Bumpity bump bump bump
Will be doing so until the cutoff point for GIVING . 
EM NEEDS YOUR PRAYERS AND KAZ NEEDS YOUR SUPPORT.
I WILL BE BUMPING THIS THREAD NIGHT AND DAY AND WITH YOUR HELP WE WILL ALL GET A CHANCE TO WISH EM WELL AND SUPPORT KAZ AS EM BATTLES THE FIGHT OF HER LIFE.
THE STRENGTH OF SILVERSTACKERS SUPPORT WILL HELP THEM THROUGH THIS TIME.
How many have told their loved one or ones they love them today
Today is all you have and tomorrow you can only hope for.
Take time to tell your friends you care, be kind to your fellow man everywhere.
Your kindness could make all the difference to someone who is in need.
I HOPE YOU WILL ALL JOIN ME IN SAYING HELLO TO KAZ AND EM, PLEASE USE THIS FORUM TO SAY HELLO TO THEM AS OFTEN AS YOU CAN.
They need their friends around them right now.
Thank you Maggie
Last edited by Maggie (2012-10-05 22:41:44)
Hi All
I originally posted this in the sydney meeting forum as did not know where else to put it but now thanks to some wonderful help I have a place to post updates and may I again say how much Em and I appreciated all of ss guys and gals support.
"Hi All
Em and I made it to the monthly meet and it was great to catch up with you all. At the time we were waiting for the BIG test to tell us if she was in remission from leukemia. Since there is now no general discussion and I am on so infrequently to know what is what I thought I would let you all know that most devastatingly we have found out that despite the chemo of the past 3 months that she is not in remission. We are temporarily shattered of course and have yet to find out what is ahead of us. As I write she is gravely ill in hospital so need to get back up there.
cheers to all
kaz"
As an update to that post Em is still quite ill in hospital but as of yesterday Tues we now know why she has not been able to keep anything including IV fluid down and why she is in such great pain. It seems for the ultrasound tests that she has such highly inflamed bowel and ulcers from top to toe that the body has been rejecting all but the minimum fluid. Now she is on pca (patient controlled pain relief) and will attempt once the pain is controlled to have some fluid orally, naturally after a week of v*%#^ she is scared to try oral but knows it has to happen.
On the failure to get into remission side we now know that she has to go to theatre when she is better and have another proceedure to allow for more chemo to be delivered. She will be put on high dose chemo (boy am I struggling with that) which will take until the end of this year, then she will be "conditioned" for a cord blood transplant. All being well and no hiccups which is highly unlikely we will be home March 2013. We are still coming to terms with this.
take care all
kaz and em
boneyard said:Once the chest is on its way.
Keep it VERY lowkey.
There can be very nasty pirates lurking around.
Shame to see the effots being pilfered by a low life lurking around.