Just life And pembrolizumab

Well after my immunotherapy treatment last Tuesday I was so tired until, at last, today I felt better. It’s the same thing each time, well that and the joint aches and itchy skin but I have meds for those. I have pembrolizumab every three weeks at the local chemo suite and have had 4 so far. CT due in July and it will be a very scary result day after that. I really hope it’s working at least to stop any further progression.

Had a chilled day and just sat crocheting blankets to gift locally to keep me busy. Also reading as usual and doing the odd review. Always try to keep myself occupied as otherwise I tend to dwell on morbid things and end up feeling sorry for myself which just doesn’t help

9.30pm so time for bed