Post by jhogan on Oct 22, 2010 13:44:38 GMT -5
Is anyone else as livid as I am over all of this media attention being given to the dangers of hormone replacement therapy as it relates to an increased risk of getting breast cancer?
I read a great post on The Today Show web page dedicated to the issue that served as a reminder that the hormone medications the doctors are prescribing cannot be called hormone replacement therapy as they are not natural and do not replace anything in our bodies, they only mimic the effects of the natural hormones. This post came from a woman who had a need for hormone therapy and was dedicated to using only natural hormones.
Anyhow, my rant stems from the fact that the media and their medical experts are reporting on this issue as if it applies only to menopausal and post-menopausal women. What about women who suffer from the disease of endometriosis and other gynecological disorders that sometimes require hormone therapy and other times result in uneducated doctors throwing hormones at them for lack of better knowledge of how to treat the disease? I want to know if there are any considerations and/or recommendations for the women who eat estrogen, progestin, and other pharmaceutical hormones that are now reported to increase the risk of breast cancer just to get through a single day without curling up in a ball with a heating pad and a bottle of Advil?
Has anyone heard any mention of how the old and the new research on this issue relates to us? One day I do hope that endometrisosis is as much of a cause as breast cancer. I am not belittling the seriousness of breast cancer with its need for chemo and its mortality rate, but, why is it so taboo to rally publicly for endo in an attempt to raise awareness and push medical professionals and researchers to become motivated to do work that sheds more light on endometriosis and other gynecological disorders that are currently labeled and described as "incurable", "mysterious", "cause unknown",
manageable depending upon severity", etc.
The new research findings about hormone therapy drugs should be expanded in scope to include ALL women who have a need for pharmaceutical hormones, and the medical community involved in the research or reporting on the research need to be able to address the issue of hormone therapy alternatives for each sect of women that are affected.
I am outraged that my physicians have NEVER had a conversation with me about the risk I take by using hormone therapy as a disease management technique for endometriosis, endometrial polyps, ovarian cysts, and heavy bleeding. I have a right to make informed decisions about my health care. I have even been told by a gynecologist that I "had to take hormone therapy to control my disease." I had elected to use holistic methods prior to that because the pharmaceutical hormones make me FEEL BADLY!
Looking for feedback and comments, would love to hear from everyone on this matter!
I read a great post on The Today Show web page dedicated to the issue that served as a reminder that the hormone medications the doctors are prescribing cannot be called hormone replacement therapy as they are not natural and do not replace anything in our bodies, they only mimic the effects of the natural hormones. This post came from a woman who had a need for hormone therapy and was dedicated to using only natural hormones.
Anyhow, my rant stems from the fact that the media and their medical experts are reporting on this issue as if it applies only to menopausal and post-menopausal women. What about women who suffer from the disease of endometriosis and other gynecological disorders that sometimes require hormone therapy and other times result in uneducated doctors throwing hormones at them for lack of better knowledge of how to treat the disease? I want to know if there are any considerations and/or recommendations for the women who eat estrogen, progestin, and other pharmaceutical hormones that are now reported to increase the risk of breast cancer just to get through a single day without curling up in a ball with a heating pad and a bottle of Advil?
Has anyone heard any mention of how the old and the new research on this issue relates to us? One day I do hope that endometrisosis is as much of a cause as breast cancer. I am not belittling the seriousness of breast cancer with its need for chemo and its mortality rate, but, why is it so taboo to rally publicly for endo in an attempt to raise awareness and push medical professionals and researchers to become motivated to do work that sheds more light on endometriosis and other gynecological disorders that are currently labeled and described as "incurable", "mysterious", "cause unknown",
manageable depending upon severity", etc.
The new research findings about hormone therapy drugs should be expanded in scope to include ALL women who have a need for pharmaceutical hormones, and the medical community involved in the research or reporting on the research need to be able to address the issue of hormone therapy alternatives for each sect of women that are affected.
I am outraged that my physicians have NEVER had a conversation with me about the risk I take by using hormone therapy as a disease management technique for endometriosis, endometrial polyps, ovarian cysts, and heavy bleeding. I have a right to make informed decisions about my health care. I have even been told by a gynecologist that I "had to take hormone therapy to control my disease." I had elected to use holistic methods prior to that because the pharmaceutical hormones make me FEEL BADLY!
Looking for feedback and comments, would love to hear from everyone on this matter!