I did get into Ipswich hospital - (a bed came available) - in ice and cold on Monday evening - ready for the chemo on Tuesday.
Tuesday - a heavy day. The complex infusions started mid afternoon and ended at half-past midnight. The morning a nightmare of wondering whether it would happen and being seen by various (helpful) people. For example - a palliative care doctor. Exhausting. The afternoon and evening - a nightmare of boredom and exhaustion, especially as the machine that handles it appeared to malfunction - in fact it was the cannula - adding an extra 2 hours to the 7 that it takes in theory.
Today - I was released in the afternoon - after various tests. Good (if somewhat exhausting) to be home.