Calling all ladies in their 20's

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  • Alyssa55
    Alyssa55 Member Posts: 4
    edited October 2011

    Hi Everyone!



    I've been trying to find a chat room with women closer to my age. I just turned 24 and am through three of my eight chemo treatments. I was 23 still when I was diagnosed and the first thing out of everyone's mouths when I would tell them my diagnosis was "but you're so young!". That got old very fast. And every group I find or blog I read seems to be all middle-aged women, so it's hard to find people to talk to that I can relate to.

  • NannaBaby
    NannaBaby Member Posts: 510
    edited October 2011

    Hey Alyssa! You will find great support here :)

  • kk11
    kk11 Member Posts: 210
    edited October 2011

    Welcome Alyssa! What chemo regimen are you on? 4 X DD AC and 4 X DD Taxol? Have you had surgery yet or will it be after you finish chemo?  I hear you on the "but you're so young!" comments. It's nice to have a group of others in our age group since we have to deal with different ramifications of having cancer, including fertility, etc.

  • BcMomOf3
    BcMomOf3 Member Posts: 80
    edited October 2011

    Hello,

    My name is Alissa and I am a 23 year old senior at Southern Methodist University. We designed this user name for my aunt Kristen, who passed away of breast cancer last October. She was 45 years old. This site was extraordinarily helpful to her and all of us. I cannot tell you the number of sleepless nights we spent on here, and each time received such hope. I commend all of you ladies for courageously fighting this battle, and my prayers are with you all. 

    As a college student I was really struck by the lack of awareness that took place on campus during October, breast cancer awareness month. Not a single pink ribbon could be found, and I quickly realized that college students do not think breast cancer effects them. The fact is 1 in 8 women will be diagnosed in their lifetime, 1 in 269 are under the age of 40. As many of you may know, there is this belief amongst young women that "it won't happen to me." Unfortunately the odds are not on our side. Until I watched my aunt find her own lump through a self exam, I never did a single breast exam, or was even really aware of the feeling of my breasts. My friends don't do them. I've asked my friends if they known people who had breast cancer and many have, but few believe that they will get it, especially so young. I believe that the way to prevent breast cancer is to start with self awareness at a young age. Women need to know their bodies, ask the questions and be aware of any changes. We are our best resources and as I learned from watching my aunt, we can only rely on ourselves to ask the questions and demand answers. 

    I am a journalism major and for one of my classes I am going to make a PSA for the Susan G. Komen foundation here in Dallas. The PSA will be played for our school morning show, The Daily Update, and linked to our school newspaper. I am hoping to interview a few young women to find out more about their disease and hopefully use them in the PSA. I would prefer to interview someone in person, on camera in Dallas, but if that is not possible, over the phone interviews with a picture or two would also work. Any help I can receive to spread awareness of this disease on campuses I would greatly appreciate. 

    Again, I commend all of you as you continue on in this fight! 

    Alissa Fitzpatrick 

    I can be contacted through this site or my email: afitzpatrick@smu.edu

  • NannaBaby
    NannaBaby Member Posts: 510
    edited October 2011

    Just found out I'm BRCA 1&2 negative!!

  • lulujune17
    lulujune17 Member Posts: 47
    edited October 2011

    Hey beautiful ladies, i just turned 29,since January last year my life hasn't been cheerful as it used to be,on January 21st last year i had an advanced miscarriage,i was 6 months pregnant,it was supposed to be my second boy(i already had a name for him)but my water broke for no reason and he was born dead the next day.since then i have been on antidepressants, and lets not forget my sweet mother in law,she made my life more miserable(she really thinks i had something to do with losing the baby)!!!!!!!! she even convinced my husband with that!!!! and for a while they were both bitching around! and then this june i was diagnosed,my onco and my surgeon thinks it has been there for a year or so,i think it happened because of the stress i had been through after i lost my baby.i didnt believe it first,had a left breast MX (no nipples saved)lol, now on FECx4,then Taxotere x4,then 5 weeks of radiation,then reconstruction(im having a tummy tuck too)Laughing

    I will take tamoxifin for 5 years ,so i think this will really put some plans on hold, i was trying to have another baby but didn't get pregnant and just when i was thinking of IVF i got the diagnosis.

    But you know what?now i appreciate everything i have,i am having more fun with my little one,i found that i have the best girlfriends in the world,very supportive and helpful and positive.

    I don't look my best now,being bald with one breast,swollen because of steroids,i tell my friends i feel i look like the Michelin Man..Lol.but from inside i am not mad,i'm not scared,i will fight it and i will live as happily as i can be,even if i become infertile,i still have lots of things to be grateful for, my husband is not helping,i get the feeling that he is mad at me for putting our little family in chaos,like i intended it or i asked for it!! But i try to ignore him and just stay positive,because i finally feel happy(can u believe that?)Laughing

    So to every young woman out there with cancer, don't be scared,try to live your life to the fullist,even if you will lose a breast or both,if this will save your life,do it, you will have new sexy boobs after reconstruction anywaysTongue out

    life is still beautiful believe me,good luck to all of you.

    Love and Hugs to all

    xoxoxoxo

  • Alyssa55
    Alyssa55 Member Posts: 4
    edited October 2011

    Hi kk11!



    I am on 4 x AC an then 4 x taxol. I actually just finished my fourth AC treatment yesterday, so I'm finally halfway done! I've been getting mixed answers though when I ask people about taxol. I had one oncologist tell me it's easier than the AC treatments, and another one tell me it's harder. Any advice? I already had surgery. On August 8th I had a bilateral partial mastectomy (essentially just a lumpectomy) with right sentinel node biopsy. I found the surgery no problem, I bounced back pretty quickly. Its the chemo that totally sucks. And to be honest, losing my hair has been one of the hardest parts. I've continued working through my chemo and even though I have a fantastic wig, I felt like losing my hair plastered a massive "I have cancer" sign on my forehead and I felt like all of a sudden everyone could tell what I was going through, ven though I hadn't told them. I'm gradually adjusting to wearing a wig and getting more comfortable in it, but it's been a lot harder than I expected!



    Lulujune17 - just wanted to say your post brought tears to my eyes. Good for you for standing so strong. And I agree, theres no point in being angry or scared about breast cancer. It sucks. It does. It totally sucks, but all that energy the could be wasted on anger and fear could be put to much better use in kickin cancers ass and getting back to life. I'm sorry to hear about your miscarriage but know that it's not your fault and I'm sure you will have a beautiful and amazing baby once this is all done. And you'll be that much more thankful and grateful to have them in your life. Good luck with everything!

  • Melanie_Ann
    Melanie_Ann Member Posts: 414
    edited October 2011

    Nanna- I think you have a case and I say go for it! We're behind you!

    Welcome to the new ones- Alyssa and Lulu.

    Alyssa- I had all three chemo's at the same time so I'm not sure how taxol is different. I just know that it can affect your  nails. I iced mine so they wouldn't fall off. It worked pretty well. They were a little tender and my toenails got some white spots on them, but I still have them. I've heard that people can tolerate just taxol better than AC together. Glad to hear you're halfway done!

    kk-how's tammi now? I've been doing it for almost 3 months now. I'm finally sleeping better. Part of it may be due to the fact that I'm unemployed now and resting better but who knows.... Still no period.

    TAC, Start Date: 2/1/2011 Cycle 6/6 <--DONE!
    Diagnosis: 12/1/2010, IDC, 2cm, Stage IIa, Grade 3, 1/7 nodes, ER+/PR+, HER2-

  • lulujune17
    lulujune17 Member Posts: 47
    edited October 2011

    Alyssa,thank you and i wish the best for you too, you will have wonderful hair once you are done with chemo,i didn't lose it all,but i didn't wait till it happen,i shaved it,but some of it is growing backLaughingi agree it really screams "i have cancer" when you lose your hair,but i always smile a really big smile to any one who gives me oh-poor-thing-she-has-cancer look,and it totally changes the way they look at me,i give them the i've-never-been-better lookLaughingit really works,try it(even if they think you are in denial)LOL  ..Just try to make the most of every day,live it to the fullist,laugh,pamper yourself(you deserve it),stay around positive people,and don't let anyone make you feel sorry for yourself,you will be okay,chemo will be over in no time and you will have your hair back,your normal life back before you know it.

    keep smiling and keep your head up sisterLaughing

    Thank you Melanie-ann.

    Good night everyone,

    Hugs to all

  • shiramg
    shiramg Member Posts: 186
    edited October 2011

    jcoutee - i've been on zoladex (same thing as lupron) for about 10 months and have felt no issues besides hot flashes.  i'm very happy i agreed to do this treatment bc it is so important for premenepausal woman to shut down ovarian function.  tamoxifen is not enough (according to my onc who is one of nyc's best)

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    Hi Ladies!

    I got my lung, bone and ultrasound results today! ALL CLEAR!! What a RELIEF!

    Thanks for cheering me on and keeping positive :)

    I don't have an explanation for the pain... it's still there :( It's been over 6 weeks.  But, at least now I'll be able to sleep knowing it's not cancer :)

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    I finally got my records from my ex family doctor!  He kept calling me and making excusses why I shouldn't see the notes... it's company policy, you won't be able to read/understand whats written, blah blah blah.  I told him to stop acting so suspicious and just give me the notes!  He got REALLY defensive! He even called me from his home to bitch me out! He didn't like it that I said it's suspicious that they are hiding my medical records... oops! LOL

    I requested my file in person 5 times! The second time I paid $50 for the size of file.  The clinical notes were only 12 pages long! For a ten year span! UGH! In his notes, he wrote "no mass palpable"?!?! My lump was 8CM!!! Yell  I don't have a case against him to sue :(  There were 2 other doctor's notes/reports in my chart that suspected b9....

  • Alyssa55
    Alyssa55 Member Posts: 4
    edited November 2011

    Hey Everyone. I had the weirdest thing happen today... I'm one week out since my last AC chemo treatment (scheduled to start my first of four taxol treatments next week) and should be coming into a few days where I feel relatively good again before my next chemo. I was at work today and basically fainted/blacked out, fell over and then started throwing up all over the place for about half an hour straight. It was crazy. My boss didn't know what was going on and called 911 so then the paramedics came and took me to emerg (at the hospital where I'm being treated - I wouldn't let them take me anywhere else). Of course when I got to the hospital they did the full workup on me because im a chemo patient but they really didn't find much. White blood cell count is low, as to be expected because I'm on chemo... Had a very low fever, but they said it wasn't high enough to give me antibiotics for.... It was just the craziest experience. I've never felt so shitty and delirious before. And I've never fainted before. Has anyone else had this happen? I don't know if my body is just run down or what... I just can't wait til I'm done with all my treatments and can finally get my body back to "normal" again! If that's even possible.



    NannaBaby - glad to hear you got your records. They legally are not allowed to ever deny you records and probably took so long getting them to you because they knew you were contemplating a lawsuit and wanted to make sure their chart had no "holes" in it so you couldn't sue them. I worked for a doctor for a couple years and sadly they're almost all the same. They keep shitty records to begin with, and it's only when they think they're getting sued that they take the time to get shit in order. I bet the note about "no palpable mass" didn't even exist until you asked for your chart. It sucks. But at least you finally have your records!





    Lulujune - thanks for the support. I actually did shave my head too. I bought a wig, and the day before my second chemo treatment, when my hair had just started falling out, I had my stylist shave it. But she said I shouldn't shave it totally bald and leave a bit of fuzz to naturally fall out. I wish she had shaved it lower than she did because watching all that "fuzz" fall out drove me nuts! It took forever and was all over everything I owned! I can't imagine if I'd have let my real hair (which was past my bra before) fall out!

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    Thanks Alyssa! I am somewhat satisfied knowing that dr finally paid attention to his shit and realized where he went wrong! That asshole didn't know how to do a proper breast exam! I used to work in the hospital teaching diets and the hospital had a policy where if there was an unmarked blank space in a patients chart, that we should mark the area with a line or x so they can't add shit to cover their asses! I know it's not a coincidence that dr notes r so broad and spaced.



    When my fuzz was falling out, I sat in front of the mirror and literally pulled it all out! I even used the cats brush! Lol

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    Oh yeah, I also had dizziness and fainting spells during chemo. Keep hydrated is what I was told... :s

  • lulujune17
    lulujune17 Member Posts: 47
    edited November 2011

    Hi beautiful ladies,

    Tomorrow is my 4th and last FEC,the 3rd was terrible,hope this one would be better.

    Alyssa,im sorry you fainted sweety,hope this never happens again, as Nannababy said,it might be dehydration,i get dizzy every now and then,and i get blurred vision(happens mostly when im driving)!!i see flies and spiders on the walls!!Laughing(i imagine them,this chemo brain is true,my onc.says there is nothing called chemo brain!!)yeah right!!

    Drink plenty of water,gatorade,fresh juices,they might help.What did your onc.say?How r u feeling today?

    When i went to shave my head at the wig shop,she said the same thing.it's better to leave little fuzz,i looked like a kiwi..LOL, it was day 17 after a i started chemo,but after my second round they started to fall out,so i did like Nannababy,i pulled them out.I just hate to wait for things to happen,if i can do it i'll do it myself.

    Nannababy,i'm glad your scans came back cleaer sweety,i can imagine what a releif it was to know that.and glad you have your records now.

    I did not let anyone c my bald head till now,not my husband,not my mom nott my friends,did anyone feel that way too?are you comfortable around ppl without covering your head or wear a wig?I can't let anyone c me bald!im always wearing my wig or a bandana. When i shaved my head,i wore a head cover,my son put his hand and felt the fuzz,he asked me where is my hair,i told him mommy is taking a medicine that makes hair fall out,but makes mommy live more,so he told me i look pretty anyway!!!it just brought tears to my eyes,i couldnt believe a 5 year old would say such a thing,but it made me feel betterLaughingGod how i love that boy!!

    I hope you all enjoy your life and health after this journey,i know i willLaughing

    Keep positive,squeeze every minute you live,be happy and keep smiling and laughing,it will be over before you know itCool

    Love you all,

    Good night

    xoxoxoxoxo

  • kk11
    kk11 Member Posts: 210
    edited November 2011

    Hi ladies - Just checking in real quick. I had my swapout surgery yesterday. I'm in a lot more pain than I anticipated, but part of that is because the binder wrap is wrapped really tightly around my chest to prevent swelling. I had a horrible night's sleep last night and don't think tonight will be much better. Just need to get to Monday when I can remove the wrapping and take a shower! I think I'll feel much better then!

    Nanna - Glad you were finally able to get your records, but sorry that it doesn't look like you have a case. I hate that it seems they are covering their asses. Congrats on the all clear on the scans and the BRCA testing! What a HUGE relief!

     Lulu - Congrats on being done with FEC! I also had a miscarriage last August (first pregnancy), though it wasn't at 6 months...it was at 10 weeks. Still, it was a complicated miscarriage (partial molar pregnancy) and I ended up needing 2 1/2 months of chemo to resolve it only to end up with the breast cancer diagnosis 2 months after that 6 month ordeal. It really sucks and I totally sympathize with you. And I can't believe your MIL tried to blame you for it and that your husband wasn't entirely on your side. That's just wrong.

    Alyssa - Taxol was easier for me in terms of nausea (had none) and overall fatigue (it was better), but it gave me other symptoms, like bone pain and neuropathy. So I guess it just depends on how well you tolerate the symptoms and it is really dependent on the individual experience. As for the hair, I felt the same way before I lost mine, but ended up quickly getting over it. I try to think of the bright side....like how I don't have to brush my hair before I leave, don't have to shave, etc. Now that I'm done with chemo for a month already, I am looking forward to getting my hair back, but I'm not paying too much attention, because then it seems like it comes back more slowly! As for fainting spells, I also got dizzy and lightheaded during chemo, but never actually fainted. If your red blood cells and hemoglobin are low, this would be the cause. Just make sure to get up slowly when you get up and like Nanna said, drink plenty of water!

    Melanie_Ann - Tamoxifen has been okay. It's been about 2 1/2 weeks and so far so good. I already had hot flashes from the chemopause, so I don't notice too much different. I am a month out from chemo and no period for me either. How long ago did you finish again?

    Shiramg - Are you also doing Tamoxifen or just the Zoladex? Also, what % were your estrogen positive? That might have factored into the decision to have you on both. I am just 10% estrogen positive, so very weakly estrogen positive. My onc is fine with just the Tamoxifen.

    Ugh....my arm is hurting from the typing. Will have to stop now!

  • MiniMacsMom
    MiniMacsMom Member Posts: 595
    edited November 2011

    I also agree that its comforting to talk to other women in my situation.  I was diagnosed on 10.25  with IDC and DCIS with a very large tumor.  They did a Right mastectomy on 11.3 because my tumor and "worrysome" tissue was about 50 percent of my right breast.  Even after the surgery the doctors still wont tell me anything.  I had some lymph nodes, with at least 2 infected, removed so now I have to get PET scans and such. 

    We started the process with a Livestrong affiliated reproductive endocrinologist to have embryos frozen, but now I am scared.  I am ER, PR + and I don't want to encourge the tumor if they are somewhere else.  My RE said that there is a special protocal for ER + patients but you still do have some ER bursts.  So now I have to decide between embryos and checking for mets and not doing embryos.  I know my health is more important and I am blessed with a husband and a wonderful son, but I just feel like the cancer has taken so much from me.  I don't want to give up my fertility.  I am 27, my birthday is in 2 weeks, and if we wait until post 5 yers post chemo, our kids will be 7+ years apart.   Thats IF: i can still get pregnant, if they let me because I am SOOO estrogen positive and If i am still around. 

     Grrrr,  I am supposed to start chemo right after the fertility stuff.  Anyone else had to make the choice.  what factored into to your decisions?  Sorry, just took a percocet for the MX pain,  they ended up taking a lot more tissue and fat than originally anticipated so my armpit kinda hurts :) more than anticipated. 

  • kk11
    kk11 Member Posts: 210
    edited November 2011

    MinimacsMom - Ask your RE about taking Femara during your fertility treatments. My RE specializes only in fertility preservation for cancer patients, so I fully trust his input. He had me on Femara to keep my estrogen levels in the blood down. They monitor your blood daily during your cycle, so you'll know how it's affecting things. I'm ER+ as well, but just 10%, so fairly weak. We have no children yet (had a complicated miscarriage last year), so we felt it was absolutely necessary to get embryos frozen. I'm 28, turning 29 in less than a week. I also don't want to wait 5 years to have a baby (I've spent the last nearly 2 years wanting one) and would like to take a break from Tamoxifen in 2 years to have one. I just have to play it by ear and see how the next two years goes. What stage are you? Is your oncologist on board with fertility preservation? I have been told that most women in our age group will get our periods back, but chemo does age our ovaries considerably, which is why I decided for the preservation.

    And try to take it easy after your MX....it's a pretty heavy surgery and you need to give yourself time to heal. I did my fertility preservation prior to my MX, so I didn't have to worry about healing from that while getting the fertility treatments. So make sure to treat your body well as it's going through quite a bit of stress right now.

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    MiniMacsMom - I had the decision to delay chemo and IVF.  But, I realized that my health is more important, and I started chemo ASAP!  I couldn't risk 3 weeks of a delay.  Plus there are risks involved in egg retrieval, which I considered because if anything were to happen, then chemo would be delayed even more! Plus their was a chance that I wouldn't ovulate, develop enough good eggs, embryo failure... etc. 

    I finished chemo in June.  I did a total of 16 infusions!  I was sure that I'd screw up my hormones and cycle for sure, but didn't!  My period is back and as normal as ever!  Chances are in your favour, because you are so young :)

  • MiniMacsMom
    MiniMacsMom Member Posts: 595
    edited November 2011

    If I start the treatments tomorrow like everything is ready for, I will  be able to get the eggs out in 14 days, which is 1 week before I want to start chemo.  I am concerned because I know who my onco is, but they won' tschedule my appt until i follow up with the surgeon on Friday.  Ugh, I am so not trusting my hospital right now.  My RE doesn't specialize in fert preservation but she is goign to put me on the femara to block the ER interaction.  I start that tomorrow after my ultrasound and the hormones on Wed.  This whole process is so scary.  After everything the RE has done to get my funding and free drugs, I feel bad backing out, but... I just don't know what to do.  I am blessed with one amazing 15 month old, already.  Sorry, very emotional after surgery. 

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    Don't feel bad backing out! It's about YOU!

    What do you mean, he won't schedule apt until u see the surgeon?  You mean your onc doesn't want you to start chemo until you see the breast surgeon? Is it because he wants to ensure it's healing properly? When did you get surgery?

  • kk11
    kk11 Member Posts: 210
    edited November 2011

    Minimacsmom- Nanna is right. It IS about YOU. I think you mentioned you just had surgery a few days ago right? I think that it makes sense to not schedule chemo until they know your surgical wounds are healing properly. As far as doing the fertility preservation, I think it's worth it if you want to keep your options open. I got the drugs free too, but still had to fork over thousands for the rest of it. Is your onc on board with you doing fertility preservation? That might help make your decision. In the end, only you can make the decision for yourself, but unfortunately you don't have much time to decide. I can't imagine having to make any major decisions like that right after my MX. Maybe sleep on it one more night? And if you have any reservations, maybe you can ask your RE and onc so that you can be 100% sure of your decision.

  • MiniMacsMom
    MiniMacsMom Member Posts: 595
    edited November 2011

    I had the surgery on 11/3.  My hospital procedure is that you see the Surgeon for the follow up and then he gives you the referal appt for the oncologist.  I seems a little backwards to me.  I want to hear my results that will affect my chemo from the doctor who controls the chemo. I think I am going to make an appt with the oncologist myself just to discuss my treatment plan.  I am only one of 4 or 5 women under 35 with breast cancer that my hospital has treated recently.  They deal with TONS of older women but not us.  I just don't think they are used to dealing with someone proactive with LOTs of questions :)  Oh well.  Yeah, I guess I will sleep on it again tonight.  I think I was at peace with my decision until my husband said "what if something happend to our son" now I definately have reservations.  i wouldn't ever replace Derek but... I'll let you know in the morning.  Man this stuff sucks! 

  • MiniMacsMom
    MiniMacsMom Member Posts: 595
    edited November 2011

    So after some serious discussions with my hubby we decided not to go through with the repro preservation. I am lucky to be blessed with a wonderful natural born son! I also didnt feel that it was worth the theoretical risk since i cant get into my onc to discuss it. On good news Vandy called today and i have an appt with a breast cancer specialist on 11.16! Good luck to all you other ladies and thanks for the support. my friends are super supportive but they dontreally understand so the different perspective was wonderful.

  • kk11
    kk11 Member Posts: 210
    edited November 2011

    MiniMacsMom - As long as YOU are happy with the decision you make, that is all that matters. I went a different route (because I don't have children yet), but totally support your decision. I might have made a similar decision had I already had a child. Everyone's circumstances are different. I hope you are recovering okay from your mastectomy. You're right that even with people who try to be supportive in your life, they don't really understand what you're going through unless they're in the same position (young and same family planning stage). In addition to this online group, I am fortunate to have found a young women's support group that is local where I go every other Tuesday for meetings. I prefer that over the idea of counseling because I'm surrounded by those who understand. It's hard otherwise, when the only people you know that have ever been diagnosed with breast cancer were already much older (and past the children stage of their life) that you.

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    MMM - I am glad that both of you decided together :)  Keep going strong! And keep us up to date with ur chemo...

  • MiniMacsMom
    MiniMacsMom Member Posts: 595
    edited November 2011

    High girls :)  looks like we made the right decision, I am stage IIIa high grade tumor.  It was a total 9x6x5cm with 4 of 13 infected lypmh node.  The one positive is my lowest clear margin is 2mm!!! They they got all they found.  I start chemo on 11/18.  They had given me three options AC/T, DD AC/T or TAC, but now they just said I get the most aggressive treatment.  I am waiting on a call from MD Anderson and I have an appt at Vandy, but I will cancel If I can get into MD Anderson in time.  Wish me luck, its gonna be a long road.

  • NannaBaby
    NannaBaby Member Posts: 510
    edited November 2011

    I'm glad you are happy with your decision! What a relief it must be! Those 3 chemo regimes are pretty much the same... Top notch aggressive stuff!  I did chemo before surgery and AC + Taxotere kicked cancers ass!

    Do you know if your cancer is hormone or HER2 positive yet?

    It will be a long road, but you will be surprised on how quickly time goes by!

    Keep in touch, and feel free to post here or PM me, if you have questions.  No matter how gross or intimate they are! LOL 

    Did they mention if you will have a port-o-cath (in the chest) or a PICC line (in the arm)?

  • MiniMacsMom
    MiniMacsMom Member Posts: 595
    edited November 2011

    I had my port "installed"during my mastectomy :)  I am ER post at 99% and PR pos at 5% and HER 2 neg.  The ER and pregnancy hormones prolly had a lot to do with the massive growth.  But i would rather have a massive fast growth than a slow growth with time to form mets!

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