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Rob your amazing, my heart soul is there for you

incredible lady and Mother. What a huge support you must have been for your Son. Sending you all the love in the world <3

I have been personally affected by MND or ALS. I know 4 people who have been struck by this horrible disease. I lost my classmate, Steve, just last month. This disease is not as rare as they would like us to think. Thank you for sharing your story and putting another face to MND. We need more people to share so that this disease will become a part of the past. God bless you and keep you. 🙏❤ Jan

You are a true warrior and an inspiration 🧡💙

Thanks for this. You are a generous woman. Please continue to ‘enjoy the smallest things’

❤

You are an inspiring warrior woman

♥

💔💔💔

Rip

A handsome guy robbed of his life by this brutal and very cruel desease. RIP Jody

I would love to volunteer

I want to volunteer

Join Alpha hour

My heart goes out to that woman.God bless her.

That’s amazing! Keep fighting the fight! 💋🥰❤️

.I'm so grateful to you Dr EHIMARE ON TH-cam CHANNEL who was able to reverse and cured my husband Al's disease with the herbs i ordered from him thank you XX Dr Ehimare ❤

What a gorgeos brave man with a gorgeous brave family.

One of MND po

Or Langer 🤷🏼‍♂️

My favourite hald back

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

Thanks Rob 🌺❤️🇳🇿7😍

This treatment to the non 13 stoners pregnant , barely able to communicate their in labour , but the men think their pretending, after sonia eastenders birth theyre .

Brought tears to my eyes…you were a wonderful mother to your lovely son.

All the best Kev what a human you you are thank you for making a difference to so many will be be cheering you on Jim and Tracy

God bless him cruel life 😢

Thank you for this wonderful centre and to everyone who has devoted their time and support to help with this terrible condition. ❤️

A lovely girl. Good on you. Sorry for your loss. Nice accent.

My school is rasing money for rouxs army at the moment I wish him all the best

Letby is nothing but the spawn of the devil 😈

I live in Australia and I have just been diagnosed with motor neurone disease, I know that there is no cure for it and I know that I am going to die possibly in the next 2 years. But I would like to talk to anyone who has mnd ,for there prospective, so if anyone knows of any online forums could you please leave the details here. Thank you 😊

Lost my mother to it.

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

Good luck. I haven't had a chance to research this, but I wish you all the best. It's an incredibly difficult, yet amazing thing you all are doing.

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

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.

Very moving, sorry for your loss.

You’re not alone. His Life had Meaning & Purpose.

I’m so sorry ❤

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.

19TH FEBRUARY 2003

18TH JANUARY.1933.

PLASHET WARD LONDON

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