Chemo in May 2014
Comments
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After this I start Taxol. I heard it is much more tolerable then the A/C, but I was reading the paperwork and one of the common side effects is queasiness - mild to moderate. UGH.
I had a small nodule on my lung when we did my pet scan and my doc said it is most likely scar tissue from something I was exposed to. They couldn't even measure it it was so small. But she wants to do another scan, now I'm scared again. WHy can't I just go through this and get on with my life? Shit.
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HomeMom - I write a popular breast cancer blog and hear from literally thousands of women who are going through or who have gone through taxol. I've only heard from maybe one or two that had any nausea with Taxol.
When I switched from AC to Taxol, it was 50% better for me - maybe more. I went from wanting to die during AC to wanting to live with Taxol. Taxol has plenty of its own challenges. But for most women, it is so much better. It is cumulative, so towards the end it adds up, but overall, so much more tolerable.
Best of luck to all of you! You will get through it and life does get better. I'm 2 years out from chemo and it is my passion to bring hope to others going through chemo!
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Had my 3rd infusion today. Reading this board and April board has me quiet concerned about how bad this might be. Except for the rash, that I most likely let go too far and ended up in the hospital, I think most SE's have been mild. So I am scared about this round. And I'm already feeling SE's today that I didn't have last time - swollen knees, headache and nausea when I was finishing up Cytoxan, sore throat, extreme fatigue in leg muscles and frequent hot flashes . Here's my #3 photo.
As bad as it is to be battling cancer, I can't imagine my baby having cancer. This is a Facebook page of a friend of a friend whose baby is starting chemo tomorrow! He's 6 months old! Can you imagine? If you're on FB look up the group created for him - Prayers for Pierce.
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Denise - thank you for the post, it makes me feel a little better! My name is also Denise, I wish I had put it in my name here. I picked up some glutamine powder today at The Vitamin Shoppe. My MO said to mix it with water or juice three times a day the first five days of the Taxol. Have heard of that? I'm also taking B6 in preparation.
Wendy - I have just been a little more severe each time and here I am three days before the last one and I still don't feel 100%. The PA told me it was cumulative and that it may just take me longer to rebound each time. So sad about the baby. I couldn't imagine as a parent having your child start their life this way. Makes you realize how lucky you have been.
I also notice the pictures everyone posts from the treatment room. My docs office has a sign that says "no photos or video allowed". I should ask why? LOL
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Glutamine helps keep neuropathy away during Taxol. I iced my hands and feet during Taxol infusions. It really works. You can read about it on my blog - all the women I know who did it had great results.
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The only thing is I will be in the chair for 2.5 hours every other week. How do you keep things frozen that long?
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Anyone have any favorite distractions during the crappy days? I watch hours of HGTV, the DH is in trouble when I'm feeling better cause I'll want everything remodeled, lol. I also like playing words with friends and cookie jam. I bought an embroidery kit, but didn't start it yet. Looks like it would require too much thought. I prefer mindless distractions.
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I had my radiation sim today, not too bad. The worst part was the needles in my sides for the tattoos. Should get started on rads in the next couples of weeks. I'm still trying to be happy about my last treatment but can't seem to get passed the punctured expander incident yesterday. Ugh! Wishing us all a good week with minimal SE's!
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debiann - I too watch HGTV non stop! Not until the afternoon though after Today show, Dr Oz, and The Chew. I play Farm Heros and Candy Crush.
Missyjean - I'm still numb under that arm pit area, so I'm hoping the "tattooing" doesn't hurt too much. Is this a permanent tatoo? I would think not.
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I started binge watching Orange Is the New Black. Terrible show. Filthy. Not something I would normally watch. And here I sit.
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I liked the first season of Orange but haven't been able to watch the second season. I don't really want to "watch" lesbian sex.I liked watching Merlin on Netflix and my 11 year old could watch it with me. Although I found that toward the end of the series it got more dark than the chemo mood could handle. It probably wouldn't have bothered me during no chemo times. Interesting how that works. Wee don't have cable so I don't watch HGTV or Foodnetwrk. Although I could probably watch online but they'd just add to a honey do list (remodel and make me this food, lol).
Baby Pierce is getting his port in as I type this :-( I just can't stop thinking about this poor baby (6 mos) getting chemo later tonight or what his parents might be experiencing. Thinking about him though has helped me not think about my own woes.
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Wendy - keeping little Pierce in my prayers
Everytime I think of my last infusion on Friday I feel queasy. I can only imagine if my SE's were worse how I''d be reacting. blah.
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The tattoos are permanent but they are very tiny. Could pass for a mole. I got three, one on each side of my chest and one marking my clavicle.
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Ugh, we had a short quick storm in our area last night that began with a big gust of wind that knocked out our power (and water since we have a well with an electric pump). It's still out and the electric company is promising everyone should be restored by Saturday. WTF? And I just had my 3rd infusion yesterday so bad days are a comin' -
Yikes, no power & water till Saturday! A couple years ago we lost ours for a week due to a bad storm. We live in a wooded area. I went home to stay with my mother, left the DH home to care for the animals. I rationalized that he could pee in the woods easier than me, lol. Do you have a generator? We have a small one. Can't light up the whole house, but kept the food from spoiling. Good luck!
I had round 4 today. All went well for me, but two people in the infusion room had reactions to the chemo. The woman in the chair next to me reacted to taxol, and it was her 7th round! The nurse told me you can react to any of the drugs at anytime. Can't wait till this is over!
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Yes, we bought a generator and a snow blower when we bought the house last year. I think those two items may have been a better buy than the house after that last winter. LOL.
Wow, a rxn after #7. Soo scary. Hate these damned drugs.
Update on Baby Pierce: They started one chemo drug at 8 and another at 9. I wonder if he's getting TC. Poor poor baby. I just can't imagine. Makes my current chemo experience nothing compared to what that would be like.
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Can't imagine what that poor baby will go through. I did hear that children tolerate chemo better than adults. Hope this is true for him.
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My mom had us over for dinner for some wonderful cheesesteaks. At least I'm told they were wonderful, kind of yucky to me. I want my tastebuds back! Just needed to vent, lol. How is everyone else doing?
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debiann I'm the same way. Office ordered pizza today and in the front of my tongue I could taste it was pizza, in the back there was nothing. T- minus 14 hours to my last A/C treatment. Let the lousy weekend begin!
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I'm scheduled for fluids on Saturday, so fingers crossed I don't feel as bad this round. My mom is hoping I feel good enough to attend a baby shower on Sunday, she said the family really wants to see me. On the way home husband questioned if I really wanted to try to go, first because its far from home, second because they'll be lots of food and everything tastes so bad now, and third because I'm kind of bitchy for the first week after tx so did I really want to be around my family, lol. Thanks for your honesty dear.
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Almost time for bed so I'd like to take this moment to vent:
I'm tired of my armpit being numbI'm tired of wearing a wig (it's only been like 3 weeks) but I'm in sales so, yeah, I kind of have to
I'm tired looking at my almost bald head - I now actually look like a cancer patient
I'm tired of chemo and the SE's
I'm tired of looking at my foob, I want to reconstruct!
I want to taste and eat whatever I want again
I'm tired of the pity looks from co workers and family/friends
I'm tired of hearing my sister say "Even when something bad happens to you something good happens to you" (Re: two new boobs) Really???
I just want to be ME again ugh!
There...done. Night night!
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HomeMom: Ditto to everything. Well said. Good night.
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Missyjean - please tell me what the "punctured expander incident" was? You are scaring me.
I met with my RO last week for planning. She said they will use Sharpie to make my marks...not tattoos. That is why we will do the SIM the week prior to starting radiation. So the marks don't get washed away. Then they will remark them with Sharpie each week during my treatments. The marks will not be permanent.
Good thoughts to everyone!
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Before starting chemo, my MO said many people are able to still work. Seriously? Is anyone one here still working and able to do their job properly? Luckily I am a teacher, so I have the summer off, but I am curious as to how others are managing. I cannot imagine working, especially at a physically demending job, which at this point would mean any job that requires standing up, lol.
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Of the 21 day cycle, I *might* be able to work 10, as long as it wasn't very strenuous and didn't require critical decision-making skills. Or mental word retrieval cuz that is SHOT!!! I just want to know if it's going to come back.
I have decided I am going to skip radiation and just have a DMX. My plastic surgeon does breast reconstruction. I am going to meet with her and see what she has to say. My husband will be coming along with me. Scared but glad I've made a decision.
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debiann - As far as work I am pretty lucky in that my boss has told me to stay home when I can't make it in and come in when I can. I pretty much am not able to go in from Friday through Tuesday every other week. I then I work from Wednesday through the the following Thursday straight to make up for the extra days off. So either I am at home sick or at work. If I feel like going home early on any given day he is ok with it, or if I need a day off that's fine as well. I am commission only and have been doing this for four years so I can work off of appointments now. PLUS I have a great partner who has been a live saver during surgery/recovery and treatments.
Sometimes thought I think an office job where I am not in contact with so many people would have been better. Nothing like showing inventory homes in Florida with a wig on!
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So happy someone can make a decision, I'm still struggling with that daily. Thoight I had settled on UMX with DEIP recon, but last night I started to get so tired of being sick, I went back to just getting the lump redo I need and rads cause it would be the fastest way through this. I'm sure I'll change my mind again a million times. What made ypu choose, surgery, reducing recurrance or avoiding radiation? I fear the se's of rads.
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lespring - If I had had no node involvement like you, my BS and the team would not have required me to go through Chemo, just rads. Did your oncotype score come back high?
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I have been trying to work through chemo. I have an office job and the first two cycles I would have treatment on a Tuesday - could work wed and thurs - then I would be off until the next Tuesday. Then I could work straight through until the next treatment. Some days it was only half a day though. But since treatment #3 I have hardly been able to work. In fact since #4 on Jul 1st I have only made it to work for 1/2 a day!! I don't what I will do for the last two - my guess is not really make it to work at all. I really don't know how anyone could work through this unless they are really lucky with the SE's. Right now I just don't have any energy at all. I stand for more than 5 minutes and I am exhausted. I dread going to the grocery store and thinking about walking the aisles.
Lespring - congrats on making your decision - it is hard to make.
Debiann - you will come to one soon. You just have to search your soul to see what sounds "right" to you. Once you do that then you know that you will never look back as it is the one that is right for you. We are all so different it what is important and what directs our actions and how we recover from things. The surgery (BMX) and the fills and stuff since has been the easiest part of my journey so far but for others not so much. Since I had surgery before treatment I really didn't have much time to think about it - maybe a week - but no regrets.
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My oncotype came back with 25% recurrence if I can't take Tamoxifen, which I can't. I'm in a "gray area" group where the benefit of chemo for me isn't known, so chemo was a coin toss. I opted for the use of whatever weapons I had available to me.
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