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Brave Finn heads back to hospital - our thoughts are with this family today.

 

 

There is a family in Queensland with whom our thoughts are with today.

A mother facing her greatest fear – and a little boy who has gone through hell bravely headed back to fight again.

Our prayers are with this family – with Mum Sarah and Dad Jason.

And we hold our collective breaths waiting to hear of 21-month -old Finn Smith’s bravery when he wakes up from surgery.

Today is the day Finn starts the next part of his journey – eight months after contracting the deadly meningococcal virus.

Today Finn heads back to hospital for vital surgery and his mother and father go through, again, what most of us could not even imagine.

Last November life changed dramatically for the Sunshine Coast family.

Little Finn had been fighting what they thought was a viral infection and they had spent a sleepless night at home. An on-call doctor had made a home visit in the middle of the night and had diagnosed the little guy with a virus, mum Sarah instructed to get antibiotics in the morning.

The next day as they were driving towards Brisbane they noticed the devastating telltale signs of meningococcal – their 13-month-old baby had three red spots across his forehead.

They made a desperate drive to the hospital where the emergency department confirmed the worst. Within hours he was fighting a life and death battle.

The Daily Mail reports that Finn was “crying tears of blood, blood was coming out of his mouth and his body had puffed up.”

Sarah told The Daily Mail “you don’t know until the spots come out and once the rash comes out the damage is done – your little boy is fighting for his life.”

Sarah, Jason and Finn survived the darkest days – Finn was in a coma for two weeks– but the septicemia that accompanies meningococcal meant he had to have amputations. Multiple amputations.

It’s difficult to even begin to imagine how Sarah and Jason survived hearing that.

It’s a tribute to them that they did.

13-month-old Finn had his left leg amputated below the knee on Christmas Eve. He then had his right arm amputated through his wrist and his right leg amputated through his ankle.

Sarah told The Daily Mail that he spent 10 weeks in hospital recovering.

Now, eight months later, it is time for Finn to return to hospital to begin the first steps towards getting some movement back in his hand – and then he will soon get his prosthetic legs.

The Sunshine Coast Daily reports that today Finn is having his hand operated on to ease some of the scars which formed when he had his index finger and partial parts of his middle, ring and pinky amputated.

He will also have a skin graft on his hand.

The aim is to give him the ability to move his hand more and pick up things properly.

His Mum Sarah wrote on their Facebook page they face 12 months of “scar management, splints and gloves to insure the scares don’t contract the fingers. This is all to allow the skin on his hand to grow with him and so he can have full function of his hand for the future.”

For Sarah today is bittersweet.

She told The Daily Mail that she dreads returning to the hospital.  “I’m not looking forward to it, we’ve been home since February and he’s sort of been getting around and doing his thing”

“Going back to hospital and the theatre, it’s hard to have to do it to him but it’s something obviously we have to do. ”

We’ll just work through it one day at a time.”

After his surgery Finn will then look ahead to the next exciting phase – when in three weeks he gets his prosthetic legs.

“These new ones are actually going to have feet and we are going to get him a walking frame so he can stand up and walk around.” Sarah said.

We look forward to hearing about this brave little boy’s first steps.

You can follow Finn’s journey and send the family messages of support at their Facebook page here.

 

Vaccinations

Sarah has pleaded with parents to have their children vaccinated against meningococcal.

She told the Sunshine Coast Daily that “those who can” should go and get the vaccine.

“It is something not worth going through, what we went through, and even worse with the possibility of losing your child,” she said. “It is just too quick. By the time the rash appears the damage is done. But it is also the only time you really know what’s going on.” “Don’t wait for the rash,” she warned.

  • The Australian Medical Association currently recommends that infants aged less than six months receive three primary doses of 4CMenB, plus a booster dose at twelve months old.
  • Fewer doses are required for older age groups.
  • For more information on Meningococcal, see the Meningococcal Australia website here.

Remember: Every hour counts, if you suspect meningococcal disease go straight to your GP or hospital.

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Top Comments

Linda in Brisbane 10 years ago

Good Luck today Finn, and to Sarah and Jason – you have
the best team on your side.

Deservedly so, Finn is the ambassador for the Channel Nine Children's Hospital Telethon, Saturday 11 October this year.

Without funding, research stops. Everything costs and together we all need to help more kids and families such as Finn's.

It used to take three days or more to test for meningococcal. With the development of the "rapid test", that was shortened to just one hour. And that has saved many lives already, including Finn's.

Leading researchers who made this discovery was Brisbane-based Professor Theo Sloots and Associate Professor Michael Nissen, and their teams at Queensland Children’s Medical Research Institute (QCMRI) which receives funding from the Children’s Hospital Foundation.

As Prof Sloots said, "Without the Children's Hospital Foundation supporters, the vaccines and rapid test we've developed would not have happened. This type of work is not funded by the government, but by donations.”

“If we are to build on what we've already achieved and create a universal vaccine capable of protecting our kids from all forms of meningococcal, their support has to continue.“

“We won't have the funds to progress without their help".

To help families such as Sarah and Jason, and little Finn; please consider donating to the Children's Hospital Foundation so we can continue to fund ground-breaking research and the best medical equipment, as well as provide family care support programs.

Good luck today Finn - you are a brave little fighter and we can't wait to see your gorgeous smile and energy again soon.

The Children’s Hospital Foundation would like to thank Sarah and Jason for sharing your journey with us and helping to highlight awareness for ongoing funding to help sick and injured kids, and their families. You are an amazing family helping so many
other families while you still have your own speed bumps.

You truly have the best team with you today. The most exciting thing is that the two professors believe that, after years of work, a universal vaccine may finally be in sight. And when people as talented as they are, tell you something like that, you have to take it seriously. After all, Theo and Michael are part of a team that has already helped revolutionise the diagnosis, prevention and treatment, of meningococcal not just in Australia, but worldwide.

To help fund research and the best medical equipment for kids just like Finn, you can donate online www.childrenshospitalfounda... or call 1300 SICK KIDS within Australia.


OSGuest 10 years ago

What a beautiful little man. His story, courage and gorgeous smile made me cry. I wish him and his family well as they go through this terrible journey. Watching my little man I cannot imagine what they are going through and will have to in the future but I am happy that they still have him for every precious day. I hope people will take the opportunity to get the new vaccination to help stop more children suffering and not listen to the anti-vaxxers and their lies. Good luck Finn, I look forward to hearing a positive update.