Anyone triple negatives that has finished all treatments

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Dahlia1966
Dahlia1966 Member Posts: 26

Hi everyone,



just wondering if anyone has finished all treatments and going on with their lives. I am currently having radiation and have been so depressed lately. I need some encouragement. I need to know that there is some kind of light at the end of this dark journey. I am paranoid and depressed. I try to be so strong for my husband and children but I am dying inside. Did anyone get some kind of proffessional counseling? And did it help at all. I think I need to seek counseling.

Comments

  • Morgan513
    Morgan513 Member Posts: 664
    edited September 2011

    Hi!  I'm almost 3.5 years out from diagnosis.  Yes, there is life after treatment but it's scary sometimes but I have to say that time does begin heal the body and the mind.

    I started counseling during treatment and I still see someone today.  I find that my anxiety levels tend to be higher than they used to be.  I guess, after all, life is not the same.  But I am very healthy and quite happy.  I exercise regularly and eat well.  

    Find someone to talk to.  You won't regret it.

    Lorrie 

  • lisaorock
    lisaorock Member Posts: 50
    edited September 2011

    Hi! I was just diagnosed last October and it has been quite a journey ever since.  I had a double mx,hysterectomy,and 8 rounds of chemo every two weeks. 4 dose dense AC,and 4 Taxol. I'm also triple negative and BRACCA 2 positive. I'm still not done with my breast reconstruction.  I just had implants placed on Aug 1 of this year. I was declared cancer free as of June 2.  My hair is coming in thick and dark. I get compliments on how it looks all the time.  I have to see my oncologist every three months for three years.  I am petrified of recurrence.  I try to exercise at least 3 to 4 times a week and eat right.  I am also going through menopause.  My husband,family,friends, have gone above and beyoond with their support.  My children have handled tis year beautifully.

     I should be happy right?  I try to be.  I have good days and bad days.  My energy level is no where near what is used to be. I am 45 and I feel like an old lady.  I just started going to a support group. It does help to talk to someone who "get's it".  I feel like a black cloud is following me.  I just want my life back.  I know it takes time because we have been through so much but I'm sick of all of it!  I just had another three month check up on Thursday.  I get my blood test results on Tuesday. I am a wreck inside.  I know exactly how you feel.  

    I just hope with time our minds and bodies will rebound from all of this and we'll be better than ever:)

    Take Care,

    Lisa

  • Dahlia1966
    Dahlia1966 Member Posts: 26
    edited September 2011

    Thank you ladies, I really appreciate your encouraging words. I think I am going to see a counselor soon. My family has been wonderful but I need something more. I am also 45 and can't wait to go back to work. Just reading your posts really made me feel so much better. I think I will also find a support group near me. Thank you again.

  • maywin
    maywin Member Posts: 49
    edited September 2011

    I'm eight and a half years out and had BMX and implant reconstruction. I still get scared sometimes but all in all, I get on with life. I come on here from time to time because it was such a kindness for people like Shirlann who posted and reassured me when I  was first diagnosed. I also was on effexor for a couple of years....it helped too.

  • Titan
    Titan Member Posts: 2,956
    edited September 2011

    Hey Dahlia...nearing the end of treatment is a scary thing..but believe me.."they" will not just say see you later...you will be followed for several years...you will be told what to watch for and you need to be diligent.

    I think sometimes our bodies bounce back quicker than our minds do..."Cancer' is such a freaking scare thing to hear...and when it means YOU ..man..it takes alot to get your brain wrapped around the fact that YOU have cancer, not your neighbor, not your friend..YOU...once you realize that fact, the healing can begin...and it will.

    Time really is a great healer...really..I'm almost 30 months out...next goal is 3 years...I can't believe how fast the last couple of year of gone..you will be that way too..really!

  • RJ70
    RJ70 Member Posts: 21
    edited September 2011

    I had my last treatment in March. and I feel great. last week I painted the out side of my house!!  At the began of summer I hated not began able to do. . I  didn't gave any  get up and go  but I push myself little bit more everyday.  I am not 100% back, but I am close.

  • AimeeMac
    AimeeMac Member Posts: 241
    edited September 2011

    Maywin, seeing that you are 8-1/2 years out is the most encouraging news. I finished chemo in March (6mos PFC yesterday), and rads in May. Did not have MX. Tomorrow I meet with my Onc.

    Dahlia, I remember feeling just the way you did. For some reason radiation was much harder than chemo. Just the knowledge that it was every damn day for 33 days, and laying on the board I could see myself in the reflection on the ceiling. I would feel like crying while I drove there and while I drove home. But day by day after you are done, it will get a little better.

    I felt much more stress and anxiety (and still do), and decided to go the pharma route rather than the counseling, but I would recommend talking to someone if it will help. Going back to work for me was the best of all. I travel for business, and being grounded for 6 months was the worst (especially during a drizzly gray Seattle winter). When you get back to the routine of work, you will find that hours go by when you don't think of cancer. Trust me, it will happen. Still haven't gotten to the point where an entire day goes by, but I have heard from people who know that this too will happen.

    These boards are a great resource and comfort; while I haven't spoken with a counselor there is so much support and encouragement here (and the ability to vent as much as you like) it has been like counseling for me.

    I hope you will post as often as you need to, and I assure you that one day in the future you will be giving support to someone who needs it as you do now.

    Aimee

  • minxie
    minxie Member Posts: 484
    edited September 2011

    I am almost 3 years out from diagnosis. Cancer is incredibly hard to get through emotionally. I saw a counselor during and after treatment. About a year after treatment I was still plagued with severe anxiety because of the cancer fears. I started seeing a psychiatrist who put me on anti-anxiety meds, which had helped my general state of mind somewhat.I still have issues but am able to enjoy life again. Don't let the stigma hold you back from seeking help - nobody can understand what you're going through unless it's happened to them. I know some people think I'm weak for not being able to deal with it all, but they have no idea what it's like to live every moment in fear, especially when you'rea mom to young kids.

  • Thepeddlerswife
    Thepeddlerswife Member Posts: 69
    edited September 2011

    My daughter is triple negative and just beginning treatment. Is radiation pretty standard treatment for Triple Negatives? I know that the weekend after my daughter was diagnosed she bought her first horse. She has spent the last two weekends riding and taking the boys with her on separate "alone" time rides. This is when she talked to them about mommy being "sick". I think this horse will be the best thing for her. Her "therapy". Horses have always been a part of our lives but this is her first "horse of my own". Animals can be amazing therapists!

  • yellowdoglady
    yellowdoglady Member Posts: 349
    edited September 2011

    Dahlia1966,

    What you will hear again and again is that each of us is unique in our diagnosis and different in our treatment and reaction to that.  That being said, I think all Triple Negs are shocked to some extent by how fast this thing comes on us.  I think all of us take it very seriously.  I've heard that TNBC patients are the best about sticking to a treatment plan, which is something that can impact our outcomes in a very positive way.  I know everyone I know like us hits those waves of wondering if "this is it" and what we could have done differently either to prevent it or to not feel so deprived of the life we expected.  The quick answer is that most of us could not have seen this bus coming when we stepped into the crosswalk as it is generally a random thing.  We can do something about making our lives better afterwards.

    Some of us lose some friends or family who are so frightened or unable to give that they can't deal with being supportive during treatment.  That can be temporary or permanent.  But you should never think you will be sent out on your own after treatment ends.  You will be watched by one or more hawks, maybe for five years from dx, and your life will get back to normal or something close long before then.

    Your hair will grow back.  Your energy will return in time, maybe not the minute you finish treatment, but you will get stronger month by month, and then your stamina will return as well.  Give yourself a few months after treatment to heal before you think to call yourself lazy.  If you have anxiety that needs attention, go ahead and get some counseling.  A professional can better understand what you have had to traverse than a friend without that experience, and most health plans will allow for several sessions a year so take advantage of that if you have it available, or join a support group.

    And just so you feel better about thinking ahead, I finished treatment two years ago in July and am just fine so far.  I'll be celebrating my first wedding anniversary next month.  Am I happy?  Yes.  Is life different than before?  Yes.  And I've taken some flack for my views on this, but I choose to look at the ways it has changed for the better.  I don't worry so much about the little things that don't matter much.  I try to enjoy every day, as I see them each as a gift I might not have had the opportunity to receive had I not chosen so much difficult treatment to have this now.

    I try to avoid those who want to howl about how cancer ruined their life.  It ruins all of our lives for a time; the choice is whether to stay there or move beyond to the goal of living happily ever after.  I choose happily ever after.  Most of us do.  And most of us get there.  Best of luck to you!           

  • mccrimmon324
    mccrimmon324 Member Posts: 1,076
    edited September 2011

    Just wanted to say that I am still in treatment, will have my last chemo in a week and a half.  After that I start radiation, I asked the be put on anti-depressants right before my first chemo and have been seeing a physcologist since the beginning also.  I am handling it much better than I thought I would but I know for a fact it's the meds and counsling.  I have really bad anxiety so I also take a xanax a day, that helps quite a bit too

    Good luck to you

  • epgnyc
    epgnyc Member Posts: 101
    edited September 2011

    I finished my treatments 3 weeks ago and it's still hard going.  This is my 2nd bout with breast cancer - my TNBC recurred 9 years later.  I remember the first time it look me 7 months to feel like my old self but this time I think it will take longer (after all, I'm almost 10 years older).  Even worse than the physical stuff (neuropathy, fatigue, aches and pains, etc.) I think it's the mental part that is the hardest afterwards.  A week ago I knew I was sliding into a depression so I called and made an appointment with a counselor who specializes in treating cancer survivors.  I think it will help.  Anyway, when I'm feeling my worst I just think to myself, "I got through it the first time  and arrived at a place where I felt well and happy and I can do it again!  Good luck and do reach out for some counseling if you feel you need it.

  • Dahlia1966
    Dahlia1966 Member Posts: 26
    edited September 2011

    Thank all of you ladies for your encouraging words. Just being able to share my thoughts and fears is so therapeutic. I really appreciate everyone here. It's amazing how just a few words from total strangers can lift my spirits. Thank you from the bottom of my heart.

  • Ranebow
    Ranebow Member Posts: 3
    edited September 2011

    Hi Dahlia, Sept 9 was my one year since I found out I had breast cancer, triple negative, lump in my breast and in my lymph nodes, 8 rounds of chemo, double masectomy, 33 radiation treatments and in 2 weeks I will have my DIEP FLAP reconstruction . Its been a rough year but through the grace of God and the support , love and prayers of wonderful family , friends and an awesome caring significant other ( he is my knight in shining armour ) I am stronger now than ever . The first 2 weeks I cried and felt so angry with it all ... cry, we have a good reason to ... I sure did ...  but then I said to myself I CAN BEAT THIS ... I educated myself with too much INTERNET information on Breast Cancer, started eating healthy, getting more rest and kept myself busy, gardening and just trying to take it one day at a time . You can do this ! Focus on the positive, find a hobby that you enjoy, pamper yourself and  think how fortunate we are that there are treatments and medicines for us . This journey has changed me forever , don't be hard on yourself, we have been dealt a nasty hand but the cancer card can also be tossed aside when you finish treatment and are told " the cancer is gone " what a wonderful day that was for me back in August when my pet scan came back clear !!!  I wish you all the best, take care of yourself, stay strong, get some fresh air and sunshine every day ...  talk to your oncologist about depression . The doctors are there to take care of you .  I hope these words help even if just a little bit . Keep us all posted please .

     Iris

  • Carla9112
    Carla9112 Member Posts: 162
    edited September 2011

    Hi triple negative sisters - I was diagnosed August 4 and since then it has been a whirlwind.  Biopsy surgery, double mastectomy, port surgery and chemo starting on 9/19 - radiation after that.  I also found out that I'm BRCA1+.  Don't get me wrong - I'm scared and hate this but my dear mother had breast cancer 29 years ago and had a double mastectomy.  She is alive and well and has been such a strong supporter for me.  She is proof that there is life after cancer.  She said for the first five years though every time she got a sneeze or pain she thought the cancer had returned.  She drove her doctors crazy!!  So, we all have to hang in there and keep moving forward to happier days in the future.

     Carla

  • Dahlia1966
    Dahlia1966 Member Posts: 26
    edited September 2011

    Ok, before I drive my dr's and myself crazy, here are my symptoms. My blood pressure is 90/60 and pulse is 103. My digestive system is all messed up. The big D everyday sometimes with a little blood. All this along with my breast cancer. No matter how positive I try to be, this really sucks!! Thanks for letting me vent!

  • lisaorock
    lisaorock Member Posts: 50
    edited September 2011

    Dahlia,

    Vent away!!! I have been eactly where you are! You are right it does suck but please believe me when I say you will get through it!!!!  I would read posts on this board while I was going through it and think I was never going to feel good ever again.  It's a tough road we all travel down but we make it through!  My last chemo was March 7 and I am feeling stronger and healthier each day since.

    I'm not going to lie and say every day has been perfect but I am happy to be alive!  Take it one day at a time! I pray that things get easier for you!

    Stay strong girl.......you can do it!!!

    Take Care,

    Lisa

  • R-S
    R-S Member Posts: 4
    edited September 2011

    Was your mother triple negative?

  • R-S
    R-S Member Posts: 4
    edited September 2011

    If you  dont mind me asking what treatments did you have to take? And how long? I was dx in June and had mastectomy in Aug. and getting ready to start my first treatment next week. They want me to start with 4 treatments of AC followed by Docetaxel. Were your lymph nodes positive? How large was your tumor and which side right or left?

    Thank you for info,

    Roxann

  • R-S
    R-S Member Posts: 4
    edited September 2011

    If you dont mind me asking what treatments did you have to have?

    Thank you,

    Roxann

  • Dahlia1966
    Dahlia1966 Member Posts: 26
    edited September 2011

    Roxanne, I was diagnosed in January with triple negative invasive cancer. The tumor was 4cm in my right breast. Lymph nodes were also positive. I had a pet scan and thank God that it did not spread any where else. I had chemo first. 4 a/c. And 4 taxol.(every other week) After chemo I chose to have a bilateral mastectomy. (that was my choice, even though there was nothing in my left breast). I responded so well to the chemo that when I got back the pathology report, the tumor shrunk to 2cm and no evidence of cancer cells. Apparently the chemo killed all of the cancer cells in the tumor and lymph nodes. The surgeon took out 22 nodes and all of them negative. I am now getting radiation treatments. (finished 8 out of 33). I can't say that this year was easy and I still have my "moments". But by coming here and reading all these encouraging words from these wonderful ladies is my therapy. I wish they knew how much they lift my spirits when I'm feeling down. Please keep posting and tell us how you are doing. Since I finished chemo already, feel free to ask me any questions and concerns.



    Diane

  • Carla9112
    Carla9112 Member Posts: 162
    edited September 2011

    Hi R-S - I assume the question about whether my mother was triple negative was for me.  Of course when she had her cancer they weren't doing genetic testing; however, she had the test a year or so ago and found out that she is too.  I only wish that I would have been tested at that time. I honestly don't know that it would have changed things though.  Telling someone to have a double mastectomy when they don't have cancer is a pretty big decision.  Plus, I had just started a new job and couldn't be out of work for a surgery that I had decided to have.

    My daughter will have to be tested at some point, but my oncologist recommended we wait until I get through all of my treatment.  She's just 19.  I hope that there will be a cure by the time she reaches her early 40's!

     Take care!

  • Meggy
    Meggy Member Posts: 530
    edited September 2011

    Dahlia, I remember nearly having a nervous breakdown at the end of radiation and then I figured out why. That last dose of Radiation is our last treatment for a triple negative.  It leaves us feeling vulnerable. I am now 3 years 7 months out from diagnosis and life is very good.  The way I got over the freaked out period after RADS was I took on my own treatment.

    My own treatment was to do all the things that they say lower recurrance for triple negatives specifically.  I ate (and still do) low fat, I think that drops the recurrance rate by 35% or so...and exercise drops the recurrance rate by a similar number.  So When I'd run and eat low fat, I'd think of it as a very effective dose of chemo...and I'd think about how I was starving all of the cancer cells by not giving them fat to thrive on...and killing them off with each step I took exercising. I would never recommend to anyone to only do diet and exercise...do chemo first of course....the low fat and exercise is there to kill off any last bits of cancer in your body.  

    Get a journal or note plad and write down what you ate that day and add up the fat...then you can feel so good and so in control.  Also write down how much you walked or ran that day.  It is ongoing treatment for Triple Negatives.  Just think how wonderful to personally starve those cancer cells right out of your body.

    Hugs sister,

    Meg

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