Dr King Calls for Immediate End to Thiomersal.

[Guest guest]

Dear Friends,

 

All disease is treated as per established medical procedure. But this procedure talks very little about accumulated toxicity as a cause of disease. As a result there virtually is no protest at the medical level to the growing use of toxins in everyday life let alone that caused by medicines.

 

In the days of GP's, there was more consciousness and also concern about the cause of disease. Patients were advised to take medicines very sparingly and advised increased fluid intake to flush out the chemicals. Rest, diet, isolation, hygiene was regularly advised.

 

However come specialisation the only concern seems to be to prescribe medicines and interventions without any doctor-patient interaction worth its name.

 

Among epidemologists the emphasis on vaccines is shocking. Vaccines were earlier an emergency measure resorted to when all else failed but today it has become a first line of defence without any worthy medical study justifying the shift. Today we have a situation where diseases are being created and panic spread via the media to help vaccine manufacturers earn profits, if more insiduous reasons are not the cause.

 

I would request every epidemologist to study in depth the ingredients of vaccines individually and also try to know what they may do in combination. Let them also recognise that there is absolutely no scientific proof that vaccines have prevented any disease. We see metastasis that is shifting of the body metabolism tro express a more deep rooted disease. Can this be termed prevention?

 

A lot of soul searching and drastic changes in curriculum is necessary to combat the falling interest in modern health care. The santitised courses should be changed to reflect the truth and not hide facts from aspiring doctors.

 

Regards,

Jagannath.

 

 

 

"Paul G. King" <drkingAll,RE: "The Rise of Autoimmune and Other Diseases in Adults"Thimerosal/Merthiolate/Thiomersal(UK) has been beingused to subacutely mercury-poison us all since the1930s!Before that, Calomel, mercurous chloride was thesubacute mercury poison of choice from the late1800s to the 1920s.That ourselves, our parents and our grandparentswere affected is no surprise to anyone who hasstudied the knowing subacute mercury poisoningrealities occurring in the English-speaking worldsince the late 1800s.In 1890s -- 1940, this poisoning was principallyeffected via teething powders and, to a lesserextent, human worming preparations -- at its "peak",sub-acute Calomel-mercury poisoning resulted inabout 1-in-500 children having a

"pink disease"diagnosis in the USA and "caused" the epidemicof "stomach cancer" in the 1950s - 1960s thatdisappeared in the 1970s.Since the 1930s in the USA, this subacute mercurypoisoning has been effected via first Merthiolateand Mercurochrome antiseptic solutions of Thimerosal(1930 - 2000/1 [finally banned from topical antiseptics & vaginal contraceptives in 1998 but with NO recall ofdistributed products and with some companies ignoringban until at least 2005).In addition, Thimerosal, used as a "preservative" inserums and vaccines (1935 -- 2009 and ongoing) has, asthe number of DOSES of those "preserved" with Thimerosalincreased, has become the sub-acute mercury poisoningvehicle of choice.In the area of serums, most use in serum product stoppedin the mid-to-late 1990s and the last Rho(D) serum product(RhoGAM) was taken off market in USA in 2001 BUT w/o recall--

so some doses available into the 2002-2003 time frame.In the area of vaccines, the MAXIMUM DOSE of Thimerosal-preserved vaccines given to pregnant women and developingchildren HAS NOT been significantly reduced or, for thatmatter, REDUCED at all.This is the reality BECAUSE, although, since 2001, thenumber of types of vaccines that can be Thimerosal-preservedhas decreased significantly, GOVERNMENT RECOMMENDATIONS(by the CDC) AND continued APPROVALS (by the FDA) of thecurrent and new sources of Thimerosal-preserved influenzavaccines HAVE COMBINED TO INCREASE the MAXIMUM VACCINE DOSEof Thimerosal (49.6% mercury by weight) that a child couldbe given IN his or her DIRECT (OR INDIRECT, when pregnantwomen are inoculated) VACCINATIONS routinely recommended(by the CDC) from conception to the age of 18 years:FROM: <500 micrograms of Thimerosal (ca. 240 mcg of

mercury FOR a developing CHILD (from conception onwards) vaccinated UNDER the 1999 CDC schedule;TO: A. >950 micrograms of Thimerosal (ca. 480 mcg of mercury FOR a CHILD VACCINATED UNERD the pre- swine-flu 2009 CDC schedule, ORTO: B. >1100 micrograms of Thimerosal (ca. 560 mcg of mercury) IF the PREGNANT MOTHER GETS: 1. Two (2) Thimerosal-preserved swine-flu shots and 2. One (1) Thimerosal-preserved human-flu shot, orTO: C. >1200 microgram of Thimerosal IF the mother is vaccinated as

in "B" and the child subsequently receives two, 0.25-mL Thimerosal-preserved human- flu shots at 6 months and 7 months and either: 1. A single 0.5-mL Thimerosal-preserved swine-flu shot or 2. two 0.25-mL Thimerosal-preserved swine-flu shots (ca. 600 mcg of mercury), orTO: D. >1250 micrograms of Thimerosal UNDER the "C" two- shots-of-swine-flu scenario BUT the two swine-flu shots are 0.5-mL.Thus, one can trace the rise to all of these virtuallyunknown (in the 1940s) diseases, syndromes, and conditionsto near-epidemic (> 1 in 5000, epidemic > 1 in 500, or,

insome instances, super-epidemic (> 50; e.g., asthma [>1 in 10])levels to the cumulative effects of increasing multi-generational sub-acute mercury poisoning of an increasingpercentage of the population with an ever increasing levelof ever more insidiously toxic: A. Compounds (from Calomel [an inorganic mercury compound] to Thimerosal [an organic mercury compound tailored to be near maximally human bioaccumulatively toxic {1}]) and/or B. Modes of administration (oral to topical to injected). {1} Sugita M. The biological half-time of heavy metals. The existence of a third, "slowest" component. Int Arch Occup Environ Health 1978; 41(1): 25-40.As was shown in a study published in 1971 {2}, the

in-uteropoisoning of developing animals produces genetic effects thatare expressed in those animals who "survive" the in-uteropoisoning long enough to reproduce their own young. {2} Goncharuk GA. Experimental investigation of the effect of organomercury pesticides on generative functions and on progeny. Hyg Sanit. 1971; 36: 40-43.Thus, none should be surprised at any of today's realities.Is sub-acute mercury poisoning the only cause?No, it is NOT the ONLY CAUSE.However, it is the ONLY CAUSE that the ESTABLISHMENT: A. REFUSES to ELIMINATE, B. INCREASES while lying to us that it has been reduced or removed WHEN the truth that the MAXIMUM exposure has been INCREASED and, if you get two SWINE-FLU shots

and they are, as most will be, THIMEROSAL-PRESERVED, WILL SIGNIFICANTLY INCREASE yet again!Hopefully, SOME of you will listen and rise up as oneand DEMAND that ALL USE of THIMEROSAL or ANY OTHER MERCURYcompound IN MEDICINE will be IMMEDIATELY STOPPED and ALLvaccines and drugs that contain ANY level of any addedTHIMEROSAL or other mercury compound will be IMMEDIATELYRECALLED and DESTROYED.Respectfully,Dr. Kinghttp://www.drking.com

"It is clear....that the government's immunization policies are driven by politics and not by science. I can give numerous examples where employees of the US Public Health Service....appear to be furthering their careers by acting as propaganda officers to support political agendas. In one case....employees of a foreign government, who were funded and working closely with the US Public Health Service, submitted false data to a major medical journal. The true data indicated the vaccine was dangerous; however, the false data" indicated no risk. - October 1999, Dr. Bart Classen, founder and CEO of Classen Immunotherapies as told to Congress.

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