from The Thinking Moms' Revolution
Posted on February 10, 2015 by Thinking Moms' Revolution
~ Jean Ghantous
I read with great interest the recent ‘measles epidemic’ articles that addressed the vaccine debate from the point of view of a cancer parent. My interest is the result of being a cancer parent myself – my little girl has been battling leukemia on and off for the past 10 years. I read these articles, and I became angry. Very, very angry. Once again, the government and drug companies are exploiting the plight of children stricken by cancer to achieve a profit-driven end without actually helping them. In fact, this profitable end could cause great harm, even increasing the rates of pediatric leukemia, if their obvious goal of a federally mandated vaccination protocol is achieved. I am a seasoned Momcologist, a term the research-driven cancer parents call themselves. We are the cancer equivalent of Thinking Moms, critical thinkers. I have done extensive reading on the etiology of leukemia, its connection to autoimmune disease, and how vaccines and natural disease may influence these sorts of childhood illnesses. Come connect the dots with me.
Clearly, I empathize with the raw fear the parents in these articles have that their immunocompromised children may contract an illness that could be devastating. I have walked for years in their shoes. I get it. However, the parents in these articles are either grossly misinformed, or their comments have been edited with bias. Let’s get some facts straight about cancer treatment and infection. One of the first things we were warned about after my daughter’s diagnosis was live-virus vaccination. No one in the family was to receive a live-virus vaccine while my daughter was on treatment because these viruses can and do shed (1, 2, 3, 4), some for as much as four weeks (5), potentially infecting the immunocompromised patient with disastrous results. That includes the measles vaccine (MMR II and ProQuad), the intranasal flu vaccine, and the chicken pox shot. In fact, my other children were able to get medical waivers not to receive vaccines because of my daughter’s illness. I know my child is much more likely to encounter a peer at school who has been recently vaccinated with a live-virus vaccine than she is to encounter natural disease from an unvaccinated child.
The most deadly threats for a child during intensive cancer treatment lie right within his or her own body. Immunocompromised pediatric cancer patients are far more likely to die from opportunistic infections that originate from overgrowths of fungi, mold and bacteria(7) than they are from vaccine-related viral infections. When I searched to find the last recorded incidence of a child dying of measles (because that is the hated disease du jour) while undergoing cancer treatment, well, I couldn’t find one. I did, however, find at least one death in the immunocompromised from the measles vaccine (8), with no indication of when it or they occurred. There hasn’t been a recorded death in the U.S. from measles in the past 10 years. (9) In fact, measles infection may actually be curative of some blood cancers (10, 11), presumably by initiating normal immune system defenses. The measles virus as an actual treatment has also been explored in other malignancies (12, 13).
There is evidence that the “hygiene theory” of the immune system may have some relevance to to vaccines. It has been found that more “hygienic” populations, i.e. kids who have had fewer exposures to everyday germs, are at higher risk for some illnesses. The idea being that the immune system needs to “learn” how to respond appropriately by coming in contact with common bugs in order to develop properly. Industrialized countries that have a decrease in infectious burden over less developed nations nevertheless show an increase in allergies and autoimmune disease. “The leading idea is that some infectious agents — notably those that co-evolved with us — are able to protect us against a large spectrum of immune-related disorders.” (14) Are we trading benign, transient illnesses that were once considered normal childhood rites of passage, illnesses that appear to be protective for more serious disease, for a lifetime of chronic illness, even death?
A discussion of the peculiarities of leukemia is in order, its relationship to the immune system, and the idea that vaccines can act as a possible trigger for the cancer itself. Leukemia begins with the development of immature white blood cells in the bone marrow, when one of these baby white blood cells mutates into an abnormal, leukemic cell. The more actively the body produces white blood cells (which are infection-fighting cells), therefore, the higher the risk of mutation. This is the explanation given for increases in the incidence of leukemia after a flu virus passes through an area (15), and why children who exhibit hyper-stimulated immune responses in the form of asthma and eczema also have increased risk for leukemia (16). It may seem contradictory to discuss infection as a preventative for leukemia when applying the hygiene hypothesis, while also pointing to infection as a cause. It’s apparently all about the maturity and status of the immune system. “Timing is critical, as early infections are likely to positively modulate the immune system thereby reducing risk of leukemia, whereas later infections in children whose immune system was less well modulated may increase such risk.” (17)
Time to stop and connect more dots. What are American children exposed to that deliberately hyper-stimulate the immune system? Vaccines. Our children are subjected to an incredibly aggressive vaccine schedule, the likes of which no other country sees, from the day they are born (and we have the highest first-day infant death rate of any first-world country, by the way) (18). Could we actually be triggering leukemia, the most common form of childhood cancer, with these vaccines? Particularly when we give them to children who already show signs of abnormal immune response?
Vaccines are not calibrated by weight or age or health-risk factors; potency levels of vaccines are standardized (19), which may cause hyper-stimulation for a child with a highly sensitive immune system. Isn’t it interesting that less industrial countries have lower rates of autoimmune disease, yet when those kids come to industrialized countries, in one generation they match our rates? (20) Could this possibly be related to the fact that these immigrants are required to submit to more aggressive vaccine schedules?
Acute lymphocytic leukemia is also less common in third-world countries, despite their children’s otherwise more debilitated state. Children in industrialized nations experience a sharp rise in leukemia between two and six years of the age, the vaccine years, which does not occur in less developed nations. (21)
It is so very obvious that this potential connection requires exploration, yet the only studies to be found merely compare leukemia in more vaccinated to less vaccinated kids. The data from children who are completely unvaccinated is critical in uncovering the true reality of overall pediatric health. We may very well find many interesting discoveries. Read this study from Germany (22), for example, which shows less acute and serious chronic illness overall for unvaccinated children, though they did not include childhood cancer. Why are we merely chasing a cure when a likely cause is sitting right under our noses?
One word: Profit. As of 1988, vaccine makers and the doctors who administer vaccines bear no liability for vaccine injury (23). They cannot be held accountable by law for adverse events from vaccination. In fact, the entire adverse event reporting system (VAERS) is voluntary! This means that the more aggressive our vaccine schedule, the more profitable it is for vaccine makers. But what about the Centers for Disease Control, don’t they direct the vaccines our children really need? Please note that the CDC uses worldwide disease data to formulate our policies, which makes no sense at all. How could one possibly compare a malnourished child living in unsanitary conditions and subsequently exposed to illness to a child exposed to that same illness in a first-world country? I invite parents to take a look at the resumes of some of the heads of pharmaceutical companies and members of the CDC like this one (24). One can very clearly see those in charge of vaccine policy have a dangerous conflict of interest with those who profit from that policy. Remember, pharmaceutical companies contributed $34 million dollars in campaign funds in 2014 (25). It would behoove anyone attempting office these days to err on the side of ‘big pharma.’
If any parent wants their child to be safe from preventable illness, it is a cancer parent. Yet I also stand with scores of cancer parents who have seen their children become stricken with leukemia shortly after vaccination. My little girl? She was diagnosed with leukemia shortly after her pediatrician “caught her up” on her shots almost 10 years ago. That “catch up” schedule matches the regular schedule for a toddler today. Unfortunately, it is nearly impossible to untangle true childhood cancer statistics or ‘cure’ (as in survival) rates (29). The SEER database includes only five states and ten cities in the U.S., and one cannot readily backtrack to the time before the mad rush of vaccines. (30)
It is time to ask the hard questions for the sake of our children. Are we actually causing leukemia and other childhood illnesses with these vaccines? Could we even prevent leukemia by allowing natural disease? The current measles “scare” is clearly a push for a federally mandated vaccine program. Measles is highly contagious, yes, but benign (even potentially helpful) for the vast majority in a first-world country. If the current vaccine schedule could be harming our children, what will happen when pharmaceutical companies are given carte blanche? Do we really want to relinquish our parental rights to a government that has shown itself to be both corrupt and callous in their treatment of our cancer kids? What data is critical to either prove, or disprove, the hypothesis that vaccines can lead to increased chronic disease, particularly those related to the immune system like leukemia? An independent study of the overall health of vaccinated versus unvaccinated children must be undertaken. It is past time to finish connecting the dots to reveal the true picture of vaccines and childhood cancer. Though it is too late for my vaccine-injured daughter, this Momcologist stands against vaccine mandates, for the health of future children.
~ Jean Ghantous
About the author: Jean Ghantous is a wife and mother of three with a background in science, who formerly held a position with a pharmaceutical company as a research specialist. She has been a Momcologist for the past 10 years, since her daughter was diagnosed with high-risk pre-B cell acute lymphocytic leukemia as a toddler. After three years of treatment, the family enjoyed years of remission until her daughter was again diagnosed with a very late relapse at nine years old. She is currently in remission and doing well.
Jean’s penchant for research led to the important discovery that transfusional iron overload had been a long-overlooked high-risk factor for adverse late effects in cancer children. “Oncologists are so focused on treatment protocols that preventative care has been neglected, universally,” said Jean. “I realized within the first 10 minutes of researching iron overload that not only did my daughter have a very grave problem, but many kids, over many years, were at risk as well. I was horrified to read the list of side effects of iron toxicity; it was eerily similar to the late effects one is told to expect from chemotherapy.” Jean pushed for treatment and preventative care. She said “No one addressed iron overload because, well, no one had NOTICED it. For decades of cancer treatment.” This led to her hospital implementing a computerized tracking program for transfusional iron deposition and its involvement in a nationwide strategy for reducing risk from iron toxicity in children with cancer.
While Jean had always been suspicious that vaccines could play a role in the development of leukemia, she was told her daughter’s diagnosis after aggressive vaccination was “coincidence.” After her third child also sustained a vaccine injury, Jean took on the additional descriptor of Thinking Mom and became more actively involved in advocating for vaccine safety. “It is abundantly clear to any parent who takes the time to do the research that there is a very real causative connection between immune system disorders, chronic disease and vaccines,” warns Jean. “American kids are sick, really sick. EpiPens, inhalers, glucometers, special diets and special-needs teachers have become normalized in our schools. Four children in my neighborhood have been granted Make-A-Wish trips for life-threatening illness. One-third of my son’s class is in need of special-needs educational support. This is NOT normal. We MUST stop this insane, profit-driven push for federal vaccine mandates. Clearly, our families’ futures depend on it.”
References
1) “Detection of Measles Virus RNA in Urine Specimens from Vaccine Recipients,” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC228449/
2) “ Vaccine Oka Varicella-Zoster Virus Genotypes Are Monomorphic in Single Vesicles and Polymorphic in Respiratory Tract Secretions,” http://jid.oxfordjournals.org/content/193/7/927.full
3) MMR II vaccine insert: “Excretion of small amounts of the live attenuated rubella virus from the nose or throat has occurred in the majority of susceptible individuals 7 to 28 days after vaccination.” http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf
4) “Chickenpox Attributable to a Vaccine Virus Contracted From a Vaccine With Zoster,” http://pediatrics.aappublications.org/content/106/2/e28.full
5) FluMist vaccine insert: “FluMist contains live attenuated influenza viruses that must infect and replicate in cells lining the nasopharynx of the recipient to induce immunity. Vaccine viruses capable of infection and replication can be cultured from nasal secretions obtained from vaccine recipients (shedding).” Study showed shedding up to 28 days post vaccination: http://www.medimmune.com/docs/default-source/pdfs/flumist_pi.pdf
6) “Influenza Outbreak in a Vaccinated Population — USS Ardent, February 2014,” http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6342a3.htm?mobile=nocontent
7) “Infections in the Neutropenic Patient— New Views of an Old Problem:,” http://asheducationbook.hematologylibrary.org/content/2001/1/113.full
8) MMR II vaccine insert: “Measles inclusion body encephalitis{44} (MIBE), pneumonitis{45} and death as a direct consequence of disseminated measles vaccine virus infection have been reported in immunocompromised individuals inadvertently vaccinated with measles-containing vaccine.” http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf
9) “There has been no measles deaths reported in the U.S. since 2003,” Dr. Anne Schuchat, the director of CDC’s National Center for Immunization and Respiratory Diseases. (Apparently, the veracity of this statement is in question, as CDC data for 2009 and 2010 both list two measles deaths, leading one to wonder why does the director of CDC’s National Center for Immunization and Respiratory Diseases not seem to know about them? Don’t you think given the current hoopla about an outbreak with no associated deaths that they would be screaming about them? Could it be that they were in immunocompromised people who got the disease either from the vaccine or from recently vaccinated people?) http://vaccineimpact.com/2015/zero-u-s-measles-deaths-in-10-years-but-over-100-measles-vaccine-deaths-reported/
10) Bluming A, Ziegler J. “Regression of Burkitt’s lymphoma in association with measles infection.” The Lancet. 1971 Jul 10;:105–106.
11) “Remission of Disseminated Cancer after Systemic Oncolytic Virotherapy,” http://www.mayoclinicproceedings.org/article/S0025-6196(14)00332-2/fulltext
12) “Measles Virus for Cancer Therapy,” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926122/
13) Liu TC, Galanis E, Kirn D. “Clinical Trial Results with Oncolytic Virotherapy: A Century of Promise, a Decade of Progress.” Nat Clin Pract Oncol. 2007;4(2):101–117. http://www.ncbi.nlm.nih.gov/pubmed/17259931
14) Hygiene hypothesis: “In countries where good health standards do not exist, people are chronically infected by those various pathogens. In those countries, the prevalence of allergic diseases remains low. Interestingly, several countries that have eradicated those common infections see the emergence of allergic and autoimmune diseases.”
“The ‘Hygiene Hypothesis’ for Autoimmune and Allergic Diseases: An Update,” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841828/
15) “Childhood Leukemia Incidence in Britain, 1974–2000: Time Trends and Possible Relation to Influenza Epidemics,” http://jnci.oxfordjournals.org/content/98/6/417.full.pdf+html?sid=b366f430-37bb-49a4-b9b0-794149a1d2da
16) “Allergic Conditions and Risk of Hematological Malignancies in Adults: A Cohort Study,” http://www.biomedcentral.com/1471-2458/4/51
17) “Timing is critical, as early infections are likely to positively modulate the immune system thereby reducing risk of leukemia, whereas later infections in children whose immune system was less well modulated may increase such risk.”
“Infection and Pediatric Acute Lymphoblastic Leukemia,” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834409/
18) U.S. highest first-day infant mortality of industrialized nations: “6 Articles You Should Read about Infant Mortality in the U.S” http://america.aljazeera.com/watch/shows/fault-lines/FaultLinesBlog/2013/9/19/america-s-infantmortalitycrisisbackgroundreading.html
19) “Potency Tests of Combination Vaccines,” http://cid.oxfordjournals.org/content/33/Supplement_4/S362.full
20) “The ‘Hygiene Hypothesis’ for Autoimmune and Allergic Diseases: An Update,” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841828/
21) “An Infectious Aetiology for Childhood Acute Leukaemia: A Review of the Evidence.” http://www.ncbi.nlm.nih.gov/pubmed/15491284. Sharp peak in ALL diagnoses in developed countries between 2 and 6 years; early infection could be protective.
22) German study on the health of vaccinated versus unvaccinated children: http://healthimpactnews.com/2011/new-study-vaccinated-children-have-2-to-5-times-more-diseases-and-disorders-than-unvaccinated-children/
23) Vaccine Liability removed: http://www.nvic.org/NVIC-Vaccine-News/March-2011/No-Pharma-Liability–No-Vaccine-Mandates-.aspx#a1
24) Julie Gerberding: “Merck Announces Appointment of Dr. Julie Gerberding as Executive Vice President for Strategic Communications, Global Public Policy and Population Health,” http://www.mercknewsroom.com/news-release/corporatenews/merck-announces-appointment-dr-julie-gerberding-executive-vice-president
25) Pharmaceutical campaign contributions 2014: “Pharmaceuticals/Health Products: Long-Term Contribution Trends,” http://www.opensecrets.org/industries/totals.php?cycle=2014&ind=H04
26) “Little Patients, Losing Patience: Pediatric Cancer Drug Development,” http://mct.aacrjournals.org/content/5/8/1905.full
27) Childhood and Adolescent Cancer Statistics, 2014: http://acco.org/LinkClick.aspx?fileticket=gAi0ji8IFPU%3d&tabid=670
28) National Cancer Institute gives 4% to pediatric cancer research: http://acco.org/Information/AboutChildhoodCancer/ChildhoodCancerStatistics.aspx
29) “Because Statistics Don’t Tell the Whole Story: A Call for Comprehensive Care for Children With Cancer,” http://acco.org/LinClick.aspx?fileticket=9egsDtJw3fw%3d&tabid=670
30) SEER database: http://seer.cancer.gov/csr/1975_2011/results_merged/sect_29_childhood_cancer_iccc.pdf
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