Chemo in June 2015

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  • AGerl
    AGerl Member Posts: 16
    edited August 2015

    Esmerelda50 - do you put anything on the sores? Are you able to see a dermatologist?

    How are your platelets? My nurse told me about skin lesions from low platelets on Friday when I was getting my blood transfusion.

    Apparently I was not doing as well as I thought last week...I had read that after TC #4 it feels like a sucker punch. And it hit me hard!

  • EnigmaticFox
    EnigmaticFox Member Posts: 54
    edited August 2015

    Hey there all! Brief post, as I'm tuckered out. We got back yesterday from a beach vacation that we snuck in between two chemo treatments. Went pretty well, though I got a fever partway and got to visit the local ER for a few hours. For a while there I thought they would admit me, but my white counts were good and they found no sign on bacterial infection, so they sent me off again.

    Today was session #6 of 8 total chemo treatments, #2 of 4 for the DD Taxol. Last time around was really rough pain-wise -- I ended up with lots of weird pain that my doc suspects is neuropathic. It was like popcorn or fireworks, dancing from one spot to another! So this time around, she wants me to take Gabapentin. We'll have to see how that goes.

    To ward against neuropathy, I am also taking B6 vitamins, L- Glutamine (the Glutasolve brand by Nestle was reccommended to me as reputable and easy to use, it's been okay if a bit chalky so far), and have been attempting to ice my hands and feet with only some success. My cancer center has cold packs, but no handy insulated mitts, so we shove the cold packs into pillowcases instead. They get warm in about half an hour. Today I also tried frozen corn packages instead, but that only lasted maybe an hour? The taxol infusion goes for several hours!

    At least I feel like I'm doing *something*, but I'm sure I could be doing this better...well, I have two more infusions to figure it out, heh. So far, I've only noticed a tiny bit of numbness in my heel -- the rest of the odd sensations seem to be connected to the changes to my nails

    Hope everyone is doing well and taking it easy!

    Take care,

    Sherri, (aka EnigmaticFox, who feels like she needs a vacation to recover from her vacation!)

  • Natejordlee
    Natejordlee Member Posts: 61
    edited August 2015

    Hey All Happy monday !! So this was my first round of Taxotere with Neuprogen shots and ended up with a neutropenic fever and an infection in the blood.. spent a couple nights in the hospital with IV antibiotics and now oral. I have had neutropenia every cycle and am feeling very frustrated. I eat well, walk, am careful around people ( starting to feel like a recluse), use antibacterial... not sure what else to do ! That's my rant for today .. good news is I feel great right now .. one week until #7 of 8 ...getting there !! Sending positive vibes out there !!

  • Esmerelda50
    Esmerelda50 Member Posts: 21
    edited August 2015

    AGerl, The doctor gave me a cream to put on the sores on my scalp and they are much better but still there. My blood work was all good, but thank you for advice.

  • Rebecca54
    Rebecca54 Member Posts: 78
    edited August 2015

    Proverbs, I haven't had a cancellation but for what it's worth my good friend did and her hubby is a big Dr. at Hopkins. She actually only did the 1st 2 of what was supposed to be 6 chemo sessions. Last month she was 5 years cancer free! Good luck!

  • gk66
    gk66 Member Posts: 6
    edited August 2015

    I've only posted once so far, way back when I started chemo at the beginning of June. I very thankfully finished #6 of 8 chemos on Thurs. It is quite a rollercoaster ride. Just when I think I know what to expect, something else comes along.

    I had 4 dose dense (every 2 weeks) of A & C and the last 4 treatments (2 of 4 done) are taxol only. Thought I would escape without neuropathy on Taxol, but nope- foot pain yesterday (heel esp) and today foot pain and mild numbness on bottom of both feet :( Took a vit B6 supplement.

    I will tell you- for those of you asking- yes Taxol is MUCH better than A+C! I have even experienced severe joint/bone shooting spasms of pain with Taxol and it is still a million times better than A&C. Very little to no nausea, stlll extremely tired, but a million times better than A+C. As a matter of fact - if I say or think about A+C I gag. :( If I see a red/pink liquid, I gag. I felt so poisoned on A+C and feel none of that with Taxol.

    I hope you are all doing well, keep your spirits up- cry when you need to, but then think positive thoughts. We will be looking at the backside of this before long.

    http://ginakarasek.wordpress.com

  • tamkay123
    tamkay123 Member Posts: 56
    edited August 2015

    I had my first treatment of DD Taxol yesterday. It wasn't bad at all but I did sleep through pretty much the entire treatment due to the Benadryl they gave me in pre-meds.

    I had an ultrasound yesterday to check on any changes in my tumor. There was significant decrease in the tumor and lymph nodes. The tumor had shrunk by 50%. Yay for good news.

  • gk66
    gk66 Member Posts: 6
    edited August 2015

    Tamkay - that's awesome! Here's to shrinking tumors!!

    I got really sick from the first benadryl with Taxol treatment. They said they dose people up (50mg) in case of an allergic reaction, but they gave it to me using a syringe into my IV and I about passed out- it made my head swim, I could barely talk- it was like I was completely drugged. Almost vomited a few times. Then I slept! It was the worst part of my 1st Taxol.

    With my 2nd Taxol- they said since I didn't have an allergic reaction they reduced the dose to 20 mg - and I asked that they give it in an IV drip rather than so quickly with a syringe, and it was much better. It still hit me after a bit, but not so badly. I hate taking benadryl unless I absolutely have to. They said next time they would look into reducing it to 12.5 mg.

  • tamkay123
    tamkay123 Member Posts: 56
    edited August 2015

    They gave mine through the IV. It wasn't long after they gave it that I could feel my eyes getting really heavy. They put me in a bed for the first Taxol dose in case of allergic reactions. I was glad to be in one considering how much I slept

  • J3nny4
    J3nny4 Member Posts: 15
    edited August 2015

    Hi all,

    I'm sure hoping that Taxol is better than AC. But, then, i didn't have nausea with AC, but i had terrible headaches, that chemical drugged feeling and exhaustion.

    For those of you who are following my treatment plan (see below) and have had at least two treatments of Taxol already, after having AC first, do you remember how you felt the days after the second treatment? I have my second treatment of Taxol on September 2nd. I will be flying across the country the day after and "running" (walking) in a 10k on day four. I know we are all different, but i thought i would get your input on how you guys felt. Thanks!

    AGerl wrote: "Another mental struggle I am having is the baldness - I am fine during the bad weeks because it reflects how I feel, but when I have my good weeks, it is another story. It is a constant reminder, and sometimes I just want to take a break from it all and not have it thrown in my face. When I feel good, I want to look like the old me..."

    AGerl, I totally understand what you are saying!!! This is SO, so true. I feel the exact same way. I just never thought about it that way.

  • EnigmaticFox
    EnigmaticFox Member Posts: 54
    edited August 2015

    Hey there, Jenny!

    I'm living it right now, though I'm on dose dense (DD) regimens so I'm not sure if it's the same for you. I've had all 4 of my AC treatments, and just had the second of 4 Taxol treatments this Monday.

    Apparently I'm one of the "lucky" ones who gets pain (nerve and joint) as the main side effect of Taxol, so right now even with gabapentin and ibuprofen and even some Tylenol + codeine, I'm hobbling around feeling like I have severe arthritis. Getting a good preview of what things will probably be like for me 20-30 years down the road (I'm 43).

    Your mileage may definitely vary though! Here's hoping that it will! :)

    Take care,

    --Sherri, aka EnigmaticFox

  • tamkay123
    tamkay123 Member Posts: 56
    edited August 2015

    I have noticed more effects from Taxol then I did A/C but I'm sure some of that could be the cumulative effect.

    Yesterday (day 3), I felt like I was getting the flu. I ended up going home from work a few hours early to lay down before I picked up my son from preschool.

    Today I feel much better but I am definitely achy. My legs keep getting these twinges of pain and I've noticed today that I feel like I have menstrual cramps...and pretty strong ones at that!

  • gk66
    gk66 Member Posts: 6
    edited August 2015

    J3nny4-

    My second Taxol was very similar to EnigmaticFox. Severe joint and bone pain (actually the 1st was worse)- I am also dose dense. On the end of day 2 (the day after chemo) I get he flu like feeling- starting in my neck, jaw, back, etc Then wakeup 3rd day with the joint and bone pain which lasts for 3-4 days. I use ibuprofen during the day and hydrocodone for a night or two. With my 2nd Taxol I got some tingling/numbness on bottom of feet and right thigh and wrist/arm. Left foot better after 2 days, but rest still an issue 8 days after treatment

  • December
    December Member Posts: 108
    edited August 2015

    J3nn4

    Hope you are hanging in there! I know about the bone pain! Thank goodness for the Hydros - although I'm going to try to avoid them as much as I can - They cause intense lower ab pains (constipation? ug) And yea, I've got drugs for that too! Blessings to you!

  • lizannee
    lizannee Member Posts: 16
    edited August 2015

    I received my last TC Monday and it hasn't been as bad as the 3rd one was. Now radiation. I am frustrated because my MO office schedules appointments without asking me if it is a good time, they have everyone come in for labs at the same time and half of the time the reception personnel is rude. This is the worst time of my life and I wish I was at an office that cared a little about me and my time. Is this normal for MO offices?

  • zzlady
    zzlady Member Posts: 19
    edited August 2015

    hi ladies,

    I have completed 4 A/C and 5 weekly taxol so far. My MO skipped chemo last week do to my neuropathy in my fingers. I'm unable to button my jeans, peel a grapefruit ect. Makes me a bit nervous because the neuropathy seems to be getting worse. Not sure what my MO will tell me this week. Anyone else have neuropathy?


  • KarenAus
    KarenAus Member Posts: 94
    edited August 2015

    Whoohoo another milestone covered in this battle. Last lot of the AC chemo done and dusted. I am told Taxol weekly is supposed to be a lot easier. Fingers crossed.

  • DayLily15
    DayLily15 Member Posts: 144
    edited September 2015

    hello :)

    yeah KarenAus and good luck with the next batch.

    Nataleejordi - sorry you had to be on antibiotics as well, i just did #2/3 of taxol and they reduced it from the first due to neuropathy in my feet, this time its is less awful.

    zzlady, my neuropathy was better after 14 days. it was scary . wishing you a good recovery from it too.

    i have been a grumpy, mess and im lucky to have good helpful friends and family. thought i was tougher than i seem to be at this point in time. rant rant .. thank you for this place to be understood.

    hugs to all :)

  • Tresjoli2
    Tresjoli2 Member Posts: 868
    edited September 2015

    I was doing so well. I had "taxol" #10 and now my feet are numb, my hands feel like they have electric current running through them. Today My doc gave me gabapentin to take at night to help? I'm miserable and I only have two more to go.erghhhhhh

  • Espanola
    Espanola Member Posts: 32
    edited September 2015

    zzlady-are you taking l-glutamine?

    Tresjoli2-i was talking to someone who had the electric current thing after her taxol and she said acupuncture helps.... Just a suggestion for after you are done. I haven't tried it yet, I have 3 more DD taxols to finish first.

    I'm so happy this part of the journey is coming to an end.

  • justmaximom15
    justmaximom15 Member Posts: 264
    edited September 2015

    It's been a while since I posted so I thought I better drop in and say Hello. Hope everyone is doing fine.

    I took a little trip this past weekend to Arkansas to visit my newest grand niece. It was a short trip but I saw almost all of my family, the youngest to the oldest (my 86 yr old aunt). Spending time with my family always makes my heart smile no matter what I'm going through.

    I had my last A/C on 8/17 and I go back a week from tomorrow to begin my 12 weeks of Paclitaxel. I'm so ready for all the chemo to be over even though I haven't had any bad SE.

    We hoped to go to Mexico in December and there's a 72hr sale right now for the first couple of weeks in December but I'm afraid to book before I see how I do with this next regimen. I can't imagine a better way to celebrate the end of chemo though.

  • Rebecca54
    Rebecca54 Member Posts: 78
    edited September 2015

    question for the group. I had my last tc on 8/17. Been having some real issues with ankles and feet swelling. I'm getting a little concerned. Any body else had this side effect?

  • gk66
    gk66 Member Posts: 6
    edited September 2015

    lizannee-

    Definitely not normal to have rude and inconsiderate personnel at your MO! Mine are incredibly kind and caring, and when my next set of appointment are scheduled- I sit there with them and we figure out what times and days work best for me.

    I am SO sorry you are dealing with people like that right now- how horrible! I know sometimes there aren't a lot of choices in an area for specialists like this :( But know that there are a lot of people who really do care (including total strangers like those of us on this board) and are very compassionate when dealing with cancer patients. So sorry!

  • LostLittle1
    LostLittle1 Member Posts: 28
    edited September 2015

    Starting DD Taxol # 3 of 4 tomorrow. My experience with Taxol #1 was awful. Severe bone pain on Days 4-7 and Dr had to double my pain meds. I couldn't walk! I had to use a wheelchair. The pain in my knees and hips was excrutiating to the point I called MO and asked to stop chemo altogether, this is the first time I considered stopping. My main complaint on A/C was acid reflux. On Taxol, my knees felt like basketballs filled with broken glass that was rubbing together. For dose #2, he dropped my Neulasta shot from 6mg to 4mg. This helped so much! I had some bone pain from Neulasta on A/C #1-4 but nothing like that. They were just achy sore feeling then but I could walk at least. So lesson learned was don't give up, call your MO! I should have done that on day 4 and not suffered like that. Dose 2 I felt better, no nausea on Taxol at all for me but also no appetite, even with the steroids. I lose 8 lbs in 2 weeks, which I am kind of happy about..Buddha belly is shrinking! With the dropped Neulasta, my WBC did not drop much as I was worried it would. It went from 10 to 6. He told me yesterday I was borderline ready for a blood transfusion if I didn't eat more red meat. Ick I hate most red meat. A burger is ok.. Guess I'm eating at Red Robin tomorrow.

    My finger neuropathy has become worse on Taxol. MO asked if it was bad at beginning and tapers off, no mine is gradually worse. During the first treatment I didn't have any problems until about a week later. Started in left hand pinky and now is all fingers and thumbs. Sometimes feet go to sleep or get really cold for no reason. MO said take B complex to help with fatigue and nerve function. I found some chewable gummies on Amazon that are good made by Nutrition Now and have strawberry flavor for $8.80 for 70.

    Good luck to all the chemo-sabe sisters in the chair this week! I have my coloring books and Kindle ready for tomorrow. xoxo


  • KickinBootay
    KickinBootay Member Posts: 38
    edited September 2015

    Anyone else do neoadjuvant therapy? I am 2 weeks post my last AC seeing my surgeon on Monday to discuss scheduling my lumpectomy. My hope is that I will not need to do the 12 rounds of Taxol isn't that all of our hopes! Hope everyone is well!

  • tamkay123
    tamkay123 Member Posts: 56
    edited September 2015

    KickinBootay - I am also neoadjuvant therapy. I have 2 more sessions of dense dose Taxol expecting my last to be on 9/28 and then I'll meet with the surgeon.

    I have an appt on the 25th with the plastic surgeon. I'm having bmx and we will discuss reconstruction options.

  • justmaximom15
    justmaximom15 Member Posts: 264
    edited September 2015

    I had my 1st of 12 Taxol yesterday and things went pretty smoothly. I didn't have that allergic reaction that I've read some people get but it seems the steriods in my pre-med really hyped me up because I never went to sleep last night and I even took Ativan and benedryl!! I'll crash hard later today I'm sure. It's odd because I've always been given the steriods in my pre-meds but it never affected me like this.


  • Tresjoli2
    Tresjoli2 Member Posts: 868
    edited September 2015

    I am DONE DONE DONE with taxanes as of today! Woo Hoo! I also had my 3 week loading dose of Herceptin. But no more CHEMO!

  • Catfurr
    Catfurr Member Posts: 69
    edited September 2015

    Hi! I started Chemo on June 23rd, had rd #4 on Tuesday. Doing TCHP every 3 wks. Was wondering if it's normal to have pain in the breast where the cancer is? Does that mean it's working?? I had no pain prior to biopsy in May, btw. I had no lumps, just cluster microcalcifications. Thanks!!

  • mama-bear
    mama-bear Member Posts: 35
    edited September 2015

    Hi all.... I am actually an August chemo starter, but I don't seem to get many answers on the other board. I am on 4 rounds of DD A/C and am going in to do number three on Thursday. My question is this.... I have had a sore throat since I started, the dr said it was not infected, or any thing to worry about. But seriously it hurts. Has any one had this and did you find any relief. Is this just a SE to deal with for four more weeks....?

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