Starting Chemo March 2016

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  • Phillipians4
    Phillipians4 Member Posts: 21
    edited March 2016

    nunn27

    In my case, I was diagnosed on 12/23 and have just now started neoadjuvant chemo on 3/17. I began with a team in my hometown who, I felt, were rushing me without doing thorough testing and I wanted to make an informed decision to prevent this from returning as much as possible. They didn't like that I got a 2nd opinion, especially the MO. Whoo! I got a bad vibe from that one! Anyway, I got a 2nd opinion at a teaching med center two hours away and am extremely glad I did. The new team actually did an mri, ultrasound on my lymph nodes (clear btw) and a mamma print test. The mri showed I have 5 tumors in my right breast whereas I originally thought I had 2. The mamma print is one of the newest tests for recurrence and helps the team decide on the best regimen. My surgeon once said to my question about this thing growing while we do all this testing and waiting..."we won't put you in any danger but want you to make the best decision for you". The waiting is the hardest part. Have confidence in your team or find another. You're not alone.

    Annette

  • Phillipians4
    Phillipians4 Member Posts: 21
    edited March 2016

    image

    Here is my new "do" when I need it here in a few weeks. What a relief to have that organized. Never know, I may not use it or I use it a lot. Time will tell. lol

  • phaila
    phaila Member Posts: 279
    edited March 2016

    in hospital with fever:(

  • NancyHB
    NancyHB Member Posts: 1,512
    edited March 2016

    Annette - you're beautiful in your "new do" - but beautiful whether you need it or not. :-)

    Today was my second treatment - 1/3 of the way through! Went well, no discussion of the infection so we proceeded as usual. My MO asked if I'd had any pain and I mentioned the few days where I need Tylenol and then broke down and took a couple of Norco left over from my surgery just so I could sleep. Without batting an eye she asked if I'd like a script, I said sure, and she gave me 40. I'll never use that many, but it's nice to know they're there if I need them. Please - if you're having pain and need something, ask for it. Just in case. You don't have to take it, but if you need it you'll be glad it's on hand.

    I've got my Neulasta button on board, am sucking down Gatorade and water as much as possible, and taking some Mirilax before I head to bed. Even with all the steroids, I'm super tired tonight. Heading in to the office tomorrow and preparing for the 8+ inches of snow and ice we're expecting over the next 24 hours.

    MFPM - I'm keeping you in my thoughts and prayers. Mention the new lump to your oncologist when you meet him; he should still be able to do a clinical exam and may want further testing, but unless it's an infection it shouldn't delay chemo. You can always request further testing after this first treatment, if need be. The school of thought is, if it IS cancer, the chemo should work on it to shrink it (which is why some of us have chemo prior to surgery). I can hear in your words how scared and worried you are about this first treatment. I concur with Candy - in general, the anticipation and waiting is far worse than the actual treatment. It sounds like your oncologist is already working to reduce your risk of side effects by splitting up your Taxotere over two weeks. I hope that helps. Please let us know how it goes tomorrow; we'll be in your pocket supporting you the whole way. *hugs*

  • NancyHB
    NancyHB Member Posts: 1,512
    edited March 2016

    Mecool - I see you're from Michigan, can I ask what area? I'm from Jackson. Are you ready for the upcoming snow and ice storm? :-)

  • Mecool
    Mecool Member Posts: 70
    edited March 2016

    I was just going to say "Hey in the Mitten" when I saw you mention snow, NancyHB! I'm actually in Grand Ledge (Lansing Area) so not far! Are you being treated at Sparrow?

    Oh, and our forecast here is just rain now! YAY! No way I was going to handle snow very well after today's sunny 60 degrees!

  • Jonsey22
    Jonsey22 Member Posts: 100
    edited March 2016

    Glad to hear it went well Pammac! Sleep and remember it gets better after the first few days.

    My hair is shedding everywhere now (day16). Starting to look like I have mange lol. Have to wear a hat to keep hair from falling everywhere.

    Best of luck tomorrow MFPM. Just breathe.!It will be okay and the stress will lessen once you know what to expect.

    Cand

  • MFPM
    MFPM Member Posts: 69
    edited March 2016

    Nancy and Candy, Thank you for the support and well wishes!  I'll be surely thinking of all of you tomorrow.  I hope to write again tomorrow night. 

  • Loretta_J
    Loretta_J Member Posts: 67
    edited March 2016

    I sent you a private message. I hope you read it before your treatment.

  • NancyHB
    NancyHB Member Posts: 1,512
    edited March 2016

    Mecool - I work in downtown Lansing; maybe we can connect for lunch or dinner sometime! I'm being treated in Jackson with my previous treatment team but did get a second opinion at UofM since this is a recurrence. I'll also be having my mx and recon at UofM this summer. I saw the revised forecast - not sure I'm loving the potential for ice now!

    Candy, when I saw the mange on my head, I decided to shave. by then my head was really render and shaving helped relieve that a lot. Good luck!

    MFPM - thinking about you this morning!
  • Seashine
    Seashine Member Posts: 24
    edited March 2016

    I am here, infusion day #1. Herceptin and Perjeta on board. No problems so far. Pharmacist came to talk with me and he was amazing, they have a pill for everything! With both Taxotere and Perjeta the balance between constipation and the other extreme can be a tricky balance. So we will see how that goes. But boy do they have the nausea meds all lined up! He said the nausea can be worse for us young folk (I'm 40).

    I will be getting Neupogrn shots, one a day for 7 days post infusion, I give them to myself! They want me to take it at night and take Claritin or Zophran for the whole time plus Tylenol. Pharmacist said that the brand new research out says that it is important for everyone on TCHP regimen of Chemo to get these shots so white count never dips. Will keep you posted as I move through these next four days which he says are the hardest. I even have a chart for my medswith everything mapped out, I will be a pill popping fool! Feels so good to get this going!

  • CJSharma
    CJSharma Member Posts: 464
    edited March 2016

    I'm barely making the gang this month. I start chemo on March 31st. I have IDC ER+, HER2- I don't know the stage yet. Because of the size of tumor (5cm) we're going with chemo first. As far as all tests show (armpit ultrasound, CT Scan and PET Scan) it has not spread and the rest of me looks pretty healthy. Because of the size of the tumor and it seemed to come out of no where, I am being put on a very aggressive chemo plan - every other week for 16 weeks.

    I will say that I feel very fortunate in that I found the tumor March 6th (while talking to my dad on the phone of all things - I lost my mom to liver cancer) and by March 11th I had been biopsied and told it was cancer (only that - we didn't have all of the results). The Her2 result was initially inconclusive so they had to send that back to the lab. I have had an armpit ultrasound, CT Scan and a PET Scan and so far it looks as if the cancer has not spread even to the lymph nodes. I get my port tomorrow, and start chemo next week. I'd like to know what to expect the first chemo session.

    My mix is dose-dense AC, adriamycin, cytoxan, with a dose dense taxol (which means every 2 weeks).



  • HRwinter16
    HRwinter16 Member Posts: 73
    edited March 2016

    Philippians- your hair is lovely!

    Phaila - are you feeling better?

    I hope everyone is doing well.

    I had my head shaved last night, feels a lot better, it had been hurting as the hairs got ready to fall out. Next chemo is Monday 3/28.

    I was reviewing some of my medical charts including an abdominal CT scan that was done just prior to my surgery and I realized the radiologist wrote in the assessment section that they noted a 4mm pleural nodule in lower left lobe of lungs and now I'm really freaked out! I contacted my oncologist to inquire if I need to have a CT scan of chest to further investigate and monitor this... I looked a little on line and it seems nodules this small are usually benign but I still feel very scared and of course now am imagining symptoms like short of breath etc. fingers crossed its nothing to worry about

  • Melgirl
    Melgirl Member Posts: 165
    edited March 2016

    welcome cjsharma. We are pretty close in diagnosis and chemo. But I did surgery first. My third AC will be on April 1.

    Sorry you find yourself here with us. Hugs

  • CJSharma
    CJSharma Member Posts: 464
    edited March 2016

    HR Winter - I had pretty much the exact same statement on my Chest XRay. I had a CT Scan done (and a PET Scan as other things were noticed) and it was nothing. I hope you have the same thing. Hugs. I get what you are saying - I had myself riddled with cancer and given 2 months to live. It's typical. Even the PET Scan showed nothing. I spent a week thinking the worst.

  • CJSharma
    CJSharma Member Posts: 464
    edited March 2016

    Melgirl - I'm sorry I'm here, too. But I'm one of those annoying eternal optimists. I'm not looking forward to dealing with this, but it is what it is. I'm sorry you are dealing with this. I'm 51 and my daughter is 22, so I have her to rely on (she's about 90 minutes away, but will be down as often as needed).

    What was the first round of chemo like? I understand it's different for everyone, of course, but I just want to talk to someone who has been through this.

  • HRwinter16
    HRwinter16 Member Posts: 73
    edited March 2016

    thank you CJSharma! Is that your kitty? Very cute! Here's mine below.

    My first chemo was not so bad - I felt ok day one and day two. Days three four and five I felt very tired and joints ached, like when you get the flu or a bad cold. Also I had to eat small meals and hanging bowel movements made me feel weak, again, like when you're sick. But overall I felt ok. I took the neulasta, Claritin, anti nausea meds and it all helped I think. I was still on medical leave so it helped I could nap. Now that I'm back at work we will see how round two goes.

    Good luck and hugs to you


    image

  • MFPM
    MFPM Member Posts: 69
    edited March 2016

    Did it and not feeling good but just took a generic Zofran, hoping it will help.  Since I had it in I.V. this afternoon, was trying to put it off 'till later but suddenly got a bad feeling, so every 8 hours it will be.  I suppose it went smoothly and almost fell asleep in the chair, guess I finally calmed down but came out of it not right, hard to explain.  Maybe a bit dazed, kinda woozy?  I'd prefer that over nausea and other things but now I'm hoping nothing else happens, plus I need for my stomach to settle.  I managed to eat scrambled eggs, bread, drinking lots of water and had some saltines.  When will they come out with something that's effective and safe?  Ugh!  I'm not a happy camper!

  • PhillipsTL
    PhillipsTL Member Posts: 4
    edited March 2016

    Hello everyone! I'm freaking out a little bit. Tomorrow will be one week since first infusion on TCHP. Side effects have been minimal, however yesterday I started breaking out with zits all over my back, shoulders and face. I was supposed to start my period last week, the day of infusion, but I started this morning, ugh. Food has no taste what so ever today. And I feel like I have zits in my throat?? Anyone else have this?? I go for my Herceptin only infusion tomorrow and I'm going to talk to the nurse and MO, just wanted to see if anyone else experienced this??


    Tracie

  • HolaSandy
    HolaSandy Member Posts: 85
    edited March 2016

    HRWinter,

    I also had 2 "non-specific nodules" noted in my left lower lobe. Mine were 3mm and 5mm and they are going to re-scan me after chemo. I'm also asymptomatic and I also read that under 2cm is usually benign. The nurse navigator told me that people are sometimes born with these things or it could be something I aspirated long ago. I also read that sometimes scar tissue shows up like this due to infections and I have had bronchitis several times. Here's hoping that ours both end up being nothing.

    Just wanted you to know that I understand your worry and I'm thinking of you!

  • ksusan
    ksusan Member Posts: 4,505
    edited March 2016

    I have a nodule that (with a positive antibody test) caused me to be treated for TB in the 1980's. When it didn't change at all, they said, "Well, it's not TB." Fortunately for me, I have years of comparison films, so when they say, "Do you know about that nodule in your right lung?" I can say, "Yeah, it's been pretty much the same since 1987."

  • Seashine
    Seashine Member Posts: 24
    edited March 2016

    No, not yet anyway. Today was my first TCHP infusion. Feel well all except for the fact that I seem to have a tight chest, like bad gas trapped? Or maybe heartburn? Gas is lower too. Anyone else? Anything help? I want to sleep, but I feel like if I lie down it gets worse.

  • HolaSandy
    HolaSandy Member Posts: 85
    edited March 2016

    seashine, heartburn is common with dexamethasone and other steroids. Did you get a prescription for ranitidine or anything? I definitely was taking mine on schedule for the first few days post infusion. You should be able to take Pepcid ac or something similar as well for immediate relief. I also had to sleep propped on 2 pillows a couple nights because it caused me issues when lying down too. Hopefully you get some rest tonight!

  • Italychick
    Italychick Member Posts: 2,343
    edited March 2016

    I took Pepcid ac and drank an entire bottle of Maalox after round 5, my guts burned so bad. Surprisingly, the Pepcid ac helped almost immediately. I'm not sure if those are the right things, but hey, they worked. I took them after spending a night sitting up while sleeping because I couldn't lay down, it burned so bad. And hit the probiotics, kefir, yogurt, activa, whatever works

    The point is, don't suffer, get some relief medication.

  • Loretta_J
    Loretta_J Member Posts: 67
    edited March 2016

    Yes Seashine. I had those same symptoms the night after my infusion. But the next 3 days for me were great. Water water water. I'm diabetic and continue to dehydrate. Stay way ahead of the nausea. Take Zofran as prescribed whether you're sick or not. My docs gave me a second one to take if I needed one before the regular Zofran dose was due.



  • HRwinter16
    HRwinter16 Member Posts: 73
    edited March 2016

    thanks Ksusan and holasunshine!

    Seashine,

    I hope things are feeling better soon - maybe your nurse or doc can give you something for the throat symptoms, there is a special mouthwash I think you can use - good luck

    And hugs to everyone, have a great day xx

  • phaila
    phaila Member Posts: 279
    edited March 2016

    I'm still in hospital and stinky as all hell!!

  • Cin54
    Cin54 Member Posts: 13
    edited March 2016

    Hope you feel better, Vicki

  • NancyHB
    NancyHB Member Posts: 1,512
    edited March 2016

    phaila, I completely missed your post about being in the hospital!! And so sorry to hear you're still there (and feeling all stinky). Any idea what's going on

  • Seashine
    Seashine Member Posts: 24
    edited March 2016

    feeling much better this morning. I chewed a few Tums and then went to bed propped up on pillows. Was bad until I fell asleep. Good nights rest was awesome. This morning I feel fine! Go figure. Thanks for all the advice. Hope everyone's day is wonderful

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