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.
Top Comments
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.
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.