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By Harriet Johnston For Mailonline 09:35 BST 14 Jan 2021 , updated 10:19 BST 14 Jan 2021
A loving son made his ALS-suffering mother's final wish come true, by wheeling her onto the dance floor at his wedding and lifting her up for an emotional mother-son dance.
Terri Hightower, 57, from Clarksville, Tennessee, was diagnosed with the degenerative disease ALS - also known as Lou Gehrig's disease – in December 2019 and by summer 2020, she could no longer walk.
But despite her ailing health, she dreamed of attending her son Scooter's wedding on October 9 and was surprised when he organised a special mother-son dance for the two of them at the event.
Terri passed away just ten days later, with a clip of the emotional dance quickly going viral online as 10 million people tuned in to watch the special moment.
Mom with ALS lifted to feet to dance with son on wedding day
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With friends and family gathered around the dance floor, Scooter and his family wheeled his mother's wheelchair into the middle of the room.
As around 150 guests watched on, Scooter cued the music and, with the help of his father lifted his mother into his arms.
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Guests standing around the edge of the dancefloor applauded as Scooter moved her gently and weeping on her shoulder.
He could be seen sobbing and whispering into his mother's ear as he cradled her in his arms during the emotional dance.
The moment was captured on video by the wedding's videographer, Neil Fox, and around the room, there was not a dry eye in the house – including Scooter's wife, Afton, 25, who had helped with the surprise.
Terri died after losing her battle with the disease less than two weeks later, surrounded by her friends and family.
Hoping to raise awareness for ALS, the family asked Neil to share the video on his Facebook page. The post has since been viewed nearly 10 million times.
Afton said of the response to the video: 'We are amazed!
'We can't believe how much of an impact it is making around the world.
'It is so amazing how many – hundreds, thousands even – have reached out to us showing their love and sympathy. Terri felt every emotion possible.
'It was a very bittersweet moment, knowing that was her goal and knowing how much it meant to her and Scooter.
'We hope this video can bring more awareness to ALS.'
There is no cure for MND and the disease is fatal, however the disease progresses at different speeds in patients.
People with MND are expected to live two to five years after the symptoms first manifest, although 10 per cent of sufferers live at least 10 years.
The NHS describes motor neurone disease (MND) as: 'An uncommon condition that affects the brain and nerves. It causes weakness that gets worse over time.'
The weakness is caused by the deterioration of motor neurons, upper motor neurons that travel from the brain down the spinal cord, and lower motor neurons that spread out to the face, throat and limbs.
It was first discovered in 1865 by a French neurologist, Jean-Martin Charcot, hence why MND is sometimes known as Charcot's disease.
In the UK, Amyotrophic Lateral Sclerosis (ALS) is referred to as Motor Neurone Disease, while in the US, ALS is referred to as a specific subset of MND, which is defined as a group of neurological disorders.
However, according to Oxford University Hospitals: 'Nearly 90 per cent of patients with MND have the mixed ALS form of the disease, so that the terms MND and ALS are commonly used to mean the same thing.'
Weakness in the ankle or leg, which may manifest itself with trips or difficulty ascending stairs, and a weakness in the ability to grip things.
Slurred speech is an early symptom and may later worsen to include difficulty swallowing food.
Muscle cramps or twitches are also a symptom, as is weight loss due to leg and arm muscles growing thinner over time.
MND is difficult to diagnose in its early stages because several conditions may cause similar symptoms. There is also no one test used to ascertain its presence.
However, the disease is usually diagnosed through a process of exclusion, whereby diseases that manifest similar symptoms to ALS are excluded.
The NHS says that MND is an 'uncommon condition' that predominantly affects older people. However, it caveats that it can affect adults of any age.
The NHS says that, as of yet, 'it is not yet known why' the disease happens. The ALS Association says that MND occurs throughout the world 'with no racial, ethnic or socioeconomic boundaries and can affect anyone'.
It says that war veterans are twice as likely to develop ALS and that men are 20 per cent more likely to get it.
As well as being known as ALS and Charcot's disease, MND is frequently referred to as Lou Gehrig's disease.
Lou Gehrig was a hugely popular baseball player, who played for the New York Yankees between 1923 and 1939.
He was famous for his strength and was nicknamed 'The Iron Horse'.
His strength, popularity and fame transcended the sport of baseball and the condition adopted the name of the sportsman.
He died two years after his diagnosis.
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Son shares first dance with his ALS-suffering mother at his wedding
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