The Ride | MND Association
ฝัง
- เผยแพร่เมื่อ 25 ก.ย. 2018
- Visit www.takeovermnd.org for more.
Imagine a terrifying roller coaster ride where every turn and loop brings you closer to death... Around 5,000 people are stuck on this ride right now in England, Wales and Northern Ireland. That's why they need your help.
Your donation can fund care support and research to defeat motor neurone disease and stop this ride once and for all.
Together, we can #TakeOverMND.
This film shows the devastating effects of motor neurone disease portrayed as a terrifying roller coaster ride. It has been produced to raise public awareness of MND and does contain scenes that some people may find upsetting.
![ตีสิบเดย์ [FULL] | คู่รักแซฟฟิก "หลิงหลิง-ออม" จากซีรีย์ "ใจซ่อนรัก"](http://i.ytimg.com/vi/zs8AfphGn2w/mqdefault.jpg)
My dad was diagnosed with MND about 4 months ago. There are some big changes in him but hes doing okay. I love him and i would take his place if god would let me. I cry most days cos we all know his time here is now limited. A beautiful hard working honest man hit hard by this condition/infliction...i feel sick cos theres nothing i can do but offer as much support as i can...my heart aches. My dad is a good man. To anybody suffering with MND or anyone who knows somebody with MND stay strong...real love never dies...be there for them. They need you...God bless
Stay strong, buddy.
Thank you sir. I wish you well....
So sorry to hear. Nobody deserves this condition. Stay strong.
Where is specialist in
My father was also suffering from mnd, I consulted number of doctors but no use.
Having lost a loved one to this horrendous disease, this is heartbreaking..
The patients with mnd are real warriors.they are the strongest people of the world.they have to face a lot of difficulties in their regular life.my husband was a patient of mnd. Doctor told him that he had only six months. But God gave him 4 years.I am proud of my husband that he spent his life so much lively and satisfied.his body became week but his will power was at the top .he life proved the example of courage ,dedication,will power and love to all.we all love him he is no more because of corona..but always will be present in our hearts .he is like a star who will always shine and guide us .love you Ehsan.
💜💜💜💜💜💜
May ALLAH give you better return
The worst disease in the world. The bravest people. Those dear people affected and also those who are there with their loved ones to the end…and beyond. It’s heartbreaking.
Rabies:
My Grandad just died from mnd yesterday. He lasted 3 and bit years with it. It is a horrendous disease
That was.....jarring. Thank you.
So cruel did you notice how quiet his 40th was. No crowds no other kids, where did all his friends disappear
They never were there
I lost my dad to this 16 years ago.
Wow, excellent ad. Recently diagnosed with mnd myself, just awful. I don't feel lonely, but I feel very alone.
Wishing you well, you are not alone. my brother just got diagnosed
@@denisehadfield7995 so sorry. Sending love xxx
I suspect most remember the Ice Bucket Challenge of 2014 and it's so easy to forget what it was all about. Watch this clip and you will remember again - and that 5 people die of Motor Neurone Disease every day in the UK. Let's all keep giving please - to help ease the lives of those living with MND and to help those searching for a cure.
Thanks for your support. It is actually now 6 people that die every day of MND. 6 people are diagnosed every day too.
@@mndassoc They say it is rare it is not! You would think in 2018 they would at least have something to slow it down.
@@pam164 I agree. I don't think it is all that rare. I personally know 2 people that have been diagnosed with it.
@@mndassoc is any use by stem cell therapy for mnd, my father was suffering from mnd since last 2 years.
Please reply me
My wife had MND didn't get a lot of help she died in 2012 after a few months the person who was supposed to help us did nothing to help us so different back than he blocked everything never went to bed for a few months glad it's better now
My husband mnd. What can I do. Pleasw
😢😢 تم تشخيص والدي بهذا المرض منذ ٧ اشهر ونحن نستمر معه بالعلاج لكن دون جدوى صحته تسوء يوماً بعد يوم😔😔
The worst illness of all
I have weakness on my left hand ..😐
Every patient of mnd must be lesson Surah Rehman three times in a day three time in a day inshallah they all will be cure its more than like a magic plz try
V
Mnd patient must be lesson Surah Rahman three times in a day inshallah they all will be cure its a more than like a magic plzzz try
Plz delete this video this is horrible.....my father has mnd 😞
Sorry to hear about your dad. This is raising awareness..
Such a good video. I know a company in India named Advancells. They provide amazing facility for als/mnd patients. They have real patients videos. For those affected with such a bad disease, i thought of providing real help by commenting.
Hi,
My dad is diagnosed with MND.. currently we are hopeless in finding a good hospital for facilitating this problem.My dad is progressing rapidly.We may not have much time to wait and understand more about these concepts
Your comment is thoughtful..Could you please suggest if there are any other resources which can be inculcated in this diagnosis..like therapies or treatments
😢😢 تم تشخيص والدي بهذا المرض منذ ٧ اشهر ونحن نستمر معه بالعلاج لكن دون جدوى صحته تسوء يوماً بعد يوم😔😔