April 2011 chemo
Comments
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Has anyone every heard of receiving Herceptin for a year after the six chemo treatments and receiving it through the port for an entire year? I laid down and went to sleep after my appointment today. Before sleeping, I left a message with the oncologist nurse about what the doctor said about the port. My husband says she called back and said that I needed the port fixed because after my six treatments are done, that I would be on Herceptin for a year every three week through the port. This is the first I have heard about this.
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Sarah: Yes, that's the standard of care for women with HER2+ breast cancer. We all get a year of Herceptin if we're lucky and have insurance that will pay for it. Herceptin is like a miracle drug for HER2 cancer. It's an aggressive form of breast cancer which used to have a bad prognosis and is now much more manageable, thanks to that year of infusions.
Look on the bright side - that's a year you won't have to worry about a recurrence. (At least that's the bright side I focus on
There are HER2 discussions on this website - take a look and you can get your questions answered there, too.
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OMG, I thought I would be getting that in pills, didn't know it was through the port.
Does herceptin even come in pills? I feel so stupid. Chemo brains I can't remember them telling me this or reading it. Thanks Windlass, and I will check that out.
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Windlass..I'm with you on the port. I do love mine, it just gave me trouble that one time. I don't have great veins, and with the lymph node surgery I only have one arm to work with. Even simple blood draws are hard on me....so the port saved me lots of pain and trouble. ( not to mention saving my arms from the bruises)
Finished number #4 TCH today. I'm feeling good and determined not to become the "decadron demon" tonight....the steroids make me a little cranky.
Sue
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Carla, that was brilliant. My husband was in the french foreign legion and watching him holding it together for me moves me to tears.
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Sudz- doing a happy dance for you to be done with #4
On ports-I don't have one. I've had 9 chemo's with out it and never had a problem. One more to go on Wed of next week, I opted out of one because I thought it would irritate me. I can not wear pierced earrings and the like so I have a high likelihood of rejecting a port. My infusions usually take 4 hours and I don't know how that compares to someone with a port, But I just make the best of the 4 hours. bring my computer, something to read, catch up on phone calls etc...
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Artiecat! YAY!!!! I'm SO glad to hear it!!!!
Carla, lovely. I teach writing, and I just think it's so wonderful when we can sit down and get some of our feelings out. You did just a lovely job. And, thanks for sharing it. Loved it.
Ah, there's more to respond to, but I read last night and now can't recall all the details. Chemo brain! I"ve also been totally naseous. I don't get it. I was FINE for 10 weeks on Taxol and Tykerb, and now I'm getting sick. I wonder if it's just because it all adds up. ugh.
Ciao for now,friends!
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I have heard others say that the last chemo made them nauseous. Its a good heads up for the rest of us to double up on the meds for that last one. SO sorry you are feeling sick Profbee.
Maybe take something to sleep? I think that would be my solution. I have lorizapan and I love it for sleep. I so not wake up in the night and that means good restorative sleep. I wake up feeling very rested and no hang over from it.
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Merilee~ my infusions are about 4 hours too, so no difference there. I'm glad you have the veins to take that many "sticks", I had one bad port week and the IV was a nightmear for me.
I don't mind my time in the chair too much. I have a really busy life working full time still and taking care of my daughters so 4 hours to myself is a good thing even under these circumstances. I bring my laptop, sometimes for work/sometimes for play.
Yesterday I had someone in the room with me on her first TC treatment. She is my age and started getting random headaches which led her to the Doctor. She had a brain tumor that came from Lung Cancer she didn't know she had...non smoker healthy life girl. We talked a lot and I told her how well i'd been doing on the same drugs.When she left...(well before me since I still had the neverending Herceptin drip to go) she thanked me and said she felt much better after talking to someone who's already in it.
I didn't get the quiet time i'd come to covet...but I got something better. It was a good day.
Today...the nasty nulasta. I can't wait to be done with that one!
Happy dance back atcha Merilee...you are almost there....ROCK STAR!
Sue
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Hi, Sarah: Herceptin is not available in pill form.
Can anyone remember the name of the movie about how Herceptin was developed? It might help Sarah (and me, too) to know more about the drug.
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Windlass, found some info on the movie (Living Proof, 2008) on the Lifetime website.
Site says no air dates in the next 6 weeks, but it does show as available on Netflix.
Hope everyone is hanging in. It's been an decent couple days post treatment, but get my Neupogen shot tomorrow...so we'll see.
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Sudz - interesting where we find lessons in this world!
So - today #4 for me...word of the day is --only two more! My wonderful daughter does with me to all appointments. After infusion we had pizza for lunch and then my daily walk today was around part of the lovely Oceanside harbor. I came home and promptly fell asleep for an hour! Feeling a little woozy (not groovy!). Go tomorrow for neulasta then acupuncture. Friday I have an appointment to check out a fitness/wellness program for cancer warriors. Gee - my dance card is full this week!!!!
Keep up the good battle everyone!!!
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I picked up a copy of a magazine called "Cure" at the onc's office. Has some interesting articles. I subscribed. There is no charge for people in chemotherapy.
www.curetoday.com
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Articat good for you for starting to think about your wellness recovery program. The walk around the ocean side sounds like a lovely start. ANd thanks for the tip about Cure, I did not know it was a free resource.
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Hi Windlass
Thank you for letting me know about the drug Herceptin not being in pill form and about the movie.
Livingproof is a movie that I must check out, thanks CarlaB76 for the link.
Thanks Artiecat for letting us know about the magazine. I love this site, I have learned a lot from you guys. You guys taught me more than my chemo doctor. The walk sounds good I could use one.
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Mighty quiet on here today...
I hope that means everyone is doing well.
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Yesterday I thought I was freaking out. I cried all day. Went for blood work and it was fine so #4 is on track for Wednesday. I asked if I could do it early maybe Monday or today and they said no. I think I am just weary of always thinking about cancer and what to do to stay functioning.
Anyone else have a day where they just cried all day? The trigger for me was picking up a scarf my daughter had made for me and I could smell her on it. It reminded me of when she was an infant and I would rock her in her sweet little jammies. I started wishing for the old days when the kids were babies and life was easy. Well, not easy, but easier than this.
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Merilee, just wanted to say that i am also finding this is getting harder emotionally as i am progressing thru treatment... and i wonder about any research on chemo and emotional responses. I dont mean steroid craziness/chemo depression, but are we also exhibiting SE of chemo on some parts of our brains, brain function ...is that stating the obvious??? i dont even know anymore because of how chemo is impacting on me intellectually..huge impact, scary. this also makes me feel really vulnerable, is another kind of baldness
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Wow Louis - emotional baldness is such a strong image! And so accurate!
I had #4 TAC this week. Actually feel better physically this time than after the others (fingers crossed that it lasts through today!). But yesterday I had a teary day too. Not out and out crying, just teariness at silly things.
I too recall rocking my little girls - now my older daughter is "rocking" me through this experience. It is funny to think about what we think as easier times. Merilee, you are right they werent really easier - just different and more "normal" - (I dont like to use that word dont think there is such a thing!).
So - we are all together in this warrior women! We can do it!!!!
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Merilee, I have days like that where I am so angry or just cry. This is an extremely stressful time for us and I think it is normal!
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I got great news, I was approved for disability SSD. I am waiting for my award letter. I am so thankful that I will be getting some income!
Feeling good today, just some strange pain from my waist and down both legs. I had that last treatment too. Goes away in a day.
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Hi ladies,
So yeah the teary days are dreadful but we are strong and must keep going with this, already half way through I'm also on round 4, I find that when the steroids have finished like yesterday the day after I am always really down and teary, basically I cry at anything, today I went to a chinese supermarket and got chatting with the sales assistant who recommended me to her uncle who does acupuncture and for some reason this kindness made me cry stupid is'nt it?? Some days I am very strong and some not I suppose we are all going through this, wish to god none of us had too go through it but thats life.
Sending lots of love and light to all
Sarah Sweety xx
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Hi everyone,
Emotional is just not a big enough word to describe what we are all going through. I think it's totally normal to cry, to cry all day, to not feel well. It's a hard pill to swallow.
On a lighter note: I know people have strong opinions of Lady Gaga (positive or negative)...but did anyone see her performance of her new song "hair"? She performed it bald. It was pretty powerful.
Taxol has been very kind to me, I am doing it weekly, and so far (fingers crossed) it has been much more manageable than the dreaded AC.
Cheers, KG
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O boy !!! emotions!! rollar coster around here!! so sweet about your daughter merilee! what about this taste thing!! i am getting so ticked off about it!!!! what taste right last cycle doesn't this cycle!!! so frustrating!!! just when you think you have it figured out....
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I hear you pawprint girl...I bought the things that tasted good last time and none of them are working this cycle. Ugh!
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Hi, April sisters!
Just popping in from the May boards. Reading about all the emotions...just wondering how you all felt about your 3rd trt? I'm up for my 3rd one this week and some say it is the worst one?
Happy a good Fathter's Day all!
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Geo-thank God for SSDI for you that is fab. I am appying and the paperwork is taking me forever to fill out because I'm so dingy. Any tips you can share on getting approved?
Emotions- Acts of kindness make me ball, thoughts of it even. Just about anything seems to set me off.
Blood work was good on Fri. So it looks like #4 will happen Wed as planned. Crossing my fingers for an easy one.
Happy dance for all who have completed #4! Surviving that is an accomplishment!
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I am curious about what everyone is eating - or not eating.
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Fresh fruit, nuts, veggies, organic eggs, Organic oatmeal, Ezekiel bread. All of the above fixed in a variety of ways.
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Eggs from my hens....lots of them!
Cashews, Watermelon, Strawberries, and plain unsweetened Iced tea.
I want to eat everything, but once I have a bite or two I don't want it anymore!
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