Treatment days 2 - 5

November 8 - 11: Treatment continued as planned. Basically, five hours on an IV waiting for fluids to drip into the veins. I feel okay through it all, just a little tired. Anti-nausea medication is working fine - I feel like eating most anything. Steriods to keep up blood cell counts deliver a side effect of being wired. They keep a permanent IV catheter in my inside forearm for easier access. But the limit is three days so on Thursday one came out and a new one was inserted on Friday.