Originally posted by suityou01
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They haven't finished counting nodes from the cat scan yet, and the scans don't show them all anyway. By this stage that doesn't really matter, the degree of spread in lymph nodes is more to do with when it's caught early and surgery to remove stomach + lymph nodes is still an option.
M number = whether it's spread. I'm M1, obviously.
My doctor(s) have been plenty aggressive and utterly fantastic at explaining what they are doing and why. Every "next" test has been lined up straight away, and they have listened to every suggestion and request, be it to use ultrasound guidance when doing the drain or just to hold off on an uncomfortable procedure for a day or two while I got my strength back from the last one.
There are actually quite a lot of them, led by a very kind faced lady who has obviously managed more suffering than you or I would really care to imagine. I have a good rapport with them and feel comfortable, I don't think you can understand just how much that counts until your going through it.
Bear in mind I have been researching this pretty thoroughly myself, it may sound arrogant but I trust my own research and opinions. I also have two friends who are doctors (although not oncologists) who I can informally ask if I have any doubts. So I don't really feel the need to take on the hassle of second opinions and further referrals which TBH probably risk delaying the start of the chemo. At the moment that is scheduled to start literally as soon as is physically possible given the wait for genetic test results.
I really am in good hands.
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