My next steps

 I met with the oncologist on Thursday and then saw my radiation doctor on Friday. I was given quite a bit of information. Nothing that I don't feel like I can't handle. I'll start with the oncologist. My oncologist I really like. I feel like he actually listens to what I am saying and wants to make sure that I am understanding everything that I am being told. He tells me that I am not a statistic but a person. Which is very reassuring to hear. It turns out that there is not a second cancer. My esophageal cancer did migrate to my brain. This is very rare. He said that he has only had this happen one other time. The treatment plan is to do radiation. If not then the chances of it coming back is 60% as where if we do radiation the chances are 10%. Of course there is chances that there are cells throughout my brain so I will have to have frequent MRI's to make sure that nothing is growing. Now onto the radiation doctor. He is a great guy too. He said because of how big the tumors were that they had been there for a while. He was surprised I was not having headaches. I never had headaches, nothing that made me think that something was wrong with my brain. We found it by a chance. Regardless.. I am going to do 5 treatments where each tumor was. Every other day. Not sure yet if they can do both areas at the same time or if we are hitting one first and then the second one. If we do both at one time then it's about a week and a half. If not then it is going to be about a month. Whatever the time length will be it is ok as long as I get it done. All of this leaves me tired still. I know that I will be tired for a while but that things will get better. They did before and they will this time. 

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