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"Do not worry about anything, but in everything by prayer and supplication with thanksgiving let your requests be made known to God." (Philippians 4:6)
Surgery, Radiation and Chemotherapy Can Debilitate the Immune System. We gratefully introduce to you a supplement (we pray and believe that it may be God's answer to your concerns, see above!) that you may want to consider:
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P.D.Q.! Recovery Dietary Supplement Pill
Brand New and Available now! :
We give God thanks that we are now able to offer a safe and magnificent dietary supplement pill which may be extremely beneficial for those fighting to recover from surgery, radiation and chemotherapy and who need their body to be as physically strong as it can be to face serious disease and WIN!
P.D.Q.! Recovery Dietary Supplement pill is comprised of an excellent blend of seven herbs and two minerals which are noted to be safe and effective. The exclusive process to produce this pill reduces the particle size of the herbal ingredients which allows deep penetration directly throughout the body!
Developed by the same top scientist that created our famous P.D.Q.! Herbal Skin Cream that has been quite successful in applications on dangerous skin lesions, this powerful pill with many patents has quite a few ingredients that you may have heard about. The list of ingredients is found below.
When someone is fighting for their life, they should do everything possible to win the battle. We have high expectations that the P.D.Q.! Recovery Dietary Supplement Pill will be of significant help in such a fight!
Editor's Note: I myself have been concerned about prostate cancer with which I was diagnosed four years ago. Our scientist guided me through a healing process using the herbs and minerals, and now I am excited, and relieved, that such a pill is going to be available. I wish I had had this pill available for my second wife who died from breast cancer. There is no promise of a cure, of course, but this sure gives me a lot of hope for myself and others. I want to give my body all the help it needs to fight a winning battle! We give a big "THANK YOU" to the wonderful scientist who developed P.D.Q.! Recovery.
One bottle contains 60 pills, to be taken four pills per day, enough for a 15 day supply. We recommend a minimum of two bottles, a one month supply. Our price is $119.97 per bottle. We also encourage you to take one bottle of our wonderful P.D.Q.! Recovery Silver Water (six teaspoons per day for eight days - $39.97) which will really give a boost to the body's immune system.
To order, our phone number is: 800-292-0003
Our email address is: luxfab@quik.com
If you peruse this entire website, you will discover that we proudly and un-ashamedly give God all the credit, praise and glory for His love for us, and for the natural ways that He has given us to have healthy bodies. We consider it a blessing to be able to offer help and hope in His name, Amen!
P.D.Q.! Recovery Dietary Supplement List of Ingredients (for more information go to lower part of page)
1. Zinc picolinate: important immune system booster for fighting disease
2. Selenium: scientific studies show it may inhibit the growth of tumors
3. Sulforaphane Glucosinolate: as found in brocoli, may help maintain the body's natural defenses
4. Saw Palmetto: probably the best known herb in alternative therapy
5. Indole-3-carbinol: powerful anti-oxidant from cabbage and brocoli
6. Ellagic Acid (from Terminalia Chebula): anti-bacterial and anti-fungal
7. IP-6 (inositol hexaphosphate): anti-oxidant may boost activity of lymphocytes
8. Milk Thistle Seed Extract: anti-oxidant may prevent free-radical damage and is an outstanding liver cleanser
9. Schizandra Berry Extract: May produce cortizon-like effect on immune system and provide an energy boost
You may find it very interesting to know that each of the above is offered by various herbal suppliers in 100% form - it would cost much more to purchase the individual herbs and minerals (and you would have to take as many as 30 pills a day!), and the key is to have the herbs in the form, size, quality and exact amount that is needed. While each ingredient may be helpful as a stand-alone, when combined together as we have in this pill the efficacy of each is enhanced.
Above all, as we say throughout the website, we believe that "Prayer is the Best Medicine". We offer prayer for each customer, over the phone if desired. We pray that you will be healthy - in Jesus' name. Blessings!
To go to the home page, click here: www.behealed.biz
To ORDER and to talk with us directly: Call us at 1-800-292-0003
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As you may know, these and any statements we make about P.D.Q.! Recovery Dietary Supplement have not been approved by the F.D.A. Please read our Medical Disclosure Statement on page 3.
ADDITIONAL INFORMATION:
Zinc:
http://ezinearticles.com/?Prostate-Cancer-Its-Preventable!&id=98568
Selenium:
http://www.newstarget.com/016446.html http://cancer.ucsd.edu/outreach/publiceducation/cams/selenium.asp
SGS™ (Sulforaphane Glucosinolate) Fact Sheet
Powerful Indirect Antioxidant "Sprouts" in Young Broccoli
Overview
Increasingly, scientists are examining the role specific natural plant compounds (phytochemicals) may play in increasing the body">Why is Ellagic Acid Important? Clinical studies are showing that Ellagic Acid may be one of the most potent ways to prevent cancer, inhibit the growth of cancer cells, and arrest the growth of cancer in subjects with genetic predisposition for the disease. The Hollings Cancer Center at the Medical University of South Carolina is conducting a double blind study on a group of 500 cervical cancer patients that has everyone excited. Nine years of study have shown that a natural product called Ellagic Acid is causing G-arrest within 48 hours (inhibiting and stopping mitosis-cancer cell division), and apoptosis (normal cell death) within 72 hours for breast, pancreas, esophageal, skin, colon and prostate cancer cells. Ellagic Acid has been demonstrated in animal models to inhibit tumor growth caused by carcinogens. Other studies have also found positive effects. A recent animal study found that Ellagic Acid protected mice against chromosome damage from radiation therapy. A separate study of Ellagic Acid indicated that it was effective at inhibiting tumor growth from esophageal cancer cells in mice.
Ellagic Acid clinical tests on cultured human cells also show that Ellagic Acid prevents the destruction of the p53 gene by cancer cells. Additional studies suggest that one of the mechanisms by which Ellagic Acid inhibits mutagenesis and carcinogenesis is by forming adducts with DNA, thus masking binding sites to be occupied by the mutagen or carcinogen.
More information: http://www.phytochemicals.info/phytochemicals/ellagic-acid.php
IP-6
Inositol hexaphosphate ( IP-6 ), is a naturally polyphosphorylated carbohydrate found in cereal grains, beans, brown rice, corn, sesame seeds, wheat bran, and other high fiber foods. It aids in the metabolism of insulin and calcium, hair growth, bone marrow cell metabolism, eye membrane development, and helps the liver transfer fat to other parts of the body. Many researchers believe that some of the health benefits may be due to the antioxidant, immune enhancing, and cardiovascular supporting activities of IP-6. In-vitro and animal research has shown IP-6 to have significant protective and growth regulating effects on various cells and tissues including those of the colon, breast, and prostate. IP-6 and Cancer
IP-6 has been reported to have in vivo and in vitro anti- cancer activity against numerous tumors, such as colon cancer, prostate cancer, breast cancer, liver cancer, chronic myeloid leukemia, pancreatic cancer, and rhabdomyosarcomas. Significant human trials are lacking and hence we do not currently know for certain whether taking IP-6 supplements are helpful in cancer prevention or therapy, but the early data look promising. IP6 and Breast Cancer
IP6 inhibits the growth of breast cancer cells; but it also acts synergistically with adriamycin or tamoxifen, being particularly effective against estrogen responsive alpha-negative cells and adriamycin-resistant cell lines.
IP6 Mechanism of Action
In addition to reducing cell proliferation, IP6 increases differentiation of malignant cells, often resulting in a reversion to normal phenotype. Orally administered IP6 is rapidly taken into the cells and dephosphorylated to lower-phosphate inositol phosphates, which further interfere with signal transduction pathways and cell cycle arrest. Enhanced immunity and antioxidant properties can also contribute to tumor cell destruction. However, the molecular mechanisms underlying this anticancer action are not fully understood. Because it is abundantly present in regular diet, efficiently absorbed from the gastrointestinal tract, and safe, IP6 holds great promise in strategies for the prevention and treatment of cancer. IP6 enhances the anticancer effect of conventional chemotherapy, controls cancer metastases, and improves the quality of life.
IP6 inhibits human platelet aggregation in vitro.Metabolism of IP6
IP6 is rapidly absorbed by rats in vivo. There is a presence of inositol and IP1-6 in gastric epithelial cells as early as within 1 h of intragastric 3H- IP6 administration. The metabolized IP6, in the form of inositol and IP1 is transported via plasma and reaches distant organs as well as tumors. In rats, the urinary metabolites of IP6 are inositol and IP1. However, in humans 1-3% of total administered IP6 is excreted in the urine as IP6. Investigations of the uptake and metabolism by a variety of cancer cell lines in vitro also demonstrate an instantaneous absorption of IP6. The rate and pattern at which IP6 is metabolized by cancer cells varies depending on the cell type. Intracellular inositols accumulated mostly (80-97%) in the cytosol as inositol and IP1-6. IP6 treatment of all the cell lines tested so far demonstrates that it is cytostatic and not cytotoxic. Along with inhibition of cell proliferation, there is enhanced differentiation of malignant cells to a more mature phenotype, often resulting in reversion to normal. The actions of IP6 involve signal transduction pathways, cell cycle regulatory genes, differentiation genes, oncogenes and perhaps, tumor suppressor genes. IP-6 Research Update
Inositol hexaphosphate ( IP6 ): a novel treatment for pancreatic cancer.
J Surg Res. 2005 Jun 15;126(2):199-203. Somasundar P, Riggs DR, Jackson BJ, Cunningham C, Vona-Davis L, McFadden DW.
Louis A. Johnson VA Medical Center, Clarksburg, West Virginia; Department of Surgery, West Virginia University, Morgantown, West Virginia, USA.
Inositol hexaphosphate (IP6) is a naturally occurring polyphosphorylated carbohydrate found in food sources high in fiber content. IP6 has been reported to have significant inhibitory effects against a variety of primary tumors including breast and colon. The effects of IP6 have not been evaluated in pancreatic cancer. We hypothesized that IP6 would significantly inhibit cell growth and increase the apoptotic rate of pancreatic cancer in vitro. CONCLUSIONS: Treatment of pancreatic cancer with the common dietary polyphosphorylated carbohydrate IP6 significantly decreased cellular growth and increased apoptosis. Our findings suggest that IP6 has the potential to become an effective adjunct for pancreatic cancer treatment. Further in vivo and human studies are needed to evaluate safety and clinical utility of this agent in patients with pancreatic cancer.Prostate cancer and inositol hexaphosphate IP6 : efficacy and mechanisms.
Anticancer Res. 2005 Jul-Aug;25(4):2891-903. Singh RP, Agarwal R.
Department of Pharmaceutical Sciences, School of Pharmacy, University of Colorado Health Sciences Center, Denver, CO 80262, USA.
Inositol hexaphosphate ( IP6 ) is a major constituent of most cereals, legumes, nuts, oil seeds and soybean. Taken orally as an over-the-counter dietary/nutrient supplement, and is recognised as offering several health benefits without any known toxicity. In vitro anticancer efficacy of IP6 has been observed in many human, mouse and rat prostate cancer cells. Completed studies also show that oral feeding of IP6 inhibits human prostate cancer xenograft growth in nude mice without toxicity. In a recently completed pilot study, we observed similar preventive effects of IP6 on prostate tumorigenesis in the TRAMP model. Mechanistic studies indicate that IP6 targets mitogenic and survival signaling, as well as cell cycle progression, in prostate cancer cells. IP6 is also shown to target molecular events associated with angiogenesis. Moreover, IP6 has pleiotropic molecular targets for its overall efficacy against prostate cancer and, therefore, could be a suitable candidate agent for preventive intervention of this malignancy in humans.Novel anticancer function of inositol hexaphosphate IP6 : inhibition of human rhabdomyosarcoma in vitro and in vivo.
Anticancer Res. 1998 May-Jun;18(3A):1377-84.
Inositol hexaphosphate ( IP6 ) is a naturally occurring polyphosphorylated carbohydrate that has been shown to suppress the growth of epithelial cancers, including those of breast and colon. The objective of this study was to investigate whether IP6 inhibits growth of rhabdomyosarcoma (RMS), a tumor of mesenchymal origin, which is the most common soft tissue sarcoma in children. We performed both in vitro and in vivo studies to evaluate the effect of IP6 on human RD cells growth. Our results show that IP6 suppresses growth of rhabdomyosarcoma cell line (RD) in vitro in a dose-dependent fashion. However, the removal of IP6 from the media, after 72 hours of treatment, allowed cells to recover their logarithmic growth. Exposure of RD cells to IP6 led to differentiation; cells became larger with abundant cytoplasm, expressing higher levels of muscle-specific actin. Consistent with in vitro observation, IP6 suppressed RD cell growth in vivo, in a xenografted nude mice model. When compared to controls, IP6-treated mice produced a 25 fold smaller tumors (p = 0.008), as observed after a two weeks treatment. In a second experiment, wherein the treatment period was extended to five weeks, a 49 fold reduction in tumor size was observed in mice treated with IP6. Histologically no evidence of tumor cell necrosis was observed. These data suggest a potential usefulness of this cytostatic, and non-cytotoxic, compound in novel therapeutic strategies for these types of tumor.Anti-HIV-1 activity of myo-inositol hexaphosphoric acid ( IP6 ) and myo-inositol hexasulfate(IS6).
Anticancer Res. 1999 Sep-Oct;19(5A):3723-6.
It is known that polysulfates have some anti-HIV-1 activity. We investigated the anti-HIV-1 activity of myo-inositol hexaphosphoric acid ( IP6 ) and myo-inositol hexasulfate( IS6 ), low molecular weight carbohydrates. IP6 and IS6 inhibited the replication of HIV-1 in a T cell line as well as that of a freshly isolated strain in peripheral blood mononuclear cells. Neither substance inhibited HIV-1-induced giant cell formation, but addition of IS6 when infecting cells with HIV-1 inhibited the replication of HIV-1. Neither substance inhibited HIV-1 reverse transcriptase activity in vitro and no influence on late stage replication was noted. Although the mechanisms of IP6 and IS6 action remain unclear, it can be speculated that they act on HIV-1 early replicative stage. Although it is not possible to develop IP6 and IS6 themselves as anti-AIDS drugs, studies of these anti-HIV agents might be expected to provide seed for eventual production of superior drugs for AIDS treatment.
Hypolipidemic action of phytic acid ( IP6 ): prevention of fatty liver.
Anticancer Res. 1999 Sep-Oct;19(5A):3695-8.
Laboratory of Nutritional Science, Faculty of Education, Hiroshima University, Japan.
Until recently, most published reports on phytic acid ( myo-inositol hexaphosphoric acid, IP6 ) have focused on the possible decreased mineral bioavailability. Because IP-6 is known to function as a lipotropic factor, studies in my laboratory were conducted to investigate whether dietary IP6 also reduces excessive liver lipids. Male Wistar rats were fed sucrose or corn starch diets, supplemented with myo-inositol or IP6 for 12-14 days. Equimolar myo-inositol and IP6 similarly depressed the rises in hepatic levels of lipids and in hepatic activities of lipogenic enzymes due to sucrose feeding. However, dietary myo-inositol and phytate did not prevent orotic acid-induced hepatic lipid accumulation, which is known to be caused by severe inhibition of hepatic lipoprotein secretion. These results suggest that IP-6 might both protect against fatty liver resulting from elevated hepatic lipogenesis.
More information: http://www.lewrockwell.com/sardi/sardi39.html Milk Thistle:To research the claim that milk thistle is useful in treating cancer, its active substance silymarin and its major compound silybin have been the most widely studied ingredients.Silymarin and silybin may protect the liver against damage from toxic chemicals by blocking toxins from entering the cell or by moving toxins out of the cell before damage begins.Silymarin and silybin have been studied in the laboratory in cancer cells as well as in animal tumors of the tongue, skin, bladder, colon, and small intestine. They have been tested for their potential to:
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- Make chemotherapy less toxic.
- Make chemotherapy more effective.
- Stop or slow the growth of cancer cells and block tumors from starting or continuing to grow.
- Help to repair liver tissue.
More Information: http://www.phytochemicals.info/phytochemicals/silymarin.php
Schizandra:
http://www.phytochemicals.info/plants/schizandra.php
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