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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 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.
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.
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
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 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
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.
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 !!
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.
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
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 ❤
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
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.
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
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.
“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.
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'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
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. 💪💙💛
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!
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.
I think it’s awesome they are using Robs situation to bring awareness. It’s got to be one of the worst progressive diseases ever, so to use oneself to help others by using his own status? Absolute legends. Oh lord…please help this man and all of their efforts in hopefully finding a cure by it. No matter what- it isn’t by any means in vane. He’s helping thousands upon thousands of people.
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
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
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.
