Ya, I'm starting cytotoxic chemo tomorrow.

 The MD/Researcher, Dr. Haverkos, called this afternoon to talk about yesterday's PET scan. It appears the first couple months the drugs held the disease at bay but the last two months, it has take off. After asking other questions I don't have the energy to share right now, he suggested I go into the hospital tomorrow and start Brentuimab and CHP. The letters all stand for drug names. 

Again, I'm struggling to stay awake so I'm not including as many details right now. 

The time in the hospital is a stretched out series of IVs, instead of the usual doing it all at once, to protect my kidneys that already seem stressed. The first round of chemo (I will do 6) kills off the most tumor load, so stretching it over a week is a good idea. 

After 2 months, we will do another PET scan to see how we are doing. 

I feel like it is time to get after this and see if we can actually get it into remission. He mentioned a Bone Marrow Transplant, which I hope we don't have to do. We shall see. 

More details to come. The doctor said that he suspects I may be one of those people who actually feel better after a couple rounds of chemo. I hope so. It's been a challenging several months. 

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