So it looks like things are moving quicker this time round. Pete is doing OK in himself, still eating & no sore mouth etc.. although he has slept all day. Not sure if it's the anti sickness meds or chemo causing this. Metroclopramide and levopromazine in syringe driver. Metroclopramide, Ondansatron and cyclozine orally. The reason I say things are moving faster is he was told today he now has to stay in his room as his neutrophils are 0.3 this is only day 2 of chemo. He has 3 days then a 2 day break then cells replaced. Last time his neutrophils didn't hit this till 3 days after having his cells back and didn't have to stay in his room till the day he had them back. I'm hoping this doesn't mean there will be an accumulated effect each time he has transplant and be worse each time but I guess we will just have to wait and see. He was so well last time so we should be greatfull for that, I just want to be greedy and have them all go so well
