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Monday, December, 01, 2008

Long-term side effects of chemo with Taxol

by  Judith Rosenthal Schwartz
Thursday, August 21, 2008
Judith Rosenthal Schwartz
Judith Rosenthal Schwartz
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Judith Rosenthal Schwartz is dealing with permanent peripheral neuropathy

I'm a mom first and foremost - my kids are 10 and 16, with older...

Judith Rosenthal Schwartz

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For the last year-and-a-half I've been really suffering with painful feet.  Now I'm not the sort of person to run to the doctor every time I sneeze, so I tried to figure it out myself.  I tried orthotic-like supports: nothing.  I t...

  1. Good news
    Maria Gifford
    Thursday, August 21, 2008 at 06:10 PM

    Hello Judith,

     

    Good news that you can once again walk, do yoga -- and dance! -- for exercise. That's great! Keep us posted on how you're doing from time to time, and above all -- enjoy the pain being gone and being active and healthier!

     

    Best regards,

    Maria

     


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  2. Glad it worked
    Phyllis Johnson
    Friday, August 22, 2008 at 06:07 AM

    I'm so glad the Neurontin worked for you.  I have neuropathy in my hands and feet, and despite the best efforts of a very good neurologist, nothing has helped me much.  I think part of the reason was that I had neuropathy for about two years before I so the neurologist.  Although sometimes neuropathy goes away by itself, I'd recommend that anyone who has Taxol-induced neuropathy see a doctor right away.  There are a variety of drugs for it now, and some people have good results from vitamin therapy.


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  3. Taxol and Neuropathy
    Marie
    Tuesday, September 23, 2008 at 09:14 PM

    I developed severe peripheral neuropathy while being treated with Taxol for Inflammatory Breast Cancer.  I was receiving the Taxol and radiation treatments at the same time to treat metastatic disease.  I started with symptoms of tingling and burning and itching within several days after my first treatment.  My oncologist prescribed Elavil and it helped but I was very lethargic.  The symptoms got much worse after the second treatment.  The itching was so severe I was using a hairbrush on my arms and hands and legs and feet.  I felt like my arms and legs were crawling or jumpy.  I found an article in an internet search that suggested that the side effects of the Taxol could be reduced by getting it in a 24 hour infusion rather than a 3 hour infusion.  My oncologist agreed to try this and it helped.  I received the same premeds and just checked into the hospital for 24 hour r&r.  The progression of the neuropathy was not as rapid as before but I did not regain any of the function that I lost earlier.  We used the longer infusion method for the remaining treatments.  I was eventually switched to Neurontin.  It has been 12 years since I completed the chemotherapy and I still have severe neuropathy.  I take 1800-2400 mg of Neurontin daily.  Even with this medication, I have bad burning pain when I am on my feet a lot or do a lot of walking.  The only solution for that has been to get off my feet and take pain medication.  Although the neuropathy is painful and limiting, I am still very thankful that I am alive. 


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    re: Taxol and Neuropathy
    amelia
    Wednesday, October 22, 2008 at 12:55 AM

    I received 6 treatments of carbo-taxol for stage 3 uterine cancer. its been 10 months since my last chemo.  I have significant pain and numbness in my feet and have since Dec of last year.  I went to my oncologist today and she told me I may have this pain and numbness for the rest of my life.  I am on gabapentin already along with some oxycodone.  After a long day at work I will be in significant pain no matter what medication  I take.  In addition, the joint pain that I am having is apparently because of the lack of estrogen because of the hysterectomy.  I cannot take estrogen because of the uterine cancer being estrogen receptive. 

     

    I am very glad to be alive, dont get me wrong, but as I am sitting here writing this I am have various shooting pains and pain in my feet.  I am overwhelmed by this diagnosis, maybe even more than the cancer itself.  I mean they went in and got it out, but I didnt think about the aftermath.  I was told most people have nueropathy for 6 months or so.  The doctors also told me that a small % of people get permanent issues.  I just didnt think it would be me.


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