Day zero is the name given to the day of your stem cell transplant. This will happen this afternoon, 48 hours exactly after my chemotherapy took place. The extra day has been to allow my kidney time to flush the Melphalan out of my body, so it won't kill the newly introduced stem cells. I … Continue reading Day Zero
The blackbird chirps away behind my window. Gladly greeting the morning. Regret not taking the sleeping tablet. It's been a steroid sleep. Wakeful hours. Toilet trips. Soon the midsummer sun will rise. A new day. An Abingdon day. Here to celebrate. A birthday. Nineteen Years on. Happy Birthday Son!
I have a new ally in the fight against sleeplessness. Following several weeks of disrupted sleep I have got prescribed some sleeping tablets. So welcome on board a new drug to be taken as and when necessary. The drug is Zoplicone. The drug has the advantage of helping me to sleep without leaving me drowsy … Continue reading Sweet Dreams
Progress is being made and I continue to remain healthy and better than I have been for several months in so many ways. The chemotherapy is working but there is a battle going on, inside a drugs war against my very own mutant cells. The bad guys, Myeloma Cells, are being taken out but there … Continue reading Drugs War
A summary of the whole process I am undergoing.
Information here is taken from various booklets received by me and interpreted in a non-expert way - they should not be taken in any other context than my own - possibly muddle opinions. Chemotherapy is not a single thing. It is not a static process but a dynamic one which combines different drugs taken over … Continue reading Chemotherapy (VCD) – Basics