Chemo May 2013

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  • elkatho
    elkatho Member Posts: 159
    edited July 2013

    Talked to MO yesterday about red itchy blotches and heavy breathing. He said hives? I said honestly I do not know, I thought hives have bumps mine are flat. He says let's get you to a dermatologist to find out wants going on. That was at 1030, nurse called at 1230 to make sure he called. She said the secretaries are working on referral. I called st 3....no they have not started the referral but took my number and would work on it and call me right back. Still nothing. I bet I can tell you what's going on.....the chemo is causing havoc on my body!!

  • Gully
    Gully Member Posts: 268
    edited July 2013

    Itiswhatitis: My appointment for round 4 is today. I am also going to ask about the 4 treatments I get and the 6 others get and the justificaiton. (reasons I have gleaned have been micrmets in lymph node of TNBC or even just ER neg or PR neg. I have LVI (not extensive) so I am a bit nervous about stopping at 4 if 6 would be better. Some papers I read said LVI can be considered a pos node? This deserves aggressive teatment and would in my mind would warrent 6 but.....  Is 4 rounds aggressive treatment in my case with no rads?

    I Was given the option to opt out of chemo completely due to 19 oncotype.... I would really rather not do six, but I will if they think its needed..I am taking in the literature I found dated 2012-2013..on the subject to see what they say. I am not sure they have seen the papers, there is so much info out there and my MO takes care of all kinds of cancer patients....He does though have a NP that is a bc specialist. So I am going to bug her about it.  Yikes..........I sure hope they can justify the 4 so I can put my mind at ease and be done!!!!!

    Good luck with everything todays ladies! I am focusing on not running out of the treatment area today,, veins are getting to be a problem!

    I wish I could take my sheperd into the treatment room with me so calms me. Guess I will have to settle for my DH,,LOL

  • Ukkate
    Ukkate Member Posts: 292
    edited July 2013

    Back at the chemo lounge. Couldn't sleep last night so I ended up taking 2 Ativan and then I was super drowsy this morning :(. I'm getting processed quick today! Already getting my pre meds

    Pat - congrats on being done with chemo. I had a single

    Mx but I would have 10 mx rather than more sessions of TCH!!!

  • AryaS
    AryaS Member Posts: 131
    edited July 2013

    Wow. You are there? I am sitting on my tush at home thinking "I don't want to go!" like a three year old.

    But I will go anyway today.

    Good luck today.

  • Ukkate
    Ukkate Member Posts: 292
    edited July 2013

    Good luck to you Ayra.  It was "speed chemo" for me today.  I got there at 8:15 and was walking out at 11:20 - it's never gone that quickly for me.  I even missed lunch!!  I pretty much slept the whole time - still feeling the effects of the double dose of Ativan and then the lovely bennydril they gave me...

  • Teresa_G
    Teresa_G Member Posts: 259
    edited July 2013

    I did take some anti nauseous meds over the weekend, eventually they helped. I think some of my problems came from the heat. I was outside for several hours both days. I was able to stay in the shade but it was still really hot. I only played one game Saturday night and went to bed. I've been camped out at my parents since because I have been so weak and exhausted. My dog (beagle mix) was even allowed to come with. My Mom really doesn't like dogs because of their germs but let me tell you this dog is getting spoiled here. I don't know what I would do without a dog, definitely worth having one. She keeps an eye on me all the time and is just there for me.



    I enjoy having my four hours at chemo with my daughter, I know I could go alone but we both like our time there together.



    Now that chemo is closer to the end for me and even though I will most likely have rads too I have been thinking about my surgery and what to do. I started with one lump in my right breast, they did a digital mammogram and an ultrasound biopsy. After they knew it was cancer I was sent for an MRI. They found another lump and did another biopsy. Of course it was cancerous as well. When we did the mastectomy an they went through all of my breast tissue there was a third lump that was cancerous as well. I am rather paranoid now that my other breast may have the same issues. I had the BRCA test done and results should be back any day. Do I have the other breast removed so I don't stress on it? I just don't know. I thought about the DIEP but I just don't think I can handle that major of a surgery so am just thinking an implant and then of course having them make my other breast look the same, it is really saggy. I'm a 42D right now. Any thoughts on removing the other breast?



    Here is to a good day for us all!

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited July 2013

    Teresa,

    I am going to get both removed and do the DIEP.

    I ruled out implants for me, sounds like discomfort and maintanence..but I could be reading not it? I will not do the Tram flap, where they use core muscle becuase I hvpave a bad back and for years have been told to strengthen my core.



    I was not happy they found surprises in the one breast after my first surgery pathology was done....I don't want to think about it.

    Because of the location of my cancer and my telling them i will be doing the masectomy I do not need to do rads. This is great for me as it cuts of 6weeks of treatment! Although my recovery from DIEP will be as long! But In The end I think my results will be better, with hopefully a lot less worry.



    Pat

  • Gully
    Gully Member Posts: 268
    edited July 2013

    WoooooooHooooo ladies talked to Mo about 4 vs 6 TC and he said no to six, no added benefit for me, so  I AM SO DONE WITH CHEMO LANDCool Get to skip the rads due to BMX, so for me its on to the TE exchange. More appointments and another surgerly etc, but glad to be switching gears so to speak. And then the Tamoxifien........Just need to get through the next few weeks of SE from round 4 to start the next leg of fun and games. 

    Could not have gotten this far without you ladies! Wishing everyone the best where ever you are in your treatments!

    Time for my gallons of water and a nap I think,,,,Hugs

  • GoWithTheFlow
    GoWithTheFlow Member Posts: 727
    edited July 2013

    Wooohoooo gully!!! So happy for you!

  • elkatho
    elkatho Member Posts: 159
    edited July 2013

    Gully.....yea to finishing chemo. Hoping for minimal SE for you!!!!



    I am seriously going to suggest only four treatments for me. That is if they can even get me in for the forth. I am less itchy than before but every now and then still have a little heavy breathing. It passes in about 10 minutes.I ended up making my own appt with dermatologists as my MO' s office took forever to call me back. We will see what she says tomorrow am. It will be nice to get another doc's opinion.

  • Ukkate
    Ukkate Member Posts: 292
    edited July 2013

    Yay gully!!!! Awesome news.

    I have my appointment with the plastic surgeon at the end of August to book the exchange surgery. And that's like the last step ( except for the next year of 3 weekly hercepten infusions!!!). I guess getting the port out is the final step. Wow - we almost made it thru chemo!!! Just 3 more weeks of taxol for me!!!

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited July 2013

    I think the one thing I won't miss about chemo is the chemo nose.

    My daughter was eating pizza from Target and I swear the cheese was rotten! Was all I could do to hold it in.

    Then came home and hubby goes to eat some leftover shrimp from the weekend. He asks "why are you saving the tails in a plastic bag, are you going to make soup?" (Do people make soup with shrimp tails!). No, I don't want to smell them in the garbage (I ate mine the day before chemo) and you can use it for your shrimp tails too.

    So I come In the house and he threw his tails in the garbage, with my shrimp Baggie of tails next to them! Eeeeew! The smell!



    Gully, congrats on being done. I still don't feel done, but guess in another week or so it will hit me I'm not going back!



    Elkatho, tell your doctor about the breathing problem.



    Ukkate, you are almost there! Yeah!



    Pat

  • Miasara
    Miasara Member Posts: 17
    edited July 2013

    Pat and Gully Yay! Happy for both of you :)

  • Teresa_G
    Teresa_G Member Posts: 259
    edited July 2013

    Congrats Patty and Gully!

  • Debwarrior
    Debwarrior Member Posts: 72
    edited July 2013

    Hi everyone,

    I've been absent for a while but following everyone's story.  Pat and Gully, big congrats on being finished with chemo.  I'm really looking forward to that day.  Four more taxols and one more carbo for me.  Carla, I'm sorry  your chemo got postponed but it sounds like a good idea to let your hand heal some more before getting knocked down again by chemo.  Angie, I feel that muscle wasting thing too.  I feel like I'm walking through mud and it even fatigues me to lift my arms up to drive, but I do anyway and I try to go for walks, but I'm slower than I used to be.  I'm anemic and neutropenic, oh boy. 
    Been eating a little more red meat and protein and that seems to help a little. This last round of carbo really knocked me on my feet and I had the worst and longest lasting nausea of the whole time.  Been taking zofran which knocks it down, but hasn't eliminated it.  My GI system also seems very messed up by all of this.  I'm tired of feeling crappy and am almost thinking about asking for a one week break from the chemo. I don't really want to extend it, but I feel like my body is suffering and may need to bounce back a little.  We'll see what my bloodwork shows.  MCGIS, I also have low hemoglobin but a little higher at 9. I bet it's lower this Thursday.  Lorrie, your comment that you will go in Thursday for them to try and kill you cracked me up and that's how I feel these days too.   I wish everyone well with this week's treatment if you have one, or with recovering from treatment.  Pat, after chemo, I'm  having bilateral DIEP also.  Anyone know anyone who has had it done at UCSF? I'm trying to decide between UCSF and Stanford.  It's all pretty daunting.  One step at a time though.

  • carla53
    carla53 Member Posts: 264
    edited July 2013

    Congratulations Gully and Patty. No more chemo for you. Now to get it out of your system.



    Minimal s.e.'s to all that have had a treatment recently. And to those who are to have treatment soon, low to no anxietys.



    Carla

  • ItIsWhatItIs2013
    ItIsWhatItIs2013 Member Posts: 541
    edited July 2013

    Got scolded today by my picc line nurse.... It's really hard not to do normal things! I'm over using my muscle causing inflammation.... Never been accused of over using my muscle before! LOL and they changed the type of dressing due to some irritation... Dang! It's only been 3 weeks.... I have 7 weeks to go! :(



    When I asked my Onc about 4 vs. 6.... He said..."that's what we do now" ??? Jeesh! He went into this long explanation of the history of chemo and it wasn't until I was walking to my car that I was like.... HE DIDN'T ANSWER MY QUESTION... And when I told him about how last treatment went, he just said " what you need is to just be done with this... You only have a few more to go"



    I go Thurs for #4 and don't want to! I was in tears when my hubby came home tonight and he says.. "well, you're the one who chose treatment."

    What does that mean??? I'm so frustrated right now. I don't even have a response for my hubby! What choices do I have? UGH!



    & my MIL is having surgery tomorrow eve... Wow! It's my GOOD few days and I'm miserable emotionally!



    Wah, wah, wah..... Thanks for letting me vent......



    Pat & Gully.... I'd say you suck for being done with chemo cuz I'm jealous, but I'm so happy that this part is over for you!!!! Congrats for doin it!



    Happy thoughts to all.....

    Lorrie

  • Gully
    Gully Member Posts: 268
    edited July 2013

    Hello Everyone,

    Thanks for all the well wishes from everyone, your right Pat it still does not seem real, go back for the Neulasta shot today.

    Itiswhatitis: I had a talk yesterday with my nurse practioner, and she gave me more info

    about 4 vs 6 TC after the history lesson as well of course. She made me feel alot better about all the choices I have made by the gut so far. She did admit one thing to me yesterday though that I have not heard from my MO the whole time. MY oncotpye was 19,  my MO gave me the option of opting out. He said he would support either way. She confessed that when she saw my stats with bilateral bc and focal LVI combined with my age 45 even with neg nodes she was really glad that I opted for the chemo! Back to 4 vs 6 TC she said there are not studies that 6 is better than 4 and that if I had need a more aggressive chemo in my case they would have went for the ACT. She said Four rounds and BMX should have taken care of the focal LVI and hopefully some of the stray cells that may be floating out there.

    Its easy to forget, but she also remined me that the hormone therpy is just as important or more important for strongly ER/Pr+ cancers as the chemo. Trying not to dwell on this yet, because it a whole new can of worms to deal with.

    My goal now is to get through Round 4 SE and on Tuesday visit with my PS to schedule my TE Exchange in Aug hopefully before school starts. Then back to the MO for the hour long introduction to hormone therapy options! Guess we still have many visits to the doc even after chemo. But at least I dont see him for a whole month! Unless I get sick in between of courseFoot in Mouth

    Good luck to everyone here with all the treatments this week. We are getting there one day at a time! I think we are all tough cookies! Something funny I noticed yesterday, I am very scared of elelvators and will walk up 20 floors to avoid them. Yesterday I said WTF and went right in one...did not die......must be the cancer courageCool

    Have  a great day ladies, have to take my roids, claritian, and zantac for the day and head for the cancer center for the neulasta! Hope your days go well!

  • Gully
    Gully Member Posts: 268
    edited July 2013

    Tereasa, 

    You of course need to make your own decision about the other breast, but it seems there have been many people with "surprises" after surgery.

    I opted for BMX firstly because if somone ever comes near me with a mammogram machine again , I will seriouly punch them. They were so painful for me. I had dense fibrocytic breast tissue and only 34 B so my sternum and ribs would be bruised after a mammo. 

    Ayway started out with a "gray" area on my left side (this way my good breast by the way) that need US and then biopsy---we all know that turned out IDC. The right side came back (on watch) as it has been for the last three years.   So went to the BS and I ask for the BMX, She asked why and I said I just did not want to deal with all the mammos anymore and deal with the (on watch breast anymore) I said if we are going to do it, take them both and I wont have to worry about it anymore! She agreed but wanted a MRI on my (watch breast) so their were no surprises.

    Went for the MRI and it picked up 3 spots in my right breast. On to US again and more biopsy...all neg on the right..thak goodness right.

    On to BMX surgery SNB on left to be done but not on right because it was deemed prophrolactic. No SNB....After surgical pathology came back ....surprise! We did find a 7 mm IDC with lobular features in the right! Bonus Bilateral BC!!! My gut turned out to be correct on this one and I am glad I am not starting over again 6 months down the road with this jouney after that (6 month watch mammo)

    Another part of my decision though was cosmetic....I thought, take these cancer bags away and give me back an upgraded symmetrical pair that I dont have to worry about as much.....also DH deserves a toy to play with after all this is over right!Surprised

    Good luck with your decision, its a hard one!

  • Ukkate
    Ukkate Member Posts: 292
    edited July 2013

    Theresa , my MRI showed absolutely no sign of cancer in my right breast but did find a 2nd tumor in my left as well as DCIS there too. So I chose a single mx. If the MRI found so much undetected stuff in the left and nothing at all in the right, then I had to trust it was thorough...

    Having said that, since going thru chemo I have been wondering if I shouldn't have opted for a double because I can't imagine doing this again!!! But my doc assured me there was no added risk by leaving this breast. It is a tough decision

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited July 2013

    Lorrie,

    I am sorry you are going through a rough emotional patch while you are on your good week.



    Husbands, can't kill them, would just lead to a jail cell! :)



    I think one of the reasons I am not "happy"...trust me, I'm not celebrating.... being done with chemo is that others are doing 6 rounds of TC...what if 4 isn't enough? There are so many doubts that come with this treatment as we all have different protocols. I know it must suck to see others getting by with less, but in the end it might be you that benefits from having more. Hope I haven't given doubt to those doing 4 treatments!



    Pat

  • lpc
    lpc Member Posts: 303
    edited July 2013

    Hi all



    Have been quite busy enjoying my son! He is currently getting a tatoos so I have some time. Have never liked tatoos and now we joke about getting my nipple tatooed. Husband says he is not sure how he feels about someone holding my breast! I said wtf do you think has beeni happening when I go to the doctors!



    Patty and Gully so happy you have finished chemo!



    Theresa mri and pet scan both showed nothing of concern in my right breast so I opted for left side only. If I had ilc probably would have done bmx as I hear that it tends to spread bilaterally. I admit in mydarker moments I worry about right side but mo continues to tell me not to worry. I actually have not quite decided to ask for the right side to be done.



    Gully did I read you went to see your daughter graduate bootcamp? How awesome and what a proud moment that must have been! What will she be doing now?



    Tomorrow I will have my 2nd of 4 taxols. So far no neurapathy but nail beds are very sore. Makes buttoning zippering or opening packages very hard. Actually any fine motor skills are difficult.



    Funny story-i threw my wig in backseat and forgot it there. I never wear it anymore even at work. I got in car the other day turned around to back up ans screamed cuz I thought an animal was in my car'



    Hope all have a good night



    Lisa

  • Gully
    Gully Member Posts: 268
    edited July 2013

    IPC: Yes my daughter graduated from bootcamp on July 3rd, she is now at AIT Heavy Transportation she is learning to drive truck anywhere from 5 to 35 tons! LOL..... She is 5 1 and 120 pounds! Anyway she chose it because it was short school in duration as she has to be back in college in the fall. It was part of her ROTC agreement with the Army (Had to complete BC and AIT in summer between Freshman and Soph years). She will start Nursing School at college in the Fall with a full tuition ride and then graduate as a 2nd leutenant as part of the Army Nursing Corp. It was a good deal for her, saves around 100,000 over four years in tuition and will get paid a smalll amount while in school. No debt upon graduation! Laughing She is a really hard worker! So proud of her.

    She wrote her freshman research paper on Breast Cancer..... so sweet, I feel really badly that she will have to start getting screened for bc in her 30's. We have no genetic family implication. I am the first lucky one, but you never know. I pray she never has to take the jouney we are on!!!

  • lpc
    lpc Member Posts: 303
    edited July 2013

    Gully one of my daughters just finished her 3rd year of nursing school. I suggested ROTC to her but she declined. Not sure i could see her in bootcamp though. I too am the first one with cancer. Did have became testing negative for both but my girls will start screening early. There is ashkenazic blood from hubby's side which puts them at greater risk.



    My Navy boy had no interest in college. Turns out he has studied harder than ever before! He reasons at least he gets paid to study. Nuke program very hard. He will be off to prototype school for 6 months and then ship out on a nuclear sub. That will be hard day for this mama!

  • Gully
    Gully Member Posts: 268
    edited July 2013

    IPC: Yes , It will be a hard day for mamma! My husband did 6 years as a Navy seal! Soooooo hard when they deploy! It is impossible to keep them home when they are driven to make it their way. It sounds like your son is doing well as well. My boys (twins) start HS this year. I dearly miss my girl though, we did everything together and she was a very amiable teen. I hated to see her go away from home for school. I could not see her in BC either..LOL now we tease her and call her cammando barbieCool

  • GoWithTheFlow
    GoWithTheFlow Member Posts: 727
    edited July 2013

    Commano Barbie - he he he.  Just so darn cute!

  • Annie54
    Annie54 Member Posts: 247
    edited July 2013

    Lorrie,

    Good luck with treatment tomorrow! I'm right there with you going in for #4 - we're on the downside now getting closer to that Aug 22 finish line. I find that the SE's are a little different everytime and hit on different days of each cycle. So I've learned to just take a lot of meds daily to try and stay in front of them. No nausea but GI problems have been the worst....stomach cramping and diarrhea after I eat. Best if I eat bland food and small portions. Found watermelon really tears my stomach up. Who would have thought! Last time I got some muscle aches...almost like having the flu, but only lasted for a couple of days.

    Instead of dreading the treatment I try to welcome it as my magic elixir that is going to keep me alive for many years to come. Hard to do but has helped me not be so anxious and roll with it.

    Another thing that has helped is watching all 3 seasons of Downton Abbey which I had not seen before. LOVE IT! Great distraction....but now I've seen all the old ones and have to wait until January for the new season :(

    Hugs to all - hope you sleep well tonight!

    Annie

  • carla53
    carla53 Member Posts: 264
    edited July 2013

    Lisa-That is funny about the wig. Soo glad you are enjoying your son. Mothing better than that.

    Lorrie-I think sometimes men are from different planets. Oh yeah...women are from venus men are from mars. They want to fix and have answers and sometimes all we want is to be listened to and nurtured. And it does get fustrating. Wishing your MIL a successful surgery. Doesn't look like you have had any me time during your feel good days. Any chance of at least a few hours for you?

    Annie-You have a great attitude.



    Carla





  • Ukkate
    Ukkate Member Posts: 292
    edited July 2013

    Annie, I watched seasons 1 and 2 of downton abbey when I was recovering from my mx. I haven't seem 3 yet.

    There are so many military mommas here!!! I agree that it's a great way to go to college with minimal debt.

    I have changed my chemo times to 3:15 in the afternoon. This way I can work most of the day and then head out to chemo. Ill miss those free lunches tho!!!

  • LJaeger
    LJaeger Member Posts: 58
    edited July 2013

    Haven't posted in a while - nothing new to update, though I'm done with all my A/C cycles - yes! Congrats to all you ladies who have completed all your chemo! <Loud Cheers!!!>

    1st taxol was yeterday (3 left now). Went by without a hitch, thank goodness. I was nervous about having a reaction, but the only reaction I had was from all the benedryl - it was like I was drunk! The nurses and my husband were laughing with me over it, and we said why bother going to a bar when I can come here to get tipsy. Ha. (trust me, I look forward to having a real drink when this is all over. I've been abstaining altogether).

    To put in a reply to some recent posts: Ukkate and Lisa- I had the same scenario. "no sign of cancer in my right breast but did find a 2nd tumor in my left as well as DCIS there too" (stolen from UKKate post). They had seen the 1st tumor and the DCIS on my ultrasound and mammogram, but the 2nd tumor was a surprise, only found in the tissue post MX.  

    Now I'm just waiting on the results from the BRCA testing. I have serious doubts that will come back positive, but if it does, it will leave a lot to think about. And will also leave me slightly annoyed that they didn't do this test before my intial MX, so I wouldn't possibly have to go back to do this process all over again on the right side. Phew. Those are thoughts for another day, or hopefully for never.

    A few pages ago folks were disussing hormonal therapy. My MO briefly mentioned that studies show 10 years of tamoxifen is better than 5 - so she wants me on 10 years (I was extremell ER positive, around 95%). I told her that someone needs to come up with a tamoxifen that is also a birth control method. She said that she could actually give me a shot at the same time, so I was pretty happy about that. I guess more info to come on that post-implant surgery and rads.

    Wishing everyone a SE-free (or as close as we can come!) weekend.

    Laura

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