it's been quite a year

Options
2456715

Comments

  • Joanne_53
    Joanne_53 Member Posts: 1,477
    edited May 2012

    I would love to join this "support group" --- pj's and all ---

    I am so not me .... I have put on weight because I allowed myself bad behaviours when I was diagnosed and then have not stopped.  I know what to do and how to do it but I cannot get motivated ....

    Sometimes I feel like I am in a daze.  My friends and family see the "up" me ... rarely do they see the real me.  I know that they have over the period of 6 months but my treatment is over and I am physically healing after radiation and life is to return to NORMAL.  What is that. 

    Thanks for this thread -- it is obvious we need it.

  • orangemat
    orangemat Member Posts: 645
    edited May 2012

    Hi Joanne. Is this thread a support group now? Well if my self-absorbed ramblings and whining make everyone else feel comfortable and better, then sure, come on in! :) though for me, I'd like to have at least just one day where I don't feel compelled to talk about my cancer history. I've never been good at ignoring the elephant in the middle of the room, so to speak, so I guess what I want is to have that elephant GONE. Or at least be in a different room than it,

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2012

    Esther- I think your ramblings, as you put it, have resonated with a lot of us who are struggling with the same feelings and issues. Call it a club, support group or whatever it sure helps to know others are dealing with the same thing. I think society and the media make it look so easy- lose your breasts and maybe your hair, bounce back quickly and within months you're running a race in your pink t-shirt good as new. For a lot of us it's nowhere near that easy so it was a relief to see it wasn't that easy for some others too. I think each thread I post on is it's own support group! :)

  • Adey
    Adey Member Posts: 3,610
    edited May 2012
    What Esther and Kate said.  Tongue out
  • camillegal
    camillegal Member Posts: 16,882
    edited May 2012

    Joanne I think most people see the feeling good us--it natural--we come here and say what's really going on. And I like that-we get it off our chests, what left of them or no chests LOL

  • Denise-G
    Denise-G Member Posts: 1,777
    edited May 2012

    Thanks, ladies, your posts all helped me!  I just finished chemo and on to rads on June 11th.  I can already see friends and family getting the glazed over look as you've talked about like, ok, get a move on.   One friend when I told her I needed Herceptin too was kind of like, "geez, did you know what you were getting into with this mess?"   and someone else said "I didn't realize this Breast Cancer was such a big deal"  Sort of like, well everyone else I know had a little treatment, why are you getting so much, kind of attitude!

     So thanks for all your posts!  Very helpful to me! 

  • camillegal
    camillegal Member Posts: 16,882
    edited May 2012

    Denise, I'm kind of laughin cuz someone said to me this morning--gee I know someone who had chemo and she was fine in less than 1 year.

    How do u even remark about all we go thru, with so much chemo and operations and rads and meds.and ood old SIDE EFFECTS--So I said everyne is different with different types of cancer.

  • Adey
    Adey Member Posts: 3,610
    edited May 2012

    Denise-  Yeah, I was at a gathering and a gal listened to my TXs and such and remarked; Isn't that a bit aggressive?  And I said yeah, I guess they want me to live!  (c:

    Cami-  Off our chests, ha!

  • 1openheart
    1openheart Member Posts: 765
    edited May 2012

    I have just finished reading through this thread and I can so relate to so much of what was said.  

     "I feel like I just cannot be the person I was before BC, but I do not know who I am yet"......I too feel this way, some days much more than others.  When I find myself thinking this, I remind myself that the universe is in constant flux and me being a part of that same universe is also constantly changing from moment to moment in ways that I cannot feel or even comprehend.  That makes the big, noticeable changes seem more manageable to me somehow.   I, too, am still in PT and I still have breast pain off and on.  It is better.  I went for over 2 weeks without any pain, but it has been back for the past couple of days.  A constant reminder every time I move my arm or flex my muscles.   I'm trying to grow and learn from this b.c. experience and hopefully come out the other side a stronger, wiser and better person.

    I just passed my one year diagnosis anniversary and my UMX anniversary is coming up in June.  Below is what I posted on my one year anniversary:

    About this very time of the afternoon last April 28th, I was sitting here on my couch much like I am today when I got the phone call that changed our lives forever.  It was my surgeon calling with the results of my stereo tactic biopsy.  I was just sure I would be in the 80% with a benign results like I had been twice before.  But, this time I was in the unlucky 20% and it took my breath away.Fast forward to this afternoon, April 28, 2012.  I have lost one breast and had a new one made, had my remaining breast lifted, had my first tattoo (areola....nothing fun) and been poked, felt up, and prodded more than I ever thought I would be in my life.  Most importantly, I have come through this year stronger, braver, more full of grace and gratitude than I would be if I had not been diagnosed with cancer.  I know I chose my friends well, because when I needed them in my darkest hours, they were there come hell or high water.  My guys, my husband and son, were so scared and worried for me, but they always put my needs before their own.  Some of my extended family were walking beside me every step of the way.....some, not so much.  But I guess I was not really surprised by that.  It just confirmed what I already knew to be true.I write this because I hope to let those of you just beginning your journey know that you will see the other side.  I consider myself "lucky" to have found my cancer on my diagnostic mammogram before it had sneaked out of my ducts and become invasive.  I had a great team of doctors who took wonderful care of me and continue to do so as we move into the follow up phase.  I cannot and will not say that I know what those of you who need more invasive and extensive treatment are going though and my heart goes out to each of you as you navigate your treatment.  I think me and my husband are going to go out to our favorite "special occasion" dinner place tonight to celebrate reaching the one year mark.  I may even take the remaining side of the  boob cake that I froze after my boob voyage party last year out of the freezer.  We only ate one side and I froze the other to eat a year later.  Maybe I'll save it to celebrate the day I became NED - the date of my UMX in June.

    I got through this because I had to and you will too.  This site was truly a life saver in rough seas.  Thanks to all of you who were there for me.  Most of you don't even know how much you helped me.   I lurked for months and only joined a couple of months ago because I felt it was time to pass it forward.  Thank you, thank you a million times over. 

  • camillegal
    camillegal Member Posts: 16,882
    edited May 2012

    Openheart---what a beautiful post--u r blessed.

  • CLC
    CLC Member Posts: 1,531
    edited May 2012

    I am only 8 months out from dx.  But I totally know what you all are talking about.  I am so profoundly different than I was.  I feel like I got my life ordered and arranged just the way I wanted it, just to wake up from bc and find I was living a life perfectly suited to someone I no longer was. 

    I cannot move on, though it seems like there isn't much left to process.  I just cannot leave it behind me.  I think, for me, it is because I am now reconstructing a new life, one that is better suited to the new me...and that is hard.  There are days that I feel crushed by the world...and there are days that the world lifts me up...but there are very few hum-drum normal days...  This has been such an INTENSE journey.

  • SelenaWolf
    SelenaWolf Member Posts: 1,724
    edited May 2012
    Sometimes I think of it as the "... Pink Ribbon Tyranny..." (not my phrase, I regret to say, I read it somewhere).  Somehow - as breast cancer survivors - we are supposed to smile, stay positive, think of others, hide how horrible treatment is making us feel (i.e., wear a wig, wear make-up, you'll feel so much BETTER), smile some more, learn something profoundly spiritual, think of cancer as a gift, and move on with our lives once it's over and never refer to again unless it's to express how grateful we are to have experienced it.

    Horsefeathers!!!

    This journey is terrifying, scarring in more than just a physical sense, incredibly difficult, and deeply wounding.  We, all, come through it in different ways and profoundly changed.  Me?  I fought my way through it - sword in hand - and feel incredibly empowered.  I learned things about myself I never suspected... like how strong- and determined I can be.  How - after years of depression and battles with self-harm - that I really, really, really want to live after all.

    But... smile my way through it?  Not a chance in hell!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2012

    Denise- I love that your friend said "geez, did you know what you were getting into with this mess?"- like you had a choice!  

    OH, I have to do all that?!?  I didn't know that!  Could I please have the less complicated treatment?  Oh, there isn't one?  Well, nevermind then.   Laughing

  • orangemat
    orangemat Member Posts: 645
    edited May 2012

    Ha, Kate!



    Hey guess what? I'm in my pajamas again... :)

  • jittersmom
    jittersmom Member Posts: 165
    edited May 2012

    Joanne 53.......

    I know what you mean, people see one thing but I feel like another person. I have also gained weight while I was on chemo, along with everything else I just feel like crap. I am 10 treatments away from being done with radiation. I don't even remeber what normal is? I will be on herceptin until Decmeber and i am still bald. it is hard for me to motivate, its like something is always hanging over my head! I am glad i can come here and vent with people that get it!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2012

    Esther- LOL!!!!  

  • Golden01
    Golden01 Member Posts: 916
    edited May 2012

    I love this thread and I am in my pajamas! Pretty ones that button up the front with a great robe. Just had my new nipples added a little over a week ago and have found everyone, including me is really tired of another surgery! I'll be coming up on marking the first year since my diagnosis in July. It is a journey.

  • camillegal
    camillegal Member Posts: 16,882
    edited May 2012

    Golden u sound good---If I would have had recon and new nipples I would want to show them to everyone-seriously. I mean other PS u show to people--I'd probably be arrested even at the grocery store. It must be wonderful to feel normal (that way) again. Godd for all of u.

  • Golden01
    Golden01 Member Posts: 916
    edited May 2012

    As far as the news ones stick out right now, everyone at the grocery store will be seeing them whether I want to show them or not! Makes me think of that old Sex in the City episode when Miranda wore fake nipples while walking through the bar.

  • Adey
    Adey Member Posts: 3,610
    edited May 2012

    Today is two years exactly post bmx.  And it's a good day!

  • orangemat
    orangemat Member Posts: 645
    edited May 2012
  • camillegal
    camillegal Member Posts: 16,882
    edited May 2012

    Golden I remember LOL

    Adey Great for u---Yay

  • Golden01
    Golden01 Member Posts: 916
    edited May 2012

    Aday, Congratulations on the two year mark! I don't think I've even been able to think of what it might be like when I do the same. Thank you for helping me look ahead.

  • 1openheart
    1openheart Member Posts: 765
    edited May 2012

    Golden....I have ONE that sticks out!  My lifted natural breast's nipple is very perky now.  The new nipple on my recon. breast has kind of flattened out already.  My natural and recon breast are really pretty even and especially in clothes, no one would ever know I had a UMX and reconstruction.

    Aday....congratulations on your two year anniversary.  So glad it is a good day for you! 

  • misswim
    misswim Member Posts: 931
    edited May 2012

    Hoping it is not too late to join.

    I thought so much about this very subject this weekend. I hit a year from diagnosis in April. Had the works, BMX, recon, and chemo, now tamoxifen. Overall, I have bounced back really well. I am exercising, eating well, feeling great. I just walked 39.3 miles two weeks ago in the Avon Walk.

    Most of my friends and family just want me to be like I was before. And I try so hard to be that person that I sometimes fool myself into thinking it so. Which, if I get too relaxed about could impede me if I am not being vigilent regarding recurrance. So I am trying to find the right "mix" of living my life and enjoying my health and also being very aware of any changes as they come about. Overall, I'd say I have done really well.

    Fast forward to yesterday. I went to a memorial service for a family friend who had been battling glioblastoma (brain cancer) for almost three years. I was sad when he passed (he was just 45) but the brevity of this is cancer and it takes lives did not hit me until this service..... and I cried, hysterically, from beginning to end. It was just a giant slap in the face that cancer has forever changed me, and my life.

    I'm trying not to let it get me down..... but biy, it sucks. I miss my life. But, I am thankful that I have place like this to come spill. I hope I haven't brought anyone down:(. Thanks for the support.

    Best to all.

  • mstrouble16
    mstrouble16 Member Posts: 198
    edited May 2012

    I am 9 months from diagnose and have had a bilateral mastectomy, diep reconstruction, chemo, and had stage II surgery in march now on this wonderful little white pill called tamoxifen with all of it's wonderful side effects. No I'm not the same person I was outside or inside. What really bothers me is 1) some people think oh, your still having issues but it's been almost a year 2) people really think this really short hair is a fashion statement...NOT! But it is a relief to know that I am not the only one that feels this way.

  • Ginger48
    Ginger48 Member Posts: 1,978
    edited May 2012

    Misswim- sorry about your friend. I think I feel it the most in those quiet moments too. This is one scary disease! Sending you hugs!

  • camillegal
    camillegal Member Posts: 16,882
    edited May 2012

    Mornin' All--I actually slept for over 5 hrs straight last night.  That's quite an accomplishment these days.I truly understand about moving beyond cancer---except for one thing---when u have a daily reminder of it with usually not sleeping, pain, confusion, diarehha (sp), headaches, LE. fatigue should I go on???

    And misswim I';m sorry for u'r loss and with those circumstances it's more complicated for u.

    I'm sorry I'm ranting, even thos I had a good nite's sleep, I guess I just feel helpless sometimes.

  • Golden01
    Golden01 Member Posts: 916
    edited May 2012

    misswim - Your words meant so much to me this morning. I am sorry for the loss of your friend and I can understand how hard the memorial service must have been for you. Your description of friends and family wanting you to be just like you were before really hit home for me. Everyone has been very supportive of me and what I've been through but I think everyone is just tired of this whole cancer thing, me included. It seems that once the surgeries were over, folks think I should be done with cancer. When I mention my fears of recurrence, there's either a blank look or a sense that I am somehow overreacting. For a couple of my family members, denial usually works for them and is one of their best coping mechanisms.

    For today, I think I'll work on SelenaWolf's ideas and look for that sense of feeling incredibly empowered. I'm not really a believer in horoscopes and don't usually even read mine but I am still in my pajamas and not going to work until these new nipples heal up so took time to read mine for today. Here's what it said "You have managed well in some respect and will do well to remind yourself. Travel back in time to connect your awareness of the 'past you' with the present, and apply what experience has taught you". I have made it from last July when I got my breast cancer diagonsis to today pretty well. There must have been some things in my "past you" that helped me do that and will help me in the days ahead.

    For today, I am also going to get out of these pajamas and head out for a three mile walk. I have another pretty set of pajamas (yes, they button up the front) to put on when I get back. Next week, I head back to work. I hope these new nipples will heal up enough to be ready for regular clothes!

  • SelenaWolf
    SelenaWolf Member Posts: 1,724
    edited May 2012

    Golden01... you GO girl!!!

    I - like you - was diagnosed last July after receiving a `negative` screening mammogram on December 12, 2010 (and 10 years of `negative` mammograms prior to that).  Argh!   You try to do everything `right` and - still - Life sometimes just bites you on the ass.  Or boob.  Or whatever...Cool

Categories