Clinical Use Report Of MSP Dr. Joseph J. from Colorado MD* Researchers have been warning the medical establishment for years that the indiscriminate use of antibiotics could spawn mutations in pathogens (bacterial, viral, and fungal), creating "Super Bugs" resistant to all known medications. The result, they warned, would create a "post antibiotic world" where common, as well as uncommon, infections would quickly escalate into fatal illnesses. The warning have been ignored; the result is that we are--right now--facing a major threat to human life from formerly* treatable infectious conditions. A friend of mine, Dr. Richard Callahan, York, NE, in a recent phone conversation remarked that, in his opinion, mutated pneumococcus bacteria and viral pneumonia will be killing thousands of Americans annually within five years. Bad news indeed. The good news is that Mild Silver Protein (MSP) may be an answer to the dilemma we are facing. I have operated a family (MD)* practice for 37 years where I have treated all types of infections in patients varying in ages from infants to over ninety. Before prescribing any treatment I believe a Doctor should determine if the patient might suffer harmful effects from the treatment. "First Do No Harm." The treatment should also offer the prospect of helping the patient recover. MSP meets both of the criteria. I started using a Silver suspension in protocols for patients with infections in January of 1992. The first patient, a female, had "walking" viral pneumonia. She was placed on one tablespoon of the silver suspension t.i.d. She was asymptomatic the fourth day into treatment. I was astounded. I thought that it might have been a misdiagnosis. Since that first experience I have treated more than 50 cases of viral pneumonia with the same positive results. Time of treatment varies, due to patient condition and severity of infection, from four days to thirty days. The outcome, however, is consistently positive; the infection is cleared. Since that first experience I have included MSP in protocols for all types of infectious diseases with positive results. MSP has cleared reoccurring ear infections in children who were scheduled for tube surgery making the procedure unnecessary. Infectious fibromayalgia (Fibromyositis) and Sjogren's Syndrome patients have benefitted from MSP therapy; MSP therapy helps many rheumatoid arthritis patients with synovial fluid infections that are causing inflammation-* to no longer need steroids. Systemic Candida Albicans is successfully treated with MSP. It is so effective we must start with small doses to control Herxheimer effect. Staph and other infections in the mouth (Gingivitis) have dramatically improved with MSP therapy. The Lyme disease spirochete (Borrelia burgdorferi) is eliminated using MSP therapy. I have records of Lyme patients who have been taking various antibiotics for three or more years who have become asymptomatic on MSP therapy after just three or four weeks of treatment. The average duration to rid the body of the spirochete is three to nine months. Systemic Candida Albicans frequently occurs in patients with Lyme; complicating the treatment and prolonging the duration of treatment. Lyme disease is far more prevalent than is generally known. Lyme has been reported in the U.S. in 43 states, and in all of Canada. I believe that reported cases of Lyme represent only about 20% of the actual number of Lyme cases. Lyme is routinely misdiagnosed as meningitis or as a "heat rash." A red rash is a typical symptom of Lyme. INVIVE 30 (30 ppm)* and INVIVE 40 (40 ppm)* are proving to be 1OO% effective in getting rid of the Lyme spirochete when they are included in the treatment protocol. The important thing about MSP therapy is that it is non-toxic. I have never observed any side effect from using MSP therapy, and I have used it in patients with all kinds of infections. In acute conditions as much as four tablespoons (60 cc/ml)* per day has been given, with no adverse reactions observed or reported. HIV positive patients have responded to MSP therapy if begun before the advanced stages of full blown AIDS. Temple University studies indicate that MSP kills the HIV virus in vitro. I believe that the HIV can be completely eliminated by using higher concentrations of MSP than can be absorbed with oral dosing. In vivo studies should be done using 250 to 750 ppm MSP administered IV. Due to the fact that MSP is non-toxic in high concentrations, this could prove to be a God-sent treatment for the millions who are suffering and dying from AIDS related illnesses. The use of AZT and other chemotherapeutic drugs, in the vain attempt to treat AIDS is, in my view, simply death by prescription. These drugs destroy DNA and the immune system; a case of "the cure being as bad as the disease." Why not use a proven to be "non-toxic" protocol with AIDS patients, rather than the present approach of hitting them on the head with a hammer to get rid of the headache? Specialists* have developed a MSP/solvent formula (INVIVE 400*). This formula, when applied to the gums, produces dramatic improvement with the first treatment. Saturate a band-aid pad with INVIVE 400* and apply to ringworm. The infection is cleared in 2 to 3 days. Psoriasis (virus in the skin) responds to INVIVE 400*, applied topically. Within 3 weeks of treatment (b.i.d.) new normal skin growth is observed. It takes three to eighteen months of MSP therapy to heal psoriasis. INVIVE 400* is so effective in treating gum diseases (Gingivitis) that, in my opinion, if widely utilized in the population, it could eradicate gum disease completely. I have seen patients with severe infections of the mouth whose symptoms included swollen gums, tongue, and cheeks (making them unable to speak or eat) improve immediately. Following one application of INVIVE 400* most could eat. These severe infections are completely cleared after two to four days of applying INVIVE 400* four times per day. We have seen excellent results using MSP therapy in Herpes genitalia. If INVIVE 400* is applied topically when itching and soreness occurs prior to vesicular eruption,* it prevents eruption in more than 50% of the cases. Eruptions are mild when they do occur. If treatment is continued b.i.d. topically to the area, the infection clears in half the usual time. Patient should also take 2 teaspoons of INVIVE 30* or INVIVE 40* orally daily and remain on 1 teaspoon per day to help eliminate future out-breaks. Herpez Zoster (shingles) has been successfully treated as well. Pain is substantially relieved and duration of eruption reduced as indicated above with h. genitalia, (same Protocol). Mild Silver Protein is not a standard colloidal silver suspension. It is made by a licensed (by the FDA) laboratory that has research to substantiate its efficacy and safety for use in vivo to control infection. Many companies have jumped on the band wagon producing colloidal silver products. Many are unstable; rendering them useless. Most are formulated with only 3 to 6 ppm. Silver suspensions are not homeopathic remedies. They are more effective in higher concentrations. INVIVE 30* is formulated at 30 ppm and INVIVE 40* is formulated at 40 ppm, as a dietary supplement, and INVIVE 400* is formulated at 400 ppm*. These are the types of concentrations I use in my practice, and they are responsible for the results achieved with patients coming to my clinic that I have shared with you in this article. If you and your doctor had access to something that would effectively kill all kinds of infections, and that was completely non-toxic with no side effects, it would be a blessing. Mild Silver Protein has proven to be that blessing in my practice.