Clinical Use Report Of MSP 
                   Dr. Joseph J. Cardot 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.