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What Depression Does To The Structure of Your Brain & How You Can Change It Back

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According to the World Health Organization (WHO), approximately 400 million people, of all ages, suffer from depression, making it the leading cause of disability worldwide.

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This is a massive target market for pharmaceutical companies, and that’s no secret. There are huge profits to be had, and drug companies are taking every opportunity to make the most of this seemingly limitless source of income — at the expense of the consumer. It is not difficult to find evidence to support this notion, and a recent study published in the British Medical Journal is just one of many compelling examples. The study showed that pharmaceutical companies were not disclosing all information regarding the results of their drug trials. Researchers looked at documents from 70 different double-blind, placebo-controlled trials of selective serotonin reuptake inhibitors (SSRI) and serotonin and norepinephrine reuptake inhibitors (SNRI) and found that the full extent of serious harm in clinical study reports went unreported.

And it’s not the first time this has happened. To read more about that and to find the study, click here.

Not feeling well can take a toll on your physical health in a number of ways; when it comes to the brain, episodes of constant depression can actually reduce the size of your hippocampus — an area of the brain involved in forming and regulating emotions and memory. This is especially concerning for teenagers, given their brains are still developing in significant ways.

There is good news, however: the damage can be reversed, and you can change your brain in a number of different ways, but to do so requires you to make the decision to help yourself and then act on it.

Depression and Your Brain

Several studies have stated that depressed people tend to have a smaller hippocampus. According to Professor Ian Hickie of The University of Sydney’s Brain and Mind Research Institute:

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[The] more episodes of depression a person had, the greater the reduction in hippocampus size. So recurrent or persistent depression does more harm to the hippocampus the more you leave it untreated.

This largely settles the question of what comes first: the smaller hippocampus or the depression? The damage to the brain comes from recurrent illness…

Other studies have demonstrated reversibility, and the hippocampus is one of the unique areas of the brain that rapidly generates new connections between cells, and what are lost here are connections between cells rather than the cells themselves.

Treating depression effectively does not just mean medicines. If you are unemployed, for example, and then sit in a room doing nothing as a result, this can shrink the hippocampus. So social interventions are just as important, and treatments such as fish oils are also thought to be neuro-protective.  (source)(source)

It’s also noteworthy to mention here that feelings of sadness and negativity can code different information into the heart’s electromagnetic field, and the heart will actually send signals to the brain that can create chaos in the nervous system. These findings come from the scientists at the Institute of HeartMath, who investigate heart and brain interaction. You can read more about that here.

Scientists have also used brain magnetic resonance imaging (MRI) data to test the hypothesis that depression changes the brain. For example, an international team of researchers found  those who suffered from recurring depression do indeed have a smaller hippocampus.

Chemical Imbalance or Not? 

Joseph Coyle, a neuroscientist from Harvard Medical School, perhaps sums it up best when he explains that this idea of a “chemical imbalance is sort of last-century thinking. It’s much more complicated than that.” And it’s true; depression cannot truly be reduced to the commonly accepted notion of  a chemical imbalance in the brain. Posed in the late 1950s, this theory essentially posits that depression is a deficiency of select neurotransmitters (chemical messengers) at critical points, like synapses. One of these neurotransmitters is serotonin; others include norepinephrine and dopamine.

As Scientific American reports, “much of the general public seems to have accepted the chemical imbalance hypothesis uncritically,” but “it is very likely that depression stems from influences other than neurotransmitter abnormalities.”

Harvard Medical School also put out a press release a few years ago stating it’s “often said that depression results from a chemical imbalance, but that figure of speech doesn’t capture how complex the disease is.” Dr. Joanna Moncrieff, a prominent author and British psychiatrist, explains further:

Of course, there are brain events and biochemical reactions occurring when someone feels depressed, as there are all the time, but no research has ever established that a particular brain state causes, or even correlates with, depression. . . . In all cases studies yield inconsistent results, and none have been shown to be specific to depression, let alone causal. . . . The fact that more than 50 years of intense research efforts have failed to identify depression in the brain may indicate that we simply lack the right technology, or it may suggest we have been barking up the wrong tree!

The most commonly cited evidence to support the chemical imbalance theory is the ability of some drugs to increase and decrease mood in human and animal models. While many antidepressants increase the amounts of serotonin and other neurotransmitters at synapses, they do not address the underlying issues or help the brain heal itself. And what we fail to realize today is that just because mood can be artificially manipulated with drugs does not mean that depression cannot be treated in other ways, or that the chemical imbalance theory is true.

We are simply incapable of saying with certainty that a human being has a chemical imbalance (to whatever extent) or identifying what neurotransmitters are involved. This is why the chemical imbalance theory of depression remains a theory. Chemical levels in the brain cannot accurately be measured or ‘looked at,’ either.

Yet much of the general public still accepts the chemical imbalance theory. A survey conducted in 2007 of 262 undergraduates at Cleveland State University found more than 80% of the participants found it “likely” that chemical imbalances cause depression. Yet according to Jonathan Leo, an associate professor of neuroanatomy at Lincoln Memorial University, this really has yet to be proven: “At best, drug-induced affective disturbances can only be considered models for natural disorders, while it remains to be demonstrated that the behavioral changes produced by these drugs have any relation to naturally occurring biochemical abnormalities which might be associated with the illness.

It’s important to keep in mind there are probably many chemicals involved, working both inside and outside of our nerve cells. As Harvard Medical School points out, there are millions, even billions, of chemical reactions that make up the dynamic system responsible for your mood, perceptions, and experience of life.

Jonathan Leo further points out that “the cause of mental disorders such as depression remains unknown. However, the idea that neurotransmitter imbalances cause depression is vigorously promoted by pharmaceutical companies and the psychiatric profession at large.”

As I hope I have made clear, the theory that depression is caused by low levels of serotonin, along with similar such theories, came into existence because scientists were able to observe what drugs do to the brain. It is a hypothesis that attempted to explain how drugs were able to fix the problem, but whether or not depressed people actually have lower serotonin levels remains to be proven. You can read more about the science here.

“The serotonin theory is simply not a scientific statement. It’s a botched theory – a hypothesis that was proven incorrect.”

– Dr. Joseph Mercola (source)

Not only is there no solid scientific proof to back up the chemical imbalance theory, many depressed people are not even helped by taking antidepressants like SSRIs. For example, a review done by the University of California in 2009 found one third of people treated with antidepressants do not improve, and a significant portion of these people remain depressed. Scientific American too points out that “if antidepressants correct a chemical imbalance that underlies depression, all or most depressed people should get better after taking them.”

That being said, there are many who do report positive benefits, but there is no way to tell if the drugs are working or if they are just working like a placebo.

Think about this for a moment: So many of us are made to believe that depression is the result of a chemical imbalance in the brain, when there is actually little scientific evidence to support that statement. Association between various brain changes and depression is large, and no studies have established a solid, cause-and-effect correlation between the brain and the disorder.

Depression science has one focus — brain chemistry — despite it being a multi-faceted problem. Focusing on this one theory and then dishing out drugs that alter brain chemistry is, as Scientific American puts it, simply “shortsighted.”

“In spite of the enormous amounts of money and time that has been spent on the quest to confirm the chemical imbalance theory, direct proof has never materialized.” (source)

I am astounded that people fail to see the irony in the situation. The only chemical imbalances we can prove exist in people’s brains are the ones being inflicted upon them by psychiatric drugs.

There Are Other Biological Factors Implicated in Depression

As Dr. Mercola points out:

Contrary to popular belief, depression is not likely caused by unbalanced brain chemicals; however there are a number of other biological factors that appear to be highly significant. Chronic inflammation is one such factor.5

Scientists have also found that your mental health can be adversely impacted by factors such as vitamin D deficiency and/or unbalanced gut flora — both of which, incidentally, play a role in keeping inflammation in check, which is really what the remedy to depression is all about.

He also talks about sugar, which is extremely toxic to the body and a catalyst for multiple diseases. You can read his article on depression and these other biological factors here.

Some Great Ways to Combat Depression

1. Neuroplasticity

Neuroplasticity refers to the idea that the brain can change and adapt. The concept is now being used to treat learning disabilities, brain damage, chronic pain, and more. A great person to learn more about this from is Dr. Norman Doidge, author of The Brain That Changes Itself. He writes:

The idea that the brain is plastic in the sense of changeable, adaptable and malleable is the single most important change in our understanding of the human brain in four hundred years. Neuroplasticity is that property of the brain that allows it to change its structure and its function, it’s a response to sensing and perceiving the world, even to thinking and imagining. Human thoughts and learning actually turn on certain genes in our nerve cells which allow those cells to make new connections between them.

Simply put, the way you think can change your brain. This is not a new idea, and it has been demonstrated by a number of experiments, ranging from quantum physics, where factors associated with conscious can change the behaviour of an atom, to placebo studies, which demonstrate the power of the mind.

For example, a Baylor School of Medicine study, published in 2002 in the New England Journal of Medicine, looked at surgery for patients with severe and debilitating knee pain. Many surgeons know there is no placebo effect in surgery, or so most of them believe. The patients were divided into three groups. The surgeons shaved the damaged cartilage in the knee of one group. For the second group they flushed out the knee joint, removing all of the material believed to be causing inflammation. Both of these processes are the standard surgeries people who have severe arthritic knees must undergo. The third group received a “fake” surgery; the patients were sedated and then tricked into thinking they had actually undergone knee surgery. Doctors made the incisions and splashed salt water on the knee as they would in normal surgery, then sewed up the incisions like the real thing. All three groups went through the same rehab process, and the results were astonishing. The placebo group improved just as much as the other two groups who had surgery.

“My skill as a surgeon had no benefit on these patients. The entire benefit of surgery for osteoarthritis of the knee was the placebo effect.”

– Dr. Moseley (surgeon involved in the study) (Lipton, Bruce. The Biology of Belief. Hay House, Inc, 2005)

The power of the placebo effect was also clearly demonstrated in a report published by the United States Department of Health and Human Services in 1999. It discovered that half of severely depressed patients taking drugs improve compared to the 32% taking a placebo. Considering all of the side effects and dangers associated with antidepressant use, this marginal difference hardly seems worthwhile. And let’s not forget that the antidepressant industry is a multi-billion dollar one.

A 2002 article published in the American Psychological Association’s Prevention & Treatment by University of Connecticut psychology professor Irving Kirsch titled “The Emperor’s New Drugs” made some more shocking discoveries. Kirsch found that 80% of the effect of antidepressants, as measured in clinical trials, could be attributed to the placebo effect. This professor even had to file a Freedom of Information Act (FOIA) request to get information on the clinical trials of the top antidepressants. Kirsch found the difference between the response of the drugs and the response of the placebo was less than two points on average on this clinical scale that goes from 50-60 points. That difference, as Kirsch points out, is clinically meaningless.

Researchers all over the world have found that placebo treatments can stimulate real biological and physiological responses — everything from changes in heart rate to blood pressure and even chemical activity in the brain. It’s been effective with a number of different ailments, from arthritis and fatigue to depression, anxiety, Parkinson’s, and more. Why are we not utilizing our brain’s own remarkable ability to heal itself more often?

2. Food

Take a look at these factors.

  • Added sugar and high fructose corn syrup
  • Genetically engineered (GE) ingredients (primarily corn, soy, and sugar beets) which, besides their own unknown health risks, also tend to be heavily contaminated with glyphosate—a Class 2A carcinogen that can also damage your gut microbiome and has been linked to antibiotic-resistance. Most conventional (non-GE) wheat is also treated with toxic glyphosate prior to harvesting.
  • By altering the balance of your gut flora, pesticides and herbicides also disrupt the production of essential amino acids like tryptophan, a serotonin precursor, and promote production of p-cresol, a compound that interferes with metabolism of other environmental chemicals, thereby increasing your vulnerability to their toxic effects.
  • Artificial sweeteners, along with thousands of food additives, most of which have never been tested for safety
    Chemicals in the food packaging, such as bisphenol-A (BPA), bisphenol-S (BPS), and phthalates, which can migrate into the food
  • Trans fats

3. Exercise 

Exercise has been shown to  effectively combat depression and help rebuild the hippocampus, and studies have shown very clear links between inactivity and depression. As Dr. Mercola tells us, women who sit for more than seven hours a day have a 47% higher risk of depression than women who sit for four hours or less per day. Furthermore, women who do no physical activity whatsoever have a 99% higher risk of developing depression compared to women who exercise.  Studies have shown its efficiency typically surpasses that of antidepressant drugs, and it also helps rid your body of stress chemicals that can lead to depression.

4. Meditation

As Forbes points out:

The practice appears to have an amazing variety of neurological benefits – from changes in grey matter volume to reduced activity in the ‘me’ centers of the brain to enhanced connectivity between brain regions. . . .

Skeptics, of course, may ask what good are a few brain changes if the psychological effects aren’t simultaneously being illustrated? Luckily, there’s good evidence for those as well, with studies reporting that meditation helps relieve our subjective levels of anxiety and depression, and improve attention, concentration, and overall psychological well-being.

Related CE article: Harvard Study Unveils What Meditation Literally Does to the Brain

For more helpful ways to overcome depression, you can check out this article.

Thanks for reading.

 

 

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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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A Statistically Strong Relationship Has Been Found Between The MMR Vaccine & Autism

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In Brief

  • The Facts:

    Dr. Brian Hooker, one of multiple people who received committed data from a CDC senior scientists regarding a 2005 MMR autism vaccine study has done a reanalysis that clearly shows a statistically significant relationship.

  • Reflect On:

    Why are negative aspects and important research/testimony regarding vaccines completely ignored? Why are people believing that vaccines are safe and effective if all of the evidence points otherwise? Why is the only response ridicule?

After four long years, CHD Board Member, Dr. Brian Hooker‘sreanalysis of the CDC’s MMR-autism data from the original DeStefano et al. 2004 Pediatrics paper has been republished in the Winter 2018 Edition of the Journal of American Physicians and Surgeons. The data, when properly analyzed, using the CDC’s own study protocol, show a strong, statistically significant relationship between the timing of the first MMR vaccine and autism, specifically in African American males. In addition, a relationship also exists in the timing of the MMR vaccine and those individuals who were diagnosed with autism without mental retardation. These relationships call into question the conclusion of the original DeStefano et al. 2004 paper which dismissed a connection between the MMR vaccine and autism.

Main Points from Reanalysis:

  • The rate of autism diagnoses has increased alarmingly in the U.S., and is about 25 percent higher in black children. Boys are far more likely than girls to receive this diagnosis.
  • As early as 2001, the Centers for Disease Control and Prevention (CDC) had data showing an increased rate of autism diagnoses in black male school children in Atlanta who received their first measles-mumps-rubella (MMR) vaccination before 36 months of age.
  • The original publication concerning the data downplayed the association, and no follow-up was conducted.
  • Dr. Hooker noted that the CDC deviated from its original data analysis plan, possibly because of unwanted results.
  • The relationship loses its statistical significance if the analysis is restricted to children with a Georgia birth certificate, which decreases the sample size by about 40 percent.
  • Dr. Hooker reanalyzed the same data set using the same methodology of conditional logistic regression but didn’t exclude children lacking a Georgia birth certificate.
  • By stratifying data for African-American males by birth year, Dr. Hooker also found a statistically significant higher risk of an autism diagnosis in children who had received the first MMR vaccine 1 year earlier, only in children born in 1990 or later. Thimerosal exposure increased in the early 1990s, and it was not removed from most pediatric vaccines until 2001-2004. Dr. Hooker suggests the possibility that there may be some interaction between increased mercury exposure and early MMR vaccination. Further study would be needed to explore this possibility.
  • Dr. Hooker’s interest was sparked, he reports, by communication with a CDC whistleblower, a senior scientist, who had retained some of the original analyses.
  • Dr. Hooker concludes that failure to follow-up on these observations represents a huge lost opportunity to understand possible reasons for the enormous increase in this devastating neurological disability.

Introduction from Dr. Hooker’s article:

“This study is a re-analysis of Centers for Disease Control and Prevention (CDC) data pertaining to the relationship of autism incidence and the age at which children got their first measles-mumps-rubella (MMR) vaccine. Statistically significant relationships were observed when African-American males were considered separately while looking at those individuals who were vaccinated prior to and after a 36-month age cut-off. CDC officials observed very similar relationships as early as November 2001, but failed to report them in their final publication. In addition, a relationship is seen when specifically considering children who received a diagnosis of autism without mental retardation. Although this was reported in the original 2004 paper, it was not discussed, nor was any follow-up study conducted. Preliminary results also suggest the possibility of a synergism between thimerosal exposure and MMR timing leading to a greater risk of autism.”

Conclusion from Dr. Hooker’s article:

“The first data set used by DeStefano et.al represents a huge lost opportunity to understand any role between the timing of the first MMR vaccine and autism. The re-analysis presented here elucidates effects that should at least merit further investigation. Specifically, increased risks of earlier vaccination are observed for African-American males and among cases of autism without MR. Both phenomena deserve additional study that could yield important clues regarding the current enormous increase in autism.”

Dr. Hooker’s Reanalysis of CDC Data on Autism Incidence and Time of First MMR Vaccination was published December 7, 2018 in the Journal of American Physicians and Surgeons.

Important Reminder From Collective Evolution

Dr. William Thompson (senior CDC scientist), who is  mentioned above as co-author of this study, blew the whistle and admitted that he was pressured to omit statistically significant data, and that there is a connection between this vaccine and autism. He released this statement in an official capacity, as explained by the Congressman in the video below. This story was an has been completely ignored by mainstream media.

Dr. Hooker and Thompson were in touch, Hooker was the one who did the reanalysis as you can see above.

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Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

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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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!

SUPPORT CE HERE!

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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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