Archive

Monthly Archives: December 2014

Luke is likely to be an angel.
He is the sum of happiness, innocence, pure joy, optimism, fun, intelligence and much more. He effortlessly makes the whole cancer thing seem so easy and a natural course of life to go through rather than a struggle. I am one lucky blessed mother.

Today is the mid point for the “interim maintainence 1” stage of his treatment. We have one more month of easy-going much familiarised chemo drugs before we hit the “delayed intensification” stage, a stage all leukaemia parents dread and loath. Oh let’s fill this month with truck loads of fun and excitement before we are hospital (and house) bound come February.

/home/wpcom/public_html/wp-content/blogs.dir/47c/42359488/files/2014/12/img_0935.jpg

/home/wpcom/public_html/wp-content/blogs.dir/47c/42359488/files/2014/12/img_0925.jpg

/home/wpcom/public_html/wp-content/blogs.dir/47c/42359488/files/2014/12/img_0918-0.jpg

Our Christmas this year in the wairarapa has been perfect in every way. Luke had so much fun in the pool, having water gun fights, sleeping on a mattress in nana’s bedroom, tenting in the backyard with the cousins. He had endless energy to burn and laughed so hard, got so wet in water, slept and played closely with m&m who’s each had a turn having some sort of stomach related bug. I consider it quite a miracle that he hadn’t got sick. Oh this resilient boy of mine, he makes us proud and happy to a point I just want to squeeze and melt him in my arms and have a good weeping cry. Christmas was perfect because he was.

Today the drive home was so lovely, here are a couple of shots of the farms we drove past. We love this part of New Zealand so much, see you next year.

/home/wpcom/public_html/wp-content/blogs.dir/47c/42359488/files/2014/12/img_0867.jpg

It’s the most wonderful time of the year, children playing, birds singing, everything we dreamed of is right here, perfection.

We are in the wairarapa this Christmas with family. Luke has not been sick two months in a row, I have to keep pinching myself. Myles walks everywhere and perpetually has a cheeky smile on his face. Nathan and I just celebrated our sixth anniversary and he is the most loving husband and father I know. What more can one wish. a jolly merry Christmas this is.

Today was set out to be a good day, nice, sunny and warm day in the Capital, we dropped off Myles at childcare centre, arrived at hospital, did the blood test, then we were told Luke’s neutrophils was zero, none, nil, non-existent. It means there is nothing in Luke’s body to fight for any type of infections, he is at risk of getting sick and being hospitalised. As a result  we couldn’t proceed with the planned chemo infusion through the portacath today, we’ll need to come back on Friday and see luke’s blood works again to see if neutrophils have recovered to a level where chemo can be resumed.

In my mind i was okay with that, then a dark cloud appeared out of nowhere and I started to feel quite depressed about Luke’s condition. I have always been feeling strong and positive about everything,taking each day as it comes, but not today. Today I felt the urge to cry. I dont think it’s possible to put down in writing what a mother feels when her son is appearing ok, but inside his body things are just not working the way it’s supposed to. I somehow felt I am a horrible mother, also I felt mentally and physically exhausted.

On top of that Myles was not eating. He has always been picky with food, but today he just wouldn’t have a bar of anything at dinner table, not milk afterwards either. Food is a big deal for me, I need my children to eat well, it’s my belief that good nutrition is the foundation of health, and when myles refuses to eat it just frustrates the heck out of me. Nathan thinks it’s no big deal, a child will never starve himself. I know that, but I can’t accept it. It might be a belief that I need to adjust, but it just added stress of my day.

Oh I need to relax, my mind is still racing, I need to now go chill out on the couch with a glass of wine and watch a movie, a movie that doesn’t involve a lot of thinking but has a nice sweet ending. At the same time cast on for my next knitting project, perhaps a miriam cardi. That might just be my de-stress strategy.

IMG_0502.JPG

IMG_0424.JPG

IMG_0402.JPG

IMG_0403.JPG
Lots of playing and laughing here when the sun is out. Myles is the most excited when he can get his hands into some water, and Luke is still on chemo treatment every 11th day, so in between treatment days he is an active fun loving normal child.
I love having him around the house, he wakes up every morning and the first thin he asks is “where are we going to today?”. If he didn’t get sick, he’d have to go to a childcare centre all day every day while I return to full time work. Now we get to hang out lots and as a result we have grown much closer. Here we have the silver lining.
But I do miss having my alone time. Maybe I should get up earlier or something to just be with myself.