So today completes the 3 days of chemo. 2 days of no treatment to follow before he gets his cells back. He has slept most of the day bless him. Waking only for the toilet and to eat. Not sure he's done all his mouth washes so hoping he doesn't get a sore mouth. Nurses changed the way anti sickness is given as apparently he can't have it through syringe driver whilst on fluids. So half of it (nonsa sonething) is given via injection. Pete thinks this is there name for the levopromazine. Odd cause he had it all through syringe driver last time and know one said any different.
Had to give up my room for the night as a man was coming from the Isle Of White to visit someone and needed a room for the night. I've got a reclining chair in Petes room to sleep on. Not that I expect much sleep worrying about him and my mom who is due her 6th camera down her throat tomorrow To do another biopsy of tumour on her duodenum. I hope to god they sort a way of removing soon before she has a nervous breakdown from the stress of going through this so many times with so many Dr's.
