Starting Chemo in October 2015
Comments
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4 down 2 to go! 2/3rds done with chemo. Let the SE's begin!
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Amy: the choir was lovely! What a memorable occasion...so glad you made it! My last infusion is also the Tuesday before Christmas. They asked me if I wanted to put it off until the following week, but I want to finish it up and move on to rads. After this last infusion, I am starting some neuropathy, as well. Just in my fingertips. That is really the only SE other than low blood pressure, after this third infusion...oh, and the fatigue. Not going to complain, though. Hope all other ladies are managing their SE's and having a good evening
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Sorry girls. I am having a pity party and you are all invited.
I have been in the hospital with pneumonia. A house guest flew in for a visit with a really bad cough. I didn't know what to do so I did nothing. I caught what ever she had so I am mad at myself.( and her )
I have been on weekly taxol for 9 wks. Only 3 more weeks to go. I have been having a flare of my rheumatoid arthritis. My hands are hot and swollen and I can't tell where the fatigue from the RA stops and the fatigue from the taxol starts. My other complaint is my neuropathy keeps getting worse. It was pretty sever before the taxol. Now I can barely feel my legs.
Well, that does feel better getting it off my chest. I will not complain in front of my children or neighbors. Thank goodness I have you all.
p.s. My hair is coming in really silver and fuzzy.
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mamabexar, i am in hospital as well, running fever last night so hubby brought me in. Xray didnt show pneumonia but that hasnt been ruled out, but definitely a bacterial infection, on IV anti biotics until blood cultures come back and we can get more specific with treatment. Really hoping this doesnt postpone my 2nd taxol next friday. Ugh!
Kim
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I am getting discharged today. I ended up having the car door attack me and the wound got infected so I got admitted on Wednesday. Wound is slightly improving with oral antibiotics, so hopefully it will keep improving.
Hopefully the rest of the hospital club gets to go home soon too.
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Ugh MamaBexar and Kim - so sorry you are both in the hospital battling infection. Anything we can do for you from afar? Sending you much strength and support across the distance.
No chemo for me today, my labs are still too crappy. We rescheduled to next week Tuesday 15th when I was supposed to be heading home and back to work. I'll drive the 4.5 hours back to AZ right after chemo while I'm still jacked on steroids. It the most sense and will keep me occupied. Happy birthday chemo for me! Spending any of my birthday in the chemo chair is not what I had in mind since I usually choose to spend that day blissfully solo hiking or snowshoeing in the mountains. Next year for sure!!
Andra xo
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MamaBexar, Skittlesgirl, and Kimmer--sorry you had to be in the hospital. Mama, what was your guest thinking??~! How dare they expose you! I hope they feel really bad now, about giving you this illness.
Kimmer, I hope you get out soon. I was in the ER last Fri, 3 days after chemo. Second time. At least this time they were able to determine that I wasn't septic, like the first time. I narrowly escaped being hospitalized over the weekend! no fun.
Skittles, I never even would have thought about getting a wound infection. Glad they hopped on it fast. Hate it was bad enough to put you in, though. I hope you'll continue to improve.
I'm feeling better now. Still having diarrhea, but that's just par for the course. No fever or vomiting, at least. Fatigue is better. Trying to get back into my old routine.
Good luck to the hospital club! May you continue onward and upward!
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oh no! skittlegirl too! Being in the Hospital is not fun. Glad you are going home today and hope your wound continues to respond to the antibiotics!
Xo
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So sorry to everyone who is in the hospital! I was in for three nights after my first round and it was so disheartening. I hope everyone has a speedy recovery and gets home SOON!!!
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I had my wires put in yesterday morning. Passed out before they were done, but they managed to finish the final placement with me sitting. Surgery went fine.
So those of you in the hospital, you went in for fever? And did they give you antibiotics, or transfuse blood? I have a feeling I will be in the same boat next month.
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I have been in twice now. First time was diarrhea and vomiting. Admitted for c diff infection. Given abx and fluids.
This time was no fever, but wound on the leg with differing opinions on how bad it was. Admitted and kept an additional night for observation after I pushed back on discharge the following day.
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hi ladies!
Thanks andra and mustlovepoodles and everyone else for your thoughts and prayers - they are felt!
Yes i had a fever last night of 37.7, and didnt want to risk it getting higher. They were happy i came in.
Turns out it is pneumonia but they are discharging me right now with oral antibiotics as they feel i will respond well and just as well if it was IV antibiotics.
Fingers crossed my counts are good next thursday and taxol #2 happens friday!
My thoughts are with others experiencing sucky effects tonight.
Kim
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When I went to the ER they tested everything--chest xray, urine testing, drew blood from the port, drew blood from the arm. Tested my blood counts and did blood cultures. The first time it happened, the blood counts revealed some kind of infection and I was very sick, weak, could hardly walk. They kept me for 4 days because my counts were all over the place and ultimately they determined that I had sepsis, a very serious infection, indeed. I was treated with massive amounts of IV antibiotics and I was discharged on powerful oral antibiotics.
The second time, last Fri, they did all the same testing. But this time, the counts were okay, decent anyway. I wasn't septic this time. They gave me a dose of Rocephin IV (pretty powerful antibiotic) and sent me home. No oral antibiotics this time. I felt bad, but I wasn't too sick this time. I recovered by the end of the weekend.
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Round 1 landed me in hospital for 4 nights too but thankfully this time I have been much better.
LoveMyVizsla just IV antibiotics for me; no blood transfusion. When you are having chemo a temp over 38 is a medical emergency.
Mine spiked at 38.6 just before I was admitted. They run all the tests including a chest x-ray and despite my inflammatory markers being high they were unable to pinpoint the exact source of infection.
I came home on oral antibiotics too.
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Knock on wood I haven't had anything that would hospitalize me. Even though my parrot had bitten me a couple of times and the usual klutzy calamities of life. I guess I have Neulasta to thank for that. Or maybe it's because I work in a hospital and I don't want to go there anymore than I have to.
Wishing you speedy recoveries.
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Thanks everyone for caring and the positive messages. I did #10 yesterday. Taxol and Herceptine. I can't remember if I mentioned that I refused steroids from day #1 and after chemo# 4 I refused the Benadryl. They given me Claritin orally before treatment. I have felt almost normal on this regime. I think the next two weeks are going to be hard. I am so weak and tired. But there is the light at the end of tunnel. I am sure that those of you just starting Taxol are going to be surprised at how easy it is. Go for weekly if that is a possibility. Keep us posted.
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Wow...sorry to all the ladies who've had to endure hospital stays! I've been lucky so far. No fevers, sicknesses, or anything that would have me at the ER/hospital! Going tomorrow to get my labs done for next week's chemo, will be #4 out of 6!
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I hope everyone is put of the hospital now and feeling much better!
Mamabexar, I really hope and pray it is easy! I start weekly taxol, herceptin perjeta on Tuesday. I am so incredibly nervous! Have you felt weak and tired the whole time?
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Hi all - I haven't been posting much but wanted to check in and compare side effects and other reactions with you all. I have done 3 out of 6 TCHP treatments and I am thrilled to be half done with chemo (I'm not counting Perception as part of chemo since that will be for a year). I wanted to check in and see if anyone else has gotten sick this winter? I caught a cold from my kids and it has knocked me out. I have had a low fever all weekend (my doc knows about it) and I just feel wretched. Also, as I read through and see that certain people are on the same regimen as me, is adding them as friends a good way to keep track of their posts?
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I haven't been sick and am praying that it continues. My middle kid came home with a fever on Friday , so I am hoping not to get what she had. She just ran a fever for a day or so and complained that her head hurt.
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SFMama, I caught a cold about a week and a half ago and am suffering now from the lingering cough and sore throat that is keeping me (and my husband) up all night. It's only at night, which is so maddening. Nothing seems to help and it's so frustrating.
I'm also on TCHP and have #4 of 6 tomorrow. My worst side effect has been diarrhea. It was so horrible after the first round that my MO reduced the dose by 20%, which seemed to help somewhat, but I think I am just going to have some diarrhea every cycle.
I also developed tinnitus in one ear, and I found in my research that the platinum containing chemo agents (like carboplatin) can cause tinnitus and even hearing loss. My MO and the pharmacist did NOT mention this possible side effect to me and I'm worried that the tinnitus and hearing loss might be permanent. Ugh!
Good luck to you!
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I hope I'm not going to offend anyone here, but I had to post a picture of the socks I got for Hanukkah last night. I'm going to wear them to the infusion center tomorrow. :-)
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Homeschool- No, I haven't been tired until the last week. Also remember I am at an age where most of my friends have the same complaints and they aren't even on chemo. I am so hoping things get better for you.
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Durham Girl- Love the socks. You go Girl,
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Durham...love the socks! If your pants hide them, you gotta make sure you show them to everyone!
Well, I believe I jinxed myself yesterday when I said I've been lucky and haven't had to go to the hospital! Went for my labs today, and there'll be no chemo for me next week. Seems my platelet count is low at 57K when normal starts at 150K, plus my hemoglobin is at 8.9 when normal starts at 11.7! MO told me if I see any external blood anywhere to go to the ER for a platelet transfusion! I should've knocked on wood as soon as I wrote that yesterday!
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Durham, LOVE the socks! Happy Hanukkah!
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How disappointing that your chemo had to be postponed igay1ord
Hoping my bloods are ok next Monday for my transfusion on Tuesday.
Lovin' the socks DurhamGirl
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Love those socks Durhamgirl!!
Yikes igay1ord! - crazy low platelets. I'm having the opposite problem...high platelets...over 500k (normal high range is 400 I think). At first they said it was normal to happen when I had that allergic reaction, but that was 2 months ago and my platelets are still high. hmmmm.
I finally felt well this weekend after my last chemo. I even went snowboarding yesterday! At first I was so short of breath (the mountain base is also 10k elevation) but found my groove after a while. I obviously didn't feel as strong or a skilled as I usually do, but it was still fun to be out there.
I sooooo don't want chemo tomorrow now that I'm finally not feeling bad. I assume my labs will be OK after having to wait 4 days because of labs and it will be a go. At least now I can start counting down the last 3 rounds to zero.
Hope everyone has a super week! xo
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Andraxo, homeschool, and everyone else who has chemo tomorrow...sending lots of positive thoughts your way! Tomorrow will be 4 out of 6 for me...officially more than halfway done...sigh...
Also...does anyone have any tricks or tips that they have found lessens the severity or duration of the "totally crappy" days after an infusion? I know the crappy days are just part of this whole awful ordeal, and I should probably just accept it, but I just thought I'd ask.
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Hi everyone! I just met with the MO, and based on new research that has come out about the effectiveness of carboplatin on HERs+ cancers, she is stopping my carboplatin effective today for my last 3 treatments. It is the likely cause of my tinnitus and hearing loss (minimal but concerning). She said that given carboplatin's high toxicity and side effects and the new research, they are recommending dropping carboplatin for HER2+ patients. For all of you HER2+ ladies out there taking carboplatin, it might be worth a conversation with your MO.
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