Starting Chemo July 2012

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  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    teeballmom, congratulations, you're over halfway thru Taxol!  I'm wishing you good results from your upcoming checkup with the ONC.

  • natL12
    natL12 Member Posts: 135
    edited October 2012

    PAEaglesFan - what a great analogy of weed killer.  I will keep that in mind when it's my turn to start radiation. I've wondered WHY must I go through that also, but figured with the aggressive nature of triple negative BC I wouldn't argue.

    Getting tired of swollen feet and ankles, chemo eyes (it's really hard to see the computer screen and correct my typos), fingernail beds hurting (how long before the nails are gone?_, and general all-over hurting and tiredness. Whining again. Only 1 more chemo to go.  :)  Nat 

  • mssunshine71
    mssunshine71 Member Posts: 162
    edited October 2012

    A week post Taxol Herceptin and I have thrush, a raging yeast infection (1st one in my life!), an unexplainable rash on my neck, and the bone pain has been almost unbearable.  Although I am so great-full not to have nausea, eating still sucks!

    Hopefully it's just a matter of reducing the dose next time.

    On a good note my hair is starting to come back :)

    I've wanted to quit this chemo thing so many times.  The only thing that is getting me through this is my 4 year old daughter who deserves to have a mother.  Her school did the Terry Fox run a couple weeks ago and she came home with this big sticker on her shirt saying "I'm running for Mommy".  I balled my eyes out!

    I thank you for letting me vent here so I can keep a smile on for her :)

  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    Nat, you're almost there!  

    Missunshine, yuck, so sorry for the infections rashes and pain.  It's good they plan to reduce your dose.  Hey my hair is sort of coming back too-- really just downy fuzz but it's encouraging.  I have one hair in front that's probably a whole inch long.  Yay!

    Well today is Taxol #3.  I decided to get my blood draw today rather than the day prior, hoping this will result in higher counts.  Last time they were below the limit and I had to get special permission for the infusion.  So I'll be driving up for blood draw, coming home, then having the DH drive me to the infusion.  Decided I'd rather just make two trips rather than making us both sit there for an hour and a half while waiting on the labs.  I barely even dread the needle sticks anymore.  I'm just bored with the whole routine!  Gonna take a book today so I don't have to rely on the rather dismal magazine selection.

  • SusanHG123
    SusanHG123 Member Posts: 414
    edited October 2012

    For those growing hair---real hair? Not the prickly scratchy barbs that catch on the pillow case? Soft hair? 

    Had Taxol 4 and Herceptin 5 on Wednesday. Last of 3 neupogen today. Bone pain increasing as steroidal high decreases. Am trying to put the steroids to better use this week--am on a true cleaning frenzy. Unlike weeks in past when I just tossed things around--am actually cleaning. Baseboards and more. 

    Emily-keep pushing for info on radiation rationale for your case. You are the mama gorilla fighting for info. I hope the therapist and groups continue to help. 

    Madelyn--black toe resolution?

    Well-I was almost "forced" to use my new pink stabber yesterday. A woman I had not seen since my diagnosis spent about 20 minutes telling me how she understood my fears etc because of her BC experience. The entire time she was talking I was trying to fight through chemo brain to figure out why I could not remember she had BC as we had children the same age who went to the same school. Finally, I said I am so sorry not to remember. And her response. It was recent and ended up being a fatty node! A fatty node! I quickly excused myself and had very bad thoughts. 

    Back to scouring and scrubbing. It is helping with some of my anger issues--which my therapist continues to say are healthy. If he only knew... :)

  • teeballmom
    teeballmom Member Posts: 322
    edited October 2012

    SusanHG123:  Yep, I have real hair.  Some are prickly but that's because I always had that wire-like Asian hair, but most are really soft.  It's coming back very white/gray (my dad was completely gray by age 40 so.....). Yuck, but it's hair.  I'm happy.  I keep waiting for it to fall out but so far so good. 

  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    I have a bunch of hair coming in.  Most of it is very fine and blond but some is brown.  The stubbles that survived the initial loss still seem to remain and are still not growing.  So it's stubbles covered with soft fine hair.  Have to admit I spend quite a bit of time admiring the fuzz, I'm so happy to see something happening.  Smile  My original hair was coarse and reddish brown.

  • emilybrooke
    emilybrooke Member Posts: 98
    edited October 2012

    PAeagles - I agree, good analogy.

    I have a bit of stubble on my head too. Plus, knock on wood, I haven't lost all of my brows or lashes from Taxol. One more round to go one week from Monday.

  • Madelyn
    Madelyn Member Posts: 93
    edited October 2012

    Hey Susan, thanks for remembering my toe. Oncology nurses just said, "yep that's what can happen." It doesn't hurt at all. No more needle feeling. It will just have to grow out. A size of a dime on the nail.....just because it gets dark, it doesn't mean it will fall off. I guess we will have to see.



    My hair is also coming back. It starts like white peach fuzz and gradually gets darker. I just scheduled my port removal surgery. I am having my last chemo and port removal on November 21st.....day before Thanksgiving.

  • Itsalltemporary
    Itsalltemporary Member Posts: 38
    edited October 2012

    Been waiting to write this sentence for a long time.....after 6 TC treatments, I am 3 days PFC (and in my sentence the "f" doesn't stand for "final"!!!). Hang in there ladies - we will get through this! I start rads on Nov 12. Meeting with the radiation onc on Tues and plan to ask about the difference between chemo and rad (love the weed killing analogy!).

    Ann -I laughed out loud when I read your sentence about analyzing your fuzz. I have been doing the same thing. I spend a lot of time looking from all angles and lots of time rubbing my head. Feels good to have heair there even if it is fine, light little duckling hair. It was somehow just a relief to see it growing back - reminded me that all will be back to normal at some time in the future.  Can't wait until we are all there!

  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    Woo-hoo!  Congratulations itsalltemporary!

  • PaEaglesFan
    PaEaglesFan Member Posts: 277
    edited October 2012

    Congratulations itsalltemporary. You're on the road to chemo-recuperation and it's all downhill :)

  • Lifeonitsside
    Lifeonitsside Member Posts: 250
    edited October 2012

    Yay, itsalltemporary!

  • mssunshine71
    mssunshine71 Member Posts: 162
    edited October 2012

    Nice to see a bunch are coming close to the end of chemo.  it must feel wonderful!!

    I have 3 more rounds of TH to go and the first one seems to be kicking my butt!

    I spent friday and saturday in the hospital with a low fever.  Many tests later, it seems I just have a respiratory virus.  I feel like death but am slowly gaining strength back.

    At least my daughter didnt have to miss her dance class.  I'm so greatful for my family, especially my sister.  I don't know what I'd do without them!  As I'm writing this my sister called to say her son has headlice and my daughter just spent a couple nights there.  Here we go again.......

  • roadwarrior28
    roadwarrior28 Member Posts: 301
    edited October 2012

    My last chemo is this Friday - 2 days before my birthday!! And no Neulasta shot for me this time since I have more time to get my WBC count back up :)

  • Madelyn
    Madelyn Member Posts: 93
    edited October 2012

    CONGRATULATIONS  Itsalltemporary and Roadwarrior28!!  Us weekly Taxol people will be there shortly.  I think TellBallmom and I finished the same day 11-21-12  and Whaevah is on our schedule too!  It's an accomplishment for sure!  

    Feel better mssunshine71.

  • Lifeonitsside
    Lifeonitsside Member Posts: 250
    edited October 2012

    My last round is Nov. 1 and I just scheduled my No Mo Chemo party for Nov. 18!



    Yay to all of you finishing up now!



    -lee-

  • _Ann_
    _Ann_ Member Posts: 769
    edited October 2012

    Congratulations in advance roadwarrior28!

    Well I feel like I'll be one of the last ones across the finish line.  My last Taxol is Dec 20, just in time for Christmas.  I'm feeling really well these days though.  The only SE's are sleeping a lot and intermittent bone pain, plus I have to eat loads of fiber to keep constipation at bay.  I'm so happy to be able to eat normally again, except I still don't want to drink plain water.  Infusion #4 this week and my first visit with the onc since starting.

  • stride
    stride Member Posts: 470
    edited October 2012

    Hi folks, I'm checking out of this thread for awhile, and will be spending some quality time in the November surgery and 2012 sisters threads. Got news today that the cancer has spread to my skin. My BS is guessing there are a couple of different kinds of cancer: one that responded to TAC and one that didn't.

    I really wish all of you the best of luck, and so happy so many people are finishing!!! For the rest of you, minimal SEs and maximum results for all!

  • TAB55
    TAB55 Member Posts: 198
    edited October 2012

    stride: So sorry about the spread of your cancer!   {{{{hugs}}}} from me to you.  

  • boobzilla
    boobzilla Member Posts: 58
    edited October 2012

    I've not been on in a while and am playing some catch up. Congrats to everyone finishing! I will have my last one Nov 1 (whew!), then meeting with breast surgeon Nov 12 to plan for MRI, surgery, etc (I am on Neo chemo). Virginia, congrats on the news of your benign results-that's great news!

    Stride, I am so sorry to hear this news-all the best with the next steps ahead-we're rooting for you.

    So much to read, but glad to hear many of you are nearing the end of the chemo journey or have already finished. What a transformative process (in many ways). I can't wait to celebrate with you all, when I pass my last one and move to the next steps. I hope the end stretch continues to give you hope and is as bearable as possible!

  • emilybrooke
    emilybrooke Member Posts: 98
    edited October 2012

    Congratulations itsalltemporary and roadwarrior!

    stride - I too am sending you a big HUG right now.

    Just confirmed my last round of Taxol - 10/29 Definitely getting excited about the last round. Still awaiting more info on the radiation front - no one has been able to produce any stats or studies for me to read. I have a follow-up with radiation onc on 11/2 so I will have to make a decision by then.

  • Itsalltemporary
    Itsalltemporary Member Posts: 38
    edited October 2012

    A No More Chemo Party - I love it! Way to celebrate the milestones Lifeonitsside!

  • Itsalltemporary
    Itsalltemporary Member Posts: 38
    edited October 2012

    Stride - so sorry to hear about the spread. Good thoughts, strength and hugs to you!

  • SusanHG123
    SusanHG123 Member Posts: 414
    edited October 2012

    Oh stride --as you step away please know we are carrying you in our hearts and praying to whom ever we each pray to daily. And, please step back and check in. I feel as if this group has become family. I look for each of you and worry when someone is missing for a day or two. Please know you are loved and cherished by your July 2012 group. And I am still planning the July 2013 Camp Hyatt escape. 

    Ann I will finish Taxol December 12th--if I do not have to miss any more weeks due to low white counts. I am hopeful to go steadily the next 8 weeks with the addition of the 3 nuepogen injections per week. If the bone pain is an indicator of white cell production I should be able to donate cells! Have a 3rd MRI next week. My 2nd one did not have the outcome the surgeon (or I) wanted--hoping for more positive results this time. Guess will be discussing when surgery will occur and what type of surgery. Radiation. When to restart Herceptin. Etc, etc, etc. 

    I met with one of my pharmacists today. I have so been stressed about taking the pain medication. As a nurse--who has worked and taught psych for years--I was really concerned about addiction. Despite my base knowledge of unlikely to become addicted when being treated for cancer. Pharmacist is also a friend who finally said--"take the *%&^$ drugs. Use the liquid morphine for break through. But take the drugs. Take the full amount. Cut in half. Cut the half in half. Bit off corners. What ever you have to do to get the edge off of the pain. Then titrate the liquid morphine for stability. If you are hurting your energy goes to pain control. Take the $%%^ drugs." All of which I knew, and understood. So took the drugs. The bone pain with round 4 of taxol and the neupogen was almost relentless this week.

    About 1/4th " strip of eyelashes gone on each eye-upper lid this morning. I used to have lashes that almost swept my sunglasses. No more. Brows very thin. And Madelyn--dark red circles on 3 fingernails today. 

    Saturday night is the Outrun Fear fund-raising event for the indigent fund my daughter, an EMS student, and a nursing student are organizing. They have worked very hard, raising monetary donations, food donations, prizes, T-shirts, etc. There will be a Zombie run for those who enjoy being scared. So hope there will be a wonderful turnout. The young women have worked so hard. And the indigent fund is in desperate need. I mentally added my EOBs over the w/end. And again said a thank you prayer for being employed with insurance. 

    Sleep well dear sisters. 

  • teeballmom
    teeballmom Member Posts: 322
    edited October 2012

    Stride: I am so sorry. Keeping you in my thoughts. Big hugs coming your way!

  • PaEaglesFan
    PaEaglesFan Member Posts: 277
    edited October 2012

    7 weeks PFC.  My eyebrows are shedding :(
    Like roadwarrior, I was allowed to pass on the final neulasta shot and felt great.  If your counts are up when you finish, I suggest asking your MO to give you a bye.  I also have an upcoming b-day that will be 8 days after I finish my radiation treatment.  I keep hoping that nothing crops up to prolong the treatments or I will be pushed into the week of Thanksgiving and I'm hoping to take some time off work just to give my brain some down time.  (I've been able to keep working thru all of this.)

    Congrats to those who are getting ready for the big finale and minimal SE's for all!!

  • CityFi
    CityFi Member Posts: 95
    edited October 2012

    Congratulations Maddie57, itsalltemporary, RoadWarrior28, on getting out of ChemoVille! I’m looking forward to joining you at the off ramp on 11/12.  Yesterday was 9 down, 3 more to go. Brings a whole new meaning to Thanksgiving, doesn’t it?  And what a great birthday present for RoadWarrior, too.

    Mssunshine, sending you love and light.

    Stride, I was upset to hear about that spread. Please keep us posted on your treatment plans.  In the meantime, sending you love and light as well.

    SusanHG123, your daughter sounds amazing. Thank you for raising such a thoughtful human being. We need more of them in the world to counter the self-absorbed @##hole like Miss Fatty Node. IMHO, you were very kind to allow her to live. ;-)

    On the issue of “Pinktober,” before my diagnosis I found the pink ribbon tsunami very unsettling. I still occasionally bought things or made donations because I thought how could I not since the # 1 risk factor for breast cancer is none other than being a woman. And since my diagnosis, nothing has changed. I’m more skeptical of it as ever. Now I do not question anyone’s good intentions.  Reasons for participating in all things like walks and runs are personal and complex. I just wish folks would (1) demand to know where the money really goes and maybe even just give directly to organizations that actually serve women like us, and (2) VOTE for programs and policies that will help women living with breast cancer, especially I this pivotal year. I recently learned, for example, that General Mills funded anti-health care reform candidates through its political action committee. General Mills owns YoPlait which had the scandalous lick-the-lid campaign that not only gave a mere 10 cents to breast cancer but also had a carcinogenic ingredient in the yogurt! I know prevention is important, but I feel like the overwhelmingly majority of breast cancer efforts have nothing to do with assisting women who have already been diagnosed. The focus is on protecting the breasts of the 7 out of 8 who will never develop breast cancer rather than saving the lives of we That Eighth Woman. 

    Emilybrooke, so glad to hear that you’ve started counseling. I wish it was something that everyone going through this had access to. I feel that it’s been a godsend to me. And to be honest, I only talk about cancer probably only ten per cent of the time lol!  Cancer has just brought other things to light for me, and as I address them, I actually find myself better able to cope with and feel more optimistic about this experience and its consequences.

    LIfeonitsside, could you post or inbox a link to your blog please?

    As for fuzz, yes, it’s coming in even as I’m still on taxol.  Even though I’ve actually enjoyed being bald, especially during the summer, bring it on I say!  I have maybe ten eyebrow hairs, and my eyelashes have become sparse so that’d be a great place to start. I feel that the eyebrows gives away that something’s afoot so that and full function of my tastebuds is what I want for Christmas.  I never fully lost my sense of taste or suffered the metallic taste, but the blandness has made it difficult to eat healthily as I search in vain for something to satisfy my palate. I lost almost 40 pounds before the mastectomy and twenty of ‘em have creeped back when my taste buds quit me and the steroids kicked in!

    Virginiaiab, thanks for the song recommendation and congrats on the benign result! ON orders of my best friend who gave me an iTunes card, I’m supposed to download an inspirational song the night before my weekly taxol infusion. My playlist is called ChemoThrive. Another song I think you’ll all love is “Not Going to Give Into It” by Olivia Newton-John. She wrote this song after a chemo session. Many of the songs that particular album were written during her breast cancer journey.

  • Lifeonitsside
    Lifeonitsside Member Posts: 250
    edited October 2012

    Here's the link to my blog. Right now, much of it is dealing with the end of my relationship with my guy but that also ties into my treatment in some ways.



    http://diaryofamidlifecrisis.blogspot.com



    You can also check out some YouTube updates and stuff at YouTube/lifeonitsside



  • FeelingtheMagic
    FeelingtheMagic Member Posts: 155
    edited October 2012

    Glancing through and happy for those who've finished their chemo! I've had my last chemo, but continue with herceptin for nine months. I think I'll feel like chemo is over after this upcoming herceptin alone really doesn't wear me out.. or perhaps when my hair starts growing back! I'll be especially excited if I can get to doing herceptin without the insane amount of steroids and 2 antihistimines that I had to have to stop the allergic reactions.  Tamoxifen begins soon as well. 

    Pretty weak legged... and get winded easily.. but dang it, I have my nails, at least 12 eyelashes, and eyebrows that look so perfect you'd think I'd had them tweezed professionally.  I'm going to keep them so well groomed, because I've discovered taking that weight off above my eyes, makes my eyes look a lot 'younger'.  So. there's a good outcome. 

    Stride, also sending hugs and healing thoughts your way.... and wishes for kick butt treatments to get that all looked after. (kicking cancer's butt.. not yours!)

    I came across a discussion on this site tonight that was pretty uplifting. Although I don't fit the diagnosis, I came across it because a friend does. Nice to read stories of people with 'tougher' diagnosis (they are all tough, I know) and doing well after many  years. http://community.breastcancer.org/topic_post?forum_id=67&id=773239&page=9

    "July women still doing chemo"... wishing you whatever you need to make it easier.

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