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"We fly a great deal and are always suffering from colds and respiratory infections. After taking your “magic drops” (Respigard™), we are no longer experiencing those infections! We will never again travel without Respigard™." Thank you!
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*User testimonials are truthful to their experience, but are not supported by clinical trials or peer-reviewed research involving products made by Natures Nurse.

 

*The products listed on this site are not to be considered substitutes for professional medical care. If you are sick, you should consult your physician. If you are currently taking any medication, consult your physician before you decide to use any herbal or other natural related products. This site and the products listed on it are not intended to diagnose, treat, cure or prevent any specific disease, nor are they appropriate as a substitute for professional care or medical consultation. These statements have not been evaluated by the Food and Drug Administration.

 


 

NATURAL IMMUNE AND RESPIRATORY SUPPORT DURING SEASONAL AND ONGOING CHALLENGES

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RespiGard™: Experience a POSITIVE RAPID IMPACT on your Respiratory & Immune System Function* through Seasonal & Ongoing Challenges

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International and U.S. based studies spanning 40+ years attest to how RespiGard’s red mangrove bark extract (Rhizophora mangle) supports natural immune and respiratory functions.

Ingredients
100% pure wild-crafted Fijian red mangrove (Rhizophora mangle) aerial rhizome
Kosher-certified USP grade vegetable glycerin
Purified water (pH neutral)

RespiGard’s™ red mangrove (Rhizophora mangle) is the main ingredient which supports our immune and respiratory systems’ function for rapid relief during seasonal stressors and when handling a wide range of other ongoing, persistent challenges – providing a natural, pure, non-toxic resolution. Users notice a rapid-response in usually 2 to 24 hours. Patent pending.

 

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SkinGard™ bottle SkinGard™: Our Exclusive Lotion Supports Healthy Skin. Caution: If you have a history of sensitivity to glycerin in skin care products, you should not use SkinGard™.

RESEARCH

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The study was conducted by Dr. Scott Carroll to follow up on, and compare results with, Dr. Ted D Anders' initial client interview study. Dr. Anders' study was the first contemporary red mangrove clinical efficacy review to evaluate products derived from his re-discovery and development of red mangrove as a viable modern nutraceutical supplement. The pertinence of Amnon Levy's (Phd) literature review to the on-going assessment of traditional herbal medicinals around the world is significant in three ways. First, it is essential that all herbal medicinals, including Rhizophora mangle, receive scientific scrutiny to substantiate claims. Second, the knowledge base pertaining to Rhizophora mangle must be expanded and substantiated as there are historical reports and recent studies from around the globe indicating potential medicinal properties (Hernandez and Perez, 1978; Duke and Wain, 1981); including significant anti-viral properties (Premanathan, Arakaki, Izumi, et.al., 1999). Third, in the case of Rhizophora mangle, it appears the plants provide a unique, reliable, naturally occurring constituent combination which needs to be more thoroughly examined to identify the primary active constituent and other identified constituents as a broad spectrum, complimentary support to primary active constituent action. Such a contribution to the arsenal of health care supplements available to humanity would be useful and noteworthy.

Methods
Selection and Description of Participants
During the 12-month time period from February, 2004 through February, 2005, Dr. Scott Caroll, M.D. conducted this initial clinical study focused on the "Fiji Titi /Fiji Tea " product created by Nature's Nurse®. The patient sample included 84 patients between the ages of 3 and 74; male and female. These patients had 2 or more symptoms related to the common cold: nasal congestion; runny nose; sore throat; headache; cough (with or without chest congestion); and malaise.

Technical Information
The recommended protocol for product use was: 2 full droppers of concentrated fluidextract to 1 cup of water, 4 times daily (morning, noon, evening and bedtime) for two days.

The fluidextract concentrates used were of two types. One was a hot water decoction. The concentrate was designed to equal the potency of the traditional dosage created from 50g of dried, crushed rhizome in 8 cups of water. The extraction was obtained with a hot water decoction, which produced a dark brown, thick liquid; the UV spectrum of which was 280nm, Abs. 0.2972. The yield was 29 ml/100g from crushed, dried Rhizophora. The final concentration was 3.4g/ml (d~1.2) or 2ml/cup of water. This fluidextract requires the inclusion of a preservative, sodium benzoate, in the finished product. The delivery system was a 1 oz. brown actinic bottle with a 1 ml capacity dropper.

The second was a proprietary glycerin-base alcohol-free fluidextract, called a '3-3-6™' processed fluidextract. The 3-3-6™ process is a serialized technology designed to produce a finished fluid extract that equals or exceeds the efficacy of the traditional dosage created from 50g of dried, crushed rhizome in 8 cups of water. The 3-3-6™ fluid extraction results in a dark brown, high viscosity liquid, with a specific gravity of 1.190, and a 3-3-6™ standardized brix density of 53 (+/- 2% ). The yield is based on a proprietary ml/g range of 29ml/Xg (noting that much less Rhizophora raw material is used in 3-3-6™ fluid extract process than that used for hot water decoction) from crushed, dried Rhizophora. The 3-3-6™ fluid extract requires no preservative (or refrigeration after opening), even claiming a labeled shelf life of 3 years. The delivery system was a 1 oz brown actinic bottle with a 1 ml capacity dropper. Approximately 50% of the patients received the hot water decoction and 50% received the glycerine-based fluid extract.

Results
Of the 84 patients from whom this researcher was able to obtain a clinical report, the following results were obtained. Seventy nine percent (79%) of overall participants had either complete resolution of symptoms before or by the end of the 48 hour treatment period (the vast majority) or in those few remaining, significant improvement. Twenty one (21%) of the patients were not improved. Of significant note is that several of the patients with recurrent sinusitis were in the 79% group. These patients thereby avoided taking antibiotics; which more of them would have been apt to do, based on prior experience in this type of patient. These results were overall concomitant for both the 3-3-6™ fluidextract and water decoction preparations, though it was noted that some respondents reported when they used half the dose for the 3-3-6™ fluidextract they still obtained results concurrent with the standard prescribed dose for this study.

Discussion
There is clear evidence that the hypothesis was supported. Rhizophora mangle L. appears to be effective for the vast majority of clients within 48 hours. Even patients with resistant, recurring sinus infections who invariably wind up on an antibiotic experienced resolution of their symptoms. Of course, these results need to be replicated in a controlled, double-blind clinical trial. Nevertheless, the impact appears to be significant and should be stimulus for further research.

References
Duke, J.A. and Wain, K.K. Medicinal Plants of the World, 3 Volumes, 1981.
Hernandez N. M. Rojas and Coto O. Perez, Antimicrobial properties of extracts from Rhizophora mangle, Rev. Cubana Med Trop, 30: 181-187 ,1978.
Premanathan, N., Kathiresan, K., Yamamoto, N., Nakashima, H. In-vitro anti-human immunodeficiency virus activity of polysaccharide from Rhizophora mucronata poir, Biosci, Biotechnol, Biochem, 63:1187-91, 1999.

* This statement has not been evaluated by the US Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

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