Brenton Smith from Campbelltown diagnosed with Duchenne muscular dystrophy married love of his life

A man who was told he would’t live past his mid-teens has defied all odds and married his former carer in a beautiful wedding ceremony. 

Brenton Smith from Campbelltown, south-west of Sydney, was only two when he was diagnosed with Duchenne muscular dystrophy, a condition which causes muscles to deteriorate leading to difficulty with walking and mobility.

Despite suffering serious medical problems his entire life, Brenton, 26 married the love of his life Chrissie, 37, on Wednesday in a stunning wedding ceremony in front of close family and friends. 

Chrissie was first to arrive and was forced to wait for Brenton who was 20 minutes late to his own wedding because he wanted to do burnouts with friends 

Brenton, 26 married the love of his life Chrissie, 37, on Wednesday in a stunning wedding ceremony in front of close family and friends 

The adorable couple were married on Wednesday after meeting in 2018 when Chrissie was employed to care for Brenton

The adorable couple were married on Wednesday after meeting in 2018 when Chrissie was employed to care for Brenton

Brenton and Chrissie were married in an intimate ceremony on Wednesday in front of family and friends

Brenton and Chrissie were married in an intimate ceremony on Wednesday in front of family and friends

Brenton was 20 minutes late to his wedding because he wanted to go out with his friends (pictured) and do burnouts

Brenton was 20 minutes late to his wedding because he wanted to go out with his friends (pictured) and do burnouts

The pair met in 2018 when Chrissie was employed to care for Brenton who is unable to eat, dress and shower by himself. 

They saw each other again at the beginning of last year and ‘hit it off’ before eventually falling in love.   

‘They became one and now they’re married,’ Brenton’s excited mother Kylie told Daily Mail Australia. 

‘She accepted Brenton the way he is and Brenton just fell over head over heels with her and so did she.’ 

Kylie, a single mother-of-four, explained she was a bit ‘stand offish’ toward Chrissie when they first met because she was ‘protective of Brenton’. 

Kylie, Brenton's mother (pictured), was excited to see her son get married on Wednesday

Kylie, Brenton’s mother (pictured), was excited to see her son get married on Wednesday

'They became one and now they’re married,' Brenton's excited mother Kylie told Daily Mail Australia (pictured: Chrissie and Brenton)

‘They became one and now they’re married,’ Brenton’s excited mother Kylie told Daily Mail Australia (pictured: Chrissie and Brenton)

The loved-up couple holding up their marriage certificate after a stunning wedding ceremony

The loved-up couple holding up their marriage certificate after a stunning wedding ceremony

‘I saw how beautiful and fantastic she was with him and how he was with her,’ she recalled. 

‘She does everything for Brenton, no carers go to him, and she does everything – feed him, take him to the toilet, dress him, turn him around at night.’

Chrissie has acknowledged that it is hard work caring for Brenton but refuses to bring in carers telling Kylie: ‘He’s my husband and I love him. I don’t want any carers.’

Brenton’s heartbreaking diagnosis came when he was just two after Kylie noticed that he ‘wasn’t walking like other children’.  

‘He couldn’t climb stairs really well, he was waddling and always falling over,’ Kylie said.

‘I didn’t think it was normal.’

Brenton's heartbreaking diagnosis came when he was just two years old after Kylie (left) noticed that he 'wasn't walking like other children'

Brenton’s heartbreaking diagnosis came when he was just two years old after Kylie (left) noticed that he ‘wasn’t walking like other children’ 

Brenton Smith

Chrissie Smith

The couple got married on Wednesday in front of their closest family and friends 

She took him to Westmead Children’s Hospital where he was diagnosed with Duchenne muscular dystrophy.  

 The family had a scare when Brenton was hospitalised at the Royal North Shore seven years ago due to a severe illness. 

‘He was intubated three times because he was really sick, I saw them revive him once and it was traumatic,’ Kylie said. 

‘They also placed a defibrillator in his chest for his heart which saved helped save him.’

Kylie and her son Brenton

Kylie and her son Brenton

'Everyone is drawn to Brenton, everyone loves him, strangers come up to him, he’s just a beautiful soul, you’ll never meet anyone like Brenton,' Kylie said (Brenton and Chrissie pictured)

‘Everyone is drawn to Brenton, everyone loves him, strangers come up to him, he’s just a beautiful soul, you’ll never meet anyone like Brenton,’ Kylie said (Brenton and Chrissie pictured)

Brenton remained in intensive care for four months and doctors told his mum that he would need a tracheostomy, an opening in the neck to help him breathe, or risk him dying if he were to be intubated again. 

‘He was only 19 and said “please mum don’t let me do it”,’ Kylie explained. 

‘I told him it was his choice and he decided against it and he hasn’t been sick like that in eight years. I’ll forever be thankful for the staff at Royal North Shore.

‘Everyone is drawn to Brenton, everyone loves him, strangers come up to him, he’s just a beautiful soul, you’ll never meet anyone like Brenton.’

What is Duchenne muscular dystrophy 

Duchenne muscular dystrophy, or DMD, is a particular type of muscular dystrophy (or wasting) caused by a mutation in the DMD gene.

The DMD gene helps produce a protein called dystrophin, which is important for muscle strength, support and repair. 

People with Duchenne muscular dystrophy don’t produce the normal form of dystrophin, which means their muscles are more easily damaged and don’t work properly. 

Signs and symptoms of DMD:

  • Toe-walking – children start walking on their tip toes 
  • Larger than normal calf muscles
  • A waddling type of walk 
  • Inability to run or climb stairs 
  • An unusual way of getting off the floor, called a Gowers sign   

 

Source: Health Direct 

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