Is There A September 2011 Chemo Group?

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  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Hey Robo.  One of the drugs that the doctor gave me was a prescribed mouth rinse in case of sores and stuff.  And one of the nurses gave me a sample size mouthwash and toothpast of bio-tene.  I thought that was pretty cool.  Any way the mouthwash that was prescribed was for mouth sores and thrush.  I am to swish and swallow.  I don't recall if they told me to start doing it right away or if I needed to wait and see if I do develope sores.  Another question for the doc Tuesday.  I have found that I do need to carry chapstick.  My lips are dry but they starting getting dry before I began chemo but still, I am proactive and keep the chapstick on there pretty much.

    Hugs!

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Belleeast I am so sorry about that.  I am really glad my port took well.  One stick and they are able to get the blood they need and do all the treatments without me looking like a pin cushion.  I hope this works out for you.  The port is really the way to go if you can.  Wishing you well!

    Hugs!

  • cupcakies
    cupcakies Member Posts: 71
    edited September 2011

    hi rjbaby69 - the prescribed mouthwash is for thrush, which i developed both after my 2nd & 3rd AC treatments..

    take it as SOON as you start seeing any whiteness on your tongue. it'll make it go away.

    The first time, i didnt knwo what it was and didnt have the mouthwash, so it got BAD. my entire tongue and tonsils were white. it was gross.

    I would only swallow the mouthwash if you have white spots on the back of your throat (like on your tonsils), otherwise I just swish for a few minutes, then spit it out and it seems to work. Swallowing was gross, and the medicine made my stomach hurt. 

    Good luck! 

  • findingsolace
    findingsolace Member Posts: 17
    edited September 2011

    Belleeast- sorry to hear about your port. It will be better in the long run so maybe just keep the port problems in perspective. It will pass, even though it is a bother right now.  Kelliregi- I have been having trouble with insurance also. What a pain. I am getting some case number where I work with one person only. I don't know if you can request that. ribaby69- your situations sounds like something that would happen to me. I went in for a surgery last year (unrelated to BC) and was in the 1% that the surgery failed, of course! The prescription mouthwash sounds like a good idea. I have Bioteen but think I will ask my doc about that when I go in. Yes, ask your doc about the 4 vs 6 cycles. I did ask mine because the size of my tumor was .8mm and no lymph node involvement but he said given its Grade 3 with HER2 + there are no good trials with only 4 cycles treating this so I am getting 6. I know you have a different history though. 

    Rain cancelled all my kids soccer games and now they are rescheduled Sept 18, with my chemo starting on Sept 16th. We already have 3 games on Sept 17th. Guess I will be a die-hard soccer mom sitting at the fields recovering from chemo!

    Have a good weekend and keep perspective everyone- I keep thinking of 9/11 and the tough time people who have lost loved ones are going through right now. We are alive and here for our families and to me, that is what matters. 

  • Rockym
    Rockym Member Posts: 1,261
    edited September 2011

    rjbaby69, I'm no MO (although with all my research I feel like one sometimes :-)).  I believe the TCx4 treatment is what my 2nd opinion guy called "chemo light."  My first MO recommended TACx6.  The TAC, I believe is for bigger, badder stuff.  Maybe larger tumors, higher grades and more node involvement.  With the TC, they are taking out what some refer to as red devil, Adriamycin.

    As for the oncotype... lower numbers usually mean that the person with no nodes and ER+ will not always have chemo do anything.  I was a 22 and in my decision making, I figured I better be a 30+ to close the deal.  If I was lower then an 8, I may have skipped chemo, but that is just with my stats.  My 2nd opinion guy didn't like the oncotype test.  He felt they needed bigger samples, especially with any node positive ladies.  Of course for me, I was questioning my node positive status until my 2nd pathology report came around.  Basically that closed the deal for me :-(.

    MOs recommend chemo very often since it's the best defense against systemic recurrence... mets.  I felt it was important for me to understand what I was getting and why I was getting it.

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Cupcakies:  Thanks for the info.  I will be looking for anything suspious in my mouth.  So far so good.  Since  I just had my first treatment, the mouth sores may not rear their ugly head until my 2nd one.  But I will be on the look out! 

    Hugs!

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Finding solace:  Can't wait to see what the next treatment brings.  I was quite comical.  I was doing all kinds of egyptian dancing and flipping and flopping like a fish.  You just had to be there!  At least it wasn't boring!!  LOL!

    Hugs!

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Rockym:  I do definitely intend to ask him about that.  I did have node involvement and I want everything I am supposed to get.  But since my score was 14 he may have decided to cut back by two treatments.  I'll be sure and get the details Tuesday when I see him.  At least  both doctors are keeping a close eye on me and that makes me feel really secure in my treatment team.  That's important for me.

    Hugs!

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Hey ladies.  Just a little update on my first day since the neulasta shot.  Got up this morning and drank coffee and read my paper.  I had a burst of energy and got busy cleaning the house.  Don't know where that came from unless it was the steriods in the treatment.  So far no bone pain but took meds according to instructions.  Still feeling a bit jittery.  Is this normal?  I have lots that I can do today so I guess I will take advantage of my energy level and just rest if I get tired.  Had a really restful night last night and was thankful for that.  No pain at all.  I don't really have an appetite right now so I am going to have to force myself to eat several times a day.  I know it's important for me to get the nutrition I need to keep my blood levels up but it's hard when you are just not hungry.  I am drinking water to stay hydrated.  Just trying to do the right things to keep me healthy and going.

    Hope you all have a wonderful day.  Talk to you soon.

    Hugs!

  • bluejay58
    bluejay58 Member Posts: 62
    edited September 2011

    Rjbaby, you are awesome! It just seems like you are powering through all this. <3

     I am on day 4 since first treatment, and wow, I guess this is the "space cadet" time I've read about on the boards.  Very slow, very fatigued, very ... flat.  *g*  Yesterday I was able to do some vacuuming around the house, not sure about that today.  Some sinus pain, tongue still feels sort of burnt/sandpapery, but no problems eating.  Also no digestive/intestinal problems and no nausea.  Just feel knocked flat, so watching college football with my husband.

     Hugs and good wishes to everyone!  I've learned so much from these forums and it really does give me strength.  :)

  • shelley2011
    shelley2011 Member Posts: 199
    edited September 2011

    Hi, ladies!  Have been reading all the posts, and I am so glad to have such good company along this journey.   Day 15 from 1st TC x 4 treatment today, and today we shaved my hair.  It was really loose, falling out everywhere, and time for it to go.  I was upset last night and this morning, and then for some reason as my son started shaving it, I felt much better!   I am sorta rocking the bald look right now, and have spent some time today playing with tying the scarves in different ways.  Discovered that I am pretty comfortable walking around the house with no head covering and it doesn't seem to bother my family at all.  They think I have a pretty head....

    Can I ask about the fingernail thing?  Anyone know if TC x 4 is at risk?  No one had mentioned that to me until I saw it discussed here.  I have #2 this Friday, and plan to ice my mouth which I learned from here, but do I need to protect the nails too?

    You are all so strong and awesome, I am proud to be part of this group!

  • CJRT
    CJRT Member Posts: 524
    edited September 2011

    Anyone having skin irritation? I don't have anything major but have noticed facial dryness and some redness. I plan to ask my doctor about any recommendations at my appointment next week but just wondering if anyone has experienced anything similar and has any suggestions about what has helped. Hope everyone is having a nice weekend.

  • Thepeddlerswife
    Thepeddlerswife Member Posts: 69
    edited September 2011

    My 30 year old daughter, Cristine, will be starting chemo on Sept. 16th. Port is being placed on Tuesday. Not sure I am ready for this but I leave for CO tomorrow and will stay until she is well. some of my friends don't understand that but I don't care what they think. I have to be there. She is a single mom with 2 boys 8 and 6 and a husband that doesn't care to be in the same state to help out. I would never NOT be there for her! I know that all of you understand!

  • geocachelinda
    geocachelinda Member Posts: 223
    edited September 2011

    Hi Ladies, I am from the April 2011 chemo group.  I just finished my chemo on August 22nd.  I had 4 rounds of A/C and then 4 Taxol.  The A/C wore me right out and after the first treatment I vomited for 5 days!  My Dr. prescribed Emend and it was great!  Taxol was the worst for me because I got severe pains in my legs about 3 days after the treatment and it lasted for nearly a week.  I had to take some pretty strong painkillers.  I did not work.  I am on disability.  I cannot even imagine working during treatment because of the exhaustion.  I did not gain weight, I have always been up and down between 190 and 200.  I started out that weight.  I had a port and my oncologist recommended I keep it in even though I wanted it out.  I'm worried it may because my chance of relapse is probably fairly high due to how my stage was 3C with 10 positive lymph  nodes.  I will be starting radiation on Sept. 19.  If anyone has any questions that I can answer I will be pleased to do so!  Good luck everyone! 

  • bluejay58
    bluejay58 Member Posts: 62
    edited September 2011
    CJRT, I've noticed some facial dryness also.  No redness, just super-dry, smooth skin.  I guess normally I'd be happy about this, but I'm more concerned with being able to keep my eyes open.  *g*  Anyway, it seems to be going away today so maybe that's the end of it.
  • Suz39
    Suz39 Member Posts: 125
    edited September 2011

    Hi All,

    My thoughts are with all you strong ladies!  It is day 8 for me, TCx4.  I got thrush a few days ago, and have been swishing and swallowing for 3 days now, which has helped a lot.  However, I have a bit of a sore throat now, and don't know if it is the thrush in my throat, or a cold.  I also got a sunburn on my neck.  I don't usually burn, so it took me a while to figure out that it was a burn, and not some other reaction.

    My treatment was changed from FECx3 + Tx3, when my oncotype score came back as 10.  So, I wouldn't be surprised if that is the same situation for you rj.

    Peddlerswife, your daughter is very lucky to have you to help her.  I think she will need it.  I am very lucky that my MIL and Mom are taking turns to help take care of me, my two kids and my husband.  It is so hard for us moms to give ourselves the time we need to take care of ourselves, the peace of mind to have somebody else there to pick up the slack is something that I am very grateful for, and your own mom knows how to do that best :-)

    stay strong everybody! 

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Hello September ladies,

    RJ - Glad you had the burst of energy today. 

    Shelley - Glad your family thinks your bald head is pretty.  I figure my hair is going to fall out and need a shave about 2 days before my 50th birthday.  I already know I have a few stork bites on the back of my head which I am not too crazy about uncovering again.  Ah, well.  I think I will probably be bald around the house quite a bit too.  Last time I was bald I did not wear a wig or a scarf ever.  I just saw a video on scarves out of old T-shirts for very simple turbans.  I am going to rip up a T-shirt today and try it for a preparedness thing.  God knows I have enough old t-shirts.  I did also request the catalogue from American Cancer Society, although that has not come in yet.

    Peddler's wife - Glad you are there to help your daughter.  I miss my mom.  She had such good taste in books and would give me the best of what she read from the library.  I have seen a lot of my mom's sister lately and some of my cousins on that side and it has helped tremendously.  They have such a great sense of humor.

    I finally found a good fix (enough for me) for going in public without breasts yesterday.  I just tucked those soft forms under a tank top mens t-shirt, then a shirt over that.  I didn't even have to pin them.  They stayed in place and I could put them in a much more natural position than with a camisole.  That's all I need for going to the grocery store or the movies.

    The other good news is I am losing a few pounds from cutting out the alcohol pre-chemo and during chemo to give my liver a break.  I picture them tracking my weight and thinking its from nausea or I am not eating properly.  I am hoping this counterbalances any tendency to gain weight from the steroids and chemotherapy. 

    Have a good weekend ladies, as best we can.  I am off to cut up a t-shirt.

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    This is the simple t-shirt turban.  Don't know what the cancer client is doing with her tongue during this video.  I found that kind of strange and distracting, but the turban is super simple. 

    http://www.youtube.com/watch?v=tNOY4cS_k7A

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    I went out and bought some colorful t-shirts, 1.50 a piece at Goodwill to see the effect.  I came home and tried it with the colorful patterns.  I was sweating bullets between the breast forms and the turban.  OMG,  OMG.  Then I googled weather.  It's 94 today in West Allis, Wisconsin.  It might work better at 70 or less, which is not too far away.

  • Kelliregi
    Kelliregi Member Posts: 138
    edited September 2011

    I got all of my pre-chemo shopping done today. I'm not sure if I hope I need it all, or hope I don't! I finally found a great place to get extra soft toothbrushes - the children's section! I am now the proud owner of several SpongeBob Squarepants toothbrushes =). I also found Biotene mouthwash, toothpaste and dry mouth spray (I thought that would be good bedside) all at CVS.

    thepeddlerswife - I'm so glad you can be with your daughter. My son, daughter-in-law and the 2 grandbabies just moved to Colorado Springs this summer. I sure do miss them. Best of luck to your daughter.

    Kimberly1961 - I never even thought about wearing breast forms! I have TE's with only one fill - not even an A-cup. I guess I'm enjoying being flat after being a D-cup most of my life. I can't believe it's still so hot in WI. It's the same temp. in Florida. I can't wait for fall!!

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Did you all get fllu shot this year?  I never had a flu shot voluntarily.  My job requires one or I will be fired, so my MO administered one.  I can't lose my job because I have cancer and I need insurance.  Years ago when vaccine was short, I was on the last tier, I was not on the list to get one.  I was not eligible.  Same thing with their TB testing.  They don't think it is important to test for TB anymore for people in my position.  It used to be they would fire you if you did not show up for TB testing. Then that stopped.  I am not really happy getting injected with virus a week before chemotherapy and immunosupressed status.  I believe the MO said the chemo would negate most of the ISP effect.  He said, want your job, take the shot, else you will be fired when they tally..  I really hate them injecting me with god knows what when I have only had flu once in 5 years and I am facing chemo in a week after the shot.  Did anyone ask you or make you get a flu shot when you were facing chemotherapy?

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Hello Ladies.  Glad to see everyone tonight.  Yesterday was wonderful. Had that burst of energy and got lots of things out of the way.  Today, different story.  Felt kinda tired all day, dragging around a bit and took a 3 hour nap.  Not like me at all, but it did help.  I have developed thrush!  Crap!  I have a prescription mouthwash and bio-tene.  Using the prescription right now.  Other than that, I am okay and just trying to rest a bit.  I am supposed to work all three jobs tomorrow.  Hope I am up to it.  I am afraid the more treatments I get, I will get more tired and will be unable to keep up with my schedule.  But I do intend to try.

    Hope everyone has a good evening.  I will talk to you ladies later.  Nite!

    Hugs!

  • Shawna77
    Shawna77 Member Posts: 28
    edited September 2011

    Kimberly: my onc told me to get a flu shot this year for sure. However, if the people at my job told me I had to get one or be fired I'm sure I'd be pi**ed off! Hope it goes well for you.

  • Kelliregi
    Kelliregi Member Posts: 138
    edited September 2011

    My onc made me get a flu shot too. My first one EVER! It wasn't too bad. I got the shot on Thursday, and spent Saturday with a raging headache and chills, no fever though. By Sunday, I was fine. Good luck with your flu shot, Kimberly.

  • BethAnnK
    BethAnnK Member Posts: 3
    edited September 2011

    Hello everyone!  I just found this forum and am completely blown away by all of you.  You seem to be such a positive wonderful group of women.  I hope I can be that way too.  I am getting ready to start chemo next Tues 20th.  I have an eccho this week and my port will be put in.  I am doing AC for 8 weeks, and Taxol for 12.  My biggest fear is "chemo brain".  I have two small children (4 and 7).  I am already about as scattered as you can imagine, my husband and I are both worried about this getting worse.  Have any of you had issues with this?  I am a little worried about the fatigue, but with young children you rest if you have to and then you move on.  I am lucky to have my parents who are retired and able to help, as well as in-laws to help on weekends when we need. 

  • Sheypres
    Sheypres Member Posts: 35
    edited September 2011

    HI Everyone,

    We decided to get more aggressive with my treatment.  I met with another oncologist who agreed with my feeling that we were not doing enough. So I get my port in a few hours then chemo starts on Thursday. 4x AC then 4x T.  After that Rads and then out come the ovaries. And finally the Tamoxifin.I feel much more at ease with this treatment even though it is "worse" for me.  I never want to ask what if?  And I certainly do not want to deal with  this again in a few years especially since my oncotype score was a 48.  That is a 32% chance of recurrance. 1 in 3 is way too high for me.  Actually picked up all my perscriptions yesterday. 10 total but at least my insurance covered all but 1 and that was only $26. I am thinking I got off pretty good at only $106 so far.

  • BethAnnK
    BethAnnK Member Posts: 3
    edited September 2011

    Sheypres - just a note on the ovaries. I had mine out a couple of weeks ago.  I am BRCA1+.  That surgery was very insignificant compared to everything else I have done so far.  My mom said I looked a little worse after it in recovery, but overall recovery was minimal.  (I had this done right after my mastectomy, so I think I was just a little tired going in.)  I have had a few hot flashes from this, but my doc said to try Vitamin E, so we will see.  Good luck with everything else this week. 

  • lwarstler
    lwarstler Member Posts: 341
    edited September 2011

    Hi ladies, my name is Lee Ann and I actually start ACT either the end of this week or next Monday...just depends on what my surgeon says. Supposed to start with dose dense AC, every two weeks for 8 weeks and then Taxol. There is a 10 percent chance my final Her2 test could come back positive and if so, they will add herceptin to the Taxol. The prior two tests both came back inconclusive, so when we get the results from the lumpextomy tissue, if it is still inconclusive he is treating it as triple negative. I have been to the cancer center and they gave me one short and one long wig, a cap and scarf. I have also cut my hair really short for the first time ever in my life because I figure it will be easier to loose hair I don't like than hair I love. I'm not sure what to expect from the chemo, but I did decide to drop my graduate classes until after chemo so I didn't have the deadline pressures. It's nice to meet you all and I look forward to walking through this with people who get it.

    Freefly, we must be pretty close to each other. I am having my chemo done at Martha Jefferson right now, but that might change tomorrow. I am getting a second opinion out of UVA and if I go with that doctor, he actually comes out here to Culpeper where we live. That will be much preferred to going in to charlottesville all the time.

    Lee Ann

  • mags20487
    mags20487 Member Posts: 1,591
    edited September 2011

    My first chemo is Sept 20th.  My Onc is starting me on Taxol first then to AC.  She does not think I need radiation since I only had 3 nodes positive, but she says to make an appt with radiation Onc to be sure.  I have yet to get a wig but have one picked out online.  I am getting a pixie cut on Wed so the change won't be so dramatic when the hair falls out.  Scared of chemo but really know I have to do anything it takes to be well again. 

    Maggie

  • mary625
    mary625 Member Posts: 1,056
    edited September 2011

    I am starting chemo on September 26.  AC for 4 treatments and T for 4 treatments, each 2 weeks apart. 

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