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Here’s Why Radiation and Chemotherapy Should Not Be The Only Two Approved Treatments For Cancer

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In the United States there are only two approved treatments for cancer – radiation and chemotherapy. Despite the fact that chemotherapy fuels cancer growth and kills the patient more quickly, nothing has changed. Despite numerous alternative treatments that are now coming to the forefront, the medical industry continues to promote and push radiation, chemotherapy and surgery as the only viable options for cancer treatment, this is simply not true.

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Major studies within cancer research have been proven as false which also suggests that the mainstream treatments we use are based on fraudulent findings and false science. It’s usually the treatments not heavily publicized and promoted that we should keep our eye on.  More researchers are catching on, not to long ago University of Michigan researchers suggested increasing public funding of research to decrease potential bias from industry ties. You can read more about that here.

Many people believe that mainstream cancer treatment is rarely effective and exists primarily for the benefit of the cancer industry itself. A study published in the journal Cancer by researchers from the department of Radiation Oncology at the UCLA Johnsson Comprehensive Cancer Center reports that radiation drives breast cancer cells into greater malignancy. (1)(2)  Malignancy is a term used to describe the tendency of tumors and their potential to become progressively worse, ultimately resulting in death.

In many cases, cancer stem cells are generated by the therapy itself, and they are resistant to conventional treatment, this may play a critical role in the development of tumors. Cancer stem sells are tumorigenic (tumor-forming) and are capable of both initiation and sustaining cancer. They are also increasingly recognized to be the cause of relapse and metastasis following conventional treatment.

Cannabis

One of the biggest alternative treatments that’s used today to treat cancer is cannabis. Why cannabis is still not an approved and recognized form of cancer treatment remains a mystery to many, especially since the anti-tumor effects of cannabinoids and THC have been demonstrated time and time again since the 1980’s.

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When scientists discovered cannabinoid receptors in the human brain, it became obvious that our body has to synthesize something that binds to these receptors. Our bodies produce these compounds in our own endocannabinoid system, which is now known to be responsible for a number of biological functions. This is why the plant has such a wide therapeutic potential for multiple diseases, including cancer.

There is study after study proving the fact that cannabis can cure cancer.*(3)*  Despite the fact that human trials have not been conducted (ask yourself, why?), there are numerous examples of patients healing themselves with cannabis. One great example is Mykayla Comstock, a young lady who has been treating her leukaemia with cannabis. She is Oregon’s youngest medical cannabis patient, and she is curing her cancer.  You can read more about her story and the details of it here.

In Oregon, when you are an adult with cancer, you have the choice to use the two recommended options or refuse them and select other methods. When you are a child, your parents do not have the option to refuse the approved way without facing legal repercussions, this is what happened to Mykayla’s parents.

Collective Evolution has also been it touch with doctors in Toronto who recently published a case study where they used cannabis to treat leukemia in a Teenage girl. (4) This patient underwent standard treatments of acute and aggressive chemotherapy as well as bone marrow transplants. It was found that none of these treatments were not effective which led the family to explore alternatives. The alternative they chose was to treat her with cannabinoids administered orally in the form of hemp oil.  You can read more about this story here

The list of examples goes on and on, below is a video of Molecular Biologist Dr. Christina Sanchez explaining how THC (one ingredient within cannabis out of multiple ingredients that kill cancer) completely kill cancer cells.

*Don’t forget to review the studies in source # 3 to help you further your research.

Royal Rife

It was in 1920 that Royal Rife first identified the human cancer virus using the world’s most powerful microscope. After identifying and isolating the virus, he decided to culture it on salted pork. At the time this was a very good method for culturing a virus. He then took the culture and injected it into 400 rats which as you might expect, created cancer in all 400 rats very quickly. The next step for Rife is where things took an interesting turn. He later found a frequency of electromagnetic energy that would cause the cancer virus to diminish completely when entered into the energy field. The great discovery led Rife to create a device that could be tuned to output the frequency that would destruct the cancer. He was then able to treat the cancer within both rats and patients who were within close proximity of the device.

To read more about this device, click here

Dichloroacetate

Dichloroacetate (DCA) is a small molecule drug that has long been used to treat congenital mitochondrial abnormalities. The mitochondria (cell power source), is vital for several reasons. One of them is acting as oxygen sensors and control, as well as controlling programmed cell death. This process is known as apoptosis. The significance here is that this process is suppressed in cancer, a disease that’s characterized by uncontrolled cell growth. Dr. Evengelos Michelakis, associate chair and medical researcher at the University of Alberta’s faculty of medicine and his team of researchers discovered DCA as a possible cure for cancer more than 10 years ago. Since then, it’s received very little attention from the medical industry,

To view these studies and read more about DCA, click here. Clinical trials (finally) are under way, and the estimated date for completion is March 2015. You can read more about the clinical trial details here.

Diet

Rarely do we consider the importance of natural, non-GMO organic fruits and vegetables. A number of them have been proven to limit cancer growth. For example, broccoli fights cancer by clearning bad tumor suppressors. (5)

Studies have shown that raw garlic cuts lung cancer risk in half. (6) Celery and artichokes contain flavonoids that kill human pancreatic cancer cells.(7)  The list literally goes on and on.

I am a big believer that diet alone can heal us from any type of cancer. So many different fruits and vegetables have a wide range of anti-tumoral effects. Taking notice of what you put into your body can play a large role in cancer treatment/prevention. We are so quick to jump to the approved treatments that we fail to realize many other factors that play very significant roles, specifically, what exactly are we putting into our bodies.

Many people have had success with cancer prevention and treatment by switching to a completely raw, vegan diet full of anti-cancer fruits and vegetables. It’s definitely something worth researching.

I could go on and on with this article, but the main point I wanted to illustrate was the fact that chemotherapy and radiation should not be the only two approved treatments for cancer.

Here’s a great video that gives us all something to think about, and some possible insight as to why multiple alternative cures have been proven effective, but don’t really see the light of day. The fact remains, there are a number of proven options out there to treat cancer, not just radiation, chemotherapy and surgery.

Cancer is a great example of how we don’t need to wait for our governing medical authorities to tell us what’s true and what isn’t. We need to turn our heads to those who have our best health interests in hand, and we need to do the research for ourselves. You always have a choice.

For more articles on cancer by CE, click here.

 

 Sources:

(1) http://www.cancer.ucla.edu/Index.aspx?page=644&recordid=560

(2) http://onlinelibrary.wiley.com/doi/10.1002/cncr.27701/full

(3) Current Research Concerning Cannabis and LeukemiaEffects of cannabinoids on L1210 murine leukemia. 1. Inhibition of DNA synthesis. (abst – 1977)

http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=Retrieve&list_uids=897352&dopt=abstractplus

Cannabinoids induce incomplete maturation of cultured human leukemia cells (full – 1987) 
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC298868/?tool=pmcentrez&page=1

Fatal aspergillosis associated with smoking contaminated marijuana, in a marrow transplant recipient. (full – 1988) 

http://chestjournal.chestpubs.org/content/94/2/432.long

Anandamide Induces Apoptosis in Human Cells via Vanilloid Receptors (full – 2000) 

http://www.jbc.org/content/275/41/31938.full

Targeting CB2 cannabinoid receptors as a novel therapy to treat malignant lymphoblastic disease (full – 2002) 

http://bloodjournal.hematologylibrary.org/cgi/reprint/100/2/627.pdf

Gamma-irradiation enhances apoptosis induced by cannabidiol, a non-psychotropic cannabinoid, in cultured HL-60 myeloblastic leukemia cells. (abst – 2003)
http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=Retrieve&list_uids=14692532&dopt=abstractplus

Cannabis-induced cytotoxicity in leukemic cell lines: the role of the cannabinoid receptors and the MAPK pathway (full – 2005)http://bloodjournal.hematologylibrary.org/cgi/content/full/105/3/1214

Cannabidiol-Induced Apoptosis in Human Leukemia Cells : A Novel Role of Cannabidiol in the Regulation of p22phox and Nox4 Expression (full – 2006) 
http://molpharm.aspetjournals.org/cgi/content/full/70/3/897

{Delta}9-Tetrahydrocannabinol-Induced Apoptosis in Jurkat Leukemia T Cells Is Regulated by Translocation of Bad to Mitochondria (full – 2006)
http://mcr.aacrjournals.org/content/4/8/549.full

Is there a temperature-dependent uptake of anandamide into cells? (full – 2006)

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1629410/

Parental marijuana use and risk of childhood acute myeloid leukaemia: a report from the Children’s Cancer Group (United States and Canada). (abst – 2006)

http://www.ncbi.nlm.nih.gov/pubmed/16466429

The effects of cannabinoids on P-glycoprotein transport and expression in multidrug resistant cells. (abst – 2006)
 http://www.ncbi.nlm.nih.gov/pubmed/16458258

Cannabis destroys cancer cells (news – 2006)
http://www.news-medical.net/news/2006/03/01/16340.aspx220

Cannabidiol inhibits tumour growth in leukaemia and breast cancer in animal studies (news – 2006)

http://www.cannabis-med.org/english/bulletin/ww_en_db_cannabis_artikel.php?id=220#2

HU-331, a novel cannabinoid-based anticancer topoisomerase II inhibitor (full – 2007)

http://mct.aacrjournals.org/content/6/1/173.long

Medical Marijuana Use and Research Leukemia & Lymphoma Society Statement (full – 2008)
http://www.maps.org/mmj/lnls-res.pdf

Enhancing the in vitro cytotoxic activity of Δ9-tetrahydrocannabinol in leukemic cells through a combinatorial approach (abst – 2008)
http://www.ncbi.nlm.nih.gov/pubmed/18608861

Marijuana’s Active Ingredient Kills Leukemia Cells (news – 2009)

http://medicalmarijuanadoctors.org/marijuana-active-ingredient-kills-leukemia-cells

Substance use and survival after treatment for chronic myelogenous leukemia (CML) or myelodysplastic syndrome (MDS). (full – 2010)http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847847/?tool=pubmed

Cannabidiol induced a contrasting pro-apoptotic effect between freshly isolated and precultured human monocytes. (abst – 2011)
http://www.unboundmedicine.com/medline/ebm/record/20471992/abstract

Tumor necrosis factor activation of vagal afferent terminal calcium is blocked by cannabinoids. (abst – 2012)
http://www.ncbi.nlm.nih.gov/pubmed/22496569

Marijuana compound could stop aggressive cancer metastasis (news – 2012)
http://in.news.yahoo.com/marijuana-compound-could-stop-aggressive-cancer-metastasis-064950912.html

Can marijuana stop cancer? (news – 2012)

http://www.examiner.com/article/can-marijuana-stop-cancer

Brain Cancer

1.  A study published in the British Journal of Cancerconducted by the Department of Biochemistry and Molecular Biology at Complutense University in Madrid, this study determined that Tetrahydrocannabinol (THC) and other cannabinoids inhibit tumour growth. They were responsible for the first clinical study aimed at assessing cannabinoid antitumoral action. Cannabinoid delivery was safe and was achieved with zero psychoactive effects. THC was found to decrease tumour cells in two out of the nine patients.

2. A study published in The Journal of Neuroscience examined the biochemical events in both acute neuronal damage and in slowly progressive, neurodegenerative diseases. They conducted a magnetic resonance imaging study that looked at THC (the main active compound in marijuana) and found that it reduced neuronal injury in rats. The results of this study provide evidence that the cannabinoid system can serve to protect the brain against neurodegeneration.

3. A study published in The Journal of Pharmacology And Experimental Therapeutics already acknowledged the fact that cannabinoids have been shown to possess antitumor properties. This study examined the effect of cannabidiol (CBD, non psychoactive cannabinoid compound) on human glioma cell lines. The addition of cannabidiol led to a dramatic drop in the viability of glioma cells. Glioma is the word used to describe brain tumour. The study concluded that cannabidiol was able to produce a significant antitumor activity.

4. A study published in the journal Molecular Cancer Therapeutics outlines how brain tumours are highly resistant to current anticancer treatments, which makes it crucial to find new therapeutic strategies aimed at improving the poor prognosis of patients suffering from this disease. This study also demonstrated the reversal of tumour activity in Glioblastoma multiforme.

Breast Cancer

5. A study published in the US National Library of Medicine, conducted by the California Pacific Medical Centre determined that cannabidiol (CBD) inhibits human breast cancer cell proliferation and invasion. They also demonstrated that CBD significantly reduces tumour mass.

6. A study published in The Journal of Pharmacology and Experimental Therapeutics determined that THC as well as cannabidiol dramatically reduced breast cancer cell growth. They confirmed the potency and effectiveness of these compounds.

7. A study published in the Journal Molecular Cancer showed that THC reduced tumour growth and tumour numbers. They determined that cannabinoids inhibit cancer cell proliferation, induce cancer cell apoptosis and impair tumour angiogenesis (all good things). This study provides strong evidence for the use of cannabinoid based therapies for the management of breast cancer.

8. A study published in the Proceedings of the National Academy of Sciences of the United States of America (PNAS) determined that cannabinoids inhibit human breast cancer cell proliferation.

Lung Cancer

9. A study published in the journal Oncogeneby Harvard Medical Schools Experimental Medicine Department determined that THC inhibits epithelial growth factor induced lung cancer cell migration and more. They go on to state that THC should be explored as novel therapeutic molecules in controlling the growth and metastasis of certain lung cancers.

10. A study published by the US National Library of Medicine by the Institute of Toxicology and Pharmacology, from the Department of General Surgery in Germany determined that cannabinoids inhibit cancer cell invasion. Effects were confirmed in primary tumour cells from a lung cancer patient.  Overall, data indicated that cannabinoids decrease cancer cell invasiveness.

11. A study published by the US National Library of Medicine, conducted by Harvard Medical School investigated the role of cannabinoid receptors in lung cancer cells. They determined its effectiveness and suggested that it should be used for treatment against lung cancer cells.

Prostate Cancer

12. A study published in the US National Library of Medicine illustrates a decrease in prostatic cancer cells by acting through cannabinoid receptors.

13. A study published in the US National Library of Medicine outlined multiple studies proving the effectiveness of cannabis on prostate cancer.

14. Another study published by the US National Library of Medicine determined that clinical testing of CBD against prostate carcinoma is a must. That cannabinoid receptor activation induces prostate carcinoma cell apoptosis. They determined that cannabidiol significantly inhibited cell viability. 

Blood Cancer

15. A study published in the journal Molecular Pharmacology recently showed that cannabinoids induce growth inhibition and apoptosis in matle cell lymphoma. The study was supported by grants from the Swedish Cancer Society, The Swedish Research Council and the Cancer Society in Stockholm.

16. A study published in the International Journal of Cancer also determined and illustrated that cannabinoids exert antiproliferative and proapoptotic effects in various types of cancer and in mantle cell lymphoma.

17. A study published in the US National Library of Medicine conducted by the Department of Pharmacology and Toxicology by Virginia Commonwealth University determined that cannabinoids induce apoptosis in leukemia cells.

Oral Cancer

18. A study published by the US National Library of Medicine results show cannabinoids are potent inhibitors of cellular respiration and are toxic to highly malignant oral Tumours.

Liver Cancer

19. A study published by the US National Library of Medicine determined that THC reduces the viability of human HCC cell lines (Human hepatocellular liver carcinoma cell line) and reduced the growth.

Pancreatic Cancer

20. A study published in The American Journal of Cancer determined that cannabinoid receptors are expressed in human pancreatic tumor cell lines and tumour biopsies at much higher levels than in normal pancreatic tissue. Results showed that cannabinoid administration induced apoptosis. They also reduced the growth of tumour cells, and inhibited the spreading of pancreatic tumour cells.

 (4) http://karger.com/Article/FullText/356446#AC

(5) http://www.scientificamerican.com/podcast/episode/broccoli-fights-cancer-by-clearing-11-01-27/

(6) http://cancerpreventionresearch.aacrjournals.org/content/6/7/711.abstract

(7) http://news.aces.illinois.edu/news/celery-artichokes-contain-flavonoids-kill-human-pancreatic-cancer-cells

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The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

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Awareness

10 Vegan Body Builders That Are Changing The Way People View Protein

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In Brief

  • The Facts:

    Many body builders and athletes have a vegan diet. Several studies are pointing towards the possibility that plant based protein might actually be a better option than protein from meat.

  • Reflect On:

    Next time somebody asks you where you get your protein from, if you're vegetarian or vegan, now you can tell them. Why are we so conditioned to believe that meat is required for building muscle?

I’m not vegan. I used to identify with this label, but now I just do my absolute best to focus on a primarily plant-based diet. I really don’t like the labels for myself, but have no problem with people who choose to use them. Despite of this, it still drives me absolutely bonkers to hear this phrase, directed at me, or any person who chooses to follow a vegan or plant-based diet, “Where do you get your protein?” It literally makes me cringe, and I will not rest until every person on this planet knows that almost all foods contain protein… and how come no one ever asks the gorilla or the ox where they get their protein?!

Anyways… people often shy away from the idea of limiting their meat consumption or giving it up entirely because they believe that in order to be strong and lean they absolutely need protein from animal sources. Fortunately, for the sake of the animals and our health, this actually couldn’t be farther from the truth. There are plenty of vegan bodybuilders and athletes, many of which have claimed that their performance actually enhanced after cutting out animals and animal products from their diets. Here are the top 10 vegan bodybuilders.

Related CE Article:  Plant Based Protein Vs. Protein From Meat: Which One Is Better For Your Body

9 Things That Happen When You Stop Eating Meat

1. Jon Venus

Jon is a popular vegan bodybuilder who shares his mission and message through his large online community via YouTube and Instagram. He has a ton of videos, workout plans, recipes and online guidance. One look at him will get you inspired to try out this lifestyle, and he proves that going vegan doesn’t mean sacrificing strength or muscles.  You can follow Jon on his journey, here.

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2. Brian Turner

Brian has a large following on YouTube, and he’s here to “relate, teach a bit and have fun with you guys” through his videos. He’s been bodybuilding for over 9 years, and has figured out a way to stay in shape while following a strict vegan diet. On his YouTube channel you can find anything from workout videos, recipe videos to acne videos!

3. Derek Simnett

Derek Simnett is a personal friend of us here at CE.  We have watched his journey unfold over the years and it has been incredible to see. TRULY authentic in his message and lifestyle, Derek is living proof that you can not only achieve big results on a plant-based diet, but you can do A LOT without lifting much weight. His primary mode of training is calisthenics. Check out his stuff here. He is also on YouTube.

4. Nimai Delgado

Once again, we have a very fit and healthy YouTube vegan bodybuilder, Nimai Delgado, an International Federation of BodyBuilding and Fitness (IFBB) Pro. He documents his journey with the IFBB on his YouTube channel and shares tips and tricks with his followers, including his workout routine. He beliefs in maintaining strength and flexibility, and not necessarily just gaining more muscle mass for aesthetic purposes. Definitely check out his YouTube channel to learn more about how this lifestyle could work for you as well!

5. Torre Washington

Torre has been Vegan since 1998! He is a bodybuilder that gets 100% of his vitamins, nutrients and PROTEIN from his diet, he doesn’t believe in supplements. Aside from his hugely successful YouTube channel, Torre also has an extremely resourceful website that can offer you much support on your path towards a fit, vegan lifestyle! Check it out here.

6. Arvid Beck

Arvid is a Vegan bodybuilder from Germany. His decision to become vegan was based largely around his moral and ethical decisions. Nevertheless he is a bodybuilding champion, redefining what it means to be a gladiator! You can check out more of Arvid’s journey here.

7. Samantha Shorkey

Samantha has a popular health and fitness blog called Jacked on the Beanstalk where she shares her secrets to success, including fitness, meal plans coaching and why she decided to adopt a vegan lifestyle and how it has helped her become so successful. Samantha was awarded her pro card in July 2014 after winning first place in the overall bikini title at the 2014 INBF South Western Natural Championships in Austin Texas. This put her on the map as the first-ever VEGAN WNBF bikini pro.

8.  Crissi Carvahlo

Crissi is a vegan fitness model, online trainer and coach, director of the Vegan Fitness International group, designer at Vegan Fitness body, Chef at Vegan Fitness body, author of Vegan Fitness Food For A lean Healthy Body ebook, and so much more! Crissi became vegan at age 38 and now makes it a huge part of her message intertwining it with the knowledge she has gained about health and fitness throughout the years. Check out her website here.

9. Ryan Nelson

Ryan is an athlete, animal lover and vegan food fanatic! Ryan is also a sponsored Posha Green super-heavyweight bodybuilder. Ryan aims to inspire others to set and achieve their goals in the weight room the classroom, sports and in real life. Ryan stands as a testament to the health benefits of a healthy vegan diet! On his website he offers online coaching and nutrition programs. Check it out!

10. Patrik Baboumian

Patrick smashes all types of stereo-types as an Iranian born, German and vegan strongman competitor. Patrick is known as a gentle giant as his concern for the well-being of animals has inspired him to become a vegan and promote this diet through his success.

Conclusion

Now, I don’t want to hear it. I believe I’ve provided you with enough information that you will no longer be asking,“Where do you get your protein?”

Much Love

We Need Your Support...

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

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Alternative News

Roll Up Your Sleeves Folks: 271 New Vaccines in Big Pharma’s Pipeline

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“No vaccine manufacturer shall be liable…for damages arising from a vaccine-related injury or death.” – President Ronald Wilson Reagan, as he signed The National Childhood Vaccine Injury Act (NCVIA) of 1986, absolving drug companies from all medico-legal liability when children die, become chronically ill with vaccine-induced autoimmune disorders or are otherwise disabled from vaccine injuries. (That law has led directly to an expected reckless, liability-free development of scores of new, over-priced, potential block-buster vaccines, now numbering over 250. The question that must be asked of Big Medicine’s practitioners: How will the CDC, the AMA, the AAFP and the American Academy of Pediatrics fit any more potentially neurotoxic vaccines into the current well-baby over-vaccination schedule?)

PhRMA (the Pharmaceutical Research and Manufacturers of America),  the pharmaceutical industry’s trade association and powerful lobbying group, says that 

“today, more than 7,000 medicines are in development globally, all of which have the potential to help patients in the United States and around the world.  According to another data source, there are 3,400 medicines in development today just in the United States, an increase of 40 percent since 2005.” (http://phrma.org/pipeline#sthash.TnxVihsT.dpuf)

PhRMA also says that today 

“the 271 vaccines in development span a wide array of diseases, and employ exciting new scientific strategies and technologies. These potential vaccines – all in human clinical trials or under review by the Food and Drug Administration (FDA) – include 137 for infectious diseases, 99 for cancer, 15 for allergies and 10 for neurological disorders.” (http://phrma.org/press-release-medicines-in-development-vaccines#sthash.rI4cQ6Tg.dpuf)

Whenever the FDA signals that it is ready to grant marketing approval for a new vaccine or drug, the first step for the pharmaceutical company’s marketing department is to promote an “educational” advertising campaign designed to instill fear in parents (and their pediatricians) about the horrible illnesses (albeit previously unknown, benign or rare) that even us doctors hadn’t yet recognized as being significant up until recently, most of us physicians have gone along with the fear-mongering that makes our practices busier while it also makes billions of dollars in profits for some unworthy CEO or Wall Street investment banker, hedge fund manager or mutual fund investor – all at the expense of America’s precious and vulnerable children who are at high risk of being sickened along the way.

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The TV commercials, medical journal articles and drug representatives will be trying to educate us about a new, unaffordable vaccine that will somehow be squeezed into an already crowded and potentially deadly group of shots that America’s already at-risk-of-vaccine-injuries infants will now be receiving at their next well-child (perhaps soon to become chronically ill).check-up.

 Recognizing this, and so as not to overload the already over-loaded well-child inoculation schedule, perhaps he CDC (the Big Pharma-subsidized and vaccine cheerleader Centers for Disease Control and Prevention) will be adding shots to the in-hospital and irrational Hepatitis B shot that it recommends be given on day one – when vulnerable mothers are too exhausted and emotionally confused to give truly informed consent.

Many state legislatures are, as we speak, considering (or have already passed laws) criminalizing the previously legal parental right of refusing vaccinations on the basis of religious or philosophical beliefs. That is happening right now in Wisconsin’s Republican-dominated legislature, Minnesota’s split GOP/DFL legislature, and California’s Democratic Party-dominated legislature – where it is already signed into law by Democrat Jerry Brown. These poorly informed – and heavily bribed politicians don’t realize that their legislative efforts will be blindly forcing unsuspecting patients to submit to every new blockbuster vaccine that successfully emerges from the pipeline. Talk about making decisions on the basis of partial information or propaganda from sociopathic corporate entities! Attention, Senators Al Franken, Amy Klobuchar and other assorted legislators. Are you listening to the real science or to the corrupted, pseudoscience of Big Pharma?

Below is a list of 146 new vaccines that were in the pipeline as of 2010. The list, PhRMA proudly tells us, is now up to 271 new vaccines as of 2013. For a full listing of these vaccine trials, go to: http://phrma.org/sites/default/files/pdf/infectiousdiseases2010%20%281%29.pdf

For parents whose infants’ brains and bodies are immunologically and developmentally immature, be aware that your children may be forced to suffer untested-for and therefore unacknowledged long term neurological, autoimmune and chronic illness adverse effects. Parents need to be aware that if their infant dies, is sickened or is made chronically ill by vaccine ingredients, they, as protective parents, will be forbidden to sue the guilty drug company (or the doctor that administered them) for appropriate damages.

Parents and grandparents of children need to be aware of the fact that many of these new vaccines will be containing contaminants (such as unfilterable viral particles, bacterial particles, monkey kidney cell fragments, human fetal cells, squalene (in anthrax and some experimental swine flu vaccines), peanut oil (a likely cause of the epidemic of peanut allergies), formaldehyde and even foreign DNA fragments) as well as known neurotoxic additives such as formaldehyde and aluminum (and perhaps even mercury), all of which are known genetic toxins and known causes of  (sometimes subtle and sometimes not-so-subtle – but always preventable) brain damage, vaccine-induced epilepsy, autoimmune disorders, the so-called, but erroneously labeled “shaken baby syndrome” (now increasingly understood to represent a vaccine-induced encephalitis), SIDS (sudden infant death syndrome), dementia, autism spectrum disorders, mitochondrial toxicity, damage to the brain’s microglial and astroglial cells (the brain’s immune system), etc.

NOTE: Much of the information in this column is derived from easily accessible books and websites, including Make an Informed Vaccine Decision for the Health of Your Child by Mayer Eisenstein, MD, JD, MPH; The Sanctity of Human Blood: Vaccination is Not Immunization, by Tim O’Shea,  DC; Screening Sandy Hook, Causes and Consequences by Deanna Spingola (an online e-book); the writings and lectures of Russell Blaylock, MD; Immunologist J. Barthelow Classen, MD; Harold E Buttram, MD, Dr Sherri Tenpenny, Dr Suzanne Humphries, Dr Kenneth Stoller, Dr Andrew Wakefield, Dr Mark Geier, and Dr Joseph Mercola, and the following two articles: http://www.vaccines.net/vaccine-induced-immune-overload.pdfhttp://www.globalresearch.ca/vaccine-induced-immune-overload-and-the-epidemic-of-chronic-autoimmune-childhood-disease/5431013.

A List of 146 of the 271 Vaccines in Big Pharma’s Developmental Pipeline (as of 2010)

 (NOTE: The corporations that have the largest financial interest in the success of the trials is listed in bold letters.)

sanofi pasteur prevention of Clostridium difficile

ACE BioSciences prevention of traveler’s diarrhea caused by Campylobacter jejuni

ACE BioSciences prevention of traveler’s diarrhea caused by Escherichia coli

sanofi pasteur diphtheria, tetanus, pertussis Phase III DTP vaccine

Aeras Global tuberculosis

Novartis Vaccines prevention of influenza A infection (H5N1 subtype)

Antigenics treatment of herpes simplex virus

BioSante Pharmaceuticals anthrax Phase I/II vaccine

Intercell USA anthrax

KaloBios Pharmaceuticals Pseudomonas aeruginosa infections

Aduro BioTech treatment of hepatitis C 

Emergent BioSolutions anthrax vaccine

AlphaVax prevention of influenza virus infections in the elderly

DynPort Vaccine botulism vaccine

Inviragen Chikungunya virus vaccine

Celldex Therapeutics cholera vaccine (live attenuated)

ChronTech Pharma hepatitis C (DNA vaccine)

Virionics prevention and treatment of hepatitis C

Vical prevention of cytomegalovirus (DNA vaccine)

AlphaVax prevention of cytomegalovirus infections

Hawaii Biotech prevention of dengue fever

GlaxoSmithKline prevention of dengue fever (tetravalent)

Acambis mild to severe dengue fever

sanofi pasteur DTP-Hep B

sanofi pasteur diphtheria, tetanus, pertussis, polio, hepatitis B, polio, Hib

Dynavax treatment of hepatitis B

Crucell prevention of Ebola virus infections

Vical prevention of Ebola virus infections

GenPhar Ebola virus vaccine

GlaxoSmithKline prevention of infectious mononucleosis (Epstein-Barr virus)

BioSolutions Escherichia coli infections

Celldex Therapeutics prevention of cholera, Escherichia coli infections

Protein Sciences prevention of influenza virus infections in adults and children

sanofi pasteur influenza virus infections (new mass production method)

sanofi pasteur prevention of influenza virus (intradermal micro-injection)

Protein Sciences influenza virus infections

GlaxoSmithKline rotavirus infections in infants

GlaxoSmithKline prevention of cytomegalovirus (recombinant vaccine)

GlaxoSmithKline influenza virus (trivalent, thimerosal-free) for children ages 3-17

GlaxoSmithKline prevention of influenza virus

GlaxoSmithKline prevention of Streptococcus pneumoniae

GlaxoSmithKline prevention of diphtheria, tetanus, pertussis, Haemophilus infections, hepatitis B, meningococcal group C infections, poliomyelitis (infants)

GlaxoSmithKline prevention of Haemophilus and pneumococcal infections

GlaxoSmithKline prevention of Haemophilus and pneumococcal infections

GlaxoSmithKline prevention of influenza virus infection in children

GlaxoSmithKline prevention of influenza A virus (H1N1 subtype) for children and infants

GlaxoSmithKline staphylococcal infections 

MedImmune influenza A virus (H5N1 subtype) intranasal

Novavax prevention of influenza A virus infection

Hawaii Biotech prevention of West Nile virus infection

Novartis Vaccines helicobacter pylori

Pfizer hepatitis B (DNA)

Emergent BioSolutions hepatitis B

GenPhar hepatitis B

Novartis Vaccines treatment of hepatitis C

GlaxoSmithKline hepatitis E (recombinant)

Dynavax prevention of hepatitis B

Pfizer treatment of herpes simplex virus infections (DNA vaccine)

AuRx prevention and treatment of herpes simplex virus infections

sanofi pasteur diphtheria, tetanus, pertussis, hepatitis B, polio, Hib

Intercell prevention of influenza virus seasonal influenza

Novartis Vaccines prevention of herpes simplex virus infections

Acambis prevention of encephalitis virus

Bavarian Nordic smallpox vaccine

sanofi pasteur influenza A virus (H1N1 subtype) in adolescents, children and infants

CSL Behring prevention of influenza A virus (H1N1 subtype) for the elderly

Baxter Healthcare prevention of influenza A virus (H1N1 subtype)

Vical prevention of influenza A virus (DNA – H1N1 subtype)

Baxter Healthcare prevention of influenza A virus (H5N1 subtype)

DynPort Vaccine influenza virus

Antigen Express influenza virus infections H5N1 vaccine

Novavax prevention of influenza virus (particle vaccine)

Dynavax prevention of influenza virus infections

Vaxin influenza virus infections (intranasal)

Abbott Laboratories prevention of influenza virus (cell culture-derived)

Intercell prevention of Japanese encephalitis in children

Novartis Vaccines malaria vaccine (U.S. Naval Medical Research Center)

Vical malaria vaccine

BioSante Pharmaceuticals prevention of malaria (U.S. Naval Medical Research Center)

GenVec malaria vaccine (U.S. Naval Medical Research Center)

Crucell malaria vaccine 

Sanaria malaria vaccine

GenPhar Marburg virus (DNA vaccine)

MedImmune parainfluenza virus infections in children and infants

MedImmune prevention of respiratory syncytial virus infections in infants

MedImmune prevention of parainfluenza virus infections in children and infants

MedImmune prevention of influenza virus (quadrivalent) for adolescents and children

sanofi pasteur Neisseria meningitidis A, C  in toddlers 9 months-12 months

GlaxoSmithKline prevention of Neisseria meningitidis groups C and Y, Haemophilus influenzae type B, and tetanus toxoid

sanofi pasteur meningitis in infants

Novartis Vaccines meningococcal group B infections vaccine group B

Novartis Vaccines meningococcal group A, C infections in children

Novartis Vaccines meningococcal group A, C infections in infants

GlaxoSmithKline prevention of malaria (recombinant vaccine)

NanoBio prevention of influenza virus (intranasal)

GlaxoSmithKline prevention of influenza virus inactivated split-trivalent vaccine

GlaxoSmithKline prevention of Neisseria meningitidis groups A, C in children

LigoCyte Pharmaceuticals norovirus infections (intranasal)

Novartis Vaccines prevention of influenza virus

Protein Sciences prevention of influenza A pandemic (H5N1 subtype)

Meridian Biosciences parvovirus infections

Crucell prevention of influenza virus infections

Pfizer meningococcal group B infections (meningococcal “plague” vaccine)

DynPort Vaccine Yersinia infections (injectable)

Baxter Healthcare prevention of seasonal influenza virus

GlaxoSmithKline prevention of influenza A virus (“pre-pandemic”)

Pfizer prevention of pneumococcal infection in the elderly (Prevnar 13 Adult™)

sanofi pasteur rabies vaccine

BioSante Pharmaceuticals ricin poisoning (“biodefense” vaccine)

Soligenix ricin poisoning

sanofi pasteur prevention of rotavirus infections

Bharat Biotech prevention of rotavirus infections

Emergent BioSolutions anthrax (Fast Track) “protective antigen” vaccine

Inhibitex staphylococcal infections

Vical prevention of severe acute respiratory syndrome (SARS) coronavirus infections

Emergent BioSolutions shigella infections

GlaxoSmithKline prevention of herpes simplex virus infections

PharmAthene anthrax (“protective antigen” – rPA)

BioSante Pharmaceuticals staphylococcal infections (“biodefense” vaccine)

Nabi Biopharmaceutical prevention of staphylococcal aureus infections

GlaxoSmithKline prevention of staphylococcal aureus infections

Nabi Biopharmaceutical prevention of streptococcal B infections

Emergent BioSolutions prevention of streptococcal infections

Novartis Vaccines prevention of streptococcal infections

sanofi pasteur prevention of meningitis and pneumonia (tetravalent)

Inviragen treatment of dengue fever

Intercell USA prevention of traveler’s diarrhea due to E. coli (“patch” technology)

GlaxoSmithKline tuberculosis

Aerus Global TB prevention of tuberculosis in young children

GlaxoSmithKline prevention of  tuberculosis in adults

sanofi pasteur prevention of tuberculosis

DynPort Vaccine tularemia

Emergent BioSolutions prevention of typhoid (live typhoid organisms – oral vaccine)

Novartis Vaccines prevention of typhoid fever

Celldex Therapeutics typhoid fever

Merck prevention of herpes zoster (shingles)

Merck hepatitis B in infants

Merck human papillomavirus infections

Merck staphylococcal infections

GlaxoSmithKline prevention of varicella zoster virus

VaxInnate prevention of influenza A virus

VaxInnate influenza A virus infections in elderly patients

VaxInnate prevention of influenza A virus (H1N1 subtype)

Inovio Pharmaceuticals human papillomavirus infections

Inovio Pharmaceuticals prevention of influenza A virus (H5N1 subtype)

Xcellerex prevention of yellow fever


Dr Gary G. Kohls is a retired physician from Duluth, MN, USA. In the decade prior to his retirement from medicine, he had spent the last decade practicing what could best be described as “holistic (non-drug) mental health care”. Dr Kohls has been actively involved in peace, justice and nonviolence issues for much of his adult life and, since he retired, he has written a weekly column for the Duluth Reader, an alternative newsweekly magazine (www.readerduluth.com). His columns mostly deal with the dangers of American fascism, corporatism, militarism, racism, malnutrition, psychiatry and other movements that threaten American democracy and civility.

This work is reproduced and distributed with the permission and request of GreenMedInfo LLC. Want to learn more from GreenMedInfo? Click here http://www.greenmedinfo.com/greenmed/newsletter.”

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Awareness

Las Vegas Man Unable to Speak, Walk, See or Breathe Just Days After Getting Flu Shot

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In Brief

  • The Facts:

    A few days after getting a flu vaccine, Shane Morgan fell ill with a disease in which a person’s nerves are attacked by the immune system, causing paralysis and, in extreme cases, death.

  • Reflect On:

    How much 'evidence' do we need that the Pharmaceutical Industry is not an advocate for human health? Can we see our way out of this system of deception?

It is starting to seem like we can write a new story every few days about someone having an adverse reaction to the flu vaccine. As I mentioned in an article from last week, ‘After Getting Flu Shot, New York State Senator Gets Sick For Two Weeks, Then Dies,’ the latest flu vaccine is being suspected of actually delivering a dangerous strain of the flu that is resistant to vaccines.

And whether or not Las Vegas’ Shane Morgan had a highly adverse reaction to the vaccine itself or actually contracted this strain of flu, it is very clear in his and his wife’s mind that his adverse reaction was caused by the flu shot. Here’s what happened, according to this Las Vegas Review-Journal article:

On Nov. 2, Shane and Monique, 31, who live in North Las Vegas and are new parents to 8-month-old Briar, got their flu shots. They were planning to see Shane’s 23-year-old daughter, Sidnee Nutter, and her 4-month-old, and Nutter requested the whole family get vaccinated to protect her infant. They typically didn’t get vaccinated, but they happily obliged.

“The only reason I took this was because I didn’t want to lie to my daughter,” Shane said. In the days that followed, Shane fell ill. He was weak and achy; he had a fever and a sore throat. By Nov. 14, he asked his wife to take him to the hospital. “That’s when we really started getting worried,” Monique said. His arms and legs were going numb.

Soon after he was admitted to the hospital, he ‘was sedated and intubated, unable to breathe on his own.’ Now, two weeks later he still ‘can’t walk. His left eye is paralyzed and shut. Tubes protrude from his neck.’

Diagnosis

The doctors have made a diagnosis of ‘Guillain-Barre syndrome.’ More on this disease from the article:

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He may have months of recovery left from the rare disease, in which a person’s nerves are attacked by the immune system, causing paralysis and, in extreme cases, death. The cause of the disease that affects one or two in a million isn’t known, according to the Centers for Disease Control and Prevention. But the disease can creep up after a bout of diarrhea, a respiratory infection or an infection from Campylobacter jejuni bacteria.

In rare cases, people come down with Guillain-Barre after having the flu or getting a flu shot, though the CDC can’t show a causal effect.

So let’s go over this slowly. The Western Medical Establishment has put a fancy name to a symptom, a person’s immune system going out of whack, and called it a disease. Of course, the CDC will say it doesn’t know what causes this disease; they are only willing to offer a few conditions which precede the onset of the disease, including having the flu or getting the flu shot. Again, this admission with the disclaimer that ‘the CDC can’t show a causal effect.’ And why? Is it perhaps because that would give someone direct grounds to sue Big Pharma?

What has the CDC really done here? They have concocted a fancy hyphenated name to de-couple immune system degradation from the introduction of pathogens into the body that would seem logically to be the cause of that immune system degradation. For an organization that prides itself on their research and commitment to objective science, they certainly pull the ‘we don’t know the cause’ rabbit out of the hat whenever it serves the purposes of Big Pharma.

Are Anti-Viral Vaccines Actually Delivering A Toxic Virus?

You may have seen in my earlier article ‘Researcher Jailed After Uncovering Deadly Virus Delivered Through Human Vaccines‘ that respected researcher Dr. Judy Mikovits had isolated a murine leukemia virus, essentially a mouse virus, in examining patients who had a variety of serious diseases such as cancer, motor-neuron disorders and chronic fatigue syndrome (CFS). It was later suggested that this mouse virus likely had been transmitted to these people through vaccines. She explains how vaccines could become infected by this mouse virus when the vaccines are being made:

What we were doing to attenuate, to make the virus less pathogenic, less toxic, is we were passing them through mouse brains, so we were passing them through the brains of mice, and every scientist who works with these viruses, and worked at the National Cancer Institute recognized the possibility that if you put human tissue and mouse tissue together the possibility is that you’re going to pick up a virus that is silent, in the mouse, that is it doesn’t hurt the mouse, but it kills the human, or causes serious disease in the human.

As discussed in that article, the very possibility that people could start to believe that vaccines are transmitting a toxic virus to those who are injected with the vaccine was such a threat to the Big Pharma’s vaccine industry that she was immediately pressured into discrediting her own study, and in refusing to do so she was immediately jailed, and told that she would be ‘destroyed.’ Such is the fate of people who look too deeply and honestly into the true causes of many of our diseases and illnesses.

Flu Strains Getting More Dangerous

The business of vaccination is certainly a huge money-making venture, such that Big Pharma continues to be willing to put out the many fires that are brought on by honest researchers as well as a population getting more sick and diseased in lock step with the increase in the proliferation of vaccines. One of those fires is the clearly documented notion that the ubiquity of the flu vaccine is the actual cause of new deadlier strains of the flu that are more resistant not only to vaccines but to the protective mechanisms of our immune system.

If you consider the fairly straightforward idea that vaccines are working against our immune system and thus are degrading our natural immunity to diseases, then it stands to reason the logical step to take would be the complete cessation of all flu vaccination in our society. My bet is that it would not be long before we would see an increase in the health in the general population, the dying off of many strains of the disease, and an increase in ‘natural immunity’ to diseases in general that parents are able to pass on to their offspring. In the video below, researcher Dr. Andrew Wakefield explains the idea of ‘natural herd immunity’ very cogently:

As far as vaccines go, I would not argue that there is absolute, definitive proof that vaccines are harmful to the average person–and that is because proper, objective testing is not being undertaken. But far more sinister than proper testing not being undertaken due to costs or proper scientific mechanisms is the indisputable fact that Big Pharma, with the CDC in their pocket, care absolutely nothing about human health. Everything they do is based on the metric of profit. They do not want the causes of human disease to be found whenever that would force them to remove pharmaceuticals from human consumption, and are willing to try to convince us that they simply ‘don’t know’ the cause of certain diseases, that they are complicated, mysterious. It’s an embarrassment.

Hypothetical Statement

Doctors and advocates in the mainstream will continue to say whatever they can, spin things in whatever way necessary, to make it seem like, despite the evidence, it’s still a good idea to take the flu vaccine. In fact, their continued livelihood depends on it. Here is the typical example from that same article:

While adverse reactions to the flu vaccine happen, it’s still considered the standard to protect against the flu, which can be dangerous and deadly, said Dr. Fermin Leguen with the Southern Nevada Health District. “The likelihood of people developing Guillain-Barre after the flu shot are very small compared to the risks of developing the flu itself,” Leguen said. “Events like this are unfortunate … but it’s a very rare condition.”

So rather than saying, ‘Shane Morgan had a serious adverse reaction to the flu vaccine and we are going to find out why so it doesn’t happen again,’ the medical establishment would hypothetically say something more like this:

‘Shane Morgan has somehow contracted Guillain-Barre syndrome. We don’t know how it got it, maybe he always had that condition and it just got triggered somehow. While sometimes people come down with Guillain-Barre after having the flu or getting a flu shot–in rare cases, it must be noted over and over again–we can’t show a causal effect. So we will treat his Guillain-Barre syndrome using our pharmaceutical wizardry, and if he survives, we expect to be treated as heroes for saving him.’

Suffice it to say that, simply on the basis of their motives and those of the industry, nothing they say can really be trusted, including the fact that they can’t show a causal effect.

The Takeaway

I personally became much healthier and much more resistant to illness when I consciously moved away from allowing pharmaceutical products to enter my body. My 4-year old son is bright, healthy, energetic, and has neither taken any vaccines nor has ever been seen by a Western doctor. And I am soundly convinced that this is a part of the reason for his good health. When we see that the Western Medicine Establishment has overly complicated and obfuscated ‘health’ to suit their own nefarious agenda and purposes, then we come to realize that completely stepping away from this industry and their synthetic products is what is really best for our health.

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