Updates from Dr. Carley: the FederalCase admitting that autism was caused by vaccines

[Guest guest]

Dear List; You have not received any updates from me in some time, as the program whichallows me to do so was sabotaged, and it took my webmaster all this time tofix it. I thank her for not giving up until she was successful, as this isone of the most important documents I have ever written. She is the best! The following is the ammo by which Big Pharma can be brought to its knees.I ask you to circulate it widely. It is time for you to DEMAND that thosepromoting mercury as the cause of autism respond to what I have writtenbelow. If the true intention of these people is to stop this epidemic inour children, then they should let go of their egos and admit that I havefigured out the true cause. Let me first encourage of all you to go tohttp://www.drcarley.com/the_big_picture.jpg;'>http://www.drcarley.com/the_big_picture.jpg; you will see that I have ALWAYSsaid it is the BIG PICTURE of assaults to our immune systems (and mercury isthere) which combine to cause disease, including autism. But it is thecorruption of the immune system caused by the inoculation of viruses whichis the root cause of all autoimmune diseases and cancer...and once thisinformation is in the hands of a critical mass of the people, we will put astop to the biggest epidemic the world has ever known...VIDS (VaccineInduced Diseases). And theindividuals who continue to promote mercury as the root cause in the face ofthis information will be exposed for being INTENTIONAL disinformers. Below is a verbatim copy of the US Government concession filed last Novemberin a Court of Federal Claims case brought by a family claiming that mercurycontaining vaccines were the cause of the child's autism that is posted onDavid Kirby's blog athttp://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-_b_88558.html. David Kirby, author of "Evidence of Harm", is one of the individualswho is distracting the public that it is "all about the thimerosol". Thetake home message therefore is that if the mercury were removed, vaccineswould be safe. A BIGGER LIE HAS NEVER BEEN TOLD; and my document"Inoculations the True Weapons of Mass Destruction" posted onwww.drcarley.com describes the corruption of the immune system caused by theinjection of viruses directly into the body, bypassing secretory IgA (anantibody in the upper GI and respiratory tracts critical for the processingof the germ by the immune system for natural immunity to occur). I was a guest with David Kirby on a radio show which is posted on my websiteat http://www.drcarley.com/kirby_vs_carley_autism.mp3,'>http://www.drcarley.com/kirby_vs_carley_autism.mp3, on which I confrontedhim with the fact that autism is actually a non-fatal case of subacutesclerosing panencephalitis caused by demyelination following vaccine inducedencephalitis, and that the name of the condition was changed to autism tohide this self evident fact. I have sent Mr. Kirby copies of the documentson my website, and asked him multiple times to be a guest on one of myinternet shows to discuss the "mercury vs demyelination" theories of autism.He will not do so. What is truly amazing is that he is now mentioning live viruses amongst aplethora of other potential problems (see # 6 athttp://www.huffingtonpost.com/david-kirby/government-concedes-vacci_b_88323.html)....but is he discussing the live viruses bypassing secretory IgA,causing vaccine induced encephalitis and subsequent demyelination? NO...heis mentioning live viruses as a cause of mitochondrial damage. So onceagain, we will now be distracted with this genetic mitochondrialdefect...perhaps develop a test to find the children with this problembefore they are vaccinated, when in fact genetic defects can also be causedby vaccines. More confusion and distraction...rather than admitting thatthere is no such thing as a safe vaccine...and the practice should beabandoned altogether, and attention placed on strengthening the immunesystem. Of course, since population reduction is the true agenda of thepowers that be, not only will the vaccine push continue...but viruses are being developed to cause disease and cancer. The mad scientists have tobe stopped...and this WILL happen once enough people have opened their eyes. I urge all of you to carefully read this decision dated 11/9/07, in whichthis young girl won her case claiming vaccines caused her autism. Notethese important points: 1. 2 days after multiple vaccines (which included the MMR, which has NEVERhad mercury), she developed a high fever, high pitched screaming, and waslethargic and irritable. these are symptoms of VACCINE INDUCEDENCEPHALITIS, an inflammation of the brain caused by injection of LIVEVIRUSES (not from mercury). 2. She also began to arch her back when she cried (a sign of vaccine inducedencephalitis, NOT mercury poisoning). 3. She developed a POST-VARICELLA VACCINATION RASH (which proves that thevaccination GAVE HER THAT DISEASE). 4. She was diagnosed with vaccine induced ENCEPHALOPATHY (degenerativedisease of the brain)...as you will see below, mercury is involved incausing the degenerative disease Alzheimer's, NOT autism). 5. She developed a SEIZURE DISORDER later on (go to the CDC website andlook for the vaccine information statement on the MMR vaccine (which hasnever had mercury), and you will see that one of the side effects is LONGTERM SEIZURES. 6. You will also note that they did genetic testing of the child and foundthat she has a genetic defect in her cellular energetics (Note that vaccinesare known to cause GENETIC MUTATION due to insertion of plasmids of DNA fromthe viruses or tissues used to culture them; in fact, this is the wholebasis on which DNA vaccines are designed). 7. You will notice that although the white coat in this case went as far asto do genetic testing in this child, there were NO ANTI MYELIN OR ANTINEURONAL FILAMENT LEVELS DONE; this IS the test that demonstratesdemyelination before it is massive enough to show up on MRI's; and this ISthe test that proves that autism is actually a non-fatal form of subacutesclerosing panencephalitis (which is why this test is almost never done). Here is the decision (but please be sure to also read what I have writtenafter it)... IN THE UNITED STATES COURT OF FEDERAL CLAIMS OFFICE OF SPECIAL MASTERS CHILD, a minor, by her Parents and Natural Guardians, Petitioners, v. SECRETARY OF HEALTH AND HUMAN SERVICES, Respondent. RESPONDENT'S RULE 4© REPORT In accordance with RCFC, Appendix B, Vaccine Rule 4©, the Secretary ofHealth and Human Services submits the following response to the petition forcompensation filed in this case. FACTS CHILD ("CHILD") was born on December --, 1998, and weighed eight pounds,ten ounces. Petitioners' Exhibit ("Pet. Ex.") 54 at 13. The pregnancy wascomplicated by gestational diabetes. Id. at 13. CHILD received her firstHepatitis B immunization on December 27, 1998. Pet. Ex. 31 at 2. From January 26, 1999 through June 28, 1999, CHILD visited the PediatricCenter, in Catonsville, Maryland, for well-child examinations and minorcomplaints, including fever and eczema. Pet. Ex. 31 at 5-10, 19. During thistime period, she received the following pediatric vaccinations, withoutincident: Vaccine Dates Administered Hep B 12/27/98; 1/26/99 IPV 3/12/99; 4/27/99 Hib 3/12/99; 4/27/99; 6/28/99 DTaP 3/12/99; 4/27/99; 6/28/99 Id. at 2. At seven months of age, CHILD was diagnosed with bilateral otitis media.Pet. Ex. 31 at 20. In the subsequent months between July 1999 and January2000, she had frequent bouts of otitis media, which doctors treated withmultiple antibiotics. Pet. Ex. 2 at 4. On December 3,1999, CHILD was seen byKarl Diehn, M.D., at Ear, Nose, and Throat Associates of the GreaterBaltimore Medical Center ("ENT Associates"). Pet. Ex. 31 at 44. Dr. Diehnrecommend that CHILD receive PE tubes for her "recurrent otitis media andserious otitis." Id. CHILD received PE tubes in January 2000. Pet. Ex. 24 at7. Due to CHILD's otitis media, her mother did not allow CHILD to receivethe standard 12 and 15 month childhood immunizations. Pet. Ex. 2 at 4. According to the medical records, CHILD consistently met herdevelopmental milestones during the first eighteen months of her life. Therecord of an October 5, 1999 visit to the Pediatric Center notes that CHILDwas mimicking sounds, crawling, and sitting. Pet. Ex. 31 at 9. The record ofher 12-month pediatric examination notes that she was using the words "Mom"and "Dad," pulling herself up, and cruising. Id. at 10. At a July 19, 2000 pediatric visit, the pediatrician observed that CHILD"spoke well" and was "alert and active." Pet. Ex. 31 at 11. CHILD's motherreported that CHILD had regular bowel movements and slept through the night.Id. At the July 19, 2000 examination, CHILD received five vaccinations -DTaP, Hib, MMR, Varivax, and IPV. Id. at 2, 11. According to her mother's affidavit, CHILD developed a fever of 102.3degrees two days after her immunizations and was lethargic, irritable, andcried for long periods of time. Pet. Ex. 2 at 6. She exhibited intermittent,high-pitched screaming and a decreased response to stimuli. Id. MOM spokewith the pediatrician, who told her that CHILD was having a normal reactionto her immunizations. Id. According to CHILD's mother, this behaviorcontinued over the next ten days, and CHILD also began to arch her back whenshe cried. Id. On July 31, 2000, CHILD presented to the Pediatric Center with a 101-102degree temperature, a diminished appetite, and small red dots on her chest.Pet. Ex. 31 at 28. The nurse practitioner recorded that CHILD was extremelyirritable and inconsolable. Id. She was diagnosed with a post-varicellavaccination rash. Id. at 29. Two months later, on September 26, 2000, CHILD returned to the PediatricCenter with a temperature of 102 degrees, diarrhea, nasal discharge, areduced appetite, and pulling at her left ear. Id. at 29. Two days later, onSeptember 28, 2000, CHILD was again seen at the Pediatric Center because herdiarrhea continued, she was congested, and her mother reported that CHILDwas crying during urination. Id. at 32. On November 1, 2000, CHILD receivedbilateral PE tubes. Id. at 38. On November 13, 2000, a physician at ENTAssociates noted that CHILD was "obviously hearing better" and her audiogramwas normal. Id. at 38. On November 27, 2000, CHILD was seen at the PediatricCenter with complaints of diarrhea, vomiting, diminished energy, fever, anda rash on her cheek. Id. at 33. At a follow-up visit, on December 14, 2000,the doctor noted that CHILD had a possible speech delay. Id. CHILD was evaluated at the Howard County Infants and Toddlers Program,on November 17, 2000, and November 28, 2000, due to concerns about herlanguage development. Pet. Ex. 19 at 2, 7. The assessment team observeddeficits in CHILD's communication and social development. Id. at 6. CHILD'smother reported that CHILD had become less responsive to verbal direction inthe previous four months and had lost some language skills. Id. At 2. On December 21, 2000, CHILD returned to ENT Associates because of anobstruction in her right ear and fussiness. Pet. Ex. 31 at 39. Dr. GraceMatesic identified a middle ear effusion and recorded that CHILD was havingsome balance issues and not progressing with her speech. Id. On December 27,2000, CHILD visited ENT Associates, where Dr. Grace Matesic observed thatCHILD's left PE tube was obstructed with crust. Pet. Ex. 14 at 6. The tubewas replaced on January 17, 2001. Id. Dr. Andrew Zimmerman, a pediatric neurologist, evaluated CHILD at theKennedy Krieger Children's Hospital Neurology Clinic ("Krieger Institute"),on February 8, 2001. Pet. Ex. 25 at 1. Dr. Zimmerman reported that afterCHILD's immunizations of July 19, 2000, an "encephalopathy progressed topersistent loss of previously acquired language, eye contact, andrelatedness." Id. He noted a disruption in CHILD's sleep patterns,persistent screaming and arching, the development of pica to foreignobjects, and loose stools. Id. Dr. Zimmerman observed that CHILD watched thefluorescent lights repeatedly during the examination and would not make eye contact. Id. He diagnosed CHILD with "regressiveencephalopathy with features consistent with an autistic spectrum disorder,following normal development." Id. At 2. Dr. Zimmerman ordered genetictesting, a magnetic resonance imaging test ("MRI"), and anelectroencephalogram ("EEG"). Id. Dr. Zimmerman referred CHILD to the Krieger Institute's OccupationalTherapy Clinic and the Center for Autism and Related Disorders ("CARDS").Pet. Ex. 25 at 40. She was evaluated at the Occupational Therapy Clinic byStacey Merenstein, OTR/L, on February 23, 2001. Id. The evaluation reportsummarized that CHILD had deficits in "many areas of sensory processingwhich decrease[d] her ability to interpret sensory input and influence[d]her motor performance as a result." Id. at 45. CHILD was evaluated by AliceKau and Kelley Duff, on May 16, 2001, at CARDS. Pet. Ex. 25 at 17. Theclinicians concluded that CHILD was developmentally delayed and demonstratedfeatures of autistic disorder. Id. at 22. CHILD returned to Dr. Zimmerman, on May 17, 2001, for a follow-upconsultation. Pet. Ex. 25 at 4. An overnight EEG, performed on April 6,2001, showed no seizure discharges. Id. at 16. An MRI, performed on March14, 2001, was normal. Pet. Ex. 24 at 16. A G-band test revealed a normalkaryotype. Pet. Ex. 25 at 16. Laboratory studies, however, stronglyindicated an underlying mitochondrial disorder. Id. at 4. Dr. Zimmerman referred CHILD for a neurogenetics consultation toevaluate her abnormal metabolic test results. Pet. Ex. 25 at 8. CHILD metwith Dr. Richard Kelley, a specialist in neurogenetics, on May 22, 2001, atthe Krieger Institute. Id. In his assessment, Dr. Kelley affirmed thatCHILD's history and lab results were consistent with "an etiologicallyunexplained metabolic disorder that appear[ed] to be a common cause ofdevelopmental regression." Id. at 7. He continued to note that children withbiochemical profiles similar to CHILD's develop normally until sometimebetween the first and second year of life when their metabolic patternbecomes apparent, at which time they developmentally regress. Id. Dr. Kelleydescribed this condition as "mitochondrial PPD." Id. On October 4, 2001, Dr. John Schoffner, at Horizon Molecular Medicine inNorcross, Georgia, examined CHILD to assess whether her clinicalmanifestations were related to a defect in cellular energetics. Pet. Ex. 16at 26. After reviewing her history, Dr. Schoffner agreed that the previousmetabolic testing was "suggestive of a defect in cellular energetics." Id.Dr. Schoffner recommended a muscle biopsy, genetic testing, metabolictesting, and cell culture based testing. Id. at 36. A CSF organic acidstest, on January 8, 2002, displayed an increased lactate to pyruvate ratioof 28,1 which can be seen in disorders of mitochondrial oxidativephosphorylation. Id. at 22. A muscle biopsy test for oxidativephosphorylation disease revealed abnormal results for Type One and Three.Id. at 3. The most prominent findings were scattered atrophic myofibers thatwere mostly type one oxidative phosphorylation dependent myofibers, mildincrease in lipid in selected myofibers, and occasional myofiber with reduced cytochrome c oxidase activity. Id. at 7. Afterreviewing these laboratory results, Dr. Schoffner diagnosed CHILD withoxidative phosphorylation disease. Id. at 3. In February 2004, amitochondrial DNA ("mtDNA") point mutation analysis revealed a singlenucleotide change in the 16S ribosomal RNA gene (T2387C). Id. at 11. CHILD returned to the Krieger Institute, on July 7, 2004, for afollow-up evaluation with Dr. Zimmerman. Pet. Ex. 57 at 9. He reported CHILD"had done very well" with treatment for a mitochondrial dysfunction. Dr.Zimmerman concluded that CHILD would continue to require services in speech,occupational, physical, and behavioral therapy. Id. On April 14, 2006, CHILD was brought by ambulance to Athens RegionalHospital and developed a tonic seizure en route. Pet. Ex. 10 at 38. An EEGshowed diffuse slowing. Id. At 40. She was diagnosed with having experienceda prolonged complex partial seizure and transferred to Scottish RiteHospital. Id. at 39, 44. She experienced no more seizures while at ScottishRite Hospital and was discharged on the medications Trileptal and Diastal.Id. at 44. A follow-up MRI of the brain, on June 16, 2006, was normal withevidence of a left mastoiditis manifested by distortion of the air cells.Id. at 36. An EEG, performed on August 15, 2006, showed "rhythmic epileptiform discharges in the right temporal regionand then focal slowing during a witnessed clinical seizure." Id. At 37.CHILD continues to suffer from a seizure disorder. ANALYSIS Medical personnel at the Division of Vaccine Injury Compensation,Department of Health and Human Services (DVIC) have reviewed the facts ofthis case, as presented by the petition, medical records, and affidavits.After a thorough review, DVIC has concluded that compensation is appropriatein this case. In sum, DVIC has concluded that the facts of this case meet thestatutory criteria for demonstrating that the vaccinations CHILD received onJuly 19, 2000, significantly aggravated an underlying mitochondrialdisorder, which predisposed her to deficits in cellular energy metabolism,and manifested as a regressive encephalopathy with features of autismspectrum disorder. Therefore, respondent recommends that compensation beawarded to petitioners in accordance with 42 U.S.C. § 300aa-11©(1)©(ii). DVIC has concluded that CHILD's complex partial seizure disorder, withan onset of almost six years after her July 19, 2000 vaccinations, is notrelated to a vaccine-injury. Respectfully submitted, PETER D. KEISLER Assistant Attorney General TIMOTHY P. GARREN Director Torts Branch, Civil Division MARK W. ROGERS Deputy Director Torts Branch, Civil Division VINCENT J. MATANOSKI Assistant Director Torts Branch, Civil Division s/ Linda S. Renzi by s/ Lynn E. Ricciardella LINDA S. RENZI Senior Trial Counsel Torts Branch, Civil Division U.S. Department of Justice P.O. Box 146 Benjamin Franklin Station Washington, D.C. 20044 (202) 616-4133 DATE: November 9, 2007 PS: On Friday, February 22, HHS conceded that this child's complex partialseizure disorder was also caused by her vaccines. Now we the taxpayers willaward this family compensation to finance her seizure medication. Surely ALLdecent people can agree that is a good thing. By the way, it''s worth noting that her seizures did not begin until sixyears after the date of vaccination, yet the government acknowledges theywere, indeed, linked to the immunizations of July, 2000, - David Kirby Now I am going to prove to you, BEYOND A SHADOW OF A DOUBT, that mercury isa distraction in the case of autism: Please go to http://healthtruthrevealed.com/audio-interviews.php, click on"inoculations the true weapons of mass destruction", and listen to theinterview I did on this very subject on 3/4/08. You will hear Greg Ciolamention research done at the University of Calgary regarding mercury'seffect on brain neurons, and I thank him for sending me a link to thisinformation. He also mentions an interview he did with John Moore, aresearcher in the dangers of mercury who himself was severely injured bymercury poisoning due to multiple amalgam fillings. His interview is postedat http://healthtruthrevealed.com/full-page.php?id=39 & & page=news. You willread on page 16 that Mr. Moore states that the research done at theUniversity of Calgary shows "the myelin sheathing simply stripped away fromthe nerve". Now, go to

this is CRITICAL.You will hear and see the effect of mercury on brain neurons demonstrated bythe University of Calgary which Mr. Moore refers to. Mercury causes DEATHof the nerve's axon, as the actin & tubulin which make up the neurofibrilsare destroyed when mercury binds to the tubulin molecules, causing theneurofibril to collapse, and some neurofibrils form aggregates or tangles.THIS IS THE KEY DIAGNOSTIC FEATURE SEEN IN ALZHEIMER'S DISEASE; NOT AUTISM!You will also notice that these neurons in a culture dish do not have myelinon then; in fact, THE MYELIN SHEATH IS NOT EVEN MENTIONED IN THIS VIDEO.(Side note - when the brains of Alzheimer's patients are studiedmicroscopically, ALUMINUM is found in the middle of these neurofibrillarytangles). I also encourage you to go tohttp://video.google.com/videoplay?docid=1803137818942286763, and hear DrBoyd Haley discuss autism & thimerosol (be sure to watch all 4 videos inthis series). Dr Haley blames thimerosol for Gulf War Syndrome (GWS) aswell as autism. I have done many shows on GWS, which has many factors; GulfWar PLAGUE (the infectious component of the SYNDROME) is due to mycoplasmaincognitas which was in the vaccines given to the soldiers. As explained inmy document "Inoculation the true weapons of mass destruction" atwww.drcarley.com, the injection of vaccines corrupts the immune system andprevents any infective agent from being eliminated from the body. GWS hasmany other aspects to it; depleted uranium, pyridostigmine pills given tothe soldiers, aspartame in their beverages, etc. To blame thimerosol solelyfor GWS is disinformation in its highest form. Dr. Haley brings up the work of Dr Andrew Wakefield, whose medical licensewas attacked because he demonstrated measles virus in the lymphoid patchesin the guts of autistic children. DR. BOYD ADMITS HE DID NOT EVEN STUDY THEMEASLES VIRUS. Although Dr Wakefield did not realize that these viruses'significance as a chronic infection is that this leads to a constantproduction of anti-measles antibody which, through molecular mimicry, thenattackes the myelin sheath (causing demyelination), he was attacked becausehis work supports my work; especially since the MMR has NEVER HAD MERCURY.Dr. Haley's work reinforces the notion that if you take mercury out ofvaccines, they will be safe. My work proves there is NO SUCH THING as asafe vaccine, due to the corruption of the immune system caused by injectionof live viruses. Dr. Haley also discusses how antibiotics further accelerate the damage inthese children. The question he does not address is why are the vaccinatedchildren on antibiotics? Answer...because they have chronic infectioncaused by inoculation of live viruses; as quoted from Harrison's principlesof medicine in my response to the CDC (also on my website), "RARELY ISPREVENTION OF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OFVACCINATION. In fact, asymptomatic infection after vaccination can serve toenhance and prolong the immune response". (And this prolonged immuneresponse IS prolonged production of anti-measles antibody which thencontinue to attack the myelin sheath, causing demyelination). As I alsoquote from Harrison's in my CDC response the symptoms of subacute sclerosingpanencephalitis (SSPE), you will see that autism is a non-fatal form ofSSPE. The way Dr. Haley gets around the fact that almost every parentreports their child descended into autism following their MMR shot is by saying that the children received OTHERvaccines containing mercury at the same time as they received the MMR. Dr. Haley also discusses how mercury is more toxic in children with immunedisorders. Where did these immune disorders come from? From the corruptionof the immune system caused by the inoculation of live viruses. He alsodiscusses that mercury can cause toxicity which affects genetics bydecreased methylation of DNA & RNA. However, no mention is made of thegenetic mutations caused by injection of plasmids of DNA from the organismsthemselves and the tissues that the viruses are cultured on, which is thewhole basis of DNA vaccines. That is why this court case focuses on thefact that the child had a genetic defect which caused mitochondrialdysfunction. Where this defect originated is not discussed...injection offoreign DNA in prior vaccines (You will note in the court decision that theparents were not tested for this defect, as that would have proven that thisis NOT an inherited genetic defect, but rather a mutation that occurred inthis child de novo). Lastly, Dr. also states that oral vaccines would be safer, but does not saythis is because of the secretory IgA causing proper handling of the antigen(as also explained in my inoculation paper), leading to life long NATURALimmunity. Of course, if all vaccines were made into oral forms, people maythen ask the hard question...SO WHY ISN'T NATURAL EXPOSURE TO THESE VIRUSESTHE BEST WAY TO GO? This question would stop vaccine production altogether,which would stop the creation of all autoimmune diseases and cancer, whichwould shut down Big Pharma. THAT IS THE POTENTIAL OF MY INFORMATION; whichis why the medical mafia has gone as far as taking my only child, not justmy medical license as they tried with Dr. Wakefield in an attempt to shut medown. Can you handle knowing the fact that all this is being done to the childrenON PURPOSE? Then go tohttp://www.republicbroadcasting.org/index.php?cmd=archives.month & ProgramID=36 & year=8 & month=3 & backURL=index.php%253Fcmd%253Darchives.getyear%2526ProgramID%253D36%26year%3D8%26backURL%3Dindex.php%253Fcmd%253Darchivesand listen to the 2nd hour of my interview on 3/5/08 with Dr. True Ott,where he discusses how the history of MediSIN goes back to the 1600's asdetailed in the Magnum Opus, with the creation of amulets by sacrificinganimals and mixing their blood with mercurial compounds TO CAST A SPELL ANDCONTROL THE MINDS OF THE POPULATIONS (Dr Ott discusses this starting at 13minutes of the 2nd hour of our interview). He explains how the origins ofthe word "pharmaceutical" in Latin is "pharmakia", which translates to"SORCERY". Yes, folks...you have now entered the rabbit hole...becausenothing has changed since the 1600's. I have been trying for 10 years to stop the vaccination holocaust on peopleand pets. I have proven, with the quoted studies and works of the "mercurycauses autism" disinformers themselves, that it is NOT MERCURY WHICH CAUSESAUTISM. I leave it up to you to forward this e-mail to all the individualsand groups which promote mercury as the cause of autism, so you will see forYOURSELVES who is intentionally misleading you, vs. who was misguided. Youwill know which is the case by whether or not they respond. SILENCE ISCONSENT that I am right; and if they do not join with me to stop thisholocaust altogether, you must then ask yourself WHY. IT IS TIME FOR THOSEWITH HONORABLE INTENTIONS TO JOIN WITH ME TO STOP THIS EPIDEMIC OF VIDS. Ihave already sent this to Dr. Boyd Haley (behaley) and David Kirby(brook200); please do so yourselves. Let's roll.... Namaste,Dr Carley --Dr. Rebecca Carleyhttp://www.drcarley.com *** Dr. Carley's information is not intended to diagnose, treat or cure anydiseases. 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