TRIPLE POSITIVE GROUP

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Comments

  • elainetherese
    elainetherese Posts: 1,640

    shelabela,

    Good to hear you're recovering from chemo. I have often thought that if I recur and do a BMX that I would consider DIEP. After my twin pregnancy, all of my weight gain ends up in my tummy area, so there's plenty of fat to use. Plus, you get a tummy tuck in the process! But, I would have to have the time to devote to surgery and recovery, and I still work full-time and have the time-consuming twins with autism to manage.

    Moodyblues,

    Steroids made me crazy, too. Ugh. That was the worst part of the Taxol infusions.

    Re: positive attitude -- it is one thing we CAN control, and it's awesome when cancer patients do adopt this approach. My health care providers have often complimented me on my attitude, probably because it makes their jobs easier and they ran out of other cheerful compliments at some point (e.g., nice wig!). But, I don't think anyone should feel pressured to maintain a positive attitude or to be a brave cancer warrior. We each come to cancer from a different place. I came to cancer as a 46 year old woman who needs to work full-time and to be there for her special needs kids, who will live in our house indefinitely. (My sons are on a 10-year waiting list for post-secondary education services and, thanks to state budget cuts, we don't know what services will be available for them when they leave school.) Getting through treatment was the least of my worries. ((Hugs)) to Denise, HapB, and everyone on this site.

  • moodyblues
    moodyblues Posts: 393

    Shelabela.  I didn't do DIEP because of the extra surgeries and pain in two areas (mastectomy and abdomen).  I also did not do DIEP as I am 54, soon to be 55 and it wasn't worth the extra time that it would take to get it all completed.  I had a unilateral MX and will have the tissue expander taken out and the implant placed before the end of the year (hopefully).   I may work on getting the other breast to match at a later time, at this point honestly I can't wait to get this all over with. 

  • kae_md99
    kae_md99 Posts: 394

    shelabela,

    if i was only a good candidate i would do DIEP flap but i am not so i would have to go with implants and i am so scared about having TEs right now but it is what it is...

  • poseygirl
    poseygirl Posts: 298

    Hi all, I think I've mentioned this before, but I'm wondering if any of you get tingling or pins and needles in your forearms and fingers on the side of your surgery? Mine is almost always there, but more pronounced at times. Wondering if this is normal??


  • Hi everyone. Haven't posted in a while as I am still waiting for my Taxol to restart. Still have a dressing on wound but hope and pray this will be the last one. Seeing my BCN tomorrow morning who will check the wound. Fingers crossed its healed and Taxol will restart next week. I notice you receive Herceptin through infusion. I am also on Herceptin every 3 weeks but it is injected into my thigh (alternating each week) and only takes 3-5 minutes - no SE so far. I assume this is new as my sister also had Herceptin on 2 occasions and at that time (4-5 years ago) she had it as an infusion with her chemo.
  • Tresjoli2
    Tresjoli2 Posts: 579

    HapB I second SpecialK. You have to slow the infusion down to 90 minutes. It makes a huge difference!!!

  • specialk
    specialk Posts: 9,299

    hap - your side effects from a 30 min infusion indicate potential benefit from dropping back to a 90 min infusion. I wouldn't suggest slowing your infusion rate, I would insist. Remember that you are the customer. Also, I believe injectable Herceptin is not yet being used in the US currently. The injectable dose is substantially larger than what you are getting with weekly IVinfusion.

  • Taco1946
    Taco1946 Posts: 630

    I really had trouble with Taxol (quit after 8) but going to a 30 minute of Herceptin worked for me. Had lots of joint pain when I started Anastrozole but it has gotten better over the last 6 weeks. Seems to just be the aches and pains of age 70 plus arthritis now. (I've already had surgery for achilles heal and for carpel tunnel). The handful of pills twice a day seems to keep growing but for now I will hang in there with the treatment. Quality of Life issues are important for me and I feel as if I don't have a very high pain threshold so I'm certain I will continue to revisit doctors' recommendations in the months and years ahead.

    Hair on my head seems to be coming in very slowly (I'm over 3 months post taxol) although not on my legs and arms.

    Just scheduled my 6 month mammogram and am certain that this Friday's visit will lead to another echo order. I resisted a bone density study pre-cancer because I had decided I wouldn't take the medication which my primary respected. Will probably have to revisit that now although MO hasn't focused on that as a SE. Will see primary again in August.

  • deni1661
    deni1661 Posts: 425

    Shelabela- glad to hear you are doing well after chemo and building up your immune system. That will help with your surgery recovery! I had Unilateral April 27 and DIEP recon May 27. My PS laid out all the options and I felt this was the best choice for me as I wanted a "one and done" recon i.e I didn't want lots of revisions. I had enough belly fat for one breast and got a nice tummy tuck out of it. I recovered from the mastectomy quickly, off pain meds and moving around pretty good in less than 2 days. My DIEP surgery was 7 hours - they monitor you closely for the first 72 hours to make sure the transferred blood vessels are flowing properly. I was in the hospital 3 days. Couldn't do much of anything for 3-4 weeks except sit in a recliner or on my deck (lots of vitamin D!) or sleep. Each day I could move around more. I was off work a total of 9 weeks. I am still tired, my breast hurts somewhat, I have cording under my arm but that's getting better, and my stomach feels tight. I am happy with the results and didn't have any real issues other than pain but even that wasn't too terribly bad. Feel free to private message me if you have questions.

    In regard to the positive attitude string, I believe faith and a positive attitude can help you get through difficult times and probably has some health benefits. Cancer is a mean monster and we're all entitled to our down days; we wouldn't be human if we didn't cry or worry or get crabby with all we're going through. Staying positive, meditation, and acceptance has helped me see the beauty in each day regardless of how I am feeling. I start my day with thanking God that I get to see another day and then I go through my grateful list. I can't really complain or be negative when I think about the many blessings I do have. I tell myself that any pain or side effects or inconvenience is only temporary - good days are ahead for all of us!

    Hugs and blessings to each of you.....


  • suburbs
    suburbs Posts: 398

    Shelabela, my BMX was last Wednesday and I have been home since Sunday evening. So far my experience mirrors that of deni1661 - pain and very little movement other than from recliner to patio to couch to bed.

    I left the hospital with 4 surgical drains, a pain ball and a Foley catheter (long story not fun!). One drain and the pain ball were removed today. Hurrah! The drains make sleep very difficult especially if you are a side sleeper.

    I have a schedule of family and friends to be 24/7 caretakers for the next 5 weeks and a visiting nurse a few times a week. Between appointments, picking up prescriptions, milking and measuring drains,and preparing meals, so far there is a lot to do and it's a full-time job. I am not helping at all. A lot of planning took place in advance.

    And to think I was going to go flat. Anyway, please feel free to pm with any questions. Also the 2017 DIEP thread has a ton of information.
  • deni1661
    deni1661 Posts: 425
    Suburbs - congrats on your surgery. Sounds like your recovery is going well, a few drains out is progress yippee! It's a long recovery but not as bad as I thought it would be.

    I might have missed it but did you get your pathology results yet? I've been saying lots of extra prayers 😊
  • deni1661
    deni1661 Posts: 425
    MLMSC - thanks so much for sharing your update. Great news, only 4 Herceptin left for you!!! I can't wait to hear the bell when you are officially done. I have 4 left as well with my last one on Aug 30. It certainly is a milestone to celebrate for us both.

    Congrats on how far you've come on your cancer journey- wishing you the best
  • deni1661
    deni1661 Posts: 425

    Sooz714 - so sorry to hear of the terrible time you're having. You are tough. Sending prayers and hugs your way. Take care

  • bji
    bji Posts: 116

    Taxol #5 done! Went good, my port cooperated and gave blood return right away. Ran some errands and stopped for supper at Texas Roadhouse. Have a busy week, 2 family birthdays and holiday weekend planned at the lake. I did take the plunge and shaved my head, the top had gotten so thin I couldn't style it. The back and side weren't too bad, I still have hair, just very short. My wig fits much better without the hair, had it cut to match mine. Out to dinner with friends on Monday and last night spent with my Bunco Babes, no one even noticed! I did get a bamboo beanie for night, just going bare headed at home. Last week brought the dry mouth, hoping nothing new this week. Have noticed slight breakout on my face, nurse said its from steroids. Still have my eyebrows and eyelashes. No neuropathy yet, nails still look good. Despite what others say, I still believe that positive attitude and faith has made my journey easier. I know I still have a ways to go, but next week will be halfway home! Another positive - I haven't shaved my legs or armpits in over a week!

    Praying for a good week and few SE, everyone have a good 4th of July!

  • specialk
    specialk Posts: 9,299

    hap - not all chemo drugs used for other types of cancer cause hair loss, however most for breast cancer do, and they do it with the first dose - that is why they say you usually see hair start to fall at about the 14 day point. With only one dose of Taxol you may only experience thinning, but not total loss.

  • specialk
    specialk Posts: 9,299

    This is a link from Chemocare.com re: Taxol - 2nd side effect listed is hair loss. I am surprised any MO would say you won't lose your hair.

    http://www.chemocare.com/chemotherapy/drug-info/Taxol.aspx

    hap - The reason I like PREDICT is because it factors in treatment for Her2+ breast cancer - other calculators may factor in the risk, but not modify it with the treatment modality.

    Here is a link to their site that explains what their numbers are based on:

    http://www.predict.nhs.uk/faqs.html

    As always, whether you recur is either 0% or 100%. Looking at those numbers will not tell you the risk you face as an individual, it will only give you a general group-based statistical prediction, which is exactly what their disclaimer says.

  • specialk
    specialk Posts: 9,299

    hap - you won't find the Taxol and Herceptin regimen, or the Herceptin alone. Taxol with Herceptin as a stand-alone regimen is too new, and usually only prescribed for those with Stage 1, or less than 1cm and node negative. Herceptin alone is not a recognized regimen, it is only done by individual oncologists in very specific situations - you won't find any data at this point. The current trials ongoing are not complete so no info has come out yet regarding efficacy of Herceptin when not combined with chemotherapeutic agents.

  • Tresjoli2
    Tresjoli2 Posts: 579

    BJI the acne is from the steroids. If u have a dermatologist, they can prescribe retin- a . They have to file a special claim with your insurance to get it approved because its supppsed to be for teenagers. Will clear it right up.

  • It's been 5 weeks since my Taxol was put on hold due to problems with my wound. After 5 Pico vac dressings it has eventually healed and I was able to have Taxol #3 yesterday with my 3rd Herceptin. So relieved to get back on track. Am keeping my fingers crossed there will be no more major setbacks. Aiming for Taxol to be finished by beginning of September and then 4 weeks radiotherapy. No SE's as yet from yesterday's Taxol - here's hoping that lasts 😊😊
  • suburbs
    suburbs Posts: 398

    Hi all. Deni1661, yes, I agree the recovery from DIEP will take more time but so far I am glad I gathered the courage and went for the more involved surgery. The time required for expanders and fills and exchanges can be spent recovering from the first big surgery. Thanks for thinking of me and leading the way by going first. So far so good!

    This week has of course been tough physically but I feel incredibly grateful. I got straight A's on my pathology report card - complete pathological response, no evidence of disease, 4 nodes biopsied with no evidence of cancer. There were no questionable margins to measure. My medical team will make a final recommendation on radiation. It looks like I may be able to avoid it. I could not have asked for a better outcome. I need to constantly pinch myself.

    I'll be recovering for weeks to come but with gratitude and hope for the future. I will need to find a way to give back and volunteer to help others once my strength returns.

    For everyone stateside, happy 4th.





  • OH Suburbs this is wonderful news.. I'm tearing up! Hugs!!

    Hugs from TN
    Denise

  • shelabela
    shelabela Posts: 327

    suburbs,

    That's great! Also thank you for your posts about DIEP surgery

  • My one and only statement on my last post before I took a break..

    I would never force what works for me or other on to someone ... That would be rude and unhelpful.. You can't force this... you can't make someone be happy and positive ..... plus its not anyone's job to do so..
    But we don't need someone jumping in and saying our opinion on what works for US is wrong... We ALL have to find what works for each of us and use it daily.

    HapB I took what you said to myself and BJl about positive attitude as a slam against what we know works for us, That having a positive attitude was not backed up by research and we were wrong and could cause hurtful feelings to someone who didn't have a positive out look..
    I think it started with your post on page 1041 to BJI.

    You may not have meant it that way..but that's how I took it ... and if you didn't I'm sorry ... and I mean that with all my heart..
    Also,after stepping back most likely it didn't help that was in the throws of chemo hell either..
    I thought it best to take myself out of the situation.... and will again if it gets too much...

    Having a positive attitude is NOT a cure...
    Yes I am a firm believer in the Mind Body connection ..I've seen it work... over and over again .. you can't separate the mind and the body
    I'm a firm believer in positive attitude or prayer ( no matter what faith or not ) or energy work or even humor, or?
    Because it has helped ME .. I don't need any research to tell me that it doesn't I'm living proof that it does....keep reading I explain why

    Do I cry?... every freaking day ... do I want give up... every freaking day ... do I get mad... yes... do I shake my fist and scream to the sky.. yes..
    I am have never been this scared in my life.. and let me tell you I've been in some pretty scary places.. a lot of dark places in my life.. This cancer has them all beat...
    But I made a promise to myself I whatever happens no matter if I live 2 years ..or 30 years ..
    I was not going to become bitter with what time I DO have. I'm not going to have my family and friends remember ME as a bitter old woman ..
    I was going to fight ....even with myself at times to be happy and positive....

    Y'all don't know me .. or my back story .. but I will say this I fight depression,anxiety and a form of PTSD everyday of my life.. I have to work at living .. Learning how to have a positive attitude was something I HAD to learn to do to just survive .
    Then BAM! Cancer... :::flipping my tumor off ::: its not going to take that hard work I've done on myself away from me.. its taken so much already .. no .. no way ...

    If what I've said or will say in the mind/body connection upsets you HapB or anyone else .. then just pass my post by..or block me.. because I'm not going to stop being who I am ...just know that I wish you well,health and happiness ... and will move on ..

    If anyone wants talk more about this with me .. I will be more than happy to take to pvt. conversation ....because this is NOT what these boards are for...
    We've got too much healing and living to do to waste our time on this .....

    Hugs from TN
    Denise


  • Well I made it through my first round of chemo ! Today I feel more like ME! Still have a little fatigue ...diarrhea ... and now my hair is falling out by the handfuls :( .... sat on the side of the bath tube yesterday holding some of my hair and cried... when I stopped crying I thought ... losing my hair is much like a snake shedding its skin.. I'm shedding the old to become something new... I know that sounds weird... but it works to get me through this process... I just hope it grows back.. I'm on Taxotere .. blahhh...

    I'm glad I'm feeling good for the 4th .... :) Then its round 2 next Friday.. I am going to insist that they do the H and P slow.. if not I will throw a hissy fit..

    My tumor does feel different maybe not smaller but flabby feeling if that makes sense ? Its under 2 cm and sometimes can be hard to find...
    Maybe its just wishful thinking ..

    Went and talked to the one of the folks at the Gild's House on Weds. Drove for the first time in two weeks... that was fun.. NOT ... lol Nashville is not a fun place to drive... but I made there and back..
    I urge everyone to find a Gild's House in your area ... they are WONDERFUL... and have classes,workshops .. support groups and such to help you with your cancer journey... and its all free.. plus your family and friends can come too :)
    In mid July I'm starting ... Qigong,Tai Chi and Mindfulness / Meditation classe! I'm excited :)

    I hope everyone has great 4th of July weekend !
    Hugs from TN..
    Denise

  • kae_md99
    kae_md99 Posts: 394

    hi all,

    can you tell me what kind of tests/ bloodworks/scans your MO did after treatment to check for recurrence? if he/she did tumor markers,what are those? and how often were these tests/ bloodwork/scans done? my MO said she will only do physical exam on me and i was surprised that she wont do more...

  • bji
    bji Posts: 116

    DeniseT

    Well said, thank you.

  • Hey..
    HapB , I'm Taxotere which if I'm not mistaken is medication like Taxol .. I think its made from the same plant alkaloids ... Special K or someone correct me if I'm wrong..
    But I had my first loading dose over 2 weeks ago... and my hair is falling out by the handfuls ... its a good thing I've got a lot of it ... if my hair was thinner I would already be bald!
    I'm just going to either get mine shaved down or even just shaved off this week...
    Also my eyelashes are falling out but only on my right eye !?! lol... too weird...

    Hugs from TN
    Denise

  • shelabela
    shelabela Posts: 327

    hapb,

    I lost my hair on Taxol, some do some only shed. Mine was coming out so fast I couldn't keep it cleaned up so I shaved after the 4th dose. My head also hurt so bad. Felt so much better after I shaved it.

  • specialk
    specialk Posts: 9,299

    denise - yes Taxol and Taxotere are both taxanes (as is Abraxane also, but without the solvents) but Taxotere is a more powerful drug - it is Taxol's big ugly cousin.

  • Great.. I get the ugly cousin.. wheeeeeeee lol

    Hugs from TN
    Denise