Taxotere, Carboplatin and Herceptin

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  • Jumpship
    Jumpship Member Posts: 305
    edited March 2015

    Two and a half months' yikes! My release to work is for Tuesday and I'm not sure I'll be able to see that well. I look like he'll

  • april25
    april25 Member Posts: 772
    edited March 2015

    CassieCat and Kthielen -- Thanks for the info on when nail problems started...

    *sigh* I'm only just in my 5th cycle, so I can still get the lovely nail lifting in future. Oh, joy!

  • Kthielen
    Kthielen Member Posts: 194
    edited March 2015

    update on the nails.....

    I finished chemo on May 28th, they were all lifted almost to cuticle by July 1st. They had fully grown out pretty much up until last week when they were really sore again. I just took my nail polish off today and yes they are all(except for the thumbs) lifted AGAIN about half way down my nail bed. What the heck!! Every time I think I am feeling better something happens:/

    At least they aren't all black and nasty looking just whitish/yellowish....back to wearing nail polish all the time

  • CassieCat
    CassieCat Member Posts: 1,257
    edited March 2015

    Oh dear...I'm so sorry your nails are lifting again. :( That is just completely unfair.

    I'd like to polish mine so I wouldn't have to see them, but I'm worried about getting polish or polish remover under the nails.

  • april25
    april25 Member Posts: 772
    edited March 2015

    Kthielen -- really? You're still getting nail lifting so long after chemo (9 months)!??? That's terrible. Do you think some of the long-term therapies are contributing to that? .. Ah, well. I hope the lifting stops and the re-growing goes quickly for you.

    CassieCat -- I hope your nails improve soon, too. ...I'd worry about getting the remover underneath, too! So far, no lifting here, but as I said, I'm only on round 5. BUT I just discovered I've got nerve damage/neuropathy. It's not painful, so I wasn't sure--but the peroneal nerve in my leg is blocked, so now I have a numb upper-foot and drop-foot! gah!

  • Kthielen
    Kthielen Member Posts: 194
    edited March 2015

    I know it's crazy!! I hope they don't lift more than they are now. They don't hurt anymore so hoping it's done!

    April, sorry to here about your drop foot:(

    Cancer sucks!!


    Kathy

  • debiann
    debiann Member Posts: 1,200
    edited March 2015

    April, So sorry to here of the drop foot. After chemo I had a long (13hour) surgery -mx with diep recon. I woke up from surgery with drop foot. It takes time for the nerve to heal, but physical therapy can also help resovle the problem. I had some neurophy from chemo too and I take B6 for that. I hope your drop foot gets better soon.

    Last week an ultrasound revealed a popiliteal (Baker's) cyst in the same leg that needs to be further evaluated with by mri. The fun never stops!

  • april25
    april25 Member Posts: 772
    edited March 2015

    debiann == Whoah--drop foot from surgery? Geesh... who knew? I hope you're doing ok, too. Good luck with the cyst, too. Hope it doesn't cause you trouble...

    Kthielen == Yeah... cancer and all the treatments for cancer definitely sucks! I keep thinking I'll manage to avoid bad SEs but things keep popping up anyway! --But at least I'm not getting the pain that comes with neuropathy. And I really do hope something can be done for my drop foot. I used to walk fast and even run around a bit, but can't do it with the stupid foot! Hopefully I can get a brace in the meantime, just so I won't trip over my foot again and re-injure it... and maybe be able to get around a bit more easily. I can walk, but I have to be careful when I do it, and I can't move quickly at all... *sigh*

  • debiann
    debiann Member Posts: 1,200
    edited March 2015

    Yes April, drop foot from surgery. They said it was from the surgical compression boot pressing on the nerve. 

    I was given a brace to wear at night to keep my foot flexed in a more natural position, otherwise my toes pointed down and caused discomfort in my calf. The physical therapy can't help the nerve repair any faster, but it keeps your muscles working normally while the nerve heals.

  • Jumpship
    Jumpship Member Posts: 305
    edited March 2015

    Another whine from me….It's 4 weeks since my last TCH. I gained 12 pounds in a few days. My feet and legs are so swollen that only one pair of pants fit. Elevating the legs doesn't help. I told the infusion nurse at Herceptin day that the doctor just didn't care. She just wanted me to wait it out. She didn't believe me. My Albumin and Protein came back low. She thought the doctor would recommend albumin (o and a transfusion, hemoglobin is low). But, true to form the doctor said wait it out. Norco doesn't touch the pain. I sleep in 90 minute shifts. This sucks! I'm just coming off of 10 days of antibiotics for an eye infection and 5 days of antibiotics for a UTI. Oh-and I still have dry mouth and my mouth tastes like (*(*)(*)(*. I knew that 6 treatments was going to suck but really, 4 weeks after the last one and I still feel like crap and have a low quality of live!


    I want to eat dinner with my husband at a restaurant (I've been quarantined for most of the last 12 weeks) and eat a meal that tastes good and that stays down. Is that too much to ask????

    God I hope tomorrow is better than today.

  • DaisyQ
    DaisyQ Member Posts: 123
    edited March 2015

    minivan: Sorry for your discomfort. It sounds like one thing after the other.. The leg swelling sounds awful. How many days are you supposed to "wait it out?" I did not bounce back as quickly as I expected either. Your mention of UTI caught my eye. I never had problems with UTI's, but since finishing TCHP I have had 3. None required antibiotics though. I do think my taste was back at about 5 weeks PFC-right around my BMX. I hope your sense of taste returns quickly and the leg/foot swelling resolves. Hang in there, you'll start feeling better!

  • CassieCat
    CassieCat Member Posts: 1,257
    edited March 2015

    minivan, one of the ladies in the August chemo group had a lot of swelling too, and I believe her MO gave her an Rx for it eventually. She did finally lose all that fluid weight, but it was slow going if I recall correctly. I hope you're feeling better soon. Cancer sucks, chemo sucks, it all sucks. But it does get better.

  • april25
    april25 Member Posts: 772
    edited March 2015

    minivan -- Sorry to hear about the leg and feet swelling. I've been getting edema, too... but I think mine is mostly from the IV drips I'm on for 2 weeks each cycle (to treat dehydration due to diarrhea). It goes away at the beginning of the cycle when I'm not on the IV drip... But it could be aided by the TCH... That stuff seems to be able to cause all kinds of SEs, so who knows? Anyway, the swelling definitely doesn't help my blocked peroneal nerve and drop foot (sigh).

    I do hope the swelling goes away for you, at least after you finish chemo, if not (preferably) before that... It seems like the docs focus on the chemo and the cancer and there could be a LOT more done for all the side effects, since they can be rather horrible... and can keep people from getting the chemo they need!

  • SpecialK
    SpecialK Member Posts: 16,486
    edited March 2015

    mini - when was your last echocardiogram and what was your LVEF? Foot and leg swelling can be indicative of chf and should not be ignored by your doc. At the very least you can have a low dose diuretic to help you get rid of the excess fluid. You need to be a squeaky wheel

  • windgirl
    windgirl Member Posts: 340
    edited April 2015

    minivan I had about 10 pounds of swelling too and mostly in legs and feet. I was told to wait it out didnt believe it would improve but magically peed it out over two distinct periods, it took 3 months to fully resolve after last chem

  • Jerseygirl927
    Jerseygirl927 Member Posts: 438
    edited April 2015

    mini, sorry about your swelling and pain, I too don't think I pee as much as I should, drink all day, and pee very little, I had my second chemo on the 19th and 1st hercepton after that and I broke out again with acne, but this time it's in the scalp too, anyone else get pimples that are sore? Another infusion Wednesday, so will bring it to Drs attn maybe I'm allergic to hercepton?

  • Jumpship
    Jumpship Member Posts: 305
    edited April 2015

    Thank you all. Special K-Muga was done before swelling….maybe 3 weeks before swelling. Every day I hope for a better day.

  • Jerseygirl927
    Jerseygirl927 Member Posts: 438
    edited April 2015

    hope that more peeing will reduce swelling under arms at surgery sites, each side from the double mast. But of course when you go for chemo or hercepton you get more hydration along with drugs that probably make you retain fluids. Still drinking but not peeing it out. Hope it won't be months later that it eventually goes, going to dr tomorrow to see if seranoma needs to be drained? It's getting uncomfortable.

  • Kthielen
    Kthielen Member Posts: 194
    edited April 2015

    jersey girl,

    I did break out on my face and scalp(as well as a few sores on my arms that were more like pustules). Are you on Perjeta? My MO thought it was from that. He ordered me Clindamycin gel and that helped sooo much! Good luck!

  • Jerseygirl927
    Jerseygirl927 Member Posts: 438
    edited April 2015

    No perjeta.... They are still telling me chemo. It seems to appear 5-6 days after the big chemo. I am putting an older cortisone cream on it and that seems to be fading them , if they weren't on my face, I might try the benedryl cream, they tell me the ones on top of the scalp are sore because of location? hydrate girls, I do feel better since drinking more. Lol. Not booze?

  • Gretagirl
    Gretagirl Member Posts: 182
    edited June 2015

    Hi

    I am brand new to this site. Username Gretagirl. I am scheduled to start treatment in a few weeks. I am trying to talk with ER PR HER2 positive ladies. I will be treating with Hereceptin Taxoterend Carboplatin. I can't seem to find any recent discussion boards (May June 2015). Also very anxious to hear any and all advice!

  • PMR53
    PMR53 Member Posts: 452
    edited June 2015

    Gretagirl

    I finished this treatment in March. I get Herceptin only now. You will be premeditated with many anti nausea meds. Chemo is hard but you can get through this. Surround yourself with caring supportive people. Ask questions to nurses and your Medical Oncologist (MO) one of the biggest things that helped me was I applied bags of frozen peas to my toes and my fingernails during the taxotere portion. It saved my nails. No lifting no change. Easy to do. Just pack a cooler and bring every tx. You will lose your hair by the 2nd tx. Get ready shave it before. Get a wig now. If you want a real hair wig which can cost up to 2000.00 or you may just do scarves. You can apply for a free wig at Lollyslocks.com.

    We are here for you. I am so sorry you have to deal with this. Please private message me if you have any more questions.

    PMR53

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2015

    Welcome to BCO Gretagirl! You picked a great place for support while going through treatment.

    My biggest tip is to stay hydrated. My biggest side effect was constipation.

    A new thread has been started for members starting chemo in June. Here is the link..

    https://community.breastcancer.org/forum/69/topic/831849?page=6#idx_152

    Also, if you go to active topics, you may find another group more specific to your treatment.

    Feel free to PM me too if you have any questions!!

    Best wishes and gentle hugs to you!!

  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited June 2015

    Gretagirl - Slow Deep has hooked you up with the group who will be going through the experience with you & that's very valuable. I also read the chemo group just before the one I joined. Below is a thread that lists most of what you'll need to prepare. Again, it's not very active but we keep "bumping" it so that new people will be able to read the advice. Good luck.

    https://community.breastcancer.org/forum/69/topic/...


  • CassieCat
    CassieCat Member Posts: 1,257
    edited June 2015

    Gretagirl, I'm sorry you have to find yourself in this position, but I'm glad you found these boards. I finished TCHP (Perjeta is the P) back in December. Being a part of the August 2014 chemo board was really helpful for me. There also a thread called Triple Positive, and a couple of new TCHP threads. Let us know what questions you have. Chemo is tough, but you get through it.

  • Teakae
    Teakae Member Posts: 3
    edited June 2015

    Hello

    I just had my first TCH treatment last Thursday and it has been a week. I was fortunate not to have severe sideeffects. But I am puzzled at a few that I did have because I didn't read about them anywhere. Can anybody tell me if they experienced them? Thanks in advance.

    Eyeball pain, pressure, vision changes where saturations seem up and everything was bright. I had to wear my sunglasses in bed. I had some nausea and I thought it was a GI symptom until I realized it was from the eye pain. After the 3rd day I took some ibuprofen and it made it all better.  A week out now, I still have some eye pain and pressure and vision changes. No watering, no focus problems, no itching or dry eye.

    Stabbing pain on head. I have a few sore spots on the back of my head that hurts like someone is stabbing me with a pencil. It is a specific areas and hurts below the skin above the bone.

    Weird jaw and teeth pain. Discomfort all along my molars and stabbing pain under my jaws. sometimes stabbing pain in ears. I also have bleeding gums now. I had my teeth checked by a dentist a few months ago everything was OK.

    Pain under my collar bone and down under the sternum. It is like someone kicked me there and there is squeezing pressure then slowly lets go. It occurred a lot after port placement, like very hour but now it is only occaisionally. It also hurts and tightens my breathing when I first lay down, then eases.

    My stomach, thighs and buttocks are cold!. I am warm elsewhere, even a little sweaty but my belly and butt are sooo cold. I use my heating pad and rotate around the areas and it never gets warm!

     


     

  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited June 2015

    Teakae - I'm sorry I'm not aware of any side effects like you're mentioning. I do think they are serious & you should call your MO immediately - do not pass go. Eyes are nothing to fool with, nor is the head pain. Since your jaws are bleeding it's even more urgent that you call right away. When you had your port installed, did you discuss the sternum pain then? I wonder if it has something to do w/how the catheter tube is laying since that is threaded through one of the large veins near your neck & down to your heart. But that is pure conjecture & you should ask your doc. You don't list where you are located, but every MO has someone on call 24 hours a day. Please do come back & let us know how you are.

  • Gretagirl
    Gretagirl Member Posts: 182
    edited June 2015

    thank you for sharing with me! I found this response by accident. How do I find any responses to my post?

  • Gretagirl
    Gretagirl Member Posts: 182
    edited June 2015

    I sent you a PM not sure if it worked. If you didn't receive please let me know on discussion board. I do not understand the ice on fingers and toes

  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited June 2015

    Gretagirl - click on the link that says "add to my favorites" when you are in a thread. Then you'll see My Favorite Threads on the left & it will show activity. I'm not sure who you're asking about the PM, but I didn't get any messages.

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