Monday, 9 August 2010
Friday, 23 April 2010
Mosiah’s surgeon, Dr Winlaw, has communicated that Westmead Kid’s heart units are desperately short of funding at the moment. Taking into account that heart disease is the biggest killer of Australian children, this is a worthy cause to support. Every donation, no matter how small can make a big difference.
Congenital heart defects in Kids, touches the lives of many. In addition to Mosiah, there are several people that we personally know who have also been affected. Here their stories:
Ava Crosbie (We can write plenty about her)
Four months after Mosiah passed away, we welcomed Ava Grace Crosbie into the world. In the minutes after she was born, the Doctors and Nurses became concerned because Ava carried some characteristics of Down Syndrome. She was also having some breathing difficulties. A few hours later her paediatrician confirmed the diagnosis of Down Syndrome. He also said that her respiratory problems were mostly likely the result of a congenital heart defect. Ava was transferred to the Grace Unit at the Westmead Children’s hospital. They were able to identify 3 holes in her heart and develop a management plan that allowed her to be moved out of an oxygen crib, remove her feeding tube and eventually come home. Ava continues to be seen by the specialists at the children’s hospital and will eventually need open heart surgery to close the holes in her heart.
Last December, Sally and I Caught up with Lorelei and Hans Anderson. Growing up, I was close friends with Lorelei. Their daughter Eliza has recently undergone open heart surgery at the Westmead Children’s Hospital to close a hole in her heart. Thanks to the expertise of the Surgeons and staff at Westmead, the surgery was a success and Eliza was back at home within a few days. Thanks to recent advances in Kid’s heart surgery, holes in the heart can usually be corrected in a single operation. After which, a child usually regains full heart function, with no complications or requirement for further surgeries.
As a teenager, Levi’s Mum Karina lived two doors from Glen and I. Her brother’s were a regular fixture at the Crosbie home… AKA neighbourhood basketball court. Karina married Ashley McCormack. Their eldest son Levi was born with Hyperplasic Left Heart Syndrome. This is the same heart condition that Mosiah had. Levi is doing well and just started school this year. He has had several successful surgeries over the years. Levi has received a lot of media attention which helps raise awareness of the challenges that these brave little kid’s face. You can follow this link to a recent 60 minutes story on Levi.
Click here to view video
Please scroll down to the next post for information on how you can help.
Donations can be made in 3 simple steps:
Go to the Children’s Hospital at Westmead Website:
Go to the donate online section:
* Fill in your details.
* In the “Company Field” enter the words “In Memory of Mosiah”
* In the “Direct my Donation to” section, select “Kids Heart Research”
* When the form is complete, click “Donate”
A receipt will be mailed to the address provided. Keep it somewhere safe, so you can claim a deduction in your next Tax Return.
THANK YOU FOR YOUR SUPPORT
Monday, 12 April 2010
Ava is growing big and strong. She's always happy and smiling (except for when daddy is late with feeding time). She's also becoming very social. .... and we can't forget how much she loves getting rasberries blown on her tummy:
Layne started school this year. Her teacher says that she is very attentive in class, listens to instructions and learns very quickly. I think the whole listening thing must be selective, because it just doesn't happen when she's asked to clean her room. hmmmm..
Jacob is now in 2nd grade and is doing very well. The soccer season also started last weekend. I think he is by far the most energetic player on the team. Its great watching the Kids burn themselves out, because it usually means a bit of peace and quiet afterwards :-)
And that's all for now. Stay posted...