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Lovely video, wishing you very well❤

My brother was misdiagnosed and treated for epilepsy. After finally getting a diagnosis he was dead in 5 days

So sad - but lovely man and great information.

This kind of exposure is illuminating. Thank you for sharing.

Kevin and your team you are an incredible and inspirational person and youur team we are all behind you kev and your team, there has been nothing on calender or look North to see how you and them are doing on this incredible challenge 🏃🏃

Wishing you the best.

Eileen, you're truly amazing - love to you, Joe and all the family ❤

This us really nice

Well done🎉

well done daniel

Rip one brave man

Rip Colm

Thank you for your courage Ollie. My mom was diagnosed in 2018. There's a lovely scripture in Revelation 21:3,4. The hope for the future is a world without suffering, no illness whatsoever.

. Hi Ollie. I just read your story on UA-cam. I wish you well. I would just like to remind you that all who are diagnosed with MND, do not die within the life expectancy and prognosis. 2 to 5 years. I got the very same diagnosis in 1977. 47 years ago. I'm still here. Badly wounded but I've still got a quality of life at 91+ years. I've known people here in Ireland who lived 30 years and another person 35 years with this disease.we never know when that breakthrough will arrive. I know that it will not arrive in time to save me. That does not worry me. I've had a good innings, and if something is discovered to arrest this disease and I'm not here to witness that. Then I will smile from the heavens above knowing that I have contributed something to this breakthrough and the people who are then diagnosed will benefit greatly. Andy McGovern. The longest living survivor in the world at the moment. Good luck Oliver. Acceptance is the key. :-)

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Wishing your family very well.

Thank you for sharing

Thank you for sharing

My name is Caleb Sheehan too. Praying for you, cousin.

Sorry to hear about your situation but you are not on your own bless ypuxxxxx❤🎉

P r o m o S M 😔

I knew Ed in New York, we worked together doing work for European TV stations like the BBC. Ed loved the art of filmmaking, I was unaware of any talent in music. Cool to see another side of Ed. I was sad to hear of his passing and actually found out because I had a dream that Ed and I were working on an independent film, where I remember saying "Ed is a really good cinematographer" and then I woke up, looked up his name on my phone only to find out he passed last year. It's been well over 20 years since I last saw Ed but it looks like he created a wonderful life for himself in Ireland. Rest in peace brother.

Thank you to all those involved for making this beautiful service available to those who were unable to join in person. Jennifer Kennedy (Brussels/Tramore)

Please help me my father is suffering from this disease

My mums called Claire Byrne I'm using her account😊😊

Rest in peace

Farewell to my old school teacher

Its a pity and at the same time maybe a good thing people only learn about MND when they need to.

Keep strong Charlie, I know it's difficult but just try and keep strong, your a good man

I hope Charlie gets to live another 5 or six years, I really hope soo

U r wonderful! We love u! Stay strong!

Incredible, fantastic voice, this is really beautiful, my mother was an MND sufferer.

We all Love you xxx And now you know it . We watched you everyday and thank you Mr Fingerless man

Beautiful ❤

All the best Charlie, MND is such a cruel disease. I have lost friends with it. My beautiful cousin is losing her lovely husband to MND here in Western Australia. I pray they find a cure sooner than later. 💙

Beautiful gesture Bono❤ Best wishes Charie❤

Nice, it feels hopeful.

Snake bono

Excellent. A track from 2009 altered a little. Good stuff, and best wishes to Charlie.

Sounds great.

Colm Murray was a Great Irish broadcaster I have alot of memories of I'm on RTE News

You are hope and inspiration for many people suffering from MND.

Farewell Roland, you and Annette will be missed by so many people whose lives you touched xxx

Good man Paul. Lovely to hear your story. I wish you well. You are indeed living with the disease, not dying from it. Here's to 2021.

I have decided to make this post or testimony public. My husband was diagnosed with Alzheimer’s ten years ago. I loved my husband very much, and it was heartbreaking to have him develop Alzheimer's disease and to stand by and watch him decline in his ability to take care of himself, struggling with day-to-day tasks. It takes away his memory and eventually the ability to do basic tasks. Alzheimer’s doesn’t just affect the person who is diagnosed - it also turns your world as a caregiver, upside down if your loved one is grappling with the condition. To be clear, there is no pharmaceutical medicine, no magic pill that has any significant effect on the progressive downhill course of this disease. Not until we use an Herbal Medicine called BRONGEE that put an end to it. He has been well and living his best life. While there may be other different options to into. Never make your own success path a secret. There should be no shame. Contact Dr. GIMMY with drgimmyharbalsolution @ gmail. com, IG page @dr_gimmy Call/WhatsApp +2347032734647 It may also help you too. HE HAS REMEDY FOR NUMEROUS DISEASES SUCH AS: *herpes cure *Lupus cure *Cancer cure *ALS *WEIGHT-LOSS *PENIS-ENLARGEMENT

I have just watched the Motor Neuron Disease Association video of the 35th Memorial service. As a long-time survivor with this disease and as a person who attended most of those 35 AGMs. I would just like to say that I was moved emotionally by the presentation and involvement of our association to make this connection with our members. (Due to the virus restrictions). Take a bow, you wonderful Association. Not only are you involved with our members, but you never forget those who have passed on, victims of this terminal illness. It is true.: "Those you love, never die.". Thank you! Andy ~

What a lovely song for a wonderful worthwhile Charity!!....and...i am so sorry to hear about your MND diagnosis (i never knew?)...remember Roy....you are always in my thoughts..you take care of yourself Buddy!!...i have Type 2 Diabetes and severe Hypertension, so i'm not in the best of health meself, and i'm on 7 x lots of meds for life...so i really feel for you, i wish i could give you a hug... :(

Great work guys x I’ll be drinking tea in June for MND

Hello Jan, my wife Patricia has M N D she is into her 3rd year, every thing has to be done for her, and in spite of all this she has the most wonderful sunny disposition, and every day this disease is talking a little bit of her away, she still laughs! she still has her speech and a little movement in her left hand, to move the joystick on her wheelchair. And she is naturally right handed, The I M N D A association off Ireland is a fantastic organization, what would we do without them, where would people be? and to her carers who are fantastic group of people, I will not praise myself, I am her husband, and there fore now ends my story on my beautiful wife Patricia! Our thoughts are with you and everyone who has this Evil disease,

Hello Paul, my wife Patricia has ''M N D, she is in to her 3rd year, as like yourself every thing has to be done for her, one thing she still has is her speech, and she has the most wonderful sunny disposition in spite of this evil disease, and every day talking a little bit of her away] she still laughs, and we cry together, when everyone is gone!