Have been having a little play around with my camera before I take my first photography lesson on Wednesday night. We have theory and then on Sunday we have from noon until 6 to do practical. Am so looking forward to it.
Have had a busy week this week. Went to a girls night in on Friday night to raise much needed funds to aid in the fight against breast cancer. I had such a wonderful fun time and cannot wait now until next year. The night ended up raising a mammoth $2372.00
Stuart and Jacob decided that they were going camping and 4w driving on Saturday so headed off for the night which just left Emma and I. Emma had a Halloween party to go to on Saturday which ended up being a sleep over. I was a bit worried how she would go as this is the first time she has been away from me since being diagnosed with cancer. I spoke to her a couple of times during the night and she was fine. I think I was worse as I just couldn't sleep knowing that I was the only person in the house. I did however get to watch two movies that I had been dying to see. "The blind side" and "letters to Juliet" both very wonderful movies.
Tonight Emma went trick or treating with Hannah and Samantha (two of her friends from our street) I don't really agree with it myself, but I guess it is just a little harmless fun and it got Emma out and about enjoying herself. I could not believe how many lollies she got. I had to end up carrying half of them. There were so many children dressed up and running around our area. Was so nice to see so many mums and dads out and about with their little ones.
As you can see from the photos, Emma dressed up as a witch. The outfit she wore was actually her big sisters.
Anyway I have loads of scrapping to get completed.
Ok well Emma decided to make some adorable little marshmallow mice and she has entered them on the Junior Masterchef website for a chance to win prizes. I am asking if you read this then could you please vote for her. It would be so nice to see her win a weekly pack with an apron etc. You vote by clicking on the stars under the photo. Click on the link below and I believe that emma is photo number 42.
The first one was to use water somehow on your layout. I decided to water down my orange paint and just let is go all over the background. I must say that I kind of like how it turned out.
The 2nd layout was for the sketch challenge, luckily it was an awesome sketch so I thoroughly enjoyed this one.
Layout number 3 was also from a sketch from the new and exciting challenge site - Get Picky. If you like to scrap with multiple photos then go take a look. There are also awesome prizes up for grabs.
Ok so yes mine is slightly different as I have done an 8.5 x 11 inch layout. I am not sure if it is allowed though so I may be out of the running already lol.
Love the flowers from little yellow bicycle, they are super cute.
Bought myself a Sunbeam Cupcake maker today after visiting a friend and seeing hers. WOW what a brilliant kitchen appliance. I can see that I am going to be hooked on making cupcakes for a while. I have already made 2 dozen. 1 dozen gluten free for Jacob and 1 dozen vanilla for Emma.
Isn't she beautiful ( her name is Clarise) LOL
Well I must go, have to get dinner ready, organise school clothes for in the morning and clean up. Stuart is in Sydney tonight for business so it will be pretty cruisy at the love shack.
Wow it has certainly been a long time between posts. We have had a lot going on around here lately so I haven't really had any time to update. Ok so what has been happening, well we brought Emma home to a hero's welcome lol, her big sister had balloons everywhere and had put a big "Welcome Home Emma" sign in the garden, you couldn't wipe the smile off Em's face when she saw it. I must say that I had a big smile too as it was so nice to be home again.
Pictures of each day Emma was in hospital, I have probably posted them before but I wanted to do this for the relatives and also to have them all together in one post.
DAY 1 - finally get to see our princess after a mammoth 10 hours in surgery (tumour was bigger than originally anticipated which caused a few hiccups for the surgeons)
Day 2 - She started her day in ICU but they then moved her upstairs into high dependency instead which was better anyway as it was a lot quieter.
Day 3 - today we saw Emma's swelling at it's worst. This child did not even look like my little baby and it was so heart wrenching to see. She was not in a lot of pain which was great as they had her on a fair dose of morphine.
Day 4 - Swelling starting to decrease quite rapidly (thank goodness) You can see where the cut starts from behind her ear and it goes almost to the other ear, they also had to cut her from the ear up to the top of her head. She also has the tracheotomy in.
Day 5 - we are finally starting to see our little girl again (praise God)Day 5 also saw another visit from her big sister
Day 6 - Wait..... do I detect a slight smile? Yep day 6 and she smiled, I am thinking it is because she finally got the trachy out.
Day 7 - Not a lot of change from day 6. She is a little happier not the have the trachy in but she is still in considerable pain and is very hungry. Hopefully she gets to take her gastric nasal tube out tomorrow. One of her surgeons told her that she was able to take it out herself which she did on day 8
Day 8 - YAH the nasal gastric tube is out and yes Emma pulled it out herself (insert gagging noises from mummy here) What a very brave little munchkin we have.
Day 9 - We were homeward bound, yep they let us out. Boy it was good to know that I would be finally sleeping in my own bed again. The hospital and staff were great but I don't think I could have slept another night in a recliner chair. We arrived home to balloons and a very happy big brother and sister.
Emma is doing really well, we saw her surgeon on Thursday and he told us that the toxicology reports were back and that none of the cancer had made it to the lymph nodes. He then went on to tell us that he has never seen a tumour as large as that in a child's head in all of his 28 years of doing this. LOL I did have to say that our Emma has never done anything by halves and she probably wasn't going to stop now. If she was going to get a tumour then it was going to be worth talking about (hehehe)
My mother has been up here for three weeks. She had to come up and make sure that Emma was indeed ok..... It has been nice having her here but she went home today which was sad. I really do wish that she didn't live so far away.
The four of us - Mishae, Mum, Emma and Me
Mishae and Mum
Emma (I was playing with the hipstamatic app on my iPhone)
All the cousins on the Love side of the family. Only 3 girls amongst that rowdy bunch of 4.5 boys.....
My Mother in law (Lee), Mishae and Mum
My Brother (Ian), Mum and Me
Stuarts brother, sister and their families came up to see Emma a week ago, so as you can see it has been a very busy time for us.
Emma is back up to the hospital on Tuesday to see the Speech Pathologist and Physiotherapist which is going to be a regular occurrence now for a few months or at least until she can open her mouth again. The tumour had wrapped itself around her jaw bone and prevented her mouth from opening very far and the muscles have not adjusted back yet.
She has been going to school for two and a half hours each morning and we are hoping that she can go back for a full day next week. She is physically ready but I am not sure if she will cope emotionally. She is a bit of a broken little munchkin at the moment but things are getting better slowly each day.
Her next MRI and CT scan are due on the 15th of November and we see her surgeon on the 18th, so until then we will know nothing more.
Ok well if you have managed to get through to the end of this post without falling asleep then well done LOL.
Am going now to try and do some scrapping tonight (if I actually remember how too)