2012 sisters

Options
1147148150152153184

Comments

  • min937
    min937 Member Posts: 37
    edited November 2012

    keetmom - So sorry you're dealing with all of this. I can relate to the unexpected surprises too. Went in for a mastectomy due to scattered DCIS in Oct. and found two small areas of IDC also. Funny how the DCIS shows up on my mammograms but not the invasive stuff. Anyway, there are a lot of great women on here with great advice, so you've come to the right place. Take one day at a time!

  • mcook301
    mcook301 Member Posts: 509
    edited November 2012

    Hello Ladies



    First of all sorry I haven't chimed in lately but I felt that I did not want to share my post chemo surgery negativities with everyone that is going through treatments right now. Then I realized this is best place to share:) It is 3 am and once again I am woking up by pain. I have been trying to work with PT and doctors but they are not really helping me at time. They gave me some at home exercises but I got what they call a frozen shoulder after surgery and it is really crappy. My range is motion in my rgt arm is pretty minimal. I guess this is pretty uncommon and they don't know what causes it so chances are none of you will get this. Funny I felt pretty good after surgery for first couple of months and this has gotten worse. I am back to work and my job has always been insane but I don't want to try and keep up anymore so after I get through my exchange surgery in jan and hopefully find a solution to my pain issues I can try and find a new life.



    I am seeing a massage therapist who specializes in this next week and I am counting the minutes so hopefully she can help me:(



    I believe I read above about the fear of remission and it is hard not to think about this but I try to not let it consume my thoughts daily but it does put it into perspective about making some choice in life to find what makes me happy and do what I love.



    My friend sent me a photo of a saying that was on a shopping cart that she saw on her vacation in Hawaii "Motto to Live By: Life should NOT be a journey to the grave with the intention of arriving safely in an attractive and well preserved body, but rather to skid in sideways, chocolate in one hand, wine in the other,body thoroughly used up totally worn out, and screaming, WOO HOO, what a ride! ...for me this may not mean drinking or eating choc but I am going to make dam sure I try and enjoy this ride as much as I can! And this does not include working 12 hour days anymore:) oh yes and I guess now the only body part that is going to look preserved is my fboobs:)





    I am sorry for all that has had to join this group but like everyone said it is the right place to be. And everyone else I have missed you and hope you are doing well. My hair is coming in crazy thick and I probably should get a trim soon. One thing about short hair it is way easier to get ready! Having long hair all my life, it is something I miss but not the hour it took to dry.



    Have a great Thanksgiving!



    Hugs

    Michelle

  • mcook301
    mcook301 Member Posts: 509
    edited November 2012

    Oh and one more thing about work...I was super women or atleast I thought I was and worked through chemo and came back quickly after surgery and if I had to do it all over again I would have not tried to do it all. It is our time to take care of ourselves and for me I did not do myself any favors trying to do it all:) I would highly recommend taking some time for yourself during your treatments and don't worry about trying to do it all. You are fighting for your life here and that is your job right now:)

  • SusannahW
    SusannahW Member Posts: 470
    edited November 2012

    Mcook, missed your posts so much, and was worried about you. It sounds like u are pulling yourself up, setting goals, and being deliberate in how u choose to live you're life. You're a brave lady, and I admire you.

  • SusannahW
    SusannahW Member Posts: 470
    edited November 2012

    I have a question for those on AIs- have any of you had gi issues, and did they get better over time? I've been on Aromasin for about 6 weeks, and the gi issues have only gotten worse, despite prescription meds from my onc.



    Would love to hear from some of you about this, I need some hope.



    Susannah

  • Scottiee1
    Scottiee1 Member Posts: 2,329
    edited November 2012

    Susannah....what kind of GI issues????

  • SusannahW
    SusannahW Member Posts: 470
    edited November 2012

    Heartburn, abdominal pain, feelings of being full too soon, queasiness.

  • Scottiee1
    Scottiee1 Member Posts: 2,329
    edited November 2012

    Susannah....as you know, I'm on Letrozole but have had none of f those symptoms, but Inhave heard some of the ladies talk about heartburn and feeling bloated. Perhaps

    you will get some advice from them. Sorry you're going through this.

  • SusannahW
    SusannahW Member Posts: 470
    edited November 2012

    Thanks Christine- and u gave me correct word to describe it-bloated-!

  • juneaubugg
    juneaubugg Member Posts: 951
    edited November 2012

    Hi ladies! I've been reading, and reading, and reading.... I'm working now and you are all posting so much that by the time I'm done reading I don't have time to post...! Yay for Sunday!!!



    First; Mcook- was thinking of you last week. Glad to "see" you; sorry about your locked arm. That absolutely sucks! It's just one challenge after another,isn't it! My hair is starting to cover my head in feel, but it's not long enough to all be seen yet. (Update your avatar would you?!)



    Those entering the black hole... (((HUGE HUGS))). I can honestly say that those holes were the worst depression of my life. Coupled with the hot flashes and other SEs... Well.... HUGS!!!! It seemed impossible at the time that I would ever feel good again, but I feel GREAT again... Finally.



    This has been such a long year. I joined this site in May. Women like 2friedeggs, soya, Tazzy, JPmom, Websister, Ramols were there to share this journey with. Since then there are so many more wonderful women here sharing in this journey. Carrying each other at times. I would send my tears off into the great electronic world and get love, support and compassion back. I would also be made to laugh out loud when no one else around me had the ability to understand my twisted cancer humor. (Well my DH was pretty good at it some days!). I also got ALL of my information and education HERE. I was prepared for every medical appointment with lists of questions based on the experiences of those who had gone before me.



    Anyway, as some of us see the light at the end of the tunnel and our busy lives intrude on our posting time, I'd like to start a new thread next month. 2013 survivors!!! I'd like to see you all there, and MAYBE next year we can plan a long weekend to meet somewhere and plan some type of retreat!! Thoughts?????



    I am now 12 days from my squishys!!! My niece thinks my boobs are too big! Lol! She is a mini me; everyone says so. My husband says she's just jealous!!! She has my small boobs. Truth is, I miss my small right boob. That boob had FEELING/sensation; but it tried to kill me so it had to go. I do worry that my left might revolt one day. I don't want to live in fear of recurrence. The feelings post treatment don't just stop. I feel great, but I'm forever changed. I hope our new forum will help us get through check ups, etc for the next 5 years. I don't think anyone else will understand my panic before that first mamo (yes I am totally projecting).



    I love you all!! I hope those USA based have a great holiday.



    Tazzy; happy trails to you as you travel across the pond!

  • teeballmom
    teeballmom Member Posts: 322
    edited November 2012

    Miranda: just wanted to pass a little tidbit our children's social worker told us when we had a thousand questions about how to deal with our 2 being so young and mommy going through treatment. She said that children are very resilient and at their young ages this time period will be just a blip on their radar. They'll remember it in simple terms like this was the year we didn't go on vacation or mommy slept a lot. I didn't believe it much at the time (although I really wanted to) but I can say that nearing the end of really active treatment, how she said the boys would handle it is pretty much what happened. Not to say that there aren't issues. Our 6 year old has not done as well in school as last year, he does act out at times in class and on the playground and our 5 year old won't stop talking in class and argues with his friends but their teachers tell me that it is all improving.



    Halfcan: All I can say is Geez!!

  • teeballmom
    teeballmom Member Posts: 322
    edited November 2012

    Keetmom: welcome to our group!



    Mcook and juneaubugg: good to see you posting. I was also thinking about all of us who started this journey together and how far we all have come. I am definitely there for the 2013 survivors group. Let us all know when the group begins.



    Been fighting a cold for over a week now. Ended up at the ONC office to see my doctor on Friday. Was worried that I might have strep, since it is going around at the boys' school right now. She put me on antibiotics to be on the safe side. I am glad. Don't want anything to stop me from getting my last Taxol on Weds. My white blood cells looked great but then again it's probably because my body is fighting something.



    As I am getting ready for Thanksgiving this week (working off a list since I can't remember anything with this chemo fog) I just wanted to say that one of the things I am thankful for this Thanksgiving is that I have all of you in my life. You have helped me get through the worst part of BC and although I am usually pretty silent in posting, I am here reading often and have found that you have given me strength and hope when I have needed it most. I share everything with my DH but there are some things about this journey he cannot understand. Knowing I can come here 24/7 and laugh, cry and vent with those who understand is a gift that I am extremely grateful for. Thank you everyone!



    Take care everyone!!

  • Outdamnedspot
    Outdamnedspot Member Posts: 297
    edited November 2012

    Though I haven't posted much, I am here several times a day.  I am very interested in a 2013 survivor's thread.  Just following others here has been tons of inspiration and encouragement

    I am so happy that this place allows us to say what we want, learn, laugh and cry.  There are so many amazing women here and I hope that there will be a get-together someday somewhere.

    This site and these threads have made this whole thing...doable.  And with lots of humour and hope.  ((HUGS)) to all.

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

    Mcook, I has problems with my shoulder and went to PT after surgery, during radiation and again a few months after treatment ... Have you tried acupuncture ... My PT can do that and it really helped.

  • juneaubugg
    juneaubugg Member Posts: 951
    edited November 2012

    Teeball: so sorry I forgot you were here when I got here!!! I know I forgot many of us.... My memory sucks!!!



  • Chrisrenee77
    Chrisrenee77 Member Posts: 1,032
    edited November 2012

    I just want to say a heartfelt thank you to all of you who have been here for each other as well as for me. I too would love a 2013 survivor thread. I don't think I would have made it through a lot of this without yall. You all have been a major support system for me. I have cried and laughed with all of you. I hope I have given the support that you all have givej me. I do not "know" all of you personally but I consider you all family. I love you all!

    Christy

  • mcook301
    mcook301 Member Posts: 509
    edited November 2012

    Hello



    I am all for a survivor thread that would be great! I am starting with a new doc next week so hopefully she can help me. I am a little scared about acupuncture? Would this increase risk of lymphdema? I am about willing to try anything at this point:)



    I will update photo as soon as I figure out how on IPad. Maybe I can have my 9 year niece teach me next week as she knows a heck of a lot more than me on this thing.



    Take care everyone! I am going to watch some football today and relax!

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

    A big FAT YES for a 2013 SURVIVOR thread.  As most have said, couldn't have got through this crap without you all.  (((hugs))))

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited November 2012

    I am in for the 2013 survivor thread but am not very techy so hope one of you will do the deed.

    SmileMarian

  • juneaubugg
    juneaubugg Member Posts: 951
    edited November 2012

    Mcook: I have had acupuncture recently. I don't think it effects lymphadema as there is no fluids being drawn or affected. BUT I'm no Dr....



    I will start the survivor thread, I promise!!!!

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

    Mcook, I asked about it and the PT checked. They do not draw blood and they are putting the needle into the muscle ... Depending on which process,they do, it doesn't hurt. One does but it does so much that the amount of discomfort is worth it.

    Will I be a 2012 or 2013 Survivor?

  • juneaubugg
    juneaubugg Member Posts: 951
    edited November 2012

    Joanne_53; who cares!!! All are welcome.... Just like here. Was it shakespeare..."what's in a name?" Lol!

  • Chrisrenee77
    Chrisrenee77 Member Posts: 1,032
    edited November 2012

    Joanna- a survivor is a survivor correct? As i was told when i made a comment that i didnt feel like i should be here, because i didnt go through all the treatment that most of you ladies have. I was told treatment is treatment, whether its chemo or rads or infusions. Its allthe same.

  • maryah930
    maryah930 Member Posts: 322
    edited November 2012

    Agree with juneaubugg and Chrisrenee: You were diagnosed, you survived. The different types of diagnosis/treatment/surgery doesn't matter, we survived. Cool

  • juneaubugg
    juneaubugg Member Posts: 951
    edited November 2012

    OK - Here it is...  2013 SURVIVORS... it's in the IDC Forum.  :-)

    http://community.breastcancer.org/forum/96/topic/796538

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

    You rock Juneau.  And I agree, we all were dx'd with cancer.  Cancer is cancer.   We all heard those words 'you have breast cancer'.

    rock on sisters !!

  • JenLex
    JenLex Member Posts: 6
    edited November 2012

    Hi, all!

    Pardon the interruption . . . This is the first discussion group that I've ever joined and the first time that I've ever posted!  I've been lurking on this site for months, though, finding information, comfort, strength and inspiration in all of your posts.  I am a 2012 sister, having been diagnosed with er+ idc bc on January 12, 2012.  I can't believe that 10 months have passed since my diagnosis.  In some ways, it seems like just yesterday and in some ways, it seems like a long time ago!  I had a mastectomy (left) in February; 4 rounds of adriamycin and cytoxan from March to May; 12 weekly rounds of taxol from June to August; and 33 radiation treatments from October to November (the last one is tomorrow!!!).  I started my 5-year regimen of tamoxifen in September. 

    I just wanted to say thank you to all of you! Your posts have made this journey much easier than I ever imagined it could be.

  • MirandaSW
    MirandaSW Member Posts: 35
    edited November 2012

    M cook--My Mom had a frozen shoulder after sugery for a broken shoulder. It is caused from a build up of scar tissue like stuff in the joint.  As you know, scar tissue is not pliable.  They had her in PT but it was so painful for her...the only option for her was surgery.  They went in and removed all that scar tissue from the joint and she is fine now.  She did not want to do the surgery, but the alternative was to continue with pain to see if maybe it would work itself out. The MAYBE wasnt good enough. Recovery from the surgery was only a few weeks as compared to the months or years it may have taken.

    Teeballmom--My 2 year old is just that...2.  He is a pain in the ass because he antagonizes  his brothers, gets into stuff, is mouthy, and just all the fun 2 year old stuff. He is pretty oblivious to my illness. My 4 year old is angry sometimes, but is actually improving his old behaviours and turning into a boy who is better able to cope with his emotions.  He used to (like 1-2 years ago) throw tantrums that would last up to 2 hours. It was maddening. Now he will actually take his own time out in his room if hes angry. He started that all on his own. My 16 year old girl. Shes fine-gets good grades, has a job, helps with kids and the house. She is a teenager so its not perfect, but pretty close.
    Now my 5 year old, Calvin, is the problem. At home he is whiny, bawls about everyting (time to shower, have to go to the store, time to put shoes on, cant wear a certain jacket), plays rough with his brothers till someone gets hurt. He is having a hard time at school, usually worse when Im chemo sick. He doesnt focus well, cant keep his hands to himself, plays too rough, impulsive, etc. His teacher is very understanding and they are trying different approaches and alternatives for him so he isnt always bringing notes home....but I dont know what else to do to help him.  He is seeing a counselor. He seemed to be doing better for a bit but all behaviors are worse again. He is in Tae Kwon Do even.  At least its only one kid I have a problem with.

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

    JenLex, be sure to join the 2013 survivors thread .. The link is above by a few posts.

  • juneaubugg
    juneaubugg Member Posts: 951
    edited November 2012

    JenLex: so glad you decided to post finally. I totally agree; it hardly seems that it's been so many months of treatment; it's like the year that wasn't. I hope you are starting to recover and feel more yourself (whatever that has become). I know my new self is not the same as the woman who was diagnosed all those months ago.



    Anyway, welcome.

Categories