RE: Dr Carley critiques the Fed Ct deci...

[Guest guest]

Can I ask the dumb blonde question here....who is Dr. Carley? I saw this on another board too and honestly don't have the patience to read all the way to the end. Can someone post the key points here? And for the scientifically challenged. : )

If she is saying that chronic disease is vaccine induced by live viruses...then what's the explanation for these genetic mutations. Is it the small pox vaccine that all of OUR moms got? Just throwing it out there.

Tami DuncanPresident and Co-Founderwww.liafoundation.orgJoin us in Fort Lee, NJ for our first East Coast Conference, Saturday, April 12th. You'll hear top doctors such as Bransfield, MD, Ray , MD, Janelle Love, MD, Warren Levin, MD, Peta Cohen, PhD, Guissepina Feingold, MD, Baker, ND, Horowitz, MD and the author of "Mold Warriors" Ritchie Shoemaker, MD. Online registration available at: www.liafoundation.org (click Spring 2008 Conference)

PERMISSION BY DR. CARLEY TO REPOST FREELY:Dr Carley critiques the Fed Ct decision admitting vaccine caused autismThe following is the ammo by which Big Pharma can be brought to its knees,and the holocaust of autoimmune diseases and cancer in people and in petsstopped at last. I ask you to circulate it widely. It is time for you toDEMANDthat those promoting mercury as the cause of autism respond to what I havewritten below. If the true intention of these people is to stop this epidemicin our 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 to_http://www.drcarleyhttp://wwhttp://www.dhtt_(http://www.drcarley.com/the_big_picture.jpg) ; you will see that I have ALWAYSsaid it is the BIG PICTURE ofassaults to our immune systems (and mercury is there) which combine to causedisease, including autism. But it is the corruption of the immune systemcausedby the inoculation of viruses which is the root cause of all autoimmunediseases and cancer...and once this information is in the hands of a criticalmass of the people, we will put a stop to the biggest epidemic the world hasever known...VIDS (Vaccine Induced Diseases). And the individuals who continueto promote mercury as the root cause in the face of this information will beexposed for being INTENTIONAL disinformers.Below is a verbatim copy of the US Government concession filed in Novemberof 2007 in a Court of Federal Claims case brought by neurologist Dr. JonPoling and his wife claiming that vaccines were the cause of their daughterHannah's autism. This decision is posted on Kirby's blog at_http://www.huffingthttp://www.http://www.hhttp://www.huffihttp://wwhttp://www.h\_(http://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-_b_88558.html\) . Kirby, author of "Evidence of Harm", is one of the individuals who isdistracting the public that autism is "all about the thimerosol". The takehomemessage therefore is that if the mercury is removed, vaccines will be safe.A BIGGER LIE HAS NEVER BEEN TOLD; and my document "Inoculations the TrueWeapons of Mass Destruction" posted on _www.drcarley.www_(http://www.drcarley.com/) describes the corruption of the immune systemcaused by the injection ofviruses directly into the body, bypassing secretory IgA (an antibody in theupper GI and respiratory tracts critical for the processing of germs by theimmune system for natural immunity to occur).I was a guest with Kirby on a radio show which is posted on my websiteat _http://www.drcarleyhttp://www.http://wwwhttp://www_(http://www.drcarley.com/kirby_vs_carley_autism.mp3) , on which I confrontedhim with the factthat autism is actually a non-fatal case of subacute sclerosing panencephalitiscaused by demyelination following vaccine induced encephalitis, and that thename of the condition was changed to autism to hide this self evident fact.I have sent Mr. Kirby copies of the documents on my website, and asked himmultiple times to be a guest on one of my internet 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 at_http://www.huffingthttp://www.http://www.hhttp://www.http://wwhttp://www.hufhtt\p_(http://www.huffingtonpost.com/david-kirby/government-concedes-vacci_b_88323.htm\l) ). But is hediscussing the live viruses bypassing secretory IgA, causing vaccine inducedencephalitis and subsequent demyelination? NO...he is mentioning live virusesasa cause of mitochondrial damage. So once again, we will now be distractedwith this genetic mitochondrial defect...perhaps develop a test to find thechildren with this problem before they are vaccinated, when in fact geneticdefects can also be caused by vaccines. More confusion and distraction. Moreconfusion and distraction.<WBR>..rather than admitting that there is no suchthing as a safe vaccine...and the practice should be abandoned altogether,with attention instead pla Of course, since population reduction is the trueagenda of the powers that be, not only will the vaccine push continue...butviruses are being developed to cause cancer under the Special Virus CancerProgram. The mad scientists have to be stopped...and this WILL happen onceenoughpeople have opened their eyes to the true purpose of vaccines.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. Note theseimportant 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 INDUCED ENCEPHALITIS,aninflammation of the brain caused by injection of LIVE VIRUSES (not frommercury).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). As explained in the quotes fromon's Principles of Medicine, 6th edition, p. 943 posted in my response totheCDC on _www.drcarley.www_ (http://www.drcarley.com/) , "RARELY IS PREVENTIONOF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OF VACCINATION. Infact, asymptomatic infection after vaccination can serve to enhance and prolongthe immune response."4. She was diagnosed with vaccine induced ENCEPHALOPATHY (degenerativedisease of the brain)...as you will see below, mercury is involved in causingthedegenerative disease Alzheimer's, NOT autism).5. She developed a SEIZURE DISORDER later on (go to the CDC website at_http://www.cdc.http://www.cdhttp://wwhttp://wwwhttp://www._(http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-mmr.pdf) ) and read thevaccine informationstatement on the MMR vaccine (which has never had mercury), and you will seethat one of the side effects is LONG TERM 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 whole basison which DNA vaccines are designed). You can read how DNA vaccines causegenetic mutations at_http://sciamdigitalhttp://sciahttp://sciamdihttp://sciamdigihttp://scia_(http://sciamdigital.com/index.cfm?fa=Search.ViewSearchForItemResultList) (youwill have to pay $7.95 to access this 1999 article fromScientific American; put "genetic vaccines" in the search engine at that sitetofind the article, and especially see p. 52 of the article). Of course, theyare purporting that this is a GOOD thing...and do not reveal that "regular"vaccines can do the same thing. VACCINES ARE THE SOURCE OF MOST GENETICMUTATIONS IN PEOPLE AND IN PETS; and once these mutations have occurred, theyarethen passed on to future generations. Thus, this insane practice has thepotential of causing the extinction of humanity itself.7. You will notice that although the white coat treating Hannah Poling wentas far as to do genetic testing in this child, there were NO ANTI-MYELIN ORANTI-NEURONAL FILAMENT LEVELS DONE; this IS the test that demonstratesdemyelination before it is massive enough to show up on MRI's; and this IS thetestthat would prove that autism is actually a non-fatal form of subacutesclerosing panencephalitis (which is why this test is almost never done). However,it is a known fact that the measles virus has similar proteins to myelinbasic protein, and thus through molecular mimicry, the anti-measles antibodyitself can cause demyelination; and, as quoted from on's above, thisproduction of anti-measles (and possibly anti-myelin and anti-neuronal filamentantibodies formed by injection of tissue culture on which the viruses aregrown) is prolonged because a chronic infection results.Here is the decision (but please be sure to also read what I have writtenafter it)...IN THE UNITED STATES COURT OF FEDERAL CLAIMSOFFICE OF SPECIAL MASTERSCHILD [Hannah Poling], a minor,by her Parents and Natural Guardians [Dr. & Mrs. Jon Poling],Petitioners,v.SECRETARY OF HEALTH AND HUMAN SERVICES,Respondent.RESPONDENT'S RULE 4© REPORTIn 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.FACTSCHILD ("CHILD") was born on December --, 1998, and weighed eight pounds, tenounces. Petitioners' Exhibit ("Pet. Ex.") 54 at 13. The pregnancy wascomplicated by gestational diabetes. Id. at 13. CHILD received her firstHepatitisB immunization on December 27, 1998. Pet. Ex. 31 at 2.From January 26, 1999 through June 28, 1999, CHILD visited the PediatricCenter, in Catonsville, land, for well-child examinations and minorcomplaints, including fever and eczema. Pet. Ex. 31 at 5-10, 19. During thistimeperiod, she received the following pediatric vaccinations, without incident:Vaccine Dates AdministeredHep B 12/27/98; 1/26/99IPV 3/12/99; 4/27/99Hib 3/12/99; 4/27/99; 6/28/99DTaP 3/12/99; 4/27/99; 6/28/99Id. 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 January 2000,she had frequent bouts of otitis media, which doctors treated with multipleantibiotics. Pet. Ex. 2 at 4. On December 3,1999, CHILD was seen by KarlDiehn, M.D., at Ear, Nose, and Throat Associates of the Greater BaltimoreMedicalCenter ("ENT Associates") At seven months of age, CHILD was diagnosed withbilateral otitis media. Pet. Ex. 31 at 20. In the subsequent months between July1999 and January 2000, she had frequent bouts of otitis media, which doctorstreated with multiple antibiotics. Pet. Ex. 2 at 4. On December 3,1999,CHILD was seen by Karl Diehn, M.D., at Ear, NoseAccording to the medical records, CHILD consistently met her developmentalmilestones during the first eighteen months of her life. The record of anOctober 5, 1999 visit to the Pediatric Center notes that CHILD was mimickingsounds, crawling, and sitting. Pet. Ex. 31 at 9. The record of her 12-monthpediatric examination notes that she was using the words "Mom" and "Dad,"pullingherself 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, andcriedfor long periods of time. Pet. Ex. 2 at 6. She exhibited intermittent,high-pitched screaming and a decreased response to stimuli. Id. MOM spoke withthepediatrician, who told her that CHILD was having a normal reaction to herimmunizations. Id. According to CHILD's mother, this behavior continued overthenext ten days, and CHILD also began to arch her back when she 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 extremely irritable 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, a reducedappetite, and pulling at her left ear. Id. at 29. Two days later, on September28, 2000, CHILD was again seen at the Pediatric Center because her diarrheacontinued, she was congested, and her mother reported that CHILD was cryingduring urination. Id. at 32. On November 1, 2000, CHILD received bilateral PEtubes. Id. at 38. On November 13, 2000, a physician at ENT Associates notedthat CHILD was "obviously hearing better" and her audiogram was normal. Id. at38. On November 27, 2000, CHILD was seen at the Pediatric Center withcomplaints of diarrhea, vomiting, diminished energy, fever, and a rash on hercheek. Id. at 33. At a follow-up visit, on December 14, 2000, the doctor notedthat CHILD had a possible speech delay. Id.CHILD was evaluated at the County Infants and Toddlers Program, onNovember 17, 2000, and November 28, 2000, due to concerns about her languagedevelopment. Pet. Ex. 19 at 2, 7. The assessment team observed deficits inCHILD's communication and social development. Id. at 6. CHILD's mother reportedthat CHILD had become less responsive to verbal direction in the previous fourmonths 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. GraceMatesicidentified a middle ear effusion and recorded that CHILD was having somebalanceissues and not progressing with her speech. Id. On December 27, 2000, CHILDvisited ENT Associates, where Dr. Grace Matesic observed that CHILD's left PEtube was obstructed with crust. Pet. Ex. 14 at 6. The tube was replaced onJanuary 17, 2001. Id.Dr. Zimmerman, a pediatric neurologist, evaluated CHILD at theKennedy Krieger Children's Hospital Neurology Clinic ("Krieger Institute"), onFebruary 8, 2001. Pet. Ex. 25 at 1. Dr. Zimmerman reported that after CHILD'simmunizations of July 19, 2000, an "encephalopathy progressed to persistentlossof previously acquired language, eye contact, and relatedness. reportedthat after CHILD's immunizations of July 19, 2000, an "encephalopathy progressedto persistent loss of previously acquired language, eye contact, andrelatedness.<WBR>" Id. He noted a disruption in CHILD's sleep patterns, persistentscreaming anwould not make eye contact. Id. He diagnosed CHILD with "regressiveencephalopathy with features consistent with an autistic spectrum disorder,followingnormal development. would not make eye contact. Id. He diagnosed CHILD with"regressive encephalopathy with features consistent with an a would not makeDr. Zimmerman referred CHILD to the Krieger Institute's Occupational TherapyClinic and the Center for Autism and Related Disorders ("CARDS"). Pet. Ex.25 at 40. She was evaluated at the Occupational Therapy Clinic by StaceyMerenstein, OTR/L, on February 23, 2001. Id. The evaluation report summarizedthatCHILD had deficits in "many areas of sensory processing which decrease[d]her ability to interpret sensory input and influence[d] her motor performanceas a result." Id. at 45. CHILD was evaluated by Alice Kau and Kelley Duff, onMay 16, 2001, at CARDS. Pet. Ex. 25 at 17. The clinicians concluded thatCHILD was developmentally delayed and demonstrated features of autisticdisorder.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 noseizure discharges. Id. at 16. An MRI, performed on March 14, 2001, wasnormal. Pet. Ex. 24 at 16. A G-band test revealed a normal karyotype. Pet. Ex.25at 16. Laboratory studies, however, strongly indicated an underlyingmitochondrial disorder. Id. at 4.Dr. Zimmerman referred CHILD for a neurogenetics consultation to evaluateher abnormal metabolic test results. Pet. Ex. 25 at 8. CHILD met with Dr. Kelley, a specialist in neurogenetics, on May 22, 2001, at the KriegerInstitute. Id. In his assessment, Dr. Kelley affirmed that CHILD's history andlab results were consistent with "an etiologically unexplained metabolicdisorder that appear[ed] to be a common cause of developmental regression." Id.at7. He continued to note that children with biochemical profiles similar toCHILD's develop normally until sometime between the first and second year oflife when their metabolic pattern becomes apparent, at which time theydevelopmentally regress. Id. Dr. Kelley described this condition as"mitochondrialPPD." Id.On October 4, 2001, Dr. Schoffner, at Horizon Molecular Medicine inNorcross, Georgia, examined CHILD to assess whether her clinical manifestationswere related to a defect in cellular energetics. Pet. Ex. 16 at 26. Afterreviewing her history, Dr. Schoffner agreed that the previous metabolic testingwas "suggestive of a defect in cellular energetics." Id. Dr. Schoffnerrecommended a muscle biopsy, genetic testing, metabolic testing, and cellculturebased testing. Id. at 36. A CSF organic acids test, on January 8, 2002,displayed an increased lactate to pyruvate ratio of 28,1 which can be seen indisorders of mitochondrial oxidative phosphorylation. Id. at 22. A musclebiopsytest for oxidative phosphorylation disease revealed abnormal results for TypeOne and Three. Id. at 3. The most prominent findings were scattered atrophicmyofibers that were mostly type one oxidative phosphorylation dependentmyofibers, mild increase 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 withoxidativephosphorylation disease. Id. at 3. In February 2004, a mitochondrial DNA("mtDNA") point mutation analysis revealed a single nucleotide change in the16Sribosomal RNA gene (T2387C). Id. at 11.CHILD returned to the Krieger Institute, on July 7, 2004, for a follow-upevaluation with Dr. Zimmerman. Pet. Ex. 57 at 9. He reported CHILD "had donevery well" with treatment for a mitochondrial dysfunction. Dr. Zimmermanconcluded 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 EEGshoweddiffuse slowing. Id. At 40. She was diagnosed with having experienced aprolonged complex partial seizure and transferred to ish Rite Hospital.Id. at39, 44. She experienced no more seizures while at ish Rite Hospital andwas discharged on the medications Trileptal and Diastal. Id. at 44. Afollow-up MRI of the brain, on June 16, 2006, was normal with evidence of a leftmastoiditis 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 region andthen focal slowing during a witnessed clinical seizure." Id. At 37. CHILDcontinues to suffer from a seizure disorder.ANALYSISMedical personnel at the Division of Vaccine Injury Compensation, Departmentof Health and Human Services (DVIC) have reviewed the facts of this case, aspresented by the petition, medical records, and affidavits. After a thoroughreview, DVIC has concluded that compensation is appropriate in this case.In sum, DVIC has concluded that the facts of this case meet the statutorycriteria for demonstrating that the vaccinations CHILD received on July 19,2000, significantly aggravated an underlying mitochondrial disorder, whichpredisposed her to deficits in cellular energy metabolism, and manifested as aregressive encephalopathy with features of autism spectrum disorder. Therefore,respondent recommends that compensation be awarded to petitioners in accordance with 42 U.S.C. § 300aa-11©( In sumDVIC has concluded that CHILD's complex partial seizure disorder, with anonset of almost six years after her July 19, 2000 vaccinations, is not relatedto a vaccine-injury.Respectfully submitted,PETER D. KEISLERAssistant Attorney GeneralTIMOTHY P. GARRENDirectorTorts Branch, Civil DivisionMARK W. ROGERSDeputy DirectorTorts Branch, Civil DivisionVINCENT J. MATANOSKIAssistant DirectorTorts Branch, Civil Divisions/ S. Renzi by s/ Lynn E. RicciardellaLINDA S. RENZISenior Trial CounselTorts Branch, Civil DivisionU.S. Department of JusticeP.O. Box 146 lin StationWashington, D.C. 20044DATE: November 9, 2007PS: 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 they were,indeed, linked to the immunizations of July, 2000, - KirbyNow 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://healthtruthrhttp://healthttp://healthtruhttp_(http://healthtruthrevealed.com/audio-interviews.php) , click on "inoculationsthetrue weapons of mass destruction", click on "inoculations the true weapons ofmass destruction"<WBR> You will hear interviewer Greg Ciola mention researchdone at the University of Calgary in Canada regarding mercury's effect onbrain neurons, and I thank him for sending me a link to this information. Healso mentions an interview he did with , a researcher in the dangersof mercury who himself was severely injured by mercury poisoning due tomultiple amalgam fillings. His interview is posted at_http://healthtruthrhttp://healthttp://heahttp://he & & page=news_(http://healthtruthrevealed.com/full-page.php?id=39 & & page=news) . You willread on page 16 that Mr. states thatthe research done at the University of Calgary shows "the myelin sheathingsimply stripped away from the nerve".Now, go to _http://www.youtube.http://wwwhttp://www.yo_(http://www.youtube.com/watch?v=85tgwh3HpsM) ; this is CRITICAL. You will hearand see the effectof mercury on brain neurons demonstrated by the University of Calgary whichMr. refers to. Mercury causes DEATH of the nerve's axon, as the actin & tubulin which make up the neurofibrils are destroyed when mercury binds tothe tubulin molecules, causing the neurofibril to collapse, and someneurofibrils form aggregates or tangles. THIS IS THE KEY DIAGNOSTIC FEATURESEEN INALZHEIMER'S DISEASE; NOT AUTISM! You will also notice that these neurons ina culture dish do not have myelin on them; in fact, THE MYELIN SHEATH IS NOTEVEN MENTIONED IN THIS VIDEO. (Side note - when the brains of Alzheimer'spatients are studied microscopically, ALUMINUM is found in the middle of theseneurofibrillary tangles).I also encourage you to go to_http://video.http://videhttp://vidhttp://video.<WBhttp://vi_(http://video.google.com/videoplay?docid=1803137818942286763) ,and hear Dr Boyd Haley discuss autism & thimerosol (be sure to watch all 4videos in this series). Dr Haley blames thimerosol for Gulf War Syndrome(GWS) as well as autism. I have done many shows on GWS, which has many factors;Gulf War PLAGUE (the infectious component of the SYNDROME) is due tomycoplasma incognitas which was in the vaccines given to the soldiers. (Infact, thispathogenic mycoplasma has actually been PATENTED by Dr. Shyn Ching Lo of theAmerican Registry of Pathology in Washington, DC, patent # 5,242,820). Asexplained in my document "Inoculation the True Weapons of Mass Destruction" at_www.drcarley.www_ (http://www.drcarley.com/) , the injection of vaccinescorrupts the immune system and prevents any infective agent from beingeliminated from the body. GWS has many other aspects to it; depleted uranium,pyridostigmine pills given to the soldiers, aspartame in their beverages, etc. Toblame thimerosol solely for GWS is disinformation in its highest form.Dr. Haley brings up the work of Dr Wakefield, whose medical licensewas attacked because he demonstrated measles virus in the lymphoid patches inthe 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 constant productionofanti-measles antibody which, through molecular mimicry, then attacks themyelin sheath (causing demyelination) Although Dr Wakefield did not realize thatthese viruses' significance as a chronic infection is that this leads to aDr. 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 a safevaccine, due to the corruption of the immune system caused by injection of liveviruses.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 infection causedbyinoculation of live bacteria & viruses; as quoted from on'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 to enhance andprolong the immune response". (And this prolonged immune response ISprolonged production of anti-measles antibody which then continue to attack themyelin sheath, causing demyelination) I also quote from on's in my CDCresponse the symptoms of subacute sclerosing panencephalitis (SSPE), and youwill see that autism is a non-fatal form of SSPE. The way Dr. Haley getsaround the fact that almost every parent reports their child descended into autismfollowing 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 by decreasedmethylation of DNA & RNA. However, no mention is made of the genetic mutationscaused by injection of plasmids of DNA from the organisms themselves and thetissues that the viruses are cultured on, which is the whole basis of DNAvaccines. That is why this court case focuses on the fact that the child had agenetic defect which caused mitochondrial dysfunction, and states that thechild has "a regressive encephalopathy with features of autism spectrumdisorder". Where this mitochondrial defect originated is not discussed...Where thismitochondrial defect originated is not discussed...<WBR>injection of foreignDNA in prior vaccines i (However, if one of Hannah's parents has thismitochondrial defect, then why don't they have autism?)Lastly, Dr. Haley also states that oral vaccines would be safer, but doesnot say this is because of the secretory IgA causing proper handling of thegerm and its subsequent elimination from the body (as also explained in myinoculation paper), leading to life long NATURAL immunity. Of course, if allvaccines were made into oral forms, people may then ask the hard question...SOWHY ISN'T NATURAL EXPOSURE TO THESE VIRUSES THE BEST WAY TO GO? This questionwould stop vaccine production altogether, which would stop the creation ofall autoimmune diseases and cancer, which would shut down Big Pharma. THAT ISTHE POTENTIAL OF MY INFORMATION; which is why the medical mafia has gone asfar as taking my only child, not just my medical license as they tried withDr. Wakefield in an attempt to shut me down.Can you handle knowing the fact that all this is being done to the childrenON PURPOSE? Then go to_http://www.republichttp://www.rehttp://wwwhttp://www.repubhttp:/ & ProgramID=36 & y\ear=8 & month=3 & backURL=index.backURL=indebackURL=indexbackURL=index.<WbackURL=indexbackURL=indbackURL=inbackURL=indebackURL=index.<Wback_(http://www.republicbroadcasting.org/index.php?cmd=archives.month & ProgramID=36 & y\ear=8 & month=3 & backURL=index.php%3Fcmd%3Darchives.getyear%26ProgramID%3D36 & year=8 & backURL=index.php%3Fcmd%3Darchives)and 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 asdetailedin the Magnum Opus by Jesuit Del Rio, with the creation of amulets bysacrificing animals and mixing their blood with mercurial compounds TO CAST ASPELLAND CONTROL THE MINDS OF THE POPULATIONS (Dr Ott discusses this starting at13 minutes 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...because nothinghas 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 individuals andgroups which promote mercury as the cause of autism, so you will see forYOURSELVES who is intentionally misleading you, vs. who was misguided. Youwillknow which is the case by whether or not they respond. SILENCE IS CONSENTthat I am right; and if they do not join with me to stop this holocaustaltogether, you must then ask yourself WHY. IT IS TIME FOR THOSE WITHHONORABLEINTENTIONS TO JOIN WITH ME TO STOP THIS EPIDEMIC OF VIDS. I have already sentthis document to Dr. Boyd Haley (_behaley@..._ (mailto:behaley@...) )and Kirby (_brook200@..._ (mailto:brook200@...) );please do so yourselves.Let's roll....Namaste,Dr Carley--_www.drcarley.www_ (http://www.drcarley.com/)Listen to "What's Ailing America?" every Thursday night at 8:00 PM EST on_www.bbsradio.www_ (http://www.bbsradio.com/) and also on_www.republicbroadcawww.repub_ (http://www.republicbroadcasting.org/) at 12noon EST everyWednesday"Inoculations are the true weapons of mass destruction, causing an epidemicof genocide" Carley, MDCourt Qualified Expert in vaccine Induced Diseases"The individual is handicapped by coming face to face with a conspiracy somonstrous that he cannot believe it exists"J Edgar HooverFBI DirectorAll TRUTH passes through 3 stages:1st - it is ridiculed2nd - it is violently opposed3rd - it is accepted as SELF EVIDENTArthur SchopenhauerIn a time of universal deceit, telling the TRUTH is a revolutionary act.1984, OrwellWARNINGAny attempts to intercept this message are in violation of Title 18 U.S.C.2511(1) of theElectronic Communications Privacy Act (ECPA). All violators aresubject to fines, imprisonment or civil damages, or both."Medical research has made such progress, that there are practically nohealthy people any more." â€" Aldous Huxley"....Perfume to you, to me is excrement."- PopeI will not have my life narrowed down. I will not bow down to somebody else's whim or to someone else'signorance. -bell hooks It's Tax Time! Get tips, forms and advice on AOL Money Finance.

[Guest guest]

WOW! Tami,

I admires this Dr. writings and believes, I

believe in his theory no Kirby, regardless that mercury is bad, of course, and

the actual truth is what he is saying!!!

I would like to meek him too.

Please let me know if you find him first.

.

From: BorreliaMultipleInfectionsAndAutism

[mailto:BorreliaMultipleInfectionsAndAutism ]

On Behalf Of Tamiduncan@...

Sent: Monday, March 10, 2008 8:10

PM

To: BorreliaMultipleInfectionsAndAutism

Subject: Re:

Dr Carley critiques the Fed Ct deci...

Can I ask the dumb blonde question

here....who is Dr. Carley? I saw this on another board too and

honestly don't have the patience to read all the way to the end. Can

someone post the key points here? And for the scientifically challenged.

: )

If she is saying that chronic disease is

vaccine induced by live viruses...then what's the explanation for these genetic

mutations. Is it the small pox vaccine that all of OUR moms

got? Just throwing it out there.

Tami Duncan

President and Co-Founder

www.liafoundation.org

Join us in Fort Lee, NJ

for our first East Coast Conference, Saturday, April 12th. You'll hear top

doctors such as Bransfield, MD, Ray , MD, Janelle Love, MD,

Warren Levin, MD, Peta Cohen, PhD, Guissepina Feingold,

MD, Baker, ND, Horowitz, MD

and the author of " Mold Warriors " Ritchie Shoemaker, MD.

Online registration available at: www.liafoundation.org

(click Spring 2008 Conference)

In a message dated 3/10/2008 7:59:10 P.M.

Pacific Daylight Time, shha2002 writes:

PERMISSION BY DR. CARLEY

TO REPOST FREELY:

Dr Carley critiques the Fed Ct

decision admitting vaccine caused

autism

The following is the ammo by which Big Pharma can be brought to its

knees,

and the holocaust of autoimmune diseases and cancer in people and in

pets

stopped at last. I ask you to circulate it widely. It is time for you

to

DEMAND

that those promoting mercury as the cause of autism respond to what I

have

written below. If the true intention of these people is to stop this

epidemic

in our children, then they should let go of their egos and admit that

I have

figured out the true cause. Let me first encourage of all you to go to

_http://www.drcarleyhttp://wwhttp://www.dhtt_

(http://www.drcarley.com/the_big_picture.jpg)

; you will see that I

have ALWAYS

said it is the BIG PICTURE of

assaults to our immune systems (and mercury is there) which combine

to cause

disease, including autism. But it is the corruption of the immune

system

caused

by the inoculation of viruses which is the root cause of all

autoimmune

diseases and cancer...and once this information is in the hands of a

critical

mass of the people, we will put a stop to the biggest epidemic the

world has

ever known...VIDS (Vaccine Induced Diseases). And the individuals who

continue

to promote mercury as the root cause in the face of this information

will be

exposed for being INTENTIONAL disinformers.

Below is a verbatim copy of the US Government concession filed in

November

of 2007 in a Court of Federal Claims case brought by neurologist Dr.

Jon

Poling and his wife claiming that vaccines were the cause of their

daughter

Hannah's autism. This decision is posted on Kirby's blog at

_http://www.huffingthttp://www.http://www.hhttp://www.huffihttp://wwht

tp://www.h\

_

(http://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-

_b_88558.html\

) .

Kirby, author of " Evidence of Harm " , is one of the individuals

who is

distracting the public that autism is " all about the thimerosol " . The

take

home

message therefore is that if the mercury is removed, vaccines will be

safe.

A BIGGER LIE HAS NEVER BEEN TOLD; and my document " Inoculations the

True

Weapons of Mass Destruction " posted on _www.drcarley.www_

(http://www.drcarley.com/)

describes the corruption of the immune

system

caused by the injection of

viruses directly into the body, bypassing secretory IgA (an antibody

in the

upper GI and respiratory tracts critical for the processing of germs

by the

immune system for natural immunity to occur).

I was a guest with Kirby on a radio show which is posted on my

website

at _http://www.drcarleyhttp://www.http://wwwhttp://www_

(http://www.drcarley.com/kirby_vs_carley_autism.mp3)

, on which I

confronted

him with the fact

that autism is actually a non-fatal case of subacute sclerosing

panencephalitis

caused by demyelination following vaccine induced encephalitis, and

that the

name of the condition was changed to autism to hide this self evident

fact.

I have sent Mr. Kirby copies of the documents on my website, and

asked him

multiple times to be a guest on one of my internet 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 a

plethora of other potential problems (see # 6 at

_http://www.huffingthttp://www.http://www.hhttp://www.http://wwhttp://

www.hufhtt\

p_

(http://www.huffingtonpost.com/david-kirby/government-concedes-

vacci_b_88323.htm\

l) ). But is he

discussing the live viruses bypassing secretory IgA, causing vaccine

induced

encephalitis and subsequent demyelination? NO...he is mentioning live

viruses

as

a cause of mitochondrial damage. So once again, we will now be

distracted

with this genetic mitochondrial defect...perhaps develop a test to

find the

children with this problem before they are vaccinated, when in fact

genetic

defects can also be caused by vaccines. More confusion and

distraction. More

confusion and distraction.<WBR>..rather than admitting that there is

no such

thing as a safe vaccine...and the practice should be abandoned

altogether,

with attention instead pla Of course, since population reduction is

the true

agenda of the powers that be, not only will the vaccine push

continue...but

viruses are being developed to cause cancer under the Special Virus

Cancer

Program. The mad scientists have to be stopped...and this WILL happen

once

enough

people have opened their eyes to the true purpose of vaccines.

I urge all of you to carefully read this decision dated 11/9/07, in

which

this young girl won her case claiming vaccines caused her autism.

Note these

important points:

1. 2 days after multiple vaccines (which included the MMR, which has

NEVER

had mercury), she developed a high fever, high pitched screaming, and

was

lethargic and irritable. These are symptoms of VACCINE INDUCED

ENCEPHALITIS,

an

inflammation of the brain caused by injection of LIVE VIRUSES (not

from

mercury).

2. She also began to arch her back when she cried (a sign of vaccine

induced

encephalitis, NOT mercury poisoning).

3. She developed a POST-VARICELLA VACCINATION RASH (which proves that

the

vaccination GAVE HER THAT DISEASE). As explained in the quotes from

on's Principles of Medicine, 6th

edition, p. 943 posted in my

response to

the

CDC on _www.drcarley.www_ (http://www.drcarley.com/) ,

" RARELY IS

PREVENTION

OF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OF

VACCINATION. In

fact, asymptomatic infection after vaccination can serve to enhance

and prolong

the immune response. "

4. She was diagnosed with vaccine induced ENCEPHALOPATHY (degenerative

disease of the brain)...as you will see below, mercury is involved in

causing

the

degenerative disease Alzheimer's, NOT autism).

5. She developed a SEIZURE DISORDER later on (go to the CDC website at

_http://www.cdc.http://www.cdhttp://wwhttp://wwwhttp://www._

(http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-mmr.pdf)

) and

read the

vaccine information

statement on the MMR vaccine (which has never had mercury), and you

will see

that one of the side effects is LONG TERM SEIZURES.

6. You will also note that they did genetic testing of the child and

found

that she has a genetic defect in her cellular energetics (note that

vaccines

are known to cause GENETIC MUTATION due to insertion of plasmids of

DNA from

the viruses or tissues used to culture them; in fact, this is the

whole basis

on which DNA vaccines are designed). You can read how DNA vaccines

cause

genetic mutations at

_http://sciamdigitalhttp://sciahttp://sciamdihttp://sciamdigihttp://sc

ia_

(http://sciamdigital.com/index.cfm?

fa=Search.ViewSearchForItemResultList) (you

will have to pay $7.95 to access this 1999 article from

Scientific American; put " genetic vaccines " in the search engine at

that site

to

find the article, and especially see p. 52 of the article). Of

course, they

are purporting that this is a GOOD thing...and do not reveal

that " regular "

vaccines can do the same thing. VACCINES ARE THE SOURCE OF MOST

GENETIC

MUTATIONS IN PEOPLE AND IN PETS; and once these mutations have

occurred, they

are

then passed on to future generations. Thus, this insane practice has

the

potential of causing the extinction of humanity itself.

7. You will notice that although the white coat treating Hannah

Poling went

as far as to do genetic testing in this child, there were NO ANTI-

MYELIN OR

ANTI-NEURONAL FILAMENT LEVELS DONE; this IS the test that demonstrates

demyelination before it is massive enough to show up on MRI's; and

this IS the

test

that would prove that autism is actually a non-fatal form of subacute

sclerosing panencephalitis (which is why this test is almost never

done).

However,

it is a known fact that the measles virus has similar proteins to

myelin

basic protein, and thus through molecular mimicry, the anti-measles

antibody

itself can cause demyelination; and, as quoted from on's

above,

this

production of anti-measles (and possibly anti-myelin and anti-

neuronal filament

antibodies formed by injection of tissue culture on which the viruses

are

grown) is prolonged because a chronic infection results.

Here is the decision (but please be sure to also read what I have

written

after it)...

IN THE UNITED STATES COURT OF FEDERAL CLAIMS

OFFICE OF SPECIAL MASTERS

CHILD [Hannah Poling], a minor,

by her Parents and Natural Guardians [Dr. & Mrs. Jon Poling],

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

of

Health and Human Services submits the following response to the

petition for

compensation 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 was

complicated by gestational diabetes. Id.

at 13. CHILD received her

first

Hepatitis

B immunization on December 27, 1998. Pet. Ex. 31 at 2.

From January 26, 1999 through June 28, 1999, CHILD visited the

Pediatric

Center, in Catonsville, land, for well-child examinations and

minor

complaints, including fever and eczema. Pet. Ex. 31 at 5-10, 19.

During this

time

period, she received the following pediatric vaccinations, without

incident:

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

January 2000,

she had frequent bouts of otitis media, which doctors treated with

multiple

antibiotics. Pet. Ex. 2 at 4. On December 3,1999, CHILD was seen by

Karl

Diehn, M.D., at Ear, Nose, and Throat Associates of the Greater

Baltimore

Medical

Center ( " ENT Associates " ) 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 January 2000, she had frequent bouts of otitis media, which

doctors

treated with multiple antibiotics. Pet. Ex. 2 at 4. On December

3,1999,

CHILD was seen by Karl Diehn, M.D., at Ear, Nose

According to the medical records, CHILD consistently met her

developmental

milestones during the first eighteen months of her life. The record

of an

October 5, 1999 visit to the Pediatric

Center notes that CHILD

was

mimicking

sounds, crawling, and sitting. Pet. Ex. 31 at 9. The record of her 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

mother

reported 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 102.3

degrees two days after her immunizations and was lethargic,

irritable, and

cried

for long periods of time. Pet. Ex. 2 at 6. She exhibited intermittent,

high-pitched screaming and a decreased response to stimuli. Id. MOM

spoke with

the

pediatrician, who told her that CHILD was having a normal reaction to

her

immunizations. Id.

According to CHILD's mother, this behavior

continued over

the

next ten days, and CHILD also began to arch her back when she cried.

Id.

On July 31, 2000, CHILD presented to the Pediatric Center

with a 101-

102

degree temperature, a diminished appetite, and small red dots on her

chest.

Pet.

Ex. 31 at 28. The nurse practitioner recorded that CHILD was

extremely i

rritable and inconsolable. Id.

She was diagnosed with a post-varicella

vaccination rash. Id.

at 29.

Two months later, on September 26, 2000, CHILD returned to the

Pediatric

Center with a temperature of 102 degrees, diarrhea, nasal discharge,

a reduced

appetite, and pulling at her left ear. Id.

at 29. Two days later, on

September

28, 2000, CHILD was again seen at the Pediatric Center

because her

diarrhea

continued, she was congested, and her mother reported that CHILD was

crying

during urination. Id.

at 32. On November 1, 2000, CHILD received

bilateral PE

tubes. Id. at

38. On November 13, 2000, a physician at ENT Associates

noted

that CHILD was " obviously hearing better " and her audiogram was

normal. Id.

at

38. On November 27, 2000, CHILD was seen at the Pediatric Center

with

complaints of diarrhea, vomiting, diminished energy, fever, and a

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 County Infants and Toddlers

Program, on

November 17, 2000, and November 28, 2000, due to concerns about her

language

development. Pet. Ex. 19 at 2, 7. The assessment team observed

deficits in

CHILD's communication and social development. Id. at 6. CHILD's

mother reported

that CHILD had become less responsive to verbal direction in the

previous four

months and had lost some language skills. Id. At 2.

On December 21, 2000, CHILD returned to ENT Associates because of an

obstruction in her right ear and fussiness. Pet. Ex. 31 at 39. Dr.

Grace

Matesic

identified a middle ear effusion and recorded that CHILD was having

some

balance

issues and not progressing with her speech. Id. On December 27, 2000,

CHILD

visited ENT Associates, where Dr. Grace Matesic observed that CHILD's

left PE

tube was obstructed with crust. Pet. Ex. 14 at 6. The tube was

replaced on

January 17, 2001. Id.

Dr. Zimmerman, a pediatric neurologist, evaluated CHILD at the

Kennedy Krieger Children's Hospital Neurology Clinic ( " Krieger

Institute " ), on

February 8, 2001. Pet. Ex. 25 at 1. Dr. Zimmerman reported that after

CHILD's

immunizations of July 19, 2000, an " encephalopathy progressed to

persistent

loss

of previously acquired language, eye contact, and relatedness.

reported

that after CHILD's immunizations of July 19, 2000, an " encephalopathy

progressed

to persistent loss of previously acquired language, eye contact, and

relatedness.<WBR> " Id.

He noted a disruption in CHILD's sleep

patterns,

persistent

screaming an

would not make eye contact. Id.

He diagnosed CHILD with " regressive

encephalopathy with features consistent with an autistic spectrum

disorder,

following

normal development. would not make eye contact. Id. He diagnosed

CHILD with

" regressive encephalopathy with features consistent with an a would

not make

Dr. Zimmerman referred CHILD to the Krieger Institute's Occupational

Therapy

Clinic and the Center for Autism and Related Disorders ( " CARDS " ).

Pet. Ex.

25 at 40. She was evaluated at the Occupational Therapy Clinic by

Stacey

Merenstein, OTR/L, on February 23, 2001. Id.

The evaluation report

summarized

that

CHILD had deficits in " many areas of sensory processing which decrease

[d]

her ability to interpret sensory input and influence[d] her motor

performance

as a result. " Id.

at 45. CHILD was evaluated by Alice Kau and Kelley

Duff, on

May 16, 2001, at CARDS. Pet. Ex. 25 at 17. The clinicians concluded

that

CHILD was developmentally delayed and demonstrated features of

autistic

disorder.

Id. at 22.

CHILD returned to Dr. Zimmerman, on May 17, 2001, for a follow-up

consultation. Pet. Ex. 25 at 4. An overnight EEG, performed on April

6, 2001,

showed no

seizure discharges. Id.

at 16. An MRI, performed on March 14, 2001,

was

normal. Pet. Ex. 24 at 16. A G-band test revealed a normal karyotype.

Pet. Ex.

25

at 16. Laboratory studies, however, strongly indicated an underlying

mitochondrial disorder. Id.

at 4.

Dr. Zimmerman referred CHILD for a neurogenetics consultation to

evaluate

her abnormal metabolic test results. Pet. Ex. 25 at 8. CHILD met with

Dr.

Kelley, a specialist in neurogenetics, on May 22, 2001, at

the Krieger

Institute. Id.

In his assessment, Dr. Kelley affirmed that CHILD's

history and

lab results were consistent with " an etiologically unexplained

metabolic

disorder that appear[ed] to be a common cause of developmental

regression. " Id.

at

7. He continued to note that children with biochemical profiles

similar to

CHILD's develop normally until sometime between the first and second

year of

life when their metabolic pattern becomes apparent, at which time they

developmentally regress. Id. Dr. Kelley described this condition as

" mitochondrial

PPD. " Id.

On October 4, 2001, Dr. Schoffner, at Horizon Molecular Medicine

in

Norcross, Georgia, examined CHILD to assess

whether her clinical

manifestations

were related to a defect in cellular energetics. Pet. Ex. 16 at 26.

After

reviewing her history, Dr. Schoffner agreed that the previous

metabolic testing

was " suggestive of a defect in cellular energetics. " Id. Dr.

Schoffner

recommended a muscle biopsy, genetic testing, metabolic testing, and

cell

culture

based testing. Id.

at 36. A CSF organic acids test, on January 8,

2002,

displayed an increased lactate to pyruvate ratio of 28,1 which can be

seen in

disorders of mitochondrial oxidative phosphorylation. Id. at 22. A

muscle

biopsy

test for oxidative phosphorylation disease revealed abnormal results

for Type

One and Three. Id.

at 3. The most prominent findings were scattered

atrophic

myofibers that were mostly type one oxidative phosphorylation

dependent

myofibers, mild increase in lipid in selected myofibers, and occasio

nal myofiber with reduced cytochrome c oxidase activity. Id. at 7.

After

reviewing these laboratory results, Dr. Schoffner diagnosed CHILD with

oxidative

phosphorylation disease. Id.

at 3. In February 2004, a mitochondrial

DNA

( " mtDNA " ) point mutation analysis revealed a single nucleotide change

in the

16S

ribosomal RNA gene (T2387C). Id.

at 11.

CHILD returned to the Krieger Institute, on July 7, 2004, for a

follow-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 Regional

Hospital and developed a tonic seizure en route. Pet. Ex. 10 at 38.

An EEG

showed

diffuse slowing. Id.

At 40. She was diagnosed with having experienced

a

prolonged complex partial seizure and transferred to ish Rite

Hospital.

Id. at

39, 44. She experienced no more seizures while at ish Rite

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 with

evidence 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 region

and

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 of this

case, as

presented by the petition, medical records, and affidavits. After a

thorough

review, DVIC has concluded that compensation is appropriate in this

case.

In sum, DVIC has concluded that the facts of this case meet the

statutory

criteria for demonstrating that the vaccinations CHILD received on

July 19,

2000, significantly aggravated an underlying mitochondrial disorder,

which

predisposed her to deficits in cellular energy metabolism, and

manifested as a

regressive encephalopathy with features of autism spectrum disorder.

Therefore,

respondent recommends that compensation be awarded to petitioners in

accord

ance with 42 U.S.C. § 300aa-11©( In sum

DVIC has concluded that CHILD's complex partial seizure disorder,

with an

onset of almost six years after her July 19, 2000 vaccinations, is

not related

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/ 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

lin Station

Washington, D.C. 20044

DATE: November 9, 2007

PS: On Friday, February 22, HHS conceded that this child's complex

partial

seizure disorder was also caused by her vaccines. Now we the

taxpayers will

award this family compensation to finance her seizure medication.

Surely ALL

decent people can agree that is a good thing.

By the way, it''s worth noting that her seizures did not begin until

six

years after the date of vaccination, yet the government acknowledges

they were,

indeed, linked to the immunizations of July, 2000, - Kirby

Now I am going to prove to you, BEYOND A SHADOW OF A DOUBT, that

mercury is

a distraction in the case of autism:

Please go to _http://healthtruthrhttp://healthttp://healthtruhttp_

(http://healthtruthrevealed.com/audio-interviews.php)

, click

on " inoculations

the

true weapons of mass destruction " , click on " inoculations the

true

weapons of

mass destruction " <WBR> You will hear interviewer Greg Ciola

mention

research

done at the University of Calgary in Canada regarding mercury's

effect on

brain neurons, and I thank him for sending me a link to this

information. He

also mentions an interview he did with , a researcher in

the dangers

of mercury who himself was severely injured by mercury poisoning due

to

multiple amalgam fillings. His interview is posted at

_http://healthtruthrhttp://healthttp://heahttp://he & & page=news_

(http://healthtruthrevealed.com/full-page.php?id=39 & & page=news)

.. You

will

read on page 16 that Mr. states that

the research done at the University

of Calgary shows

" the myelin

sheathing

simply stripped away from the nerve " .

Now, go to _http://www.youtube.http://wwwhttp://www.yo_

(http://www.youtube.com/watch?v=85tgwh3HpsM)

; this is CRITICAL. You

will hear

and see the effect

of mercury on brain neurons demonstrated by the University of Calgary

which

Mr. refers to. Mercury causes DEATH of the nerve's axon, as the

actin

& tubulin which make up the neurofibrils are destroyed when mercury

binds to

the tubulin molecules, causing the neurofibril 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 myelin on them; in fact, THE MYELIN SHEATH

IS NOT

EVEN MENTIONED IN THIS VIDEO. (Side note - when the brains of

Alzheimer's

patients are studied microscopically, ALUMINUM is found in the middle

of these

neurofibrillary tangles).

I also encourage you to go to

_http://video.http://videhttp://vidhttp://video.<WBhttp://vi_

(http://video.google.com/videoplay?docid=1803137818942286763)

,

and hear Dr Boyd Haley discuss autism & thimerosol (be sure to watch

all 4

videos in this series). Dr Haley blames thimerosol for Gulf War

Syndrome

(GWS) as well as autism. I have done many shows on GWS, which has

many factors;

Gulf War PLAGUE (the infectious component of the SYNDROME) is due to

mycoplasma incognitas which was in the vaccines given to the

soldiers. (In

fact, this

pathogenic mycoplasma has actually been PATENTED by Dr. Shyn Ching Lo

of the

American Registry of Pathology in Washington,

DC, patent #

5,242,820). As

explained in my document " Inoculation the True Weapons of Mass

Destruction " at

_www.drcarley.www_ (http://www.drcarley.com/) , the

injection of

vaccines

corrupts the immune system and prevents any infective agent from being

eliminated from the body. GWS has many other aspects to it; depleted

uranium,

pyridostigmine pills given to the soldiers, aspartame in their

beverages, etc.

To

blame thimerosol solely for GWS is disinformation in its highest form.

Dr. Haley brings up the work of Dr Wakefield, whose medical

license

was attacked because he demonstrated measles virus in the lymphoid

patches in

the guts of autistic children. DR. BOYD ADMITS HE DID NOT EVEN STUDY

THE

MEASLES VIRUS. Although Dr Wakefield did not realize that these

viruses'

significance as a chronic infection is that this leads to a constant

production

of

anti-measles antibody which, through molecular mimicry, then attacks

the

myelin sheath (causing demyelination) Although Dr Wakefield did not

realize

that

these viruses' significance as a chronic infection is that this leads

to a

Dr. Haley's work reinforces the notion that if you take mercury out of

vaccines, they will be safe. My work proves there is NO SUCH THING as

a safe

vaccine, due to the corruption of the immune system caused by

injection of live

viruses.

Dr. Haley also discusses how antibiotics further accelerate the

damage in

these children. The question he does not address is why are the

vaccinated

children on antibiotics? Answer...because they have chronic infection

caused

by

inoculation of live bacteria & viruses; as quoted from on's

principles

of medicine in my response to the CDC (also on my website), " RARELY IS

PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OF

VACCINATION.

In fact, asymptomatic infection after vaccination can serve to

enhance and

prolong the immune response " . (And this prolonged immune response IS

prolonged production of anti-measles antibody which then continue to

attack the

myelin sheath, causing demyelination) I also quote from on's

in

my CDC

response the symptoms of subacute sclerosing panencephalitis (SSPE),

and you

will see that autism is a non-fatal form of SSPE. The way Dr. Haley

gets

around the fact that almost every parent reports their child

descended into

autism

following their MMR shot is by saying that the children received OTHER

vaccines containing mercury at the same time as they received the MMR.

Dr. Haley also discusses how mercury is more toxic in children with

immune

disorders. Where did these immune disorders come from? From the

corruption

of the immune system caused by the inoculation of live viruses. He

also

discusses that mercury can cause toxicity which affects genetics by

decreased

methylation of DNA & RNA. However, no mention is made of the genetic

mutations

caused by injection of plasmids of DNA from the organisms themselves

and the

tissues that the viruses are cultured on, which is the whole basis of

DNA

vaccines. That is why this court case focuses on the fact that the

child had a

genetic defect which caused mitochondrial dysfunction, and states

that the

child has " a regressive encephalopathy with features of autism

spectrum

disorder " . Where this mitochondrial defect originated is not

discussed...

Where this

mitochondrial defect originated is not discussed...<WBR>injection of

foreign

DNA in prior vaccines i (However, if one of Hannah's parents has this

mitochondrial defect, then why don't they have autism?)

Lastly, Dr. Haley also states that oral vaccines would be safer, but

does

not say this is because of the secretory IgA causing proper handling

of the

germ and its subsequent elimination from the body (as also explained

in my

inoculation paper), leading to life long NATURAL immunity. Of course,

if all

vaccines were made into oral forms, people may then ask the hard

question...SO

WHY ISN'T NATURAL EXPOSURE TO THESE VIRUSES THE BEST WAY TO GO? This

question

would stop vaccine production altogether, which would stop the

creation of

all autoimmune diseases and cancer, which would shut down Big Pharma.

THAT IS

THE POTENTIAL OF MY INFORMATION; which is why the medical mafia has

gone as

far as taking my only child, not just my medical license as they

tried with

Dr. Wakefield in an attempt to shut me down.

Can you handle knowing the fact that all this is being done to the

children

ON PURPOSE? Then go to

_http://www.republichttp://www.rehttp://wwwhttp://www.repubhttp:/ & Prog

ramID=36 & y\

ear=8 & month=3 & backURL=index.backURL=indebackURL=index

backURL=index.<WbackURL=indexbackURL=indbackURL=inbackURL=indebackURL=

index.<W

back_

(http://www.republicbroadcasting.org/index.php?

cmd=archives.month & ProgramID=36 & y\

ear=8 & month=3 & backURL=index.php%3Fcmd%3Darchives.getyear%26ProgramID%3

D36 & year=8 & backURL=index.php%3Fcmd%3Darchives)

and 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

as

detailed

in the Magnum Opus by Jesuit Del Rio, with the creation of amulets by

sacrificing animals and mixing their blood with mercurial compounds

TO CAST A

SPELL

AND CONTROL THE MINDS OF THE POPULATIONS (Dr Ott discusses this

starting at

13 minutes of the 2nd hour of our interview). He explains how the

origins of

the word " pharmaceutical " in Latin is " pharmakia " , which

translates to

" SORCERY " . Yes, folks...you have now entered the rabbit

hole...because nothing

has changed since the 1600's.

I have been trying for 10 years to stop the vaccination holocaust on

people

and pets. I have proven, with the quoted studies and works of

the " mercury

causes autism " disinformers themselves, that it is NOT MERCURY WHICH

CAUSES

AUTISM. I leave it up to you to forward this e-mail to all the

individuals and

groups which promote mercury as the cause of autism, so you will see

for

YOURSELVES who is intentionally misleading you, vs. who was

misguided. You

will

know which is the case by whether or not they respond. SILENCE IS

CONSENT

that I am right; and if they do not join with me to stop this

holocaust

altogether, you must then ask yourself WHY. IT IS TIME FOR THOSE WITH

HONORABLE

INTENTIONS TO JOIN WITH ME TO STOP THIS EPIDEMIC OF VIDS. I have

already sent

this document to Dr. Boyd Haley (_behaley@..._ (mailto:behaley@...) )

and Kirby (_brook200@..._ (mailto:brook200@...) );

please do so yourselves.

Let's roll....

Namaste,

Dr Carley

--

_www.drcarley.www_ (http://www.drcarley.com/)

Listen to " What's Ailing America? "

every Thursday night at 8:00 PM

EST on

_www.bbsradio.www_ (http://www.bbsradio.com/) and also on

_www.republicbroadcawww.repub_ (http://www.republicbroadcasting.org/)

at 12

noon EST every

Wednesday

" Inoculations are the true weapons of mass destruction, causing an

epidemic

of genocide "

Carley, MD

Court Qualified Expert in vaccine Induced Diseases

" The individual is handicapped by coming face to face with a

conspiracy so

monstrous that he cannot believe it exists "

J Edgar Hoover

FBI Director

All TRUTH passes through 3 stages:

1st - it is ridiculed

2nd - it is violently opposed

3rd - it is accepted as SELF EVIDENT

Arthur Schopenhauer

In a time of universal deceit, telling the TRUTH is a revolutionary

act.

1984, Orwell

WARNING

Any attempts to intercept this message are in violation of Title 18

U.S.C.

2511(1) of the

Electronic Communications Privacy Act (ECPA). All violators are

subject to fines, imprisonment or civil damages, or both.

" Medical research has made such progress, that there are practically

no

healthy people any more. " †" Aldous Huxley

" ....Perfume to you, to me is excrement. " - Pope

I will not have my life narrowed down

.. I will not bow down to somebody else's whim or to someone else's

ignorance. -bell hooks

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[Guest guest]

Dr. Carley is giving us an introduction into the "cellular theory" of disease.

One that is NOT taught in medical school. Western physicians are trained in

the "germ theory"...which is wrought with inaccuracies.

Anyone who really digs into it's concepts, will find it incredibly simple compared

to the "germ theory".

Truth is obvious and pure...Lies are complicated.

Perhaps that is why it takes so long to earn a medical degree?

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