Round 8

We are back in ward C2 for round 8 of chemo. This is 24hrs of chemo followed by 24hrs of hydration. That, combined with pre-hydration, means the earliest we can get out is Sunday evening.

Holly was good last night. No sickness and a good night sleep (although numerous toilet trips).
Today has been a bit rougher. Holly felt fine this morning and managed a 2 course breakfast. It then went downhill and the sickness kicked in. She has only been sick twice but the constant feeling of nausea has been making her a little grumpy! She did, however, manage to find some energy to do some arts and crafts. The bed is now covered in glitter, as is Holly and the floor! She is even feeling hungry and has sent Dad and Kirsty to the supermarket for more supplies.

The doctors are really pleased with how well Holly is doing and the way she is tolerating all the treatment. Amos (doc) explained that the next step will be to decide whether to do surgery. This will be decided after all her scans which will take place over the next couple of weeks. Her GFR test showed her kidneys are working normally. If she does have surgery then the next step will be very high dose chemo and a stem cell transplant. This is very tough on the body and will require at least 3 weeks in hospital (most of which will be in isolation). If she doesn't have surgery then the stem cell transplant will just be brought forward. It is very strange to know that Holly won't be having any chemo throughout May, her body should have a good chance to recover (and her weight a good chance to build up!).

Whether we get to go home tomorrow depends on Hollys blood results. If she needs platelets then they will be fitted in tomorrow. If she needs blood then they will run into the night, so it will be Monday before we get home. Please keep fingers crossed as it is my gorgeous little Harrys 1st birthday tomorrow and we are having a party for him on Monday. They are coming to visit tomorrow so that should be interesting (if a little noisy).