DETOXIFICATION
detoxification , in general is the removal of toxic substances from the body.
Using our detox program your skin will become more brightening , the cell will be regenerated, full of energy and ready .....
TARGET AGE : 20-100y
TARGET AREA : body and face
ACTIVE:
deetox for heavy metals
detox for chelating
eliminate s the toxins from environments and from inside of your body
FINAL GOAL: Purified the cells for all type of toxis. Recreate the brightening , the relaxation and the hapinees of your body.
Detoxification has to be done each month for 1 day
Detox working in combination with a healty and also with our regenerate water ( special water with a cocktail of vitamins and plants extract).
Products:
FACE:gentlecleanser/ exfolienting product/heat program follow by the mask / serum / healing cream ( day/night)
BODY: exfolienting cleanser/ foot mask/ detox shower gel/ a healing body lotion
aromatherapy blend
Regenerative Water
Detox cocktail
Kurzweil
Aging is not one thing. There's a number of different processes involved and you can adopt programs that slow down each of these. For example, one process involves the depletion of phosphatidylcholine in the cell membrane. In young people the cell membrane is about sixty or seventy percent phosphatidylcholine, and the cell membrane functions very well then—letting nutrients in and letting toxins out.
The body makes phosphatidylcholine, but very slowly, so over the decades the phosphatidylcholine in the cell membrane depletes, and the cell membrane gets filled in with inert substances, like hard fats and cholesterol, that basically don't work. This is one reason s that cells become brittle with age. The skin in an elderly person begins to not be supple. The organs stop functioning efficiently. So it's actually a very important aging process, and you can reverse that by supplementing with phosphatidylcholine. If you really want to do it effectively you can take phosphatidylcholine intravenously, as I do. Every week I have a I.V. with phosphatidylcholine. I also take it every day orally. So that's one aging process we can stop today.
Another important aging process involves oxidation through positively-charged oxygen free radicals, which will steal electron s from cells, disrupting normal enzymatic processes. There are a number of different types of antioxidants that you can take to slow down that process, including vitamin C. You could take vitamin C intravenously to boost that process.
Advanced Glycation end-products, or AGEs, are involved in another aging process. This is where proteins develop cross-links with each other, therefore disrupting their function. There are supplements that you can take, such as Alpha Lipoic Acid, that slow that down. There is an experiment al drug called ALT-711 (phenacyldimenthylthiazolium chloride) that can dissolve the AGE cross-links without damaging the original tissues.
Atherosclerosis is an aging process, and it's not just taking place in the coronary arteries, of course. It can take place in the cerebral arteries, which ultimately causes cerebral strokes, but it also takes place in the arteries all throughout the body. It can lead to impotence, claudication of the legs and limbs, and like most of these processes, it's not linear but exponential, in that it grows by a certain percentage each year.
So that's why the process of atherosclerosis hardly seems to progress for a long time, but then when gets to a certain point it can really explode and develop very quickly. We have an extensive program on reducing atherosclerosis, which is both an aging process and a disease process. We cite a number of important supplements that reduce cholesterol and inflammation—such as the omega-3 fats EPA and DHA—as well as the Statin drugs. Supplements like Curcumin [Tumeric] are helpful. Supplements that reduce inflammation will reduce both cancer and the inflammatory processes that lead to atherosclerosis. There are a number of supplements that reduce Homocysteine, which appears to encourage atherosclerosis. These include Folic Acid, vitamins B 2 , B 6 , and B 12 , magnesium, and trimethylglycine (TMG).
So you can attack atherosclerosis five or six different ways, and we recommend that you do them all, so long as there aren't contraindications for combining treatments. But generally these treatments are independent of each other. If you go to war, you don't just send in the helicopters. You send in the helicopters, the tanks, the planes, and the infantry. You use your intelligence resources, and attack the enemy every way that you can, with all of your resources. And that's really what you need to do with these conditions, because they represent very threatening processes. If you are sufficient proactive, you can generally get them under control.
David: What are some of the new anti-aging treatments that you foresee coming along in the near future, like from stem cell research and therapeutic cloning?
Ray: It depends on what you mean by “near future,” because in ten or fifteen years we foresee a fundamentally transformed landscape.
David: Let's just say prior to nanotechnology, and then that will be the next question.
Ray: is the next frontier is biotechnology. We're really now entering an era where we can reprogram biology. We've sequenced the genome, and we are now reverse-engineering the genome. We're understanding the roles that the genes play, how they express themselves in proteins, and how these proteins then play roles in sequences of biochemical steps that lead to both orderly processes as well as dysfunction—disease processes, such as atherosclerosis and cancer—and we are gaining the means to reprogram those processes.
For example, we can now turn genes off with RNA interference. This is a new technique that just emerged a few years ago—a medication with little pieces of RNA that latch on to the messenger RNA that is expressing a targeted gene and destroys it, therefore preventing the gene from expressing itself. This effectively turns the gene off. So right away that method ology has lots of applications.
Take the fat insulin receptor gene. That gene basically says ‘hold on to every calorie because the next hunting season may not work out so well.' That was a good strategy, not only for humans, but for most species , thousands of years ago. It's still probably a good strategy for animal s living in the wild. But we're not animals living in the wild. It was good for humans a thousand years ago when calories were few and far between. Today it underlies an epidemic of obesity. How about turning that gene off in the fat cells? What would happen?
That was actually tried in mice, and these mice ate ravenously, and they remained slim. They got the health benefits of being slim. They didn't get diabetes. They didn't get heart disease. They lived twenty percent longer. They got the benefits of caloric restriction while doing the opposite. So turning off the fat insulin receptor gene in fat cells is the idea. You don't want to turn it off in muscle cells, for example. This is one methodology that could enable us to prevent obesity, and actually maintain an optimal weight no matter what we ate. So that's one application of RNA interference.
There's a number of genes that have been identified that promote atherosclerosis, cancer, diabetes and many other diseases. We'd like to selectively turn those genes off, and slow down or stop these disease processes. There are certain genes that appear to have an influence on the rate of aging. We can amplify the expression of genes similarly, and we can actually add new genetic information—that's gene therapy. Gene therapy has had problems in the past, because we've had difficulty putting the genetic information in the right place at the right chromosome . There are new techniques now that enable us to do that correctly.
For example, you can take a cell out of the body, insert the genetic information in vitro—which is much easier to do in a Petri dish—and examine whether or not the insertion went as intended. If it ended up in the wrong place you discard it. You keep doing this until you get it right. You can examine the cell and make sure that it doesn't have any DNA errors. So then you take this now modified cell—that has also been certified as being free of DNA errors—and it's replicated in the Petri dish, so that hundreds of millions of copies of it are created. Then you inject these cells back into the patient, and they will work their way into the right tissues. A lung cell is not going to end up in the liver.
In fact, this was tried by a company I'm involved with, United Therapeutics. I advise them and I'm on their board. They tried this with a fatal disease called pulmonary hypertension, which is a lung disease, and these modified cells ended up in the right place—in the lungs—and actually cured pulmonary hypertension in animal tests. It has now been approved for human trials. That's just one example of many of being able to actually add new genes. So we'll be able to subtract genes, over-express certain genes, under-express genes, and add new genes.
Another methodology is cell transdifferentiation, a broader concept then just stem cells. One of the problems with stem cell research or stem cell approaches is this. If I want to grow a new heart, or maybe add new heart cells, because my heart has been damaged, or if I need new pancreatic Islet cells because my pancreatic Islet cells are destroyed, or need some other type of cells, I'd like it to have my DNA. The ultimate stem cell promise, the holy grail of these cell therapies, is to take my own skin cells and reprogram them to be a different kind of cell. How do you do that? Actually, all cells have the same DNA. What's the difference between a heart cell and pancreatic Islet cell?
Well, there are certain proteins, short RNA fragments, and peptides that control gene expression. They tell the heart cells that only the certain genes which should be expressed in a heart cell are expressed. And we're learning how to manipulate which genes are expressed. By adding certain proteins to the cell we can reprogram a skin cell to be a heart cell or a pancreatic Islet cell. This has been demonstrated in just the last couple years. So then we can create in a Petri dish as many heart cells or pancreatic Islet cells as I need, with my own DNA, because they're derived from my cells. Then inject them, and they'll work their way into the right tissues. In the process we can discard cells that have DNA errors, so we can basically replenish our cells with DNA-corrected cells.
While we are at it, we can also extend the telomere s. That's another aging process. As the cells replicate, these little repeating codes of DNA called telomeres grow shorter. They're like little beads at the end of the DNA strands. One falls off every time the cell replicates, and there's only about fifty of them. So after a certain number of replications the cell can't replicate anymore. There is actually one enzyme that controls this—telomerase, which is capable of extending the telomeres. Cancer actually works by creating telomerase to enable them to replicate without end. Cancer cells become immortal because they can create telomerase.
As we're rejuvenating our cells, turning a skin cell into a kind of cell that I need, making sure that it has it's DNA corrected, we can also extend it's telomeres by using telomerase in the Petri dish. Then you got this new cell that's just like my heart cells were when I was twenty. Now you can replicate that, and then inject it, and really rejuvenate all of the body's tissues with young versions of my cells. So that's cell rejuvenation. That's one idea, or one technique, and there's many different variations of that.
Then there's turning on and off enzymes. Enzymes are the work horses of biology. Genes express themselves as enzymes, and the enzymes actually go and do the work. And we can add enzymes. We can turn enzymes off. One example of that is Torcetrapib, which destroys one enzyme, and that enzyme destroys HDL, the good cholesterol in the blood. So when people take Torcetrapib their HDL, good cholesterol levels, soar, and atherosclerosis dramatically slows down or stops. The phase 2 trials were very encouraging, and Pfizer is spending a record one billion dollars on the phase 3 trials. That's just one example of many of these paradigm : manipulating enzymes. So there's many different ideas to get in and very precisely reprogram the information processes that underlie biology, to undercut disease processes and aging processes, and move them towards healthy rejuvenated processes.
tURMERIC ANTI-CANCER, ANTI -INLFLAMATORY SEEE WEKEPIDIA.
Turmeric is currently used in the formulation of some sunscreens. Turmeric paste is used by some Indian women to keep them free of superfluous hair. Turmeric paste is applied to bride and groom before marriage in some places of India , where it is believed turmeric gives glow to skin and keeps some harmful bacteria away from the body.
The Government of Thailand is funding a project to extract and isolate tetrahydrocurcuminoids (THC) from turmeric. THCs (not to be confused with tetrahydrocannabinol , also known as THC) are colorless compounds that might have antioxidant and skin lightening properties and might be used to treat skin inflammations, making these compounds useful in cosmetics formulations.
Turmeric makes a poor fabric dye as it is not very lightfast (the degree to which a dye resists fading due to light exposure).