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Health Kiwi man tries to stay positive as body turns to stone

22:26  14 november  2017
22:26  14 november  2017 Source:   msn.com

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Kiwi man tries to stay positive as body turns to stone . An Auckland man is suffering from a debilitating disease that slowly hardens his skin and internal

An Auckland man whose body is turning to stone thanks Kiwis for connecting with his plight. stuff.co.nz. · 14 ноября в 17:43 ·. 'I try to stay positive ': Rare disease turns Auckland man 's body to stone .

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An Auckland man is suffering from a debilitating disease that slowly hardens his skin and internal organs, effectively turning his body to stone . "I get sick very easily but I stay positive ."

Callan Fabian suffers from the auto-immune disease scleroderma, which is rapidly turning his body to stone . An Auckland man is being progressively paralysed due to a rare and incurable disease. "I thought I was going to die at times but I stay positive ," he said.

An Auckland man is suffering from a debilitating disease that slowly hardens his skin and internal organs, effectively turning his body to stone.

Callan Fabian has gone from a fit and strong young man working as a stonemason to living in constant pain, due to Scleroderma, a rare condition that has no known cure.

Due to the tightness of his skin, Mr Fabian is unable to sit upright for long and ulcers have broken out across his body, which are unlikely to heal.

"I'm losing all of my movement and my ability to do everything," Mr Fabian told NZME.

a man standing in front of a building © Provided by MediaWorks NZ Limited

"I get sick very easily but I stay positive."

His internal organs aren't functioning properly, and Mr Fabian will not recover from the progressive condition.

'Every morning, I would wake up to clumps of hair all over my pillow.'

  'Every morning, I would wake up to clumps of hair all over my pillow.' By Madeleine Compion I first got Alopecia Areata five years ago, when I was 29 years old. It was when my husband and I made the decision to immigrate to Australia from South Africa. Some specialists refer to this as the triggering event – a really stressful situation that may trigger the start of Alopecia. … ContinuedI first got Alopecia Areata five years ago, when I was 29 years old. It was when my husband and I made the decision to immigrate to Australia from South Africa. Some specialists refer to this as the triggering event – a really stressful situation that may trigger the start of Alopecia.

Callan Fabian was expected to live until Christmas, but passed away early.

Breathe with your belly and focus on just your in-breaths and out-breaths for a minute or two to calm your mind and body down. Refocus. shrishti. Adding on to this great post about how to stay positive , what’s helped me most through trying times is to take a step back from situations where I

The 44-year-old has no family in Auckland, however an RSA volunteer has struck up a friendship with him - dipping into his own pocket to help to care for him.

Scleroderma Auckland, a charity that supports sufferers of the disease in New Zealand, has set up a Givealittle page to support Mr Fabian to continue to access care and support.

"It is unacceptable that a volunteer caregiver needs to use his own funds to care for someone in such a condition," the group said.

"As Callan is in constant discomfort and pain and is now unable to sit upright for extended periods of time due to the tightness of his skin he now requires an ambulance just to attend hospital appointments."

Almost 300 people have donated since the page was set up.

Scleroderma is not contagious, infectious, cancerous or malignant and it is usually not hereditary. Around 1000 people in New Zealand are believed to suffer from the disease.


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