CDC and ADA Advise Against Fluoride

by Suzanne Somers 8/23/2011 1:58:00 PM

Dear Friends, 

I was discussing the fluoride issue with Dr. Garry Gordon, a doctor I am iterviewing for my new book.  Last fall, a new study in the Journal of American Dental Association reported that fluoride is actually bad for teeth.  Of course, those of us who understand it is a toxin already know that - but now the CDC and AMA say that this recent study shows intake of fluoride during the first few years of life is significantly associated with fluorosis, and they now warn against using fluoridated water in infant formula.   

The Centers for Disease Control and Prevention (CDC) is of a similar opinion. According to their website: "Recent evidence suggests that mixing powdered or liquid infant formula concentrate with fluoridated water on a regular basis may increase the chance of a child developing ... enamel fluorosis." 

Sources:   Journal of the American Dental Association;October 14, 2010;  141(10):1190-1201;CDC May 28, 2010 

Fluorosis causes spotting on teeth, and in severe cases can cause orange or brown mottling of the teeth.  Sadly, that's just the tip of the iceberg when it comes to the damage that can be caused by fluoride.  In my opinion, these agencies who have been telling us it's safe for so long can't completely back track and announce, "Whoops! That toxic waste will kill you!"  So instead they find a gentle way to let us know it's best to avoid with the most vulnerable, like infants. 

Here is Dr. Gordon's response. 

 

Suzanne,  

Fluorine is very toxic for many patients and the dangers go far beyond the dental fluorosis issue, but at least that alone suggests proof that over 30% examined children have excessive fluorine already. We all need to know that fluorine is another mistake made by governmental agencies and now we even have CDC and ADA admitting that there are issues about fluorine excess showing up. 

Believe me when I tell you that ALL fluorine should be destroyed, as the toxicity goes far beyond what you have been told. For one example, please know that fluorine makes the bones look white and dense and strong but they fracture easily. This means that by the time someone is being told they have osteopenia, what is being seen is often far worse than the x-ray reveals because the fluorine we all get and almost cannot avoid is making everyone's bones appear not too bad. 

But we have new knowledge today that what matters is elimination of fractures and now we see this bone health picture gets complex but bone health is essential for longevity. FACT: bones are breaking even when the bone density appears normal; in fact bone density is a poor predictor of future fracture risk. 

The more you study this fluorine issue, the more you will see we must add this to our growing long list of reasons we are all unhealthy today compared to what we could be. That list can get very long when we include GMO foods inducing leaky gut and unleashing an epidemic of food sensitivities, along with other toxins like the mandated flame retardants now in everything, PBDE (polybrominated diphenyl esters), dangerous vaccinations, and coal burning power plants polluting everything with lead and mercury.

Fortunately, we were born with lots of resilience so we appear to handle all the above for a time, but finally all this and the other contributing factors covered in my FIGHT program all come home to roost. 

Garry F. Gordon MD,DO,MD(H)

 



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We need your voice!

by Suzanne Somers 7/18/2011 8:54:00 AM

Hi Friends – Please read the following post from Dr. Nick Gonzalez.  He has outlined the important developments on the recent “consumer protection” bill which would make it virtually impossible to buy supplements without a prescription.  WE NEED YOUR VOICE!  This bill does NOT protect us.  It violates our rights.  
 
 
Dear Friends:
 
I am writing to alert you of two assaults against nutritional supplements against which we all need to mobilize.  Over the years I have witnessed many serious threats to supplements proposed by members of Congress and the FDA, always presented in the guise of “consumer protection.”  Invariably the proposed legislation or regulations have been onerous, repressive, and apparently intended to eliminate or seriously curtail the availability of most nutritional products, forcing the US into a European style situation where nutritionals are either forbidden (as in Norway) or become prescription items, and as a result, to the glee of pharmaceutical companies, their drugs become the primary option.  In the past, we here in the US have been able to mobilize to stop such intrusions, such as the ill-conceived McCain bill of a year ago.  But once again, the anti-nutrition forces have organized and mobilized, in ways I have not previously seen.
 
The first threat is Senator Durbin’s noble sounding Senate bill S1310, the "Dietary Supplement Labeling Act," ostensibly prompted because of a recent episode of melatonin tainted brownies.  Senator Durbin has long been an aggressive, vocal opponent of supplements and their availability as over the counter products.  He has long supported a “strong” FDA and the pharmaceutical industry.  In any event, this bill would give the FDA a new set of powers that could easily be used to badger honorable, honest supplement manufacturers providing  legitimate and useful products.  The FDA needs no new authority in terms of labeling, because it already has enormous power to regulate additives to food, and remove harmful or dangerous supplements from the marketplace.  Furthermore, the FDA has already mandated very stringent "Good Manufacturing Practice" regulations that promote standards and require manufacturers of nutritional supplements to provide the highest quality, legitimate products to consumers.  I believe this new legislation is part of an ongoing pattern to eliminate the availability of legitimate supplements so that Americans have no choice in their health care.


Senator Durbin, true to form, presented his legislation on the Friday before the July 4th weekend, presumably hoping that no one would notice. But the ever vigilant Alliance for Natural Health learned of the bill almost as soon as it was available, and sent out a much needed warning to begin mobilizing to stop it in its tracks. I would suggest you contact your Senators and Representatives, either by phone or e-mail, expressing your strong opposition to this bill.  Public outcry has stopped many similar bills in the past, and we can do it again, but it takes pressure, and effort, and energy.  Of course, be polite, but explain that the FDA already has sufficient power to regulate supplements, their labeling, and food additives.  And, express your wish that supplements be kept available for your use. Of course no one wants dangerous products in the marketplace, but most manufacturers are honest and honorable, providing health-promoting, high quality supplements.
 
About the same time Senator Durbin proposed his legislation, the FDA itself announced its plans to enforce an entire new set of regulations on supplement manufacturers that are so onerous, I doubt any company could comply or remain in business. In 1994, Congress passed the “Dietary Supplement Health and Education Act” (DSHEA), which in once sense did protect nutritional supplements available at the time from FDA over regulation, and protected manufacturers from overt FDA harassment. However, the bill also gave the FDA enormous power over any new supplements that might be developed after 1994, with the authority to require the expensive, and time consuming process normally reserved for synthetic pharmaceuticals before these new supplements could be made available to consumers.  Basically, if implemented, supplements would remain stuck in 1994, with manufacturers unable to provide new products in response to ongoing research in the field.


Furthermore, by enforcing this provision in DSHEA, the FDA could require supplements available prior to 1994 that have undergone any change whatsoever to undergo review, with the possibility that these products might be removed from the market until the lengthy review was completed.  Apparently, even if the particle size of a supplement has changed since 1994, the manufacturer would be required to petition the FDA for approval of the product.   As I read the new, complicated regulations, in my opinion any supplement manufacturer might be at risk and few could financially survive should the FDA enforce to the letter the regulations that it presented last week.
 
Nutritional supplements, because of the concern and integrity of the great majority of manufacturers, are extraordinarily safe and the FDA knows this. Our supplements for example are manufactured at an approved facility in compliance with the strict FDA Good Manufacturing Practices.  These products have been life-saving, proving effective even against advanced cancer.  We need these supplements for our patients.
 
The FDA already has the power it needs to "protect" the consumer.  These regulations are unnecessarily onerous and unreasonable.
 
For further information I suggest you consult the following website:  http://www.anh-usa.org/
 
I suggest you write your Senators and Representatives protesting both the Durbin bill and the new FDA regulations.  Always be polite.  But we need to stop Senator Durbin's bill and fight for the continued availability of nutritional supplements.
 
Below is a letter I sent my own Senators.  Feel free to adopt it as your own
 
 
Re:  Opposition to Senator Durbin's bill S1310, the "Dietary Supplement Labeling Act."
 
Dear Senator Gillibrand:
 
I am writing because I need your help.  On the Friday before the July 4th weekend, Senator Durbin - hoping his actions would not be carried in the media before a major holiday - introduced the above referenced legislation, the "Dietary Supplement Labeling Act."  Though couched in terms about consumer protection, the bill really seems designed to give the Food and Drug Administration extraordinary new levels of regulatory authority over dietary supplements, which it does not need to perform its job, and which will add new onerous regulatory hurdles onto legitimate, honest supplement manufacturers in this country.
 
The FDA already has the authority to supervise supplement manufacture and remove harmful or dangerous supplements from the marketplace, It has already put in place very stringent "Good Manufacturing Practice" regulations that promote standards and require manufacturers to provide the highest quality, legitimate products to consumers.  I believe this new legislation is part of an ongoing pattern to eliminate the availability of legitimate supplements so that Americans have no choice in their health care.
 
Americans by the tens of millions use supplements daily, and want these products to remain available to them.  As a physician who uses specially designed supplements in his practice, I know the value of properly formulated nutritional products. The supplements I utilize are specially designed according to very strict specifications, and quite literally, the lives of hundreds of my patients depend on these products.
 
At the same time Senator Durbin proposed his legislation, the FDA itself announced its plans to enforce an entire new set of regulations on supplement manufacturers that are so onerous, I doubt any company could comply or remain in business.  It appears, judging by what I have read, the FDA seems intent to use harmless sounding regulations that do not require Congressional approval to eliminate the supplement industry from this country. I can think of no other rational explanation.
 
Nutritional supplements, because of the concern and integrity of the great majority of manufacturers, are extraordinarily safe and the FDA knows this.  The FDA already has the power it needs to "protect" the consumer.  These regulations are deliberately onerous and unreasonable.
 
For further information I suggest you consult the following website:   http://www.anh-usa.org/
 
Please help stop Senator Durbin's bill.  Please reign in an out-of-control FDA.  My patients need their supplements.
 
I would be happy to talk to any of your aides, I would welcome a visit to my office to show the results of our practice, and our desperate need that our supplements remain available. .
 
Sincerely,
 
Nicholas Gonzalez, MD


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LifeWave and Nanotechnology

by Suzanne Somers 5/25/2011 10:08:00 AM

Dear Friends, 

I like the natural approach to health.  I also am very excited about cutting edge, non-drug solutions to everyday common complaints.  Nanotechnology is not only the future, but nanotechnology is now. What seems like inaccessible therapies are now available in simple non-drug patches.  Years ago I started interviewing scientist, David Schmidt, who developed the LifeWave patches utilizing nanotechnology.  Since that time I do not recall ever reaching for an over the counter or pharmaceutical method for pain relief.  The patches are non-transdermal, meaning nothing enters the skin.  In the simplest terms, you could say they work similarly to accupressure by stimulating the light waves in your body.   

If I pull a muscle or have a headache, I put on my LifeWave IceWave patches and usually within 15 minutes the pain is gone.  When I work out with weights,  I put on my LifeWave Energy Enhancer patches and I have much more energy and endurance and find my workout to be so much easier and more effective.  Everyday I wear a LifeWave Y-Age Glutathione patch to detox my body from the environmental assault.  At night I wear a Y-Age Carnosine patch to repair any cellular damage that might have occurred during the day from toxins or chemicals.  If I gain a little weight, I'd never reach for diet pills, I just wear my LifeWave SP6 Complete patches which diminishes my appetite. 

I don't agree with sleeping pills as a means to get needed sleep because as I've written about in my books, sleeping pills do not promote real sleep. Instead, you go into a suspended state where none of the healing hormone work your body needs can happen.  I have never taken sleep medications, but every night I have a ritual....I turn down the lights in the house, (this lowers cortisol), light candles, play soft music, take a hot bath, put on my LifeWave Silent Night patch, chew a couple of GABA tablets (turns off the noise and the lists), take my Sleep Renew (time-released melatonin), and within 15 minutes I am gone for the next eight hours. Good, real, healing, quality sleep.   

Every time we take pharmaceutical or over the counter medicines we are putting chemicals into our bodies.  The toxic assault has reached catastrophic proportions and in order to save ourselves from the damage done to us by the environment, finding non-drug remedies is especially appealing and life affirming.  Think of all the chemicals I am avoiding by the remedies I described above.  I am the ambassador for LifeWave.  I volunteered for the job because I think these patches are so appealing. 

CLICK HERE for more information on LifeWave or to order the patches (this link allows you to order directly). Use them for a month and see how much better you feel. I can't say enough about the benefits of LifeWave. 

Sincerely,  

 

Suzanne Somers

 

 

For more information, visit SuzanneSomers.com.

 


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My Response to New York Times Article by Tara Pope

by Suzanne Somers 4/6/2011 2:43:00 PM

Hi Friends,  

This is my response to Tara Pope’s article yesterday in the New York Times.  I have no idea if they will print my letter but I thought you'd like my perspective.  Her article follows my response.  

Sincerely, 

Suzanne Somers 

 

Half Right...by Suzanne Somers 

Tara Pope reports in today's New York Times that estrogen has benefits of lowering the risk of breast cancer and heart attacks.  This information has been available for some time.  

But, Ms. Pope ignores the existence of biodidentical hormone replacement therapy.  Ms. Pope explains that Premarin is 'chemically similar' to female human estrogen.  Yet bioidentical estrogen is ' biologically identical', an exact replica, of female human estrogen.  Premarin is made from pregnant mare's ( horse) estrogen.  A horse has 34 different estrogens, NONE of which is identical to a human female.

Why would any woman want to take a chemical that is 'similar', when the real thing exists? 

With the population of the world being bombarded by the greatest environmental assault in the history of mankind, do we really need to add yet another chemical to our already toxic bodies?

How long are we going to ignore true natural hormone replacement?

The Women's Health Initiative blew the whistle on synthetic hormones; Premarin, Prempro, Provera, in 2002.  It spotlighted the 'dangerous, harmful, and even fatal' effects of these unnatural synthetic drugs and in particular the use of progestins, which actually gave women breast cancer.  As a result the WHI urged women not to take these dangerous hormones.

Bioidentical hormones give back quality of life to women and men.  They are not used by most doctors out of ignorance.  They were not taught in medical school and are too lazy to do research to see the tremendous benefits.  THERE HAS NEVER BEEN ONE RECORDED INCIDENCE OF CANCER WITH ANYONE TAKING BIODENTICAL HORMONES.

Synthetic hormones cannot make that same claim. 

Our medical schools teach allopathic medicine only.  This is because of tremendous funding from pharmaceutical companies to our universities.  Big pharma is not interested in non-patentable medicines of any kind. 

I have been on bioidentical hormones for 15 years.  My health has never been better as well as my quality of life.  I have written several books on the subject, all of which have appeared on the New York Times Best Seller lists.

If the New York Times is truly fair and balanced then Ms. Pope needs to be challenged.  She has written a book on synthetic hormone replacement.  Let her read the many studies and efficacy on biodidentical hormone replacement therapy and report fairly. 




April 5, 2011, 4:02 pm

Estrogen Lowers Breast Cancer and Heart Attack Risk in Some
By TARA PARKER-POPE

Photo: Andrea LaCroix of the Fred Hutchinson Cancer Center in Seattle found that estrogen lowers breast cancer risk in some women.

In a finding that challenges the conventional wisdom about the risks of some hormones used in menopause, a major government study has found that years after using estrogen-only therapy, certain women had a markedly reduced risk of breast cancer and heart attack.

The research, part of the landmark Women’s Health Initiative study, is likely to surprise women and their doctors, who for years have heard frightening news about the risks of hormone therapy. But most of those fears are related to the use of a combination of two hormones, estrogen and progestin, which are prescribed to relieve hot flashes and other symptoms of menopause, and have been shown to increase a woman’s risk of breast cancer.

The new findings, reported Tuesday in The Journal of the American Medical Association, come from 10,739 women in the Women’s Health Initiative study who had previously had a hysterectomy, the surgical removal of the uterus. Nationwide, about one-third of women in their 50s have had a hysterectomy.

While other women in the study were taking combination hormone therapy, women without a uterus took estrogen alone or a placebo for about six years and were followed for nearly 11 years. The estrogen-only group was not given progestin, which is prescribed only to protect the uterus from the harmful effects of estrogen. Although all the women in the estrogen study stopped using the treatment in 2004, the investigators have continued to monitor their health, as is typical in large clinical trials.

The most surprising new finding relates to breast cancer. The women with hysterectomies who used estrogen alone had a 23 percent lower risk for breast cancer compared with those who had taken a placebo. This is in stark contrast to the higher risk of breast cancer shown in the estrogen-progestin part of the trial.

“The decreased risk of breast cancer in this group is something we totally didn’t expect when we started the W.H.I. hormone therapy trials,” said Andrea Z. LaCroix, the study’s lead author and a professor of epidemiology at the Fred Hutchinson Cancer Research Center in Seattle. “This study differentiates estrogen alone from estrogen and progestin in a very big way. I hope it gets across to women, because we are not reversing ourselves.”

Indeed, the investigators emphasized that the results do not change recommendations concerning combination hormone therapy for the two-thirds of menopausal women who still have a uterus. The Women’s Health Initiative data have consistently shown that the combination of estrogen and progestin raises breast cancer risk, and the treatment should be used only to relieve severe menopause symptoms, using the lowest dose for the shortest possible time.

An accompanying editorial in the journal was skeptical about the results, arguing that the design of the Women’s Health Initiative, which is skewed toward older women and stopped all forms of hormone treatment after several years of use, does not match the way doctors typically prescribe treatment to women in their 50s at the onset of menopause.

Dr. Graham Colditz, an author of the editorial and professor of surgery at Washington University School of Medicine in St. Louis, said he thought data collected from observational studies that show a higher risk of breast cancer associated with estrogen use were more reliable than the data gathered from the Women’s Health Initiative clinical trial.

“The finding doesn’t reflect how hormones are used in the U.S. at the moment,” Dr. Colditz said.

The trial has, however, been held up for years as the gold standard for medical research, and its findings linking combination hormones to breast cancer and heart problems led to significant changes in the way doctors around the world treated menopause.

A major caveat in interpreting the new estrogen data is that the study used conjugated equine estrogens, which are estrogen compounds derived from the urine of pregnant mares and marketed by Wyeth Pharmaceuticals under the brand Premarin. The brand has fallen out of favor with many women who are choosing treatments that contain estradiol, which is chemically similar to a woman’s natural estrogen. It is not known whether the benefits of estrogen shown in the Women’s Health Initiative would be replicated using a different type of estrogen.

Nobody knows why estrogen treatment alone appeared to lower breast cancer risk in the study, but one explanation may be that in menopausal women with low levels of natural estrogen, the effects of estrogen drugs induce cell death in existing tumors. Nobody is suggesting that women start using estrogen to prevent breast cancer, but the finding opens a potentially new avenue of research in the prevention of the disease.

“We need to look closely at these findings to see if we can learn more about ways to prevent breast cancer in women,” said Dr. JoAnn Manson, a Women’s Health Initiative investigator and an author of the study who is chief of preventive medicine at Brigham and Women’s Hospital in Boston.

In the estrogen-only group in the trial, use of the hormone was not associated with any significant risks or benefits pertaining to blood clots, stroke, hip fracture, colon cancer or overall death rates.

But there were surprising differences in the risks and benefits of estrogen use on heart risk when comparing the youngest and oldest women in the study. Women who were in their 50s when they first started using estrogen also had significantly fewer heart risks, including almost 50 percent fewer heart attacks, compared with those assigned to the placebo group.

The data indicate that for every 10,000 women in their 50s, those using estrogen would experience 12 fewer heart attacks, 13 fewer deaths and 18 fewer adverse events like blood clots or stroke in a given year, compared with those taking a placebo.

But the risks of estrogen use were pronounced in older women. For every 10,000 women in their 70s, using estrogen would cause 16 extra heart attacks, 19 extra deaths and 48 serious adverse events.

“The big message there is that the data look much more favorable for younger women and much riskier for older women,” said Dr. LaCroix.

Dr. Rowan Chlebowski, another author of the study and a medical oncologist at Los Angeles Biomedical Research Institute, said the findings underscore the fact that the risks and benefits of menopause hormones change depending on a woman’s health status, her age and the type of hormone used.

Dr. Chlebowski previously led research that showed cancer risks associated with combination hormone therapy, but he says the new data on estrogen alone show that in certain women, estrogen use to relieve menopausal symptoms is a “good choice.”

“When you look at the debate, people are saying hormones are good or not good — it’s been all or nothing. This calls attention to the fact that there are differences,” said Dr. Chlebowski. “I hope that separation will become clearer now.”


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Radiation Exposure - What you can do to Protect yourself.

by Suzanne Somers 4/4/2011 8:15:00 AM

Hi Friends,

In watching the news and given my passion for detoxification and relieving the toxic burdens carried in our bodies , naturally I was concerned about radiation contamination affecting the USA  as a result of the nuclear meltdown of their reactor in Japan.  This horrible tragedy imposed upon the incredible nation of Japan is dangerous to all of us.  I asked my dear friend and renowned neuroscientist, Dr. Russell Blaylock what we could do to protect ourselves.  

If you want to know more please order his book "Nuclear Sunrise",  www.blaylockwellnesscenter.com.  

His response follows.

 

Sincerely,

 

Suzanne Somers  

 

Suzanne,

I thank you for your eternal vigilance. Yes, there are a number of things people can do to protect themselves from radiation exposure. The children are most in danger from I-131, which is taken up by the thyroid and can not only induce thyroid cancer, but a whole host of thyroid diseases, including autoimmune thyroid disease, hypothyroidism, etc. This isotope has a relatively short half-life of just 8 days and by 2 weeks it is of much less danger. Adults seem to be resistant to thyroid cancer from I-131. The other isotopes being released, such as strontium-90 and cesium-137 are more of a problem. They have very long half-lives—about 30 years, meaning that they will remain a danger for at least a hundred years or more. Both of these isotopes easily enter the body and remain for long periods.  While taking I-131 tablets (Iodoral is the least toxic and best tolerated, even for children) will greatly reduce risks of thyroid disorders, it must be given before exposure.

A number of newer compounds are being found that offer tremendous radioprotection against the harmful effects of these isotopes against every organ and tissue in the body. Remember, Iodine only protects the thyroid. The other beneficial compounds include curcumin, quercetin, resveratrol, garlic extract, white tea and many more. In tests using animals exposed to massive, normally100% fatal gamma radiation levels, several of these flavonoids have dramatically improved survival—as much as 50% to 70%. They have also been shown to dramatically reduce the risk of a person developing cancer from the radiation, and again this has been tested using extremely high levels of gamma radiation, the most damaging form.  Most interesting is the finding that unlike iodine, which has to be taken before exposure, these flavonoids offer high levels of protection even days after exposure.

Beta-1,3/1,5-glucan, an immune stimulant, has been shown to powerfully protect the bone marrow, the most sensitive tissue in one’s body to radiation damage. It is suppression of the bone marrow immune white blood cells by the radiation that is responsible for most deaths from radiation, so this is a significant protecting supplement. The government, over the years, has been secretly dispensing this supplement to nuclear plant workers who are at the greatest risk. High purity beta-1,3/1,6-glucan can be purchased without a prescription—but it has to be of high purity.

Most of what we know about radiation protection by natural products has been learned through research funded by the defense department and NASA.

Russell




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Are We Prepared?

by Suzanne Somers 3/15/2011 12:38:00 PM

 

As we sit and watch our televisions and computers, horrified at the death and destruction of Japan, I’m sure we all wonder what would we do in the event of a disaster in our own backyard?  

I know after the Northridge earthquake, many of us in California put together our emergency kits.  I think mine must have gone up in smoke when my house burned down. 

How can we be prepared?  What do we need?  

Here is a list of essentials – feel free to add suggestions for more.

  • Bottled water
  • Canned food
  • First aid kit (include sanitary pads for wounds)
  • Cash, travelers checks, change
  • Sleeping bag or blanket for each family member
  • Change of clothing, long sleeved shirt, long pants, sturdy shoes
  • Medications and supplements (especially my hormones and calming supplements!)
  • Glasses
  • Infant formula and diapers
  • Pet food
  • Copies of insurance policies, identification, bank account records (in waterproof, sealable container) 
  • Household chlorine bleach and medicine dropper: When diluted nine parts water to one part bleach, bleach can be used as a disinfectant. Or, in an emergency, you can treat a gallon of water with 16 drops bleach.  Do not use bleach with scented, color safe or added cleaners.
  • Fire Extinguisher
  • Matches in waterproof container 
  • Feminine supplies, personal hygiene, toilet paper 
  • Mess kits with cups, plates, utensils, paper towels
  • Paper and pencil
  • Books, games, activities for kids 
  • Potassium iodide – in the event of nuclear fallout 

 

Take all of these items and place into a sealable trash can, taped closed, for safe keeping.  Hopefully you will NEVER need to use them.   

As for the Potassium Iodide – right now we are not in imminent danger of the nuclear fallout from Japan, but this is an important product to have on hand in the event of a nuclear emergency close to us.  High concentrations of radioactive material can be fatal and can increase the risk of thyroid cancer. This inexpensive product is an FDA approved compound that can help protect you and your family from radioactive iodine. 

As I said, in this country we are not in danger right now.  Most suppliers are sold out right now, but you can place an order to have this product on hand for the future.  

For more information on health concerns from nuclear fallout and dosages of potassium iodide, please CLICK HERE

Sincerely,

Suzanne Somers

For more information, please visit www.SuzanneSomers.com


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Dr. Nick Gonzalez – Dateline Response to KNOCKOUT Alternative Cancer Treatment

by Suzanne Somers 2/24/2011 4:11:00 PM

Dear Suzanne: 

You had suggested that I respond to the NBC News Dateline program of Sunday, February 20, 2010.  I am happy to do so, to set the record straight in terms of the information regarding myself and my nutritional approach to cancer. 

As a general point, the idea that I have been less than transparent, either with NBC during the production of this show, or within our profession, is simply preposterous.  For the past year, I have provided the Dateline producer, Ami Schmitz, with whatever documentation she requested about any aspect of my therapy, no matter how strange I might think the request.  For example, during our first phone exchange, she asked me about my finances and income, and asked to see my income tax returns – which I happily provided her, probably to her disappointment because my income is so modest.  I doubt very much that she similarly asked to see income tax returns when she interviewed Dr. Cassileth, Dr. Weil, the American Cancer Society spokesman, or the oncologist criticizing Dr. Burzynski.  To this day I have no understanding of the relevance of my income to the science behind what we do.   

During the past year, I spent hours on the phone with Ms. Schmitz, e-mailed often at great length on countless occasions, sometimes several times a day, and provided a stream of documents demonstrating the scientific rationale from the conventional medical literature for much of what I do.  Ms. Schmitz asked for case summaries and records of ten patients with appropriately diagnosed advanced cancer who did well under my care, with proof of response.  I wrote up 15 case studies including several diagnosed with pancreatic cancer and gave her the requested records, though not one word of this effort, or these patients, made its way into the show.  I provided the requested documentation about my training, job offers at Sloan-Kettering that I turned down, even information about my family genealogy.  My grandfather, an accomplished cellist from a very well known musical family in Mexico, was very active in one of that country’s failed democratic revolutions, and Ms. Schmitz wanted the background on that.   

In terms of my transparency within the medical profession, I have been accumulating data and presenting such data on the enzyme approach to cancer since I was a medical student, beginning with my discussions with Dr. Robert A. Good, my mentor at Cornell University Medical School who first encouraged my initial research efforts. I have presented repeatedly at the NIH and at the NCI, have presented at numerous scientific conferences over the past 23 years, have published clinical results and co-authored basic science research in the peer-reviewed medical journals.  I have opened my offices to the scientists of major corporations, all of which Ms. Schmitz knows, such as Procter & Gamble and Nestlé, who provided millions of dollars in research funding. When the National Cancer Institute offered a grant to test my approach in patients diagnosed with inoperable pancreatic cancer, I accepted without hesitation, though the study would ultimately be undermined at many levels.  So, the accusation that I have been less than forthcoming with anybody, including NBC, is nonsense.  

Throughout, the Dateline producers and editors effectively colored their story to minimize the positives about me and my treatment approach.  For example, though Ms. Schmitz, Dr. Snyderman and I spoke at length about my training and background, none of that appears.  I would think the audience would like to know that I have respectable educational credentials, Phi Beta Kappa, magna cum laude at Brown, postgraduate studies in science at Columbia, medical school at Cornell, fellowship in cancer immunology under Dr. Good, the most published author in the history of medicine and the “father of modern immunology,” as the New York Times obituary of him claimed. I think the audience would have been interested to know that under Dr. Good’s tutelage I actually was trained in bone marrow transplantation, about as conventional and aggressive as oncology gets. 

I just do not understand why Dateline focused on a peripheral aspect of my treatment, the “hair test,” which we use as an adjunctive evaluating method but never as a primary diagnostic tool.  First of all, we do not accept patients unless they have been previously diagnosed by conventional methodologies.  Virtually all our patients arrive having been extensively evaluated and in most cases extensively treated by conventional physicians.  We continue to require conventional testing as appropriate for each case – as Ms. Schmitz well knows.  We do also use a hair test which is little known, and considered worthless in some circles, as the critics claimed during the show.  This is their opinion, which I think is ignorant.  I have been studying this test now for close to thirty years, since I first began working under Dr. Good and with his approval, and have found it very valuable in fine tuning nutritional protocols.  As the show claimed, it can give a tumor marker I find in general far more accurate than standard blood tumor markers. 

The hair test does seem unusual at first glance, as it did to me when I first learned about it from Joan, the woman featured on the show. However, its history, as Ms. Schmitz again knows, goes back 100 years to Dr. Abrams, a neurologist at Stanford, who first became convinced that our cells, tissues and organs have an electrical field that can be measured and that can in turn yield considerable information about the state of the body and its various components.  Those that followed in Abrams’ footsteps, including a former Chairman of Anatomy at Yale, and a group of scientists in England, developed a simple instrument that seemed able to translate this electrical field into meaningful data about various biochemical and physiological functions, as well as disease states.  However simple the test may seem, at times in science the simple ideas prove most valuable.   

Joan is one of the few Americans ever accepted into the rigorous training program in England, which she completed before I even met her.  She had the time, energy and resources to study the method and is the only operator I know of in the US performing the test properly.   

Before I considered using this test with patients I subjected it, and the operator to rigorous evaluation.  During the mid-1980s, when I first became interested in its possibilities, I sent multiple samples for testing with no information provided about the patients whatsoever.  Joan with nearly 100% accuracy was able to pinpoint each patient’s specific problem and its severity.

Since I opened my practice in 1987, I have used the test primarily to give information about each patient’s nutritional status.  Patients have never been charged for the test, though I pay Joan a modest monthly amount for which Joan works seven days a week with us because she so believes in our approach.   

She has a personal reason for such dedication, as Ms. Schmitz knows but chose to leave out of the story.  Joan became interested in alternatives when in 1977 her husband was diagnosed with acute myelocytic leukemia, one of the most aggressive of cancers.  When chemotherapy at a major academic center failed to put his disease in remission, Joan and her husband sought out treatment with my controversial predecessor, the late Dr. Kelley.  With Kelley’s help, the disease regressed completely, enabling him to live another seven years before he died of causes unrelated to his cancer. 

Yes, Joan does run a day spa on her extraordinary property.  Dateline left out that she also maintains an extensive sculpture garden, has hosted scientific meetings in her convention center, and runs much of her land as a nature preserve in trust with the Nature Conservancy.  Her father was a famed inventor, her first husband was a World War II and Korea fighter pilot, a Ph.D. astrophysicist graduate student and test pilot who died during a flight, leaving Joan with five children to raise.  She later remarried a wonderful lawyer from an old Louisiana family with three children of his own.  The idea that Joan is just a housewife from some small town broaches on idiocy. 

The show included a dramatic segment showing a woman’s long locks of hair being shorn from the top.  I have no idea where this hair cutting was done for the show, but it certainly wasn’t done in my office.  Contrary to the portrayal on camera, we need only a snippet of hair the size of a pencil tip, which we always take from the back of the neck, not the large bunches of long strands shown being cut at the top of the head.  I wonder if that wasn’t done in a studio, again with the purpose of making the test, and in turn, me, look bizarre. 

Though Ms. Schmitz spoke with at least seven patients at length, including a patient with stage IV colon cancer now with me eight years, and a woman with stage IV breast cancer, now with me five years, the show featured only two in any detail, a new patient just beginning the program, and Sarah Ann Cooper, the woman with pancreatic cancer.  Though two others did appear on camera, they seemed to provide only background, as there was no discussion of their medical history. 

I thought that even Ms. Cooper’s segment had been edited so precisely to make her story less memorable.  For example, I believe it would have been useful to mention that the pathology department at the Mayo Clinic in Rochester, Minnesota confirmed her diagnosis of the most aggressive form of pancreatic cancer.  Ms. Cooper underwent no standard therapy, not even surgery, only our treatment.  She is now ten years out from diagnosis (not nine as the show states), and is in excellent health. I also would have thought the show would have at least mentioned how extraordinary such survival is for a disease that usually kills within six months.  But the producers and writers left that up to the audience to figure out. 

Dr. Snyderman refers to Ms. Cooper “whose stage IV cancer he says (referring to me) has shrunk and stabilized” as if this were my opinion only.  First of all, though Ms. Cooper’s long-term survival for such a deadly disease is itself proof of treatment effect, in fact multiple conventional CT scans over the years have shown a gradual shrinkage of her pancreatic tumor, and more recently, stabilization.  It’s the radiologist reading the scans who says this, not I, and NBC had all these records.  While Dateline allocates considerable space to the “hair test,” there were no experts discussing the extraordinary nature of Ms. Cooper’s ten-year survival from her diagnosis of aggressive pancreatic adenocarcinoma. 

During the show, Dr. Snyderman, in discussing costs, remarked that my therapy costs $12,000 for the first year.  This in general would be correct, but it wasn’t made clear that the costs lessen after that first year, and the greatest expense are the supplements, not our own office fees.  And though my colleague Dr. Isaacs and I have designed many if not most of the supplements we prescribe, we have no financial relationship, either directly or indirectly, with the company that sells the products to our patients.

I was disappointed in the “experts” chosen by Dateline to offer ongoing commentary throughout the story on Dr. Burzynski, myself, and alternative medicine in general:  Dr. Barrie Cassileth from the Memorial Sloan-Kettering Cancer Center (MSKCC), and Andrew Weil, MD, a well-known alternative medicine guru.  Dateline presented both as experts on alternative medicine without question, and the viewer would certainly be left with the idea that these two are experts specifically in alternative cancer therapies.   As Dr. Burzynski points out in his letter, neither are trained as cancer specialists, neither treats cancer and to my knowledge neither has ever treated a cancer patient as the primary caretaker.  The show failed to make that point, though each was presented as a voice of knowledge and wisdom.  But the producers and editors left out much more. 

The show identified Dr. Cassileth as the Director of the Memorial Sloan-Kettering Integrative Medicine Service, and referred to her repeatedly throughout the hour as “Dr. Cassileth” without once defining just what kind of “Dr” Dr. Cassileth might be.  The viewer could easily have assumed Dr. Cassileth is an MD, but in fact, Dr. Cassileth is not an MD, but a Ph.D.  Of course, one would argue, a Ph.D. out of Sloan-Kettering and Director of their Integrative Medicine Service speaking on cancer on Dateline must be some sort of impressive basic scientist.   

The MSKCC website includes lengthy biographies of all its staff members, including Dr. Cassileth.  I assume she provided her own biography since it is written in first person, but interestingly enough, she doesn’t mention the field in which she earned her doctorate – unlike most of the other Sloan-Kettering staff.   

When Dr. Cassileth and I had the good fortune to be seated next to each other at a dinner event some years back, we had ample opportunity to chat, in an informal way.  Dr. Cassileth was extremely pleasant and respectful, even offering some condolences on some of the battles I’ve had to fight over the years.  During that conversation, I learned a lot about Dr. Cassileth, including the nature of her education.  She explained to me when I asked that her Ph.D. was in sociology. 

There is no “transparency” to use the Dateline term on the show that Dr. Cassileth’s graduate studies were not in hard science, but in sociology.  I think, especially since Dr. Cassileth so often assumes the role of expert the field of cancer research and alternative medicine cancer treatments, that in the future her training should be made clear. 

Dr. Cassileth’s lack of formal medical training has never stopped her from offering opinions about cancer medicine or cancer research.  Yet in her own interview on Dateline she mocks Suzanne Somers stating the actress is “not qualified to have an opinion about cancer treatments.”  Dr. Cassileth, trained in neither medicine nor hard science, apparently believes those without medical training have no right to an opinion, except apparently in her own case. I disagree with the premise; in this country, even an actress has a right to an opinion about anything.  That’s why we’re such a great country. 

In any event, Dr. Cassileth presented many unsubstantiated claims.  For example, in referring to alternative medicine practitioners, she states as fact “these people tend to make a lot of money.”  How does she know?  Has she done a study?  I did not see her present a single piece of evidence to support her claim. 

I do know that while my entire treatment for the first year, including supplements (which I do not sell) costs in the range of $12,000, a Whipple procedure – the standard operative treatment for pancreatic cancer, can cost in the range of $50,000 per operation for the surgeon – not bad for a few hours’ work though it most often fails to control the disease.  Medicare which shortchanges everyone last I checked, allows $31,000 to the surgeon for the operation – still not a bad bit of change. 

Dr. Cassileth makes the blanket statement “anecdotes don’t matter.”  My mentor Robert Good who was the Director of Sloan-Kettering would disagree.  Dr. Good frequently stated that nearly all great discoveries in medicine began with anecdotal observations, not controlled clinical studies – such as Dr. Jenner’s simple observations that milkmaids exposed to the mild cowpox seemed immune to the very deadly smallpox. It was an anecdotal observation of profound import.   

More recently, Dr. Fleming observed that no bacteria grew in proximity to the penicillin fungus growing on a contaminated petri dish.  From an instance of sloppy lab technique sprung the whole antibiotic industry. 

And as I have written before, the FDA has itself approved cancer treatments, such as interleukin II, based on anecdotal patient responses.   

Dr. Cassileth states, referring to alternative medicine practitioners, they “go after vulnerable helpless cancers patients with a claim something will help, and have never tested it to prove its benefit, is the problem.”   

Early in my discourse with Ms. Schmitz, I suggested before she proceed with her story she get a copy of the wonderful book “False Hope” and read it to help open her mind.  This wonderful tome tells the story of not some fringe alt med treatment, but the use by conventional oncologists of bone marrow transplant in the treatment of women with advanced or poor prognosis breast cancer.  To sum up a long, tragic and complicated story, during the 1990s, the conventional oncology world promoted bone marrow transplants as a powerful high-tech treatment for women with advanced or poor prognosis breast cancer - despite the lack of any evidence that the treatment worked.  No controlled clinical studies had been completed or even proposed when the treatment took hold.  But despite the lack of supportive data, working astutely with the media and trial lawyers, oncologists were able to force insurance companies to pay for the procedure, which could cost up to $450,000 a transplant in those days.   

The procedure not only was expensive, but also very toxic, responsible for killing 10-30% of those willing to undergo the treatment.  But woman with breast cancer, presumably exemplary of the “vulnerable, helpless cancer patients” Dr. Cassileth references, lined up for the therapy.  The enthusiasm for the treatment was so great in the profession that by the mid-1990s it became standard of care, again in the absence of any legitimate evidence of efficacy. It became the approach of the day in hospitals all over the country, and profit-making centers were set up just to provide the procedure. Fortunately a few honest oncologists kept insisting studies should be done to determine whether the therapy actually worked, but leaders in the profession insisted no trials were necessary.  Finally, five studies were completed; four showed the therapy was no more effective than standard chemotherapy against breast cancer, one was very positive but ultimately proved to be completely fraudulent. The treatment was discredited, but not before 40,000 women underwent transplants for breast cancer, and thousand had their lives shortened unnecessarily.   

In response to the host’s questions, Dr. Cassileth categorically states hair testing has “never” shown any value in the diagnosis or treatment of any disease.  I was surprised such as incorrect statement would appear on the Dateline piece.  Before the story aired, when I realized our hair test was going to be front and center, I sent Ms. Schmitz an article appearing in the March 1999 issue of Nature – an esteemed conventional scientific journal – entitled “Using hair to screen for breast cancer.”  In this report, a group of Australian researchers described their findings showing that molecular changes in hair structure could be used to predict breast cancer occurrence with uncanny accuracy. 

In my library I have a book entitled “Drug Testing in Hair” from CRC Press presenting extensive evidence that hair serves as a very accurate tissue to assess past drug use – findings now accepted by the FBI. 

Now let us turn to Dr. Andrew Weil, author of bestselling books on healing, and breathing, and using water filters and whole grains, Director of the Arizona Center for Integrative Medicine, successful enough to end up on the cover of Time Magazine.   

I met Dr. Weil twice, the first time when I spoke at a conference in Washington DC some thirteen years ago, and he was in the audience.  We talked very briefly after my presentation.  About a year later, I encountered Dr. Weil by chance at the New York Book Fair held annually on Fifth Avenue.  Dr. Weil was at a booth promoting his books, I went over and said hello and we talked for about a minute. I have never spoken to him since.  He has never expressed any interest in my work, in the science behind what I do, my results, nothing.  Consequently I was quite surprised that Dr. Weil would feel himself an expert in my treatment.  In fact he clearly knows very little about what I do.  I myself stopped taking him seriously as a scientist when I happened to be in Bloomingdale’s looking for a gift for my wife some years ago and happened upon a rather large poster of Andrew Weil, announcing the Dr. Weil line of pots and pans – arrayed on counter after counter. 

Dr. Weil, as does Dr. Cassileth, apparently sees the non-expert opinions of someone like Ms. Somers dangerous, stating on camera that people like her and me in terms of what we preach can “lead people to make not good decisions. “  Be that as it may, apparently like Dr. Cassileth, Dr. Weil thinks we must rely only on the opinions of conventional scientific researchers like those who promoted the use of bone marrow transplant for breast cancer. 

I did chuckle to myself, I must admit, when I listened to Dr. Weil’s dismissal of coffee enemas, a mainstay of our therapy, which he derided as “an old hippie treatment.”  Though I have been studying coffee enemas for some thirty years, I am completely unaware of hippies using them.  I also found Dr. Weil’s mockery of something as “hippie” quite ludicrous – this is the guy who wrote his undergraduate thesis at Harvard on the narcotic properties of nutmeg, and who was a regular contributor to High Times.  I would humbly suggest that if Dr. Weil wishes to once again reinvent himself and deny his own hippie roots, that he ditch the beard. 

Dr. Weil seems totally unaware that coffee enemas do not come out of Haight-Ashbury (the original San Francisco 1960s hippie heaven) but the conventional medical literature. During my year talking to Ms. Schmitz, I presented her with the copious documentation showing that coffee enemas were part of mainstream medicine right through the first half of the 20th century.  They were recommended in many major nursing texts and were included as a useful therapy in the Merck Manual, a compendium of conventional therapeutics, right up until the 1970s.  My alternative mentor Dr. Kelley first began prescribing coffee enemas after reading about them in the Merck Manual, not in High Times. 

Though the Dateline producers presented Dr. Weil and Dr. Cassileth as if they were experts about my work and devoted considerable time to their opinions, they deliberately edited to a brief mention their interview with the one person trained in oncology who truly understands the nature of my practice and my treatment.  As Dr. Snyderman states, the Medical Board in New York assigned oncologist Dr. Julian Hyman to review my methods and supervise my practice in 1995.  Though arriving from the opposition camp, he quickly discovered, as he has written, “miracles” in my office.  After a year of regular review of my charts, patients, medical knowledge and ability, he ended up a strong supporter, defender, and close friend.  I was honored to sit at his table during his recent 85th birthday celebration. 

Dateline producers interviewed Dr. Hyman at his lovely home in New Jersey, then Dr. Snyderman interviewed him at length in Manhattan.  Subsequently, Dateline sent a team to his home to photograph his wonderful and extensive art and print collection.  Dr. Hyman, now retired, is not only an eminent oncologist, but also an expert nature photographer whose work has been exhibited in galleries.  He is the former President of the New York Print Club, and a friend to many a well-known artist. 

Dateline left out other significant information about Dr. Hyman that would have made his support of my work even more significant.  Dr. Hyman comes from a family of doctors: his late brother, with whom he shared a practice, was an oncologist and Professor at Columbia College of Physicians and Surgeons.  Julian’s son Steven, a research psychiatrist trained at Harvard Medical School and former director, National Institutes of Mental Health at the NIH in Washington, currently serves as Provost of Harvard – the second highest position in the University. 

I think it’s disappointing that Dateline chose to marginalize Dr. Hyman.  His defense of me, based on his exhaustive review of my practice, says more about my treatment than the long discourses of Dr. Weil and Dr. Cassileth, neither of whom have set foot in my office, neither of whom have reviewed a single one of my patient charts, and neither one of whom has ever expressed to me any interest in learning about the scientific underpinning of my therapy.   

After his interview with Dr. Snyderman, Dr. Hyman called me, somewhat distressed over the tone and direction of the conversation.  He couldn’t understand why Dr. Snyderman asked him multiple questions about the hair test, which Dr. Hyman observed during his stint in my office.  He felt she should be concentrating on the patient successes, not an ancillary test. 

As for the reference to my National Cancer Institute clinical trial conducted out of Columbia, I am astonished that Dateline would devote so little time to uncovering the truth of what really happened during the study.  The Office of Human Research Protections, a government oversight group, after their investigation found the Principal Investigator had admitted 42 out of 62 patients improperly, including 40 improperly consented – hardly trivial paperwork issues.  Because of these findings, OHRP required the team at Columbia undergo retraining in research methodology.  This is on the OHRP website for all to see. I would have thought that Dateline would find such a turn of events newsworthy, since it was the alternative doctors, myself and my colleague Dr. Isaacs, who insisted the trial be run properly, and the Columbia team who messed up.

I gave Ms. Schmitz a copy of an official letter from the NIH written in January 2005, documenting that so many patients had been admitted by Columbia for our treatment who could not or would not follow the prescribed treatment, the data had no meaning.  NBC had a copy of that letter but chose to ignore it. 

The Principal Investigator at Columbia, we later learned, helped develop the treatment regimen that was being used against us – a conflict of interest that should have precluded him from serving in that role, and again raises very serious questions about the validity of any of the data. 

On my website at www.dr-gonzalez.com/jco_rebuttal.htm, some time ago we posted a 13,000 word document that describes the many failings of the study.  I have also posted the NIH letter stating the data had no meaning, and a link to the OHRP findings of mismanagement.  I offered for NBC scrutiny a copy of the 750-page manuscript I am preparing for publication that tells the story of the clinical trial fully and honestly, but Ms. Schmitz declined the offer.  And Dateline made the choice not to ambush the Principal Investigator, whom Ms. Schmitz told me refused to talk on camera  – though they did fly a team to question Joan. 

I could go on, but I suspect I’ve gone on long enough.  Anyone still trust the mainstream media?  

Sincerely,  

 

Nicholas J. Gonzalez, M.D.  


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Cancer | Health and Hormones

Dateline KNOCKOUT - Dr. Burzynski Response

by Suzanne Somers 2/22/2011 1:14:00 PM

I received the below letter from Dr. Stanislaw Burzynski regarding the omissions from the Dateline story, which aired this past Sunday night. Dr. Burzynski is a serious scientist and I believe will one day be regarded as the Jonas Salk of our times.

 I am reminded of the Arthur Schopenhauer quote on the three stages of truth.  "Every truth passes through three stages before it is recognized.  In the first it is ridiculed, in second it is opposed, in the third it is regarded as self-evident."  Regarding the truth about cancer and alternatives, we are deep into “violent opposition.”  

Please read Dr. Burzynski's letter in response to his appearance on Dateline. As you will clearly see, he was misrepresented there was no mention that he has completed Phase II clinical trials in compliance with the FDA! Knowing this would have been very convincing to the viewing audience but, unfortunately, it was omitted. I personally have seen, and/or spoken with many, many of Dr. Burzynski's “cured” patients. Sadly, their stories were also omitted. Many of these patients are written about in KNOCKOUT.

If ever you or a loved one are in the terrible situation of being diagnosed you will be grateful there are doctors like Dr. Burzynski and Dr. Gonzalez who offer other options.

Sincerely,

 

 

Suzanne Somers  

Dear Suzanne,

Dateline is known to expose criminals, and they are good at this.  There is no doubt that for them to produce the story at all, which we saw on Sunday, is our success.  The interviews with you and the patients were great, and with Dr. Gonzalez and me, not too bad. The photographic part was also very good.  What was absent was investigative acumen of the two women regarding the experts presented, who are simply crooks.  Their lies and half-truths should be exposed.  First of all, there was no doctor on the show who knows anything about the treatment of brain tumors.  One of the experts was not an oncologist and not even a medical doctor, (the woman from Sloane Kettering, Barrie Casselith is a PhD, Chief Integrative Medicine Service), and the other doctor has nothing to do with the treatment of patients. The third “expert” recently changed places from M.D. Anderson to Cancer Treatment Centers of America, and certainly, he has never treated brain tumors in his life.  Dateline was reluctant to give the credentials of these experts, yet, on the other hand, they refused to present our sources, who actually work in the field.


I repeatedly mentioned Dr. Julian Whitaker to them as an excellent expert, and who would have been much better than Dr. Andrew Weil, an M.D. who has no expertise in cancer or oncology.  Because Dateline did not include the experts who were on our side, I felt the story was poorly balanced.  The doctors featured knew very well that we have numerous successful Phase II clinical trials, which show statistics of patient responses; therefore, these are not "anecdotal case reports", as he said.  The producers of Dateline are also aware that we are now in Phase III clinical trials, which clearly proves that the treatment is safe and efficacious.  At the beginning of last year we made a public announcement about Phase III clinical trials conducted in Japan, which compares the results of antineoplastons with standard chemotherapy in colon cancer (killing the argument of the doctor from M.D. Anderson that the treatment was not compared with standard therapy).  When he looked at our publications he purposely picked up the abstract from the Congress of Neuro-Oncology as proof that we have only published abstracts, and not full-length, peer-reviewed papers.  He knew very well that the stack of the papers, which he had in front of him, consisted of peer-reviewed papers as well as book chapters.  At that same time, the Dateline reporter (Dr. Nancy Snyderman) knew very well what was going on, yet did not expose it as a pack of lies and half-truths. This goes poorly with such refined investigative reporting.  My belief is that the "experts" were working on behalf of the American Cancer Society to desperately cover the truth and defend their losing ground.  


Dateline raised the issue of "transparency of our records."  During their visits to our clinic they had unlimited access to patients whom they interviewed, and their medical records and scans. After they left, they requested that we send all of our films of the scans of successfully treated brain tumor patients to them so that their experts could review them.  We informed Dateline that according to the rules governing clinical trials, we have to keep the originals in well-organized archives.  They could not be sent to Dateline for review, but we would be glad to make them available for their experts if they wanted to visit our clinic.  One of our radiologists would accompany them, and we would assign a special office for them.  We told them they could stay as long as they wished.  We were surprised to hear that the experts refused to do it, because they were too busy. Subsequently, Dateline requested that we make copies of the x-rays to send to them.  We immediately contacted an imaging center, which promised to do it within approximately six weeks, for $14,000 (we are talking about hundreds of x-rays which needed to be either copied or converted to CDs).  The time and the amount of money to proceed with this project were unacceptable to Dateline.  They narrowed down their request to a smaller number of x-rays, but still the amount of money necessary to do it was in the range of $2,000.  Subsequently, the project was dropped by Datelin

Anyway, smart people will know very well what is going on.  Congratulations to you.  I have no doubt that the next story will be much better.

Stanislaw R. Burzynski, M.D., PhD.
Burzynski Clinic
9432 Katy Freeway, #200
Houston, TX 77055

www.BurzynskiClinic.com  


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Cancer | Health and Hormones

Bioidentical Hormones...the Studies that Back Up Efficacy and Safety

by Suzanne Somers 1/4/2011 9:39:00 AM

Americans are becoming more and more aware that there is a new approach to aging.  We now have tools and knowledge available teaching us new ways to begin the reversal process. 

As I've written about in  many of my books disease prevention and successful aging begins and ends with bioidentical hormone replacement. The effects of real hormone replacement are so remarkable and life altering (for the better), that it threatens big business.  As a result the opposition continues to discredit the theory of restoration to optimal health through hormone replacement. Big business realizes that if we all get to feel this good on real hormone replacement then we won't need many (or any) of their drugs.  But as information infiltrates (hopefully in part due to my books) millions of people are now choosing restoration and in doing so realize that we can not only turn back the clock but in  many cases eliminate degenerative disease risk---and with it the subsequent need for hospitalization, toxic drugs, and nursing home confinement.

I am constantly attacked for offering information on this 'other way' to age, through hormone replacement, avoiding pharmaceuticals unless absolutely necessary, and eating good, real, nutritious food.  It makes one wonder what I am espousing that bothers everyone so much.  They say there are no studies for the facts presented in my books. So to quiet all those in big business who would like to discredit and dismiss the information and education I have so meticulously researched  and rather than provide legitimacy to any particular group whose interest is ensuring that Americans predictably succumb to horrific age-related pathologies, I have chosen to take the high road and publish a meticulous rebuttal. The data was compiled by scientific experts who disagree with the absurd notion that aging humans should stand by and do nothing to reduce their risk of degenerative disease. What follows is my rebuttal to the inaccurate and misleading claims that have been made against the natural approaches I advocate to maintain optimal health.

My position: I have long stated that bioidentical female hormone replacement offers significant safety and efficacy advantages over conventional hormone replacement therapy.

What my critics say:  There are no published studies in peer-reviewed journals showing that bioidentical hormones are safer than other menopause treatments.

My rebuttal to the critics: I have always said that based on the peer-reviewed data, that non-bioidentical progestin increases cancer risk, while bioidentical progesterone does not. A review of the peer-reviewed literature supports this position.

In fact, at least thirteen studies document that non-bioidentical progestin significantly increases estrogen-stimulated breast cell replication and growth.{References: Climacteric. 2002 Sep;5(3):229-35.; J Steroid Biochem Mol Biol. 2005 Jul;96(2):95-108.; Breast Cancer Res Treat. 2001 Aug;68(3):187-98.; J Clin Endocrinol Metab. 1999 Dec;84(12):4559-65.; Cancer Res. 1992 Dec 1;52(23):6539-46.; Mol Cell Endocrinol. 1994 Jun;102(1-2):45-52.; Cancer Res. 1990 Dec 15;50(24):7858-62.; Biochem Biophys Res Commun. 1987 Jun 15;145(2):706-11.; Br J Cancer. 1993 May;67(5):945-52.; Breast Cancer Res Treat. 2007 Jan;101(2):125-34.; Breast Cancer Res Treat. 1998 Apr;48(3):221-9.; Am J Obstet Gynecol. 1996 Jan;174(1 Pt 1):93-100.; Cancer Lett. 1986 Feb;30(2):213-8.}

In stark contrast, at least seven studies have shown that bioidentical progesterone does not induce estrogen-stimulated breast cell proliferation. {References: Fertil Steril. 1995 Apr;63(4):785-91.; Fertil Steril. 1998 May;69(5):963-9.; Climacteric. 2003 Sep;6(3):221-7.; Jpn J Cancer Res. 1985 Aug;76(8):699-704.; J Gynecol Obstet Biol Reprod (Paris). 1990;19(3):269-74.; J Steroid Biochem Mol Biol. 2000 Jun;73(3-4):171-81.; Breast Cancer Res Treat. 1986;8(3):179-88.}

Numerous studies have demonstrated an increased risk of breast cancer with the use of non-bioidentical progestins. {References: 25. Int J Cancer. 2005;114:448-54.; JAMA. 2003 Jun 25;289(24):3243-53.; Cancer Causes Control. 2002 Nov;13(9):847-54.; Br J Cancer. 2005 Jun 6;92(11):2049-58.; Br J Cancer. 2005 Apr 11;92(7):1293-7.; Cancer Epidemiol Biomarkers Prev. 2002 Jul;11(7):593-600.; Int J Cancer. 2004 May 1;109(5):721-7.; Maturitas. 2004 Sep 24;49(1):44-50.; Int J Cancer. 1999 May 5;81(3):339-44.; JAMA. 2000 Aug 9;284(6):691-4.; J Natl Cancer Inst. 2000 Feb 16;92(4):328-32.; Am J Obstet Gynecol. 2004 Apr;190(4):1141-67.;  Obstet.Gynecol. 2002 Dec;100(6):1148-58.; JAMA. 2003 Jun 25;289(24):3254-63.}

However, the use of bioidentical progesterone has not been associated with an increased risk of breast cancer. Quite the contrary, research has revealed that bioidentical progesterone decreases the risk of breast cancer.

For example, in a study published in the journal Breast Cancer Research and Treatment, 80,000 postmenopausal women using various forms of HRT were followed for more than 8 years. Women who used estrogen in combination with non-bioidentical progestins had a 69% increased risk of breast cancer, compared to women who had never used HRT. However, for women who used bioidentical progesterone in combination with estrogen, the increased risk of breast cancer was eliminated with a significant reduction in breast cancer risk compared with non-bioidentical progestin use. {Reference: Breast Cancer Res Treat. 2008 Jan;107(1):103-11.}

In another investigation, researchers found a 40% increased risk of breast cancer for women who used estrogen with non-bioidentical progestin. Interestingly, in women who used estrogen combined with bioidentical progesterone, there was a promising trend toward a reduced risk of breast cancer, compared to women who had never used HRT.{Reference: Int J Cancer. 2005;114:448-54.} In essence, bioidentical progesterone appeared to protect women against the development of breast cancer. These findings confirm work done six years earlier that found a trend toward a reduced risk of breast cancer in 1,150 women using bioidentical progesterone, compared to non-users of progesterone. {Reference: Cancer Detect Prev. 1999;23(4):290-6.}

My position:  Estriol is an essential natural estrogen missing from FDA-approved estrogen drugs. It is available as a topical cream from compounding pharmacies that will usually start a woman off with a compound cream containing 80% estriol and 20% estradiol. There is evidence showing estriol may help protect against breast cancer and provide other benefits.

What my critics say:  Estriol tablets (not cream) when given orally to 24 women with breast cancer showed tumor growth in six women and two developed endometrial hyperplasia--a precancerous condition of the uterus.

My rebuttal to the critics:  It is an unfair and inaccurate inference to suggest that I advocate the use of oral estriol tablets. I advocate the use of transdermal applications, not oral hormone tablets, which are metabolized differently in the body. Giving oral estriol tablets to women with existing breast cancer is different than healthy women taking it. Yet after my encounter with breast cancer, I choose to take an estriol-based cream, natural progesterone and numerous other natural therapies to boost my immune system to reduce the odds of my cancer returning.  Endometrial hyperplasia will develop in some women who are given an estrogen compound without natural progesterone. This is common medical knowledge, yet my critics attack the inappropriate delivery of estriol (in the form of tablets and not cream) given without natural progesterone in a high risk group to claim that estriol is harmful. This is like comparing apples to oranges, but my critics use it to discredit the proper use of bioidentical hormones nonetheless.

A 2004 study was published in the International Journal of Cancer reported on the use of hormone replacement therapy (HRT) and breast cancer incidence in 31,451 postmenopausal women. The analysis of the data determined that women who used estriol did not have an increased risk of breast cancer, compared to women who never used HRT.{Reference: Int J Cancer. 2004 Oct 20;112(1):130-4.}

Additional evidence of estriol's safety was provided by a study that compared use of HRT in 3,345 women over age 50 with breast cancer to 3,454 women without breast cancer. Those women who used non-bioidentical estrogen (like Premarin(r)) had a risk of breast cancer that was double that of women who never used HRT. However, women who used low-dose oral or topical estriol did not have an increased risk of breast cancer, compared to women who never used HRT. {Reference: Int J Cancer. 1999 May 5;81(3):339-44.}

The increased risk of uterine cancer in users of non-bioidentical estrogen is well-established in the scientific literature.{Reference: Engl J Med. 1975 Dec 4;293(23):1167-70.; Am J Obstet Gynecol. 1977 Mar 15;127(6):572-80.; Am J Epidemiol. 2009 Jul 1;170(1):12-23.}

In contrast, the use of topical lower-potency estriol is not associated with an increased risk of uterine cancer.{Reference: Lancet. 1999 May 29;353(9167):1824-8.} A review of 12 studies determined that the use of intravaginal estriol did not result in endometrial proliferation (abnormal overgrowth of the cells lining the uterus with the potential to become cancerous). {Reference: Fertil Steril. 2003 Jan;79(1):221-2.}

Although several studies suggest that the oral route of administration of estriol (in tablet form) appears relatively safe over the short term (e.g., less than five years), topical application is preferred for long-term use. For example, one study found an increased risk of endometrial atypical hyperplasia and endometrial cancer with oral use of estriol, but not with topically applied estriol over a five-year period. Compared with individuals who did not take estriol, those who took oral estriol for at least five years had a significantly greater risk of uterine cancer, and women using topical estriol for at least five years did not have any increased risk. {Reference: Lancet. 1999 May 29;353(9167):1824-8.}

As I mentioned earlier, women taking any kind of estrogen should balance it with the appropriate dose of natural progesterone (and definitely NOT synthetic progestins that have been shown to increase breast cancer risk).

I do not advocate the use of oral hormone formulations as critics sometime erroneously claim. I suggest the use of transdermal applications because of the safety benefits associated with topical (through the skin delivery) rather than oral hormone tablets.

My position:  I strongly advocate for bioidentical hormone restoration therapy in the context of healthy lifestyle choices to include beneficial nutrients found in cruciferous vegetables shown in peer-reviewed, published studies to support healthy estrogen metabolism and high doses of supplemental vitamin D.

What my critics say:  There still is not solid proof that bioidentical hormones won't cause some of the problems associated with FDA-approved unnatural-to-the-body estrogens and progestins.

My rebuttal to the critics: Estrogen is not one compound. It comprises different forms that metabolize in the body to ones that can either promote cancer or protect against it. Compounds found in cruciferous vegetables (such as cauliflower, broccoli, cabbage and Brussels sprouts) help neutralize an estrogen metabolite called 16 alpha-hydroxyestrone that promotes hormone-dependent tissue growth.

For example, major reductions in cancer risk and specific protective mechanisms against hormone-responsive cancers like breast cancer are observed with cruciferous vegetables {References: J Nutr. 2004 May;134(5):1134-8.; Nutr Cancer. 2002;42(1):1-9.; Cancer Res. 1999 Aug 15;59(16):3991-7.; Cancer Epidemiol Biomarkers Prev. 2000 May;9(5):477-85.; Mutat Res. 2007 May;635(2-3):90-104.; Cancer Res. 2005 Sep 15;65(18):8548-57.; Cancer Epidemiol Biomarkers Prev. 2000 Aug;9(8):773-9.; J Natl Cancer Inst. 1997 May 21;89(10):718-23.; J Cell Biochem.Suppl. 1997;28-29:111-6.}

Studies have also found a strong correlation between blood levels of vitamin D and the risk of breast cancer. A case-control study comparing 1,394 postmenopausal breast cancer patients with 1,365 controls showed that low blood levels of vitamin D were significantly related to breast cancer risk. In fact, women with the highest levels of vitamin D had a nearly 70% reduction in their risk of breast cancer, compared to women with the lowest vitamin D levels. {Reference: Carcinogenesis. 2008 Jan;29(1):93-9.}

Similar research examining the relationship between blood levels of vitamin D and breast cancer risk revealed that women with blood vitamin D levels of approximately 52 ng/mL had a 50% lower risk of breast cancer compared with women who had vitamin D levels below 13 ng/mL.{Reference: J Steroid Biochem Mol Biol. 2007 Mar;103(3-5):708-11.}

In another study, the effects of administering 1,100 IU a day of vitamin D were evaluated in 1,180 postmenopausal women. After only four years, the risk of developing any cancer was 60% lower in the vitamin D group, compared with those in the control group. {Reference Am J Clin Nutr. 2007 Jun;85(6):1586-91.}

We know that cancer results from the accumulation of mutations in genes that regulate cellular proliferation. As we age, we develop more of these mutations, thus placing us at far greater cancer risk. Vitamin D favorable effects hundreds of cell proliferation regulating genes and by this mechanism, confers substantial protection against breast and other cancers.

So in summary:

Given the above evidence, aging women should feel confident that bioidentical hormone replacement, when appropriately prescribed, offers a safer and potentially more effective alternative to conventional hormone replacement than with non-bioidentical hormone drugs to help relieve menopausal symptoms and optimize long-term health. The addition of several proven nutrients (such as vitamin D) to a bioidentical hormone regimen can help optimize estrogen metabolism and reduce cancer risk further offering a balanced approach to health maintenance.

Those critics who advocate that aging women can do nothing to forestall normal aging processes are condemning their followers to becoming statistics in mainstream medicine's anticipatory revenue assembly line. Drugs for symptoms. Continued aging requires more drugs. More revenue. Instead, I personally prefer to take affirmative steps to guard my health rather than do nothing but wait for premature disease and aging to strike.

I live by the rule of example...if others want what I have relative to health and vitality, then they can feel safe in doing what I do. Because as you can see from the research above, I do my homework.

   

Sincerely,

 

 
Suzanne Somers

 

For more information, please visit www.SuzanneSomers.com.

 


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Cancer | Health and Hormones

JAMA Study on Hormones - Here we go again

by Suzanne Somers 10/25/2010 11:20:00 AM

Dear Friends,  

Well they are at it again.

Trying to scare us away from our quality-of-life-giving  hormones.  The deception is mind boggling.  Please know, the hormones they are referring to in the JAMA study are once again, Premarin and Provera; dangerous drugs, which in my opinion should be outlawed. These so called hormone drugs made from horses' urine were reported by the Women's Health Initiative 2002 "to be dangerous, harmful,  and even fatal, and would be better to take nothing at all than to take these drugs."  My sentiments exactly. 

I have exposed from the research I have done and interviewing hundreds of cutting-edge doctors that natural bioidentical hormones can be individualized to perfectly restore each woman to optimal health according to her individual needs. A horse has 34 different estrogens and we have 4, none of which are compatible with a horse. Synthetic hormones are chemicals.  Why would a woman take a drug when she could take a natural exact replica of what her body makes or once made?

Natural hormones keep you healthy, give you quality of life, and are cancer protective.  In fact, there has never been one reported incidence of bioidentical hormones causing cancer.  Natural hormones, along with a good diet, good nutrition, quality sleep, and a positive mind-set allow you to live out the second half of your life with pleasure.  Because I replace my hormones with natural bioidentical hormones, and have done so for 13 years, I do not require one single pharmaceutical drug. If all women felt as good as I do as do those on the bioidentical regimen then we wouldn't need their drugs unless absolutely necessary.

I asked my friend, Bill Faloon, Editor of Life Extension magazine, along with the help of his scientific advisory board, to give me their thoughts on the flawed and deceptive JAMA report (see below).

Follow the money. If they can scare you away from hormones, then you will need all their various drugs to take away the debilitating symptoms. Connect the dots.

I've got your back!

 


Suzanne

 

For more inforamtion on bio-identical hormones, check out my Lecture at the Movies coming to a theater near you on November 4th and 9thFor more information and to watch newly posted clips from the movie, click here.

Dear Suzanne, 

This JAMA study corroborates everything we know about horse-urine derived estrogens and synthetics progestins. We said back in 1994 that they increase breast cancer risk and the WHI study proved us correct. You have also criticized the use of these unnatural hormones (Premarin® and Prempro®) in your books. You have recommended individually-dosed compounded natural estrogen (estriol and low-dose estradiol) and natural progesterone (which is completely different than synthetic progestins (Provera®), We have persuasive evidence that estriol may protect against breast cancer, as well as findings indicating a possible protective effect for natural progesterone. 

The one flaw to this study (and all others for that matter) is that they don’t properly account for confounding factors such as 25-hydroxyvitamin D blood levels and cruciferous vegetable intake. To protect you against criticism from the ignorant mainstream, we compiled an article years ago detailing what diet-nutrients a woman adhere to if she is taking any kind of estrogen replacement therapy. The most up to date version of this is embedded in the extensive White Paper we compiled on the safety of bioidentical hormones that you can access  in our October 2009 edition of Life Extension.  Our position is that natural hormone (bioidentical) replacement therapy is safe when combined with the wellness program that we both advocate. 

For longer life,  Bill Faloon

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Health and Hormones

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About Suzanne

Suzanne Somers is one of America’s most popular and beloved personalities. In a multifaceted career, she has achieved extraordinary success as an actress, New York Times bestselling author, entrepreneur, singer, comedienne, and lecturer. Suzanne has authored 20 books, including eleven New York Times bestsellers, as well as five of which were #1 New York Times bestsellers. There are currently more than 10 million copies of her books in print. As one of America’s most informed and dedicated health care advocates, Suzanne has been acknowledged for her leading role in bringing information on today’s groundbreaking anti-aging medical protocols, preventive care, long-term health, and hormone replacement therapies to women and men across the country.

Click here for Suzanne's full biography.