Amyotrophic Lateral Sclerosis ALS, Motor neurone disease MND

[jessyjessy4]

very interesting video thanks

[msjessypp]

love the video really good

[abhaymude]

This is MND, tack care and love to her, Swami Samarth, bless you

[Richardluvsjesus1]

You are so pretty.. I feel sorry for you.. I wish i could do something. but great you have a lot of spirit. I love you..

[Germenguy5545]

OMG have i gone madd why the fuck am i giggling to my self this is sad now that i think of it damn man im so very sorry i respect those with MSD and ALS sorry for my rudeness i really am it just happened :(

[raphaelcornwell]

I found out today that my mother has ALS.....

Thank you for posting this video, and I wish you all the best in your

fight against this disease.

raphael

[The391956]

Very nice sweet husband, lucky lady their

but unlucky to have ALS.

Their are ALS patients who feel blessed

to find a nursing home because their

loved ones abandoned them leaving them

in a hospital.

That is sad

[brebesh]

@penguingirl24 i pray that you get better.

[connaught2008]

God Bless ya

[topbombing2007]

Good to see you can still walk with assistance. I was diagnosed with ALS leg onset less than three months ago and already I am wheelchair-bound and my arms and hands are very weak. I am worried at how fast my progression is going with this horrible disease.

[jujubagirl]

I will have u in my paryers tonight, u are amazing.

[phoeniximperator]

she almost resembles my own condition.

[kitty591]

wish you the best !! my dad was diagnosed with ALS july '07, went into a coma due to respiratory failure october '07 passed away july '08. he was 51 . I was 17. im now in college. my research paper for my Bio class is on ALS. Keep it strong. hold on to whatever is left. =)

[ozyush]

I wish you all the best

[JohnTthefirst]

Thanks for trying (Ledbythelamb) but Lymes disease is quite different to ALS/MND.

I've had ALS for nearly 6 years now and I've looked ALL alternatives and believe me I'd do anything to have one of the alternatives.

But it isn't quite as simple as you make out.

[Guitarsolage]

@JohnTthefirst how can you get this disease can you get it from lack of sleep?

[JohnTthefirst]

@Guitarsolage Hi there no you don't get MND by lack of sleep although I suppose that in a very indirect way it could be a contributing factor.

the truth is that nobody knows yet what causes MND. The scientists are working like mad to find the cause and of the CURE.

aLLT HE BEST

JohnT the first

[Guitarsolage]

@JohnTthefirst alright thanks i was afraid because i stay up all day about 2 days of the week and I really dont get a full 8 hours of sleep on a daily basis

[thestrokessss]

You are an inspiration to me. Please keep up the amazing work! :oD

[hairless25]

stay strong! my mom has ALS and I have see it with my own eyes.

[kolakbanana]

@hairless25 : my dad got diagnosed with ALS last year.. he passed away 3 weeks ago.. we did everything we could but nothing could save him

[hairless25]

@kolakbanana Truly am sorry for your loss of your dad, my mom past away on 9-19-09...this disease is truly nasty...I do pray you are doing well...I am hanging in there she was my bf and i dearly miss her..

[katie1741]

@kolakbanana my aunt was diagnosed with ALS 2 years ago. she died march of this year. i miss her alot, i was rlly close with her. it was hard to see her like that, i remember one time visiting her, she spelled out "i want to die" with her little speling board thing. it killed me and my little cousin to hear my mom read that out. it was rlly hard when i went to visit her cuzz evry time i jus wnted to cry, cuz i wnted her to go back to the way she was before. i misss and love her soo much.

[zcharh5]

You are remarkable. Well done, it must have taken great courage and good-will to post this video.

[LedByTheLamb]

Thanks for the informational video. My doctor (neurologist) has found that a lot of people with ALS dont really have it.. they have long term Chronic Lyme disease. ALS patients have gotten better on long term antibiotic therapy. It's always worth looking in to. :)

[bobinalong1]

my brother has had mnd fore 4 years now he is 47 its very sad to see him as disabled as he is now, he has had his leg amputated last year but strangly this did not bother him one bit. the neurological centre where he lives also has the hospital social club about 100m away and he goes there evry night and is now part of the furniture. are you in england??? The one and only advise i can give to anyone with mnd is that you must get what you need now and dont wait for nhs to supply takes to long

[lyndouninette]

that's the first time i see someone who had the same als as my mom had, i found some similare expressions in her face, and the way she laughs i know now that those expressions weren't my mother ones but the desease ones.

[tjmyers321]

Many blessings from America.

[millie73]

Bless you for posting this :-)

[Schizomanicman]

Great to see you're doing so well! :)