REFUSAL OF VACCINES FORMS

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you should probably print this out and keep it .......I am not sure how long this URL will stay activehttp://www.geocities.com/Heartland/Ranch/4172/VacRefuse.htmlREFUSAL OF RECOMMENDED VACCINESPatient Name_______________________________Birthdate_______________As the parent/guardian of __________________________,I have investigated the risks and benefits of the followingvaccines and diseases. I am aware that there are documentedcases of people contracting diseases for which they areclinically fully immunized and that the manufacturers of thevaccines do not guarantee 100% efficacy. I am also awarethat VAERS (Vaccine Adverse Events Reporting System)documented cases of over 54,000 adverse reactions fromvaccines in a 20-month period. The National Vaccine InjuryFund, created in 1986 to compensate those damaged byvaccines has paid out over one billion dollars in compensationto date.POLIO: I have been informed of the risk of my childdeveloping paralytic disease and meningitis associatedwith poliomyelitis. I understand that even under epidemicconditions, natural polio produces no symptoms in over 90%of those exposed to it.[those who get enough vitamin B don't get polio](1) I understand that there have been no cases of wild polioin the US in the last 20 years and that those cases which havebeen documented have been caused by the vaccine.(2) I understand the following side effects for the vaccine arepossible: Killed virus polio: temperature of *102 in up to38%, sleepiness, fussiness, crying, decreased appetite, vomiting,Guillain-Barr* Syndrome and allergic reaction in those allergicto neomycin, polymyxin B and streptomycin. Precautionsinclude those who have had a previous negative reaction,pregnant women, and possibly those with HIV/AIDS orotherwise compromised immune systems.Live virus polio: Reactions include contraction of polio bythose who have received the virus and by those who have comeinto contact with body fluids and wastes of the immunizedperson. Paralytic symptoms may follow contraction of polio.Live virus is reportedly shed for up to 8 weeks after theinoculation. Guillain-Barr* Syndrome has also been noted.Not recommended for use in households where someone hasa compromised immune system, for pregnant women, or wherea previous reaction has been reported.(3) Killed virus Ipol¨ is grown on monkey kidney cells,contains formaldehyde, and triple antibiotics. Poliovax¨ isgrown on cells from an aborted baby, contains formaldehyde,cow serum and triple antibiotic solution.(4) The monkey kidney cells used in the original killed poliovaccine contains SIV-40 and has been found in tumor cells ofchildren whose parent's were vaccinated against polio using thecontaminated virus.(5) The live vaccine is grown on monkey kidney cells,antibiotics and calf serum. HEMOPHILUS INFLUENZAE B:I have been informed of the risk of my child developingmeningitis (although this vaccine will not protect the child frommeningitis from all other forms such as pneumococcus, andmeningococcus, viruses, and fungi), pneumonia, and infectionsof the blood, joints, bone, and soft tissue associated withHemophilus Influenzae B. I understand that this disease ismost likely in children up to 15 months of age and is fatal in3-6% of children who contract it. Incidence of this diseasetoday is low and the vaccine has not proven to be highlyeffective in 41% of cases, according to some studies.(6) Treatment is available.The vaccine is often combined with the DPT which has thehighest reaction rate of any vaccine available today. Reactionsinclude: contracting HIB, localized pain, erythema andinduration, fever >100.6¡, irritability, lethargy, anorexia,rhinorrhea, diarrhea, vomiting, cough, when administered alone.Reactions occurred in up to 30% of patients. Whenadministered in conjunction with the DPT, reactions includelocal tenderness erythema and induration, fever >100.8¡,irritability, drowsiness, anorexia, diarrhea, vomiting, persistentcrying, seizures, urticaria, hives, renal failure, Guillain-Barr*Syndrome and death. Reactions occurred in up to 77.9% ofpatients.(7) The vaccine contains yeast, thimerosal (mercury derivative),and diphtheria toxoid when given alone.(8) PERTUSSIS: I have been informed of the risk of mychild developing whooping cough, pneumonia, convulsions,inflammation of the brain, and death associated with pertussis.I understand the disease is rarely fatal, with a 99.8% recoveryrate. It is most serious and life-threatening in children under 6months old, but there are adequate methods of treatmentavailable.(9) The vaccine is most often given in conjunction withdiphtheria and tetanus as the DPT or as the DaPT. Pertussisvaccine may cause: fevers >106, pain swelling, diarrhea,projectile vomiting, excessive sleepiness, high--pitchedscreaming, inconsolable crying bouts, seizures, convulsions,collapse, shock, breathing problems, brain damage and SIDS.One in 600 suffer a severe reaction in one study(10) and 1 in 875 suffered shock-collapse and convulsions.(11) Those in the 2nd study were only tracked for the first 48hours following immunization. A more recent study indicatesthat 1 in 100 react with convulsions, collapse, or high-pitchedscreaming and 1 in 3 of those cases sustained permanent braindamage.(12) In a study of 103 children who died of SIDS, 70% diedwithin 3 weeks of the DPT vaccine and 37% of those diedwithin the first week.(13) The DaPT is recommended as a safer option forvaccination. Side effects of the DaPT were only tracked for72 hours and included: tenderness, erythema, induration, fever>102.2¡, drowsiness, fretfulness, vomiting, upper respiratoryinfection, diarrhea, rash, febrile seizures, persistent or unusualcrying, lethargy, hypronic-hyporesponsive episode, urticaria,anaphylactic shock, convulsions, encephalopathy, mono- andpolyneuropathies and death.(14) Not recommended for children under 15 months or forthose who have not had 3 injections of the DPT. Either formof the vaccine contains thimerosal (mercury derivative),formaldehyde, and aluminum phosphate.(15) DIPHTHERIA: I have been informed of the risk of mychild developing paralysis, heart failure, or respiratory failureassociated with diphtheria. I have also been informed that therehave only been 5 cases reported annually since 1980.(16) I am also aware that diphtheria is rarely fatal and treatedwith antibiotics and bed rest.(17) The Diphtheria component is most often given within theDPT or DaPT and includes the same side effects and reactionsas those listed for pertussis. TETANUS: I have been informedof the risk of my child developing fatal neuromuscular diseaserelated to tetanus. I understand that the incidence of tetanus islow, and there is an antitoxin, should we decline the immunization.I understand that contracting tetanus does not provide life-longimmunity, and neither does the vaccine. I understand that toprevent more severe reactions from the vaccine, the tetanuscomponent has been so significantly "diluted" that it is clinicallyineffective.(18) I understand that the death rate for properly treated casesof tetanus may be as high as 20%.(19) Side effects of the tetanus vaccine alone include: highfever, pain, recurrent abscess formation, inner ear nerve damage,demyelinating neuropathy, anaphylactic shock and loss ofconsciousness.(20) Tetanus given in the DPT or DaPT shot include thesame side effects and reactions as those listed for pertussis.RUBEOLA (MEASLES): I have been informed of the risk ofmy child developing pneumonia, encephalitis (inflammationof the brain), degenerative disease of the nervous system withconvulsions (subacute sclerosing panencephalitis) related torubeola. I understand the death rate for measles is .03 in100,000.(21) I understand that since 1984, over 55% of documented,confirmed cases of measles have been in fully immunizedpersons.(22) I understand that the greatest risk of the measles vaccinemay be to push the incidence of this disease into the late teensand adulthood where it is more likely to be fatal or cause moreadverse and long-term effects.(23) The measles vaccine is a live vaccine, and carries the riskthat it will cause the patient to contract measles. Other adversereactions include: stinging or burning at the injection site,anaphylaxis, fever up to one month following injection, rash,cough, rhinitis, erythema multiforme, lymphadenopathy,urticaria, diarrhea, febrile convulsions, seizures, thrombocytopenia,purpura, vasculitis, optic neuritis, retrobulbar neuritis, papillitis,retinitis, encephalitis and encephalopathy, ocular palsies, Guillain-Barr* Syndrome, ataxia, and subacute sclerosing panencephalitis.(24) Measles vaccine is most often given as a part of the MMRwhich includes the following side effects: burning or stingingat injection site, malaise, sore throat, cough, rhinitis, headache,dizziness, fever, rash, nausea, vomiting, diarrhea, erythema,induration, tenderness, lymphadenopathy, parotitius, orchitis,nerve deafness, thrombocytopenia, purpura, allergic reactions,urticaria, polyneuritis, arthralgia, arthritis, anaphylaxis, vasculitis,otitis media, conjunctivitis, febrile convulsions, seizures, syncope,erythema multiforme, optic neuritis, retrobulbar neuritis, papillitis,retinitis, encephalitis and encephalopathy, ocular palsies, Guillain-Barr* Syndrome, ataxia, subacute sclerosing panencephalitis,(25) and a recent study from Europe indicates that there may bea link between the MMR (measles/mumps/rubella) vaccine andautism and irritable bowel syndrome.(26) Measles vaccine contains chick embryo cells, neomycin,sorbitol and hydrolyzed gelatin. MMR contains all livevaccines, chick embryo, cells from aborted babies, neomycin,sorbitol and hydrolyzed gelatin.(27) MUMPS: I have been informed of the risk of my childdeveloping inflammation of the testicles, joints, kidneys, and/orthyroid, and hearing impairment related to mumps. I understandthat mumps is rarely harmful in childhood, and that most of theabove risks occur when mumps is contracted in adolescence oradulthood.(28) I understand that there is a Mumps vaccine which posesthe following risks: contraction of mumps from the live vaccine,burning or stinging at the injection site, anaphylaxis, cough,rhinitis, fever, diarrhea, vasculitis, parotitis, orchitis, purpura,urticaria, erythema multiforme, optic neuritis, retrobulbarneuritis, syncope, encephalitis, febrile seizures, and nervedeafness.(29) Mumps is usually given in the MMR and may causethose side effects and adverse reactions as noted in the measlessection above. Mumps vaccine is live and should not be givento pregnant women. It is cultured in chick embryos andcontains sorbitol and hydrolyzed gelatin.(30) RUBELLA (GERMAN MEASLES): I have beeninformed of the risk of my child developing inflammation ofthe brain or joints, and of the risk of birth defects (includingeye defects, heart defects, deafness, mental retardation, growthfailure, jaundice, and disorders of blood clotting) in infantsborn to mothers who contract rubella during pregnancy, relatedto rubella. Therefore, I understand that the greatest risk to mychild may be if she never contracts rubella as a child, but whenshe is pregnant and it damages her unborn child. If she contractrubella in childhood, she is immune for life, and prior to thevaccine 85% of the population was immune.(31) I understand that if she is not immune as an adult, shecan choose to take the vaccine prior to becoming pregnant. Iunderstand that many of those who contract rubella have beenimmunized (up to 80%).(32) Adverse reactions from the vaccine among teenage girlsis 5-10% and 30% in adult women.(33) Adverse reactionsinclude: contracting rubella from the live virus in the vaccine,burning or stinging at the site, lymphadenopathy, urticaria,rash, malaise, sore throat, fever, headache, dizziness, nausea,vomiting, diarrhea, polyneuritis, arthralgia, arthritis, localpain and inflammation, erythema multiforme, cough, rhinitis,vasculitis, anaphylaxis, syncope, optic neuritis, retrobulbarneuritis, papillitis, Guillain-Barr* Syndrome, encephalitis,thrombocytopenia, purpura, and Chronic Fatigue Syndrome.(34) Rubella is most often administered in the MMR and maycause those side effects and adverse reactions listed undermeasles. Rubella is cultured on the tissue of an aborted child.This child was the 27th child aborted and tested by researchersdue to exposure to rubella in a pregnant woman. It containsneomycin, sorbitol and hydrolyzed gelatin.(35) HEPATITIS B: I have been informed of the risk of mychild developing Hepatitis B viral infection which can causechronic inflammation of the liver leading to cirrhosis, livercancer, and possibly death. I understand that my child's risk ofdeveloping Hepatitis B is low if I am not a carrier or infected, ifmy child does not engage in promiscuous sex or use drugs. Iunderstand that there is antibiotic treatment for HepB and thatmost of those who contract it recover.(36) I understand that the HepB vaccine only contains strainsof HepB and is not effective against HepA, C, D, E, F, or G.I understand that the HepB vaccine has the following sideeffect and adverse reactions: induration, erythema, swelling,fever, headache, dizziness, pain, prutitus, ecchymosis, sweating,malaise, chills, weakness, flushing, tingling, hypotension,flu-like symptoms, upper respiratory illness, nausea, anorexia,abdominal pain and cramping, vomiting, constipation, diarrhea,lymphadenopathy, pain or stiffness in muscles and joints,arthralgia, myalgia, back pain, rash, urticaria, petechiae,sleepiness, insomnia, irritability, agitation, anaphylaxis,angioedema, arthritis, tachycardia/palpitations, bronchospasm,abnormal liver function tests, dyspepsia, migraine, syncope,paresis neuropathy, hypothesis, paresthesis, Guillain-Barr*Syndrome, Bell's Palsy, transverse myelitis, optic neuritis,multiple sclerosis, thrombocytopenia, eczema, purpura, herpeszoster, erythema modosum, alopecia, conjunctivitis, keratisis,visual disturbances, vertigo, tinnitus, earache, and dysuria.(37) The studies only followed patients for 4 dayspost-vaccination. The most commonly used HepB vaccinecontains thimerosal, although a relatively new release doesnot contain thimerosal. The vaccine also contains: aluminumhydroxide, yeast protein, and phosphate buffers.(38) VARICELLA (CHICKENPOX): I have been informedof the risk of my child developing chicken pox which couldpotentially result in pneumonia, secondary skin or generalizedinfections, or, if caught during pregnancy, birth defects in thebaby. I understand chicken pox is generally benign in children,but results in significant lost hours at work for parents. Chickenpox in adults often manifests as shingles, a chronic and painfulcondition. I also understand that contracting chicken pox later inlife may increase my risk for herpes simplex.Side effects and adverse reactions for the chicken pox vaccineinclude: contracting chicken pox from the live vaccine (27%),pain and redness at site, swelling, erythema, rash, pruritus,hematoma, induration, stiffness, upper respiratory illness,cough, irritability/nervousness, fatigue, disturbed sleep,diarrhea, loss of appetite, vomiting, otitis, diaper rash/contactrash, nausea, eye complaints, chills, lymphadenopathy, myalgia,lower respiratory illness, headache, teething, malaise, abdominalpain, other rash, allergic reactions including rash and hives, stiffneck, heat rash/prickly heat, arthralgia, eczema/dryskin/dermatitis, constipation, itching, pneunonitis, febrileseizures, and cold/canker sore.(39) Varicella vaccine is cultured on cells from aborted babies,and guinea pig cell cultures. It contains live virus, monisodiumglutamate (msg), sucrose, phosphate, processed gelatin,neomycin and fetal calf serum.(40) HEPATITIS A (HAV): I have been informed of the riskof my child developing HAV which could potentially result inprolonged or relapsed hepatitis, but will not result in chronichepatitis disease.(41) HAV usually causes mild "flu-like" illness, jaundice,severe stomach pains and diarrhea; and, in rare cases mayresult in death. Infection confers lifelong immunity.(42) I understand that the CDC admits that good personalhygiene (handwashing) and proper santitation can preventHAV.(43) HAV infection is spread by contaminated water orfood, infected food handlers, unsanitary conditions followingnatural disasters, ingestion of raw or undercooked shellfish,institutionalized individuals, children not yet toilet trained,blood transfusions or sharing needles with infected people.Transmission is most likely in developing countries wheresanitation is poor and infection rate of children under 5 is 90%.Fatality rate is less than .6% overall, and 70% of those inpatients over 49 years, many of whom have underlying liverdisease.(44) Other at-risk populations include those living on AmericanIndian reservations and in Alaskan Native villages, homosexuallyactive men, IV drug users, people using clotting factorconcentrates and international travelers.(45) Side effects and adverse reactions from the vaccineinclude: injection-site soreness, headache, fever, malaise,induration, redness, swelling, fatigue, anorexia, nausea, pruritis,rash, utricaria, pharyngitis, upper respiratory tract infections,abdominal pain, diarrhea, dysgeusia, vomiting, arthralgia,elevated cratine phosphokinase, myalgia, lymphadenopathy,hypertonic episodes, insomnia, photophobia, and vertigo.(46) Aborted fetal tissue is an ingredient in the Havrix¨ Hep Avaccine, as is formaldehyde, aluminum hydroxide and2-phenozyethanol.(47) There is currently a combination Hep A and B vaccine,Twinrix¨, being tested in the UK.(48) Twinrix is grown in human cell cultures, contains2-phenoxyethanol, neomycin sulfate, polysorbate, tromentamoland formaldehyde. (49) PNEUMOCOCCAL: I have been informed of the risk ofmy child developing pneumococcal disease which could resultin meningitis, blood infection, pneumonia and/or ear infections.Iunderstand studies indicate that this vaccine may only decreaseear infections by 9%, and only result in a 20% reduction inchronic ear infections and ear tube insertion in that group. Iunderstand that my child has a 7.5:5,000 chance of deveopingthis disease if he or she is under age 2 and a 1:5000 chance ofdeveloping it if over age 2. Risk factors for developing thisdisease are: immunoglobulin deficiency, nephrotic syndrome,Hodgkin's disease, congenital or acquired immunodeficiency,some upper respiratory infections, splenic dysfunctions,splenectomy or organ transplant. This vaccine (PCV) wasoriginally marketed for immunocompromised children.(50) This vaccine is contraindicated to children withthrombocytopenia, coagualtion disorders, or sensitivity todiphtheria toxoid.(51) Possible side effects and complications from the vaccineinclude: erythema, induration, tenderness, interference of limbmovement, inflamation, fever, irritability, drowsiness, restlesssleep, decreased appetite, vomiting, diarrhea, fussiness, rash,hives, bronchitis, asthma, pneumonia, otitis media (earinfection), sepsis, seizure, anaphylaxis and death.(52) Recipients were followed for 3 days and almost 10%of the subjects made a visit to the emergency room in thefollow-up period. There were 8 cases of SIDS in the 17,066subjects involved in the trial.(53) Note: Children in the studies' control group receivedanother experimental vaccine, so there have been no trialstudies done with children who received no vaccine.(54) Prevnar contains .125 mg of aluminum sulfate, proteinpolysaccharides from 7 strains of strep. pneumoniae bacteria,diphtheria toxin, casamino acids, yeast extract. Studies indicatethat it may interfere with the safety and efficacy of othervaccines. ~~~~~~~*::<<¤Ø>>::*~~~~~~~Complied by Kathryn E. Rateliff, CCD, CCCE, SM October,1999 and revised January, 2001 Questions and comments canbe addressed to her at: titus2.Want to know more about the issue of vaccine choice?Titus 2 Birthing has a 42-page packet to help parents look atsome of the issues regarding vaccine choice. This packetincludes the above form plus many other helpful documents.Topics include: vaccine safety, disease frequency in the US,exemption information and worksheet, religious concerns aboutvaccines, immunization registry information, vaccinations andpremature babies, vaccines and immune supression, the AmericanAssociation of Physicians and Surgeons policy on mandatoryvaccines, additional resources, and Jock Doubleday's challengefor immunization providers to drink a vaccine additive cocktail.If you are interested in getting a copy of this packet, contactKathy at <titus2 and she will be glad give youall of the details. Note that there is a cost for this packet. ~~~~~~~*::<<¤Ø>>::*~~~~~~~(55) Reference List 1. M. Burnet and D. White, The NaturalHistory of Infectious Disease (Cambridge, 1972), p. 16. 2.Strebel, et al, "Epidemology in the U.S. One Decade After theLast Reported Case of Indigenous Wild Virus AssociatedDisease," Clinical Infectious Diseases, (Center for DiseaseControl, February 1992), pp. 568-79. 3. Physician's DeskReference (PDR), 50th Edition; Medical Economics, 1996, p.1388-1390. 4. Ibid, p. 885-886 and 891-892. 5. J. Butel, et al;"Molecular Evidence of Simian Virus 40 Infections inChildren", The Journal of Infectious Diseases ; September1999;180:884-887. 6. PDR, 50th Edition, p. 872-875. 7. Ibid.8. Ibid. 9. Richard Moskowitz, M.D., "Immunizations: TheOther Side," Mothering, (Spring1984),p. 34. 10. Immunization:Survey of Recent Research, (United States Department ofHealth and Human Services, April 1983), p. 76. 11. "Natureand Rates of Adverse Reactions Associated with DPT and DTImmunizations...," Pediatrics, Volume 68, No. 5 (November1981). 12. Walene James, Immunization the Reality Behind theMyth, (South Hadley, Massachusetts: Bergin & Garvey, 1988),p. 14. 13. W.C. Torch, "Diptheria-pertussis-tetanus (DPT)immunization: A potential cause of sudden infant deathsyndrome (SIDS)," (Amer. Academy of Neurology, 34thAnnual Meeting, Apr 25 - May 1, 1982), Neurology 32(4), pt.2. 14. PDR, p. 875-879 and 892-895. 15. Ibid. 16. RobertMendelsohn, M.D., How to Raise A Healthy Child...In Spite ofyour Doctor (Chicago: Contemporary Books, 1984), p.223. 17.Ibid. 244-246 18. Isaac Golden, Ph.D., Vaccination? A Reviewof Risks and Alternatives, (Geelong, Victoria, Australia: ArumHealing Centre, 1991), p. 31 19. Richard Moskowitz, M.D.,"Immunizations: The Other Side," Mothering, (Spring1984),p.34. 20. Isaac Golden, Ph.D., Vaccination? A Review of Risksand Alternatives; p. 71 21. R. Mendoholson; How to Raise aHealthy Child; p. 217. 22. John Frank Jr., M.D., et al."Measles Elimination - Final Impediments," 20th ImmunizationConference Proceedings, May 6-9, 1985, p. 21. 23. InfectiousDiseases (January 1982), p. 21. 24. PDR, p. 1610-1611. 25.DR, p. 1687-1689. 26. Sara Solovitch, "Do vaccines spurautism in kids?", San Jose Mercury News, 5/25/99. 27. PDR,p. 1687-89, 1610-1611. 28. Richard Moskowitz, M.D.,"Immunizations: The Other Side," Mothering, (Spring1984),p.35. 29. PDR, 1708-1709. 30. Ibid. 31. R. Mendoholson; Howto Raise a Healthy Child; p. 218. 32. Dr. Beverley Allan,Australian Nurses Journal, (May 1978). 33. Hannah Allen,Don't Get Stuck: The Case Against Vaccinations..., (Oldsmar,FL: Natural Hygiene Press, 1985), p. 144. 34. DR, p.1697-1699. 35. Ibid and Attenuation Of RA 27/3 RubellaVirus in WI-38 Human Diploid Cells; Amer J Dis Child vol118 Aug 1969 and Studies of Immunization With LivingRubella Virus ; Arch J Dis Child vol 110 Oct 1965. 36. JohnHanchette, "Safety of controversial hepatitis B vaccine at centerof debate" Gannett News Service, 5/18/99. 37. PDR, p.1744-1747, 2482-2484. 38. Ibid. 39. PDR, p. 1762-1765. 40.Ibid. 41. CDC Viral Hepatitis A - Fact Sheet, 9/29/00;www.cdc.gov/ncidod/diseases/hepatitis/a/fact.htm 42. CDCHepatitis A Vaccine Vaccine Information Statement; 8/25/9843. CDC Hepatitis A Facts, 11/16/00 44. Mosby's GenRX¨,10th Ed., Hepatitis A Vaccine (003158) as posted onMDConsult website 45. CDC Hepatitis A Vaccine VaccineInformation Statement; 8/25/98 and CDC Hepatitis A VaccineVaccine Information Statement; 8/25/98 46. Mosby'sGenRX@, Hepatitis A Vaccine 47. Ibid. 48. "Combinedhepatitis A/B vaccine offers fast protection," Reuters Health,4/12/00 49. Vaccines and Their Ingredients, 6/24/99;www.909shot.com 50. Michael Horwin, MA; "Prevnar: ACritical Review of a New Childhood Vaccine" 9/19/00. 51.Prevnar package insert, Wyeth Lederle, 2/17/00 52. Ibid. 53.Horwin; "Prevnar: A Critical Review" 54. Dr. Erdem Cantekin,Ph.D.; "Pneumocaoccal Vaccine and Otitis Media", NVIC's2nd Intl. Public Conference, 9/8/00. 55. Horwin; "Prevnar: ACritical Review"Complied by Kathryn E. Rateliff, CCD, CCCE, SM October,1999 and revised January, 2001 Questions and comments canbe addressed to her at: titus2.Want to know more about the issue of vaccine choice?Titus 2 Birthing has a 42-page packet to help parents look atsome of the issues regarding vaccine choice. This packetincludes the above form plus many other helpful documents.Topics include: vaccine safety, disease frequency in the US,exemption information and worksheet, religious concerns aboutvaccines, immunization registry information, vaccinations andpremature babies, vaccines and immune supression, the AmericanAssociation of Physicians and Surgeons policy on mandatoryvaccines, additional resources, and Jock Doubleday's challengefor immunization providers to drink a vaccine additive cocktail.If you are interested in getting a copy of this packet, contactKathy at <titus2 and she will be glad give youall of the details. Note that there is a cost for this packet. «¤»¥«¤»§«¤»¥«¤»§«¤»¥«¤»§«¤»¥«¤»§«¤»¥«¤»§«¤»¥«¤«¤»¥«¤»§«¤»¥«¤»§«¤»¥«¤»§«¤»¥«¤»Paranormal_Research - Scientific Data, Health Conspiracies & Anything Strange Paranormal_ResearchSubscribe:... Paranormal_Research-