September 2013 Chemo Group

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  • lighthouselady
    lighthouselady Member Posts: 752
    edited January 2014

    Audra - I had neoadjuvant chemo for a couple of reasons.  My tumor was large and close to the surface, so my surgeon would have had to remove a lot of skin during surgery, leaving my plastic surgeon with not a lot to work with.  (She ended up taking quite a bit of skin anyway, to have clean margins, so I just think how much worse it would have been)  Also, I had 1 node biopsied and it was positive... with the cancer grade 3, they wanted to attack it fast so the aggressive cells didn't have time to spread anywhere else.  Surgery would have removed the known cancer, but then it would have delayed chemo that much longer, which attacks ALL the cancer hiding elsewhere.  

    Some women have chemo first in order to shrink the tumor in hopes of having a more breast conserving surgery....if they have a good response, they may only need a lumpectomy.  Since I'm BRCA+ I knew a bilateral mx was my only surgery option, but I'm still glad I did chemo first.

    KJ - you're a crazy lady.  LOL

  • kjsimpson
    kjsimpson Member Posts: 445
    edited January 2014

    For those of us with inflammatory breast cancer (IBC), they do neoadjuvant chemo (chemo before surgery) as a matter of course.  First chemo, then surgery, then radiation.

  • audra67
    audra67 Member Posts: 521
    edited January 2014

    Aha=  thanks you all for the information.  I thought I had researched and know it all by now...lol.

    That is nice that you see the tumor shrinking with chemo...proof! 

    I am going on faith and hoping the chemo killed any little thing in my body and that nothing will ever come back!  - as I am praying all of ours did!

    You all are awesome !

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2014

    Kathryn - thank you so much for all of the drain info. I'm finding I've got lots of anxiety before my pre-surgical appt with SO tomorrow and it's good to be prepared, ahead of the surgery.

  • Miss_Mama_Bear
    Miss_Mama_Bear Member Posts: 252
    edited January 2014

    BetterDay: so sorry to hear about your news. It is tough to say what to do first. Both ways have advantages and disadvantages. They did chemo first on me because they thought it was in my nodes and my tumor was fairly large for my breast size. All we can do is to hope and pray for our team of doctors to make the right decisions. I will be praying for you to have a positive outcome no matter what route they take.

    OY! Always a roller coaster! I saw my BS today and she freaked me out by telling me she is 100% certain I did have cancer in my lymph nodes before chemo (and there is the downfall to doing chemo first). She still isn't recommending rads though because it was completely gone at the time of surgery. Still really freaked me out and makes me wonder if maybe I should have rads anyway. The final say is up to the RO, I guess.

    My PCP office called today to say that my bloodwork came back indicating that my nipple discharge is not due to a tumor on my pituitary gland. I didn't talk to my doc, just her nurse, but she said that doctors notes said that she thought my discharge was due to my cancer. Well...it is bilateral and I am still having it... What does that mean?! So, then there goes any remaining doubts about having a BMX, but again, I am freaked out.

    I did talk to my surgeon about a nipple sparing today and was debating that. The thought of the possibility of the discharge bringing cancer cells up and them settling in the nipple worried me so I was going back and forth about it still. She said I had about the same chance of that happening as I did of getting killed in a car accident when I left her office. Well... a chance is a chance, right? Have you ever heard me say that I hate making decisions? lol. I was happy that she said she could do incisions either around the nipple or under the lower breast fold. That makes me happy because I have the two 3" incisions already on my side boob area. I am hoping they can do something during surgery for that one, like you said LHL. I forgot to ask. 

    Oh yeah, I forgot I changed my name on here, if you didn't already figure that out lol. I plan on posting pics in the lumpectomy section. It can be a kind of worst case scenario lol. My surgeon apologized for beating the crap out of me. Her assistant came out and asked her what the heck she did to me during surgery. Funny because I was at least 1000x worse before. In addition to the crazy bruising (from lower bra band to above my armpit area and encompassing my entire breast all the way back to where my side turns into my back-nearly solid bruise at one point, except under the arm) I have a massive hematoma where my tumor was. She drained what she could of it, but it was only about half. I am still down a good full cup size, and OMG it felt soooo good. Anyone who has ever nursed will know what I mean, I feel like I got emptied after total engorgement. A lot of the numbness has gone away too. I guess the whole side of my breast wasn't supposed to be numb lol. At any rate, I think the whole thing has given me a little taste of what the BMX will be like. 

    Oh, and the guy. I don't know lol. I guess we will see what happens. I think we are both in a position where we want to take things really really slowly. 

  • Cougarlicious
    Cougarlicious Member Posts: 114
    edited January 2014

    Betterday - lots of hugs.  I got my first MRI this weekend and am worried I will have similar results.  My tumor (over 3cm to start) shrank quickly to a nub on AC, but then started to grow in size by the last one.  Once on Taxol it shrunk back down to about 1cm, but now that I'm on 9/12 Taxol, it seems like it's grown again.  The whole thing has made me swing from 90% having a lumpectomy to now I am at 90% for sure getting a BMX.  I'm worried about future recurrence and new cancers growing as fast as this bugger (grade 3, 95% KI-67).  I'm nervous that the docs are going to recommend more chemo if they still see cancer lurking in there.  But I suppose we want to attack this thing with everything we can, right?

    Miss Mama Bear (dig the name) - I missed it, why are you doing lumpectomy first and then BMX?  My surgeon told me if I decide on a BMX just to do it once as opposed to two surgeries.  Or did they get bad margins and you decided to change course?

  • lighthouselady
    lighthouselady Member Posts: 752
    edited January 2014

    mamabear - your bruising sounds like me after my biopsy. My whole breast turned purple and I had a hematoma... Just from a biopsy!! I didn't bruise at all from my bmx.

    Waiting to go in for my rads consult. I'm nervous. Don't know why. I've been through so much and so many appointments... why is THIS one freaking me out?  Stupid cancer. LOL

  • Art123
    Art123 Member Posts: 115
    edited January 2014

    hope you ladies are doing well.

    So much for having an uneventful time after end of chemo and before surgery. The antibiotics they gave nat after root canal made her sick and she missed 2 days if work, she didn't miss a day during chemo. Then last Saturday, we had to go to her pcp, he drained an abscess. She went back Monday for a small boil on her abdomen. She us doing better, no fever or other symptoms, the first abscess is healing well. Supposedly chemo makes u susceptible to this stuff, don't remember this on the list. He did get it cultured and sent out to make sure it's not MRSA. I wasn't thrilled to hear about that possibility and I have finally stopped looking stuff up because I'm in a state of worry. 

    MRI tomorrow, and Friday she has follow up with pcp, hopefully it will be nothing and all healed.

    I just hate seeing her upset. She was off yesterday and said it felt good to relax. 

  • Miss_Mama_Bear
    Miss_Mama_Bear Member Posts: 252
    edited January 2014

    Oh my LHL! I am glad that you didn't have a bad response with the BMX as compared to your biopsy. I wonder why it was so bad?! I wonder if my platelets dropped or something after I had pre-op bloodwork. That scares me with having a BMX. I am glad to know that it sounds like a BMX is better than my experience with the lumpectomy on THAT front, anyway lol. I hope your rads appointment goes well. It seems like ROs are really good people and everyone has a good experience with them. The one I saw (and will see if I need rads) was such a wonderful guy. I could tell that he knew his stuff, he was very thorough and wanted the best possible care for ME, and I felt very good in his care. I hope that your RO is just as wonderful and makes you feel better about the whole experience.

    Cougar: Don't worry, I've got everyone confused (myself, too sometimes) lol. Such a mess lol I will try to do Reader's Digest version. I was going to have DIEP flap done. Those surgeons wanted a node biopsy done first to determine the need for rads. They won't do a DIEP if they know rads need to be done after; they want rads done first. So, we scheduled the node biopsy and she said she would go ahead and do a lumpectomy as well since my tumor was near my armpit and she thought she could get them both with one incision. She also wanted to give me the option of doing a lumpectomy instead of a BMX. I was still kind of back and forth on that; if I had positive nodes and had to do rads anyway, I might have decided on postponing the BMX until later or not doing it at all. So, even though I have since decided to do tissue expanders/implants, I thought it was the right road to go on. Maybe, just maybe, it will make the BMX a little bit easier if I don't have to deal with getting lymph nodes pulled, too. That has been the worst part about the lumpectomy, in spite of how it all looks lol. I had so much pressure from the hematoma that it was mostly numb on one whole side. 

    Oh, and my BS was cracking me up. She was jokingly trying to talk me out of using the PS I chose. Remember, the jerk I posted about? She agrees lol and kept saying "I'm going to have to work with him?" and "I keep trying to get him to straighten up his act". She did also agree that with his quality work, he can afford to be, I guess. I would like to some how be able to hear what they are saying when they are operating on me lol. 

    And KBee that reminds me of your post about being a nude model during surgery! Dang it! I was trying so hard to remember what I was going to respond to, and even went back through the posts several times to try and find it...chemo brain! ANYWAY! I LOL'd at that! It does kind of freak me out to think of being completely out and what is going on around you and even with your own body. I suppose it is better than the alternative though!

  • Miss_Mama_Bear
    Miss_Mama_Bear Member Posts: 252
    edited January 2014

    Oh Art, so sorry Nat is having a rough go of things. Not on the list...my list only had about 5 things on it lol. I think it needed at least 3 dozen more. I just dealt with a MRSA situation with a friend of mine, and I will say that what you are finding on the net is probably worse than the reality of the situation (I know that is what happened to me). The net can be a wonderful thing but also a horrible place to fuel our worry. Take a deep breath and wait for the results. The facts. Then deal with it. You guys have enough to deal with already. And with her not taking a day off through chemo, she deserves one! Glad she was able to relax a bit. 

  • lighthouselady
    lighthouselady Member Posts: 752
    edited January 2014

    Art - {{hugs}} to you & Nat.  I'm sorry she's had such a rough go of it.  That's like adding insult to injury, going through chemo and ending up dealing with that afterward!  Ugh.

    So my RO consult was good.  Don't know why I was so anxious.  He's a kind-faced, older Asian man and was very thorough.  He took his time with us, going over my recent health history (before BC) and then going through the timeline step by step from when I found the lump until now.  In a way I felt like I was reliving it, which is something I don't really want to do!  LOL   But I guess he wants to get the whole picture, which is good.  He examined me and said as long as my MO and PS were ok with delaying rads (so I have time to fill the expanders) he was ok with it, but he never really did give us his opinion on it.  I'm thinking he might have leaned the other way & would want me to start sooner.  I know cancer takes precedence over reconstruction, but I'm not really sure how much a few weeks either way matters at this point, since I've already had the surgery and chemo.  Something to ask my PS next time I guess.

    Anyway, I'm temporarily scheduled for my "simulation and mapping" on March 20th, and I'll start rads the next week.  So that gives me 8 weeks to get some energy up and heal completely from my surgery, as well as give my PS time to fill my expanders.  One part of me is just READY to get on with it, but I can't make my body heal faster than it does, and I would like to end up with nice looking breasts when all is said and done.  

  • KBeee
    KBeee Member Posts: 5,109
    edited January 2014

    Art, So sorry for all Nat is going through.  Enough is enough; she deserves a break!  I hope she heals soon.

    Mama, Hooray on the guy front!  Sorry the bruising is so bad; that sounds awful.  I had much more bruising with biopsy than with BMX.  I had even less with the exchange, though more and more bruising seems to show up each day.  My PS does not have the best bedside manner either, but he is very agressive and particular about infection control (which I heard from various nurses) and does good work.  he is who all of the nurses on the cancer floor use for family members going through it...and nurses know best!  My tumor was close to the nipple, so nipple soaring was not an option.  I will just let them rebuild or tattoo it.  Seems there are always more steps, aren't there?

    LHL, I hope the rads consult goes well...one step closer to the finish line.

    Cougar, Praying for favorable results from your MRI.  How's that baby doing???

    Chickchick, Hope the appointment goes well.

    Audra, i also did surgery first then chemo.  It is a toss up as far as far as advantages and disadvantages; my tumor was on the small side though...1.9 cm.

    Knightzoo, Cool picture!!!!

    Betterday,  Sorry to hear about the results.  We are in your pockets during every battle of this war.

    Warrior70, Yahooooooooooooooop for last chemo!!!!  i hope the side effects are few and do not stick around.  let the healing begin!

    KJ, how are you feeling?  Hooray on getting rid of a few drains.  they are sooooooo annoying.  Sounds like you had good news on your pathology report.

    Simplelife, Hope you got your dance class in.  Sounds like fun.

    I am feeling really good after the surgery.  I have not taken anything other than plain tylenol since getting home, and have not taken Tylenol in 2 days.  I am having a little pain, but if I took tylenol and killed all of the pain, I would do more than I should, which would be bad...trying to be a good girl.  The most annoying is having to wear this surgical bra 24-7...especially after not wearing a bra at all for the past few months with the TEs.  thr strap is right on the incision which is especially annoying.  Looking forward to my appointment on Friday to see when i can ditch the surgical bra.  Of course, I will have no bras that fit, so I will need to find somewhere to actually get a fitting since I do not know the first thing about how a bra should really fit...especially over foobs.  I know I am not supposed to need one eventually, but I probably should have a couple on hand.  hope everyone has a good day.  gor me, today is "piles" day...tackeling the "piles" of papers that seem to accumulate.  Fun.

  • audra67
    audra67 Member Posts: 521
    edited January 2014

    Kbee-

    MY PS told me no need for bra either but mine are large and they feel heavy...I think I would like to wear a bra...and they sortof show through tops - like obviously not wearing a bra....Next week I will go out and get sized and all and see what size I am now and get a bra...I know mine also said NO underwires....not sure why...so that could be challenging too.

    Feeling sad today as my husband has been home with me pretty much through all of this- he has a sales job and can work from home and does very well so when he can he doesn't work....anyhow he has meetings the next few days here in town and I am feeling like a baby...I have become dependent on him and now feel downright pouty about him going somewhere!  I know it is wrong, but it scares me to be 'done with chemo' and now 'alone' ...it is all so new and weird and adjustment I guess...


  • josgirl
    josgirl Member Posts: 231
    edited January 2014

    Mama - I met my (now) fiancee only two months before diagnosis and going thru all this crap has put a strain on our relationship big time.  I mean he barely got to know me before I became engulfed in cancer land!  But I think at the end of the day I know if we got thru this and he stayed we can get through other tough times.  And this caused some things to progress fast in our relationship but others to progress very slowly.  And I am the person to jump in real quick so forcing myself to progress slowly has been really for the best.  I am wishing you the very best - if nothing else having this sense of possibility and mutual attraction is life affirming and wonderful.  It seems to us that we are lacking what we had just 6 months ago but I think we misjudge the strength and perspective that we have now.  I know that I am a different person and a lot of crap that I was worried about and would stress me out just doesn't anymore (or as much....lets be honest).  And I think that is attractive.  Also boobless and hairless.....if they know you that way from the beginning there is only up to go :)  But you have been through a lot single parenting through BC so I think that strength shows through even though you don't see it yet.  Just take it slow and don't jump to all the expectations we planning ladies like to :) 

    Audra - also estrogen in fat cells - just another reason to exercise and maintain healthy weight!

    KJ - great idea about the fanny pack!  I put my drain around my necklace in the shower and it was out of the way and not where I would accidentally pull on it while showering.

    LHL - I think your MO is the person to judge how fast YOUR cancer is going to move in regards to when to do rads or not.  I loved my rad onc but I think their knowledge is very specialized and your personal timeline better judged by your MO who has seen all your scans and the reduction of the tumor thru chemo.  And I understand about the shock the MO apt in regards to more chemo.  I guess it is the benefit/disadvantage of not having a single team.  I take it as a benefit although it can be upsetting and maddeningly frustrating too.  I saw so many docs at the beginning and still now I have an MO, a naturopath onc, and a naturopath who all tell me slightly different things...not to mention my acupuncturist who is also a nutritionist and specializes in cancer treatment.  There are so many opinions out there but I feel just knowing and being mentally aware of the other opinions is so helpful.  Food for thought I guess and then you have to make your decision.   Seems like they never end....

    About the Port removal - I kinda felt like I was tempting fate having it removed so quickly after chemo was complete but the alternative was going back and getting it flushed every 4-6 weeks or so.  If there had been no follow up apts needed maybe I would have kept it in (finally stopped hurting and being annoying).  But strangely enough for that surgery they got the IV started on the first try.....go figure!

    Art - I know it is crazy when 'normal' things happen.  It's like "REALLY".  My daughter scratched my cornea halfway thru chemo - thought I should be immune to everything non-cancer but it is the opposite.  And no days off during chemo - wow I am impressed with that.  This is her body saying slow down for a second! Our body does take awhile to recover fully - my white blood cell count is still very low - normal to expect after chemo but have to be very careful not to get exposed to germs....at least I say that....whether I follow my own advice....Here's to a quick recovery and feeling better.

    KBEE - yes on feeling great after surgery! 

    Better Day - Research is a good way to cope as well as to be proactive in your care.  Hugs from me.....

  • audra67
    audra67 Member Posts: 521
    edited January 2014

    All-

    I just got scheduled for port removal Monday!  That will be 18 days post last chemo!  When was yours removed JOS????

    I will be THRILLED!!!  I guess they have to check blood first but I am having it removed at hospital where they put it in by interventional radiologist... MY port still bothers me...I tend to hunch that shoulder even and tighten that muscle...and I think it's on a nerve so I get zings down my arm and to my neck...from the very day they put it in....HATEIT!!!  SOOO EXCITED!

    You are all so good to mention everyone in posts...I am too tired...

    I just had a salad with tuna for lunch and then wanted a pudding...took me like 3 minutes and severe agony to each thumb to finally get the little pull tab pulled!!! OMG!!! Those are my scary nails too that have pulled off on one side...thought I might lose one but I NEEDED that pudding!!! :)

    I know fat and the brain adds more estrogen but I think main supply is ovaries...I am seeing a gyn/mo end of month and we will see if her feelings match the MO and the other gyn I just saw...who said no removal necessary.

    I am questioning my MO in regards to wine...he said on Tamoxifen I could drink wine and the estrogen it produces would be blocked??? Does that sound right??

    Cause I thought Tamoxifen was selective and didn't block the uterus even??

  • josgirl
    josgirl Member Posts: 231
    edited January 2014

    Audra - Mine was removed just over a week past my last chemo.  It was fast but I wanted it out in time to heal before starting rads - which I also did quicker than normal..only two and a half weeks pfc.And lol about the pudding...sometimes we don't care what gets in our way....glad the nails held up!

  • BabyRuth
    BabyRuth Member Posts: 264
    edited January 2014

    Wow!  it is hard to keep up with everyone and what is going on with them.  Just know that I am always thinking of you all.

    Betterday-so sorry you did not get the results you were hoping for. Sending good thoughts your way!

    Art-hope Nat is feeling better!

    I got stuck in the snow storm(only 2 to 3 inches) that took over Atlanta yesterday.  I left my work for my usual 20 minute drive home and did not get there until 7 hours later.  I finally ditched my car about 3 miles from home and started walking because the roads were backed up with people stuck in their cars.  My goal was to get to Waffle house and eat and then come up with a game plan.  I only walked for about 10 minutes when a man offered me a ride.  I just jumped in  the car with a perfect stranger, I was so grateful.  He took me about halfway home and then I got out because he  needed to try to go back and  help his wife and kids who were stuck at school.  I then walked for about 5 minutes and someone else came by and offered me a ride.  Yet again another stranger willing to help out.  Mind you there were tons, and I mean tons, of people stuck everywhere.  All sorts of people and families were walking home. This gentleman got me all the way to within a block of my home.   I am so grateful for the kindness of complete strangers.  The whole time I was stuck in the traffic nightmare I keep thinking " if I can beat cancer now for the fourth time, this little bit of snow will not stop me."    

  • josgirl
    josgirl Member Posts: 231
    edited January 2014

    BabyRuth, Heard about Atlanta all day - wow what a rough evening for everyone impacted.  Glad the kindness of strangers is what stood out in your mind.  We humans certainly have the capacity to rise to the occasion and be heroes! 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2014

    Thanks, KBee. The SO appt. did go well (thanks to Xanax) and as I figured, mastectomy was the best option for me, since the tumor is still at 4.5cm. Right now I want as few surgeries as possible, but it's nice to know recon can be done in the future, if I change my mind. I'm glad your recovery is going well and it looks like I'll soon know the thrill of the post-surgical bra, too ;) The fun never ends in this cancerland.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2014

    BabyRuth - 7 hours to get home, YIKES! What a blessing to have so many people offer to help you out. I was at a tile convention in Atlanta in 2013 and found that the people there were so nice. If you just asked someone for directions, they insisted on walking you there. Very sweet.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2014

    Audra and others, My nails were coming apart and peeling and getting caught on things - - two months after chemo ended ! I couldn 't take it anymore so I got my FIRST manicure + fake nails on Saturday !  Fake hair , fake boob, fake nails..I'm on a roll!!!!!

    image

  • VintageGal1111
    VintageGal1111 Member Posts: 705
    edited January 2014

    Oh My Goodness, you gals have been chatty! I love reading all your posts. But I can't go back right now & reply to each. Though wish I had the time.

    I feel bad when I read of some of you getting not so good news, & I am glad when I read of one of your milestones like finishing chemo or finally getting surgery. 

    All your posts are so helpful, this is where I have learned & acquired most of my info on this journey.

    Thanks

    VintageGal

  • KBeee
    KBeee Member Posts: 5,109
    edited January 2014

    BabyRuth, Glad you got home safely!

    Audra, Yahoo for port removal!

    Running, Love the nails!

  • kjsimpson
    kjsimpson Member Posts: 445
    edited January 2014

    Everyone sure has been busy this week!  Myself included.  This was supposed to be a week of rest. HA!

    Met with the Radiation Oncologist this afternoon for the consult.  She is saying 6 weeks, not 7 weeks of rads.  Not sure why.  Might have something to do with their newer technology. She said the sunburn is going to get very intense, especially towards the last two weeks.    She was very patient, then suggested that we could get started on February 10th and be done by my vacation the last week of March, if we could get the markings and simulation appointments done this week and next.

    So, she had them do the markings today.  It involved a mark-up of my chest, a CT, and placing the tattoos.  My body is tired, even though all I did was lay on a table for most of the time.  On February 6th, they will do the simulation.  Then, if all goes well, get started on February 10th.

    I haven't been taking Percocet except sometimes at night for most of the week.  Just got home, took one and some additional Tylenol and am exhausted.  Something tells me I might have a mental meltdown day tomorrow... that was stressful.

  • lighthouselady
    lighthouselady Member Posts: 752
    edited January 2014

    Pretty nails!!!  Mine survived chemo, but they just can't seem to stay looking nice.  I'm taking biotin for hair & nails, and they seem strong, but then all of the sudden they start chipping and I have to file them way down.  Ugh.

    Who has last chemo tomorrow?  Someone, but I can't remember who!

    Babyruth - thank GOD for the kindness of strangers!  I'm so glad you were able to make it home.  What an ordeal for everyone in the southeast.  I saw on the news the kids sleeping in their schools two nights in a row... I would be frantic if I was a parent!  

  • hockeymommy
    hockeymommy Member Posts: 77
    edited January 2014

    holy smokes I think I am caught up on all that's going on!! I have been so busy this last week with kids hockey games,  wrestling tournaments, life guarding practice,  dr appointments, the twins writing their first set of exams. ..I am exhausted.  but I have to say I feel so much better with these drains out! I get these zingers every once in a while and man do they hurt. The incision is healing up nicely and I am proud to say I love being flat!  lol. I hope everyone is doing well and taking it easy!  I may not post a lot, but I think about all of you daily!!

  • kjsimpson
    kjsimpson Member Posts: 445
    edited January 2014

    TANTRUM TANTRUM::  I want my Drains out!!  I want my Drains out!!  ::TANTRUM TANTRUM

    (carry on)

  • SpecialK
    SpecialK Member Posts: 16,486
    edited January 2014

    audra - Tamoxifen does not suppress estrogen, or its production, it blocks the receptors on the cells.  The aromatase inhibitors suppress estrogen by interfering with the enzyme aromatase that converts androgens into estrogen.

  • simplelife4real
    simplelife4real Member Posts: 563
    edited January 2014

    ClickChick, are you going to have more chemo after surgery?  My MO and I had talked about doing that when my TNBC tumor wasn't shrinking. Since I thought I was going to be where you are, I had given a lot of thought to what I would do.  I would be making the exact same choices you are in terms of surgery.  I would want to be not dealing with reconstruction either.  You can do that down the road, but right now it's about focusing getting rid of cancer.  I'm in your pocket every step of the way.

    Mama, I'm glad your nipple discharge turned out to be okay.  I'm thrilled you like your new PS.  I wish my PS was a woman.  All my other doctors are and I feel like they all "get" what it's like to go through this.  With my PS, I feel like it's just a job...and why would a 61 year old woman (me) care about how she looks or if her sex life is good?  I just don't care for him much, but I feel too tired to look for someone else and I don't want to delay my LX and ALND.

    Lighthouse, my biopsy left a horrible bruise and swellling too.  It took weeks for all that to go down.  Getting the port in was a piece of cake compared to that.  It's amazing your biopsy bruised worse than your BMX.  Getting rads kind of freaks me out too.  I think it's because I'll be getting so much radiation every day for weeks....all our lives, we are told to try to avoid radiation, and now we are being told to get lots of it.  I just have trouble wrapping my head around that part of treatment.  So many people freak out about chemo, but I felt like chemo was the thing that's going to save my life.  I didn't like chemo, but I'll gladly take more of it if it kills my cancer.  The thing that helps me with rads is looking at the differences in recurrence rates with and without them.  That makes me pick rads every time.  I'm glad you ended up liking your RO.  He seems like a nice guy.

    Kbee, that's great that your pain levels are so low!   Hope you get to ditch that surgical bra soon...that's what sounds like the real pain.Happy

    Audra, my husband has been my rock and constant companion too throughout this ordeal.  He had just retired a month before I got diagnosed.   I miss him when when he's gone for more that a few hours.

    Jos, hooray for your new  guy hanging in there and your engagement!  I'm really impressed with any guy that does that.  He didn't have any idea what he was in for when you first started dating.  BC puts a stress on any relationship.  It's a stressful thing for everyone concerned.

    Audra, it is amazing how fast they take out ports.  I'm getting mine out with my surgery.  I really didn't expect that, but it will be nice to have it out.   Mine bothered me a lot too.

    BabyRuth, I'm sorry you had such a hard time getting home, but I love your story of all the help you got from strangers.  It reminds me of NYC on  9/11.  I really like how you kept thinking that if you could get through so many bouts of cancer, you KNEW you could get yourself home.

    Running, great nails!

    KJ, does it hurt when they do the tattoos?  You had a long day yesterday, but they got a lot accomplished.  Rest easy today!  Tantrum acknowledged!

    I had a good day yesterday.  My energy levels are really starting to come up after finishing with  AC 15 days ago.  I think my red blood cell count was low and it's really starting to rebound.  I've been drinking lots of fresh veggie juices and making sure I have adequate protein.  My heart rate was skyrocketing when I would try to do anything, but yesterday it stopped doing that.  I was able to work out on the elliptical without it going bonkers.  Big difference.  My surgery is in exactly two weeks.  I feel a lot more confident that I'm going to be physically ready for it now.  Mentally...it's a different matter.  Still working on that.  It will be okay, I know.  It just takes me some time to adjust to each change that comes with dealing with cancer.

  • lighthouselady
    lighthouselady Member Posts: 752
    edited January 2014

    Can I just say that I'm jealous of all of you getting your ports out???  I hate mine, and MO wants me to keep it in until I'm done with EVERYTHING this year.  <sigh>  That makes me want to throw a tantrum with KJ.

    I was surprised at my MO appointment the other day that my blood levels are still low.  My WBC were still hanging around 4000 and I'm still slightly anemic.  I know it can take a long time to get back to normal, but I feel really good most days.  I guess I still need to be careful about watching how much I do and how many people I'm exposed to.

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