Hi Melissa, Terry, Ash & Tyler, Hope our little man is still doing well....Amy is jealous because you met the Wiggles, Mark & Alex because you met Fatty, me because you met Andrew G & Neil because you met Lady Luck. So you guys had it pretty well covered as far as we are concerned!!! The whole of Amy's school has said so many prayers for you guys, I have lost count & you know how well God listens to little children!!! I'll get them to keep it up Be strong, be brave lol Neil,Vicki,Mark,Alex & Amy
Am still unable to update website so I thought I'd just give a quick one here.
We have our boy out with us tonight for the first time in 8 weeks!! Got discharged this afternoon & have clinic Thurs & quick chemo treatment Fri (a 9 day booster shot pretty much).
So far all is going well, however, it's all a bit surreal. The docs probably thought we were a bit strange as we weren't overly excited at discharge - we just wanted gate leave!! The whole 'unknown' is all a bit scary!!
Just a very quick message to send all of our love. We think of you all everyday - and love looking at this wonderful website! All of our questions get answered without us having to nag! Tyler's website shows just how special you all are - and just how much you are loved and cared for. Catch up soon.
Lots of love and kisses always Uncle Ton' , Aunty Nean and Jack xoxoxoxox
This is Jay's darsly mum - he is feeling a little unwell but he wanted me to come tell you he is thinking of you each and everyday and he wishes you can get better real quick. I know you probably don't understand what is happening to you and why you have to be poked and prodded alll the time but believe me it is so you can get better. Jay trevels that same journey as you and understands what you have to go through & that is why he wants to let you know that it can be beaten - Jay always says "The word CANcer spells CAN" and I CAN beat Neuroblastoma - he also says "CAN't is not a word becuase it spells CAN - and I can do anything I set my mind to.So you all stay positive and strong always believe in your dreams and keep that smile on the dile (face). Jay sends you lots of his strength & courage and hopefully we will all get together and all say we survived Neuroblastoma - it will happen. Sending you lots of big big big big koala hugs from (JAY & his darsly mum)
As everyone says - you're all always in our thoughts and prayers. That breather seems to be exactly what you needed to prepare for round 2. Hope it's going as best it can.
Hey Tyler, Its your cuz Taleisha. Miss ya heaps!!! your doin soo well, your such a brave little boy Cooper says WOOF lol Luv ya heapsssssssss!! from Taleisha
To Tyler and family I have seen your pictures and i feel so sorry for what you have to go through i am looking at your pictures every week. I hope you get better and always know that i am thinking of you.