Chemo today. Had my oncologist check-up yesterday, and she gave me some more drugs for the excruciating joint pain that I get with this chemo. I told her I'd been eating some magic brownies, and she was fine with that. She said that we live in BC, after all. Hey, whatever works. Last time I had chemo, I had an immediate allergic reaction to the Docetaxel drip--I got really hot right away and had chest pains. So they stopped the drip and pumped me full of steroids and Benedryl via IV. Then they started the drip again. So this time, I'll get premedicated with the stuff to prevent the same reaction.
I gather from my nurse and doc that what I experienced with the last chemo is only going to get worse, as the effects are cumulative. But the good news is that after this chemo, I only have 2 more! I should be finished with chemo in the second week of January.
Then comes the radiation. We met with the radiation oncologist on Monday, and it was explained to us that the benefits of radiation are good and proven, that the chances of secondary cancer is less than 1%. So starting at the end of January, I will go in every day for five and a half weeks to get my radiation. I was told that it's like going out in the sun, that I will tan on the radiated area. Folks, I don't tan--I burn, like within ten minutes of being in the sun--with 50 SPF sunscreen. But if I get bad skin irritations, they will, of course, give me yet another prescription.
This morning, before I go in for my chemo this afternoon, I'm going to do the whole home spa thing. Long hot bath, good reading (I'm reading Inventing Victor, which is a collection of short stories by my friend Lisa's friend, Jennifer--and it's great!), sitting in my new massage cushion (DH bought me a new wonderful massage cushion yesterday at Costco, which has a rolling function, a shiatsu function, and a heat option!). I'm hoping that after chemo, I won't be too wiped out to go to the end of the term Creative Writing party on campus. I haven't seen a lot of my creative writing cohort in a while.
I want to write about all the fun stuff that's been happening in the past two weeks and try to forget all the crappiness (since that will be soon revisited anyway). Lisa and Vicki's visit was a godsend, if only a little too short for my taste! It was so wonderful to hang out with my best friend from home and her mom, and take them to all my favorite restaurants and places in Vancouver. Luckily, the weather wasn't shitty the entire time, as we were blessed with some wonderful sun. I think they really enjoyed it, and I hope they come back soon. When I'm not a lazy ass, I will download some of the pictures and post them.
Then we had two wonderful events for the book I edited that came out of the workshop that I taught back in February and March. The book is called Eating Stories: A Chinese and Aboriginal Potluck. I went on CBC on Friday morning to talk about it, then three of the authors went on CBC on Sunday morning for an interview, and other authors and folks are going to appear on radio, tv, and in print about it. People seem really excited about it! So I celebrated my birthday at our launch on Sunday, with song and cake and flowers (thanks, everyone!). And then we had dinner with DH's folks and sister and her family (before the launch we went out to brunch with DH's parents at Cafe Pacifica in the Pan Pacific Hotel). Then DH and I went to see Beowulf on 3D Imax (which would have totally blown chunks if not for the impressive 3D effects). It was a great day!
Last night, our pals Michael, Anne, Debora, and Lynda brought over a fantastic dinner (sushi from Hiroshi's, noodles that Michael made, and salted cod that Debora made), and frozen soups. We had great conversations, enjoyed the food, and it was just so great to see my pals.
But the best thing that happened in the last few weeks was when we were at our family doctor last week, getting our flu shots. While we were waiting for her to come into the exam room, Chloe grabbed my head and pulled it to her ear and said, "Mama, I can hear the ocean. I can hear whales." Granted, it's like she's saying I'm empty-headed, but it was wonderfully poetic to me.
Showing posts with label doc update. Show all posts
Showing posts with label doc update. Show all posts
Wednesday, November 28, 2007
Monday, October 29, 2007
Natural Highs, Liquid Lows
I walked miles and miles last week. One day, I walked from the cancer agency, across Cambie Bridge, along the seawall where all the Concord Pacific condos are, all the way to English Bay. I sat there for a while, waiting for DH to come join me. About two hours as a matter of fact, but he got caught up in the office. It wasn't exactly warm outside, but there were moments of sunshine here and there, and I watched people fly kites and do tricks. I watched people walk their dogs. I watched leaves flying around. Here's the view I had:

And here's the bench I sat on. There's something magical about memorial benches.

I want to do more physical activity, but I find myself getting tired more quickly, especially on one of my long walks. I feel the need to nap more. And yeah, I shouldn't be drinking alcohol like I'm accustomed to. I did that on Saturday night with DH, his sister and her husband at Parkside restaurant, and I was paying for it all night long. You know how these prescriptions say not to drink alcohol while taking the drugs: I forgot to pay attention to that. I had a really awful, painful pukefest all night. I hate not being normal.
Today, we're meeting with the oncology surgeon again. Hopefully, this time around, she has our info and will have a more informative meeting with us. I actually got a copy of my chart on Friday just so there are no excuses. I remembered that DH's brother had to get his chart to make sure about the situation because when you have to deal with so many doctors and specialists and their staff, something is always bound to get lost in the cracks. So it was a good idea to get the chart.
This week I also have an ECG, an ultrasound and a core biopsy. Next week I start the new chemo. Fun.

And here's the bench I sat on. There's something magical about memorial benches.

I want to do more physical activity, but I find myself getting tired more quickly, especially on one of my long walks. I feel the need to nap more. And yeah, I shouldn't be drinking alcohol like I'm accustomed to. I did that on Saturday night with DH, his sister and her husband at Parkside restaurant, and I was paying for it all night long. You know how these prescriptions say not to drink alcohol while taking the drugs: I forgot to pay attention to that. I had a really awful, painful pukefest all night. I hate not being normal.
Today, we're meeting with the oncology surgeon again. Hopefully, this time around, she has our info and will have a more informative meeting with us. I actually got a copy of my chart on Friday just so there are no excuses. I remembered that DH's brother had to get his chart to make sure about the situation because when you have to deal with so many doctors and specialists and their staff, something is always bound to get lost in the cracks. So it was a good idea to get the chart.
This week I also have an ECG, an ultrasound and a core biopsy. Next week I start the new chemo. Fun.
Labels:
activity,
bad daze,
coping,
doc update,
good daze
Monday, September 24, 2007
Bright Light, Dim WBC's
I went on CBC this morning and gave an alright interview: CBC Brandy Interview . . . It's hard to think of what to say that early in the morning. Oh yeah, and you need Real Player to be able to listen to the interview.
Anyway, then I had my usual lab work done this morning to check how my white blood cell (WBC) count is going. After I got poked, I noticed that my band-aid was slipping off because I was bleeding profusely from the tiny prick. So I went back to the nurse, who cleaned me up and gave me another band-aid.
Later, I had my appointment with the oncologist. They told me that my WBC count was low enough to be concerned, and that from now on, I'd have to inject myself with a drug that would help boost my WBC count. So starting with the cycle tomorrow, I have to give myself an injection every other day, and this will last through the remaining chemo treatments. Sounds like it sucks, but I'm sure I'll get used to it. It was kind of a bummer though, because I was hoping that with my good energy levels and me exercising and taking good supplements, that I'd be strong and all that. But it seems that my body has other plans in mind.
Good news is that the chemo seems to be working. The oncologist said that the lump feels smaller, so that's a positive sign for sure! So the experiment that is my life continues.
Anyway, then I had my usual lab work done this morning to check how my white blood cell (WBC) count is going. After I got poked, I noticed that my band-aid was slipping off because I was bleeding profusely from the tiny prick. So I went back to the nurse, who cleaned me up and gave me another band-aid.
Later, I had my appointment with the oncologist. They told me that my WBC count was low enough to be concerned, and that from now on, I'd have to inject myself with a drug that would help boost my WBC count. So starting with the cycle tomorrow, I have to give myself an injection every other day, and this will last through the remaining chemo treatments. Sounds like it sucks, but I'm sure I'll get used to it. It was kind of a bummer though, because I was hoping that with my good energy levels and me exercising and taking good supplements, that I'd be strong and all that. But it seems that my body has other plans in mind.
Good news is that the chemo seems to be working. The oncologist said that the lump feels smaller, so that's a positive sign for sure! So the experiment that is my life continues.
Subscribe to:
Posts (Atom)