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Old 08-27-2006, 09:10 AM
EarlyBird EarlyBird is offline
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Default Lung Cancer

August has been a horrible month where my friends' health
is concerned.



My friend Marge called me this am to tell me she has early
stages of Lung Cancer, and will begin Chemo treatments
this week.

Besides Vit C in large amounts, Flax Oil , selinium and vit E
[thanks Gerry] what else should I get for her to take? Also, besides Brocolli, cabbage, what foods would be good to suggest to her? I am really upset!

Thanks All
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Old 08-27-2006, 03:20 PM
bifrost99 bifrost99 is offline
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Vitamin B-17!

It's mainly for prevention, but if we all have cancer going on in our body all the time, as explained in the trophoblast thesis of cancer, then the prevention is actually ongoing cure.

A list of foods rich in B-17:

http://worldwithoutcancer.org.uk/aspreventative.html

The Unitarian or Trophoblastic Thesis of Cancer:

http://worldwithoutcancer.org.uk/thesis.html

Better to explore the whole site, itself:

http://worldwithoutcancer.org.uk

Of course, there's immune system stimulation with glyconutrients from mushrooms, lactobacilli, aloe vera gel, coconuts, brewer's yeast. Zinc would also be a mineral to consider.

It would be better, too, if you can convince your friend to forego chemo. It really wrecks the immune system. Acetogenins from graviola or paw paw, as well as artemisinin, may replace the chemo.

Gerry
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Old 08-27-2006, 10:57 PM
Aardvark Aardvark is offline
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Okay, let's try this again. A thunderstorm just knocked me off line and my post got lost.

To Gerry's suggestions I would add Ellagic Acid, Cat's Claw (Una de Gato) and visual imagery, along with the Budwig Protocol of flax oil and cottage cheese. Whatever she can do to bring her immune system to maximum activity is helpful, because she'll need all of her immune resources to not only fight the cancer, but also to fight the chemo's negative effects.

It's critical to keep a positive attitude, to stay physically active and to enhance immune activity by having some intense fun like riding roller coasters and bumper cars at an amusement park. Of course, it goes without saying that she needs to minimize, if not altogether eliminate, her intake of processed sugars, processed carbs and processed foods in general.

Please keep us informed regarding what she's willing and able to do.

Learn. Fight. Win.
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Old 08-28-2006, 12:54 AM
Josy Josy is offline
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Default lung cancer

EarlyBird, I am so sorry to hear about your friend. I can't believe how many lung cancer cases I am hearing about lately! One thing I have heard is it is linked to the chlorine you inhale while showering or in spas. So I would suggest that she buys one of those filters you put on the shower head to filter the chlorine out. You know you inhale that stuff with the steam.. Ok this is not going to heal her, but no sense in continued exposure.

Keep us posted...

Josy
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Old 08-28-2006, 05:23 AM
nightowl nightowl is offline
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Very sorry to hear about your friend's illness EarlyBird! I have been reading about this study a lot lately, at the following link and I would definately try it if I were in that condition.

http://www.drrathresearch.org/lab_re...0401_0506.html

This is a link to a product that has three of the ingredients listed, all except a high EGCG green tea.

Http://www.drrathvitamins.com/products/pdprolysin.html

I would use Mega Green Tea Extract from the Life Extension Foundation (LEF) with the supplement above, unless you know of another brand that is standardized with a dependable amount of EGCGs. LEF has 725 mg of Green Tea, powdered extract (leaf), 246.5 mg EGCG, and 674 mg other polyphenols. They also have the same potency in a decaffinated form. I wanted to give you a direct link to the tea but they are updating the search engine right now. You can find it later at http://www.lef.org or www.lifeextension.com . I believe the article mentioned, or I read in another article, that when all four ingredients were used together it was much more effective. I know this study wasn't on humans but it also worked on tissue in lab tests and to me it would be worth a try.

Also, one of the first things I would do is get IV treatment with Vitamin C.

Good luck and prayers for your friend.

nightowl
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Old 08-28-2006, 06:17 AM
EarlyBird EarlyBird is offline
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Default Lung Cancer

Thanks Everyone for your great suggestions. I'll read each link and copy as many as I can for margie to read. She has no computer, no Ins except for medicare, is quite poor and lives in Gov subsidized housing.

Except for foods which she can buy, I'll be supplying the supplements, teas, etc. for her.

I'm just so afraid the Chemo will get her before the cancer does. I doubt at this point I can talk her out of it, as the doca are giving her hope, saying it's Early Stages, and she's believing them. I can't take that away from her right now.

My main hope at this time is to try to help her build up her immune system and to eat the best foods for her body to fight both cancer and chemo with. Plus the supplements.

Marge is such a good, caring person. She uses her own Gov commodities and meager money to buy foods to fix meals for others who are sick or elderly, where she lives. She uses her gasoline to take some of them to Dr. appts or to get their meds I've called her St. or Mother Marge for years.

Thanks again, I've got to get to my reading the links, making a list, etc. and get to the HFStore.
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Old 08-28-2006, 08:16 AM
Marcus Marcus is offline
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Lack of Oxygen is the main factor that cancer occurs. Otto Warburg (nobel prize winner two times) figured this out a long time ago but even alternative people continue to ignore it.

Ozone is the best way to reactivate enzyme processes, reawaken cellular metabolism and respiration and get the oxygen delivery system funcioning correctly at the cancer site.

I do not recommend the Enlay ozone generator these days because I can not verify its levels of ozone but I have read testimonials from people who use them with success. Enlay is a very inexpensive ozone generator, about $50. You can set up a system for about $350 to $400 using medical grade ozone, (supposedly) with an Enlay. Includes oxygen tank, regulator, tubing, olive oil bubbler. This would enclude all the equipment you need. And since the tumor is in the lung you will be getting the ozone where it needs to go pretty easily. All directly inhaled ozone must be bubbled through olive oil and there is equipment for that. She could also insufflate her ears with ozone taking the gas directly to the brain, the location where most lung cancers tend to met. to and hopefully prevent this problem from occuring. People have cured brain cancer with ozone applied as such.

The second option is to purchase and use Homozon. Each teaspoon of homozon given in water equals the oxygen carrying capacity of 750 drops of H202 (though an ozone delivery system of ozone bound to magnesium developed by Nicholas Tesla) but with out the stomach upset. 6 teaspoons divided through the day would be needed.


In either case she should be taking extremely high dosages of digestive enzymes with meals and between meals. These also helps to break up tumor tissue and toxins released as the healing process goes on. It will soften severe herximer reactions.

Along with this I would use the arteminsin. And murphy's cocktail IV. (did I remember the name of that right?) In fact, a full protocol of Clarks parasite cleanse is in order and should be repeated every few months. I will post an article on arteminsin following this. Arteminsin also provides needed oxygen through peroxide and the article will tell some on this.

Homeopathy is always good but don't count on it as the cure all. Few homeopaths in the US are skilled enough.

Money is always an issue when it comes to chronic disease. I do think it is planned genocide for the ill, the disenfranchised, as well as those with money. They will ream your insurance company for every sent possible, take your house, your life savings and leave no foundation for future generations. Who are they? The pharmaceutical companies and their paid cronies, Medical Doctors and the hospital industry.

There are two choices. You can either get angy, get motivated, fight back, generate the money to do what needs to be done or she can write her last will and testiment.

Sorry to sound so harsh. But it is the truth.

Arrow
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Old 08-28-2006, 08:21 AM
Marcus Marcus is offline
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Article:


Wormwood (Artemisinin)
I first encountered wormwood in 1979 as the primary component in herbal capsules known officially as "42's" and informally as "gut bombs." My naturopath, Dr. Harold Dick, made them up in his clinic and used them for digestion and elimination remedies. For digestion, one just had to empty 2 capsules in warm water and drink it down--easier said than done, considering they taste somewhat like watered-down horse manure. But for someone with indigestion or having just consumed "food intolerances" that otherwise make them very ill, these foul-tasting concoctions have proven to be a blessing. (They are also rumored to be like "salve on a sore" for a hang-over.)

For bowel cleansing or constipation, one or two capsules taken straight down work amazingly well. When married in 1981, a visit to my naturopath on the way to Alaska via the Alaskan highway was a condition of marriage for my new husband, who had suffered from a lifetime of bowel problems. He decided to "pop a couple of capsules" driving down the road and lived to regret it. Four times that afternoon he had to pull over to the side of the road and run for the woods, toilet roll in hand. Thankfully, we were in the Canadian wilderness by then and there were nice soft snowbanks to plow into when he cranked the wheel. We're still laughing 25 years later, and he's still singing the praises of wormwood. (It might have looked ridiculous, but it felt good.)

More recently, I decided to do the liver-gallbladder flush recommended by Hulda Clark and others, but according to her advice one must at least always do a parasite cleanse first. That involves 3 products--cloves, black walnut hulls, and wormwood. I followed instructions and did the prerequisite cleanse just to get to the flush, not expecting anything to happen. However, on the day I did the largest number of product before tapering off, chronic pain in my neck and right shoulder that had tormented me for 15 years and cost thousands of dollars for chiropractic care over that time as well as putting me out of the free lance engraving art work I did for many years suddenly disappeared! I thought the pain was work-related and gave it up. I've never had another treatment for the problem that caused me countless sleepless nights and miserable days in pain. I still can't believe it. Love that WORMWOOD--DJT

(From an internet source

"A cancer cure from the ancient past?
Plant compound sparks chain reaction that kills tumor cells.

Chinese folk medicine has yielded a promising new approach for treating cancer. Using a dash of logic and modern lab techniques, Seattle scientists have shown that a compound extracted from the wormwood plant seeks out and destroys breast cancer cells, while leaving healthy cells unscathed.

IN LABORATORY experiments, the compound killed within 16 hours virtually all human breast cancer cells exposed to it in the test tube, reports Dr. Henry Lai, a bioengineering researcher at the University of Washington. Just as importantly, he says, nearly all of the normal cells exposed to it were still alive. And a dog with a type of bone cancer known as osteosarcoma so severe that it couldn't walk across the room made a complete recovery within five days of receiving the treatment. X-rays showed the animal's tumor “had basically disappeared,” says Lai, adding that he believes the dog is still alive two years later.

“Not only does [the drug] appear to be effective, but it's very selective,” Lai says. “It's highly toxic to the cancer cells, but has a marginal impact on normal cells.”
So what is this “novel” anti-cancer compound?
It's called artemisinin - and actually, it isn't new at all. Chinese folk practitioners extracted it from the plant Artemesia annua L., commonly known as wormwood, thousands of years ago for use in the treatment of malaria, Lai says. After a “secret recipe” for the treatment was discovered on a stone tablet in the tomb of a prince of the Han Dynasty during an archaeological dig in the 1970s, artemisinin re-emerged as a therapy for the mosquito-borne disease, Lai recalls. In fact, a purified form of the plant compound is now the drug of choice for treating malaria in many areas, particularly where chloroquine-resistant strains have emerged, he says.

"Nightly News: Predicting breast cancer

WHY IT WORKS
Experiments into why artemisinin works as an anti-malaria agent led to its tests as an anti-cancer drug. The key turned out to be a shared characteristic of the malaria parasite and dividing cancer cells: high iron concentrations.When artemisinin - or any of its derivatives - comes into contact with iron, a chemical reaction ensues, spawning charged atoms that chemists call free radicals. In malaria, the free radicals attack and bind with cell membranes, breaking them apart and killing the single-cell parasite. Cells, too, need iron to replicate DNA when they divide, Lai says. And since cancer is characterized by out-of-control cell division, cancer cells have much higher iron concentrations than do normal cells.On their surfaces, cancer cells also have more so-called transferrin receptors - cellular pathways that allow iron to enter - than healthy cells. In the case of breast cancer, the cells have five to 15 times more transferrin receptors on their surface than normal breast cells, Lai says.And so entered the dash of logic: About seven years ago, Lai reasoned, why not target cancer cells with the anti-malaria treatment? Working with assistant research professor Narendra Singh, Lai devised a strategy and obtained funding from the Breast Cancer Fund in San Francisco. The work appears in the November issue of the journal Life Sciences.

THE ANTI-CANCER STRATEGY
The thrust of the strategy, according to Lai, is to pump up cancer cells with even more iron and then introduce artemisinin to selectively kill them. In the experiments, Lai subjected sets of both breast cancer cells and normal breast cells to either: A compound known as holotransferrin, which binds with transferrin receptors to transport iron into cells and thus further increases the cells' iron concentrations;
A water-soluble form of artemisinin; or
A combination of both compounds. Cells exposed to just one of the compounds showed no appreciable effect, Lai reports. But the response by cancer cells when hit with first holotransferrin, then artemisinin, was dramatic, he says. After eight hours, three-fourths of the cancer cells were obliterated. By 16 hours later, nearly all the cancer cells were dead. Just as importantly, he says, the vast majority of normal breast cells did not die, showing the safety of the treatment.The success is particularly noteworthy in that breast cancer cells that were resistant to radiation were utilized in the experiment, Lai adds. “So that means this approach might work for cancer resistant to conventional therapy.” As might be expected, more aggressive cancers such as pancreatic and acute leukemia - which are characterized by more rapid cell division and thus higher iron concentrations - respond even better, Lai says. In a separate study, the therapy eliminated leukemia cells in the test tube within eight hours, he says.The next step, according to Lai, is further animal testing, followed by human trials. First the patient would be given iron supplements to raise iron concentrations in his or her cancer cells, he says, and then the compound would be given in pill form. While human tests are still years away, the treatment could revolutionize the way some cancers - particularly aggressive, fast-growing ones - are approached if it lives up to its early promise, he adds. But remember: Not every drug that shows promise in the test tube pans out in human tests. “The fascinating thing is that this was something the Chinese used thousands of years ago,” Lai says. “We simply found a different application.”The application certainly makes sense. There's a wealth of research linking iron and cancer: One study, for example, showed that three times as much iron could be extracted from malignant breast tissue as from benign tissue, according to Ralph Moss, author of the “Healing Choices” reports for people with cancer. Elevated iron storage was found in 88 percent of the breast cancer patients studied. Given this shared characteristic of malaria and cancer cells, why did it take so long to think of it? That, Lai says, is a mystery - 'Maybe people just don't think of simple ideas.' "

From: http://www.townsendletter.com/Dec200...isinin1202.htm
Artemisinin: From Malaria to Cancer Treatment
by Robert Jay Rowen, MD Editor-in-Chief, Second Opinion

Artemisinin, the key ingredient obtained from Artemisia annua, has a long history of use as an antimalarial remedy. Artemisia annua, or “sweet wormwood,” is mentioned in the Recipes For 52 Kinds Of Diseases found in the Mawangdui Han Dynasty tomb, dating from 168 B.C. In that work, the herb is recommended for use for hemorrhoids. It is also mentioned in the Zhou Hou Bei Ji Fang (Handbook of Prescriptions for Emergency Treatments) written in 340 A. D. The major active principal was first isolated in l972, and investigators at the Walter Reed Army Institute of Research located and crystallized the active component in l984.1

Artemisinin and two synthetic derivatives, artemether and sodium artesunate, were evaluated in the l970's. A number of the tropical countries have conducted trials. In China in 1979, wherein 2,099 patients infected with P. viva and P. falciparum, Artemisinin had good therapeutic effects and improved or cured all patients. Furthermore, the treatment with Artemisinin was without any obvious side effects. Artemisinin is also effective in cerebral malaria. Body temperature of patients normalized within 72 hours, and asexual parasites were eliminated within 72 hours. However, there was a relapse rate of 21%.2

In clinical trials in Vietnam, children ages 1 to 15 years were randomly selected to receive artemisinin suppositories or oral quinine. The results indicated that the suppositories rapidly cleared asexual P. Falciparium parasitemia in children and confirmed the problem reoccurrence rates.3

Artemisinin has been extensively researched for malaria, and has been used on over a million patients, mostly in China and Vietnam. It is very helpful for drug resistant malaria. Extensive review articles are available documenting the extensive testing that has been done.4-6

Various oral dosage regimens have been adopted in treating over one million patients. Early studies suggested that an optimum total dosage of 3 grams (about 50 mg/kg) was administered over a 3 to 5 day period. In most cases parasite and fever clearance times were in less than two days. Recurrence were much more common with tablets than with parenteral formulations. Because of the very rapid clearance time of fever and parasites, the use of artemisinin was favored, and recurrences, which were common, were treated with artemisinin again or with another drug.7

About twelve years ago, Dr. Leo Galland and Dr. Herman Bueno worked together in New York City and began using artemisinin as a broad spectrum antiparasitic agent.

“Artemisinin is a powerful oxidant. I have used it orally to treat small bowel bacterial overgrowth, Clostridial overgrowth and (along with other herbal extracts, such as berberine, grapefruit seed extract and oregano oil) as a treatment for intestinal parasites.” Leo Galland, MD.

Very recently, news reports have trumpeted Artemisinin as a leading treatment for malaria. Affected nations are calling for it to be accepted as the number one first line treatment, but the USA has blocked its acceptance as the primary treatment, alleging yet more studies are needed.

For the past ten years, the Hoang medical family, with three generations of sophisticated physicians, have used artemisinin in combination with several other herbs to treat cancer, and eliminate necrosis material from the body; for example, from wounds; from intestines of people who have ulcerative colitis, and from Crohn's disease. The efficacy of the artemisinin compound is very impressive for the treatment of breast cancer and possibly to prevent it. It is not only because of direct anticancer activity, but also due to hormonal balancing properties of the artemisinin. Herein, doses of 300 mg twice per day were adequate with other herbs.8

“The herb itself, Artemisia annua, is one of the best things for PMS, cramping, excessive bleeding and all symptoms of hyper-estrogenemia and hyperprolactinemia.” Dr. Hoang, MD.

Artemisinin contains an internal peroxide group. Due to this group, reactive oxygen is already present in the molecule. This belief is in agreement with the observations that derivatives of artemisinin lacking the peroxide moiety, are devoid of antimalaria activity.9

Additional support for oxygen-mediated toxicity of artemisinin is generated from other studies. The antimalarial activity of artemisinin in vitro, against P. falciparum, could be enhanced by increased oxygen tension. Drugs such as miconazole and doxorubicin, which are known to work via oxygen radical effects, enhance the activity of artesunate, a derivative of artemisinin. The effectiveness of artemisinin is reduced by catalase, dithiothreitol and alpha tocopherol.10

Furthermore, Levander, et al. found that manipulation of the host antioxidant defense status could provide prophylactic or therapeutic enhancement for the control of malaria. In this study, mice were fed with diets deficient in vitamin E or a diet supplemented with cod liver oil, which would deplete antioxidants. Vitamin E deficiency enhanced the antimalarial action of artemisinin against P. yoelii, but selenium deficiency did not. A diet containing 5% cod liver oil had a very strong antimalarial action.11

Artemisinin has been shown to work through oxygen and carbon based free radical mechanisms. Its structure includes an endoperoxide bridge. Peroxides generate free radicals in a Fenton type reaction when exposed to unbound ferrous iron. Malaria, which grows in the erythrocytes, has the opportunity to accumulate much excess iron which can spill into the unbound form. Electron microscopy has confirmed destruction of plasmodium membranes with morphology typical of free radical mechanisms.

With the knowledge of a high accumulation of iron in cancer cells, researchers Henry Lai and Narenda Singh of the University of Washington became interested in possible Artemisinin activity against malignant cells. In 1995, they published a paper in Cancer Letters concerning the use of artemisinin against numerous cancer cell lines in vitro. This article has mobilized interest in artemisinin as an addition to anticancer treatment.12

There are a number of properties shared by cancer cells, which favor the selective toxicity of artemisinin against cancer cell lines, and against cancer in vivo. In addition to higher rates of iron flux via transferren receptors than normal cells, cancers are particularly sensitive to oxygen radicals.13

A subsequent article appeared in Life Science in 2001 by Singh and Lai on the selective toxicity of artemisinin and holotransferrin towards human breast cancer cells.14 In this article, rapid and complete destruction of a radiation-resistant breast cancer cell line was achieved when the in vitro cell system was supported in iron uptake with holotransferrin. The cancer cell line was completely nonviable within 8 hours of combined incubation with minimal effect on the normal cells.

Artemisinin becomes cytotoxic in the presence of ferrous iron. Since iron influx is naturally high in cancer cells, artemisinin and its analogs selectively kill cancer cells under conditions in vivo. Further, it is possible to increase or enhance iron flux in cancer cells using the conditions that increase intracellular iron concentrations. However, intact in vivo systems do not need holotransferrin, the living body provides all the necessary iron transport proteins.

A third paper, by Efferth et al., published in Oncology in 2001 stated that the antimalarial artesunate is also active against cancer.15 This article described dramatic cytotoxic activity against a wide variety of cancers including drug resistant cell lines. Artesunate (ART) is a semi-synthetic derivative of artemisinin, and has been analyzed for its anticancer activity against 55 cell lines by the Developmental Therapeutics program of the National Cancer Institute, USA. ART was most active against leukemia and colon cancer cell lines. Mean growth inhibition 50% (GI 50) 1.11microM and 2.13 microM respectively. Non-small cell lung cancer cell lines showed the highest mean (GI50 26.62 microM) indicating the lowest sensitivity towards ART. Intermediate GI 50 values were obtained for melanomas, breast, ovarian, prostate, CNS, and renal cancer cell lines. Most important, a comparison of ART's cytotoxicity with those standard cytostatic drugs showed that ART was active in molar ranges comparable to those of established antitumor drugs. Leukemia lines resistant to either doxorubicin, vincristine, methotrexate, or hydroxyurea were tested. Remarkably, none of these drug resistant lines showed resistance to ART. The theorized reason for this is the absence of a tertiary amine in ART, present in virtually all other chemotherapy agents, which is required for cellular transport systems to usher the drug outside the cell.

Cancer Cells Are Deficient in Antioxidant Enzymes

Cancer cells are notoriously deficient in antioxidant enzymes - both forms of superoxide dismutase, the manganese form in mitochondria, and the copper zinc form in the cell cytoplasm are generally low in cancer cells. Cancer cells are grossly deficient in catalase and glutathione peroxidase, both of which degrade hydrogen peroxide. It is these deficiencies in antioxidant enzymes which lead to the use of many of the common chemotherapeutics which are superoxide generators.16

The higher iron fluxes, especially associated with the reproductive phase of tumor cells, should render these cells even more susceptible to oxidative damage via hydrogen peroxide and superoxides. Normally, the profound catalase deficiency in cancer cells is credited with creating vulnerability to oxidants, in relationship to IV vitamin C or IV hydrogen peroxide. However, since all of these protective antioxidant enzymes are most often deficient in transformed cells, the oxidant vulnerability should be enhanced dramatically, and further so, due to enhanced unbound iron during cell division.

Dr. Hugh Riordan has suggested that very high doses of IV vitamin C can kill cancer cells via conversion of vitamin C to hydrogen peroxide, and due to deficiency of catalase. For this procedure to work, very high levels of IV vitamin C are required to reach “kill concentrations.” IV vitamin C may be one of the best-documented alternative cancer treatments.17

Artemisinin may be a most effective method, and certainly one of the easiest, of delivering a knockout oxidative stress to cancer cells.

Artemisinin is appealing for oral use in that the pharmacodynamics, dosage and toxicity have been well studied for use in relationship to the treatment of malaria. Artemisinin is relatively safe with little side effects even at high dosages (70 mg/kg per day) in short term malaria use.

Artemisinin has two semisynthetic derivatives. Artesunate is a water-soluble derivative with no reported toxicity at usual levels. However, its serum half-life is relatively short. Artemether is a lipid soluble derivative, effective in cerebral malaria, and therefore may be more effective in brain cancers by better penetration of the blood-brain barrier. Artemether, however, has been reported to cause some neural toxicity in laboratory models in rather high doses. Artemisinin has an intermediate half life and can cross the blood-brain barrier. The two semisynthetic derivatives are available overseas in both oral and injectable for artesuante and artemether.

As mentioned, Lai used holotransferrin, which is iron-loaded transferrin, to further sensitize tumor cell lines to the oxidizing properties of dihydroartemisinin, which is derived from the parent compound metabolically in vivo. A human leukemia cell culture, Molt-4-lymphblastoid cells, and normal human lymphocytes were used in this experiment.

A significant decrease in cell count was noted with artemisinin alone, with p<.035. Greater effects were noted when transferrin and dihydroartemeisin were used together. In combined treatment, considerable tumor cell death was observed at a concentration of dihydroartemisinin of 1 uM after 8 hours of incubation. Furthermore, there is reason to believe that artemisinin can work at lower concentrations in vivo than in vitro, due to destruction of the artemisinin molecule in vitro.

Lai suggests that this procedure would be most effective for the treatment of aggressive cancers, in which large numbers of transferrin receptors are expressed on the cell surface. It may not be effective for T cell leukemias, which have defective internalization of transferrin receptors, and therefore may not be susceptible to this treatment.12

Case reports

1. Patient D.A. a 47 year-old mechanic who presented with a 4.5 cm. Non-Hodgkin's lymphoma on the right side of his head, with gaping incision from a recent biopsy, and tremendous inflammatory erythema. Artesunate, 60mg was administered IM 14 consecutive days and he switched diets to high protein/vegetable (Kelley parasympathetic type diet). At the end of two weeks, a depression appeared at the apex of the tumor. Four weeks later, the mass was completely gone, skull surface smooth, incision totally healed and erythema virtually cleared. Apparantly cancer-free as of this writing 6 months later.

2. Patient V.M. an 83 year old Toronto resident. Healthy most of her life, she now had a non-small cell lung carcinoma in the right lower lobe, considered non-resectable because of heart failure and circulatory problems. She received Artemisinin 500mg BID from Allergy Research Group and Carnivora oral, via nebulizer, 5cc BID. In 4 months the tumor shrunk to 1x2 cm and her oncologist felt this represented scar tissue and declared her cancer free. (Her heart condition improved considerably with CoQ10, 600mg daily).

3. Patient D.E., a 47 year-old Alaska resident with stage 4 breast cancer and metastases to T1 with significant pain, vertebral collapse and local neurological impairment. First seen May 2001, she received a series of IPT (insulin potentiation therapy-low dose chemotherapy), high dose vitamin C infusions, supplements, and dendritic cell vaccine, dietary management (Kelly sympathetic type diet), and detoxification strategies. Most symptoms had cleared within 4 months (October 2001). In January 2002, she received artesunate IV (source: mainland China), plus oral artemisinin 300 mg BID (ARG and Wellcare Pharma) which has been continued. Six months later she was happy to report she has no symptoms whatsoever and is living a normal life. Her local provider believes the regressed mass is now scar tissue.

4. Patient F.A., an 81 year-old Californian with multiple skin cancers including one active recurrent quarter-sized lesion that had been burned 4 times previously. Topical artemisinin (one capsule ARG artemisinin in 50% DMSO) applied twice daily caused the large lesion to fall off within 5 days and other smaller skin cancers to regress. His wife reported the same with her skin cancers.

5. L.L. is a West Coast woman in her 40's with breast cancer and extremely painful metasteses all over her spine. She had received limited radiation therapy to reduce the pain in the thoracic spine prior to consulting me. She began artemisinin, and a variety of complementary strategies, including diet, detoxification and Kelly type proteolytic enzymes (from Allergy Research Group). Immediately, her energy exploded. Her pain level took a dive when she received treatment from an Edgar Cayce Foundation healer. Her comment after two weeks on artemisinin was "Last week I thought I was dying, and today for the first time in months, I believe I am going to live." Four months into therapy using oral supplements alone (no IV therapy), diet and detoxification strategies, a PET scan, the most efficient and sensitive study for spread of cancer, did not show any activity anywhere in her spine, even in places that were present before and not radiated! Further, the scan did not confirm definite cancer activity anywhere else!

All patients who took oral artemisinin did so in the morning and evening on an empty stomach with either conjugated linoleic acid and/or omega 3 supplements and/or some full fat cultured organic dairy product to enhance absorption. Simultaneous iron in the stomach might neutralize its effectiveness.

Conclusion

Artemisinin has been used for about 30 years in Vietnam and China for cancer treatment. And the experience with artemisinin for this purpose is increasing. This history probably led to the recent cited cancer research with artemisinin.

The fact that artemisinin's direct antineoplastic effects closely resemble that of high-dose intravenous vitamin C is intriguing. The potential benefit of artemisinin in cancer treatment should be further explored because it is simple, safe, well-understood, and capitalizes on the multifold weakness in cancer cells to defend themselves against oxygen radicals. Enhancing the oxidant activity with other oxidation agents (such as carnivora, ultraviolet blood irradiation, H2O2, or higher oxygen tension itself) may add significant synergism. Adding artemisinin to low dose chemotherapeutic regimens inducing cytotoxicity via free radical mechanisms (such as doxorubicin), may safely add to the effectiveness of such treatment.

Dr. Singh, in a personal communication to me, has shared that he has been following a series of cancer patients with nearly universal improvement on artemisinin or its derivatives. He believes artemisinin will prove to be the most powerful, yet extremely inexpensive and safe, chemotherapeutic agent yet found, and effective orally for home use. However, like myself, he and the Hoang family of physicians, believes it should only be used in a professional atmosphere together with complementary strategies employing detoxification, diet, immune support, spiritual work, etc. This use of complementary strategies and professional supervision cannot be emphasized enough, especially since long term use of artemisinin and/or its derivatives has had little study. The Hoang family has indicated to me a 50-60% long-term remission in over 400 cancer patients utilizing artemisinin together with a comprehensive cancer strategy, and with no observed toxicity.

References

1. Klayman D. Qinghaosu (Artemisinin): Antimalarial Drug from China. Science, 1985, Vol. 238, May 31, p.1049

2. China Cooperative Research Group on Qinghaosu and its Derivatives as Antimalarials. J. Trad. Chin. Med 2, 17, 1982.

3. Keith Arnold, Tran Tinh Hien, Nguyen Tran Chin, et al. A randomized comparative study of artemisinine suppositories and oral quinine in acute falciparum Malaria.

4. Transactions of the Royal Society of Tropical Medicine and Hygiene (1990) 84:499-502.

5. Bharel S, Gulati M, Abdin P, Srivastava S. Structure biosynthesis and functions of artemisinin. Fitoterapia Vol LXVII No 5, l996.

6. Gulati A, Bharel S, Srivastava M, Abdin MZ. Experimental Studies on Artemisia, an herbal remedy for malaria. Fitoterapia Vol LXV11 No 5, 1996.

7. Hien T, White N. The Lancet 1993 Vol 341 March 6 p 603-651.

8. Personal communication from Dr. Hoang, M.D., 2002.

9. Ames JR, Ryan MD, Klayman DL. Charge transfer and oxy radicals in antimalarial action. J. Free Rad Biol. Med 1985, 1:353-61.

10. Krungkrai SR, Yuthavong. The antimalarial action of Plasmodium falciparum of qinghaosu and artesunate in combination with agents which modulate oxidant stress. Trans. R Soc. Trop. Med Hyg 1987, 81:710-4.

11. Levander OA, Ager AL, Morris VC. Qinghaosu, dietary vitamin E, selenium and cod liver oil: effect on susceptibility of mice to the malarial parasite Plasmodium yoelii. Am. J. Clin. Nutr. 1989; 5:346-52.

12. Lai H., Narendra S. Cancer Letters, 91:41-46, 1995.

13. May WS. J Membr. Biol., 88:205-215, 1985.

14. Singh NP, Lai H. Life Sci Nov 21, 70(1):49-56, 2001.

15. Efferth T, Dunstan H, Sauerbrey A, Miyachi H, Chitambar CR. Antimalarial artesunate is also active against cancer, Oncol. 2001, Apr;18(4):767-73.

16. Levine SA, Kidd PM. Antioxidant Adaptation: Its Role in Free Radical Pathology. Allergy Research Group, San Leandro, California, 1985.

17. Journal of Orthomolecular Medicine, Special Edition, 1999.

***

Wormwood is an integral part of Dr. Hulda Clark's parasite cleanse for cancer, and an herbal mixture called "42's" used by Dr. Leticia Watrous and her father, the late Dr. Harold Dick, for digestion and bowel stimulation-cleansing.

Inexpensive bulk herbs (not in capsules): herbalcom.com
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Old 08-29-2006, 05:45 AM
EarlyBird EarlyBird is offline
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Default Lung Cancer

Thanks again All.

Right now, I'm trying to find bulk PawPaw for Margie. If anyone knows of a source in the US, please post it.

I'll let you all know how she does - she's to begin Chemo next week.

Aardvark - I sure hope your area got more rain than mine. Ohio and Indiana sopped up most of ours. And it's still miserasbly humid :x
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Old 08-29-2006, 02:46 PM
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Quote:
Originally Posted by EarlyBird
Right now, I'm trying to find bulk PawPaw for Margie. If anyone knows of a source in the US, please post it.
The cancer-active compounds in paw paw are the acetogenins. These were first discovered as the active ingredients of graviola. So if you can't get paw paw, graviola can be a substitute, though some have shown that you'd have to take about 3 to 4 times more graviola than the equivalent of paw paw. It's probably because graviola products are usually the whole leaf while paw paw products are extracts. Me, I prefer the whole rather than the extracts, even if it means taking more.

I find Swanson's to be the cheapest source of supplements (so far):

http://www.swansonvitamins.com

They have graviola and artemisinin, but still do not have paw paw (graviola was a recent addition). They also have seed products which can be a source of vitamin B-17, though they don't market it as such. But she could just keep eating nuts. :wink:

I would recommend their mushroom product (Immune Essentials) and aloe vera products for immune stimulation. Of course, this stimulation should be followed up with lots of protein from the diet.

(I am just a client of Swanson. No commercial interest. 8) )

Gerry
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Old 08-29-2006, 02:52 PM
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Early Bird, my husband has prostate cancer which spread to his bones. For the past three years he has been taking graviola, which I get from Rain Tree. I buy the bulk powder, but you can get it in capsule form too.
http://www.rain-tree.com/graviola-capsules.htm

Husband became symptom free in a few months and remains so. I don't know what tomorrow brings, but today is good!
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Old 08-30-2006, 07:33 AM
EarlyBird EarlyBird is offline
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Thanks, Jo. Did you see where their Graviola has
Brazillian PawPaw in it?

I'll try to order some today. So many thanks to you, Jo.

Thanks to you too,Gerry. I'll check out Swansons
plus your other suggestions.

You ALL are just so SPECIAL
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Old 08-31-2006, 05:57 PM
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I just received this article in a health e-letter from Swansons today. Again, it wasn't a human trial, but sounds worth a try, especially since silibinin is so available. If she does use it, be sure she gets a standardized version.

~~~~~~~~~~~~~~~~~~~~~~~

Silibinin, a flavanone of milk thistle, inhibits lung tumor growth in mice and “merits investigation as a chemopreventive agent for suppressing lung cancer progression,” researchers wrote in a study published in the Journal of the National Cancer Institute.

Scientists at the University of Colorado, Denver decided to examine the effects of dietary silibinin on the growth, progression and angiogenesis of lung tumors in mice, noting that silibinin “inhibits the growth of tumors in several rodent models.”

Researchers injected mice with urethane to induce lung cancer. The rodents then received diets containing various doses of pure silibinin for 18 or 27 weeks. The researchers have been studying both silibinin and silymarin, another component of milk thistle, for over a decade in conjunction with their efficacy against various forms of cancer.

Mice receiving silibinin had “statistically significantly lower lung tumor multiplicities” than those fed a control diet. In the case of mice receiving a one percent (wt/wt) dose of silibinin for 18 weeks, there were 93% fewer large tumors compared to those in the control group.

Journal of the National Cancer Institute 98(12):846-855, 2006
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Old 08-31-2006, 09:20 PM
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Earlybird:

From what you have said I realize that your friend has been “sold” on chemo by her doctor and he wants her to start treatment in a week. Of course we all know that the chemo has an equally good chance of killing her before the cancer would. So being that she is still in the “early stage” I would do everything in my power to convince her to hold off on the chemo at least for a while. She has time to try the suggestions offered here and they will have a better chance of working if they do not have to be also fighting against the chemo.

By all mean give her printouts of what has been written here so she can see that there are real alternatives to what she has been told is the "only way".
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Old 09-05-2006, 06:00 AM
EarlyBird EarlyBird is offline
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Default Margie and Cancer

Just wanted to let you all know, that Margie has gone
solely Allopathic, and will NOT consider anything else,
even to NOT taking the Vit C I took her. Her Dr told
her that her 1 multiple vit daily will be sufficient.

Thanks to All of you for your advice and info, but Margie's
in God's hands now, and all I can do is pray for her,
and keep in touch.
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