April 2015 Chemo Crew... Starting in April? Please join us!

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  • lovlilynne
    lovlilynne Member Posts: 405
    edited July 2015

    Hi April Ladies,

    Just checking in, I have been reading, but haven't had time to respond. I've been thinking of everyone, wishing all positive thoughts.

    Ankledolphin, my surgeon did a really good job of explaining everything, and I didn't have any questions. Once I read the pathology report, though, I saw that she noted that there was a "hot" node, and it haunts me - why didn't she take that node out? I'm glad she didn't take multiple nodes out, and I get why they just take the one, but I wonder why if she saw one that looked "hot" why wouldn't she remove it. So, I guess my suggested question would be - if you see another lymph node that looks like it might be unhealthy, will your surgeon take it out? And if not, why?

    I don't think I ever was able to respond to your question about the process - I had my tumor guide wire placed in a regular mamography room. They put your breast in the machine, then place the tube, wire, while checking the pictures for placement. The only difference was that I was in a chair (probably because a lot of women would pass out if they had to stand). Then, they called down for the radioactive material, and that was shot into my nipple area for the sentinel node tracer. It did sting (they warned me), but it was bearable. The nurse and doctor kept up a constant chatter and distraction from what was going on.

    Best of luck on your appointment.

    Lynne

  • lovlilynne
    lovlilynne Member Posts: 405
    edited July 2015

    I've been having an ok post-Taxol vacation. My bf and sisters usually walk every morning, and I've been able to do 2.5 mile walks. I started with numb/tingling in fingers and feet early - Tuesday. My DS gave me my Neulasta shot on Tuesday, and I started with the bone pain and aches by Wednesday. I am so out of shape. I have to climb a hill up to the main building, and I am winded by the top. I am happy to walk, but then I'm exhausted later. The bone pain/aches have lasted longer this time. Last night as I tried to settle to sleep, my feet and legs were aching and jumpy. I feel it in my wrists too.

    Still, I'm happy that I've been able to mostly enjoy our vacation like we usually do. We've had a couple of really nice beach days (today included), and we've spent time at the pool, and spent time with my family. My DD2, though, has been driving me crazy. She just fights me on everything, and she is relentless.

  • samaileko
    samaileko Member Posts: 13
    edited July 2015

    Better late than never ;)

    Aloha, everyone! I started chemo (Taxotere/Cytoxan x 4) on 15 Apr 15. I did not really utilize this site until I had bad hives about a week after my third round + Neulasta shot.

    I found out we are the experts on SE :) When I asked my Nurse Practitioner if the hives were normal, her only response was, "Any abnormality is not normal..." Well, that and her "what a stupid question" look!

    I am a 43 year old Air Force Reserve pilot. I found my 1.2 cm lump on my right breast while I was deployed in Dec 2014. Diagnosed in Jan. (ER+, PR+, HER2- IDC) Sentinel Node Biopsy in Feb: 0/7 involved :) I had already decided on BMx/chemo/Hysterectomy before finding out I am BRCA2+.

    Bilateral NSMx was accomplished 16 Mar, with right nipple removal one week later due to pathology report showing DCIS in areola area. My unaffected breast tissue showed three additional <1mm IDC. PET Scan on 9 Apr was clear.

    I just finished 4/4 rounds of TC on 18 Jun. I meet with my Gyno Onco on Weds and have my post chemo blood test/MO appt on Thursday.

    I have tissue expanders in and was planning on expanding during chemo, followed by implant swap out, but an incision on my right breast became an open wound after my 1st round...will need a DIEP flap. I have a bilateral DIEP flap surgery scheduled for 24 Aug.

    Since I started chemo, I began walking with my female Doberman Pinscher. I keep pretty active with my three little boys, 3, 4, and 6.

    I often pray for patience. I get frustrated sometimes because it takes so much effort to do nothing...I was so used to being healthy.

    I wish I would have joined this page sooner, instead of dealing with everything on my own. My rehab people were very supportive, but I finished last week.

    I am here to gain/give insight and share positive energy. I am happy, yet anxious about my next few steps. I'm blessed and very happy to be alive!

    What a perfect weekend to come across this group...celebrating Independence Day, especially with KSusan's inappropriate picture!!! LOL!!!

  • ksusan
    ksusan Member Posts: 4,505
    edited July 2015

    #27: I am grateful for drives in the country that end with fruits and vegetables.

  • KBeee
    KBeee Member Posts: 5,109
    edited July 2015

    Samaileko, Welcome !! I'm glad you found us. I hope you are feeling better and better every day now that chemo is done. How scary to find your lump while deployed.

    Lynne, Your vacation sounds fabulous! I am glad you've been able to enjoy it.

    MO is gone chemo day all month, so I see him a day early... Which is annoying because it means 2 co-pays! So..... Blood work today, Taxol tomorrow. Predicting higher hemoglobin but lower whites. We'll see!!! Hoping numbers are high enough for chemo

  • KBeee
    KBeee Member Posts: 5,109
    edited July 2015

    I was scheduled to see the doc today and chemo tomorrow ... They said I could do chemo today to save the extra co pay. That's great, but I do not have my ice with me, or anything else other than my phone!!!!! I hope my battery lasts so I have my entertainment!!!

  • Addie29
    Addie29 Member Posts: 307
    edited July 2015

    so beyond mad right now. Got a sitter for my 3 kids to attend the look good feel better program. Drove 30 minutes away with squeaky van rotors and the program director never showed up for the program. I'm so mad! What a waste of gas and resources.

  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited July 2015

    Kbeeee, how is your cold?? Fingers crossed you can get dosed today!

    Good Luck everyone going to the chair today!

    Samailako, Welcome! Yup, we got the side effects down to a science here- sorry you have to be here, but you couldn't ask for a better group!

    Lynne, glad you had a good vacation! I still can't believe you still felt like going so soon after chemo. You are tough! :)

    Grrrf, its Monday. Baaaaaad crash after getting dosed on Thursday. Had to cry all weekend. I'm so happy I only have one more of these! Feeling little shooting pains in my shoulders, thought it was my port, but its on both sides. Wonder if its the range of motion stretches the PT gave me? Giving myself a "Get your shit together, Ryan" pep talk right now...

  • gingeel
    gingeel Member Posts: 102
    edited July 2015

    Welcome Samaileko, glad you found us, and happy that you are finished with chemo!

    KSusan, that picture is great. It's wonderful news that having your port out is as good as I imagine. lol

    Lynne, your vacation sounded perfect! How old is your DD2? My son is 11, and I've noticed how defiant he's become. It's like he's found his voice, and he's gonna use it! Argues about everything!

    KBee, hope chemo treats you well, glad they saved you a copay.

    Littleblue...how you feeling today? I laugh at you for complaining about letting your upper body go....hello!? You hike 3-5 miles with a pack! Girl, give yourself some credit. I've never really been hiking, but I can't imagine its light work!

    Had a great 4th of July. Was feeling so bad Friday....crying, hurting, exhausted.........then woke up Saturday still a little weak and light headed, but it's like the fog lifted by midday. I imagine that my counts were low Friday thru Saturday morning, and then Boom! they were up, cause I felt like a million bucks Saturday night. Went to 2 bbq's and watched Fireworks and even danced with my kids under the stars. I was so grateful to have felt good. And still am! Those moments of feeling so good, when you've felt so damn bad, really stand out. That's just me feeling happy to be alive.

    Happy Monday, ladies!

  • gingeel
    gingeel Member Posts: 102
    edited July 2015

    Sorry, Addie and Littleblue for the crappy morning.

    How can they not show up? I would have been furious! Well, you should keep your sitter and run your ass to the mall for some therapy shopping, or better yet, get a massage.

    Hope you feel better Littleblue. I cry more now on Taxol than I did with AC....guess it's the steriods.

    Gotta go.....I'm not paying attention to my kids, and my little one is having a fit.

  • Positive_spirit
    Positive_spirit Member Posts: 218
    edited July 2015

    Littleblue and Gingeel - Awww... sending you both a hug! The emotional reactions to all the meds, cancer, etc..are huge.

    Addie - Oh, that sucks about the program director. What an idiot to not show up for something like Look good, Feel good. UGH! Hope the day turns out better

    Alibeth and Ksusan - nice photos

    Lovlilynn - you inspired me with your vacation talk to get ourselves out of town. It did wonders for us!

    My best friend of 26 yrs drove down from Canada to visit and another friend is coming on Thursday. Feeling loved and giving love back. Yeah for tried and true friends. Wishing everyone going through chemo or rads this week an uneventful session.

  • KBeee
    KBeee Member Posts: 5,109
    edited July 2015

    positive spirit, so glad you can see your friends!!!

    Gingeel, those bad days are bad, but you are right... They sure make you appreciate the good ones!

    Little Blue, I sure hope you are starting to feel better with less pain.

    Addie, I can't believe they did not show up. That is absolutely horrible!!!! I hope you call and give them a piece of your mind!

    My counts were up a bit from last week. Yay! Premeds going in now. Not going to know what to do with my free Tuesday!!! My bad days this week should be Friday/Saturday. That means I should feel better by Sunday... Yahoo!!! I work tonight, Thursday, and Sunday, so that makes me happy to feel good on my work days

  • StacyMc329
    StacyMc329 Member Posts: 48
    edited July 2015

    last chemo tomorrow. So very happy about that.!. The SE have been really getting to me lately. Really bad numbness/tingling in my right hand and both feet. And starting to feel the same on my upper back too. I'm hoping to get back to my regular work schedule in Aug but I just don't know what to expect from rads. Anyone have any help in that area? I have all my appointments set up already for after chemo and would love to Know what to expect

  • ksusan
    ksusan Member Posts: 4,505
    edited July 2015

    I hope everyone has a better day today!

  • Rpayton
    Rpayton Member Posts: 235
    edited July 2015

    Kbee: hooray for counts being up! Hope your week is good when working.

    Addie: WOW I can't believe they didn't show. That is such a great program and a full class, well at least over by me. I hope they can make it up to you somehow.

    Lynne has inspired all of us to get away for a bit! Hooray!

    Gingeel: glad you are better too. Yeah it changes how we look at those good days and really appreciate them. I try to take a few minutes to be grateful each day for little things to stay positive.

    Starting 2nd week of disability and starting to relax and forget and forgive the work drama I was going thru. Much better for me. Taking this time to really go thru some drawers and cleaning when I can as that will make me feel like I'm accomplishing something. And I'm getting involved with the cancer wellness center for yoga and other programs available. Hoping to also volunteer as I can too. Back to the chemo spa on Friday for me.

    Everyone praying for a good week for all!

    Renee


  • gkodad
    gkodad Member Posts: 188
    edited July 2015

    First DD Taxol was great Thursday and Friday...then Saturday and Sunday leg and foot pain was beyond bad. Couldn't sleep and nothing stopped the pain. Today is better - just achy.  But I already have finger numbness and numb spots on feet.  Since Taxol is, at best, only borderline effective for post-menopausal ER+, HER- women, has anyone else stopped when the numbness got bad?  And how bad?  I'd like to make at least one more, and MO says it's my call [unless he decides I have to stop].  

  • SueH58
    SueH58 Member Posts: 632
    edited July 2015

    gkodad, could you try weeklly taxols instead of DD?

  • KBeee
    KBeee Member Posts: 5,109
    edited July 2015

    Gkodad, I am surprised your MO thinks Atac is only borderline effective for that category. My MO pretty much said the opposite!

    Renee, Enjoy your time off so you can just focus on you!

    Stacey, congrats on last chemo tomorrow!!!

    Home from Taxol #7. Glad to have another done! Of course I do wish I was doing dose dense... Then it would be my last! 5 more though... I can now count them down on one hand!!!


  • AndreaC
    AndreaC Member Posts: 220
    edited July 2015

    Good morning all!

    Not sure if I should still be here, having finished chemo...but I love you guys! And I am just 3 days post chemo so am still having SE's. So far not bad...just the usual steroid crash and a tingly tongue...waiting for the sores to start popping up. I gave myself the Neulasta this morning, I can expect leg pain tomorrow.

    Samaleiko, welcome! It's so awful you have to be here but this is a great support and wonderful women here. (And the occasional husband!)

    Addie, that sucks about the program being cancelled, and your car issues. Sheesh...about time you caught a break!

    Kbeee...re co-pay - it is a totally foreign concept to me. In Canada our health care is free...well, we do pay for it but it's on a sliding scale so if someone can't afford it it is free. For those of us working stiffs, it's taken off our pay but it's inexpensive and we don't even notice it. It is actually illegal in Canada to be without health insurance, and there is no reason to not have it. But I don't want to get into a political discussion. Suffice to say that it's nice going to hospitals and doctor's offices without ever worrying about bills.

    We have been having such a hot dry spring/summer and there are forest fires all over. Our sky has gone from brilliant blue to orange/grey thanks to the smoke. The fires aren't anywhere near us but there is a huge smoke cloud hovering over southern Vancouver Island.

    However...I am off to a big music festival up island on Wednesday. My husband is coordinating the volunteer performer shuttle this year. We both volunteer at it every year, but this year I'm opting out due to chemo. But as a coordinator he gets a ticket for me including a backstage pass! Lyle Lovett, Buddy Guy, and Graham Nash are the headliners. Looking forward to it! We are camping on site so if I get tired I can go lie down in the van.

    Have a great week everyone

    Andrea


  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited July 2015

    Yay, Stacy! Congrats on being done with Chemo!

    Wow, Kbeee, only 5 more??? Awesome! Glad you could stay on track today, it would be terrible to get behind, I agree.

    Addie, really???? I would be so pissed off! I hope you felt up to doing something else fun with your time..

    Positive-Spirit, Thanks for being here and being so encouraging!

    Ok, so what got me down is my Mom. She is the best, she comes over for every treatment and stays with me for at least 2 days, but she can really say some disturbing shit. This weekend was " Well, dear, when you were born, I had a dream that there were two souls present. One of them was 17. I always had the feeling you were born 17. So, really, you are 51 right now, and these old lady problems (cancer and infertility), make sense". And then she said she hoped I had 17 more years left. This, on top of her asking what doing Radiation would do to my work schedule. She always drops stuff like this. She also told me once she debated having an abortion with me. Don't know why its getting to me, but it really is..sorry, needed to vent...

  • gkodad
    gkodad Member Posts: 188
    edited July 2015

    littleblue - I think you're triple neg - research says Taxol is exactly right for you.   I'm ER+, post menopausal - research says taxol after A/C doesn't add much in the way of benefit unless you're Her+, which I'm not.    So I'm in the gray area - it's still the "gold standard" but the ER+ piece is now looking like it should be a big factor in the decision. Also I'm older, so the age factor is there as well.  I asked him straight out for the numbers - 50/50 chance it has NO benefit.  Now - don't everyone start questioning your Taxol decision - we're all different and both age and ER/PR/HER are big variables in what works and what doesn't.

    I want to get through at least 2 - maybe there's SOME benefit.  We'll see what he says next week - I suspect I'll do 2, but he's already said we stop if neuropathy becomes a problem.  

  • gingeel
    gingeel Member Posts: 102
    edited July 2015

    Congrats Stacy for almost being done!

    Positive, hugs back, girl!

    RPayton, I'm happy that you are able to take time from work to be home and focus on you. Relax and enjoy it!

    Gko, like Sue said, maybe try weekly Taxol?

    KBee lucky you! you're almost done! I still have 8 more left. Well, actually, after tomorrow...7.

    Andrea, of course you should still be here. You stay as long as you want. I know I will. And, I'm glad you're not staying home and going to that music fest! You need to get out, girl! Why let hubby have all of the fun?

    Littleblue, hmmm....moms. I don't blame you for being miffed about what she said. I would have been, too. Sometimes people say things without really thinking about what they are saying. They don't have a filter. You just have to excuse things like that.

  • littleblueflowers
    littleblueflowers Member Posts: 2,000
    edited July 2015

    Glad you are feeling good, Gingeel! And thanks for the pep talk about my Mom. You are so right- she has no filter. Guess its her old lady street cred LOL.

    GKO, I hope you can find whats right for your system. You are awesome, and you give great advice and write really well.

    Andrea, DON'T LEAVE US!!!!!! Just kidding, but you are such a great voice here, please never question your place! And the music festival sounds so fun..I love me some Lyle Lovett! He's got such a sexy voice..

    I'm a snot factory

    and I'm ok

    I snurff all night

    and I blow all day...

  • Rpayton
    Rpayton Member Posts: 235
    edited July 2015

    Andrea: hope you don't leave us! Stay in touch here. We all learn from each other. What dies your MO have you do next?

    Gingeel: my mom has no filter either. LOL I get it. In some ways I think I have to make her feel better. She is in her 70s and I know this is hard for her and my dad.


  • gkodad
    gkodad Member Posts: 188
    edited July 2015

    Thanks for the writing compliment, littleblue...this is a great group.  I have no one locally who is going through this and my family, while concerned, do not really grasp the situation.  My mother also has no filter....but let's don't get started on that!   I enjoy my MO and nurses, but if I don't ask the question they may not provide the information, so you guys help with the right questions..  And while I'm an oldster here, in my chemo setting I'm younger than most, so it's nice to get the perspective of people who are young and active. 

    As for Taxol, I'll hang in there until my gut tells me the risks outweigh the benefits, especially at my age.  I'm a watercolor artist and I don't want to learn to hold the brush with my mouth!   Those of us who are ER+ will move on to possible radiation and  5 or 10 years of hormone therapy, so it's not like chemotherapy is the end of treatment. 


     

  • Addie29
    Addie29 Member Posts: 307
    edited July 2015

    tomorrow I go back to the chemo bar. #4 taxol for me and I'm losing my eyelashes super fast. This is depressing me severely. I've felt so sad lately. Cancer is taking all my beauty away from me. I know it will come back but still- I feel hideous and today was not a good day for me after missing out on look good feel better program I had to have my van towed because the brake caliper went in one of my rear tires- so I sat in the parking lot for 2 1/2 hours until my hubby leave work a little early to get me. I cried the whole time I waited- like I said emotional- maybe it's the chemo pause. Woe is me. Side effects from taxol aren't too bad for me. I feel decent. Not too tired but super emotional- I just want my bed and maybe a bubble bath. Take me away Calgon. Hope everyone's Monday was better than mine.

  • Stephmoen
    Stephmoen Member Posts: 563
    edited July 2015

    ugh Addie the same thing happened to me the first time I went to attend the feel better program I was almost there when they called and cancelled it although my story isn't as bad as yours I was still pissed! I went last month got some cool stuff only had 2 other older women there and one kept talking about how lucky she was that she didn't have to do chemo although I don't understand why she didn't she said she had a tumor that doubled to the size if a golf all in a couple weeks! Anyways I hope everyone is well I haven't been on here too much I started Exeffor I think it's helping on my 2nd week with it I had a very rough time last week I read in one of my reports that my lymph node looked suspicious on anultrasound loss of hilium fat my pet scan was negative and my mo is still saying stage 1 but I'm afraid it's spread further than I originally thought I hate neoadjuvant chemo because I don't know my full status and it's very difficult for me

  • ThePrincess
    ThePrincess Member Posts: 424
    edited July 2015

    Ladies! Late to the party on the exercise - but I've also been doing bootcamp - my surgeon said I can do anything that doesn't hurt (ie: stop IMMEDIATELY if something hurts) and make sure I don't fall (so I don't do any jumping exercises or anything that seems risky) so I do weights and pushups (girl style as my arms are weaker and I'm a wee bit afraid of doing too intense of a chest exercise) intervaled with running.

  • ThePrincess
    ThePrincess Member Posts: 424
    edited July 2015

    KSusan - love that pic!!!

    KBeee don't get a cold!!!! Wishing the germs away!!!!

  • KBeee
    KBeee Member Posts: 5,109
    edited July 2015

    Addie, I hate that it was such s tough day. Those steroids can wreck havoc on us emotionally. Not to mention that cancer does too. Sometimes you need a good cry. It does sound like a good night for Calgon.

    Andrea, Don't leave us!!!! The time when chemo is done can be even more challenging than chemo emotionally... We're all here as friends for the long haul. Please stick around!!!!!!

    Little Blue, uuuugh on the mom. I love my mom dearly, but I had to tell her she could not come out until I am near the end of chemo. My parents are great, but they always fight, try to tell me what to do and are "never" wrong. When I have appointments, my BP is always about 20 points higher when they are here. They mean well, but..... I have started calling them out when they say things that bug me. That has helped. Do not be afraid to call her out on it.

    Gkodad, post a picture of some of your paintings!!!!!!

    Rainy, dreary day here, so a good day to get chemo done

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