Hey Everyone:
So my appointment was today with my Urologist, Dr. Peter Lau (kidney/urinary tract specialist)... there will be a few days delay in my posting this blog entry because I don't intend to post it before going to my parents house and then speaking with my brother and sister, but I want to give you all an update as well.
My appointment was at 10:45 this morning (Wednesday morning, November 24th) and unfortunately Joel couldn't come with me as he is at a work function in Regina, so my friend Michelle came along with me instead. Michelle just happened to already know Dr. Lau as she is a research nurse and has worked with him in the past. It was nice to know from her that he was a very patient and kind man who would take the time necessary with me and not rush through things. She was totally right. He was awesome and so was she. I can't thank her enough for coming with me and making herself available to me while Joel was away. Thanks Michelle!!!
Anyway, he started off by showing me the CT images of my kidney. Doesn't mean much to someone like you or I, but I got to see them and he explained as best he could about them and showed me where the tumor was on my kidney.
He went on to explain that they couldn't tell for sure what it was unless it was removed and examined by a pathologist (doctors who study and diagnose disease). Biopsies on kidneys aren't particularly effective and are rarely used because they can give a lot of false negatives - showing that you don't have cancer when you actually might. So, they remove them - pretty much all of them. Mine is to be no different. I will have surgery. The mass and part or all of my left kidney will be removed.
Kidney masses/tumors/growths - whatever you want to call them - mine included - have a bad rap, and for good reason. In my particular case, given the size of the tumor, my age, and overall health etc. there is about a 70% that it is malignant (cancerous). If it were kidney cancer and it spread to other parts of the body (metastisizes), traditional cancer fighting therapies like chemotherapy and radiation do not work.
That being said, there is some really good news in my particular case. My tumor is very small. About an inch around. Whatever it is was caught by fluke, and also caught very early. I had a chest x-ray done at my Urologist appointment - it was normal - if it is something that can spread - it hasn't. For these reasons we have to be extremely thankful. Also, because the tumor is so small, they can do a laprascopic surgery, meaning 4 very small incisions (no bigger than about 1cm each) are made to insert a camera and the surgical equipement. This means quicker recovery for me. With this type of surgery there is always the chance that they might have to convert to an open surgery (traditional/old school/normal surgery with a larger incision and more healing time etc) if there were any complications during the laprascopic process. My surgery will likely be sometime in January although I don't know a specific date just yet.
Chemo is only ever used on cancers that have spread, so even if it was effective in treatment of kidney cancer, I wouldn't need it, and I'm also happy that I won't need radiation. I won't lose my hair, I won't destroy my immune system... I'll just have surgery - a surgery that the Saskatoon Urologists do often and have lots of experience with.
The thing about kidney cancer is that if it is caught early, it's one of the more "ideal" cancers to have, because they cut it out and you're basically cured. Even if they remove my entire kidney, I have another one that works just fine and can more than manage to do it's duties for the rest of the 70ish more years I intend to live. It is when kidney cancers are caught late and have spread, the outcome can be much worse and 5 year survival rates go from about 95% to as bad as 5%.
One interesting thing I thought of today was that by the time I know 'what I have' - I won't have it anymore! And for some reason to me, that seems pretty good. Say if it is cancer - by the time I know it's cancer, I won't have cancer anymore. It will be totally removed in the surgery. I'll just be tired and pretty sore with 3 - 6 weeks of unwanted and unpaid time off work... and we were getting so close to paying off our last loan!
Anyway, I'm doing okay - better than I thought I would considering I found out less than 12 hours ago. Maybe I'm still in denial, but I don't really think so - I just think I've already accepted it because my mind went to worst case scenario after my CT Scan 3 weeks ago. Don't get me wrong - the actual surgery scares me more right now than whatever it is that might be every slowly growing inside of me to be quite honest. The thought of a catheter that I'll have for a day or so toally grosses me out, and I read they're uncomfortable, and I'm not super stoked to have 4 little reminder scars on my belly and left side for years to come.
The hardest part though is yet to come. I cannot imagine the worry I am going to cause my family when I tell them about all of this on the weekend. More than anything, I wish I didn't have to tell them. I wish I didn't have to tell my mom that I might have the same cancer as her good friend - who wasn't so lucky as me to catch it early.
If anyone has questions, please let me know. This can be scary for those of you that know me well too I'm sure and I'm happy to answer any questions that I can. Please try to stay positive and remember that this is not necessarily cancer (30% chance!) even though what I talked about focuses largely on that diagnosis. I tried to cover as much as I could, but I'm sure I forgot some important detail somewhere! Email me or post a comment and I'll get back to you.
Luv, Kristie














