Friday 23 March 2018
School again!!!!
I managed to have a morning at school today after finishing chemo on Wednesday morning! When I came home at 12pm I realised that it probably wasn't a great idea to go to school as I got really tired and when I got home in the afternoon I was in bed for the rest of the day. I just have to remember that it is still only 2 weeks since my surgery!
Monday 19 March 2018
"Clean up" chemo round 1!
Today is my dads birthday! Happy birthday dad!!!!
Like usual I wasn't bored because I always found my self something to do like.....
Painting easter chics, writing notes on the whiteboard, eating, sleeping, colouring in pencil cases and counting my beads of courage.
Thursday 15 March 2018
Time to Shine
I have been nominated for an award "Child of Courage "
The awards evening is at Chorley Town Hall tonight.
All the children who had been selected for the final got an award and I was one of them!
When we got there we realised it was being hosted by Steve Marsh from the Rock FM Breakfast Show!
He was also BIG COOK in children's program Big cook Little cook!
I was really excited to meet him as I listen to him every morning on the radio!
During the interval I got to meet him and he promised to give me a shout out on the radio!
The awards evening is at Chorley Town Hall tonight.
All the children who had been selected for the final got an award and I was one of them!
When we got there we realised it was being hosted by Steve Marsh from the Rock FM Breakfast Show!
He was also BIG COOK in children's program Big cook Little cook!
I was really excited to meet him as I listen to him every morning on the radio!
During the interval I got to meet him and he promised to give me a shout out on the radio!
A big thank you to Kirsten and her Mum Gill for nominating me....
Tuesday 13 March 2018
Feeling much better
They are removing the pumps one at a time and I am feeling better! There's no stopping me now!!
I did a lap of the ward and I am now feel really tired.
We decorated my room's window.
I pack all my stuff up and go home! ALL DONE!
Wednesday 14th March
Today I am just resting at home, I am really tired!
Monday 12 March 2018
Fish and Chips!
Today I am feeling much better and had Fish and Chips for my lunch!
The Surgeon came to visit me and said I looked fab! He said I could have my catheter removed today so I will be more comfortable!
Dr. Farrelly, my surgeon
The Surgeon came to visit me and said I looked fab! He said I could have my catheter removed today so I will be more comfortable!
Sunday 11 March 2018
Sunday - Mothers day
Today my mum is in hospital with me and I have sneeked a card in for her.
They said I was doing so well that they can remove the drain pipes in my back YAY!
Taking the pipes out REALLY HURT!!!!!!!!!!!!!!
But I feel better without them! Step nearer going home!
They said I was doing so well that they can remove the drain pipes in my back YAY!
Taking the pipes out REALLY HURT!!!!!!!!!!!!!!
But I feel better without them! Step nearer going home!
Saturday 10 March 2018
Recovering from my operation!
Friday 9th March
At 5am this morning my temperature spiked to 38.2. this is not good!
The doctors started giving me lots of antibiotics and paracetamol every 6 hours!
Because my temperature keeps going above 38 they are worried about infections and low immunity due to chemo, so they are moving me from a ward with 4 beds to an isolation room with just me in it!
This is much better as we have more space and our own bathroom!
The pain in my back and lung is really bad, so they are giving me paracetamol, morphine and ketamine also chirocane is being pumped directly into my back!
I also have 2 drain lines going into my back to take the fluid out of where my lung should be.
So I have 7 pipes connected to me! Very hard to sleep at night because of the pain, all the pipes and the pumps beebing all night!
Milly came to see me this morning.
Saturday 10th march
I am starting to feel a little better and the nurses have turned the painkiller pumps down a little!
This afternoon I had a chest X-Ray to check there is no fluid in my lung. My nurse said it would be better for me to try sitting up more today so the lungs will naturally clear any fluid. I managed to sit in a chair for 45 minutes.
Milly visited me again today and she cheered me up!
At 5am this morning my temperature spiked to 38.2. this is not good!
The doctors started giving me lots of antibiotics and paracetamol every 6 hours!
Because my temperature keeps going above 38 they are worried about infections and low immunity due to chemo, so they are moving me from a ward with 4 beds to an isolation room with just me in it!
This is much better as we have more space and our own bathroom!
The pain in my back and lung is really bad, so they are giving me paracetamol, morphine and ketamine also chirocane is being pumped directly into my back!
I also have 2 drain lines going into my back to take the fluid out of where my lung should be.
So I have 7 pipes connected to me! Very hard to sleep at night because of the pain, all the pipes and the pumps beebing all night!
Saturday 10th march
I am starting to feel a little better and the nurses have turned the painkiller pumps down a little!
This afternoon I had a chest X-Ray to check there is no fluid in my lung. My nurse said it would be better for me to try sitting up more today so the lungs will naturally clear any fluid. I managed to sit in a chair for 45 minutes.
Milly visited me again today and she cheered me up!
Thursday 8 March 2018
In Recovery
At 2.10pm the surgeon came to the ward to tell us that Sally was fine & was now in recovery.
He explained that the operation had all gone according to plan. He had removed only the one rib & a 50p piece size of the lung. He said he could see nothing else that needed removing. Everything had been sent to Pathology for testing. We then had to wait another hour before we could see her.
He explained that the operation had all gone according to plan. He had removed only the one rib & a 50p piece size of the lung. He said he could see nothing else that needed removing. Everything had been sent to Pathology for testing. We then had to wait another hour before we could see her.
Surgery!!!!!
We set off at 6.10am in the snow. We had to be there for 7.30am. This time I am on Ward 77.
The anaesthetist came to see me first, then Dr. Farrelly & his team. He drew an arrow on my back.
(By Mum)
At 9am Sally was walking to theatre with mum, dad & our nurse for the day, Daniele. (With one l). Only one of us was allowed in the pre-operative room so dad stayed in the waiting room.
When they were putting Sally to sleep she remembered to count this time & managed to get to 9!!!
I then had to leave Sally in their capable hands.
We now had time to kill. Dr. Farrelly had said the op would be 3-4 hours minimum.
So what do mum & dad do for the next few hours?
Well, Richard has a couple of machines on his work schedule for March at Manchester hospital & he suggested that he could do them today! Obviously, I wasn't too impressed at the idea until he suggested I go with him. A chance to see the machines he works on? Why not? It'll fill some time. Better than pacing the floor!
The anaesthetist came to see me first, then Dr. Farrelly & his team. He drew an arrow on my back.
(By Mum)
At 9am Sally was walking to theatre with mum, dad & our nurse for the day, Daniele. (With one l). Only one of us was allowed in the pre-operative room so dad stayed in the waiting room.
When they were putting Sally to sleep she remembered to count this time & managed to get to 9!!!
I then had to leave Sally in their capable hands.
We now had time to kill. Dr. Farrelly had said the op would be 3-4 hours minimum.
So what do mum & dad do for the next few hours?
Well, Richard has a couple of machines on his work schedule for March at Manchester hospital & he suggested that he could do them today! Obviously, I wasn't too impressed at the idea until he suggested I go with him. A chance to see the machines he works on? Why not? It'll fill some time. Better than pacing the floor!
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