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Motor neurone disease – two heartbreaking stories

Polio_spinal_diagramMotor Neurone Disease (MND) is a progressive disease that attacks the motor neurones, or nerves, in the brain and spinal cord. This means messages gradually stop reaching muscles, which leads to weakness and wasting.

MND can affect how you walk, talk, eat, drink and breathe. However, not all symptoms necessarily happen to everyone and it is unlikely they will all develop at the same time, or in any specific order.

Although there is currently no cure for MND, symptoms can be managed to help you achieve the best possible quality of life.

 

Sir Chris, who conquered Everest back in 1985, is now caring for wife Wendy who is suffering with motor neurone disease

Sir-Chris-Bonington-3128937.pngFrom Daily Mirror UK

Challenge: Sir Chris admits that caring for wife Wendy is the hardest thing he’s ever done

World-famous adventurer Sir Chris Bonington has said he is facing the toughest ­challenge of his life – caring for his dying wife.

The 79-year-old explorer, who conquered Everest in 1985, is main carer to Wendy, who has been diagnosed with motor neurone disease.

The couple have been together for more than 50 years and have two sons.

Sir Chris, a veteran of 19 expeditions to the ­Himalayas, said: “It’s the hardest thing I’ve ­experienced in my life.

“It’s a truly terrible disease. It’s also a very rare ­condition, so there’s not much ­incentive for big drugs companies to research treatments.

“I’ll be working with the MND Association to help raise awareness.”

For more on this story go to:

http://www.mirror.co.uk/news/uk-news/explorer-sir-chris-bonington-admits-3130536#ixzz2uiGJwGMp

 

A legend’s fight

140226112422-joost-van-der-westhuizen-2013-vertical-galleryBy Sarah Holt and Robyn Curnow, CNN

Joost van der Westhuizen: ‘Invictus’ legend vows to fight motor neurone disease

Joost van der Westhuizen is a legend of South African rugby who has been battling motor neurone disease since being diagnosed in 2011. He is now confined to a wheelchair but continues to travel the world promoting the J9 foundation, which raises money and awareness of his incurable disease.

Joost van der Westhuizen is a former South Africa rugby player fighting motor neurone disease

The scrum-half was part of the team which won the 1995 Rugby World Cup in South Africa

The team’s achievements were immortalized in the film “Invictus”

140226114636-joost-van-der-westhuizen-2003-horizontal-galleryHe has set up his own foundation J9 to raise awareness of motor neurone disease

The life of rugby player Joost van der Westhuizen is the stuff films are made of — literally.

The 43-year-old was part of the South Africa team which won rugby union’s World Cup on home soil in 1995 and received the trophy from the late president Nelson Mandela as the post-apartheid era dawned.

140226111756-van-der-westhuizen-hong-sevens-horizontal-galleryThe story of that victory was immortalized in acclaimed film “Invictus” and now, as he battles a life-threatening illness, Van der Westhuizen is drawing inspiration from that Latin word which means undefeated; unconquered.

Van der Westhuizen was diagnosed with motor neurone disease, also known as ALS, in 2011.

The man that famously muscled New Zealand rugby giant Jonah Lomu to the turf in the closely-fought 1995 World Cup final now uses a wheelchair to get around.

140226114906-joost-van-der-westhuizen-1993-vertical-galleryHis body is too frail to walk because the debilitating disease effects all physical movement, including speech.

And the light and shade between his former glories and his present battle with illness is not unsurprisingly proving frustrating.

“It is,” Van der Westhuizen told CNN’s South Africa correspondent Robyn Curnow in a television interview where Van der Westhuizen’s slurred speech has been subtitled. “But then again, that’s how my life is.”

The memories of his stellar career — the Springbok jerseys and silverware — line the walls of Van der Westhuizen’s home in South Africa.

When he retired in 2003, he was the country’s most capped player with a reputation as one of the most brilliant, and toughest, scrum halves in the history of the game.

Francois Pienaar, who captained South Africa to success in 1995, described Van der Westhuizen as “a phenomenal athlete.”

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“What Joost did on the rugby field was incredible,” Pienaar told CNN. “He was probably the best number nine to play the game, and that’s saying something.”

Tough and tenacious on the rugby field, Van der Westhuizen is having to apply those skills in his fight to stay alive and help find a cure for motor neurone disease.

“I am,” he assured CNN. “Without a doubt. I am a self-confessed bad loser and I want to beat this not just for myself but for everyone with ALS around the world.”

Van der Westhuizen has started a foundation called J9 to raise money and awareness of motor neurone disease.

The foundation offers support and advice to patients and their families as they come to terms with a disease which has no clear cause.

A J9 legends team — boasting over 500 international caps between them — was cheered on by Van der Westhuizen in the veterans’ tournament at November’s Dubai round of the HSBC Sevens World Series.

He still travels around the world, often connecting with his old rugby rivals for fundraising events as well as making regular medical research trips to the United States.

It isn’t just Van der Westhuizen’s global mission which keeps him pressing on with his crusade.

“I am doing this to give my children a dad for longer,” he says. “My daughter is eight, my son 10. They need a dad.”

It is for this reason that Van der Westhuizen has revealed that he has decided to be artificially ventilated when his lungs are no longer able to function on their own.

It is a huge step for Van der Westhuizen given it’s not common practice in his native South Africa.

“I am going to live as long as possible — to help find a cure, to give my kids a dad,” he said, confirming that he has made a decision about using an artificial ventilation machine, which will aid his breathing and help him stay alive

“There is nothing wrong with my brain or my heart. I am still alive.”

Already a figure in one of South Africa’s most historic sporting events, Van der Westhuizen is determined to defy the odds and help make history a second time.

For more on this story go to:

http://edition.cnn.com/2014/02/26/sport/joost-van-der-westhuizen-motor-neurone-disease/

 

 

0 COMMENTS

  1. We all did our best to seek help for this disease, no medications they prescribed worked ,we were all scared we might lose him due to his condition, as he had been his brother’s caregiver a few years earlier for the same disease before he passed. doctor recommend natural treatment from multivitamincare .org for his ALS we have no choice to give a try on natural organic treatment ,this herbal cure has effectively reverse my father condition ,losing his balance which led to stumbling and falling stop  after the completing the herbal supplement which include his weakness in his right arm and his speech, home remedies from multivitamincare .org is the best although their service is a little bit expensive but it worth it, they save lives.

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