I had breast cancer - but I got better.... A posse is a group of people who ride out with you into the teeth of trouble. They generally have your back. This blog contains notes for all those who have watched and supported my ride...
Mar 14, 2010
An Interesting Weekend
I'm not at all sure what's happening this weekend. I go the new chemo agents (Taxol and Herceptin) on Friday but I didn't get the side effects I expected. The confusion started on Friday morning in the Infusion Center when the nurse declared that my 'orders are all wrong'. Not a comforting thing to hear. Apparently, she could alter some of the orders, but I was still getting the Taxol and Herceptin, just like I thought. At the time, it didn't seem necessary to go into the ask-a-million-questions mode. Some of the things that the oncologist said seemed to be contradicted by the nurse. Like - I wouldn't need a Nulasta shot on Saturday, which they sent me for anyway. The Nulasta shot helps support the immune system, which is blasted by chemo. I was told, though, that Taxol doesn't need Nulasta but I went to get the shot anyway, like the nurse said, b/c it can't really hurt. I'm wondering about that thought right now because my bones and joints are aching big time! To add to the fun, the Nulasta nurse, on Saturday, said that I got the 'dense' dose of Taxol which is given every other week. I'm supposed to get Taxol every week. So, do I feel so lousy because I got too much Taxol?? Sooo, tomorrow morning, I'll be getting back into commando mode; getting answers! Look out Sinai!
Mar 2, 2010
My Big Feet
Hey, looks like I haven't blogged in a while. Guess that's because, until a few days ago, things were pretty quiet - or maybe I'm getting used to the 'chemo effect'. What a crappy thing to get used to! I'd much rather be getting used to sitting on the nice, hot beach under an umbrella with a cool drink. But, then something comes along to jolt you out of your stupor. My feet and hands have revolted - and they are revolting to see! Red, somewhat swollen and tender. I keep bashing my hands into things and the cuts take ONE MONTH to heal. Can't walk right and I have these attractive blisters on my hands. Bubonic Plague, anyone? Oy! So, I talked to the Oncologist. She's going to postpone my next chemo treatment until my extremities behave. What the heck happened? One minute I'm the poster girl for getting through chemo, the next minute I'm down for the count. Down, for now maybe, but not out! I will sit down and put my feet up for a few days and carry on with the program as soon as possible. Gotta keep hammering those cancer cells!
Feb 20, 2010
Debbie's Book
Props to my wonderful sister-in-law Debbie Godfrey. The book she gave me at the beginning of my treatment is now the only 'cancer' material that I read. The book is called "What Helped Me Through: Cancer Survivors Share Wisdom and Hope" by Julie K. Silver, MD. It's mostly quotes from survivors about non-medical issues; things that 'helped them through'. I don't look at articles about cancer or treatment. I don't read any of the other books that the hospital gave me. I don't surf the net. I don't read the handouts about the medications I'm being given. This is a little odd because I've spent my entire career as a Nuclear Medicine Technologist reading journal articles, going to continuing ed. seminars and in general learning, in detail, about everything new and known about the studies that we do. But, as a cancer patient, my only source of info about treatment and drug side effects are my oncologist and the nurses in the Infusion Center. The nurses, especially, are the best filter about what to expect with each treatment. Having seen and heard about all side effects, they tell me about only the effects that are likely to happen, not every possible one. Lots less stress!
Feb 18, 2010
The Night Before
So, I'm sitting here at quarter past eleven stuffing my face! Tomorrow, and for 5-6 days after, I won't be able to eat whatever I want so I'm enjoying the last moments of indulgence. But, oh, WAH! I sound like such a baby, worried about not eating everything in sight! I have real things to dread and real things to celebrate. First, the dreaded part, just to get the whining out of the way: Tomorrow will be perhaps the worst chemo I'll ever have. It's the very last really nasty one with Adriamycin and Cytoxan. Last week, when I was still feeling bad from the last one, I cried every time I thought about having to do this again this week! Please don't drag me down to the dungeon again! I do feel a bit more ready to run the gaunlet again now, though. Now that I'm back to normal and feeling strong, I can take anything they throw at me! Especially with the great finding this week, which brings me to the thing to celebrate.
Earlier, I wrote about not being able to feel the lump in my armpit. Well, I saw the oncologist today. After she examined me, she said "Jane, I want to make sure that you come in for your treatment tomorrow. The lesion is gone - sometimes my patients decide not to come back". She confirmed my own findings! The doctor even said it!! I told her that there was nothing that could keep me from the rest of the treatments. Bring it on! Let's stomp on every last one of those cancer cells!
There's one more thing to celebrate. It's the thing that I celebrate all the time now. It's the thing that amazes me and humbles me and makes me cry (in a good way). It's all the love, concern, prayers and good thoughts that are being sent my way. It's truly awesome! Life is beautiful and so are my friends and family! Thank you, thank you, thank you...
Earlier, I wrote about not being able to feel the lump in my armpit. Well, I saw the oncologist today. After she examined me, she said "Jane, I want to make sure that you come in for your treatment tomorrow. The lesion is gone - sometimes my patients decide not to come back". She confirmed my own findings! The doctor even said it!! I told her that there was nothing that could keep me from the rest of the treatments. Bring it on! Let's stomp on every last one of those cancer cells!
There's one more thing to celebrate. It's the thing that I celebrate all the time now. It's the thing that amazes me and humbles me and makes me cry (in a good way). It's all the love, concern, prayers and good thoughts that are being sent my way. It's truly awesome! Life is beautiful and so are my friends and family! Thank you, thank you, thank you...
Feb 15, 2010
A Victory!
Well, I felt it two days ago, but wanted to wait and try again, just to be sure. I cannot feel the lump in my armpit any longer. If I press and press deeply, there might be something small and dried up deep down but the big round lump that I found back in December is G-O-N-E!! Woo-hoo! Your prayers and thoughts for me are working! Not to mention the yuckky chemo treatments. Now, I'm not saying or thinking that my cancer is gone. Nobody is saying that, yet. I haven't had any tests or imaging recently to backup my self-exam. The cancer exists in my body on the cellular level and demands that every treatment my oncologist has get thrown at it over the next months. LOTS more chemo, radiation and surgery are the weapons we will blast the bad cells with. But, OH BOY, do I feel good right now!!!
Feb 12, 2010
Nothing new
Hi! Just a quick update. Nobody wants to read a bunch more stuff about how I feel bad. Each day post-chemo is better, but each treatment takes a little longer for recovery. Thankfully, I have just one more really bad chemo. Then, it just continues until the end of May. And not a hair on my head! Makes showering so fast! No shampoo, no combing or styling and I just take the face cream all the way up and over...
Feb 5, 2010
Just Crush It With Your Car
Had another chemo today. There are 3 marbles in the dish and only one more of the really bad treatments. One more Adriamycin and Cytoxan, then we move on to Taxol and Herceptin and weekly treatments with less side effects. Yay! The Nurse Practiotioner and the Nurse told me today that the treatments I'm getting are really hard and that I am doing really well! That was so good to hear. I know I am strong and that I am moving through the program with a minimum of bad effect, compared to the old days when chemo was truly brutal. But I do feel pretty yucky (it's a medical term) for longer and longer after the chemo. So, I got some confirmation that I am not a whiny weakling. Nobody's saying that, but I feel like it sometimes!
I asked my nurse today if I could have the gigantic empty syringes that the Adriamycin comes in so that I could take them outside and run them over with my car a few times. But she said, surprisingly, NO! Darn, it's so rewarding to destroy the inanimate thing that has caused you misery. I have taken out and sledge-hammered the occasional recalcitrant blender or printer that has caused me nothing but grief. I put on my safety goggles and smash the crap out of it. Satisfying! I'm not up to swinging a sledgehammer right now, so I thought my car could fill the bill. But, the empty Adriamycin syringe would contain traces of a dangerous biohazard. When the nurse is giving it to me, she is swathed in a fluid-impermeable gown, wears a mask and eye protection and thick rubber gloves. So, she is safe (which is very good), but taking the syringe outside might hurt the poor road that I would smash it on! Somebody walking by might get a miniscule droplet on their shoe! But, yeah, that stuff gets pumped right into me - through my port, then it dumps into my heart and gets circulated to every cell in my body. Well... these are not good thoughts for me to be having right now so I'll be chanting these phrases as I go up to bed: I LOVE my chemo!! It is saving my LIFE!! Go, chemo, go!!
I asked my nurse today if I could have the gigantic empty syringes that the Adriamycin comes in so that I could take them outside and run them over with my car a few times. But she said, surprisingly, NO! Darn, it's so rewarding to destroy the inanimate thing that has caused you misery. I have taken out and sledge-hammered the occasional recalcitrant blender or printer that has caused me nothing but grief. I put on my safety goggles and smash the crap out of it. Satisfying! I'm not up to swinging a sledgehammer right now, so I thought my car could fill the bill. But, the empty Adriamycin syringe would contain traces of a dangerous biohazard. When the nurse is giving it to me, she is swathed in a fluid-impermeable gown, wears a mask and eye protection and thick rubber gloves. So, she is safe (which is very good), but taking the syringe outside might hurt the poor road that I would smash it on! Somebody walking by might get a miniscule droplet on their shoe! But, yeah, that stuff gets pumped right into me - through my port, then it dumps into my heart and gets circulated to every cell in my body. Well... these are not good thoughts for me to be having right now so I'll be chanting these phrases as I go up to bed: I LOVE my chemo!! It is saving my LIFE!! Go, chemo, go!!
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