October 2013 Chemotherapy

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  • lgkgde13
    lgkgde13 Member Posts: 164
    edited November 2013


    ladies - I just want to thank you for all the support over the last few months. It has helped me tremendously. To know I can log in and speak with others that get it had been incredible. Everyone is so knowledgeable. Thank you again :) we will get through this.


    I am sure you all know what my wish was for my birthday!!

  • TeamKim
    TeamKim Member Posts: 568
    edited November 2013


    great cake, lgd!!! Yum!!!

  • lonnie713
    lonnie713 Member Posts: 236
    edited November 2013


    I haven't been on in a while. You ladies are awesome. Congrats to those finishing up this week. I get my 3rd AC on tmrw and the neuropathy shot on thanksgiving day. There goes thanksgiving, although I can't taste anything anyway. I will be home in bed. I feel so bad for my hubby. I usually cook every TG. Have a wonderful holiday all.

  • Pam358
    Pam358 Member Posts: 294
    edited November 2013


    Wrenn - I'm doing OK - it's now my good week. But unfortunately from last Wed through the weekend and even some on Monday I was just dealing with side effects. I'm hoping that when I begin Taxol next week that I'll recover quicker. I hope your side effects have been kept to a minimum.

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    I had a feeling you were feeling some side effects. I hope it is better for you with Taxol. I am feeling pretty lucky so far. I had a bit of heartburn and upset stomach the first evening but cleared with metoclopromide. Sleeping pill took care of steroid jitters and so far the neulasta shot (injection yesterday) has not caused any pain at site or bones. I didn't use Claritin. I am feeling pretty good so far.


    I hope things improve for you soon. Take care of yourself.

  • travlmom
    travlmom Member Posts: 90
    edited November 2013


    I first want to wish everyone a good Thanksgiving - we are doing a very simple day all premade foods. I thought I might feel up to making sides but no way. I went to work yesterday to only cover lunches in the office 3 hours - at the one hour mark I knew it was going bad. Told my co worker that I would not make it. Got up to go to the bathroom and passed out in the hall. Luckily my husband works from home and was able to get my in 10 minutes. Off to the ER and my potassium was low along with my hemoglobin - but I only got a potassium treatment. I know I am not eating enough because it all tastes like crap. Came home and ate skillet steak and a sweet potato then off to bed.


    Today was herceptin day and I asked the nurse for a full bag of fluids as I still felt off - she started off so snotty I was in tears. They did another blood test and my potassium was lower so I got a 3 hour infusion of potassium and 4 pills of potassium. I still feel off. But she told me I need to be drinking less water and more juices like cran apple mixes and gingerale to keep my electrolytes up. I must say it tastes better than water!!!! I am so tired of sending hubby to the store every day for this or that... I hate this week after chemo. Next round I am not even leaving the house for this week. "Only" 3 more pity weeks and then I will be off this damn train. Only good news is that my BP meds are working and my heart no longer beats out of my chest. But I did not take it in the am because I already felt like crap and it was in a good range. I will take it before bed and hope to sleep.


    Gobble Gobble!!

  • naiviv
    naiviv Member Posts: 535
    edited November 2013


    My Dear BC Friends/Family,


    I wish all of you and your families and friends a Very Blessed, Health filled, Bountiful and Happy Thanksgiving Day. You have all entered and affected my life in many different ways, from your heart wrenching dx's, surgeries, chemos, survival tips, sharing life's precious moments and everday anecdotals.


    I am thankful to each and every one of you, for sharing and helping me and so many others through our anxiety, worries, tears, chuckles, laughs, rants,vents, pity moments.....the list continues.


    You will each be at my Thanksgiving table,


    Vivian

  • Gramof2boys
    Gramof2boys Member Posts: 194
    edited November 2013


    Hi BC friends,


    Just wanted to wish everyone a Happy Thanksgiving! I have learned so much from everyone here, making my cancer journey a little more tolerable. I actually have one whole week of NO doctor visits or appointments until next Friday! I'm so excited about that! I hope everyone enjoys tomorrow and will be able to at least eat some yummy food. I am thankful for my family and friends who have been supportive during this bump in the road for me. I will continue to fight this, become a survivor and continue to live my life as I knew it!!!! We can do this!


    Julie

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    Happy Thanksgiving to my American neighbours. Hope everyone does ok on this very different thanksgiving. Next year will be better I bet.

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    just curious. In general how long does the bone pain last? Yikes

  • LiLi1964
    LiLi1964 Member Posts: 331
    edited November 2013

    Wrenn - it can last several days to a week.  I'd take the Claritan now, although it might not be very effective since it works best if taken the day before the Neulasta injection and then for about 5 days after.

    Yes, YIKES is a good way to put it.....!!!!! 

    FYI - Peppermint Oil is a good alternative to anything internal.  Works great for nausea either in a diffuser or can be used topically.

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    Thanks Lisa, I will definitely take it pre injection next time. I feel silly for bragging about how easy it was this morning. I guess I still had steroids in my system. It really hit hard by noon. The nausea seems ok with the metoclopromide thankfully. I am so relieved to have this forum to know that these things are not unusual.


    I hope you have an ok Thanksgiving Lisa. I won't say "happy" but at least minimally uncomfortable.

  • LiLi1964
    LiLi1964 Member Posts: 331
    edited November 2013

    Thanks, Wrenn. 

    Here is a little info I got from my MO this last chemo on the horrible fatigue....she asked me "does it feel like you just fall off a cliff physically and fatigue sets in suddenly and through the entire body"? - to which I said YES!  She said it is sometimes associated with the sudden stoppage of the Dex.  So, after I take 2 pills a day for 3 days following chemo, she had me take an additional 1 pill a day for 3 more days.  It helped some.

    Your description of how you felt this morning vs later today makes me wonder if perhaps you might talk to your MO before your next chemo and see if adding a few more days of Dex at a low dosage might help you out. 

    Feeling better today so hoping I've "turned the corner" for this round and hoping for a Happy Thanksgiving tomorrow.  Still not up to eating but we've planned a very low key appetizer day w/just hubby and I.  The big turkey dinner will have to wait til Christmas.....

    Hoping the bone pain doesn't set in too bad.  If it does, don't hesitate to call MO for suggestions.

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    Thanks Lisa. That is a good idea about the dex. I will bring it up. I will also take the claritin pre injection. Enjoy your quiet day. Goodnight

  • TeamKim
    TeamKim Member Posts: 568
    edited November 2013


    Wrenn -- so sorry you are having bone pain. I take the Claritin, but still get some pain in my feet and ankles, and it is worse at night. Don't feel bad about saying you were doing well this morning, -- you didn't know you would feel worse as the day went on. The steroids tide you over for a couple days. And then it sets in. Day 3 and 4 are usually worst for me. My MO said I could take Motrin and Tylenol, alternating every 3 hours for the pain -- but I know some MOs don't OK Motrin. Hang in there -- and if need be, call the MO on call to see what you can take for the pain.

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    thanks teamkim. It is mostly lower legs. I am taking tylenol and will for sure take the claritin next time. I hope you have an ok Thanksgiving

  • Pam358
    Pam358 Member Posts: 294
    edited November 2013


    Wrenn - My bone pain was the worst the first time and although it's showed up the other three times once the dex wore off it wasn't as bad. The nurse told me that was not unusual, so maybe that will be the same for you. I have not taken the Claritin as the pain has been manageable with Tylenol. I do suggest though that you take the pain meds on a schedule so you can stay ahead of the pain, that helps me.

  • Pam358
    Pam358 Member Posts: 294
    edited November 2013


    Happy Thanksgiving Everyone! You are certainly counted among my Blessings!

  • Malakies
    Malakies Member Posts: 40
    edited November 2013


    Happy Thanksgiving to all !! I am blessed to have a 'good' week and am able to EAT!! I've lost 7lbs since I started chemo on 10/7 ( I could use to lose it he he) but today I will probably gain half back! YIPEE!!


    Enjoy the day as much as you can!! <3

  • Furfriend2
    Furfriend2 Member Posts: 299
    edited November 2013


    Happy Thanksgiving ladies! Gobble Gobble! Thank you for being here for me. It is like having a hug every time I check in.


    All the best (((HUGS)))

  • Furfriend2
    Furfriend2 Member Posts: 299
    edited November 2013


    Wrenn,


    I saw your post about the bone pain. I too took Clartin for 3-4 days with my shot and after. I did feel some of the pain but it is doable w/Claritin. I am able to take Tylenol as well but no aspirin due to my tx regimen.


    I start Taxol Monday. Getting anxious just thinking about it. I am going in for another echo this week to boot.


    Still awaiting results on my follow up ultrasound from my cyst and polyps(sp). Can you believe it has been 2 weeks and my Dr. still has not read my results? Yikes! First time I have had to wait for so long?

  • SchoolCounselor
    SchoolCounselor Member Posts: 452
    edited November 2013


    I have gained weight on chemo, about 15lbs. But prior to my BC diagnosis, I was working out with a trainer, running, and seeing a nutritionist...not too worried about it. I will take it off again. Now that might change now that everything tastes like mud and the only thing I like is oranges!


    Fur I would call the doctors office, it might have slipped off their radar.


    Happy Thanksgiving to you all!!!

  • Hydavis42
    Hydavis42 Member Posts: 52
    edited November 2013


    Happy Thanksgiving relocatedtarheel. Yes Taxol is much better than a/c at least for me. I did 4 rounds of a/c which was tough but doable. The side effects were rough some days but I made it through. I am going for my 3rd round of 4 on Taxol and I can tell you the only aggravating side effect I have had is constipation and a little fatigue. Taste buds and appetite is back which was almost non existant on a/c for me. I wish you well and minimum se when you begin taxol.

  • Headeast
    Headeast Member Posts: 619
    edited November 2013


    DebDylan, I have gained 25lbs since my mastectomy, particularly in my waist. I used to take diuretics, so that is one reason, I am not taking them now. The other reason is because I am eating carbs and protein shakes with bananas for the potassium and minerals. I am not exercising as much as before either. I started walking some this week, but have to increase my exercise time to burn those calories.

  • VintageGal1111
    VintageGal1111 Member Posts: 705
    edited November 2013


    Good Morning


    the morning after the big feast....hope you all had a wonderful Thanksgiving. We had way too much food, but for the most part I was able to taste it. Wasn't keen on desserts though. Just never know what those taste buds are going to do. Thursday are normally my *bad* day, this being my 2nd weekly Taxol I expected some pain & fatigue from being anemic but it was a good day.


    I hope all of you had a decent day. Anyone get a bit emotional? That realization of here's the holiday season & here I am with cancer going though chemo lurks in the corners of the brain.....


    VintageGal

  • LiLi1964
    LiLi1964 Member Posts: 331
    edited November 2013

    Vintage Girl - funny you mentioned emotional.....I spent most of the day crying.  The holiday hit me very hard - that I'm lucky to be here, lucky my cancer was found.....lucky to be alive.  Then saddened that I feel so awful from chemo that I can't enjoy the day.  Then wondering if I'll be "cured" after chemo and if I'll see another Thanksgiving....

    It was a very rough day.  I had expected to be Thankful on this Thanksgiving but ended up being an emotional wreck......

  • VintageGal1111
    VintageGal1111 Member Posts: 705
    edited November 2013


    LiLi1964


    I understand....I had all those thoughts & emotions too. We put up a brave front but it can be a struggle.


    Hope you're doing ok today.

  • TeamKim
    TeamKim Member Posts: 568
    edited November 2013


    Since there was only me and DH, and I can't taste anything anyway, we didn't have a TG dinner.... I just made a nice soup in the crockpot and made some biscuits. The soup was good -- though I couldn't really taste it, healthy veggies and warm broth was cozy. Kind of sad to miss the feast this year, but reminded myself that the whole idea of this is to be around to be thankful for many Thanksgivings to come. DS will be home in 3 weeks... 10 days after my last chemo tx.... Counting the days and planning the Christmas feast...... I think I will start decorating for Christmas today! since my energy is starting to return. Blessings to you all, sister warriors!

  • Headeast
    Headeast Member Posts: 619
    edited November 2013


    VintageGal, Thanksgiving brought way too much food! I don't have taste buds issues, I actually am really hungry all day.


    I don't feel sad but I am sure it has to do with having my last chemo treatment next week and right after three weeks is Xmas. I am wondering if I want to have a Xmas tree or not though. I am worried about getting any type of infections and trees come from who knows where.


    What are your thoughts? I know I am oaranoic with infections...

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2013


    Yowza, i visited hell for 2 days. I don't know how you manage to go to work or take care of families. I pretty much stayed in bed and felt sorry for myslef. I still have stomach pain and headache but legs are not as bad and i was able to eat a bit.


    My BMX incisions hurt more than they ever did post op. I guess this shows me just how lucky i have been so far to never have experienced this before. If it is improving now though then i guess 2 or 3 days of hell is ok.


    I hope everyone got through Thanksgiving ok xo

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