What Is Narconon Redwood Cliffs

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  • #10157 Reply


    Narconon Rehab Center on the Pacific Coast

    Situated on nearly 30 acres of land in the Santa Cruz mountains overlooking the Pacific coast, Narconon Redwood Cliffs offers an ideal location for a drug addiction rehab treatment center. The center was founded more than 20 years ago, and since then they have been helping people to overcome their addictions and make a fresh start in life. The center is surrounded by forest and offers a peaceful and beautiful environment for those who have been struggling with addiction and want to achieve meaningful and lasting recovery. During their time at the Redwood Cliffs center, students (as patients are referred to in Narconon) can enjoy a variety of recreational opportunities including:

    • Running trail
    • Swimming pool
    • Exercise equipment including weights
    • Basketball, volleyball, horseshoes
    • Foosball and ping-pong tables
    • Television lounge

    The center serves three meals per day and snacks in between meals, and the menu features highly nutritious foods that assist in the process of physically recovering from the ravages of addiction. Meals feature lots of fruits and vegetables harvested from the local farms, with produce grown in California soil that is among the richest and most productive in the world. The menus also include steak, chicken, pork or seafood, as well as options to accommodate a vegetarian or vegan diet.

    About the Narconon Redwood Cliffs Program

    The program at Narconon Redwood Cliffs does not approach the problem of addiction as an incurable disease. In other words, a Narconon graduate is not told that he or she is a “recovering addict.” Instead of treating addiction as a disease or an inherent fault in the person’s character, the program works by assisting the student to discover the underlying cause of his or her addiction, and to build up the person’s ability and confidence so that he or she can quit and remain stably sober. Redwood Cliffs is not a 28-day rehab. Students can stay at the center for as long as necessary to achieve the full recovery that they came for, and most complete the program within 90 to 120 days. The program involves several components including a sauna detox, the use of nutritional supplements and moderate exercise, counseling and life skills courses for a full rehabilitation of the person. This comprehensive approach to rehab treatment produces one of the best success rates in the field of addiction treatment, with a recovery rate of around 70% in terms of program graduates who maintain sobriety and avoid relapse.

    Narconon Redwood Cliffs Reaches Out into the Community

    Over the course of more than two decades, the team at the Redwood Cliffs center has assisted many people in recovering from addiction. They have also invested enormous amounts of time, energy and passion into the cause of preventing addiction before it starts. For example, they have delivered drug prevention education lectures to more than 50,000 elementary and high school students since 2004. They have appeared at schools in the Monterey Bay area, as well as throughout Central and Northern California. The organization also regularly engages in community outreach activities, such as by organizing holiday season toy drives and working with the Salvation Army to host Thanksgiving dinner for the homeless. They recently had a booth at the annual Strawberry Festival in the nearby beach city of Watsonville, passing out The Truth About Drugs booklets and getting local young people to sign a pledge to live drug-free and crime-free lives. For the past three years, they have co-hosted the National Night Out event along with local law enforcement agencies. In everything they do, the team at Narconon Redwood Cliffs is committed to helping to reduce the devastating impact that drugs have on society.

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    #68068 Reply


    Vancomycin INN /v??k??ma?s?n/ is a glycopeptide antibiotic acquainted with in the prophylaxis and treatment of infections caused by means of Gram-positive bacteria. Vancomycin was key eremitical in 1953 at Eli Lilly, from a begrime sample nonchalant from the upland jungles of Borneo nearby a missionary. It is a consequently occurring antibiotic made past the soil bacterium Actinobacteria species Amycolatopsis orientalis(formerly designated Nocardia orientalis). It is a complex chemical mix and an archetype of a comparatively rare haloorganic reasonable compound, containing two covalently bonded chlorine atoms.
    The compose was industrially produced by fermentation and assumed the generic name vancomycin, derived from the term “vanquish.” The original indication for vancomycin was in behalf of the treatment ofpenicillin-resistant Staphylococcus aureus, a consume kept alive for many years beside the fact that formulate had to be given intravenously and as follows provided bacteria fewer opportunities to evolve intransigence, and the happening that organisms were somewhat boeotian to evolve to reshape to it, orderly in experiments.
    For various years since its initial make use of, vancomycin had traditionally been unsocial as a psychedelic of “last resort” apposite to premature observations of its nephrotoxicity and ototoxicity as well as its intravenous dosing requirements.<>] Recently, however, vancomycin unaffected organisms are becoming common. Thus, vancomycin is increasingly being displaced from this role during newer antibiotics such as linezolid(Zyvox), daptomycin (Cubicin), and quinupristin/dalfopristin (Synercid).
    Vancomycin was sooner cloistered in 1953 by Edmund Kornfeld (working at Eli Lilly) from a tarnish try composed from the personal jungles of Borneo by a missionary.<>] The being that produced it was when all is said named Amycolatopsis orientalis.<>] The aboriginal clues instead of vancomycin was in the interest the treatment of penicillin-resistant Staphylococcus aureus.<>]<>]
    The multiply was initially called compound 05865, but was eventually prearranged the generic namevancomycin, derived from the arrange “vanquish”.<>] One gain that was fast ostensible is that staphylococci did not develop significant freedom fighters undeterred by serial verse in culture media containing vancomycin. The brisk development of penicillin resistance nearby staphylococci led to the parasynthesis’s being fast-tracked for endorsement about the Rations and Narcotic Administration (FDA) in 1958. Eli Lilly oldest marketed vancomycin hydrochloride controlled by the patrons name Vancocin<>] and as COVANC from Nucleus, India.<citation>needed]
    Vancomycin never became the first-line treatment for Staphylococcus aureus recompense specific reasons:
    1. It possesses insolvent uttered bioavailability; it must be given intravenously instead of most infections.
    2. β-Lactamase-resistant semi-synthetic penicillins such as methicillin (and its successors,nafcillin and cloxacillin) were afterward developed, which bear better activity against non-MRSA staphylococci.
    3. At cock crow trials cast-off at the crack impure forms of vancomycin (“Mississippi gombo”), which were create to be toxic to the ears and to the kidneys;<>] these findings led to vancomycin’s being relegated to the position of a psychedelic of mould resort.<>]
    In 2004, Eli Lilly licensed Vancocin to ViroPharma in the U.S., Flynn Pharma in the UK, and Aspen Pharmacare in Australia. The plain expired in the primeval 1980s; the FDA authorized the in stock of sundry generic versions in the USA, including from manufacturers Bioniche Pharma, Baxter Healthcare, Sandoz, Akorn Strides and Hospira.<>]
    An vocal ceremony of vancomycin was originally approved nearby the FDA in 1986 for the treatment of Clostridium difficile induced pseudomembranous colitis. It is not orally immersed into the blood and remains in the gastrointestinal tract to eradicate C. difficile. This effect is currently marketed by means of ViroPharmain the USA.<>]
    From suzhou pharmaceutical technology co.,ltd.

    #69785 Reply


    Thyroid hormone drugs are natural or synthetic preparations containing tetraiodothyronine (T4, levothyroxine) sodium or triiodothyronine (T3, liothyronine) sodium or both. T4 and T3 are produced in the human thyroid gland by the iodination and coupling of the amino acid tyrosine. T4 contains four iodine atoms and is formed by the coupling of two molecules of diiodotyrosine (DIT). T3 contains three atoms of iodine and is formed by the coupling of one molecule of DIT with one molecule of monoiodotyrosine (MIT).

    Both hormones are stored in the thyroid colloid as thyroglobulin.

    Thyroid hormone preparations belong to two categories: (1) natural hormonal preparations derived from animal thyroid, and (2) synthetic preparations. Natural preparations include desiccated thyroid and thyroglobulin. Desiccated thyroid is derived from domesticated animals that are used for food by man (either beef or hog thyroid), and thyroglobulin is derived from thyroid glands of the hog. The United States Pharmacopeia (USP) has standardized the total iodine content of natural preparations. Thyroid USP contains not less than (NLT) 0.17 percent and not more than (NMT) 0.23 percent iodine, and thyroglobulin contains not less than (NLT) 0.7 percent of organically bound iodine. Iodine content is only an indirect indicator of true hormonal biologic activity. Cytomel (liothyronine sodium) (liothyronine sodium) Tablets contain liothyronine (L-triiodothyronine or LT3), a synthetic form of a natural thyroid hormone, and is available as the sodium salt.
    From http://www.tcsindustry.com – TCS INDUSTRY LTD

    #70324 Reply


    Moxidectin (Milbemycin B[1 – ) kills parasites, so is second-hand on the restraining and supervise of heartworm and intestinal worms, and can be originate in treatments prescribed in place of animals such as dogs, cats, horses, livestock and sheep. Diligence methods an eye to moxidectin alternate not later than treatment, and include voiced, topical, and injectable solutions. Cydectin Spew out On is a swap choose for a formulation for urgency on cattle and red deer.
    Moxidectin is a semisynthetic imitative of nemadectin [2 – which is produced past fermentation before Streptomyces cyano-griseus. This Streptomyces species was discovered in a defile specimen from Australia in the past due 1980s unperturbed alongside an agronomist working for the American Cyanamid company.
    Moxidectin treats and controls some of the most unrefined internal and outward parasites on selectively binding to parasites?? glutamate-gated chloride ion channels. These channels are vital to the function of invertebrate nerve and muscle cells; when moxidectin binds to the channels, it disrupts neurotransmission, resulting in paralysis and cessation of the parasite.
    Studies of moxidectin posture the side effects restyle at hand animal and may be contrived beside the product??s formulation, application method and dosage. The products are usually recommended around a veterinarian to insure chasten avail oneself of and application. Herding dogs may be avermectin-sensitive, but avermectin-sensitive dogs can permit example doses looking for heartworm prevention. Moxidectin is manifestly harmless as far as something collie breeds. As a heartworm preventative, moxidectin can be injected at one time every six months covered by the brand name Proheart6, or every 12 months lower than drunk the brand name Proheart SR 12.
    Moxidectin is the referred to of a trial to assess its suitability, as an another to ivermectin, to remedying onchocerciasis in humans.[3 –
    From http://www.fmyykj.com – suzhou pharmaceutical technology co.,ltd.
    From http://www.tcsindustry.com – TCS INDUSTRY LTD

    #70718 Reply


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