Suzanne Somors hormone replacement???
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Hi, Artsee:
Talking about Herceptin. I am delighted that it saved your dear friend's life. It is comforting to hear good news in the world of breast cancer.
I attended the Premiere of the movie "Living Proof" here in my area (http://www.mylifetime.com/on-tv/movies/living-proof). Got to meet Renee Zellweger, guest of honor. Na!!!!
Of course, this is the story of Dr. Dennis Slamon, the inventor of Herceptin. I did have very high hopes when I set out to attend that fund-raising party (benefiting, it goes without saying, breast cancer research).
But what a disappointment it was!
The movie is inaccurate due to the way that it "cutesyfies" breast cancer. Dr. Slamon is portrayed as some kind of mad genius. Makes it sound like he just discovered the antibiotic, or created the anti-polio vaccine (there is actually a scene at the end of the movie showing him entering a stadium running like an Olympic champion, and in the stadium are the "ghosts," I guess, of millions of women who died before the "fabulous" invention of Herceptin was out, cheering him on his victory lap on the tracks. No kidding.)
This is light-years from reality, of course, when one knows that antibiotics and the anti-polio vaccine, among others, went on to save literally millions of lives worldwide. Whereas the absolute benefit on Herceptin is 0.76 percent (of course, the relative statistic is, I believe 73%; I work for an organization whose job is to establish development statistics for different countries in the world, so I know something about how statistics can be made to say just about anything you want them to say for political reasons).
And I am not even going to start talking about the side-effects.
This movie has women with Stage IV cancer (all looking absolutely lovely and ravishing right through chemotherapy, radiation, etc...) first despondent over their health, of course, letting go of life in a torrent of heart-wrenching tears................. And so on and so forth (you get the idea: Typical Hallmark Channel type)...
But by the end of the movie, here they go: riding into the sunshine (post-Stage IV), all cured after a few weeks on Herceptin, some going on to marry Prince Charming, and now in the pinkiest of health, just like breast cancer never ever entered their lives.
This movie is an insult to the intelligence of anybody who is fighting Breast Cancer. It certainly is an insult to women. But what makes me even angrier is that, by attending it, I participated in yet another fund-raiser for breast cancer. Big business, which has been making billions and billions for corporations (some of them actually guilty of spreading cancer through pollution and the use of dangerous chemicals, including pesticides). And cancer rates are still increasing (here again, some statistics show that they have declined: that's because of the WAY said statistics are presented).
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This forum sure has gotten interesting...I am the person who experienced a growth of her breast cancer on bio-identical hormones and a reduction in the tumor when I went off of it...everything I read at the time had convinced me they were safer than regular HRT and for me they turned out not to be. HOWEVER...things are never simple. I do NOT believe that BHRT caused my cancer--I believe that it fed my cancer...I also know that many studies have shown that women on HRT have lower grade cancers and better survival rates than women who did not. That certainly was true for me as I had a very low grade tumor that had a very low proliferation rate. Was my HRT in some form protective? I don't know. I would not choose to go back on any form of estrogen--but I would consider bio-identical progesterone to balance my estrogen. I also know that I feel better with some estrogen and was miserable on an Aromase Inhibitor. Also a recent clinical trial showed success in treating stage 4 cancer with estrogen when inhibitors had stopped working--to "confuse" the tumor. Sooo, perhaps we all need to be a little humble about what we know and don't know and very respectful of the hard choices we all have to make. God Bless you all as you make these tough decisions!
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Yazmin: it's interesting what you got out of the movie and what I did (having met the man).. IMO the movie was an attempt to show how difficult it is to do research, how many obstacles he had to jump thru for the pharmacutical companies (and FDA) he tried to work with (and did work with), the incredible help one women can be to helping - in this case the women who's life he had saved and her attempt to make that gift of life available to the rest of the world. How DIFFICULT it is to be a person determined to help, for alturistic reason, any one person or any one disease. How she turned his life around by making people listen to her about his medicine (yes she did have pull with Avon). It is a wonderful drug - though even Dr. Slamon I sure would suggest he is not some hero and but that this country needs to change it's policy on science and our goal of real healing.. That's what I got out of that story "based on real life", but yes I'm sure it was glorified to some degree.. but that man goes out of his way when he hears that someone's life is in trouble - I know this from personal experience. How could that be a bad thing for breast cancer patients.. I think he has moved us into the real world where we know how difficult and sometimes impossible to take even the best of science and apply it and that all of the money collected for bc research is not moving us any closer to a cure and yet he was able to move MOUNTAINS with a little help from his friends. Also, that was a trial they showed in the program and so not all the women were "saved".. but indeed it was Hollywood! The man deserves his 15 minutes of fame and so did the women who "tested" that drug for the rest of us.. It was also a real testiment to how we should all try to be in "trials" if at all possible, how we should all try to do our part in helping not only women with bc but everyone within our circle of influence.. THis is just my interpretation of the movie - not challenging anything else you might have said about where we are with medicine etc.. just my commentary on your commentarry. Best
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sarabhealed:
I pasted your previous post further up in this thread, because we were all frantically looking for you, at some point.
This new post of yours is extremely interesting. It sounds to me like there is a new school of thought burgeoning right beneath the surface, according to which estrogen is NOT the culprit, after all. This would be awful for all the people who have been enduring SERMs, AIs, etc..
.......But it has happened before. After I had already been put through 5 rounds of the abominable TAC chemotherapy, it became official, in 2006, that ER+, PR+, HER- tumors do not benefit from chemotherapy, after all, and I did not complete my chemo course........Meanwhile, of course, myself and a few million more women had gone through dangerous and devastating chemotherapy during the past 20+ years, supposedly to reduce recurrence.
And all they have to say to us is: "Sorry: there is no benefit from chemotherapy for your type of tumor." [little cynical voice]
Frankly, I insist that research teams need to start including patients on the different approval panels to help navigate research directions. Right now, research is too money-and-pharmaceutical-companies driven.
Perhaps that's why cancer seems to be more prevalent than ever, despite all the pinkwashing.
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Sarabhealed, your post really interested me because you said that you would consider progesterone, since that is what I am thinking too. What do you think about estrone, which I have read is considered a protective estrogen as opposed to estradiol which is not? Have you any advice about finding doctors who understand BHRT to monitor use?
I think I saw part of this movie. Was it on TV recently?
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prettyinpink100, you wrote: If you can't trust the drug companies how do you trust those that are making millions without ANY guidelines or requirements?
Again, I reiterate what I am actually saying, which is: there are good and bad products on both sides. I firmly believe in doing one's own research before choosing to take either a supplement or a regular drug. I do deplore the OVERPRESCRIPTION of drugs, NOT their use. Example: Tamoxifen is a good medicine, it is saving (for another 5 years) the life of a friend of mine, who is battling uterine cancer. But I personally turned it down, because I feel this excellent drug should target a minority of women (in view of its potentially serious side-effects). To slap everybody with every drug available is not simply wasteful (which is why insurance rates keep on shooting up on us), it is also dangerous for many patients (it was just discovered recently that Tamoxifen actually FUELS HER+ tumors; thankfully, it also does absolutely nothing one way or the other for yet another portion of the patients). Herceptin is also a life-saver. But not for everyone. Unfortunately for many patients, all they will get out of it is heart disease (without the benefit of being cured from cancer). And for those patients for whom IT DOES WORK, AND THERE ARE SOME one can only count on that benefit for about 1 year or 2.
All I am saying is: Let's aim research at overall survival (as opposed to 1-2 years "extensions" and temporary tumor shrinkage, which is currently an obsession for researchers); let patients have a say in the way that drugs are developed (as advocated by NBCCF). Let's make it a priority to find tests which reveal who really benefits from which substance (as opposed to giving everything to everybody). And let's make sure that the drug-approval process is completely independent.
Someone is implying further up that she feels I don't like doctors and that I am simply against conventional medicine. Nothing could be further from the truth. I am advocating a reform of conventional medicine to take patients into consideration and to reduce financial pressures on research. I actually have a wonderful oncologist, a great GYN, and I just love my General Practitioner.
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Vivre, is this the estrogen you're thinking of? This is the one Dr. Jonathan Wright uses: This article was excerpted in part from the book What Your Doctor May Not Tell You about Breast Cancer, by John R. Lee, M.D., Dr. David Zava and Virginia Hopkins, which has a detailed chapter on estriol and a complete list of references on estriol research.
Estriol, the Safest Estrogen
Estriol is a Safe and Effective Hormone for Menopausal Women with Hot Flashes and Vaginal Dryness
Estriol is a type of estrogen made by the ovaries. It is one of the primary hormones of pregnancy and as a hormone replacement therapy it has been used in Europe for many decades. Until the advent of bioidentical hormone replacement therapy (BHRT), estriol was rarely used in the U.S., because the pharmaceutical industry here is not interested in a nonpatentable medicine, no matter how safe and effective it is.
In a review of estriol in the 1980s, Dr. Robert Greenblatt, one of the foremost researchers in hormone therapy at the time, commented that "the ability of estriol to relieve vasomotor symptoms [hot flashes] and to improve vaginal maturation [prevent vaginal dryness] without inducing notable side effects, is sufficient reason for it to be included in the management of the postmenopausal syndrome." In other words, he felt that estriol should be considered as an effective and safe form of HRT because it prevents menopausal symptoms like hot flashes without causing side effects so common to conventional estrogen replacement therapy.
Estriol Protects Against Breast and Uterine Cancers
That estriol is a very useful form of ERT wasn't news to Professor Henry Lemon. He and other clinical scientists had been saying this for over 30 years. In fact Dr. Lemon stated in a 1966 article published in the Journal of the American Medical Association that "Estriol offers a nontoxic, physiologic antagonist for ovarian estrogens, inducing little or no endometrial proliferation in postmenopausal women, which together with progesterone might simulate the protective effect of pregnancy upon subsequent breast cancer risk." In other words, estriol could be used as a form of ERT to protect the uterus and breast from cancer.Estriol as a Replacement Estrogen in Breast Cancer Survivors
Dr. Lemon also researched how effective estriol is in treating women who already have breast cancer. His rationale was that estriol, unlike estradiol or estrone, had not been shown in animal studies or human clinical trials to stimulate the uterus or breast cells, therefore making it an ideal candidate for ERT in very high risk women whose breast tumors were estrogen sensitive. A clinical trial of 2.5 to 5 mg per day of estriol therapy in 28 premenopausal and postmenopausal breast cancer patients demonstrated that estriol induced remission or arrest of metastatic tumors in six (37 percent) of the women.Estriol Prevents Vaginal Atrophy and Urinary Tract Infections
At menopause a common problem is degeneration of the vaginal lining, which can make intercourse painful, and renders the vagina more susceptible to invasion by bacteria, causing urinary tract infections. Several studies clearly show that a vaginal estriol cream can prevent such urinary tract infections in postmenopausal women, and this is estriol's primary use in Europe.Estriol Does Not Cause Blood Clots
A very serious problem with using estradiol or estrone in a minority of women (1 out of 5,000) is that it increases the risk of death due to deep vein thromboembolism, which means the formation of life-threatening blood clots in the veins. Estriol, on the other hand, has very little effect on the blood clotting factors. Doses as high as 8 mg per day have not been found to increase the risk of blood clotting. Dr. Lemon also noted that estriol did not cause any problems related to thromboembolism in his clinical study exploring the use of estriol for treatment of menopausal symptoms in breast cancer patients. This was also the consensus of a review committee that met in the 1980s to review the clinical efficacy of estriol.Estriol Protects the Skin From Aging
It is well recognized that the time around menopause is associated with more rapid aging of the skin. Estrogens are important for the structural proteins collagen and elastin, which give the skin elasticity and structure, as well as hyaluronic acid, a naturally occurring "moisture retainer" under the skin. Studies published in the mid to late 1990s demonstrated that estriol, applied as a skin cream directly to the face, remarkably reversed wrinkling and other problems of skin aging associated with the onset of menopause.How to Take Estriol
The typical oral dose used in Western Europe is 2 to 5 mg daily, but because much of it is "dumped" by the liver immediately, this may only ultimately amount to ½ to 1 mg of estriol actually getting into the body.Many clinicians use an estriol cream that delivers 2 to 5 mg. When made as a cream, the pharmacist should indicate on the container how much cream it takes to provide the 2 to 5 mg of estriol. When you deliver estriol to your body via a cream, it is delivered in a much steadier fashion, whereas given orally it is subject to all the variables of how the digestive system and the liver are working from hour to hour.
An estriol cream that delivers 0.5 mg, used every other day, has been shown to be very effective for treating vaginal atrophy and urinary tract infections. Published studies show that 0.5 mg estriol delivered every other day for 2 weeks, is adequate for most women, and this is how estriol is used by most women in Europe. The reason that estriol is used only every other day is because it doesn't clear from the body as fast as the other estrogens and therefore one dose will last for two days. Using it every day can result in excessively high levels. Although estriol does not absorb through the skin as rapidly as estradiol or estrone, studies have shown that topical delivery of estriol is about twenty times more efficient than oral delivery.
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Deirdre1:
Yes, perhaps I am being a little tough on living proof. I tend to be overly, overly sensitive about everything related to breast cancer. I have little mercy on research, etc...
Now that I have read your (very different) impression, I plan to go get a copy of this movie and view it again at home with an open mind.
You are absolutely right in saying that the (real) Dr. Slamon is a man who goes out of his way to help his patients.
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Yazmin--I know what you mean about chemo and I turned it down too...at least they have the oncotype dx test to help people make the decision now--but how awful that so many have put up with the side effects AND after-effects when it didn't help but only compromised their immune systems.--I am on your wave length about meds--some are lifesavers for the right situations, but they are overused in others.
Vivre--love your posts! I know estriol is considered the "good" estrogen and I like Lee's stuff BUT my bio-identical hormone was 80% estriol and the cancer still grew. I know I have been estrogen dominant over the years and had great success with progesterone suppositories for PMS years ago. Now that the Femara is out of my system and I'm starting to have more estrogen I plan to test levels and see...my compounding pharmacist actually knows more about it than most doctors, but there is a wholistic doctor in town who does this stuff and my oncologist is fine about working together with her. I still am confused about saliva testing (which I've done for years and Lee recommends) and some recent stuff that says blood serum levels are better after all...still researching that, but interested in info that others might have. I also use flax seeds, calcium d-glucarate, and am getting cruciferous complete to take instead of I3C which I have been taking.
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Herceptin reduces recurrence of Her2 positive breast cancer by 50%. Why would anyone quote "absolute" statistics? It is completely irrelevant. When you have Her2 positive disease, anyone in their right mind would take a 50% reduction in recurrence. This type of bc is virulent in its ability to grow and spread. It used to be a death sentence.
What side effects? The tiny percentage of heart related problems MOST OF WHICH resolve if the drug is discontinued or delayed for a time? My LVEF started at 71% when I began Herceptin and was 77% when I ended. It is thus for most women. Vastly most women.
Herceptin is literally a miracle drug for Her2 positive women.
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Sarahb-what is cruciferous complete? Sounds interesting. I read that saliva testing is more viable when we are premenopause, because hormones fluctuate more then. But the blood tests are more accurate and are the best for menopausal women. There is so much info out there that the key is estrogen balance with progesterone. I sure hope they start to give more credence to this. It just seems so much more logical. I just can't get past the fact that the incidence of bc goes up, as our estrogens go down as we age. Yet we are still estrogen dominant because we have no progesterone. I wish they would get this all straight!
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Hi Yazmin,
Just wanted to say that overprescribing is one problem with antibiotics, but the other side of that is non-compliance in the general population of completing the meds. Many people start to feel better and do not take the whole term of the prescription. This in turn leads to the 'bug' being able to replicate and become resistant to that antibiotic. And even worse - resistant to the whole of the 'family' of which that antibiotic belongs to. I worked in a large suburban hospital and we continually saw abcessed wounds of those, sadly, drug addicted. They would come for treatment, get an antibiotic, discontinue it and be back again because the wound had abcessed worse or yet again, and at that point, many antibiotics wouldn't work. So it isn't always just over-prescribing. I do believe that antibiotics have been overprescribed, and I think a lot of that has to do with people demanding them of their doctors and not knowing that antibiotics don't help everything - like a cold. And sadly, doctors themselves are to blame in some of those cases. A quick fix, the patient is happy, and everyone goes on their merry way thinking everything is fine. I heard recently that there is some thought that the overprescription of antibiotics and the overuse of antibacterial everything has caused an inability of our children to have the natural good bacteria in their systems to fight some common things like colds.
Just my own observation.
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At this point, I'm reluctant to move forward with hormone therapy. I really should talk to my naturalpathic doctor first. One year ago my pathology report read only 3+ estrogen and 1 + progesterone. That seems very low. I wonder if my estrogen level had anything to do with my cancer? And does dcis differ in receptors? Does dcis have estrogen receptors? Since its not invasive cancer would the hormones effect it? All I hear about dcis is that they know so little about dcis. It gets thrown in the whole cancer catergory. Perhaps it reponds differently to hormones?
Forgive me for being a little dense when it comes to hormone therapy. I' have only looked into this since hearing of Suzanne Somers interview with Ophra.
Like I said before, if bioidentical helps, why not consider it...just unsure right now. B Barry
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>> Why would anyone quote "absolute" statistics? It is completely irrelevant.<<
I don't think it's irrelevant. I think we are constantly bombarded with information that is inflated and purposely designed to deceive, and it starts in the grocery store. If the pool of people benefitting is 40,000, then 50% would be 20,000. If it's only 20 people, then 50% is only 10.
With an annual bc death rate of approximately 40,000, anything benefitting less than 400 people is less than one percent of the total death rate per annum. And by the way, the statistics from the Journal of the American Medical Association (JAMA) report a death rate of approximately 140,000 people per year are the result of taking pharmaceuticals. So yes, I think if a doctor is going to convince me that I can prevent a recurrence by 50% if I just take a pill, I'd want to know 50% of what. Then I'd want to know the side effects.
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abinneb: You are 100% right about non-compliance and the role of the doctors themselves in helping create resistance to drugs that were absolute miracle drugs when they were discovered a few dozen years ago. Thank you for clarifying this point.
althea: Your analysis is so........right to the point. Nothing to add.
barry: My understanding is that they are not EVEN sure DCIS is actually a cancer; Some oncologists definitely don't see it that way at all. They know little about DCIS (and about everything else), but you are in very good shape with a non-invasive "cancer" (if we end up accepting that it is, indeed, cancer). I would play it safe, maybe? (if all I had to worry about was a DCIS, that is).
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I may be wrong, but I believe that as we go into menopause our hormones continually flucuate. They do not just gradually lessen. It is those flare ups of hormone that cause havoc on our systems.
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Here is was Dr. Reiss says about hormone levels and menopause:
onset menopause-This category refers to the first few years of menopause, where women still experience large fluctuations from time to time, yet less frequently than during perimenopause. There is no menstral cycle. This is when symptoms of deficiency are at their peak.
midmenopause-This category refers to the next 5 years of menopaus, that is, women who are three to eight years into the change. Estrogen fluctuations still occur however, they are minimal. There is a significant reduction of symptons such as night sweats and hot flashes at this time.
late menopause-This group generally includes women over 60. They have been in menopause for 10-15 years or more. There have been barely any fluctuations in their estrogen.
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I had very few symptoms of low estrogen during menopause, no night sweats and only occassional and mild hot flashes. This is what Dr. Reiss says about women like me and why I am so concerned about my low levels of progesterone:
"There is a reason for concern here. The relatively higher level of estrogen at this stage implies the existance of estrogen dominance. Remember, there is no progesterone in the body to balance the estrogen. In medical terms, we say the estrogen is "unopposed". We have to be alert to a potentially threatening imbalance that could lead to cancer and have negative long term effects on a women's health."
I continue to ask: If doctors know this, then why do they continue to block estrogens, and not balance hormones???
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Actually, this discussion has got me thinking harder. I just realized that I have not been giving enough thought to the issue of hormonal BALANCE. The more I read this thread, the more convinced I am that I have to make it a priority to look into it, and I now plan to discuss it with my general practitioner (I could never get my oncologist to "deviate" one millimeter from the literature, although I would not call that deviation, but innovation. But He!).
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Vivre and interested others:
Cruciferous Complete was recommended by my Chiropracter it is a whole food substance that gives you all of the phytochemicals in organic cruciferous vegetables. I've been concerned about the controversy around I3C and DIM and I think taking the whole food might be better...Metragenix also did a study--small but impressive--about it's detoxing effects. Metragenix also has a urine test that looks interesting that can monitor what estrogen is being excreted. Here is one of many articles you can read if you google it...
Women, Cancer and Vegetable Powder
Health Alert, October 2008, Volume 25, Issue 10
Most women know that too much estrogen is related to higher risks of breast and uterine cancer. That is why the breast cancer rates fell dramatically for the first time in history when women stopped taking their doctor prescribed estrogen. But what if your own body makes too much estrogen?Normally your organs of detoxification (kidneys, liver, etc) eliminate excess estrogen. That is one reason why detoxification or purification, which enhances the way your body detoxifies, is important, especially in cancer cases or for those prone to cancer. The liver and other organs of detoxification use phytochemicals from vegetables (especially whole cruciferous, brassica vegetables such as brussels sprouts and kale) to enhance liver detoxification.
A recent study clearly showed that consuming a special dried vegetable powder made up of organic Brussels sprouts and kale significantly increased the detoxification and excretion of excess estrogen. Estrogen excretion was measured by what is known as its best marker-the 2/16 hydroxyestrogen ratio. And this is important for premenopausal women who have breast problems, breast cancer in the family, or who already had a breast or uterine cancer.
This study was done by the Metametrix Institute on a vegetable powder, Cruciferous Complete, grown and processed by Standard Process. Metametrix does not sell this product and is therefore unbiased. Almost all subjects showed increased rates of excess estrogen excretion while consuming 3.6 grams of Cruciferous Complete daily. Those with the highest excess estrogen showed the greatest increases in detoxification-averaging 500% (or 5x) greater than normal.
So if you are a premenopausal woman with any of the breast or uterine cancer markers, you can now lower your excess estrogen risk easily, safely, and without drugs. Simply take 6 Cruciferous Complete capsules daily for 4 months, followed by 3 daily thereafter until menopause. This study confirms all our previous hypotheses and protocols (such as our Purification Program). It is now a fact that using cruciferous vegetables for detoxification and to lower cancer risk works. It also provides women with proof that they can use cruciferous brassica vegetable powder (Cruciferous Complete) to help them prevent estrogen-induced cancers.
As Always-The Whole Plant Is Best
There are all kinds of fractionated cruciferous supplements on the market. But this study clearly showed that the entire plant supplement worked best. The authors concluded that "single compound extracts (fractions) may lose effectiveness through the lack of potential benefits from the entire range of natural compounds found in whole crucifers (vegetables)." They also concluded that super-high doses of fractionated products from vegetables often fail to get into the body and convert to the disease-fighting molecules needed.In fact, just as reported in Health Alert, the study showed that the whole food product produced responses 100 times greater than much higher doses of fractionated products. This proves once again that whole food phytonutrient complexes are much more effective in absorption and conversion into needed disease-fighting molecules. And they actually produce the measurable results we are after.
This whole study came as a slight surprise to me. I always use cruciferous vegetables to aid in detoxification, but have not emphasized Cruciferous Complete for women with estrogen-related cancers. I have used this product (3-4 daily) for its other beneficial compounds (flavonoids and hydroxycinnamic acids) to help people with macular degeneration. Based on my macular degeneration study, we now know that improvements in macular degeneration perhaps also come from improved detoxification, and not just the effects of increased levels of flavonoids, etc. on the eyes.
Either way, this product serves as an anti-macular degeneration product as well as an anti-estrogen product for premenopausal women at risk for breast or uterine cancer. Let's hear it for two vegetables that most people do not like to eat. And for phytonutrient products, organically grown and processed without heat or chemicals to maintain the life force of the plants.
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I am persuaded by the need to balance excess estrogen with progesterone--but here is my dilemma: If being menopausal with symptoms like hotflashes means my body wants more estrogen and since progesterone is a precurser to estrogen and can be converted by the body if it needs it, how do you know when it might actually create estrogen rather than balance it???
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I want to chime in with some information as it pertains to underactive thyroid. Even though my internist told me my thyroid is 'fine' with a TSH of 4.2 (never mind that the 'new' normal of .3 to 3.0 went into effect seven YEARS ago), I have done enough research to believe that I am hypothyroid. Radiation is notorious for knocking our thyroids out of balance, and yet, here I am 4 years later with ZERO help from my doctors on this subject. but I digress...
Cruciferous veggies are to be avoided when suffering hypothyroidism. Also, I've read just recently that progesterone can stimulate thyroid activity. That sure makes me want to try some, but I won't -- just yet anyway. I just ordered a supplement that I believe comes close to what doctors prescribe for hypothyroidism. I've been hoping for 3+ years that my fatigue will exit my life, trying this that and the other thing every 4-6 weeks in the interim. ..but maybe this time it will finally happen. I think I might be adding progesterone to my list of things to try someday though. Haven't had the problem of running out of things to try yet.
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Also on my mind is an article entitled 'High estrogen associated with breast cancer recurrence' quoted on page 3 of this thread. The summarizing paragraph states "Researchers found that higher estradiol concentrations, in all forms, significantly predicted cancer recurrence."
I am in complete agreement with anomdenet as a I look at that conclusion with puzzlement. First of all, why wasn't progesterone included in the study? As I recall Dr Christiane Northrup's explanation of these two hormones, estrogen is in charge of cells cycling in and progesterone is in charge of cells cycling out (aka apoptosis).
I have to wonder, do estrogen and progesterone travel around in pairs? What if they did, and what if the proliferation of estrogen really represented the proliferation of progesterone? Then, you might have, sharp intake of breath, something similar to white blood cells being associated with infection! Or, better yet, you might have something like fire trucks being associated with scenes of fires!
If the high level of estrogen turned out to also be a high level of progesterone, then it could be an indicator of our bodies trying to get some cells to cycle themselves out. I REALLY hope there's a research scientist way ahead of me on this one.
And even though I'm not a scientist, or doctor, or anything close except as a patient, I just have this feeling in my heart that estrogen is not the evil culprit here. To jump from 'associated with' to 'predicting recurrence' is a might big leap if you ask me. In fact, it doesn't really indicate anything at all as far as cause is concerned. It makes as much sense as an assertion that fire trucks cause fires due to the association between the two.
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I'm not a scientist either Althea, but I am as concerned as you are about this quandry of progesterone being identified, but identified as doing what? Many of us are PR+ and if we take that at face value that it means the same thing as ER+ then progesterone grows cancer??? Yet I can't find any studies stating this and I don't know one doc who really understand what PR+ means.. so why identify it at this stage if no one really know what it means. It's is a very confussing predictor, or not a predictor at all! IMO
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Althea-your analogy was very interesting to me. Since my son is a fireman, does that mean we are more likely to have a fire?LOL But I do get your point because after all the reading I am doing on hormones, I am beginning to think the same thing. Wouldn't it be a huge controversy if it is found that too much estrogen does not cause bc, but lack of progesterone does? As I said, this would make the fact that bc risk goes up as we age and our progesterone levels drop to nil. I would not put it past drug companies to pull one over on us, in the prospect of making a buck. Could you imagine the lawsuits? No wonder they lobby extensively to get natural hormones off the market. No wonder they block any research on natural hormone replacements. There are a lot of doctors out there using them successfully. There are a lot of studies in other countries proving they are safe, yet the FDA refuses to approve it here. I smell a rat.
As to your comment on thyroid; Where did you here that cuciferous veggies were bad for the thyroid? I can see how it could be true that the thyroid is affected by rads. That could be why women have such fatigue. My last thyroid test shows mine is low, yet I do not have any fatigue and I also had none during rads. I just attributute this to my daily exercise routine. I have read that low progesterone affects the thyroid too, so I am getting very close to going this route. I just have not found a good doctor yet to regulate it. I do believe it is very important that we have doctors monitoring us before doing hormone replacement. It is essential to get only as much as needed.
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A very interesting thread. Sarabhealed asks a good question about the progesterone. If you look at the steroid hormone cascade, of the 3 important hormones the ovaries made (estrogen, progesterone and testosterone), progest and testosterone can both convert to the "more dangerous" estradiol and estrone. The only hormone that does not have the potential to convert to new hormones is estriol (deemed the less potent, safer form or estrogen in Dr. Lee's books).
And then there was a study, that was reported recently (can't remember the name) that suggested that in the progesterone/estrogen arm of the study there were more women who developed breast cancer than the estrogen ALONE arm. Maybe someone will remember the name of the study and particulars such as dose, forms of hormones given. -At any rate makes you wonder how much of a role progest might have in br. cancer?
Very frustrating to find out what if any, at what doses and what type (estriol vs estradiol), might eventually be suggested as feasable for us survivor's to try.
Julie
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althea:
Your analyses are truly thought-provoking..... This is like reading a fairly long mathematical equation leading up to yet another problem to solve (one has to concentrate in order to follow the process). After reading your thought progression a few times, I can see how this logic could end up leading to the question of whether estrogen is actually the culprit. I know some breast cancer advocay groups (such as Breast Cancer Action) have already asked themselves this same question.
I, too, have asked myself this question before, but this is the first time I can see a logical path in that direction. I have wondered elsewhere whether there might be an emerging school of thought in which estrogen is not considered the culprit in this matter, after decades of hormonal treatment.....
.......And what a "revolution" that would be! But not impossible, when you realize that Tamoxifen was only recently found to actually fuel HER+ tumors (http://www.nature.com/nature/journal/v456/n7222/full/nature07483.html).
.......And when you know that after putting millions and millions and millions of women (just like myself) through chemotherapy, it has now been discontinued for our cases, because it was found to do absolutely nothing good (and much to the contrary) for ER+, PR+, HER- tumors.
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Can someone here direct me to some good current info on Thyroid issues? I just read an article that surprised me about thyroid and menopause. And while my doc really didn't blow me off about my low-normal thyroid, I am interested now in knowing more about it. My mom had (?) Stage 1 thyroid cancer..... I need to investigate that better too.
Thanks so much, Amy
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Breastcancerchoices.org has a lot of info on thyroid and breast cancer. I have also found some info in Dr. Reiss' book, Natural Hormone Balance. While we have always heard a lot about the problems with high thyroid, low thyroid is finally becoming more in focus. So back we go again to the fact that even though we may pooh pooh celebrities because they tend to make a lot of money from us, it is celebrities like Oprah and SS who bring this information out of the closet that is actually making a difference. Sad but true.
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pod,
You are thinking of the Women's Health Initiative study. The women who took the horse-based estrogen with a SYNTHETIC progesterone (Provera) had a slightly higher risk of breast cancer. But this synthetic progesterone SUPPRESSES our natural protective progesterone. So, it seems fitting that synthetic progesterone would be dangerous.
But there was an arm of the study of women who had hysterctomies taking horse estrogen alone: These women GOT SIGNIFICANTLY LESS BREAST CANCER and colon cancer. They never took synthetic progesterone.
There are several follow up analyses identifying synthetic progesterone as the culprit. I think Oprah's website has some scientists and practitioners discussing this.
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