TRIPLE POSITIVE GROUP

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  • cherry-sw
    cherry-sw Posts: 784

    debiann, I am deeply moved by your post, thank you. I actually red it when I woke up in the morning after I called my husband whether he has landed yet, he was on the business trip this week. Then I red about HapB's incident and just thought, oh, no.

    Thank you so much, I really felt better for so many reasons. I understand that the old life is over but I do not know what the new one is supposed to be and how to find the meaning in it and most importantly how to hold to it, where to find this strength. I do not think or believe it anymore, I know that I am a worrying kind, this is completely useless but I worry a lot about what is there to come and that I am not prepared. Your tag pops in my head now and then when all these thoughts consume me. Yours and another one I saw on these boards that is actually Hagrid's quote, from Harry Potter, "No good sittin' worryin' abou' it. What's comin' will come, an' we'll meet it when it does."

    I cannot say I am thankful for this bc, I am not, not there yet, I am not sure I ever will be. I am completely shocked I got it, maybe now ,after I have red a lot and start landing in my diagnosis, I understand that I had some risk factors like relatively large very dense breasts, late pregnancies, eating some pholate pills, maybe too much wine consumation, but on the other hand, I was exercising a lot lately, ate a lot of vegetables, we had this combucha mushroom that is considered to possess some anti-cancerogene qualities. So, here I am prepared to do any chemo they offer me and want to know how to prevent it from coming back and feeling no power and no control. And even worse, I regret the past so much, what I did, what I should have done, or that it is gone and life will never feel the same. Yesterday I was looking at the pictures from my birthday three years ago when we took a shorter city trip, I burst into tears that this feeling of security and happiness is completely gone and over and oh, I looked so beautiful. I remember it so well, I asked myself whether I could enjoy it more than I did and I couldn't, it was so perfect. Never in my life I thought that I will be going through all the pictures trying to remember the good old days so soon in my life. My youngest looks so little on these pictures, i am afraid she would not remember much and I may not be around to tell her, my husband's memory is not that reliable. I took my life for granted before and now it is threatened. I keep telling her that I love her and that she always must remember that. I do not know why I am doing it to myself, I want to believe it is a part of the acceptance process.

    I also remember you once wrote about a woman in your neighborhood who got hit by a car and died when you got diagnosed. All you wrote about a lot of things being worse than bc is true and I am grateful for what I have but as all of us I am afraid to lose it. I am grateful for all advise and will try, like deni1661, to make a list in my head and to recite it every morning, things I am grateful for, my kids, my husband, for my mom who has stayed with us since my surgery, it must be so hard for her, my job and my manager, for my cat that is there by my side as often as she can with her enigmatic look in her eyes, the fact that I moved to a country that can provide the best available treatment for me, for my oncologist who in spite of me being so PITA , she did very politely admit that the last time, in spite of that she looked at me and said that her one and only goal is to make me free from this disease, and she wished she could give me a 0,000001 risk but she couldn't but in any scenario they will not just let me go. And I am so grateful for your endless patience with my constant ranting and for any token of compassion I will receive in the future.

    SpecialK, when we were discussing my further treatment and all pro/cons for starting EC I red to her what you wrote to me regarding my possible treatment change. And my oncologist answer was: well, I am impressed that this lady took her time to write to you a so competent and detailed answer. My oncologist is not just a doctor, she is a consulting doctor, a grade between a specialist and a professor.

    Sorry for the rant, again, thank you for your reaction

  • Kim, I had very little neuropathy and it is now gone. I used the elasto gel gloves and booties. You can google the study for instructions. Worked like a charm

  • Hap ... Please get medically checked after your incident.

    Make sure your car is still aligned and the frame is not damaged.

    Vicky


  • KimCee
    KimCee Posts: 170

    HapB. Oh my gosh... I must have missed the original post. As Coach said, please get checked and have you vehicle looked at. Glad to see you will see the doctor. Thank God you were one of the miracles that walked away. Sending you hugs.

    Thank you Bird of Light. I will look into those gloves and socks for sure.


  • PauletteK
    PauletteK Posts: 1,279

    HapB you should be in shock, did you able to get some shut eyes last night? Yes we are blessed every morning, there are so much crazy things going on, we can get into any kind of accident. Take care your body have it check up please.

  • suburbs
    suburbs Posts: 398

    Wow. This board has been quite busy.

    HapB, please seek medical care to be safe if only to confirm the existence of angels.

    Cherry-sw, keep on talking things out. It's therapeutic and should help. Never imagine there is an allotment on how much you can share. There is no score card here. That's what is so amazing about the triple positive board - judgement free zone. It's my life line too.

    Debiann,thank you for those words of wisdom.

  • HapB I was so sorry to read about your accident. I really hope you are okay and not suffering from any serious after effects?

    Cherry-sw I know exactly how you feel. The thoughts about re-occurrence and getting worse are with me too. I try to stop them in their tracks and a lot of the time I do, but there are plenty of days when I can’t shake them off. I am hoping as time moves on the negative thoughts will lessen and the positive thoughts will take over. We are still in the very early stages of coming to terms with our illness. I have to believe in the days and months ahead life will be better for all of us.

    I haven’t posted for a while on here as I don’t want to always complain and moan about the issues I have had with my wound. And that’s what I feel I have been doing constantly.

    It’s 7 months since my first surgery followed by a 2nd lumpectomy 2 weeks later and my wound still has a dressing on it. It has never healed “properly” and since my radium finished over 2 weeks ago I have been told there is an infection and I am now on 2 different antibiotics. I feel worse now than I ever have since the start of my treatment. And to really rub salt in the wound I am supposed to be going to Glasgow for a few days break next week and have been looking forward to it for so long. Now it looks like my sisters and Mum will be heading off without me.

    Ever feel like running away people??? I hope tomorrow is a better day 😔😔
  • T-Sue
    T-Sue Posts: 207

    Hap, thank goodness you came out of that accident unscathed! Please let us know how you are doing after a Dr. check and some rest.

    Glascowgirl, I'm so sorry to hear that your wound hasn't healed yet. What a pain! Just as you advised Cherry, no limits as to what you can share here! Complain all you like. I hope your double antibiotics knock out that infection and allow you to join your family on a trip.

  • cowgirl13
    cowgirl13 Posts: 817

    GlasglowGirl, please don't stay away because you think you are complaining and moaning. It is very important to be able to talk and put things out there. Having your feelings and talking about them is exactly what will move you forward.

  • cherry-sw
    cherry-sw Posts: 784

    Hi GlasgowGirl99, I am sorry your wound wouldn't heal. What does the doctors say? Radiation does certainly not help the healing process, I red about it, it takes longer time. And I am sorry you are not able to go to Glasgow because of that, a trip may take your mind out of this bc thing, I hope you can join your mon and your sister the next time. Please moan and complain here as much as you want, I am doing it to often as it seems but only when I really have to pour it out which gives you an idea how I really feel and I am on a mild anti-depressive, maybe I need some heavy stuff. If I could choose I wish it never happened to me and my family but it did and I want to understand how I can make the best of this situation and so far I have not figured it out how to do it. I mean I have been given advise and I know in theory but I am still not there but I am trying because there is simply no any other way. I hope your wound will heal soon and I am sorry you are feeling low, hang in there, clouds move, there must be some better days ahead.

    I always feel like running away, driving actually. When I drive to an appointment or to the store I always think if I could just keep driving somewhere for really long time and come to another city away from all this stuff.

    Hugs from chilly Stockholm,

    Cherry

  • cherry-sw
    cherry-sw Posts: 784

    HapB, did you see your doctor? I hope you have not sustained any injuries, please keep us posted

  • About moaning and complaining ...

    What a wonderful supportive forum to pour everything out! No one judges us here because everyone can understand what the 3+ journey is like.

    The Nurse Practitioner on my MO Team shared that she thought the 3+ treatment was the hardest of all cancer treatments because it lasts so long. It is. For me it was 2 months of surgeries and healing. Afterwards the chemo time was 22 August 2016 thru 14 Aug 2017. Doing ANY medical treatment for that long would have moaning and complaining as a side effect!

    Bring it on! Pour your hearts out.

    Vicky


  • HapB,

    Wow! what an ordeal. Yes, sometimes we just should feel doubly-blessed. Last night, a tornado hit a concert my daughter was attending. No injuries, just damage to the roof on the building, thank God.

    Glasgowgirl -- Ugh about the lack of healing! How frustrating for you. Yes, just vent as much as you want. You, too, Cherry! Better to just let it all out to some sympathetic ears.

    coachvicky, triple positive is truly a marathon that tries the patience and the goodwill of all of us. I sometimes think it helps if you break it down into segments, mentally. "Radiation done! Got that checked off the list."

    My best to all!

  • hi ,I hope someone can answer this question

    I take anastrazole ( Arimedex ) daily

    Can i take antiacid ?

    I heard that antiacid ( zantac )

    Will reduce the absorption of the Arimedex

    Any feedback would be greatly appreciated

  • deni1661
    deni1661 Posts: 425
    Glasgow - so sorry to hear your wound hasn't healed yet. That sounds like a terrible ordeal. 7 months is a long time and I can only imagine how frustrating this must be.

    As the others said before me don't ever feel like you're complaining. This is the best place to share what you're going through. I find this group to be the most comforting resource I have since most people in my world cannot relate to what I'm feeling. We're in this together for the long haul.

    Sending prayers that things get much better for you soon. Hugs
  • PauletteK
    PauletteK Posts: 1,279

    HapB - thanks God you are fine! Yes we need to live life fully everyday even under chemo.

  • suburbs
    suburbs Posts: 398

    HapB, haut les coeurs!

    Glascowgirll99, what an ordeal! Please feel free to rant lots and often. Very frustrating for you. Sending positive healing thoughts. Please keep up posted.

  • Thank you all for your words of encouragement ☺️☺️. Good to know I can come here and let all my frustrations out without being judged. My 2 sisters and Mum are heading off tomorrow morning while I am going to the hospital to have my wound checked again. I am hoping they may give me the go ahead to go to Glasgow on Tuesday but at the same time want to be close to my own oncology team in case things worsen 😐.

    So glad to hear you are ok HapB.

    Cherry - we will get those better days very soon 😊

    Hugs to each and every one of you dear ladies 🤗🤗
  • la1986
    la1986 Posts: 4

    Good evening,

    Happy Sunday night! I just started chemo this week and wondered if anyone who has taken L Glutamine during TCH chemo can share what their dosage was if they took it everyday during treatment or just a few days before and after? Appreciate it, thank you very much. My oncologist is on board but I am curious about the protocols. I have seen recommendations for 4 days afterwards to the entire course of treatment

  • T-Sue
    T-Sue Posts: 207

    Thought you all would get a kick out of this. My son and I tested out Halloween costumes for a "Boo at the Zoo" event today. My shirt says "It was never a dress" and I have a red cape and my headscarf to compliment it. 😀

    image

  • PatinMN
    PatinMN Posts: 784

    LA1986 - I took l-glutamine four days a week on weekly taxol. 15 grams in the morning and 15 grams in the evening. 15 grams is about a heaping tablespoon. I also took 100 mg of B6. It seemed to work for me - or maybe I wouldn't have gotten bad neuropathy anyway. Who knows? The chemo nurse suggested waiting until I had symptoms before starting since neuropathy doesn't hit everyone. I ended up with just some mild tingling.

  • T-Sue
    T-Sue Posts: 207

    Thank you HapB! The "It was Never a Dress" campaign was started by a breast cancer survivor to bring awareness to the hidden powers of women. It's not just a rah-rah thing, I believe that she promotes girls in coding and engineering classes and careers. You can read more about it here:

    https://itwasneveradress.com/about/


  • specialk
    specialk Posts: 9,299

    hap - glad you're ok, that had to be scary!

    la1986 - I had 6 TCH and took both L-Glutamine and B6. I took 30g of L-Glutamine in 3 daily servings of 10g each. I dissolved it in a cold, non-acidic drink - heat and acid can denature the powder. It is pretty tasteless so you can disguise it easily, but don't mix it with pudding or applesauce and try to eat it. Trust me on this, lol! I took a 100mg capsule of B6. I took both of these supplements throughout chemo.

  • CCNC
    CCNC Posts: 26

    Question for everyone on TCHP or Herceptin, how often is your oncologist checking your heart throughout the year(s) of treatment? How many echocardiograms have your had during your treatment?

    Thank you

  • CCNC

    My heart had a baseline and checked two other times. My scores increased each time so I did not have a final one.

    Coach Vicky


  • cherry-sw
    cherry-sw Posts: 784

    HapB, this accident sounds horrible indeed, you were luck

  • cherry-sw
    cherry-sw Posts: 784

    T-Sue, love the picture and the spirit, your boy looks just like you, very sweet. How old is he, if I may ask? Those who are posting pictures actually look good, I really look bad, completely unrecognizable to myself. Yesterday I cut what was left of my hair, it was not much I kind of looked like Gollum but some hair stuck out when I had my hat on. Now it is gone and I do look hideous, so sick and aged like 10 years

    Cherry

  • cherry-sw
    cherry-sw Posts: 784

    Hi everybody, I got another question. Prior chemo did your oncologist asked you about exposure to any kind of radioactivity?

  • T-Sue
    T-Sue Posts: 207

    CCNC, I also had a baseline eccocardiogram before herceptin. My MO requests an ecco every three months while on herceptin for a year. 

    Cherry, thanks! My son is 9yo. I had a Gollum look for awhile too - I think the buzz cut looked better. Getting some colorful scarves and new, bright lipstick helped me look better and feel better. Also, I don't recall my doctor's asking about radiation exposure.

  • cherry-sw
    cherry-sw Posts: 784

    T-Sue, this is definitly your collor.

    I also wonder if anyone had been exposed to any radiation in their teens