Health & Wellness
According to a new study published in the Lancet journal, there is unequivocal evidence of high failure rates of metal on metal hip replacements, especially in women.
The data showed that on more than 400,000 hip replacements, metal on metal types needed revising more often than other types. Those found in women were especially prone to failure.
The researchers say that tiny metal ions, made of cobalt and chromium, break off the implant and leach into the blood. This causes muscle, bone and possibly neurological damage.
The British Medicines and Healthcare products Regulatory Agency (MHRA) issued new guidelines for the devices, according to The Guardian, 50,000 patients in the UK will need to have annual MRI's and frequent blood checks, for heavy metals in the blood.
The research found that metal to metal hip replacements have a five-year revision rate of 6.2 percent. Whereas ceramic on ceramic devices have a 2.3 percent five-year revision rate. And plastic on metal types only have a 1.7 percent revision rate.
Ron Rosedale says to keep your cells sensitive to leptin, insulin and other hormones for better health.
He gave this talk at the American Society of Bariatric Physicians (ASBP) meeting Oct 31, 2006. They're medical experts who work to reduce obesity. As part of the 2006 presentations, the ASBP included a special segment that featured low-carb diets, researchers and scientists who are connected to the Nutrition and Metabolism Society. Special thanks to Instatapes for recording this presentation.
SPEAKER'S INTRODUCTION: Dr. Ronald Rosedale is an internationally renowned expert on the biology of aging. He was at the International Conference on Aging Medicine at Rio de Janiero, and the first European Conference on Longevity Medicine and many more. He is the author of The Rosedale Diet: Insulin and its metabolic effects. He will be speaking to us this morning on the detrimental effects of too much protein. Please welcome Dr. Ronald Rosedale.We might give a different view on protein intake and nutrition and actually health in general. First, you hear a lot about paleolithic nutrition, the idea being that ancient man can tell us how to be healthy. That we need to go back to our ancient roots and eat like they did, and then we'll be healthy. But you have to go back even further and understand what Nature is after. And there are two prime prerogatives of all life, since the beginning of life. And they both involve making more life.
How do you make more life? Reproduce. What do you do to reproduce? You have to eat. You have to eat and reproduce. It's all life does, and we evolved with those dictums.
We can't use Paleolithic Man. We evolved with a diet to not allow a man to live a long healthy life.
Nature does not care about us living a long healthy life, or any life, for that matter. Nature wants "Life" to live.
It's like, you don't care if there's a little cell on your hand that dies, as long as the whole remains. Nature doesn't care if you or I dies, or if all mankind dies. Nature wants life to live. The diet that ancient man grew up with was to maximize reproductive sense. Not necessarily the life of each individual.
We do know, there is a powerful connection between energy stores, reproduction and longevity. Certainly, we know that it takes a lot of energy to make babies. And if there was not a lot of energy around, Nature would put off reproduction, and it is that trick that we want to use. It puts off reproduction by allowing the organism to live longer. It appears that all organisms have genetic mechanisms to delay aging, to delay dying so that the organism can reproduce at a future more opportune time. And generally this is genetically controlled, and it's controlled by the availability of nutrients, whether it's good to reproduce now or put off reproduction into the future.
"It [is] like putting a bullet in your mouth, and then just waiting for the day it might kill you."Let's first draw the picture - in living color - for you to look at closely before you choose to do a root canal(s) in your mouth.
~ A Dental Consultant after years of observing the ravages of root canal 'treatment'
This routine procedure involves the following technique every time the endodontist or general dentist gets busy in your mouth making canals in your teeth, some of which may be stubs at that point.
First the dentist removes all the dental pulp from the tooth. "The dental pulp is the part in the center of a tooth made up of living connective tissue and cells called odontoblasts." This vital pulp, which is necessary for a living tooth to remain living, is full of blood vessels and nerve tissue. When this blood supply and network of nerves is extracted, the tooth is essentially devitalized, aka killed. The tooth is then completely unable to perform all the normal activities which are required for normal tooth health.
So, the first question any rational person would ask themselves is: "Why would I want a dead tooth in my mouth ... for the rest of my life?"
Good question! Answer: You don't want a dead tooth in your mouth for the rest of your life.
Please show us - The Health Coach - another instance in your body where a dead organ, tissue, limb, digit, etc. is purposefully kept in or attached to your body by the Medical Practitioner. Show us just one example.
Our experience has been that wherever an organ dies, the doctor removes it pronto. Whenever a limb becomes gangrenous, the surgeon amputates post haste. If your eye were to "die" due to some traumatic injury which became infected, the ophthalmologist would completely remove the eye leaving an empty socket cleaned out of all infected tissue, yes?
Why then does an endodontist go out of his way to keep your white shiny tooth in place even though he has just killed it?! The only reason he is able to get away with this extremely dangerous procedure is because of our ignorance often coupled with vanity, together with his/her 'compelling' sales pitch as to why you don't want to lose the tooth (that's another very long story for another dental coaching session).
Mercury in Skin Creams?
That was the headline-grabber last week, when an FDA investigation found imported skin creams may contain toxic levels of mercury and other heavy metals. The risk is serious; people are actually getting sick from mercury contamination from these products.
The list of dangerous skin creams is fairly long, but - so far at least - contains only products you'd purchase from an import store or Latino, Asian or Middle Eastern market, and no American-made brands or products. The creams are intended primarily for "skin lightening" and anti-aging and include Stillman's skin bleach cream, Diana skin lightening formula, and numerous products with labels in Chinese, Hindi, and other languages.
If you've been using a lightening skin cream that's imported from China, India, Mexico, or some other exotic locale, check the label for mercury. But be aware the ingredient might also be listed as "mercurous chloride," "calomel," "mercuric," or "mercurio." If there is no list of ingredients, don't use the product. Symptoms of mercury poisoning include tremors, memory problems, irritability, and changes in vision or hearing. The creams have turned up in seven states so far, and several cases of serious mercury poisoning have been reported.
Many of the chemicals in sunscreens have been found to cause phototoxic, photoallergic or photogenotoxic (DNA altering) effects. PABA (Paramino benzoic acid) has been found to increase the development of a particular DNA defect in human cells. When this occurs in people who lack the mechanism to repair the defect, they are more susceptible to skin cancer. When exposed to sunlight, PABA also readily generates oxygen radicals which harm DNA strands . An ester of PABA, amyl paradimethylarninobenzoate (Padimate A) was found to cause phototoxic reactions. Padimate A reacts with UVA to produce symptoms widely resembling sunburn. The similarity between sunburn and a phototoxic response has led people to mistakenly believe that the sunscreen causes sunburn. An ingredient commonly used in sunscreens, 2-phenylbenzimidazole-5-sulfonic acid (PBSA), strongly absorbs UVB radiation, thus becoming energised and capable of affecting adjacent skin tissue by damaging the guanine base sites of the cell's genetic material. This may increase the risk of developing skin cancer.
It's easy to visualize how fatty foods raise blood cholesterol, which, despite being a large inert molecule, somehow precipitates out to infiltrate the inner lining of the coronary arteries, where it forms fatty atheromatous plaques.
These plaques slow the flow of blood and eventually completely obstruct it to cause the death of myocardial tissue. This sequence of events was similar to the gradual buildup of lime and rust in pipes, and the terms coronary occlusion, myocardial infarction and heart attack are still often used as synonyms.
What is hard to believe is that there is no evidence much less proof to support this entrenched lipid theory of coronary atherosclerosis. In point of fact, it has been completely refuted by numerous scientific studies. Consider the following half dozen examples:
Studies have found that in general, the optimal temperature for sleep is quite cool, around 60 to 68 degrees Fahrenheit. For some, temperatures that fall too far below or above this range can lead to restlessness.
Temperatures in this range, it seems, help facilitate the decrease in core body temperature that in turn initiates sleepiness. A growing number of studies are finding that temperature regulation plays a role in many cases of chronic insomnia. Researchers have shown, for example, that insomniacs tend to have a warmer core body temperature than normal sleepers just before bed, which leads to heightened arousal and a struggle to fall asleep as the body tries to reset its internal thermostat.
In the event that the public becomes too informed and savvy about toxic additives in our food supply, what's a multi-billion dollar industry to do? The first step is to create another more toxic version of the additive. The second step is to collude with regulatory authorities such as the FDA to convince the public that the new, more toxic additive is safe. The third and final step is to prevent the toxic additive from being listed on any ingredient labels. From the folks that brought us Aspartame, meet Neotame, a deadly sweetener that you'll never see on a label because...well that's just the way the FDA wants it.
Neotame is officially marketed as an inexpensive artificial sweetener made by NutraSweet, which is a former division of Monsanto and original manufacturer of aspartame.
Eighty percent of all Food and Drug Administration (FDA) complaints pertain to aspartame's adverse reactions. These reports include: grand mal seizures, brain tumors, blindness and other health-related problems, including deaths. Monsanto's Nick Rosa stated in 1998, that Neotame is "based on the aspartame formula."
It is up to 13,000 times sweeter than sucrose (table sugar). The product is very attractive to food manufacturers, as its use greatly lowers the cost of production compared to using sugar or high fructose corn syrup (due to the lower quantities needed to achieve the same sweetening).
Neotame is aspartame plus 3-di-methylbutyl, which can be found on the EPA's list of most hazardous chemicals. The aspartame formula is comprised of Phenylalanine [50%], which caused seizures in lab animals and Aspartic Acid [40%], which caused "holes in the brains" of lab animals -- bonded by Methyl Alcohol, or Methanol [10%] which is capable of causing blindness, liver damage and death.
It's common knowledge that too little sleep can increase our odds of getting sick, but a new study sheds light on just how direct the connection is. Researchers found that the body's circadian clock controls an essential immune system gene in mice -- a gene that helps the body ward off bacteria and viruses.
"People intuitively know that when their sleep patterns are disturbed, they are more likely to get sick," study author Erol Fikrig, professor of epidemiology at the Yale School of Medicine, said in a press release. "It does appear that disruptions of the circadian clock influence our susceptibility to pathogens."

This figure shows 50 nm carboxylated polystyrene nanoparticles (green) interacting with a cell culture model of the intestinal epithelium (red). Oral exposure to these particles was shown to affect iron transport.
According to lead author of the article, Gretchen Mahler, assistant professor of bioengineering at Binghamton University, much of the existing research on the safety of nanoparticles has been on the direct health effects. But what Mahler, Michael L. Shuler of Cornell University and a team of researchers really wanted to know was what happens when someone gets constant exposure in small doses - the kind you'd get if you were taken a drug or supplement that included nanoparticles in some form.














Comment: Light also plays an important part in quality sleep. Why Too Much Bright Light Before Bed Harms Sleep