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Wednesday 27th January 2016
Hello
Yesterday I had my Long Chemotherapy Treatment day. This is what happened....
Tuesday 26th January 2016
9am My Long Chemotherapy Treatment day happens today. It was cancelled last week because of my PICC line problem and removal. So with my new Hickman line (which has a wider bore on the line. Less chance of blocking) installed in my chest, there should be no problems. No problems at all.
(so I thought)
My chemo nurse tried to take bloods from my new line, to make sure it is clear for todays chemo infusion. No blood flowed from my body. I was asked to cough alot, wave my arms, walk on the spot, etc. to get my blood flowing. Nothing happened. She tried teasing any blockages with a saline line flush injection. My bloods still did not flow.
A second nurse was asked over to have a try. Nothing. So I was put horizontal on a bed, same try again to take blood. Nothing still. Was asked to turn my head and cough alot again (throat was in agony), waving of arms, turning of my body.
Nothing still!
So I was given (surprise, surprise) 'urokinase' injected into my new line, and wait one hour for it reduce any line blockages. That means my chemo treatment is put on hold till the nurses see what develops in an hours time.
10:30am Blood flowed super fast into my nurses syringe. We are all happy. That means they can go ahead with my treatment.
Later on I was wearing a woolen jumper with front zipper, to make my new Hickman line more accessible for the nurses. Was feeling the heat. I should wear lighter tops for my treatments. Nose and eyes were watering and throat was raw from earlier dry coughings.
Later on in the afternoon the ward doctor had a look at my now-improving cuticles of my fingertips/big toe. She is really happy, and I have to continue with the meds I get to take home. Good stuff!
5:10pm I got my chest pump attached. It is the same as the previous arm pump. 46 hours of meds are pumped into me, at home, and I go back to the hospital to get it disconnected at 4pm on Thursday (a few days later). Then the nurse said I could go home. I grabbed a coffee from the reception machine, and half an hour later my brother picked me up to go home.
So I will be back in the hospital on Thursday afternoon.
............................................................................................
All the best,
Muz xxxxxxxxxxxxxxxxxxx
Hello
Yesterday I had my Long Chemotherapy Treatment day. This is what happened....
Tuesday 26th January 2016
9am My Long Chemotherapy Treatment day happens today. It was cancelled last week because of my PICC line problem and removal. So with my new Hickman line (which has a wider bore on the line. Less chance of blocking) installed in my chest, there should be no problems. No problems at all.
(so I thought)
My chemo nurse tried to take bloods from my new line, to make sure it is clear for todays chemo infusion. No blood flowed from my body. I was asked to cough alot, wave my arms, walk on the spot, etc. to get my blood flowing. Nothing happened. She tried teasing any blockages with a saline line flush injection. My bloods still did not flow.
A second nurse was asked over to have a try. Nothing. So I was put horizontal on a bed, same try again to take blood. Nothing still. Was asked to turn my head and cough alot again (throat was in agony), waving of arms, turning of my body.
Nothing still!
So I was given (surprise, surprise) 'urokinase' injected into my new line, and wait one hour for it reduce any line blockages. That means my chemo treatment is put on hold till the nurses see what develops in an hours time.
10:30am Blood flowed super fast into my nurses syringe. We are all happy. That means they can go ahead with my treatment.
Later on I was wearing a woolen jumper with front zipper, to make my new Hickman line more accessible for the nurses. Was feeling the heat. I should wear lighter tops for my treatments. Nose and eyes were watering and throat was raw from earlier dry coughings.
Later on in the afternoon the ward doctor had a look at my now-improving cuticles of my fingertips/big toe. She is really happy, and I have to continue with the meds I get to take home. Good stuff!
5:10pm I got my chest pump attached. It is the same as the previous arm pump. 46 hours of meds are pumped into me, at home, and I go back to the hospital to get it disconnected at 4pm on Thursday (a few days later). Then the nurse said I could go home. I grabbed a coffee from the reception machine, and half an hour later my brother picked me up to go home.
So I will be back in the hospital on Thursday afternoon.
............................................................................................
All the best,
Muz xxxxxxxxxxxxxxxxxxx
Murray - update
Hello everyone, this is Murray's brother Donald.
I know Murray was using this journal to keep you updated on his progress. It breaks my heart to have to write this but he sadly passed away last Friday evening. He had been hugely strong throughout these last three years and is now at peace.
His health deteriorated quickly over the last week and he died peacefully at the Marie Curie hospice in Fairmilehead, Edinburgh with his family around him. I know he had a lot of friends on here who gave him loads of support and for that I thank you.
I want to make sure his legacy is preserved on here and will need to work out the best way to do that.
Haemoglobin Levels
Thursday 12th July 2018
Hello there.... :wave:
I got a phone call from the Cancer Clinic yesterday morning, from one of their nurses. It seems my 'Haemoglobin' levels have not changed (after they studied my blood sample taken by my GP on Tuesday). The nurse is happy that the level has not dropped, but still wishes to get another blood sample, next Tuesday via my GP (the week before my next cycle of chemotherapy treatment). If it does drop, they may give me another blood transfusion. We shall see what happens. The earlier they know, the easier it will be for the clinic/hospital to book me bags of blood for the possible transfusion.
--------
Update on Chemo
Friday 6th July 2018
Hello,
Yesterday was a bit muddled!! I shall continue...
----------xXx----------
Thursday 5th July 2018
At 11:30am I got a taxi to the the Cancer Clinic. I met the Cancer Doctor that I had the chat with about the results of my recent CT-SCAN. I quickly mentioned my current gastric 'PLUG' problem thing which had bothered me for a while. It had fantastically disappeared/moved out the night before. So my sleep positions were back to normal and I could get more sleep with less soreness. Only pain when sleeping would be my right-hand side where my tumour is (it swells my liver up also). I avoid that side. We were both hap
Summoned
Tuesday 3rd July 2018
I gave blood at 10:20am today (same every third Tuesday, a few days before my next cycle of chemotherapy treatment on Thursday). It went ok. Because of my recent anemia I felt ancient getting a bus up the road home instead of walking.
12:00 noon I got a phone call from a nurse at the cancer ward asking how I have been coping. I explained my gut/tummy pain (opposite to liver/tumor side) which has been very uncomfortable, especially when I attempt to sleep. I also told her of my anemia creeping back like before.
She phoned back later requesting me to go into the cancer ward in a few hours for a checkup by a ward doctor.
© 2016 - 2024 muzski
Comments11
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Heyo, installation problems!
Glad your nurses and doctors got it to work right, and your cuticles are less of a pain
I have mental images of you flailing your arms and hacking like cat with a furrball hee hee.
Keep truckin' trooper!
Glad your nurses and doctors got it to work right, and your cuticles are less of a pain
I have mental images of you flailing your arms and hacking like cat with a furrball hee hee.
Keep truckin' trooper!