Taxol Chemotherapy
Comments
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I just had my first Taxol infusion, the first of twelve, last Thursday. Tomorrow I am scheduled for round #2. The first went surprisingly well...soooo much better than the A/C. I found that on Day 3 I was fatigued and exhausted, but without the severe aches and pains like I had with the A/C. And I wasn't nauseous at all, which I gotta say was a very pleasant surprise.
Now....my concern....like you, chapter4, I have numbness in my face. It showed up on Day 6. It feels like I've had a novacaine shot that is just starting to wear off. It's just in my chin. What IS that? Since I'm so new in the Taxol game, I'm a bit alarmed and concerned. Of course, I'm going to ask my doctor when I see him before my next round tomorrow, but I wondered what you all may know before I head in,and if this will in any way derail my current 12-step program. -
CSmommy- my dr didn't seem concerned about the numbing of my chin and around my mouth. I have my last taxol is on Tuesday....the numbing comes and goes...sometimes it's more intense than others.
Steroids....they just may be the worst part of taxol for me....they drive me crazy too...I'm dreading this next round....but it is my last! The radiation....then they tell me I have to wait 6 months to a year for reconstruction! Great....... -
My doctor wasn't too concerned about the numbness, either. He gave my mouth a good once-over to check how my teeth &j jaws were faring, and just said to keep an eye on it. He mentioned something about the mental nerve that goes down the jaw line, and that it may be affecting that, or I could be having some "normal" jaw and teeth problems that is doing it (I have notoriously bad teeth...began 2012 with a root canal. Sheesh....shoulda known 2012 wasn't going to go well). Like you, it comes and goes with the severity as well. Like at this moment, it feels just fine. Bizarre.
Congrats to you on nearing up the end of your taxol!! -
I will be joining yo ll next Tuesday. I have read thru the thread to re-aquaint myself with this stuff. I did six TCH last summer and really dkidn;t do bad til the last 1. Lost my hair right at 2 weeks last time-hating the very thought of that again. Glad to see some of you are working full time. My onc isn;t in favor of it but I am going to try. I work in a factory where the temps have been averaging 110 degrees most days. The one thing i do remember from last summer was the fatigue part of it-and the bad tastebids. i have stocked up on lemonade and chicken. they were my go=tos last year.
I will have to get some of the gltamine and acetyl carnitine too. I did ice last year and never lost a nail but i would really like to find out where to buy some of the fancy gloves/socks i stead of the ice or pea bags.Anybody got a web site for that?
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Tweetyb422, I am in the same boat with you (and I'm sure many others!)!! I've never been so down, weepy, and overwhelmed in my whole life! I will be on my 2nd round of DD Taxol this Wednesday and I think it's soooo much harder than DD A/C!! The nausea was horrible on A/C but that's about all I dealt with. Now I deal with debilitating bone pain, (at times) overwhelming sadness, extreme fatigue, and insomnia, to name a few. My Onc team claimed Taxol would be "sooo much easier!!" I meet with them before my 2nd round so I will have a few choice words for them! On A/C I would be knocked down for 1 week, then I'd have a whole week to feel good and normal. It took over a week and a half to feel even partially normal and now I'm starring down the barrel of another Taxol treatment in 2 days... NOT FAIR!!
I'm trying so hard to take each day as it comes... because when I think about what is coming up in a couple of days I just want to quit. But we can do it!! My new motto (thanks to a fellow chemo patient), "put on your big girl panties and deal with it".
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Hi all I'm 17 days out from my last DD Taxol. Feeling much better energy wise and mentally! Had surgery on the 19th even. It does get better!
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Need some more input from everyone. Couldn't finish my 12 treatments of Taxol. Had 3 blood transfusions and my neuropathy got worse. Did complete 8 of them. My doctor is recommending a month for my body and mind to heal. My neuropathy has left me with loss of motor control, weak muscles, burning and tingling hands and feet. Some loss of vision too. I need to know what is out there working for you with shoes and relief for symtoms. Also, what is working for you when it comes to hormone therapy. Pros and cons.
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Sonant,
Sorry to hear you're having such a hard time with Taxol. But glad to hear your doctor has taken you off the drug to give you time to regroup.
For my Taxol-induced neuropathy, which affects my feet, cushioning is the most important thing. For the gym or walking outside (I'm able to do this with support--on a treadmill or with a hiking stick, in part because I also have arthritic knees), I wear New Balance running shoes. I'm no runner, but they give me better cushioning and are lighter than their walking shoes. The WR840 work best for me. Like walking on a trampoline.
I can also recommend Mephisto cork-bed sandals and Finn Comfort sandals (the Finn Comforts have removeable and replaceable cork-based footbeds). Both expensive, but when your feet are a problem and you want to walk for health and enjoyment, expensive footwear it is.
I take Femara for hormone therapy. I have a lot of complaints related to achey joints and lack of stamina, but I think they're related to my arthritis. Age is also a factor. I'm 61, and achey joints are common complaints among my friends who DON'T take hormone therapy. In any case, I don't think Femara is causing my joint pain. If it protects me in any way from the possibility of recurrence, I'll gladly take it.
These can be hard situations to adjust to. I know that for many women, the neuropathy is short-lived and resolves after treatment ends. I hope that's the case for you! But please try not to get discouraged. If the Taxol keeps the cancer at bay, well, it's a good thing.
Wishing you good health and peace of mind.
Ann
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Taysmama - I was right exactly where u are now, feeling the same way. I finished taxol last week & I do feel better. The emotional roller coaster ride was the worst for me especially after infusion. Taxol is known to depleted the neurotrsmsitters in yur brain that regulate the emotions, but they will level off. My second infusion was the worst emotionally.. it will get better but it totally sucks along the way. So many woman have talked about everything leveling off once they are done..it is the getting done part that takes the longest. My onc office also told me taxol would be easier, but it wasent for me either, just a different bag of se. Hand in there, u can do this!
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Sinant- I am done with 6 treatments and had to have an infusion. I am getting very nervous ad to how many more I will need. Could you please tell me how often you needed infusions. Please PM me if you would prefer that. Any insight you can provide will help.
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Quick question for those that have had neuropathy with their hands and feet. I just finished my fourth Taxol infusion yesterday, and noticed that I'm getting the pins and needles tingling in my feet. Is this the beginning of neuropathy, or do I just need to stop sitting so funny? Apparently, I'm a criss-cross-applesauce sitter. If I get up and walk around, while it's painful, it does eventually go away. Just wondering if this is the beginning, or if I just need to change my sitting habits.
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When did you all begin to lose your hair? I am Day 15 and no signs yet. Now that I've said that aloud, you know it will start!
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Lauren,
I had A/C before Taxol, and lost my hair at....about 15 days! I noticed it when I would tuck my hair behind my ears, and it fell out in my hand instead.
I didn't lose my eyebrows/eyelashes with A/C, but now that I'm on Taxol I'm losing those. I counted 23 eyebrow hairs yesterday morning, and now 16 this morning. I'm currently 22 days out on Taxol.
Hope that helps.
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CSMOMMY,
That is how my neuropathy started. The first couple of weeks I had it, I had that pins and needles sensation for just a few days after the Taxol, then it resolved. I'm getting ready for Taxol #12 on Monday, and at this point, the pins and needles sensation is there all the time. I feel it from my fingertips to my just above my elbows with some mild numbness in a couple of fingers. I feel it in my toes up to my ankles with some moderately numb toes on each foot. Sometimes there is a mild stinging like pain in my toes, but for the most part, it is has just stayed as more of an annoying sensation.
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Hi Hopeful,
My first and second blood transfusion was during my third, and after my fourth A/C treatment. Had four treatments. Every other Thursday. My last blood transfusion was during my Taxol. After my fourth treatment. Was going every week for Taxol. Had to take a week off because of my blood count going down. I was able to recoup and continue without another transfusion. Only made 8 treatments because of the neuropathy. My doctor was afraid the damage would become permanent.
Just hang in there. Everyone is different. Hopefully you won't go through the same thing I did. Will add you to my prayer list. Actually everyone with cancer and dealing with chemo and treatment are on my prayer list!
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Sonant- thank you so much. I am done with the AC and done with 6 Taxols, 6 more to go. It appears that Taxol makes my counts go down quite a bit each week. I had one transfusion. Thank you so much for adding me to your prayer list. We all need the prayers to get us through this.
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Hi My onc has assured me that Taxol would be a breeze compared to the nightmare I experienced with AC--I was bedbound with severe fatigue and stomach issues for 11 out of 14 days.
My onc has said that neither taxol or herceptin are immuno-suppressive chemos so I was wondering why the need for the blood transfusions. Also, for those who are experiencing low blood counts with taxol, did you also have that problem with Ac?
Thanks in advance
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hi did you also have low blood counts with Ac?
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I just finished my last of 12 Taxol cycles yesterday. My hemoglobin dropped from 12.8 to 9.0 with the Taxol. My oncologist said that count could continue to drop for another several weeks before stabilizing. My hemoglobin dropped from 14.0 to 12.8 while on the Adriamycin/Cytoxan. My white count and platelets dropped on the A/C but they stayed within normal limits while on the Taxol. I had Neulasta with the A/C but not with the Taxol.
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My WBC counts have remained above normal on Taxol, and even after I dealt with an infection last week they were still above normal. My A/C rounds, on the other hand, had them all a mess. I received the Neulesta shots with the A/C. I was looking at a graph of my WBC just the other day and marveled at the wackiness during A/C, but the Taxol has remained relatively stable.
This time around, however, my RBC are below normal. I didn't have that issue with A/C. But it hasn't become an issue yet.
I apologize if this question has been asked before, but regarding the neuropathy with Taxol, does it come and go? I just finished up Taxol #5 today, and I noticed this evening that for the first time the heels on my feet were numb. I've had pins and needles off and on for a few weeks, but never noticed numbness until today. It lasted a couple of hours and went away. Is that normal?
As if anything with cancer and chemo is normal.
Including the darn insomnia I get on chemo days. Holy Moly. -
Interesting to see that I am not alone. During AC my WBC went down, but managed to get though without Neulesta. Rbc dropped a little but remained stable. Weekly Taxol made my RBC drop from 10 to 7.2 in five weeks. My WBC is low but stable with Taxol.
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Hi weekly taxol group
I have just finished my 3rd weekly infusion of taxol/herceptin. Main side effects are fatigue and loss of appetite starting on 3rd through 6th day in.
But I have also been experiencing abdominal/bowel cramping before bowel movements. It is not diarrhea or constipation just incomplete cramping bowel movements --sometimes many of them. not only is it painful but it makes it hard to plan on doing anything because I fear I will have to rush off to public restroom and sit for a long time with these cramps and unusual bowel movements--not an ideal way to spend the day.
Anyone have this experience? my mind is going to bad places--do I have colon cancer?--and my onc just brushes it off as a side effect of taxol. If I knew what is causing in maybe I could try some meds or diet to relieve it.
Amyone?
Thanks Carol
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I too get those cramps in the early days. They are way low in my gut and almost feel like menstrual cramps-sometimes they are sobad I cann;t stand up straight. I use heat and take Tlenole and just wait them out. Sorry I can;t be more helpful but I know jusy what you are talking about
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Hello ladies,
Hope all is well with everyone. My neuropathy still continues. If you have any tingling in hands and feet, make sure you tell your doctor. I waited and made mine worse. Lesson learned and passing this on to all of you! My hair is starting to grow back. Eye lashes and eye brows have returned. Wahoo! I start on hormone therapy next. I can start finishing up with my tissue expanders. My port has been removed. Starting to feel a little more rejevinated. God has really been good.
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I haven't had any adverse side effects from the Taxol, which I started 1st on April 12, 2013. I'm on week 6 of 13. Going every Friday. I've been energized and feeling better than I have felt in 1-2 yrs. I do start having rib pain one day prior to next chemo. Most of all the posts are doing Taxol after the Cytoxan & Adriamycin. Not sure why my onc chose to do it 1st. Has anyone else had this regime? My hair started falling out rapidly after the 4th session of Taxol so I had it shaved. Now 2 weeks post baldness I have folliliculitis, which is tiny red bumps all over. My chemo nurse said its because I shaved it before it all fell out. And it's also due to the chemo. Any suggestions for getting rid of the bumps? She rec OTC hydrocortisone cream.
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Mommacharb, there is a "weekly taxol" thread with more up-to-date postings. Check there and you will be more likely to get a response.
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I was told to that Alra hair conditioner is the way to go. My local hospital carries it but it is available online for a few dollars more.
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hello to all
I'm having tomorrow my #7 taxol treatment of 12. but I'm really terrified because I have rectal bleeding as side effect. The truth is that started after 5th treatment and constipation that I had. I have red blood on the toilet paper. I know i have hemorrhoids for sure because I had a colonoscopy back in 2010. My onc doesnt seem very concerned about this he told me to eat properly for the constipation and to take a gel for the area in case there is a tear...
Also my GI doc told me that taxol has that as SE. Also I've an IBS because of my anxiety. Has anyone has this as a SE of taxol? I also have nose bleeding (not so much).
Thank you for reading
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NoteRed—you should re-post this over in the Weekly Taxol thread. This one has been dormant for five years.
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Thank you I'll do that
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