Rob Burrow's journey with MND 

Rob is a complete legend in the game and a amazing inspiration. His wife is showing complete devotion to her family and us a fantastic beacon of light

The man is an absolute legend. I've seen him play numerous times. What an inspiration.

What an amazing wife a true keeper.

Lost my dad last year to this awful disease. Stripped him to the bone. 94kgs to 38 when he died. If i was diagnosed id immediately move to a country where I could easily overdose or dignitas. Watching him slowly disappear was terrible for all those involved. Dad never talked about it much in the first year and then he lost his speech, he was a brave man. It has scared our family and I personally will never recover from this disease. A broken soul stares from a pair of watering eyes is my lasting vision of pops.

Lost my Dad 4 years ago with this disease, I don’t want to tell how he was suffering during those years, only things i wish to find the cure ASAP🙏

An old friend of mine passed away 8/11/21 from MND at Pilgrims Hospice Margate. With their care he managed to get home for a few days to see his family. This Leeds Centre will be a good safe haven for family and patient .

What an amazing Man, his wife is so supportive alone with this children and his parents. The medical team are doing a great care with him I admire them all

Inspiring man who was n is a fantastic role model with a beautiful devoted wife n kids god bless you all

Nothing but respect for this guy.

It makes my guts turn to see what's happened to the guy from being so fit ,its truly frightening, I have a connective tissue desease so never know what may come , MND is my worst fear as I have noone to care for me , such a brave man and family to deal with this the way they have ,especially Rob who could of just shut himself away ,👏 36 billion was spent on a track and trace app yet the government fund no research for MHD as they don't for many other illnesses and things need to change,having the attitude to fund and support the limited number of people through the illness until they die rather than fund a cure is not a good attitude ,and people like Rob are mostly helped by charities and fund raising ,

Ive run marathons and thank god for that. The love surrounding rob and his family is so touching so great to see the leeds marathon named after him. I breifly met kevin sinfield in Jersey last year what a great guy, his love for his mate moves me to tears. God bless yiu both.

Rob burrows absolute hero amazing on the pitch and amazing off you keep on fighting this mate your an inspiration to everyone absolutely incredible man

I grew up loving Wigan. When super league started I could not get over Rob he could turn on a sixpence and what a player. I love you Rob I really wish you all the best and although you may not benefit you are doing so much for those who come after you. You truly are a LEGEND

Behind every great man is an amazing woman 💯❤️🇳🇿

What an inspiring fella Rob is.just finished his book.incredible

What an inspiring man , and Mr Winfield , good luck to all xxx

I really feel for Rob nice bloke good family behind him his wife is a rock and his kids this should not happen to good people❤️❤️

Imagine if we spent the amount of money on mnd that we do on covid

My favourite hald back

Rip

Lost my mother to it.

Thanks Rob 🌺❤️🇳🇿7😍

God bless him cruel life 😢

My mum had this disease.

💙

How sad to have this awful disease he so young too

Or Langer 🤷🏼‍♂️

I am happy to share with you all that I am completely free from ALS

I read some patients can live 20 years with ALS? Why do doctors tell people they have 18 months to live? HuH?

Genetic illnesses are not recognised by the NHS. How do I know I’ve got one I’ve got Ehlers-Danlos I’ve met Rob indirectly I was in a shop where he was his wife pushed him by in a wheelchair which I use a wheelchair as well. I didn’t know what to say. I’d love to be sat there and spoke to him, but Rob needs to actually scream out and say there’s more genetic illnesses were made looking at I have a Ellens Danlos syndromes a genetic disorder, which is now taking my mobility. I am in desperate need for a new wheelchair. The NHS have told me to go and find it myself I’m on benefits I’ve been told I can never go back to work. I would love to go back to work. I spent 10 years in a uniform for the crown and the people in the land and this is our offices gets rewarded after 10 years service phone onto the rubber sheep. . To Rob’s wife, you are amazing woman my partner kicked me out after seven days. After being told, I have cancer the cancer treatment treatment as accelerated me EDs I have no one now no partner no friends no nothing I don’t even physically have a home because the local council keep on abusing me. Bolsover district Council absolute racists I have taking him to the Ombudsman, I was successful they were in my favour, but still the abusive Cancel carries on abusing at the beginning of the month. They sent contractors in who stole approximately £5000 worth of keys because things about to be changed and items about to be re-purchased. I am sick and tired of this. I do if I the police, the police tell me they work for the council Bolsover district which is actually illegal because the council are not government and the police are not supposed to work for the government they’re supposed to work for three things the land the people in the crown don’t get me wrong the crown or not the Royals there is a job title only my friend, I know this may seem hard but we need to take back our rights as disabled people. I do not class myself as disabled. I class myself as enabled because the so-called normal people in this world are more mental and have more illnesses. then the people are classed, disabled or enabled like myself. Rob keep your chin up and your beautiful wife, give her a cuddle because you will deserves it. Thank you for your time peaceloving to everybody.