Hi everybody,
My name is Livia and I do not post very often but I read every single email I receive.
Just a little bit about me. I was diagnosed in February and I am on Gleevec 600 mg. Sometimes they put me on 400 and after they change it to 600. I do not experience many side effects. I am from
I do not know what to do. If to go back to my country or stay here. I miss my family and their support, my friends, peaceful and slower life over there, BUT there is not Gleevec. So far I know they are testing it. So basically I can?t go home. I have never felt so powerless in my life. Young, full of ambitions, helping other with problems and now I feel like I can not help myself.
I also have a doctor who is not a specialist for CML. I am frustrated. In order to change a doctor, I have to change my insurance, which is possible in January 2006. I hate it so much !!! Are there any possible consultations with doctors who are specialists?
I am thinking about the future and I can?t help myself, I just can?t. Everybody says, do not worry about it, just live life from a day to day. Yes, but after I can not think about having a baby, about going back to my native country, and many other things.
Any help is appreciated. I also do not know what it is RDW. When they take my blood the only result which is a little bit high is RDW. On Monday I have a bone morrow biopsy and I am scared. It is so uncomfortable and she wants to take also a piece of bone. I can?t sleep a week before I am supposed to have it. Some of you wrote some percentages and that you are in PCRU or CR? I do not know where I am and how my results are. My blood counts look fine though.
I think it is enough for today. I am sorry for mistakes and maybe I repeated some sentences as usually, but I am at work and a little bit frustrated today : )
Hugs and blessing to everybody,
Liv
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