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Red Marine Algae Supports Us and Our Immune System

Maintaining a strong, healthy immune system is of the utmost importance. The ease with which so many individuals acquire infections and are subject to viral conditions suggests that we are all relatively weak in our ability to resist pathogens. When the immune response is inadequate to meet the challenge of an invading pathogen, the agent escapes destruction and is able to multiply and chronically persist in the tissues.

Red Marine Algae is capable of working on multiple levels to strengthen the body and solidify its primary defense system. This is accomplished in several ways:

First and foremost, returning to whole foods from the ocean can help realign our bodies to the ancient life-giving balance. Any immune disorder causes a severe mineral deficiency. Red Marine Algae is rich in minerals and is organized in such a way that the body can utilize them easily. Minerals and trace elements are the key to restoring and maintaining proper acid-alkaline balance in the body.

When a proper acid-alkaline balance is not maintained, the body falls into a state of degeneration. Acid conditions develop which create a chronic stage of disease. Too much acidity allows yeast, viruses, rebellious cancer cells, and various other parasites to thrive. Acidity also lead to conditions such as chronic fatigue, AIDS, arthritis, and allergies. The effect of Red Marine Algae is to create an alkaline reaction in the tissues in order to rebuild healthy tissue.

Red Marine Algae provides a nutritional base for improved digestion. Improved digestion enhances organ function and thereby nourishes the colon, liver, and adrenals. Proper function of these organs reduces tension, helps us live with stress, and enables our bodies to maintain a more constant vitality.

Red Marine Algae - A Key to Wellness

Red Marine Algae can restore nutritionally what we need in order to function on basic levels. This is very important because it allows a body's internal balance to naturally affect the growth of pathogenic bacteria, fungi, and viruses before they become harmful. We cannot completely stop pathogens from living in our body; however, we can inhibit their activity. We can accomplish this goal by preserving a healthy climate within our body where fair weather and sunny skies are the order of the day. This is extremely important as bacteria, fungi, and viruses thrive in dark, moist, contracted areas of the body. The ancient life-giving balance we receive from red marine algae takes on new meaning when understood as a major step towards strengthening our immune system.

Further information about Red Marine Algae can be found at the following:
Red Marine Algae as a super food
Red Marine Algae as an alternative medicinal treatment
Red Marine Algae general information


1. Baba et. al., "Mechanism of inhibitory effect of dextran sulfate and heparin in replication of human immunodeficiency virus in vitro." Proc Natl. Acad. Sci 85:6132-6136. 1988

2. Barbul, A. et al., "Arginine stimulates lymphocyte immune response in healthy human beings. Surgery 90: pp 244-251. 1984

3. Cole and Sheath, (Ed.), Biology of the Red Algae, Cambridge University Press, Cambridge, 1990.

4. Dieg et. al., "Inhibition of herpesvirus replication by marine algae extracts," Anitimicrb. Ag. Chemother. 6:524-525. 1974

5. Dieg et. al., "Evaluation of extracts of marine algae for antiviral activity in experimental herpes simplex infections of infant mice." In Fifty-second Technical Progress Report, Section 4, Naval Biosciences Laboratory, School of Public Health, University of California, Berkeley. 1977

6. Dieg et. al., "Development of dermal lesions in adult mice infected with herpes simplex virus: application of the model in the evaluation of antiherpesvirus substance from marine algae." Office of Naval Research, University of California Sea Grant Program. Unpublished.

7. Ehresmann et al., "Antiviral properties of algal polysaccharides and
related compounds," In H. A. Hoppe et. al., (ed.), Marine Algae in
Pharmaceutical Science, W. de Gruyter, N. Y.: 293-302. 1979

8. Ehresmann, et. al, "Antiviral substances from California marine algae," J. Phycol. 13: 37-40. 1979

9. Gonzales et. al., "Polysaccharides as antiviral agents: antiviral activity of carrageenan," Antimicrobial Agents and Chemotherapy. 31: 1388-1393.  1987

10. Hallinan et. al., "Inhibition of reverse transcriptase by polyvinyl
sulfate (PVS)," Cancer Biochem. Biophys. 98:97-101. 1981

11. Hatch et. al., "Chemical characterization and therapeutic evaluation of anti Herpesvirus polysaccharides from species of Dumontiaceae," In H. A. Hoppe et. al., (ed.) Marine Algae in Pharmaceutical Science W. de Gruyter, N. Y. 346-363. 1979

12. Mitsuya et. al., 1988 "Dextran sulfate suppression of viruses in the
HIV family: inhibition of virion binding to CD4 and cells,"
Science 240:646-649. 1988

13. Nakashima et. al., "Antiretroviral activity in a marine red alga: reverse transcriptase inhibition by an aqueous extract of Schizymenia pacifica" Journal Cancer Res. Clin Oncol 113: 413-16. 1987

14. Neushul, "Antiviral carbohydrates from marine red algae." Hydrobiologia 204/205:99-104. 1990

15. Pitchford, Paul, Healing with Whole Foods, North Atlantic Books,
Berkeley, California, 1993

16. Richards et. al., "Antiviral activity of extracts from marine algae,"
Antimicrob. Agents Chemother. 14: 24-3-. 1978

17. Schaffrath et. al., "Interactions of glycosaminoglycans with DNA and RNA synthesizing enzymes invitro," Z. Physiol Chem. 357:499-508. 1976

16. Solomon et. al., "Inhibitory effect of heparin on Rous Sarcoma virus," J. Bact. 92:1855-56. 1966

18. Straus et al.,, "Suppression of frequently recurring gential herpes"
N Eng J of Medicine, Vol 310 No. 24 pg. 1545-50. 1984

19. Douglas et al., "Acyclovir and Genital Herpes" N Eng J of Medicine,
Vol. 310 No. 24 pg. 1551-56. 1984

20. Thomson and Fowler, "Carrageenan: a review of its effects on the
immune system,: Agents and Actions. 11: 265-273. 1981

21. Ueno and Kuno, "Dextran sulphate, a potent anti-HIV agent in vitro
having synergism with sidovudine," Lancet 1:1379. 1987