Is bimari ne meri ma mere to kho lai 😢

My mother also a MND patient

Visited here trying to u destand otuoma Kenya

My former partner passed from MND. He had been a Special Forces squaddie and a real outdoors man. We would do survival holidays etc. Within 8-9 months he simply faded away until he could have been lifted up, caught by a gust of wind. The reason why it became so difficult to obtain these medications was because they were used by the gallon in the "Land of the free" to murder innocent people based on evidence obtained using "The Reid Technique" and lie detector tests (which are horribly flawed and totally inadmissible in courts almost everywhere else

So is this drug available in the market. Hope you reply.

Not one MND sufferer on this a

DIVINO !!!!!!!!!!!

RIP Dad 🕊️❤

It should be important to emphasise that not all MND's are life shortening. In my case of PLS (Primary lateral Scelerosis) where lifespan is not shortened, just more difficult to negociate each year. PLS is very rare, and and still only a very small proportion of MND cases, and because of its rarity few healthcare professional have even heard of it.

G’day from Australia, you have both done a fabulous job 👏

My uncle, Norman, had Motor Neurones Disease, diagnosed in 1974 I think. He went from an active man, a mechanic, someone who valued his ability to complete practical tasks above all in his business, a best friend and a good father to just... nothing. It was about 3 years before they had to tie his head to chairs because he couldn't hold it up on his own anymore, and a matter of months until, on the 8th November 1977, he died due to the complications.

Thanks so much for uploading this ep Peter and Daniel r a joy 2 watch together and they were incredible on corrie in this storyine will miss Paul and billy were best corrie couple😊😊☹️❤️❤️🧡💙🧡💙

Thanks for this upload. These are 2 brilliant actors especially Peter ash. They have played out the story in a realistic and believable manner. Well done to them both!

Thank you so much for doing this campaign. It is so important that there is more awareness of MND amongst the general public. Great work.

Amazing campaign 😭💔lost my mum to MND

So sad 😢😢

my brother was diagnosed in July 2024

She seems like such a sweetheart, I hope she is still doing well, although the prognosis is very poor.

Absolutely brilliant, even Heads of State globally got involved, raising awareness is key to diagnosis. Project Mind such a brilliant research project 👍

What an incredible man. Sam, you've already won at life to have the outlook and strength you already have. Sending all my love to you 💕

Great advise to others Nicky, stay positive, my thoughts are with you & your family. Lovely horses too x

Amazing story, such a brave lady.

I really appreciate this video as I have just been diagnosed last week and it is really scary. I can only deal with each day, as it comes.

How do you think you got it? I got mnd swear i gotta it through a infection

My mother is going through this phase. May God provide peace and strength to the ones and their families who are going through it.

God bless them all , hopefully there’s some light on the horizon xx

its the saddest thing ever.. to watch helplessly as someone you love dies slowly... its devastating.. my mum got diagnosed today

Just found out my 32 year old brother has just been diagnosed with MND this morning. Just seems so unfair

Such a horrible disease ,why can't we just all get old and go to sleep, who created all these cancers and diseases, can we blame God as he created us

It's the most unfair, cruel , hideous disease.

brixton bully slide with the botty man leave 2 in your hoodie

Did you take the vaccine ,as there is a link between the vaccine and MND and other neurological conditions

MND is the worst illness of all

I lost my dad to this 16 years ago.

The worst illness of all

Cruel disease but having Sam's attitude is the way to deal with it. Wishing this lovely guy all the very best

Its so unfair how anyone goes through this

My naned izzy, I'm 20 years old and my dad was diagnosed with mnd two weeks ago. This is probably just a shout into the void but im looking go feel less alone?

This information is amazing .....Yogendra ras from Planet ayurveda are very good results on Motor neurone disease.

Don't Trust Any Doctors they are Scammers, make your disease more worsen, they're taking advantage of incurable ALS, Official it can be stopped or slowed to 15 years, when regular exercise, healthy and rich diet is preferred NOTE:- Any type of Vaccination can cause Rapid Progression and death, preferred not to take any vaccination

I wish you well Sam. I am the longest living survivor in the world at the moment 47 years since I was diagnosed in St Vincent's Hospital, Dublin. With motor neuron disease. It was hell. The first few years. Then I started to accept my condition. I still got some abilities that I treasure. I wish you the same life expectancy. Andy McGovern.

A basic and common error in this video unfortunately. The DST is a decision support tool not a decision making tool. It must not be used prescriptively or mechanistically to decide eligibility by scoring. The decision is made by the MDT using their professional judgement after they have used the DST as a structured evidence gathering tool. The domain weightings are a guide only and not having a high enough score does not necessarily mean you are not eligible. Paragraph 161 of the 2022 Framework and Coughlan case law test (in annex B) explain this principle.

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