Starting Chemo in October 2015
Comments
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BellaV, I am on day 2 of my ac and I'm just weak and tired. Are you taking any anti nausea meds around the clock? I am so prone to nausea that I am taking compazine, then 4 hours later zofran, then 4 hours later compazine and so on. I am hoping to prevent the nausea from occuring.
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Tessu, please stick around, these wonderful ladies here provide always amazing support!
Dmckinley, welcome to our community! We hope you are finding the forums helpful too. Best wishes,
The Mods
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skittlegirl: I'm not sure the white tongue is bad enough to be thrush... going to read up on that.
homeschool: And I was not taking the meds for nausea until I felt I needed to. Probably waited too long? I don't know. I have Zofran 4mg. every 6 hours.
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BellaV , yeah they told me it's much easier to prevent the nausea than get it under.control.once it starts. Try to start taking it regularly the day before you got sick this time.on your next cycle.
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round 2 of the red devil.. urine infection was put on cipro.. feel not to bad yet. I had a lot of digestion and jaw pain round 1..
2 left of this beast .. 4 of tax..
I never lose cancer will not win..
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Hi everyone! I was wondering if people are wearing masks when out and about to prevent infection? I see some people going through chemo wearing masks whenever they are in public, but I wasn't sure...I have an event to go to next weekend with 300 or so other people, and I don't want to be stupid about it, but I have a hard time with the feeling of a mask covering my mouth and nose.
Thanks!
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I was supposed to start chemo on Thursday the 22nd but after the tumor board met they decided I had 1 more node they wanted to remove. So I was already scheduled for my port on Friday so they went back in through the same old incision from 3 weeks ago and removed the node. Then I had another spot on the opposite side of the same breast removed at the same time and the port put in on the right. So now I pretty much look ready for Halloween! My chemo will be set back probably 2 weeks because of it so now I"ll probably start on the 4th of Nov. Did anyone else have trouble with the port? Mine is 2 days in and it is so sore that I can't really lift my head too far. It hurts even when I open my mouth and chew. When I do raise my chin up any the vein in my neck pops out. Any advice?
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Durhamgirl I haven't started chemo yet but my MO told me that I would have to wear a mask at school (I'm a teacher) days 7-10 of each treatment when my WBC would be the lowest.
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DurhamGirl: My friend who is an infectious disease specialist said those paper masks don't protect the wearer from sick people in group gatherings, because the microscopic holes that let air through are too big. But keep them at home and make any visitors with respiratory infections wear them while inside your home --- best is to not let anyone infected visit, but that is not always practical.
What DOES help protect you is hand disinfection: warm soapy water at home, that liquid stuff while out and about. Door handles, shopping cart handles, pens used by tons of people harbor bacteria for hoirs after contamination, and we touch our faces multiple times a day without realizing it. So keep your hands clean
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I'm thinking the mask might be a good idea...
Jamigb: I had the same experience with my port- it did get better by day 4 or so, much faster than the lumpectomy. Advil helped too.
I am at day 6, and starting to feel a bit better. The bone pain from the Neulasta shot was really bad day 3 PM through day 5AM. Now just tummy issues and light-headed.
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No, I am not wearing masks and no one has said anything about avoiding crowds.
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hi ladies
About the white tongue, i had it on days 3-6 after my first chemo treatment - i used saltwater 3-5 times per day, followed by a swish of Biotene mouthwash-helped cleared it up nicely, and hasnt returned.
My main goal is eating enough protein rich foods each day, i cant afford to keep losing weight!! I have an incredible appetite and a little worried if i keep this up i will be rolling into the hospital for treatments, but that would be a good problem to have.
Looking ahead to #2 chemo treatment this friday, neupogen (neulasta) shots have not given me any side effects yet, i feel really good. As i know what to expect now, my days 4&5 after chemo were the worst for me.
Since day 7 i have been out walking and feeling stronger each day, and praying for each of you facing treatments this week, for low side effects and much strength!
Kim
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Back to the chair for me. This will be my second trip. My original Dx was 5/13 and I belong to the June 2013 group as well but I thought I would join you ladies too. I will be getting a slightly different chemo regime this time around. No time to fit in port placement before my first treatment so I will take Taxol, Herceptin and Perjeta IV on Friday. Perjeta wasn't out of trials when I was first treated so if anyone has started taking it this month, I am interested in hearing how you are doing.
Thanks,
Tracy
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Hey everyone! Had my second chemo this past week. AC. I actually have felt better than the first. But wicked night sweats; up changing pjs three times and bed sheets once. Is that normal? It seems to be diminishing each night; very little last night. I've been hungry, but I don't feel like eating. I live alone and my MO has advised I limit my adventures among the public, so I'm a bit stir crazy. My MO also advised a face mask if out in public. Hair is all but gone. I haven't heard anyone mention it, but is anyone experiencing gut issues, like loose stools, diarrhea? This is going on for days after treatment.
Durham girl, I'm over here in Raleigh. Nice to see a neighbor!
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Tracy, I just wanted to tell you I am so sorry you have to start chemo again. How are you holding up emotionally?
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Ncsue927,
I too have the night sweats. I didn't know if mine was postpartum from losing the baby last week or chemo. I know chemo throws your hormones out of whack too, so I bet it's both. I also had diarrhea starting the day after treatment and have read that both diarrhea and constipation are normal. I think the chemo causes diarrhea and zofran and other pain meds cause constipation.
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Day 3 after AC and I just feel weak and a slight headache. And lots of heartburn. Will I hit a wall tomorrow, day 4? Has that been most of your experiences?
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Homeschool: Thank you for asking. I am disappointed that my first treatment wasn't a cure. I'm thankful that this treatment will give me additional length of life. I am angry that cancer is such a disruption to my life. I am humbled by God's plan for me. Emotional roller coaster would be the simple answer.
I notice that we have similar pathology, it is not a common pathology at all. Would you share what your oncologist has told you about it? My breast tumor in 2013 did not have this pathology. My oncologist is considering putting me on Arimidex but I am reluctant as SEs are pretty miserable and the benefit for PR+ has not been demonstrated. There is some consideration about why PR testing is done as it's not considered a reproduceable breast cancer subtype.
ncsue927: D-> is a pretty standard SE of chemo as it kills all rapidly reproducing cells indiscriminately. That's why many get mouth sores. Epithelial calls are among those rapidly reporducing and replaced cells. They cover all surfaces that have an opening to the outside of the body. That is why intercourse can painful during chemo too. D-> was probably my most significant SE during my first Chemo treatment.
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hey homeschool
For me day 4 was the worst, so hang in there! I was on anti nausea drugs through day 3, so with no meds day 4 at all, your body is feeling the full effect of chemo with nothing to mask it. I also had heartburn for those 3 days but the nurse said that would happen from the steroids. My next time around i plan to take a gentle laxative on day 3 to help with mild constipation, but had no trouble with diarrhea (nurse said that would be normal though).
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Tracy, I was only like 9% positive for pr so basically they have ignored it so far. But also I was pregnant upon diagnosis (just lost the baby a few days ago at 13 weeks), so they haven't addressed everything about my cancer that they would have had I not been pregnant. Friday was my first chemo and the resident basically said I probably have stage 4 and wanted me to get all kinds of scans. This was 2 days after delivering our stillborn son and I kind of freaked out on him. I can't handle any more bad news right now. I know the scans eventually need to be done so I am shooting for after Christmas. What chemo did you have the first time?
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Hello Ladies! I have been following the discussion boards for the past few weeks and felt that it was time to jump in and take the plunge. I had my port placed two days ago and will start chemo on Tuesday, October 20th. I had been placed on Arimidex for the time being, as I had a few delays along the way. After being diagnosed with BC, and having a scan, they found thyroid cancer and that had to be addressed first. I am happy to find an online support group, such as yourselves
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One more question for everyone...I can't shake this headache I've had for two days. Not getting worse but not going away either. I thought it was from the Zofran, but I'm not on Zofran anymore. I've tried both Ibuprofen and Aleve, with no relief. I am trying to stay away from Tylenol. Anyone have anything that has helped with headache?
Thanks!
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Durhamgirl, are you drinking enough water?
Homeschool, I cannot fathom the horror you have faced over the past months. I am brought to tears just thinking about it never mind living it. I am so sorry for such a significant loss. Prayers that you are not stage IV---it may not feel like it but miracles are granted.
The first time I was treated with six rounds of Taxotere, Carboplatin and Herceptin and then Heceptin alone for 11 additional treatments. PR+ is between 40-60%.
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Hey biscuits. It's nice to see another E. WA gal. I am down in the Tri-Cities. Good luck on Tuesday. I go in for round 2 on Wednesday.
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Biscuits, we'll be starting chemo on the same day, 10/20. I get my port tomorrow morning (10/19). Not looking forward to any of it, but I'm resigned to it now--got my chemo bag packed and in the car.
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Mustlovepoodles, mind if I ask what you packed in your chemo bag?? I start this week slso, Thursday the 22nd
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I packed a bag and ended up using nothing from it. I was too terrified of everything going on and they were always pretty much doing something with me. Switching medicines and stuff.
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round 2 seemed a little better .. I did it Friday, I feel OK today .. I have a urine infection so I am on cipro..
The port Hurt for 2 weeks and I was really bruised. Now I forgot it's there . I have it in my arm as it wasn't good in my chest to close to my implant . I am tiny .
My hair is falling out, it's the only real time i have cried .. we will all be ok, look for the light ..
Cancer will not beat me..
Xxt
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I commute to NYC and i wear a mask on the bus.
People Have NERVE.. THEY Ask If I Have hiv..
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I start chemo October 22.
MsYelv
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