I have been diagnosed with CLL from February 2021. My doctor started me on Calquence shortly after diagnosis. My white blood cell count Shot up to 66K and has now been trending lower and is now at approximately 24K. I have been reading some posts about interpreting blood tests and I need some help understanding what levels are important to watch and if there are other blood tests or any tests I should ask my doctor for. It appears as though many folks here talk about mutations and other markers that are very confusing. I’m sure that I can understand the information if it is presented to me, but I need to know what I don’t know.
My doctor just keeps relying on the overall white blood cell count but as I read this Forum, it appears as though there are many other things I need to look for to determine my chances of a long life and also other helpful information
Thanks in advance for any help