2012 sisters

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  • MaddyMac
    MaddyMac Member Posts: 75
    edited June 2012

    In the interest of getting to know one another: I'm 48, a California native, writer/editor by trade - I haven't published the novel I finished recently, but I have been able to keep a roof over my typewriter with tedious financial writing. I have a 15 year old border collie/coyote hybrid dog named Dancer who is closer to me than my shadow, and who saves me all the time in one way or another.



    My D and only H died on New Year's Eve in 2009, a week shy of our 13th anniversary. He had a rare brain condition that showed up when we'd been married for six years, and it was unusual enough that his docs couldn't tell us whether he'd die in a day or a year or a decade. This kind of uncertainty was very hard for me to deal with, and I developed a positive, tough superwoman facade I did so well that I couldn't stop doing it, which is why I asked about singing the blues earlier. I'm trying to let myself have some feelings, and I figured you guys would get it.



    People really do say the most hideous things with good intentions - my own story on this one was that when DH got sick, several people took me aside to tell me that it was a good thing we didn't have any children for me to worry about, when we had desperately wanted them. Someone just did it again on learning about my illness. Maybe I'll just clock the next person who does it!!



    OK, that's the most you'll hear out of me in a minor key. I have terrible trouble keeping track of everyone at first, a condition in am choosing to call pre-chemo brain, so sorry if I mix anybody up.



    ;-)

  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012

    Welcome Karen - to the club no one wants to be in.   Nice co-worker ?!   You will find that we talk about everything
    under the sun.   We laugh, cry, share stories - it's a great bunch of women here.

    You really do have to shake your head at people's comments too.   Also I noticed when I first had to tell co-workers that I had bc they would tilt their heads to the side and lower their voices - like I was about to drop dead.  

    I never realised there were 2 vballmom's.. 1 or otherwise... and I am blaming chemo brain whatever anyone else says.Smile

    Vickilind61... sleep well.  Oh! and I heard someone say ‘cancer, the gift that keeps on giving'... aint that the truth.

    Wishing everyone a good evening and peaceful sleep.

  • vballmom
    vballmom Member Posts: 426
    edited June 2012

    Hi everyone!  I am the "original" vballmom Cool and I did NOT start this thread!  I am not surprised that you are confused, because when I saw it I was confused, too!  I really thought I was losing it.  That being said, I am a 2012 sister and obviously a volleyball mom. I have two girls that will be playing in college in September.  I am very  irritated that BC is interrupting my empty-nest plans.  I want nothing more than to be at every game!

    I found my lump myself, in the shower. It was, of course, a shock. I have been getting mammograms since I was 35 due to family history. I just figured one day the technician would say, "Oh, we see a suspicous area...blah blah blah..."  Never did I expect NOT to find it early.  I was three months overdue for my mammogram.  I have no excuse, other than being busy and procrastinating. I try not to beat myself up anymore.  What's done is done.  I can't change things, although I am a nag to my friends.  Living with that guilt is the worst feeling ever.

    I hang out mostly at the April/May chemo group and lurk on the Triple Positive!  

  • 2FriedEggs
    2FriedEggs Member Posts: 640
    edited June 2012

    As far as what people say-Not too many people know whats been going on with me. I didn't want it interferring with some of their  plans and others I just didn't want all the questions and opinions. I have one friend from out of town that calls all the time to chat and last fall I told her I was going in for a core biopsy. Although she is well meaning, she is still asking if I'm feeling ok from that. So glad I didn't tell her everything that followed that biopsy. lol I do have one close friend, who is also out of town that I've confided in. She is the "perfect friend" just listens and laughs with me when I laugh(when all of this started she cried when I cried but I really don't cry about it anymore.) I do get uncomfortable though when I'm out and someone glances at my chest. Since I've been enhancing these 2friedeggs with lots of padding I worry that they may shift and that I may be wearing one up under my neck and one down by my belt- that would be a total giveaway!  When I'm at the doctors office and one of the staff asks how I'm doing,  I don't know if its my imagination, but they always seem to look at my chest after they ask.The one day I went in to the docs, it suddenly started pouring down rain and one of the girls behind the desk said "wow, you made it in here through all this rain, how are you doing?", then obviously looked at my chest.  I immediately looked down at myself and said "oh I was worried there- I have so much stuffing in these foobs, and no umbrella, that i didn't know if they got water logged and were out of place." Told her all I could think of as I ran in from the parking lot was when I'm on the highway and I see a pick up truck hauling a set of mattresses and it starts to rain.  She cracked up laughing and said " oh no you look great " but has never looked down at my chest since. Funny when you're going through this bc crap, the various things we "see" and "hear" coming from others who have no idea how sensitive we are to their words and actions. I have to admit, it's made me more aware of what I say or do now. I'm sure it's just instinctive to look at a womans chest, particularly when you hear the word mx, but I'm pretty sure I won't do it again. Now though that these friedeggs are starting to get filled and I don't need as much padding, I'm going to switch my way of thinking if someone looks  to "boy they must be looking good!" lol 

  • teeballmom
    teeballmom Member Posts: 322
    edited June 2012

    I really wonder about some of my family and friends.  I get stories from "Oh, her cancer came back after one year" to the best one the other night "I know someone who had BC and she died and left 2 really small children without a mother, so sad".  I wanted to smack her silly (and she knows I have a 6 and 4 year old so not something I want to hear).  Last night I sent an email out to friends and family requesting that if they don't have something encouraging to tell me, please at least refrain from telling me the horror stories because my mind can come up with those stories on its own.  I don't think that specific email account has ever heard the sound of crickets churping.  Complete silence from everyone.  Kinda nice but wondering "O.K. who did I irritate now".

    2FriedEggs (I love your name):  When I read your post this morning it reminded me of a conversation I had with our 6 year old last night.  Our 6 year old had a tummy ache and asked me to sit with him in the bathroom, then he kept looking at my chest.  I asked him what he was looking at.  He asked if he could see my scars.  I told him they were private and only me, Daddy and the doctors were allowed to see them.  He asked if they were scarey.  I said not really.  He asked if they would make him run away.  I said I don't know but Mommy's not going to let him find out.  A couple hours later he looked at me in the eyes and asked if my chest was going to grow back.  I told him no, they won't grow back.  Then he said to me that he hoped he would be brave like that someday and then went and played.  After that comment I just about choked up.

    Take care everyone!

  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012

    Vballmon the original... welcome - ha ha !   With chemo brain really doesn't take a lot to be confused... actually didn't take much before chemo, but now I have an excuse Laughing  Feel free to lurk amongst the rest of of 2012 girls. 

    2FriedEggs... that is one funny story and yes next time you should think to yourself... "boy they must be looking good"... I mean why not eh?   This bc crap knocks our confidence for six as it is... why shouldn't we still think with look the dogs B's with it... ha ha !

    Well ladies I will check in later on.  Off to meet my RO for the first time and at least get that plan of action into place.

    Enjoy your days, hope it is sunny where you are... still raining there ?!

    Peace & hugs xxxxxxxx

  • DianaNM
    DianaNM Member Posts: 281
    edited June 2012

    Teeballmom, your story choked ME up. Kids can say some really profound things. 

    Was supposed to meet with my MO today, but the Oncotest is not back yet. Kind of sweating that one out. Really don't want to do chemo, somewhat willing to try HT but will ask about DIM. I am right at that cut off point where the study says limited benefit for women over 60 HT, I am age 59.  

    Been down with an infection, but doubling up on antibiotics seems to have cleared it up. I hope it stays away.

    Haven't noticed anyone looking at my chest. I've got like a little girl bra i got from a mastectomy site, and it has some fiberfill foobs that velcro inside. It's that or a foob pinned inside a vest since I still can't wear a bra or cami! It's a little lumpy. 

  • Soyaandpepper
    Soyaandpepper Member Posts: 368
    edited June 2012

    Hi to vballmom! I was wondering about that myself, whether it was the same person and now I guess its confirmed that its not. Now I'm wondering who is the person that started this thread and where is this person? She only had 1 post when she started this and she has not been in the thread at all since she started. 

    2FreidEggs-That was a funny story! I understand that you are really conscious about other people looking at your chest and its hard on us who went through a mastectomy. To tell you the truth, I think the same way when someone ask me how I going? I'm wondering if they're looking at my chest too and my chest looks about the same as before. 

    Teeballmom-Your story made me teary eyed!!!!! And yes I think that some people are so insensitive about our situation sometimes, I like the fact that you sent an e-mail stating what you want, I'm sure all of them are scratching their heads now! 

    Tazzy-Good luck on your app. and hope that you get your plan of action. Keep us posted! 

  • jpmomof3
    jpmomof3 Member Posts: 643
    edited June 2012

    I am glad to see so much activity! I had to take notes as I read...  chemo brain, fatigue brain or just plain air headedness.

     Tazz, my last chemo is the 25th, i am right there with you.  just counting them down.  I can't wait.  Your story about your SIL was great.  I hope the venting on her was therapeutic.  These poeple mean well and most people just want to hear the canned "i am good" answers, but they shouldnt ask a cancer patient that without expecting a real answer from time to time. 

    Kjberty your story about your hives and co-worker's response is classic too, people are in their own little worlds most of the time.  sometimes i just want to give people some perspective.  I hear them complaining about things that dont seem all that import in general but obviously concern them.  I think "at least you dont have cancer..." I want to say it but dont.  we never know what it is like to walk in someone elses shoes and we dont have all the information.  I have to remember not to judge, even though I want to sometimes.

    I work in an urgent care and had a 19 year old perfectly healthy girl come in with cold symptoms and she complained about how tired she was... I wanted to shout at her, you have no idea what tired is... but i didnt.  I get surprised sometimes.  she was fine but i have been surpised when blood work shows a severe anemia or thyroid problem- in that case they do know what tired is.

    My husband has been a rock for me through this, couldnt do it without him.  When I am feeling sorry for myself and express it he brings me back to reality and checks those negative feelings.  but man, sometimes i just want to shout out how crappy i feel and how horrible this situation is and get some sympathy.  My mom is good for that and thank goodness for websites like this.

    MaddyMac, so sorry to hear about your DH and those horrible comments about the kids.  They meant well i suppose. But people really just dont know how to respond to hearing such bad news about other people.  My father was diagnosed with a brain cancer at the age of 29 and died when he was 32.  Its the worst.

    2friedeggs I laughed when I read your story about the doctors office worker.  I am glad you brought it out in the open like that.  humor helps everyone and sounds like it broke the ice. Its normal to feel self concious about all thesse body changes we are gong through and it will get better soon.  probably people arent looking as much as we think they are but who knows.  This country is obessed with boobs. 

    I slept better than expected last night with the steroid, yay Ambien!  Slogging through a 12 hour shift at work now...

  • 2FriedEggs
    2FriedEggs Member Posts: 640
    edited June 2012

    My husband always tells me I look great and just like before the surgery. He said no one could ever tell and that I am too self-conscious about it. I always tell him " ok just make sure you tell me if you see any white stuffing hanging out around my neck or waist." He promised he would and told me to quit thinking about it. lol He has been great through out this whole thing. Don't know what I'd ever do without him.

    DianaNM that's funny- a little girl bra.I wore the one I got after surgery for quite a while until I went to the PS for one of my checkups and said I can't wait to get rid of this thing. She said well you know there is nothing sacred about this bra. As long as it isn't a compression bra, I don't care what bra you wear. I was like really? and went out and got the Genie bra because it was soft but held my bandages in place but had pockets I could stuff with batting to hide my pittiful little fried eggs.

    Tazzy let us know how the Ro visit goes; think of it as another piece to the puzzle. As for the chemo brain, I can't use that excuse so why am I the way I am ? lol

    Teeballmom Let us know how extensive the "fall-out" is over your email. Lol  Good for you telling them that - we should all get together and write a book "how to talk and act around cancer patients FOR DUMMIES. We know some on your list are probably trying to justify their dumb insensitive comments to each other with things like "well you know, she probably just wrote that because she's just moody because she had cancer" or something else stupid. But your talk with your son is really something. If only we knew what was going on in their little heads all the time. It reminds me many moons ago when my son was about 6 , I had to have some exploratory surgery  for some "suspicious" tissue seen around my ovary. I hadn't really said anything to my son much except that Mommy was going to go into the hospital for a day or two the following week and that the doctor was going to look into my belly with a special tool. He went to a Christian School at the time and on Fridays they always had a little prayer session. Well Friday afternoon, I got a call from the principal telling me that they prayed about my surgery and she wished me the best. I was so floored and said "how did you know?." She said that before the prayer, my son raised his little hand and ask if they could pray for his mommy because she might have something bad in her tummy, like cancer or something, that the doctor was going to look for. I was devastated that he had picked up on my fear because I never said anything to him about cancer and had tried to be upbeat around him. Anyway it allowed me the opportunity to talk more in depth with him and allay some of his fears. After I got home and told him all was well, he went skipping back into school all happy and told everyone that their prayers worked. You did good talking to your son though and gave him some great answers as well as allaying his fears about the scars, etc. - who knows maybe the fact that he is asking if your chest will  grow back, will lead him to a scientific or medical career and he'll figure out a way for it to happen. Bless his little heart.

    JPmomof3 you are so right about judging people even though sometimes its not easy to hold back. I mean before bc, if something was hurting me or I didn't feel good, it was still important to me just like it is to others who haven't had anything major. Infact others on here like those of you going thru so much with chemo etc etc. could say, that about some of us who have had bc but haven't had to go thru as much and I sure as heck wouldn't blame you. Every now and then I have to catch myself and think  everyone has a right to feel sorry for themselves because there is something going on with them that takes them out of their own "comfort zone" even if it's just a headache. Doesn't mean though that I haven't wanted to scream at them and tell them to quit whining. I guess one thing this cancer has taught me is that we are entitled to occasionally feel bad for ourselves but that no matter how sorry I  might feel for myself at times, I need to feel blessed because there are so many more people out there that have it way worse.

    Well I'd best go get some work done. Hope everyone has a good day.

  • MaddyMac
    MaddyMac Member Posts: 75
    edited June 2012

    Hi -



    I have a general question: does anyone NOT have a sentinel node procedure instead of going directly to axillary dissection these days?

  • jpmomof3
    jpmomof3 Member Posts: 643
    edited June 2012

    Maddymac, Don't know for sure but from what I have read the sentinel nodes procedures are much more common these days as the recurrence rates are the same with full axillary node dissection vs sentinel nodes.  There are fewer side effects with the sentinel node procedure- much lower lymphedema rates and less likely to have pain and nerve damage etc. 

  • jpmomof3
    jpmomof3 Member Posts: 643
    edited June 2012

    Whoops didnt finish my thoughts on sentinel node procedure vs axillary dissection.  The studies are showing that women with no evidence of metastisis to the nodes or women with positive sentinal nodes but no evedince of involvement of other nodes did just as well with recurrence rate and survival rates whether they had just the sentinel node procedures vs axiallary dissection.  if there is evidence of more extensive metastasis like matting or clumping of the nodes then those women would need axillary dissection.  Only your surgeon and oncologist can determine which is best for you since everyone is different.  But ask ask ask. 

  • kjiberty
    kjiberty Member Posts: 1,385
    edited June 2012

    Maddy:  I had the sentinel node.  My BS said it reduces the risk of lymphedema.  I feel fortunate.

  • MaddyMac
    MaddyMac Member Posts: 75
    edited June 2012

    Thanks much, JPMom. I met with my surgeon shortly after my MRI, for which I had been tranquilized like a horse, and I'm not sure I remember everything - like whether she will be doing the sentinel prcodeure or not. I will indeed ask. And ask and ask!

  • 2FriedEggs
    2FriedEggs Member Posts: 640
    edited June 2012
  • kjiberty
    kjiberty Member Posts: 1,385
    edited June 2012

    jpmomof3:  The same gal (aka idiot) called me today to ask me a work-related question.  Again, she started out with "how are you?".  I told her I was doing just okay and she said, Great!  How nice.

  • jpmomof3
    jpmomof3 Member Posts: 643
    edited June 2012

    kjiberty, you got it thats all they wanna hear.  everything else goes through one ear and out the other without hitting brain tissue in between...

    Teeballmom and 2friedeggs, those stories about your sons are just precious.  kids really are amazing.  My three year old looked at my newly shaven head a few months ago and said "I dont like it, I want you to wear your new hair"  it took me a minute to realize that he had seen the wig I had bought and wanted me to wear it.  He likes to pet my new fuzz now though... I am always surprised at what they pick up and how much they understand.  Sometimes it looks like it bounces off of them but the something like what happened to you guys makes you realize they understand a lot.

  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012

    Teeballmom... that story choked me up - cant imagine how it made you feel.  Kids can be so precious eh?

    Jpmom... here's to us and the June Chemo Grads - cheers !

    2fried eggs...loved that story - thank goodness for humour eh?     And you have chemo brain because you are empathetic to your sisters on chemo Wink  And I love the "How to talk and act around cancer patients FOR
    DUMMIES" idea.

    Kjiberty... good to know you are doing OK - ha ha !!

    So I had my meeting with my RO today - she is a sweetheart and has all the time in the world to listen and answer questions - phew ! that for me is a biggie.     She believes that I will be having my rads before surgery, but is waiting for my BS to confirm, which he will do when I meet him tomorrow.  Anyway I will likely be having six weeks worth - 5 days per week, with weekends and stat days off.  She told me about the possible side effects - hopefully I wont get them all or that bad.   If I am having them before surgery will likely start around end of July... so after last treatment on June 22...there may be a few weeks before rads when I can feel ‘normal' again -
    and I don't do normal.....but you know what I mean.   I have a lot of literature to read and a DVD to watch. She told me all about the planning and mapping session I will have beforehand, and which I said she made me sound like a local Council meeting for a new bus route - she laughed.

    I hope you all had good days and will have enjoyable evenings.

  • VickieDallas
    VickieDallas Member Posts: 6
    edited June 2012

    Hello all!  Thanks for the best wishes!!! 

    What do you think about this:

    ER 3+  95%

    PR 3+  92%

    HER 2 Neg

    Ki67  70%

    Size 1.9cm

    IDC

    I think it is Crazy!!!

  • MaddyMac
    MaddyMac Member Posts: 75
    edited June 2012

    Tazzy, great that you like your RO. That seems critical to me. After encouragement from a woman I keep bumping into at the imaging suite (sisters everywhere!) I worked up the nerve to fire my MO, whom I really didn't like. I guess one could work with a doc she didn't like, but we're going to be seeing a LOT of these folks on our teams.

  • sammistar509
    sammistar509 Member Posts: 23
    edited June 2012

    I love reading all the posts here but lose track sometimes and there are a lt of posts in one day!

    I am high school math teacher, geometry and algebra2/trig outside of Albany, NY. I have been married four years to my amazing husband Mike. We don't have kids, two cats and a dog :) both our families are from ths area so it has been great living here!

    I was actually being tested fr some abdominal issues before my diagnosis. My dad has had some weird intestinal studs so I figured it was that. Turned out I had ovarian cysts (nothing cancer related) and a lump is some sort. I had a hysterectomy three years ago, at 35 I opted to keep my ovaries, and I hadn't been back, I took a lot of heat frm docs, nurses, family....... So when I went to Obgyn for annual they asked about self-exams, with DD's it's not easy so I mentioned that I thought my left was different. She said it felt dense, no lump, but I am close to 40 so she sent me for mammogram. I also had an abnormal pap (good for now, back in July). My level two ultrasound on ovaries showed they were functioning but there is something there they are watching and after those two vists I was feeling pretty good. The next day I was diagnosed, that was Jan 24, and it has been quite the journey!!

    I also had to shush the gloom and doomers - maintaining a positive attitude can be a challenge and I don't always have it in me to listen to stupid commens. I don't always explain things well, including the potentially ovary removal but until I see my oncologists in two weeks I can't offer any additional info. I do know that I had three tumors and they found a fourth when they sent my tissue to pathology. Two of those tumors are being tested so I am waiting to see what comes next.

    My family and friends have been amazing but not all are patient, at least not with this. Bummer for them!!!!! I am feeling good, that is enough for now. My list of questions grows everyday and when the time comes my husband and I will make the best decision for us.

    Thanks for sharing!!!!!

  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012

    Sammistar it is hard to keep up with sometimes...espcially with chemo brain ha ha !!   I have to say that in school you would've been my biggest nightmare - I could never every grasp algebra or trig.. still cant actually.

    Yeah my MO is just so sweet, very quiet spoken and gentle and looks you in the eye - that's what I liked.   Good for you getting rid of the one you didn't like - we are going through way to much as it is not to have a healthcare team with like and trust.

    MaddyMac... I  dunno how I missed your post at the beginning of this page.   I am so very sorry for the loss of your DH. And now you have to go through this crap.. and put up with the most insensitve and stupid of comments.   I think you restrained yourself very very well in fact.    And you sing those blues baby anytime you feel the need.  That's what we are here for.

    I think for all we are going through and all we will go through we should have one day a month where, if anyone upsets us or makes a really stupid comment we can tell them (with no repercussions) that off is the direction I would like them to fu*k (hope I dont offend anyone here.. and if I did sorry !).  

    OK that's my rant for the evening, enjoy the rest of yours.  And for those whose days start before mine... enjoy the day.

    Peace & Hugs xxxxxxxxxxx

  • Moonflwr912
    Moonflwr912 Member Posts: 6,856
    edited June 2012

    Wow, I missed three days and 5 pages to catch up. Welcome to everyone I haven't met here, and sad you have to be here. In the interest of getting to know me, I am 57, have 4 grown kids, no grand kids, was Dx in Dec, with Dcis, IDC in the breast I insisted they remove if they were taking the other one. I will have been married 39 years in October. My DH was not very good to me the last ten years, but since this Dx, has been incredible and more like the man I married. Ok, way too much info for you all, LOL. Much love to all.

  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012

    Morning

    Hoping you are all having a really great day and if on treatment very few SE's.

    Moonflwr happy to hear your DH is once again a DH.

    Off to the BS today - fingers crossed for me girls.  

    Peace and hugs to you all xxxxxxxxxxxxxxxxx

  • 2FriedEggs
    2FriedEggs Member Posts: 640
    edited June 2012
    Tazzy Fingers and toes are crossed for you today. Let us know how it goes! Funny thing real quick though I went to my bs yesterday and she did a check up on these fried well more like poach eggs now and said "are you done or are you going to go bigger?." Told her definitely going to have more fills- I atleast want to have bigger breasts than my husband. (Can't imagine anyone stopping with these lil things LOL) Again good luck today.
  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012

    Thanks 2FriedEggs.  That is a very funny story.  So many decisions to make eh? But least I will come away from the appt. armed with my options instead of just wondering what they are.  

    Hope you are having a really great day.

  • kjiberty
    kjiberty Member Posts: 1,385
    edited June 2012

    Tazzy:  Good luck today

    2friendeggs:  You crack me up!  Thanks for a good laugh! 

  • MissAngie
    MissAngie Member Posts: 29
    edited June 2012

    Hello there!  I've been lurking on this site since I was diagnosed and really wished that I joined these discussions a lot sooner.  Reading all of the posts has been inspiring and informative.

    My connection with bc began with my friend going through aggressive bc treatment in 2009.  She unfortunately passed away one year later at the age of 41.  She really made me think about getting a mammogram and to convince myself to get one, I told myself last year that it would be my birthday present.  I was quite shocked to know that they could already see my tumour on my first mammogram.  I couldn't feel a lump at all.  I had more follow up mammograms and two ultrasounds for the rest of the year.  And finally had a core biopsy before Christmas.  I was notified that I had an appointment with a breast surgeon. That's what really freaked me out.  In my mind, it was a sign that something was wrong and that I had bc.  I met with my breast surgeon after the new year and she gave me the diagnosis.  It was devastating and I cried even before she gave me the diagnosis. She said she couldn't feel the tumour either. The day I was diagnosed is the day my sister was having a hyserectomy for endometrial cancer.

    I had my lumpectomy in January and finished my radiation at the end of April. I've been on Tamoxifen for a month now and am trying to live with the side effects. 

    I feel grateful that I have a very supportive boyfriend and family and good friends that are helping me through this.  Its funny that friends and/or family mean well, but say the most insensitive things.  My SIL recently asked me how I was doing.  I told her I wasn't feeling very well and that I had back pain because of the Tamoxifen.  She asked if it was because I was "lying around"!  I told her that I don't lie around and that I actually do things around the house.  She said it must be nice to be off work.  I told her that I don't want to be off work because of bc.  She said you're cancer free, aren't you?  I got mad and hung up on her.  Who knows if I am cancer free? I will only know that for myself once I have my folllow up mammogram.  Oh well... some people just don't understand.

  • Tazzy
    Tazzy Member Posts: 2,546
    edited June 2012
    Hi MissAngie, glad you got the courage to come out of the shadows... took me a while too, but now, think I am one of the worse chatterboxes on here Laughing  You will find so much comfort and support here.   Great you have a supportive boyfriend... makes all the difference really it does.   you've been through a lot this year.  As for the SIL... think ours must be related.  Mine called us on Sunday and I was feeling pretty crappy, when she asked how I was I said had better days, she aske me why what is the matter?   I let her have it too... bet they both will think twice before being so bloody insensitive.  No, people do not understand - that's why here is good... everyone understands.

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