Starting Chemo in October 2015

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  • ncsue927
    ncsue927 Member Posts: 57
    edited November 2015

    Thanks, Andra! As soon as my taste returns to normal, I am making the sweet potatoes! They sound absolutely yummy! Something to look forward to!

    My white count is still down; more neupogen today. Hopefully I will be up for my AC on Tuesday. After this one, only one more to go!

  • TinaB71
    TinaB71 Member Posts: 17
    edited November 2015

    very nice. My son say to me dad 2.0. , he has yet a little bit more hair how I.

  • marylc
    marylc Member Posts: 13
    edited November 2015

    yes--feet are peeling and "burning" sensation. Helps if you can avoid walking. Cream helps. Actually put feet on ice packs to help hot feeling. Getting better as days go on

  • DurhamGirl
    DurhamGirl Member Posts: 100
    edited November 2015

    Hi everyone! Been offline for a few days but I'm back. I finally ventured out to synagogue this weekend after avoiding it since starting chemo. I've been afraid of getting sick again. And because my husband is the rabbi, I'm in a sort of public position there, so I always get bombarded by people (they all mean well--it's just a bit overwhelming). I also really didn't want to have the answer the same questions over and over again. Most people were lovely and respected my need for a little distance, although there were a few who didn't get the message about "chemo etiquette" and bombarded me with hugs.

    And the post-mastectomy bras and silicone prosthesis I ordered from the cancer center boutique arrived right in time for the formal wedding I'm going to this afternoon. It's quite comfortable actually and I feel and look almost "normal" again. Grateful for the small things!

    On to chemo #3 on Tuesday...good luck to my fellow Tuesday crew and, of course, to everyone else as well!

  • Jclc83
    Jclc83 Member Posts: 246
    edited November 2015

    Welcome back Durham! Glad you can get out a little. :

  • mustlovepoodles
    mustlovepoodles Member Posts: 2,825
    edited November 2015

    Whoopee for going to synagogue, Durhamgirl. I'm not the wife of a pastor, but I do sing in the choir. It's been disappointing that I haven't been able to attend church or rehearsals much since I started chemo. Sometimes I'm just too tired to fool with it. But I have had a burst of energy the last 2 days, so I dragged myself out of bed this morning and went to church. Even sang in the choir, too. One of the best things about singing in the choir is that we're in the front of the church, behind the pastor. It limits the number of people I'm exposed to and there's not shaking hands. Win!

  • Kimmer33
    Kimmer33 Member Posts: 386
    edited November 2015

    hi ladies!

    I dont want to grumble today, but feel i need to ask this. Since beginning your chemo treatments have you had second thoughts or questioning your decision to do chemo?

    I had one node positive out of 17, grade 1, and my oncotype came back at "9", which translates to a 5% chance of recurrence with hormonal therapy. Yet my oncotype also showed a 7% chance of recurrence with hormonal therapy AND chemo, so my choosing to do chemo has actually given me more of a chance of cancer recurrence. I am 100% er & prg.

    Would love to hear your thoughts!

    Kim

  • Smurfette26
    Smurfette26 Member Posts: 730
    edited November 2015

    Wow Kim. That seems crazy. Your oncologist still recommended chemo? And yes I'm day 5 in hospital after my first chemo. Questioning it and wondering how I will get through the next 3.

  • Kimmer33
    Kimmer33 Member Posts: 386
    edited November 2015

    smurfette, you will get through it, i didnt think i would either, but it does happen. I think chemo was recommended due to my one infected lymph node - that gets you on the fast track to chemo, however when i think about how the hormonal therapy will starve these rogue cancer cells anyways, chemo is a tough pill to swallow and get through, you know?

    Kim

  • Sloan15
    Sloan15 Member Posts: 896
    edited November 2015

    Just popping in from August chemo....

    I was scheduled for 4 rounds of TC, but I only did 3 because I was getting really bad neuropathy in my fingers. It's normal to feel tingles for a few days, but when it doesn't resolve after several weeks, that is when you and the docs have a talk. There are MANY options if you start having bad side effects, and if you are doing it prophylacticly like me, you can stop if things aren't going right. (By the way, my neuropathy completely resolved itself after a few months!)

    ALSO, my hair didn't fall out until DAY 30, so don't do anything too extreme until you are sure it's going to fall out! Once it started coming out, I got it cut into a cute 1' pixie so I could try out a cute short cut. I'm 8 weeks after chemo--finishing radiation next week-- and it's starting to grow back now (so don't get discouraged!!).

    You can do this!!!!

    I don't have this thread saved as a favorite, but you can private message me if you have any questions. Good luck.

  • homeschool4us
    homeschool4us Member Posts: 255
    edited November 2015

    I thought this article really described perfectly the see saw of emotions we are dealing with:

    I can't get the link to work, but the article is called, Living with cancer Curses and Blessings

    Here is an exerpt:

    Like someone with bipolar disorder, I see-saw between irritability and elation, depression and euphoria. As a cancer patient, I cycle through curses and blessings at a hectic rate.

    The real horror lies within, in my capacity for bilious envy. Why am I scared and scarred, when all those others are not? Why am I positioned toward a dire future when all those others take for granted the pleasures of the present? Why am I fulminating about a friend who has neither phoned nor visited? Nasty side effects of cancer, malice and venom, must not poison my days I determine over and over again.

    On the other hand, the cessation of pain or of baleful side effects produces wonders like nothing else. I marvel at the hot water of a shower or the melodious sonata on a CD. I say, "Thank you, deer," when I see a deer, "Thank you, dog," when I see a dog and "Thank you" to another friend who does phone or visit. Often, I stand in awe of the moon in the night sky struck dumb with its beauty. And this month, regardless of the blood marker, I will give thanks to the lightning bugs, because who would not want to thank each and every lightning bug?

  • biscuits
    biscuits Member Posts: 3,304
    edited November 2015

    Thank you homeschool4us! I found that exerpt to be very profound. I think we can all see ourselves in some of those statements.

  • MamaBexar
    MamaBexar Member Posts: 102
    edited November 2015

    I did # 7 of my weekly taxol on Fri. Still not much in SE's. I have a house guest for a couple of weeks. I will be out and about more than usual. It finally got cold enough to wear my wig today.(62 degrees) I went to the theater and dinner with friends. Wishing every one a good week.

  • Kimmer33
    Kimmer33 Member Posts: 386
    edited November 2015

    thanks homeschool, that is beautiful!

    Mamabexar, i start DD Taxol next friday (dec 4).nice for you side effects are minimal!

    If you could give your chemo side effects a rating on a scale of 1-5, 1 being minimal to nil and 5 being the worst what would it have been? Also if you could do the same with Taxol, i wiuld love to see the difference for you so i can anticipate some relief possibly. Dont forget to include the fatigue!

    Thank you!

    Kim

  • PatRN10
    PatRN10 Member Posts: 332
    edited November 2015

    Hi Everyone,

    Just popping in to say hi. Had TC #3 Thurs 11/19 and still not feeling well and out of work through Thanksgiving. Kudos to everyone who went to the Look Good Feel Better class. I loved mine a got a lot of great tips.

    Stubble is also driving me nuts. I like the idea about shaving it down again and will ask my daughter to do that.

    Take care everyone!

    Pat

  • MamaBexar
    MamaBexar Member Posts: 102
    edited November 2015

    Kimmer, Weekly Taxol is the only chemo I am getting, so I can only rank that. I do get Herceptine every 3rd week but I can not tell any difference between week with or week without. My worse SE's might be a1+ or maybe a 2 with fatigue. I don't pay much attention to the things like minor nosebleeds, hair falling out or minor aches and pains. They do not influence my life style very much. I found that going out without hair almost a plus. People are nicer, smile at me, hold doors etc. And it is always nice to see the innate goodness of most people.

    I was most concerned about nausea as a SE. So my MO made sure I had plenty of meds on hand. I only needed 1 on day 2 of first chemo. I don't know your age but I am sooooo much older than every one in these groups that it may not be correct to draw comparisons. I just spent a year of the past year and a half, recovering from a total knee replacement. If I spend another year being treated for BC, that could be conceivably 20 to 25% of my remaining time on this earth. So I have opted for gentler but still prudent treatment.

    I can not evaluate my own brain fog so I have no real assurance that any thing I have just said makes sense. I do hope so. You all have become very important to me. Best wishes.

  • Jclc83
    Jclc83 Member Posts: 246
    edited November 2015

    That was really sweet MamaBexar! We're all in the same club Friendships come in all forms.

    PatRN you and I are on the same schedule still. I got my 3rd round of TC Thursday too. I might actually try to do a few things tomorrow. I can't imagine being any more exhausted

  • Kimmer33
    Kimmer33 Member Posts: 386
    edited November 2015

    thanks mamabexar

  • Prettyblueyes
    Prettyblueyes Member Posts: 28
    edited November 2015

    Hello,

    I'm about to start carboplatin/abraxane too. I'll be going once a week for 2 weeks then labs and then two weeks on- labs until a scan shows activity again.

    I just finished 4 rounds of A/C. I was diagnosed in August.

    Hugs to you

  • Prettyblueyes
    Prettyblueyes Member Posts: 28
    edited November 2015

    Hello,

    I'm about to start carboplatin/abraxane too. I'll be going once a week for 2 weeks then labs and then two weeks on- labs until a scan shows activity again.

    I just finished 4 rounds of A/C. I was diagnosed in August.

    Hugs to you

  • homeschool4us
    homeschool4us Member Posts: 255
    edited November 2015

    My mouth sores have gotten horrendous this round again. Ugh. Hoping they lessen by Thanksgiving.

    I just wanted to put this out there also; If anyone would like to friend me on Facebook, please feel free to message me. I would love to keep up with you all through the years, after we may stop posting as often here.

  • DurhamGirl
    DurhamGirl Member Posts: 100
    edited November 2015

    homeschool4us...how do I find you on Facebook? Do you use a different name? I'd love to keep up with how everyone is doing after this crazy journey...

    Good luck to everyone going in for treatments tomorrow

  • homeschool4us
    homeschool4us Member Posts: 255
    edited November 2015

    Durhamgirl, I messaged you my real name!

  • ncsue927
    ncsue927 Member Posts: 57
    edited November 2015

    homeschool....I had horrible mouth sores the treatment before this last one. Then I read where someone had said if you suck on ice cubes during the whole infusion, you won't have mouth sores. So last infusion, I sucked on ice cubes from beginning to end of the infusion. I did not have mouth sores at all after that. I have my ice cubes ready for my #5 AC tomorrow. I also found baking soda rinses to be helpful. I must say, that week that I had the mouth sores was the worst SE I have had. It was all I could do to suck down some mashed potatoes. Now, I still have the metallic taste, but at least I can eat and chew.

    Good luck to those getting treatment tomorrow!!!

  • Autumn121
    Autumn121 Member Posts: 29
    edited November 2015

    Regarding mouth sores: I have had two treatments of AC so far, and both times the nurse had me suck on and/or chew ice cubes while infusing the red devil. I had a cup and a spoon and chewed and sucked on the ice for those 12 minutes trying to numb freeze my mouth while she infused. She said the ice reduces the size of the capilaries in your mouth, so the chemo can't affect them.

    I have done ice both times and have not had any trouble with mouth sores. If you are not offered it, maybe you could ask next time.

    It can't hurt, and may help!!!!!!

  • homeschool4us
    homeschool4us Member Posts: 255
    edited November 2015

    I didn't do ice the first time, but I did the next 2 times. I got mouth sores all 3 times. The last time wasn't as bad because they weren't on my tongue. I should say that I have had trouble with canker sores all my life so I am obviously predisposed to getting them for some reason and the chemo just makes it all the worse.

  • Jclc83
    Jclc83 Member Posts: 246
    edited November 2015

    When I was first diagnosed I decided to ask for suggestions for my bucket list on Facebook. Mind you I usually don't post much because I'm a pretty private person. None of my "friends" on FB know I have cancer. Anyway I got a total of three suggestions, two of which weren't age appropriate. Visit the National Parks was the third suggestion which I liked since I'm a nature girl. I deleted the post after a few days because it makes me feel so vulnerable. But Iwould love some ideas from all of you of things you would want on your bucket list.

    On a funny note I thought if I could get to 100 friends on FB that would really be something! So if any of you are truly interested in becoming a FB friend private message me please. Maybe I'll break a new record!

  • MamaBexar
    MamaBexar Member Posts: 102
    edited November 2015

    On my bucket list- see the northern lights

  • mustlovepoodles
    mustlovepoodles Member Posts: 2,825
    edited November 2015

    Hmmm, on my bucket list...several things. Does "become a grandmother" count? So far my kids are not cooperating with that one. How about "learn to make really good gravy"? See a state or national park in all the contiguous 48 states?

  • Jclc83
    Jclc83 Member Posts: 246
    edited November 2015

    Can you see Northern lights in the summer? I'm about to be a grandmother for the fourth time in early January. They are all three or less. I love being a Grandma and want to be as close to them as I was to my Grandma. That's why I'm fighting cancer for them. I suck at making gravy. I honestly never thought about becoming proficient at it. The parks are definitely on my list.

    I reallynever thought about having a bucket list before BC. Maybe once when I saw the movie.

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