In a completely unrelated note, you have no idea how happy it makes me to have taken a pretty picture again. :) Settings are ISO400, f3.2, 1/250 SS taken with my 35mm lens, straight out of camera
This makes me happy for so many reasons! One of which is that I find it reassuring that Rory sweats about as much as our two girls. Must be a Korean thing :)
Anonymous said…
Wonderful!!!!
Briar sweats in the exact same place on her nose. :O)
In the past 48 hours I've received 9 emails asking how I'm doing. I've been debating writing this post for more than 48 hours, and I may regret it later, but I'm tired of pretending that I'm fine so I'll just answer you all here. While I don't feel well physically, emotionally I feel completely battered. I knew this was going to be hard, but I clearly underestimated how hard it would be to face the reality that chemo is now my way of life. That I'm never going to get to quit. That there is no hope of a cure. That I am probably not going to see my children grow up or grow old with my husband. That physically, this is as good as it gets. I know I should look at chemo as a gift. It's supposed to kill cancer. But chemo hasn't proven to kill my cancer; it just makes me sick. I'm tired of being an "inspiration." Tired of choosing joy, choosing gratitude. Tired of not knowing where we'll live or work. Tired of waiting on God...
Knowing my recent health history, you're not expecting good news, right? As I suspected, it was not pleasant to hear how difficult my physical situation is. Basically, the doctor told us that the best we can hope for is to keep the cancer stable, and I will remain on chemo indefinitely. I could not make myself ask how long that might be. Despite the bad news, I realized after several hours of reflection (and by reflection I mean crying and resisting the urge to scream at someone, something) that God did answer our prayer. We asked to feel calm, and we asked that the choice would be clear. The cancer center treated us very well; the staff was compassionate; the doctor spent a full hour with us giving us more information on ovarian cancer and treatment than we have received in the last 7 months. My treatment would have been the same at Vanderbilt as it was with Dr. W. The Taxol/Cistplatin/Carboplatin is the standard treatment. Ovarian cancer is rare enough and complicated enough th...
Talked to my nurse today and Dr. W wants me to come in so he can discuss my scan. This is a little bit of new territory for us because he's never discussed before - just put me on a new treatment plan. The nurse said there was a note on the scan saying that there were no new masses and my original nodules remained unchanged, but my CA125 was 19.4 this month so that means an increase 2 months in a row. If I had to guess, I would say that Dr. W is going to tell us that he's got nothing left in his chemo arsenal to try since I've now had a total of 6 different chemo drugs and they have had no effect. I suppose I should feel lucky/grateful for a slow-growing cancer. I would rather feel grateful for no cancer, but that is clearly not going to be my story. Unfortunately, because of the office/hospital switch, his earliest "discussion" appointment isn't until January 22. The nurse is going to try to fit me in so I don't have to wait for 2 weeks, which I ...
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One of which is that I find it reassuring that Rory sweats about as much as our two girls. Must be a Korean thing :)
Briar sweats in the exact same place on her nose. :O)
My father is going through treatment for lung cancer......I will add you to my many prayers.