‘I am one of the far too many girls who have been affected by the HPV Vaccine, “Gardasil”, It has rendered my life very difficult. I am lying here in bed, when I should be in school preparing for leaving certificate. My cognitive function is so bad, i can’t even manage home schooling at the moment
My symptoms include chronic fatigue, chronic pain, severe headaches, dizziness, short term memory loss, very poor concentration, food intolerances, cysts, heart and breathing difficulties, both light and noise sensitivity. and menstrual disruption.
I’d like to think I’m an intelligent girl, and was aiming to study Psychology in Trinity, I was playing basketball & kayaking,…I had so many friends, and wanted to travel the world. Now all these things have been taken from me. You have no idea how horrible this is.‘ Another teenage victim of the Gardasil Vaccine
In practical terms, a synergy factor inevitably occurs when combining multiple ingredients such as heavy metals, live viruses/or strands of DNA-RNA “heat treated virus”, anti-biotics, formaldehyde, detergent, diploid cells (aborted fetal tissue), mycoplasma, phenol dye & excipient buffers together in a vial mixture.
Once injected into deep muscle tissue or subcutaneously (either route which literally bypasses one’s natural barriers altogether), a cascading degeneration known as Ischemia, a singeing of the neural pathways from toxic overload which prevents vital oxygen from reaching the brain, literally inhibiting normal development, often occurs.
The viscosity of this toxic sludge resulting from vaccines clogs/singes the vast network of arterial veins & capillaries leading to the brain while accumulating in the organs (ie. heart, liver, kidney), joints, meninges – 3 layers of protective tissue called the dura, arachnoid, & pia mater that surround the neuraxis (axial unpaired part of the central nervous system), intestines, along the neural pathways, veins & capillaries interlacing the entire body (resulting from “stagnant” blood). Anaphylaxis, a system-wide allergic & functional breakdown, described as ‘a severe, whole-body allergic reaction to a chemical that has become an allergen‘, and Encephalitis, inflammation of the brain & meninges (Meningoencephalitis) manifesting as ‘diffuse and/or focal neuropsychological dysfunction‘, inevitably follow.
The Myelin Sheath is a critical (electrical) insulator of the brain cells, ‘the protective sheath around axons (A long fiber of a nerve cell/neuron that acts somewhat like a fiber-optic cable carrying outgoing/efferent messages) in the nervous system…often referred to as ‘white matter’, containing a variety of fatty substances (lipids), and at least ten distinct chemicals‘; ‘formed by concentric layers of Schwann’s cell (peripheral) or oligodendrocyte (CNS) membranes – which serves to speed up neural conduction‘.
‘Myelination is an essential part of human brain development. Nerves can only conduct pulses of energy efficiently if covered by myelin. Like insulation on an electric wire, the fatty coating of myelin keeps the pulses confined and maintains the integrity of the electrical signal so that it has a high signal-to-noise ratio. When the insulation on a wire is damaged or destroyed, the flow of electrical current may be interrupted and a short-circuit occurs. Oligodendrocyte cells give white matter its color by manufacturing myelin. If myelin falls into disrepair, nerve axons cease to function, even though they themselves aren’t damaged. Protecting oligodendrocytes after brain or spinal cord injury might keep nerve cells intact. At birth, relatively few pathways have myelin insulation. Myelination in the human brain continues from before birth until at least 20 years of age. Up until the age of 10 or so, vast areas of the cortex are not yet myelinated.‘
“Almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.” Charles Posner, Harvard Medical School Department of Neurology, 1947
Two primary factors here, in determining the extent of vaccine derived neurological & corresponding neurodevelopmental damage (including the host of typical auto-immune failure responses) which are often overlooked in Medical circles? Timing & synergy.
Timing is CRITICAL. A newborn lacks sufficient protection to guard against premature damage to the blood barrier (physiological mechanism that alters the permeability of brain capillaries so that some substances, such as certain drugs, are prevented from entering brain tissue, while other substances are allowed to enter freely) on the brain – so that vital, unfinished area is still completely raw. The Myelin Sheath, a casing or insulator which protects the baby’s basic cells, is also under-developed. In fact, a baby undergoes continuous Myelin formation well after birth. Similarly, the Meninges layering is designed to insulate the brain & spinal cord from injury – notwithstanding the accumulative barrage of synergistic toxicity associated with early childhood vaccines. “Probably no field in embryology has been less explored than that relating to the meninges.”
Note: Early Onset Autism, which occurs anywhere from 12-18 months, coincides precisely with most intense period of standard immunization. By 15 months the average child in most developed countries, has received a minimum of 25 injections. This results in severe heavy metal toxicity interfering with the earliest stage of development, particularly during the first 6 months after birth.
The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient toxicity “sludge” targets 3 primary core “electrical grid” stations encasing the nerve center/brain – kin to throwing water over a main keyboard operating system. Once the blood barrier, Myelin sheath & meninges are breached, neuro-developmental disorders inevitably follow. A master Electrician knows more about overall functionality of the human body than your average Pediatrician.
The human body is bio-electric, a huge bio-conductive circuit board that runs throughout the entire body enabling all your systems to function & co-ordinate. You have 60,000 miles of blood vessels coursing throughout the body, a vast array of highways & byways & tributaries that are all inter-connected. The neurons in your brain rely on these ions to generate messages. from your brain throughout the body & back; the regulating of organs, your bloodstream, Heart, Kidney, Liver function – chelating & sequestering, the operation of one’s senses & warning signs, everything related to overall system co-ordination is managed via this delicate bio-conductive process. Enter Aluminum.
Aluminum is a positively charged bio-conductive element, 64 times more positive than colloidal blood products (ie. anything suspended in your blood) are negative; with the properties of a coagulant. It literally draws in all other metals & toxins in its path. Once injected subcutaneously into deep muscle tissue, this neurotoxin gets redistributed via the bloodstream, consisting of 90% water, to areas of fatty tissue (highly electrical tissues – negatively charged) throughout the body, builds up over time in these delicate centers; primarily in the Brain, Spinal cord, Myelin sheath, cardiac cells, breasts & ovaries in women, prostate in men, kidneys, liver & bowels.
This “sludging” is activated when Aluminum interacts with Hemoglobin in flow, in the negatively charged environment. This causes the negatively charged blood products to “attract” towards the larger, more massive positively charged Aluminum, causing clumping or “sludging”. This restricts blood flow, and it changes the Zeta Potential to change from -15mv (minus 15 milivolts) towards -10 mv (minus 10 milivolts), or possibly closer to zero. This is an increase in Zeta Potential, from a negatively charge towards neutral. (This is somewhat analogous to a change in state of water as it turns to ice – it’s a change in viscosity, affecting blood flow).
“Your blood has no method of excretion; Heavy metals & live viruses, formaldehyde are redistributed by the blood to areas of fatty tissue (highly conductive/electrical tissues) – found in the gray matter of the brain, the Myelin Sheath, neurons, the meninges/spine, cardiac cells, breasts & ovaries (in women), prostate (in men). Blood is made of water. When you stick aluminum in your blood, anything that’s toxic debris is going to bond to and coagulate and cause a congestive coccidiosis and this stuff gets caught in the tiny highways & byways. So you have the big gushing arteries & veins but they byfricate and branch into streams like a river; and they branch in again to the tiny arterial & capillary bits. That’s where the blockages are occurring, the brain, the spine, (the intestines/bowel) fingers & toes – which turn blue, choking of the micro-vessels from all the sludge that gets caught from all these repetitive hits/vaccinations, over & over. There are 60,000 miles of blood-vessels in one body.They run through every part of your muscle, your bone, your brain. Anywhere you stick an inter-muscular injection it goes into the blood.” Dr. Gary Tunsky
Two excerpts from closed door meeting conducted by the CDC in 2000: “But from all of the other studies of toxic substances, the earlier you work with the central nervous system, the more likely you are to run into a sensitive period for one of these effects, so that moving from one month or one day of birth to six months of birth changes enormously the potential for toxicity. There are just a host of neurodevelopmental data that would suggest that we’ve got a serious problem. The earlier we go, the more serious the problem.” Dr. Weil
“Aluminum & mercury are often simultaneously administered to infants, both at the same site & at different sites. However, there is absolutely no data, including animal data, about the potential for SYNERGY, additively or antagonism, all of which can occur in binary metal mixtures that relate and allow us to draw any conclusions from the simultaneous exposure to these two salts in vaccines.” Dr. Johnston
Multiple Sclerosis (like Amyotrophic lateral sclerosis/ALS, Lupus, Parkinson’s & Huntington’s Disease) is one of the most debilitating neuro-developmental disorders resulting from this breach of the body’s delicate nerve center (Blood-Brain barrier, Myelin sheath & Meninges). There is a scientifically verifiable link between vaccine derived sludge-toxicity related damage to these vital centers (in addition to post-vaccination ‘prescribed’ drug adverse reactions) & the onset of MS.
‘About 250,000 to 350,000 Americans have multiple sclerosis (MS), and women are affected almost twice as often as men. MS is characterized by scarring of the myelin in the brain and spinal cord, causing varying degrees of neurological impairment depending on the location and extent of the scarring. Although the cause of MS is unknown, scientific evidence increasingly suggests that genetics may play a role in determining a person’s susceptibility to MS. There are several treatments to alleviate the symptoms of MS but no cure.‘
‘Physically, the brain and the spinal cord are involved. Specifically, degeneration of myelin, a material which is composed mainly of fats and serves as an insulation for the nerves, much like the covering of an electric wire, degenerates. This fatty insulation allows a nerve to transmit its impulses with lightning-like speed, enabling people to move almost without thinking. The loss of this myelin insulation causes what is, in effect, a short-circuiting so that a person loses the ability to make smooth, rapid, and coordinated movements.
Thus, MS is a demyelinating disease. With multiple sclerosis, the loss of myelin appears to the naked eye as a hardened sclerotic (scar) area. These areas are multiple within the central nervous system, thus the term multiple sclerosis. Different areas of the brain and spinal cord are responsible for different kinds of movements. For example, the cerebellum, an out-pocketing of the brain, is responsible for making coordinated movements. When an area of demyelination occurs in the cerebellum, coordinated movements become difficult. The neurological deficit is quite dependent on the region of the brain or spinal cord that has been affected.‘
Glycoproteins involved in Myelin sheath formation, maintenance and degeneration: ‘Because glycoproteins are prominent components of plasma membranes, it is not surprising that they have important roles in the formation, maintenance and degeneration of myelin sheaths. The emphasis in this review is on four integral membrane glycoproteins. Two of them, protein zero (P0) and peripheral myelin protein-22 (PMP-22), are components of compact PNS myelin. The other two are preferentially localized in membranes of sheaths that are distinct from compact myelin. One is the myelin-associated glycoprotein, which is localized at the inside of sheaths where it functions in glia-axon interactions in both the PNS and CNS. The other is the myelin-oligodendrocyte glycoprotein, which is preferentially localized on the outside of CNS myelin sheaths and appears to be an important target antigen in autoimmune demyelinating diseases such as multiple sclerosis.‘
The HPV vaccines, Gardasil & Cervarix, contribute to “immune-mediated reactions to the nervous system” resulting in “Motor Neuron Disease” throughout the brain; and for those young teens whose threshold cannot withstand the toxic assault, due to a prolonged, compromised immune system (coupled with pre-existing medical conditions) stemming from the long-term accumulation of vaccine/anti-biotic/bad food choices inflicted erosion/saturation of the brain & gut, the eventuality of “multifocal or atypical demyelinating syndromes” (ie. Multiple Sclerosis).
‘Destruction of myelin and oligodendrocytes leading to the formation of large demyelinated plaques is the hallmark of multiple sclerosis (MS) pathology.‘ Journal of Neuropathology and Experimental Neurology
‘Post-mortem evaluations revealed widespread infiltrates of T lymphocytes and macrophages in the grey and white matter at all levels of the spinal cord. The researchers also reported extensive demyelination (MS symptoms) and severe loss of motor neurons (post) immunization with Gardasil. Lead investigator Maria Bouktsi from the Interbalkan European Medical Centre in Thessaloniki, Greece told Medscape Neurology that her team is questioning whether the immunostimulatory effects of the HPV-like particles of the vaccine are triggering adverse effects in vulnerable patients. It is the same question that researchers asked in a recent issue of Multiple Sclerosis (2009). Ian Sutton, MB ChB (Hons), MRCP(UK), PhD, FRACP from St. Vincents Hospital, New South Wales, Australia, and his team have reported five cases of multiple sclerosis after vaccination with Gardasil. The team reported that patients presented with multifocal or atypical demyelinating syndromes within 21 days of immunization. These researchers have also noted that this was an unusually rapid development of disease that is not normally seen in the general population.
It is the same question that researchers asked in a recent issue of Multiple Sclerosis (2009;15:116–119). Ian Sutton, MD, from St. Vincent’s Hospital in New South Wales, Australia, and his team reported 5 cases of multiple sclerosis after vaccination with the drug. The group reported in January that patients presented with multifocal or atypical demyelinating syndromes within 21 days of immunization. No definitive conclusions can be made based on this report, Dr. Sutton and his team noted. “It should not be overlooked that several epidemiological studies indicate that viral infection is associated with a threefold increase in the risk of a multiple sclerosis relapse,” write the researchers. 7 More Cases: Lead investigator of the second group presenting on this topic said that he agrees that postmarketing pharmacosurveillance is necessary to improve safety. “[Human papillomavirus] vaccines elicit a strong inflammatory systemic immune response,” said Til Menge, MD, from Heinrich-Heine University in Düsseldorf, Germany.His group suggests that it was this inflammatory response that may have triggered a case of fulminant neuromyelitis optica in a previously healthy 17-year-old girl.’ Dr. Lucija Tomljenovic, PhD
CNS demyelination and quadrivalent HPV vaccination: ‘Vaccination is generally considered safe in patients with multiple sclerosis (MS). We report five patients who presented with multifocal or atypical demyelinating syndromes within 21 days of immunization with the quadrivalent human papilloma virus (HPV) vaccine, Gardasil. Although the target population for vaccination, young females, has an inherently high risk for MS, the temporal association with demyelinating events in these cases may be explained by the potent immuno-stimulatory properties of HPV virus-like particles which comprise the vaccine. A prospective case-control study of patients with MS or clinically isolated demyelinating syndromes receiving the Gardasil vaccine may provide relevant safety data in this population.’ Sutton I, Lahoria R, Tan I, Clouston P, Barnett M, Department of Neurology, St Vincent’s Hospital, Darlinghurst, New South Wales, Australia, 09/19/08
‘Report of Motor Neuron Disease After HPV Vaccine: Investigators are reporting a case of motor neuron disease after immunization with the quadrivalent vaccine Gardasil. The Merck product is designed to prevent infection with several types of human papillomavirus.
Presenting here at the 134th annual meeting of the American Neurological Association, researchers describe a case of rapidly progressive disease leading to the death of a 14-year-old girl.
‘The cervical cancer vaccine Gardasil has triggered multiple sclerosis (MS) symptoms in some girls after being inoculated: Doctors said the victims were either teenagers or women in their early 20s who may have been predisposed to MS or who had a prior history of symptoms. St Vincent’s Hospital neurologist Dr Ian Sutton reported five cases in a journal article in January. Another five have since emerged. “Gardasil vaccination is not the cause of MS; whether or not it was a trigger for episodes of inflammation in the brain in these rare cases is unclear,” Dr Sutton said. All cases were in women aged under 26, the target group of a vaccination program that began in 2007. Symptoms began within three weeks of vaccination and lasted from weeks to months. “We have raised the question: has the vaccine modified what may have occurred anyway or just been an additional trigger?” Dr Sutton said.
The Therapeutic Goods Administration (TGA) last week said six million doses of Gardasil – created by scientist and former Australian of the Year Ian Frazer – had been distributed in Australia, and 1476 suspected adverse reactions had been reported to the regulator. “The TGA is also aware of a small number of cases in which neurological symptoms, similar to those experienced in patients with a dedemyelinating disorder such as multiple sclerosis, have been reported shortly after HPV (human papillomavirus vaccination),” the regulator said. The cases involving neurological symptoms have been investigated by an independent panel.
Specific role of Polysorbate 80 coating on the targeting of nanoparticles to the brain (causes a blood/brain barrier breach) “Partial coverage was enough for Tween-80 coating to play a specific role in brain targeting of nanoparticles; concerned with the interaction between T-80 coating and brain micro-vessel endothelial cells. Therefore, the specific role of T-80 coating on nanoparticles in brain targeting was confirmed.” Department of Material Science and Engineering, Huazhong University of Science and Technology, China Study, 2003
The mainstream Medical channels would have you believe “immune modulators/interferons” such as Copaxone greatly benefit those stricken with Multiple Sclerosis (or those exhibiting MS-like symptoms). Copaxone, in particular, has been singled out as a wonder drug with minimal side effects; unanimously endorsed by the US National Multiple Sclerosis Society, FDA, National Institute of Allergy and Infectious Diseases, & Medical Review Board; “(Copaxone) should be considered as soon as possible following the definite diagnosis of multiple sclerosis”…”(Copaxone) does NOT produce any flu-like symptoms, potential liver damage, any effects on white blood cells or thyroid functions nor possible links to depression as all interferons.” In addition, adverse drug interactions to vaccines (ie. Gardasil) have been deliberately glossed over; in fact the use of Gardasil in combination with Copaxone has been given official FDA green light approval – ‘not believed to contraindicate vaccination with Gardasil.’
‘Copaxone® for Modulation of Central Nervous System Autoimmune Disease – NIAID-supported scientists used an MS mouse model to explore how the FDA-approved drug Glatiramer acetate (Copaxone®) reduces the symptoms of MS. They showed that Copaxone® promoted the development of a specific type of anti-inflammatory immune cell called type II monocytes. These cells, in turn, modified their output of inflammatory molecules, which led to the generation of T regulatory cells, a type of immune cell that can ameliorate MS-like symptoms and central nervous system inflammation. This improved understanding of how Copaxaone® works may lead to the development of new and more effective forms of this drug. (Nat Med: 13: 935-43, 2007).‘
‘Copaxone (glatiramer acetate) is a compound made up of amino acids. These amino acids, which are also found in myelin, are thought to help switch the immune system from causing inflammation around lesions to reducing inflammation.‘
The National Multiple Sclerosis Society recommends that treatment with a “disease-modifying” (glatiramer acetate-type) medication, such as Copaxone, ‘should be considered as soon as possible following the definite diagnosis of multiple sclerosis with active, relapsing disease, and may also be considered for selected patients with a first attack who are at high risk of multiple sclerosis.‘
The immune modulators approved by the FDA for use in Multiple Sclerosis which are not believed to contraindicate vaccination with Gardasil include:
• Glatiramer acetate (Copaxone®)
• Interferon beta1a (Avonex® and Rebif®)
• Interferon beta1b (Betaseron®)
Copaxone marketing: ‘Copaxone is a non interferon based treatment for Relapsing Remitting MS (RRMS) that unlike the other CRAB (Copaxone, Rebif, Avonex, Betaseron) does NOT produce any flu-like symptoms, potential liver damage, any effects on white blood cells or thyroid functions nor possible links to depression as all interferons. On the other hand, the medication is given every day via subcutaneous injections, making it the most frequent of all MS treatment therapies and the injections themselves can have a fairly serious sting to them. The most common side effect of Copaxone is that it can leave fairly itchy/painful welts (lipoatrophy) a skin reactions (taking up to 5 days to disappear). ‘
‘Copaxone (glatiramer acetate) is a different formulation than the other CRABs, which are interferon-based. Therefore, it has different side effects — it does NOT have the flu-like symptoms, possible links to depression, potential liver damage or effects on white blood cells or thyroid function of the interferons. This makes Copaxone a popular choice for people working full-time, mothers of young children or other people who cannot afford down time due to side effects.
However, Copaxone is injected every day, the most frequent of any MS therapy, and the injections themselves can have a fairly serious sting to them. They also can leave fairly itchy/painful welts (which can take up to 5 days to go away), which is the most common side effect. Copaxone also can cause lipoatrophy, a destruction of fat cells in localized areas where it has been injected. This looks like a depression in the skin and underlying tissues and is permanent.‘
Contrary to all the Industry fanfare praising the drug, it turns out Copaxone adverse effects ranging from Respiratory Arrest, Tremors, Cardiovascular Disorder, Suicidal Ideation, Shock, Cardiac Disorder Thrombosis, Renal Disorder & Multiple Sclerosis (58 Cases of Multiple Sclerosis Relapse) to numerous incidents of deaths were deliberately buried from Press Publications; while references to negative test results in mice from early Clinical Trials were also conveniently omitted.
‘Israeli generics giant Teva Pharmaceutical Industries is suffering a couple of Copaxone-related headaches. First, Israel’s health ministry appointed a special committee to probe a trial of the MS drug. Allegedly, Teva tested Copaxone on ALS patients–despite the fact that previous trials on mice had failed. Teva maintains that testing Copaxone in human ALS patients was perfectly safe despite the deaths seen in mice taking the drug, because Copaxone had already made it through plenty of human trials for its approval as an MS drug. But an internal investigation by the health ministry’s comptroller found that the company didn’t submit all the necessary info before trial approval. So the special committee will take a look at the evidence to see whether the ministry and/or the company did anything wrong.’
Copaxone (Glatiramer) – Adverse Event Reports – All Cases – 58 Cases of Multiple Sclerosis Relapse
Copaxone (Glatiramer) – Adverse Event Reports – Serious Event – Death: Reported by a consumer/non-health professional from United States
Copaxone (Glatiramer) – Adverse Event Reports – Non-death related Serious Events
This pattern of systemic ignorance/silence within the Medical Establishment filters down to family clinics & hospitals throughout the community; the administering of prescription drugs, such as Copaxone, to post-HPV vaccination victims. How is it possible that such a widespread scandal involving Copaxone should go unnoticed by mainstream doctors working within the system; as young teens, experiencing adverse reactions to Gardasil (ie. MS-like symptoms) are having their health further undermined by serious drug interactions post-vaccination? This is tantamount, in legal terms, to ‘Assault & Battery On A Child Under 14 Causing Bodily Injury‘.
‘The HPV vaccine (Gardasil®, Cervarix®) can potentially interact with many drugs. Some of the drugs that may lead to HPV vaccine interactions include Immunosuppressants/biologic medications, such as: Glatiramer (Copaxone®)’ MedTV
Startling testimonial by previously healthy Gardasil victim indicates post-vaccine drug treatment with Copaxone linked to onset of MS-type symptoms: ‘I have been told about a girl who was 12 getting MS – possibly triggered from Gardasil…MS generally starts effecting people from 20 onward, as I guess you probably know but the fact anomalies are happening around the Gardasil shots (you would think) would be enough reason to investigate properly or raise more awareness….I still have symptoms – it gave me an auto immune disease and chronic illness.
It started this time last year, vertigo, a 4 month migraine, Diploplia – I was hospitalized cue a bunch of CT scans and MRIs etc…then IV drips of steroids to take the swelling down. They made it seem like I had a brain tumor, told me there was something in my brain stem and needed to start Steroids asap…just a horrible year – couldn’t drive til recently, lost a job, relationship etc etc across the board just horrible and n ow I am on daily injections and at the moment I have numb hands (have since Jan) I find it hard to type and do things like count money at work etc., Sore eye – the one that had the Diploplia and rolled up creating double vision, fatigue, etc etc.
I knew nothing (about Copaxone), was told it was the oldest MS drug they had and my condition had gotten worse in the last 5 months between the MRIs that was about it. I brought up the Gardasil/MS correlation with the appointed nurse who told me that there was no such thing etc and I didn’t bother arguing as she kept bringing it up saying she’s been in the field since the 70s etc I actually freaked out when they slammed my 4 choices in front of my being Copaxone, Avonex, Beta interforn 1b and then get this – REBIF made by MERCK.
My condition has worsened since we last spoke too. I now have Optic Neuritus in both eyes (worse in left one at the moment) and my numb hands have become more fatigued and unfeeling at the fingertips. My doctor told me to go to the Emergency room to get more steroids through a drip and I really did not want to so I’m at home, kinda hoping it just gets less inflamed…
I guess Gardasil has effected my life by triggering an auto immune /chronic disease for me. I suffered Vertigo, a 4 month long migraine, dizziness, Diploplia, muscle spasms in my hands, numbness in my fingers…I was hospitalized because of the CIS at the time and the demyelination had caused swelling in parts of my brain.
It has stolen over a year of my life at present, I had my birthday and it was like…Wtf happened…I don’t know where 365 days went among all the scans/MRI, blood tests and bad news etc.
Healthwise – my life is now a guessing game. Every time something weird happens I wonder if its related to my disease. I have anxiety over my possible future.
Psychologically – I keep going from “bring it on, I will fight what this did to me” to “Why did I do this? I’m so stupid. I know so much about NWO but this snuck by me and I don’t know why I fell for misinformation and aggressive marketing, the fact it was free in my country in 2008 and only for a limited time…and realising that taking the shots is the only regret I have in my life. I worry about any eventualities and whether I will be able to do the things I wanted to do in my life. While other girls my age want to go to University or get married etc I’m wondering if I will be able to walk in 10 years.
Work – I am now “disabled”, on disability and I’m not sure, if I don’t get better somehow that I will ever be able to earn enough money to do the things I need to .
Relationship/friendships – Not many of my friends know the full extent. I don’t want to be seen differently. My partner (I am extremely lucky) is dealing with the challenges but I feel like its too much for other people sometimes and I hate putting it on them so I stress over picking and choosing how much to share.
So I kinda feel on top of the things I need to tackle with the disease and what Gardasil has done, there’s all these little things that surround it. It’s a vaccination that has caused physical pain to my body but has effected every other part of my life.’ Ongoing correspondence with VRM
Note: The young woman behind this powerful testimonial was subjected to multiple CT scans & MRIs while undergoing tests in hospital. ‘A single CT scan of the chest is equal to about 350 standard chest X-rays.‘ 3 X 350 = 1050 chest X-rays.
‘A Melbourne woman who suffered an auto-immune and neurological attack after being injected with the cervical cancer vaccine Gardasil is leading a class action against its manufacturer. Seven other Victorian women who are considering joining the court case against Merck say they have suffered anaphylaxis and physical breakdowns as a result of the vaccine. One has attributed a miscarriage to the injections.
Naomi Snell, 28, said her life was put on hold for more than two years after she lost the ability to walk, battled crippling back and neck pain, and suffered convulsions that started soon after her first injection in July 2008. “I never attributed it to my vaccine so I went back for my second and third dose,” she said. “My doctors were baffled. They did diagnose me with multiple sclerosis, but have since retracted that and said it was a neurological reaction to the vaccine.”‘
Vaccine/Drug-injury related testimonials: ‘I am a 23-year old female. In March, my PCP had me get the first injection of Gardasil (the HPV vaccine). About 10 days later, I had symptoms of visual disturbances, numbness, and headache that lingered for a week. My MRI taken days later showed white matter lesions. In early June, I had a follow-up MRI that showed increased white matter lesions. I had the second Gardasil injection in late June. In late July, I had my second MS “attack” this time complete with significant twitching. Some of the twitching persists now, one month later. My official MS diagnosis is in a holding pattern until next week when I see my neuro again. As I am set to get the third and final injection of Gardasil next month, I am clearly concerned about not only if I should get the injection, but also if it has caused my neuro problems. I have read about instances of Guillain-Barre being associated with Gardasil. As it is a demyelinating disorder, it doesn’t seem to be a stretch to think that MS could also be linked.’
‘I have a friend whose sister and another friend have both been diagnosed with MS after receiving the Gardasil vaccination, within a month of each other. Both girls began having symptoms after their second doses. My daughter had received her first and I am not going to continue the vaccination. I should have researched this before just trusting that it would be OK.’
‘I chose Copaxone as well. I wound up in the hospital. What started out as a site reaction, within a month became an allergic reaction to the drug. I wound up in the hospital and almost died because of Anaphylactic (sp?) Shock. I stopped breathing. Copaxone is a wonderful drug for those who can take it…however for those of us who can’t- it can be awful. Everyone I know who had the same site reactions, eventually gave up. They don’t usually get better, and in fact can get worse.’
VRM is committed to uncovering the full extent of this scandal, by educating as many parents & young teens as possible throughout the community, as to the imminent dangers posed by HPV vaccine uptake. We need your input now. How many teens out there who unfortunately got the Gardasil/Cervarix series (or parents of teens who got the shot) were subsequently prescribed COPAXONE (or a similar drug) for Multiple Sclerosis type symptoms?
VRM Worldwide Autism Study
VRM: The Problem With Vaccines Part 1
VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body
VRM: Vaccine Clinic – A Concise Compendium To The Problem With Vaccines
VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting Body
VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body
VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body
VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus http://vaccineresistancemovement.org/?p=9431
VRM: The Rise of Mutagenic Viruses http://vaccineresistancemovement.org/?p=13124
VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460
VRM: 5 Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642
VRM: The Flu Report http://vaccineresistancemovement.org/?p=9226
VRM: 5 Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642
VRM: L-Histidine, Squaline, & Human Chorionic Gonadotrophin In Vaccines – Nature Off Balance
VRM: Vaccine Ingredients
VRM: Safe Alternatives to Vaccines
VRM: Family Charts Gradual Decline Of Daughter
VRM: Autism – Steps To Take Toward Prevention
VRM: Health Matters Part 1
VRM: Health Matters Part 2
VRM: Alternative Cancer Cures That Work
VRM: Pregnancy Tips
VRM: The Vanishing Sperm Count
VRM: Dr. Andrew Wakefield Being Crucified By Big Pharma
VRM: Dr. Wakefield’s Imminent Vindication – Turning Of The Tide
VRM: Media Spin & Swine Flu Hysteria
VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t & WHO – Cost To Taxpayers Exceeds 2.5 Billion
VRM: Flu Death Statistics – WHO & The Big Lie
VRM: Canada’s 2010-11 Flu Vaccine A Deadly Concoction
VRM: United States 2010-11 Flu Vaccine Afluria – Buyer Beware
VRM: Australian Vaccine Scandal
VRM: Polio – United Nations & The Great Cull
VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) http://vaccineresistancemovement.org/?p=10091
VRM: Weaponized Polio & The African Green Monkey Conundrum http://vaccineresistancemovement.org/?p=10727
VRM: Mandatory Vaccinations – How They Will Be Implemented http://vaccineresistancemovement.org/?p=11806
VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460
VRM : Vaccine Industry Deception, Propaganda & Media Collusion
VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios
VRM: H1N1 Bio-weaponry Incorporated
VRM : Aids & The WHO Connection – Criminal Intent
VRM: Morgellons Syndrome & Chemtrails
VRM : Council On Foreign Relations 10/16/09- Major Influence on Government Vaccine Policy
VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines
VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario
VRM : World Health Organization & Vaccine Manufacturers Implicated In Massive H1N1 Financial Scam Involving Kickbacks & Cover-ups
VRM : Former Pharmaceutical Representative Gwen Olsen Exposes Systemic Industry Fraud
VRM: Britain’s National Health Service – Criminal Syndicate Swindling Billions While Rapidly Destroying Health Care System
VRM: UK Institutes Brand of Medical Martial Law With ‘Super-Vaccination’ Day
VRM : The Awakening Has Begun
VRM: Medical Martial Law In The US – Sleeping Giant Of Tyranny
VRM : Multi-Virus Vaccine Quinvaxem Proving Deadly
VRM: New Generation Cancer Vaccine Will Cause Infertility
VRM: CDC-Gate Exposes A Trail of Fraud Behind Autism Studies
VRM : Squaline – The Military Agenda Comes Home
VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis.
VRM Live – 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk.
VRM Live – 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis.
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