- Si continua a discutere sull’incremento dei casi di autismo e sulla sua correlazione con frammenti di DNA umano.
- Gli scienziati del Sound Choice Pharmaceutical Institute (SCPI) hanno trovato che l’aumento nella diffusione dell’autismo corrisponde all’introduzione di vaccini che utilizzano cellule umane fetali abortive e contaminanti retrovirali.
- la Dr Theresa Deisher; il suo studio succede a quello pubblicato dal Dr. Brian Hooker, il quale ha trovato un 340 per cento di aumento del rischio di autismo nei bambini afro-americani che ricevono il vaccino MMR (morbillo-parotite-rosolia).
Dr. Theresa Deisher
La Dr. Theresa Deisher, un dottorato di ricerca in Fisiologia Cellulare e Molecolare presso la Stanford University.
- “E ‘possibile che questi frammenti contaminanti potrebbero essere incorporati nel genoma di un bambino e perturbare la funzione del gene normale, portando a fenotipi autistici.”
Si può leggere lo studio completo QUI .
La Dr. Theresa Deisher ha trascorso oltre 19 anni nel settore della biotecnologia con varie aziende come la Genentech, Repligen, Amgen e le sue scoperte hanno portato a sperimentazioni cliniche per patologie multiple.
L’importanza di una ricerca indipendente
Quando si parla di studi scientifici in materia di vaccini, siamo bombardati da studi sponsorizzati dalle case farmaceutiche, studi che sono sponsorizzati dai produttori di vaccini stessi.Questi sono gli studi utilizzati per giustificare la sicurezza dei vari vaccini ricevuti dai bambini poco dopo la loro nascita e nella loro infanzia.
E’ aberrante come le molte pubblicazioni scientifiche peer-reviewed, antiche e recenti, indichino chiaramente i molteplici pericoli associati ai vaccini ma nonostante ciò,il pubblico è bombardato pesantemente dalla mala informazione. Sappiamo che grande giro d’interesse ci sia.
La verità è, una gran parte della folla “anti vaccinazione” comprende scienziati, PhD, e professori. Movimenti “anti-vaccinazione” sono supportati da una enorme quantità di scienza.
Questo è esattamente il motivo per cui la ricerca indipendente è così importante. I documenti ottenuti da Lucija Tomljenovic, (un altro scienziato e indipendente ricercatore che ha fatto luce su fatti importanti circa le vaccinazioni) PhD, del Gruppo di Ricerca Neurali Dynamics presso il Dipartimento di Oftalmologia e Scienze Visive presso l’Università della British Columbia rivelano che i produttori di vaccini, farmaceutica le imprese e le autorità sanitarie hanno saputo di più pericoli associati con i vaccini, ma ha scelto di trattenere loro dal pubblico. Questa è la frode scientifica, e suggerisce che questa pratica continua fino a oggi. ( fonte ) Un recente informatore del CDC ha recentemente ammesso che il CDC ha omesso dati che collega i vaccini per l’autismo, si può leggere di più su questo qui .
ASTRATTO E FONTE
The vaccination policy and the Code of Practice of the Joint Committee on Vaccination and Immunisation (JCVI): are they at odds?
Lucija Tomljenovic, PhD Neural Dynamics Research Group, Dept. of Ophthalmology and Visual Sciences, University of British Columbia, 828 W. 10th Ave, Vancouver, BC, V5Z 1L8, lucijat77@gmail.com
Introduction
No pharmaceutical drug is devoid of risks from adverse reactions and vaccines are no exception. According to the world’s leading drug regulatory authority, the US Food and Drug Administration (FDA), vaccines represent a special category of drugs in that they are generally given to healthy individuals and often to prevent a disease to which an individual may never be exposed [1]. This, according to the FDA, places extra emphasis on vaccine safety. Universally, regulatory authorities are responsible for ensuring that new vaccines go through proper scientific evaluation before they are approved. An equal responsibility rests on the medical profession to promote vaccinations but only with those vaccines whose safety and efficacy has been demonstrated to be statistically significant. Furthermore, vaccination is a medical intervention and as such, it should be carried out with the full consent of those who are being subjected to it. This necessitates an objective disclosure of the known or foreseeable risks and benefits and, where applicable, a description of alternative courses of treatment. In cases where children and infants are involved, full consent with regards to vaccination should be given by the parents…
ALLEGATI
“E ‘possibile che questi frammenti contaminanti vengano incorporati nel genoma di un bambino e vadano a perturbare la funzione del gene normale, portando a fenotipi autistici.”
Si può leggere lo studio completo QUI .
FONTE
http://edgytruth.com/2015/04/01/stanford-scientist-proving-dna-fragments-in-vaccines-cause-autism-great-read/#
ALTRA NOTIZIA CORRELATA
B-lymphocytes from a population of children with autism spectrum disorder and their unaffected siblings exhibit hypersensitivity to thimerosal.
Abstract
The role of thimerosal containing vaccines in the development of autism spectrum disorder (ASD) has been an area of intense debate, as has the presence of mercury dental amalgams and fish ingestion by pregnant mothers. We studied the effects of thimerosal on cell proliferation and mitochondrial function from B-lymphocytes taken from individuals with autism, their nonautistic twins, and their nontwin siblings. Eleven families were examined and compared to matched controls. B-cells were grown with increasing levels of thimerosal, and various assays (LDH, XTT, DCFH, etc.) were performed to examine the effects on cellular proliferation and mitochondrial function. A subpopulation of eight individuals (4 ASD, 2 twins, and 2 siblings) from four of the families showed thimerosal hypersensitivity, whereas none of the control individuals displayed this response. The thimerosal concentration required to inhibit cell proliferation in these individuals was only 40% of controls. Cells hypersensitive to thimerosal also had higher levels of oxidative stress markers, protein carbonyls, and oxidant generation. This suggests certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like the vaccine preservative thimerosal…
La presenza di elementi come il thimerosal nei vaccini,responsabile (per diversi nella comunità scientifica)dello sviluppo di disturbi dello spettro autistico (ASD) è di intenso dibattito, così come la presenza di mercurio (amalgame dentali e l’ingestione di alimenti che lo contengono da parte delle madri in gravidanza). Abbiamo studiato gli effetti del thimerosal sulla proliferazione cellulare e la funzione mitocondriale da linfociti B studiati e prelevati da persone con autismo, e dai loro fratelli non autistici. Undici famiglie sono stati esaminate e confrontate con controlli .
Le cellule “B” sono state coltivate con livelli crescenti di thimerosal, e vari esami (LDH, XTT, DCFH, etc.) sono stati effettuati per valutare gli effetti sulla proliferazione cellulare e la funzione mitocondriale. Una sottopopolazione di otto persone (4 ASD, 2 gemelli, e 2 fratelli) da quattro delle famiglie ha mostrato ipersensibilità verso il thimerosal, mentre nessuno dei soggetti di controllo ha confermato la medesima risposta…
FONTE
This figure shows the typical responses of a family of cells to thimerosal, measured on day 5 postinoculation. ASD = black, Twin = red, Sibling = blue, Control = green. (a) The percent control LDH values are plotted against increasing thimerosal concentrations for the 4 cell types. Arrows indicate LDH-G50 values with ASD = 314 nM, Twin = 648 nM, Sib = 373 nM, and Cont = 1000 nM. (b) The percent control XTT values are plotted against increasing thimerosal concentrations. XTT-G50 values are obtained using the mitochondrial XTT assay. (c) The percentage of cellular LDH that is accessible to lactate (i.e., percentage of dead and dying cells) is plotted against thimerosal. (d) Cell number and XTT reduction rates as a function of increasing thimerosal concentrations are shown. The plots obtained are “hockey stick” in shape.
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders.
Abstract
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed countries, including Denmark and Israel where the vaccine was added to their national vaccine programs in 1993 and 1994, respectively. There have been marked increases in the reported prevalence of autism spectrum disorders (ASDs) among children in the US beginning with birth cohorts in the late 1980s and in Denmark and Israel starting approximately 4-5 years later. Although these increases may partly reflect ascertainment biases, an exogenous trigger could explain a significant portion of the reported increases in ASDs. It is hypothesized here that the introduction of the Hib conjugate vaccine in the US in 1988 and its subsequent introduction in Denmark and Israel could explain a substantial portion of the initial increases in ASDs in those countries. The continuation of the trend toward increased rates of ASDs could be further explained by increased usage of the vaccine, a change in 1990 in the recommended age of vaccination in the US from 15 to 2 months, increased immunogenicity of the vaccine through changes in its carrier protein, and the subsequent introduction of the conjugate vaccine for Streptococcus pneumoniae. Although conjugate vaccines have been highly effective in protecting infants and young children from the significant morbidity and mortality caused by Hib and S. pneumoniae, the potential effects of conjugate vaccines on neural development merit close examination. Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response. This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.
