The results are in and not good. I seems I have extensive liver mets. We are looking at chemo. I will know more when I see the head of the oncology department. We are trying to get that appointment as soon as possible, maybe even next week. I want to start treatment as soon as possible. I don't want to delay at all. The sooner treatment begins the better.
I asked about liver biopsy but with so many mets (too many to count) there doesn't seem to be any point.
I asked about a PET scan, that is an out of pocket expense and means travel to the US. Not an option for me.
I asked about surgery but with so many mets, how can we be sure to get them all and still leave me with a liver?
I did tell her the nausea has been ongoing since I started the aromasin. It gets no better nor worse, just stays the same, there all the time.
Radiation for bone mets is an option but will wait on that until I know what else I am facing. I may be able to do that after chemo.
The hydromorph contin is back in place with a dose right now of 9mg twice a day, along with maxeran to control the nausea. If the maxeran doesn't work I am looking at taking zofran long term.
All I can say right now is I am angryand saddened
by what I learned today. I will be talking with my SIL and letting her know what is happening. My children will not be told until I know what the treatment plan is. Until then I will keep things pretty close to my heart.
Thanks for all your prayers and support. Love Lana.


and saddened
by what I learned today. I will be talking with my SIL and letting her know what is happening. My children will not be told until I know what the treatment plan is. Until then I will keep things pretty close to my heart.
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