I am tired of being strong

Options
13»

Comments

  • beceen
    beceen Member Posts: 15
    edited April 2010

    Anyone do any research on traumatic events in your life at the time cancer started?  From the information I was given on my 4 mm DCIS, it said it would have taken 7-8 years to become that size which coincides exactly with a totally unexpected divorce from a 30 year marriage which was the height of a traumatic experience in my life.  Couldn't have turned my whole any more upside down than it did.  So I was just wondering if anyone else has found a past event to coincide with the start of their cancer. 

  • robinlbe
    robinlbe Member Posts: 585
    edited April 2010

    I, too, was curious...my doc said mine had been there 5-7 years....which was when my dad was diagnosed with a very aggressive form of lymphoma, and died five months later....

    Supposedly, though, from some stuff I've read, unlike other cancers, BC isn't so much affected by stress.....but I just don' tknow...

    blessings...robin

  • Katey
    Katey Member Posts: 733
    edited April 2010

    The only real stress in my life is this stupid BC (other stuff just doesn't compare).  I had been told this first time which put me at 22 for trauma.  Hmmm, graduation, off to Europe, having a blast with friends, few responsibilities.  This time puts me at 45, successful business, happy, healthy ( I thought), great daughter and husband.  I get tired of all the reasons blaming us for our BC, it's not our fault!!  There must be a zillion suggestions of things that cause it.

  • 1965sally
    1965sally Member Posts: 113
    edited April 2010

    I think it's natural to wonder.  My cancer might have been growing up to 10 years, I was guessing, and at that time in my life, age 32, I was 1 year past a miscarriage and in the process of divorcing.  But I'm not sure I believe that's any more than a coincidence.  I sure would love to know though.

     Robin, thanks so much for your encouraging words!  I haven't been back to the boards for a few days because I was feeling better.  "It's all swings and roundabouts," as my English friends used to say, whatever exactly that means!  Ups and downs, I guess.

  • xiaomei
    xiaomei Member Posts: 43
    edited April 2010
    I hear you dsj. I made the same mistake when I first told my brothers. Instead of telling them the truth (such as fear, anxiety, etc), I tried to comfort *them* by saying don't worry, it's pre-cancer and I'd be fine. Then I hardly ever got calls from them checking on me. Two month later one of my sister-in-laws said to me "I thought you don't have cancer". By then, I was smart enough to correct her "yes I do have cancer. Why else I had surgery and why else I do radiation?"

    What I learned? Never tell anyone I have DCIS again. Just tell them I have cancer. If they care to ask, tell them it is early stage, but I still have to do surgery and radiation. I feel scared. I feel tired. I am not the usual strong person anymore.
  • mercurialqueen
    mercurialqueen Member Posts: 31
    edited April 2010

    beceen...yes, my husband left us, me and my daughter, two years ago and I have been dealing with a lot of depression and sadness.  I was diagnosed with DCIS last friday.

     When I told my family and friends that I may have breast cancer, they were so scared that I was the one reasuring them that I was going to be ok. 

    I guess that these people saying "it's ok, everything's going to be fine" or whatever is a self defence mechanism, so I wouldn't be so hard on them.

  • Suecee
    Suecee Member Posts: 6
    edited April 2010

    I had a similar experience with trying not to worry family with my diagnosis, emphasizing it was very treatable, prognosis is good and all of the other things the doctors say to you to help you pull it together after diagnosis. I think after the initial shock of hearing the word "cancer", most of them seemed to get the idea that it wasn't that big of a deal for me.

    After more tests and reading, I mentioned I was planning on a mastectomy and people were really surprised. I have had to emphasize that I really need their support, that this is very hard and that even a phone call can be very helpful to my husband and I.

    Unfortunately, we are not geographically close to any family anymore. Five years ago, hubby's job transferred us to Florida from California and we don't really have many friends here....more like acquaintances. It worries me a little since everything I read says let family and friends help. Ahhh well.....I am stockpiling casseroles in the freezer and trying to streamline the house in preparation for recovery. 

     I miss having close friends who live nearby so much though, and I really appreciate being able to read other women's experiences on the boards. I found several local support groups and that has helped me feel less isolated, but I think they will be even more help after surgery as I learn to live with the idea of this lifetime risk of having cancer again.

    I have some family and one dear friend who call me often, bless their hearts. It's amazing how much a phone call can life your spirits. On the other hand, one of my oldest friends, a friend since childhood, can not bring herself to call me at all. Her sister has had breast cancer twice and both her parents died of cancer so I'm guessing its more than she wants to deal with. I'm not really sure, but am focusing on the positive and getting past the hurt.

    I'm also starting to realize that most people I know don't know much about breast cancer and the diagnosis and treatment details just confuse them. I think back to the people I've known who have fought breast cancer and realize how little I really understood about what they were facing, so I understand and I'm even more grateful for the few in my life who do want to know more and will listen to all the details because it really helps me process this emotional roller coaster ride. 

    More and more I'm starting to think that the most helpful support is from another cancer survivor. I don't feel strong and brave either and I never know what to say when people ask "How are you doing?" I miss who I used to be and I wonder if I'll ever see a "self" I recognize again.

    But, If I can just get a reconstruction plan worked out to my satisfaction with the PS and have my surgery at least I will have taken the first steps.

  • flickyd
    flickyd Member Posts: 5
    edited April 2010

    Oh, I so get this - and I am tired of feeling so alone with this. I had to see my GP the other day as I have bronchitis - just to add insult to injury. I really wanted to talk to him about anti depressants as I have reached the point where I just can't deal with anything any more ( 8 weeks after three surgeries in six weeks) and his reaction was that I was so lucky and everything must be back to normal by now and ushered me out. HE'S lucky I didn't burst into tears right there - I waited til I got to my car! I have to be upbeat and positive all the time, and people don't realise that NOTHING WILL EVER BE NORMAL AGAIN. So I save my tears for when I'm at home, but there are days when I don't know how I'll start the day, let alone get to the end of it.

    I've always been the sort of peron who passes things off with a joke and a laugh, so I guess it's my own fault, and that's how people expect me to be but, dammit, I want some sympathy and real support!

    Have you noticed that once the immediate surgery is over and the results are ok, all support fades, cos everyone thinks you're on the mend and all better? I get comments like 'How can you still be sore after 2 months? You need to move on' and so on...

    But venting is good, so thanks for letting me do so!

  • beceen
    beceen Member Posts: 15
    edited April 2010

    You are right.  Things will never be the same as they were before.  We will never feel as safe as we did before we were diagnosed with cancer.  But what choice do we have?  We go from here I guess.

     I think I am a bit like you in that I try to make light of any serious situation involving myself.  I don't want to be the center of attention in that way at all.  But along with that, I think I was in a lot of denial and that's why it's been so difficult emotionally.  Today was the first of my 11/33 treatments where I didn't have any tears while I was at the clinic and didn't cry all the way home.  Maybe I'm coming to grips with it finally.

  • olivia218
    olivia218 Member Posts: 257
    edited April 2010

    Beceen, 

    I am with you. I make light of anything that has to do with me but inside I feel alone. I don't want to be the center of attention either, it makes me uncomfortable. I am 10 weeks post surgery and still have massive crying spells. My husband says Mondays are the pits because he can look at me and see pain in my eyes. I am lucky he is supportive and gets me but I feel bad that he sees it.  

    I finally told my Dr I am not wonder woman and this is hard. He said, I am glad to hear you say that because this is tough.  

    Hugs to everyone!!!

    Olivia 

Categories