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We are so on our own. Sure they tell you that Tamoxifen might cause cervical cancer and osteoporosis, but do they tell you that it also essentially makes sex excruciatingly painful? It's like they assume that you are simply a carcass and not a living breathing human. Don't get me going!. But Paul Levy is trying to help http://runningahospital.blogspot.com/
he did a great post on the side effects of Zeloda and how the drug company refused to acknowledge that a simple henna remedy could work

Yes, we are on our own. I fought the battle with Tamoxifen for two years. Night sweats, fevers, insomnia, you name it... I had it. I had some luck combining effexor with Tamoxifen to help reduce the hot flashes, but I didn't like the idea of taking medications to combat side effects from other medications! What a rat race. After two long, painful years, I stopped taking it. Sometimes the cure is worse than the disease. Hang in there. I hope you find the best dosing/timing that works for you. Take care - all the best, @stales

This same feeling is coming into my life with my wife. She's now on nearly half a dozen medications for various things. The web sites don't have any help, the doctor's don't have any suggestions, and the it seems like the only one that might is a pharmacist. And they can only give general advice. Why is it so dang difficult to give some advice?

Hi,
Wow Nice blog,Itgives very good information on side effects of breast cancer treatments.It's really very helpful to that people who doesn't know about the breast cancer.

I'm an invasive breast cancer survivor on Tamoxifen, and at 35, am enjoying the splendor of night sweats and zero sex drive. Gah. I've definitely given up on finding a solution to these issues, but I'll stick with the medicine.

Hi,
Nice post.It gives very good information on side effects of breast cancer treatments.It's really very helpful to that people who doesn't know about the breast cancer.

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About My Cancer

  • Invasive Lobular Carcinoma
    My form of breast cancer is less common than others. In fact only about 6 to 8% of cases of breast cancer are the invasive form that is based in the lobules, not in the milk ducts.

    Invasive, sometimes called Infiltrating, is a scary word. In most cases this form of breast cancer has been present for 8–10 years when detected by a mammogram or physical exam.

    In my case there was clearly an area that felt thickened or dense on December 6, 2007. A mammogram the next afternoon was not able to detect it but it clearly appeared on ultrasound and was confirmed by multiple biopsies the same day.

    During those 8 to 10 years the cancer took to become apparent to me, there has been plenty of opportunity for those invasive cells to get out of the breast and spread to the rest of the body.

    It is after all, by definition, an invasive form of cancer.

    Each year about 190 thousand women are diagnosed with invasive breast cancer in the US and about 40 thousand women will die of the disease. The larger the mass is when discovered the more risk. Mine had tentacled almost 5cm into the surrounding tissue and two other areas in the breast were discovered as well.

    My chances of living another 10 years without cancer in another area are about 40%. The likelihood of one of my other underlying health conditions doing the job before that is 20%. it took a few months to get used to that idea.

    Now though my attitude is that at least I know what I'm facing. It's just not what I expected. Life changes in an instant.

Funding Cancer Research


  • We Will Not Apeas Cancer

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