January 2016 Chemo!

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  • LovesToFly
    LovesToFly Member Posts: 1,133
    edited April 2016
  • Valstim52
    Valstim52 Member Posts: 1,324
    edited April 2016

    Congrats Zinny

  • LovesToFly
    LovesToFly Member Posts: 1,133
    edited April 2016

    Day 4 after docetaxel. Yuck. I expected yesterday to be bad but it was OK, today is crappy. I feel tired and achy and buzzing, and of course I have to get ready for Passover! Grrr

  • MissBee123
    MissBee123 Member Posts: 186
    edited April 2016

    I'm so happy for all of you who are wrapping up!!! Looks like there are still a group of us who have a little ways to go. I just had #7 yesterday and will finish Taxol May 26th.

    Am I the only one here who will continue with Perjeta/Herceptin for another 9 months? I won't officially be done with infusions until next March!

    Small but happy news today: I have actually managed to lose some weight! All the steroids from chemo, lack of mobility from surgery, and hormones from egg retrieval helped me to put on a whopping 25lbs. Finally, 6 weeks into Taxol and only one tiny bag of steroids, the weight is slooooowly starting to come off. I am hoping once I'm done with Taxol then it will really skim off, but for now I'm just thrilled the scale is going back in the right direction. It's not a vanity thing, I just want to feel like my old self again. Hair loss, weight gain, surgical scars, etc...where did I go???

  • Maya15
    Maya15 Member Posts: 323
    edited April 2016

    LoveMyVizsla, what's your eye pain like? Since starting Taxol I've had occasional shooting pain/headache that lasts just a few seconds when I move my eyes. I just figure it's the Taxol. Also had blurry vision which they said was due to neulasta. Sure enough it went away when I stopped having neulasta and came back a bit with neupogen. MO advised me to wait till I was done with chemo for the ophthalmologist because any changes should go away.

  • Maya15
    Maya15 Member Posts: 323
    edited April 2016

    MissBee, just saw your post. I'm also in for Perjeta/ Herceptin for another 9 months till next March. I still have a lot ahead of me--surgery, recon, maybe rads etc.

  • Valstim52
    Valstim52 Member Posts: 1,324
    edited April 2016

    MissBee

    I still have surgery next month then rads. 33.

  • LoveMyVizsla
    LoveMyVizsla Member Posts: 813
    edited April 2016

    Maya, I hadn't started taxol yet when the head pains and eye pain started. It was 3 & 4 weeks after my last AC, so that long after the last Neulasta. It feels like the muscle behind the top of my eyeball is pulling. I can kind of feel it go way back toward where my brain was hurting on top. Weird. She said we'll do the MRI first and then maybe she would sent me to an eye doc. I will have three doses of neupogen starting tonight. Then they will reevaluate after my counts next week. :-

  • Myraknits
    Myraknits Member Posts: 264
    edited April 2016

    2 more TCHP then surgery and rads in June and Herceptin till next Feb.

    Can I just admit that I'm so sick of feeling sick at this point. 11 days post infusion #4 and I'm not bouncing back as easily as I was. I'm sleeping or watching tv most of the time. It's hard to swallow anything but liquids and everything tastes like poop...no appetite either. Days like these make me wonder if I'll ever feel like myself again.

  • zinny
    zinny Member Posts: 281
    edited April 2016

    Myra, you will get back to yourself. Little by little… And it SUCKS to feel sick all of the time. It is totally ok to say that.

    Thrush, maybe? That's a long time for a sore throat…Can you tolerate smoothies? Something like Rumble to get you some protein? I got "The Cancer Fighting Kitchen" cookbook which has lots of brilliant ideas for fussy tastebuds on chemo - worth a look?

    I thought that my taste would change with Tamoxifen, so i was eating all of the yummy stuff before it tasted awful. Well, I gained 10 lbs and it all still tastes ok - oops. Weird how it is different for everyone.

  • Ivegotthis
    Ivegotthis Member Posts: 28
    edited April 2016

    Miss Bee, I'm in for Herceptin until January. What is that? Ahhh, it's nine months! (Had to count on my fingers). You are not alone. I have my sixth and final chemo on Wednesday. I'm looking forward to it and dreading it equally at the same time.

    Myra, the one thing I always hold onto is that every day gets better after chemo. Okay, so I'm an optimist, but it's true. One day this will all be behind us. You can do this. So should I complain four days post chemo, please copy and paste my comment right back at me.

  • LifeAloft
    LifeAloft Member Posts: 150
    edited April 2016

    Myra, I could have written that post, I'm feeling the same way. Sick and tired of feeling sick and tired. I have 7 more weeks of Taxol/Carbo to go and it seems like forever. Dare I say that I think the dose dense AC was easier, at least I felt like myself for a week inbetween. My biggest thing is the exhaustion, and lately I feel like I'm letting everyone down because I AM always tired. They just don't get it.

    I was told that I have thrush this week, I thought I was coughing and everything tasted bad because everything is so dry, but the thrush medication is definitely helping, it may be worth checking into.

    One day at a time...

  • Milwmama
    Milwmama Member Posts: 115
    edited April 2016

    Spend way to much time watching tv on the couch. Between headaches, fatigue, and general felling shittiness, its about all I can do. Food is for survival, not taste. Have lost 40ish pounds since the start sometimes 4 or 5 a week. Had maintained for a bit but losing again. So yes, sick of being sick.

    Good news is my hair is starting to come back slowly. 👍 No neuropathy or nail problems noticed.

    Halfway through Taxol on Thursday if the counts are up. Woot! When I get it to one hand countdown I'm going to get excited. Looking forward to getting back to "normal".

    The sun is shining, but the warmth is not there. Maybe tomorrow. Spring in WI, 40 one day, 70 the next :/

  • buttaflydiva
    buttaflydiva Member Posts: 88
    edited April 2016

    I will be on herceptin until Jan 2017


  • LoveMyVizsla
    LoveMyVizsla Member Posts: 813
    edited April 2016

    Have I mentioned how much I HATE giving myself injections? It's worse with neupogen because it's day after day. At least Neulasta was once a treatment. I would not make a good diabetic.

    I was awake from 3:34am-10pm yesterday. To make up for that, I took a long nap today, then went for a hike. That wiped me out.

  • Cathytoo
    Cathytoo Member Posts: 667
    edited April 2016

    SO TIRED ‼️ I'm two days from getting my 5th TC infusion. I have only been tired days 4,5 & 6. After that everything has been normal. But, today I can barely walk a few steps without feeling totally exhausted. Wonder if my blood count has dropped. Anyone experienced this. Tomorrow I go to see Hamilton on Broadway. Hope I don't fall asleep

  • JCS28
    JCS28 Member Posts: 153
    edited April 2016

    Cathytoo -- I AM SO JEALOUS THAT YOU ARE SEEING HAMILTON!!! Please let me know how much you loved it! Enjoy!!!

  • jensgotthis
    jensgotthis Member Posts: 937
    edited April 2016

    Cathy, my fourth TC cycle was definitely my most fatigued. I started eating beets, spinach and some red meat and felt a little better - found my counts had dropped a little more than usual when I had my blood levels checked. My 5th and 6th rounds have been much easier though. Even went to Disneyland 6 days after round 5 and walked 24 miles Over two days and felt great

  • Cathytoo
    Cathytoo Member Posts: 667
    edited April 2016

    jensgotthis...It's so weird. My MO let me go 4 weeks between infusions, so I'm actually on my fourth week since infusion #4. Saturday I walked through the airport coming home from Florida. Sunday I had 22 people for dinner. Felt great. Today, I can hardlywalk to the kitchen. Feels scary because this feeling is new to me. JCS28...don't feel jealous. I'll think of you and maybe you'll get some Hamilton vibes‼️


  • EstelaLorca
    EstelaLorca Member Posts: 98
    edited April 2016

    Cathytoo - I'm going for treatment every 3 weeks (Taxotere) , but I definitely felt the accumulative effects on the 3rd week of my 5th round (2nd week was better). I'm completely retaining water, my feet are swollen and I'm having difficulty breathing when I'm laying down. Legs feel like lead, and rashes now. I try to get out for walks but it's hard cause I get so winded and of course legs heavy...but I force myself to because I think it helps.

    It's absolutely scary, and not to scare you....but when there are such huge changes in your body your mind goes into overdrive. Mention it to your MO. I did, and I got a mugga (spel?) and an EKG but she thinks it's all due to the water retention. Now I have to take a water pill.

    Hope you feel better soon!

  • fightergirl711
    fightergirl711 Member Posts: 300
    edited April 2016

    buttaflydiva I'll have 13 more rounds of Herceptin, but not sure when they start after AC, surgery, etc. At one point I looked at the calendar and roughly estimated April 2017. I got a bit depressed. It is what it is.

    Cathytoo I'm fried too. This week not so bad but go for #3 of AC this week and dreading it. the only consolation is that there is only one more after that on May 12. Up until last week I was doing relatively ok. But HAMILTON! I'm with JCS28 - SO JEALOUS! :)

  • Valstim52
    Valstim52 Member Posts: 1,324
    edited April 2016

    Cathytoo, Hamilton is worth it even if you sleep a little. lol

  • Cathytoo
    Cathytoo Member Posts: 667
    edited April 2016

    HAMILTON... I wish you all were coming with me tomorrow. But, I'll be sure to give a review when I come back.

  • zinny
    zinny Member Posts: 281
    edited April 2016

    Ugh. 4th DD Taxol hardest by far, struggling to get back to normal!!


  • buttaflydiva
    buttaflydiva Member Posts: 88
    edited April 2016

    im dealing with the cumulative effects of weekly taxol...im so freakin tired lol. I push through the tiredness and do what I gotta do but sometimes I get to the point where I feel like every ounce of energy is drained from my body and I just have to stop and rest

  • LifeAloft
    LifeAloft Member Posts: 150
    edited April 2016

    Zinny and Buttaflydiva, I totally understand, weekly Taxol is kicking my butt! Finally felt OK yesterday, just in time for another infusion today, #6 of 12...ugh. This is more difficult for me than AC, with AC at least I had a week to feel almost normal.

    My bf is not being very supportive or tolerant of my tiredness either which isn't helping. He "jokingly" called me lazy the other day, then told me that a lot of it could be in my head. I'm still angry.

  • Valstim52
    Valstim52 Member Posts: 1,324
    edited April 2016

    Dose Dense Taxol really zapped my energy and bowels. I had my last one 4/18 and am just now feeling near human. Glad it's over. AC still made me the sickest but comparing awful to awful i don't know. I was able to do a lot, but so exhausted.

    '

  • songbird72
    songbird72 Member Posts: 68
    edited April 2016

    I had my last dose dense Taxol on the 19th. I am so glad to be done with chemo but struggling to get my energy back this time. It has been such pretty weather here and I want to be outside planting flowers but a little activity just does me in! I also have three more weeks until I start rads (I have to drive 80 miles one way to get to treatments) and want to make the most of it.

    Is anyone else struggling with swelling? My fingers are swollen and the last two days at the end of the day my ankles/feet and my arm around my elbows were a little swollen. It has been pretty warm here the last couple of days but it was doing it before it got warm and a search of Taxol and swelling revealed this has been a side effect of some women. Anyone? I think I'm putting in a call to the ONC today just to make sure there isn't something else I need to do.

  • EmilyJane7505
    EmilyJane7505 Member Posts: 25
    edited April 2016

    songbird72 - I did get some swelling in my fingers and fingertips - it was accompanied by redness and pain, my MO said it was Hand and Foot syndrome. Would be interesting to see what your doctor says because it doesn't sounds like you have any pain associated and you have swelling in other areas than your hands and feet. I also had my last dose dense Taxol on the 20th and I am finally feeling myself today - I'm glad for no nausea but it's definitely not a cake walk. I have been trying to walk a little everyday even if it's just around the yard - might be all in my head but I feel like it helps with the achiness and just helps how I feel inside to get outside.

    So - has anyone's face broken out? I have a face full of zits similar to when I was a teenager! So beautiful :) I was debating whether to call my MO or not for advice. I'm going to give it another week or so to see if it clears. Trying to keep my skincare regimen very gentle.

    Also - a very sensitive topic, I'm just going to go for it ;). I have started into a chemical menopause from the chemo - have been getting hot flashes on a regular basis. Something else is that I noticed that I am noticably dry 'down there' and sex is painful. Is this typical of menopause or is this a Taxol side effect?

  • Maya15
    Maya15 Member Posts: 323
    edited April 2016

    For me too Taxol is kicking my butt. I switched from weekly to dose dense because I didn't have the energy for hospital visits 3 times a week for chemo/neupogen shots. Dose dense definitely has more side effects (bowels, tiredness, bone pain), but it gives me some time when I feel myself. My MO said Taxol is much easier than AC but that hasn't been the case for me.

    EmilyJane -- I'm having a breakout too. MO says it's folliculitis: Taxol attacking cells in the skin that keep bacteria in check. They gave me a prescription for clindamycin, but it didn't work. I have the same side effects also from chemical menopause. I'm hoping the dryness and pain is from Taxol because the rest of my skin is the same. I get blisters from walking in my normal shoes and I start bleeding whenever there's any friction on the skin. Can't even wear earrings cos the holes just bleed as soon as I put them in. So, let's hope it goes away when we finish. In the meantime, I use lubrication and it helps a bit.

    As I crawl toward the finish line, I just got confirmation that it's all WORTH IT: went for MRI yesterday and they just phoned with the results. Bit of background, I'm having neo-adjuvant chemo and at diagnosis there was cancer all over my breast and in the lymph nodes, multiple tumors, very aggressive, etc. MRI shows "marked response to treatment", lymph nodes have gone back to normal size and "no definite residual malignancy in the breast"!

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