Sarah's Story - MND Association 90"
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All Comments (35)
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I have recently stared experiencing MND symptoms, and this ad scares the shit out of me!!!!! it's hard to watch!!!
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People, look up Low Dose Naltrexone on the Internet. It has been helping people with any number of autoimmune and neurological conditions. It's supposedly good for Motor Neuron Disease too.
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This is a truly shocking view on MND but spot on I'd say. My nanna had MND and it is a horrific thing to see someone you love go through. I am a photography student and did a documentary project on her, rephotographing old photographs and made it into a video which can be viewed on my channel if anyone would like to see please feel free and any feedback would be appreciated. thankyou.
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@StTudno I lost my grandad to MND in 2006, it was horrible as no one had heard of it and i couldnt explain it because i got upset. People need to be made more aware of this horrible disease.
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Good Grief! What a harrowing truthful advert, Very Well Done. My Grandad has M.N.D. and has only been given a couple of months to live. I had never heard of the diease before adverts like this should definatly be shown to make people aware of what its like. xx
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Damn! Even though this is an ad, its still a nightmare to watch, no matter how many times watched.
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The Motor Neurone Disease Association is campaigning for a national strategy for this much neglected disease. Please visit the MNDA website and add your signature to the petition online.
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This ad needs to be shown, people need to understand what it is like to suffer from this disease!
Someone very close to me, in my immediate family, was diagnosed two years ago and unfortunately very few people know of the disease itself, of how it can effect families and individuals.
I personally found this very hard to watch, but the MNDA need help in spreading the message
This needs to be seen!!
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Why was this ad banned from the TV? When we are surrounded every day with visions of war (real and imaginary) and the violence done by man to man, why would this offend? We need more real life images like this not less - maybe then less people will live in isolation and ignorance. Sarah, well done girl.
I lost my dad on 11th June 2008 from MND. It was bloody heartbreaking .I had to keep explaining what he had as no-one had even heard of it. I see the expression on his face from the morning he died every night before I go to sleep.
StTudno 2 years ago 3
This is amazing - it really captures the pain and feeling isolated and trapped. Not a lot of people know about MND, and im so glad people are raising awareness. My Dad died of MND, and I miss him everyday, but the work that this association is doing is phenominal. Everyone involved should be so proud of themselves.
HannahCostello123 2 years ago 3