Afi

Forgive me.

I realise I havent written in over a month and for that I am sorry. I have no real reason or explaination to give you. Maybe a little writters block? Its not to say that I havent anything to write about I think its maybe more to do with the fact that I have had a lot of processing to do over the last few weeks and have had alot that has been on my heart that I just havent known how to share.

So I will begin with Afi.
Afi is one of the sweetest and coolest 5 year olds I have ever met, she has totally stolen my heart and she knows it. She came to us with a tumour in her mouth that was begining to obstruct her airway and had to be sent to theatre urgently to have a tracheostomy placed to allow her to breathe properly. She spent the next few weeks in the ward adjusting to breathing thru a tube in her neck and waiting for the results of the biopsy we took of her tumour. During that time of waiting for the results she contracted a nasty infection in her sputum and had to have several rounds of antibiotics to try and clear it up. After the fourth round we were finally successful and got the infection. After weeks of waiting the results came back saying it was a malignant cancer. Oh gosh. What do we do? Do we send her back home with palliative follow up? Do we attempt to take the tumour out and hope for the best?

Fortunately for Afi a head a neck specialist was due to arrive on the ship the following week so Dr Gary our resident maxilo-facial surgeon who is a very talented and humble man decided to wait for him and they would attempt to do the surgery together.

Im so grateful they did. Afi went to surgery over a week ago and is doing amazingly well, they were able to remove all of the tumour and are pretty postive that it wont return. It was news that nurse needed to hear. They removed her trach tube and she was able to breathe without any problems, she can eat properly again and be a normal 5 year old.

Awesome.