I don't know what to say really. I cannot comprehend the courage, selflessness, and love that Rob and his family have. I played rugby league for a year as a scrawny teenager, but couldn't take the pain and head knocks so gave up. Rob, who is much smaller than me, not only played for many years but did so magnificently at the highest level. Now, he is taking on, while putting himself aside for his love of others, the cruellest of diseases. An inspiration to all. 💪💙💛
Never been the biggest Rugby League fan and used to think why do these doughballs at Leeds call Sinfield, Sir Kev? He's been unreal. What an absolute colossal of a man and leader.
Absolutely brutal watch this 😢
Strength, love and sending the light to Rob and his wife and children and extended family ❤🙌🏽🙏🏽🙏🏽
Keep fighting rob you are a legend.
I'm 60 n this story has got me gripped it's soso sad to see a lovely decent man with lovely wife n kids n loving parents with this illness but also on other hand it's inspiring how rob n others are trying to help others it's certainly helped me see life in a different light + when I'm out running n feel tired I think of rob n his truly great friend Kevin sinfield n I keep going god bless all these lovely genuine decent people
Half way through his book which I had for Christmas.so inspiring.so positive.makes me want to do something to help. Top bloke
“A heart is not judged by how much you love; but by how much you are loved by others”. L. Frank Baum, The Wonderful Wizard of Oz. My word this man was loved. He was clearly a very, very special person. RIP Rob.
A teacher of mine died of mnd some years ago. It was painful to visit him. To pick him off the floor when all he wanted to do was go over a style to walk in the countryside. For Rob .... To be loved and to have family & friends around him at this time, is the greatest gift of all. It is an honour to stand by anyone who has a journey like this to endure .. to help & to watch! Just to be there!
Good luck Rob , keep fighting.
So sad, I've known 2 people to pass from this disease, it's so horrible!
Keep fighting Rob.
Keep going strong Rob, everyone is with you. 💪👍🏉🏉
I am so sorry and you are an inspiration. Xx
You sir are a legend God bless
proud to say he played for my team growing up as a kid
Rob Burrow what a man!
Have only watch Rob Burrow documentary now oh sad it is but what an incredible man family and friends he has my husband is very sick with a lot of illness but you would ask at times why but my god the day you get up is a good day terrible in 2024 and not a significant indication of any break through yet please god in the coming years somewhere the will find it 🙏🙏🙏
Wigan fan in peace...... Just watching this again now. I only booed you because you were a pain. You kept scoring and creating tries. A real great in my eyes. Keep scoring tries against the stronger team and running through the biggest guys.
Anyone arguing the toss about whether they should comply with social distancing rules and wear masks should just think about people like Rob, who have missed out on important therapy needed to help them live the best lives possible
My great uncle died of MND. He was a much older man at that time and his children were grown up with children of their own. It is so awful to see this happening to such a young man, how devastating - we must find a cure for this disease. Or at least some treatment to slow or halt its progression so people can enjoy more time.
So sad what a fantastic man and lovely family ❤️😢
Keep fighting. Love you Rob❤️
My late husbands twin sister died of this age 60. It took many years to be diagnosed . She was 60 . Also very brave as was Rob and the other brave people ❤
Rest in peace, legend.
It’s not just athletes that get mnd. It strikes all folks from every walk of life.
Teary eyes here in Papua New Guinea... RIP Champ...😢😢😢
As a life long St Helens supporter I watched rob a few times playing against us , and wished he wasn’t going to play because he was that good , that all I can say a one off.
so sad made me cry
Respect rob he is a legend he got my respect ✊
Lovely man keep strong rob xx
Keep fighting Rob
So sad. Wonderful rugby player and human being. Hert breaking for his wife and children!
Such a cruel fate. RIP 🙏
Such a shame,gutted for Rob and all his family and friends. So sad.
Fight on Rob lad
fev rovers.. 5 mins walk from my house. hope your still doing good., best wishes
Я рос на твоих играх, Роб, и вырос в фаната регбилиг. Покойся с миром, дорогой друг.
Rugby doesn’t cause MND. Everyone, anyone can get it. Anytime. You. Me. It is a lot more common than you think. Pray for a cure. Soon.
Would not wish this disease on my worst enemy.
From Leeds, live abroad, just watched it now, makes me so pissed off, at the end the BBC taking the credit.... Billions spent on the "CONVID" fucking discrace.... God bless YOU Rob and family.
Well Kev & Burrow family really grateful to bbc, he don’t need bad vibes.
Rip in Rob
🙏❤️🙏
Sorry Rob ..... best of luck mate.
Sometimes the BBC do good things ..... very rarely.
Nuff said
What is causing this kind of illness ( tragedy ) ???? Why ??? 😢
What causes any awful illness? sadly Bodies can go wrong
🙏
♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ ♥️ I
Why is there still no progress to a get a cure? What research is going on at this time? We are ALL at risk of this.
The COVID-19 pandemic has had such a widespread impact, both direct and indirect. Get vaccinated when you can!
Thank you for the inspiration rob burrow now RIP mate
😆😆