Connect with us

Awareness

How Pharmaceuticals Came To Be The 4th Leading Cause Of Death In America

Published

on

lisaPrescription drugs are the 4th leading cause of death in America. (1) People know this to be true, they know it to be appalling, but it’s still seen as incomprehensible and absurd. How could medicine hurt so many people? We all know that side-effects happen, but they are thought to be rare. They must be rare, right? We all know some good, kind, generous, thoughtful doctors who want nothing more for their patients than health and happiness, so they certainly aren’t giving their patients drugs that hurt them, are they? We know that the FDA is a federal bureaucracy, so it must be too restrictive of the pharmaceutical industry, right? And the FDA is supposed to protect consumers, so we’re as safe as we can be, right? And people can sue, so the legal system must be keeping the bad aspects of the medical system in check, right? All of these questions, and many more, bring up some cognitive dissonance for people when they’re faced with the fact that prescription drugs, used as prescribed, kill an inordinate a number of people. It brings up the questions –

advertisement - learn more

How do prescription drugs get to be the 4th leading cause of death in America? How does that happen?

Here is a tale of how prescription drugs, used as prescribed, kill people.

Kerstin (age 30) comes down with a urinary tract infection. It’s a Saturday so her regular doctor’s office is closed. Urinary tract infections are painful so she knows that she can’t wait ‘til Monday to get treatment. She goes to an Emergency Services Clinic close to her house. She tells them that she has a urinary tract infection and they write her a prescription for Cipro (Ciprofloxacin – a fluoroquinolone antibiotic). They do not culture her urine because they don’t have the time or capacity to do so. It doesn’t matter what kind of bacteria is in her urine though, they know that Cipro will kill it because Cipro is a broad-spectrum antibiotic and it will kill all the offending bacteria in her urinary tract, plus some.

Kerstin is relieved. Her painful urinary tract and bladder are about to be healed.

Kerstin takes two 500 mg. pills of Cipro two times a day for a week. On the 5th day of taking Cipro, Kerstin starts to feel a bit off. Her bladder feels full even when it isn’t, she has dark “floaters” interfering with her vision and she feels anxious. She doesn’t think anything of these things. They’re strange, but not too worrisome. She doesn’t think for a second that they could be due to the antibiotic that she is taking. Kerstin finishes the seven day course of Cipro. Her urinary tract infection is gone and she is pleased about that. Her bladder fullness, floaters and anxiety come and go and she doesn’t think much of them.

advertisement - learn more

Ten days pass in which Kerstin feels fine. On the eleventh day after she has finished taking Cipro, she starts taking ibuprofen to treat menstrual cramps. On the thirteenth day after she has finished taking the Cipro, it feels as if a bomb goes off in her body. Her hands and feet swell to twice their normal size. It becomes painful for her to walk or to do anything with her hands. Her knees are burning as if every tendon in them is inflamed. She is weak. She develops hives all over her body. Her anxiety levels are sky-high.

Kerstin goes to the doctor. The doctor says that the hives are a result of an allergic reaction and tells her to take Benadryl. Kerstin asks the doctor why she can barely walk when she was going to the gym daily just a few days earlier. The doctor says that she doesn’t know, but that she will run tests.

Kerstin takes Benadryl but it doesn’t seem to help. She goes back to the doctor for something stronger. She is put on prednisone.

The swelling in her hands and feet goes down, but her other symptoms worsen. She develops insomnia. She sprains her wrist while opening a jar. Intermittent pain throughout her body, but especially in her legs, begins. She loses her memory and has trouble concentrating.

Her test results come back. They are all “normal.”

Her pain worsens. She is diagnosed with Fibromyalgia. She asks the doctor who diagnoses her with Fibromyalgia how she could have gone from being healthy and active to being disabled and in pain, now with a diagnosis of Fibromyalgia. The doctor mutters something about mysterious diseases and unexplained symptoms. Kerstin asks if her symptoms could be related to any of the medications that she took – Cipro, ibuprofen and prednisone. The doctor says no. More tests are run to see if there are other causes of Kerstin’s symptoms.

Kerstin is put on Lyrica to help her with her Fibromyalgia pain.

The Lyrica seems to help some of her pain but her mental symptoms get worse while she is on it. In addition to her already existing memory and concentration problems, Kerstin develops brain-fog. She feels slow, stupid and like she is living in a dream. She gains 15 pounds in two months. Her hair starts to fall out. She feels suicidal. She is taken off of Lyrica by her doctor.

Kerstin continues to have problems in her joints, especially her wrists, knees and ankles, so she is not surprised when she is diagnosed with Rheumatoid Arthritis. She starts seeing a Rheumatologist who puts her on Humira. Humira decreases some of her inflammation symptoms but many of her other symptoms remain. She receives Humira treatments for 2 years.

After two years of Humira treatments, Kerstin is diagnosed with hepatosplenic T-cell lymphoma – cancer. She dies on the operating table when her surgeon attempts to remove the lymph nodes on her neck that had been affected by the cancer. She is 34 years old when she passes away.

Kerstin’s story is fictionalized, but it is far from fantasy. Stories like hers happen every day. A large portion of her story is my own and it was both true and horrifying to experience. Stories that are significantly worse, where a doctor’s injection site turn into a staph or MRSA infection to start the whole process, or where anti-psychotic medications that the patient are put on drive her to homicide or suicide. And I didn’t delve into the PAIN that comes with Fluoroquinolone Toxicity (Cipro is a fluoroquinolone and the others are just as bad, if not worse), so it’s a light fictionalized version – with the hope that you’ll find the horror to be believable, because it is very, very real for too many people.

The Explanations, Journal Articles and Facts behind Kerstin’s Story

I don’t expect you to accept the story above as fact without some thorough explanation. Here is the information behind my assertions:

The antibiotic that Kerstin took is Cipro (Ciprofloxacin). Cipro is a fluoroquinolone antibiotic, along with Levaquin, Avelox, Floxin and a few other less commonly used drugs in the fluoroquinolone class. Fluoroquinolone antibiotics are the “big guns” of antibiotics. They are broad spectrum antibiotics that will kill all bacteria in their path. (2) They are frequently prescribed to treat urinary tract infections (3) because they penetrate kidney tissue well (4).

Cipro, and all the other fluroquinolones, have terrible side-effects. Many of the awful side-effects that can be experienced, often all at once, are listed on the Cipro Warning Label. However, many things are left off of the warning label, they are listed on http://www.ciproispoison.com/.

Additionally, here are articles backing up Kerstin’s symptoms:

  • Vision Floaters – The JAMA article entitled “Oral Fluoroquinolones and the Risk of Retinal Detachment” notes that fluoroquinolones increase the incidence of Retinal Detachment (5). If the connective tissue in your eye is damaged, visual disturbances, including floaters, can result.
  • Anxiety – The Journal of Neurosciences in Rural Practices’ article entitled “Levofloacin-induced Acute Anxiety and Insomnia” notes that Levofloxacin (another fluoroquinolone – Levaquin) can induce anxiety and insomnia (6) Cipro/Ciprofloxacin can do the same.
  • Bladder fullness – This is a symptom that I experience, along with many other people suffering from Fluoroquinolone Toxicity. I’m not completely sure what it stems from, but here are a couple of possibilities. This article in the Journal of Urology entitled “Role of Mitochondria in Ciprofloxacin Induced Apoptosis in Bladder Cancer Cells” notes that Cipro disturbs the mitochondria in bladder cells and causes apoptosis (cell death) (7). It is also possible that the feeling of bladder fullness is a result of dysglycemia as it is noted in an article in Medscape Medical News that fluoroquinolones increase the risk of severe dysglycemia in diabetics. Additionally, “one fluoroquinolone antibiotic, gatifloxacin (Tequin, Bristol-Myers Squibb), was already withdrawn from the US market in 2006 due to the risk for severe dysglycemia” (8)
  • Pain and swelling in hands and feet – This symptom can be more succinctly described as peripheral neuropathy. The FDA issued an update to the labels for fluoroquinolones noting that PERMANENT Peripheral Neuropathy is a possibility in August, 2013 (9). This neuropathy may stem from destruction of the Myelin caused by the fluoroquinolone.

There are likely other causes and reasons for Peripheral Neuropathy being a result of Fluoroquinolone Toxicity, including the production of neurotoxins caused by the drugs (10) and the fracturing of DNA (11).

  • Skin problems like hives/uticaria/rashes are listed on the warning label
  • Tendon pain/tear/strain/rupture – This adverse effect is so well documented that fluoroquinolones carry a black box warning about the danger of rupturing a tendon on the top of the warning label. An article in Musculoskeletal Medicine entitled “Musculoskeltal Complications of Fluoroquinolones: Guidelines and Precautions for Usage in the Athletic Population” notes that young, healthy, athletic people’s muscles and tendons are adversely effected by fluoroquinolones (12)
  • Fibromyalgia – Mysterious, sometimes intermittent, sometimes constant, pain is common among those with fluoroquinolone toxicity. The information above about peripheral neuropathy should ring a lot of bells for those diagnosed with Fibromyalgia.  Additionally, Carboxylic Acid is attached to the quinolone molecule (13). It is a known neurotoxin. (14 and 15) Also, a quinolone studied in the article “Cytotoxcicity of Quinolones toward Eukaryotic Cells” notes that quinolones “kills cells by converting the (topoisomerase) type II ezyme into a cellular poison.” (16) Cellular poisons can lead to pain.
  • A diagnosis of Rheumatoid Arthritis – Per Toxicologist, Professor Joe King, “when a cell is malfunctioning (due to a mutation caused by a toxin or radiation) the body deems it alien and begins and autoimmune response as a defense mechanism. Thus producing positive autoimmune antibodies in lab tests, but in actuality you don’t really have the disease, it is bad cells. For example I test positive for rheumatoid arthritis (RA), but I don’t have RA, I have Fibrillan Connective Tissue destruction upon biopsy. But the doctor reads the lab report for RA and recommends anti-inflammatory steroids. Bad diagnosis, because the problem is not RA but Fibrillan and steroids will dissolve the Fibrillan faster.” Also per Professor King, “the cells in your tissue, organs, etc. are not functioning correctly, there is a mutation in there somewhere and the body is reacting to this weird cells as alien, thus producing an inflammatory process (which is painful).” Additionally, it should be noted that Cipro was found to cause chromosomal abnormalities in immune system cells. (17)

I mentioned NSAIDs and steroids. Both NSAIDs and steroids are contraindicated with fluoroquinolones (18 and 12). Please note that Kerstin didn’t take NSAIDs or steroids at the same time as the Cipro. Both NSAIDs and steroids are contraindicated for any person who has ever experienced an adverse reaction to a fluoroquinolone, likely because of the production of acyl glucuronides, “which are chemically reactive electrophiles formed by carboxylic acid-containing drugs” (15) and/or because of the depletion of the CPY450 enzymes by quinolones/fluoroquinolones that leave the body unable to metabolize other drugs (19 and 20).

How do fluoroquinolone ANTIBIOTICS cause all that harm? The harm that they cause is in the essence of the way they work. They are the “first antibacterial agents that efficiently inhibited DNA replication.” (21) Antibiotics in the penicillin and cephalosporin classes, by comparison, work by disrupting bacterial cell walls, not by doing anything to bacterial, or human, DNA. Fluoroquinolones also form “a poisonous adduct on DNA” (21). Fluoroquinolones cause chromosomal abnormalities in human cells (17) and also have tumor killing qualities (22). While that might sound great on the surface, if you read between the lines you’ll note that if these drugs kill tumor cells, they kill human cells. Fluoroquinolones cause apoptosis, programmed cell death, at a massive rate (23). Patient studies have shown, through a DNA Adduct Mass Spectrogram Analysis, that quinolone molecules have adducted to their DNA. Adducting to and breaking human DNA can cause every single one of the problems that Kerstin experienced, all of the problems listed on the FDA warning label for these drugs, and more. It’s a bad idea to mess with human DNA and chromosomes – a look back at the history of Agent Orange will tell you why this is true.

The consequences of the DNA destruction done by fluoroquinolones is yet to be established. An article was published in Nature in September, 2013 connecting topoisomerase inhibiting drugs (fluoroquinolones inhibit topoisomerases II and IV (24)) with triggering the expression of autism related genes. I wrote about this on CE – http://www.collective-evolution.com/2013/09/18/a-horrifying-cause-of-autism-dna-damage-from-synthetic-antibiotics/ Of course, more studies need to be done to determine the implications of this study.

Studies of the DNA make-up of Gulf War Veterans and their children may also be revealing as all 1991 Gulf War Veterans were given Cipro prophylactically because of fear of anthrax (25). Likewise, in 2001 United States Postal Workers who took Cipro prophylactically, also to prevent anthrax, and any ensuing health issues that they have (57% reported side-effects –26) may be related to their exposure to fluoroquinolones.

Fluoroquinolone antibiotics are dangerous drugs that have been used recklessly since their introduction to the market as a first-choice broad-spectrum antibiotic. They are likely responsible for many of the “mysterious” illnesses that have been on the rise since the early 1980s when Cipro was patented by Bayer and Levaquin was patented by Johnson & Johnson. Everyone who has Fibromyalgia, Chronic Fatigue Syndrome, Thyroid Dysfunction, any Autoimmune Disease, Gulf War Syndrome, Leaky Gut Syndrome, Dysautonomia, etc. should look at their medical records to see if they have ever taken a fluoroquinolone. If a fluoroquinolone is in your past, fractured genes may have resulted, and thus your pain and suffering. Please note that adverse reactions to fluoroquinolones are often delayed for weeks or sometimes months or years after administration of the drugs has stopped and there is a tolerance threshold for metabolism of these drugs (20) so most people do not react to their first dose.

Lyrica and Humira

Here is the warning label for Lyrica – (link – Source 27) Please note that suicidal ideation is one of the acknowledged adverse effects caused by this drug. Weight gain, difficulty concentrating, etc. are also listed on the warning label. Patient reports (these people aren’t lying) can be found on askapatient.com – Lyrica.

Humira, Enbrel and other TNF inhibiting drugs CAUSE CANCER. This is well documented and known. The warning labels for both Humira and Enbrel state in a big black box warning that various cancers are associated with use of those drugs. In case it needs to be spelled out, cancer can be deadly.

Here is an excellent blog post about how Humira can kill, and how it is marketed – http://davidhealy.org/welcome-to-the-humiraverse/

Conclusions

It is often noted as people are bemoaning the unwillingness of the pharmaceutical industry to create more antibiotics, that there isn’t enough money to be made from antibiotics to encourage their production. (28) While there may not be much money to be made in selling antibiotics directly, there is a whole lot of money to be made in treating autoimmune diseases. Humira reached $7.9 Billion in sales (29) in 2011 despite the undisputed fact that it causes cancer. If a class of antibiotics can cause the body to react as it would if it had an autoimmune disease for an extended period of time (the ill effects of fluorouquinolones can be permanent but they typically last from 6 to 36 months), and therefore a person gets diagnosed and treated for an autoimmune disease, though they don’t actually have the autoimmune disease, they actually have an autoimmune reaction to a poisonous drug, the pharmaceutical industry has effectively taken an acute problem, an infection, and converted it into a chronic problem, an autoimmune disease. Chronic conditions mean repeat customers and the pharmaceutical industry makes billions. (I doubt that this process is a conspiracy or even planned on the parts of the people in the pharmaceutical industry. Rather, I think that it is caused by willful ignorance among those in the medical professions, encouraged by greed and a complete lack of checks and balances on the pharmaceutical companies, those that have the most to gain in creating repeat customers.)

People are being hurt by their medicine and it is unacceptable. If harm is impossible to avoid completely, it should be minimized. There is zero effort on the part of Doctors, Pharmacists, the FDA or anyone else to minimize adverse effects of drugs. If an effort were being made, we would not be in the tragic situation that we’re in, with the pharmaceutical industry being the 4th leading cause of death of Americans.

The mantra of “all drugs have side-effects” has been so ingrained into the collective consciousness that we have come to think of it as acceptable that drugs have side-effects, and for drug side-effects to be devastating. In accepting this “better someone else than me” / “it can’t happen to me” attitude, we have given permission to the FDA to be inept, incompetent and lazy. In their ineptitude, they have ignored 15 years of research noting that commonly prescribed ANTIBIOTICS are damaging our DNA. We can only hope that this oversight caused by laziness and incompetence is not consequential to us all. Because I can accept the possibility that it may be worth it for society for me to be sacrificed so that we can have powerful antibiotics, but no drug of any sort, no matter what good it does, is worth sacrificing our collective DNA.

Post Script:  The author’s web site, with more information about fluoroquinolones, is www.floxiehope.com

Sources:

1.Donald W. Light, “Risky Drugs: Why the FDA Cannot be Trusted,” Harvard University, The Lab @ Edmond J. Safra Center for Ethics. http://www.ethics.harvard.edu/lab/blog/312-risky-drugs?layout=default#stay-informed

  1. Jane E. Brody, “Popular Antibiotics May Carry Serious Side Effects,” New York Times, September 10, 2012. http://well.blogs.nytimes.com/2012/09/10/popular-antibiotics-may-carry-serious-side-effects/?_r=1
  2. Web MD, Antibiotics for Urinary Tract Infections (UTIs) http://www.webmd.com/a-to-z-guides/antibiotics-for-urinary-tract-infections-utis
  3. DANA E. KING, M.D., ROBB MALONE, PHARM.D., and SANDRA H. LILLEY, PHARM.D., East Carolina University School of Medicine, Greenville, North Carolina, “New Classification and Update on the Quinolone Antibiotics” American Family Physician http://www.aafp.org/afp/2000/0501/p2741.html
  4. Mahyar Etminan, et. al., “Oral Fluoroquinolones and the Risk of Retinal Detachment” JAMA, April 4, 2012—Vol 307, No. 13 http://211.144.68.84:9998/91keshi/Public/File/40/307-13/pdf/joc25028_1414_1419.pdf
  5. Arun Kandasamy and D Srinath, “Levofloxacin-induced acute anxiety and insomnia” J Neurosci Rural Pract. 2012 May-Aug; 3(2): 212–214. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410005/
  6. OLIVIA ARANHA, et. al., “ROLE OF MITOCHONDRIA IN CIPROFLOXACIN INDUCED APOPTOSIS IN BLADDER CANCER CELLS” The Journal of Urology
Volume 167, Issue 3, Pages 1288-1294, March 2002 http://www.jurology.com/article/S0022-5347(05)65283-4/abstract
  7. Lisa Nainggolan, “Fluoroquinolones Up Risk for Severe Dysglycemia in Diabetes” Medscape Medical News, http://www.medscape.com/viewarticle/809442 Based on this article http://cid.oxfordjournals.org/content/early/2013/07/23/cid.cit439.abstract
  8. 08/15/2013 FDA Drug Safety Communication: FDA requires label changes to warn of risk for possibly permanent nerve damage from antibacterial fluoroquinolone drugs taken by mouth or by injection http://www.fda.gov/Drugs/DrugSafety/ucm365050.htm
  9. David A. Jernigan, “Lyme Toxins The Primary Cause of Your Symptoms” Townsend Letter. April, 2007. http://www.benbrew.com/lb/lyme5.pdf
  10. G. Palu, et. al., “Quinolone binding to DNA is mediated by magnesium ions” Proc. Natl. Acad. Sci. USA Vol. 89, pp. 9671-9675, October 1992 Biochemistry http://www.pnas.org/content/89/20/9671.full.pdf
  11. Mederic M. Hall, MD, Jonathan T. Finnoff, DO, Jay Smith, MD, “Musculoskeletal Complications of Fluoroquinolones: Guidelines and Precautions for Usage in the Athletic Population” 2011 by the American Academy of Physical Medicine and Rehabilitation, Vol. 3, 132-142, February 2011 http://www.levaquinadversesideeffect.com/wp-content/uploads/Documents/Hall-2011.pdf
  12. NAI-XUN CHIN AND HAROLD C. NEU, “Ciprofloxacin, a Quinolone Carboxylic Acid Compound Active Against Aerobic and Anaerobic Bacteria” ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Mar. 1984, p. 319-326, 1984, American Society for Microbiology http://www.ncbi.nlm.nih.gov/pmc/articles/PMC185508/pdf/aac00192-0027.pdf
  13. José Antonio Vázquez, et. al. “Evaluation of toxic effects of several carboxylic acids on bacterial growth by toxicodynamic modelling” Microbial Cell Factories2011,10:100 http://www.microbialcellfactories.com/content/10/1/100
  14. Urs A. Boelsterli, “Acyl Glucuronides: Mechanistic Role in Drug Toxicity?” Current Drug Metabolism (v.12, #3) p. 213-214 http://www.chemweb.com/journals/journals?type=issue&jid=13892002&iid=12003
  15. Sarah H. Elsea, et. Al, “Cytotoxicity of Quinolones toward Eukaryotic Cells: IDENTIFICATION OF TOPOISOMERASE I1 AS THE PRIMARY CELLULAR TARGET FOR THE QUINOLONE CP-115,953 IN YEAST,” The Journal of Biological Chemistry, Vol. 267, No. 19, Issue of July 5, pp. 13150-13153 http://www.jbc.org/content/267/19/13150.full.pdf+html
  16. PS Ambulkar, et. Al, “Genotoxic and cytotoxic effects of antibacterial drug, ciprofloxacin, on human lymphocytes in vitro” Nepal Med Coll J 2009; 11(3): 147-151 http://www.nmcth.edu/images/gallery/Editorial/xRZVmps_ambulkar.pdf
  17. S. Mannino, et. al., “NSAIDs, Quinolones and Convulsions: An Epidemiologic Approach” Post Marketing Survellance 1992 p. 119-128 http://213.4.18.135:48080/10.pdf
  18. HJ Xie, et. al., “Alteration of pharmacokinetics of cyclophosphamide and suppression of the cytochrome P450 genes by ciprofloxacin” Bone Marrow Transplantation (2003) 31,197–203. http://www.nature.com/bmt/journal/v31/n3/abs/1703815a.html
  19. Dean P. Jones, et. al., “Mechanisms of Pathogenesis in Drug Hepatotoxicity Putting the Stress on Mitochondria” Mol Interv. 2010 April;10(2): 98–111. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895369/
  20. Arkady B. Khodurskyand Nicholas R. Cozzarelli, “The Mechanism of Inhibition of Topoisomerase IV by Quinolone Antibacterials” October 16, 1998 The Journal of Biological Chemistry, 273, p. 27668-27677.http://www.jbc.org/content/273/42/27668.full
  21. Yi Xia, et. al., “Recent Advances in the Discovery and Development of Quinolones and Analogs As Antitumor Agents” Current Medicinal Chemistry, 1999, p. 179-194 http://books.google.com/books?hl=en&lr=&id=SJoxUN91vK4C&oi=fnd&pg=PA179#v=onepage&q&f=true
  22. V Talla and PR Veerareddy, “Oxidative Stress Induced by Fluoroquinolones on Treatment for Complicated Urinary Tract Infections in Indian Patients” J Young Pharm. 2011 Oct-Dec; 3(4): 304–309. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249743/?report=printable
  23. 2013 FDA Warning Label for Ciprofloxacin (Cipro) – http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/019537s082,020780s040lbl.pdf
  24. Patricia Kime, “New FDA warnings on Cipro may tie into Gulf War illness” Air Force Times, November 1, 2013. http://www.airforcetimes.com/article/20131101/NEWS/311010018/New-FDA-warnings-Cipro-may-tie-into-Gulf-War-illness
  25. “Postal Workers Sue Bayer Over Cipro” http://www.yourlawyer.com/articles/title/postal-workers-sue-bayer-over-cipro
  26. Lyrica Label http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021446s013s014lbl.pdf
  27. Garcia Rey-C, “The role of the pharmaceutical industry. Why aren’t new antibiotics being marketed?”  2010 Nov;28 Suppl 4:45-9. http://www.ncbi.nlm.nih.gov/pubmed/21458701
  28. Ben Comer, “Brand of the Year: Humira” PharmExec.com February 1, 2012 http://www.pharmexec.com/pharmexec/article/articleDetail.jsp?id=757392

Help Support Collective Evolution

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!

cards

Advertisement
advertisement - learn more

Awareness

My 400 Days Without Candy & What I Learned About Sugar Addiction

Published

on

At the end of 2017 I decided to temporarily say goodbye to my dietary Achilles heel.

While I’m certainly not suggesting that I am some beacon of ideal healthy eating, I have always been someone who, for the most part, makes what I’ve found to be healthy choices. Except for my one glaring weakness… candy.

In particular, the really sour and heavily sugar coated kind, but you’d be hard pressed to find me turning down even those better classified as sweet, with all of their sugar fused within the confines of the chew. Cherry Blasters, Sour Patch Kids, Fuzzy Peaches, Sour Punch Straws, you name it, I ate it, and usually with a big smile on my face.

But no matter how much my tastebuds loved this stuff, I’ve always known that it’s not good for me (I can’t imagine that there is anyone out there who actually thinks it is), so I decided to listen to my body, just as I had already done with a number of my other dietary changes. I opted to no longer ignore the stomach and headaches that would often come shortly after my sugary indulgences and give it up.

What started as a one month challenge quickly evolved into a three month challenge, followed by a one year challenge, and then a 400 day challenge simply because I liked the sound of the number. Here’s some of what I learned from this journey:

advertisement - learn more

The First Days Are Undeniably The Hardest

The old adage that it takes approximately 21 days to break a bad habit or make a new one in this case certainly held true. It was right around the 3 week point that I started to find myself far less tempted and far less frequently on the search for something to satisfy my sweet tooth. And believe it or not, the longer I went on, the less appealing the idea of eating candy became. It almost felt as if the memory in my tastebuds that had controlled so many of my past decisions had gradually faded away.

Mindset Is Everything

While I will fully admit that my quest to 400 was helped by it naturally feeding into another one of my “addictions” (a great joy in setting records and tracking analytics), I found that so much of the temptation to consume these sugary, salty and greasy foods really was incredibly temporary. Challenge yourself to at least not let it win once and you’ll likely see just how quickly its strength can fade.

It Paid Dividends

While I didn’t completely cut sugar out of my diet, as many people have so admirably done and documented about, I can say that cutting back even as much as I did felt really good for me. Some may be quick to chalk it up to the placebo effect, and understandably so, but I can honestly say that the above mentioned stomach and head aches occurred far less often over the 400 day span.

Real-Time Analysis: After The First Bite

Having now officially consumed my first piece of candy since 2017, believe it or not, it tastes different. Is it still tasty and did it satisfy me at some level? Absolutely. But it also tastes way more sugary and foreign to my body than it once did. It’s as if my body really wanted to make it clear by saying, “are you sure you want to bring this stuff back into the picture?”

Side Note: For those that are curious, since it’s the most common question I’ve been asked since embarking on this journey, the candy I chose to eat as my first piece was a Vegan Wild Cherry Belt by Squish Candies. (And no I’m not getting paid to brand-drop, and no I don’t make any commission should you choose to buy any at that link… unfortunately LOL).

Where I Go From Here

While I don’t see myself going completely cold turkey on candy again, I also cannot see myself consuming it nearly as much as I once did. And I do so happily, not out of punishment. While I’m also certainly not qualified to be giving out dietary advice, I am comfortable challenging all of you to give up something you know to not be good for you. See how your body feels both without it and after you re-introduce it.


For more brutally honest personal development content designed for those who actually want to change be sure to subscribe to my YouTube Channel and to follow me on Instagram. And to receive my free eBook on 5 Simple Daily Hacks For A Genuinely Happier Life click HERE.

Help Support Collective Evolution

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!

cards

Continue Reading

Alternative News

Big News: Costco To Become First Major Retailer To Stop Selling Roundup Herbicide?

Published

on

In Brief

  • The Facts:

    According to the non profit group Moms Across America, Costco is set to stop selling Roundup herbicide.

  • Reflect On:

    Despite the fact that harmful products continue to be approved across North America, the ultimate power to stop their use is us. When we become aware, we stop buying, and their profits drop. We are the ones that use it. Vote with your dollar.

It’s hard to even know where to start with the herbicide Roundup. Despite years of science exposing the inarguable health and environmental consequences of Roundup, federal health regulatory agencies in North America are still approving the herbicide, while multiple other countries have banned it and made its use illegal, citing various health and environmental concerns. Sri Lanka, for example, banned it five years ago due to its link to deadly kidney disease.

Furthermore, the countries approving it are doing so with massive amounts of corruption. These approvals come as a result of corrupt regulatory agencies here in Canada as well as the US, specifically the Food and Drug Administration (FDA) and the Centres for Disease Control and Prevention (CDC). The list of examples is very long when it comes to corruption and government connections to corporations like Monsanto, the corporation that created and sells Roundup. This is the only way these products get approved. It’s not science, it’s simply because of lobbying efforts and shady politics.

“It is commonly believed that Roundup is among the safest pesticides… Despite its reputation, Roundup was by far the most toxic among the herbicides and insecticides tested. This inconsistency between scientific fact and industrial claim may be attributed to huge economic interests, which have been found to falsify health risk assessments and delay health policy decisions.” – R. Mesnage (et al., Biomed Research International, Volume 2014 (2014), article ID 179691)

The latest approvals of glyphosate, the main active ingredient in Roundup, came from within Canada as well as Europe.

EU regulators recently decided to relicense glyphosate, a decision that was based on an assessment plagiarized from industry reports. It’s quite backwards that, for years, health regulators have been relying on the scientific reports from the companies that manufacture these products instead of seeking out independent scientific studies.

A group of MEPs decided to commission an investigation into claims that Germany’s Federal Institute for Risk Assessment (bFr) copy-and-pasted tracts from Monsanto studies. You can read more about that here.

advertisement - learn more

In addition, Monsanto colluded with the Environmental Protection Agency (EPA) to stifle cancer research that had any connection to their products.

The corruption is never-ending when it comes to the link between corporations and government agencies. In fact, only a few years ago, more than a dozen scientists from within the CDC put out an anonymous public statement detailing the influence corporations have on government policies. They were referred to as the Spider Papers.

Related CE Article: Robert F. Kennedy Jr. Explains How Big Pharma Completely Owns Congress

Costco

The corruption that plagues our federal regulatory agencies runs deep, and no matter how obvious the science becomes, like the dangers of Roundup, products that negatively impact our health seem to often get approved anyways. But something special on planet Earth is happening, and that’s massive awareness. We are finally starting to see through the veil that’s been blinding the masses in so many different areas within human life.

Sure, these products may continue to get approved, but we are the ones who are constantly choosing to do so. We don’t have to buy them, and that is why awareness is key.

Zen Honeycutt, the leader of Moms Across America, announced this week that Costco will not be selling the glyphosate-based weed killer Roundup Ready.

In a live video update posted on Facebook, Honeycutt stated that she received word that Costco was no longer selling Roundup or glyphosate-based herbicides.

While she’s allegedly not received any official word yet from Costco, she stated that she has talked to various people at the headquarters and regional offices confirming this news. This is huge news because, according to a 2015 article in National Geographic, Roundup is the second-best-selling herbicide in the U.S. for home lawn and garden use. Under a lucrative contract with Monsanto, Scotts Miracle-Gro owns the exclusive right to market Roundup in North America and much of Europe. Scotts distributes about $154 million worth (5.5 percent of the company’s total sales) of Roundup each year to retail giants including Amazon, Home Depot and Walmart.

So let’s hope it’s true.

I asked for an official statement and was told that usually, Costco does not issue press releases, etc discussing which items they have discontinued. Despite not hearing back from the Costco PR department, I decided to announce the information anyway. I told them that the 89,000 people who signed a petition to Costco, Home Depot, and Lowe’s deserved to have an answer. I knew that they would be happy to know that Costco was doing the right thing. – Honeycutt (source)

It’s weird how this is even a debate in some circles. This has been known for a very long time, and we’ve seen similar happenings with DDT in the past.

“Children today are sicker than they were a generation ago. From childhood cancers to autism, birth defects and asthma, a wide range of childhood diseases and disorders are on the rise. Our assessment of the latest science leaves little room for doubt; pesticides are one key driver of this sobering trend.” – October 2012 report by Pesticide Action Network North America (PANNA) (source)(source)

Glyphosate is really getting a bad name, as this new information regarding Costco is coming off the heels of some bad press for Monsanto (Bayer) as the case regarding school groundskeeper Dewayne Johnson was the first lawsuit claiming that glyphosate causes cancer to go to trial. There are thousands upon thousands of similar pending cases. Any jury that reviews all of the scientific evidence will not be able to rule in favor of Monsanto, and Johnson’s case was a great example that showed glyphosate caused his cancer.

The Takeaway

At the end of the day, it’s us who decide to use these products. Obviously, we’ve been misled and made to trust our federal regulatory agencies who are supposedly in charge of protecting us from these harmful products. It’s the complete opposite, and what these agencies do is actually quite criminal. This is why conscious media is so important. The same powers that control these corporations have a tight grip on mainstream media as well.

This is why this issue goes largely ignored, and the fact that so many people rely on mainstream media for information about what’s really happening in the world with regards to health, environment, finance, politics, etc. is why a lot of people are still completely unaware of important issues. This is also why governments have started a war on ‘fake news,’ which seems to be a cover for protecting corporate and government interests.

Help Support Collective Evolution

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!

cards

Continue Reading

Alternative News

New Study Links Acetaminophen (Tylenol) To Attention Deficit Disorder with Hyperactivity

Published

on

Another damning study indicates it is simply time to pull the plug on this outdated drug.

The study just published in JAMA Pediatrics once again indicated that women who take acetaminophen during pregnancy are more likely to have a child with attention deficit hyperactivity disorder (ADHD). The researchers also found that prenatal exposure to the medication was associated with a higher risk of having children who exhibit other emotional or behavioral symptoms.

Recent detailed analysis of clinical studies on acetaminophen (Tylenol) have concluded that this popular drug was ineffective for low back pain and provided no significant clinical relief of hip or knee osteoarthritis (OA) pain, while quadrupling the risk for liver damage.

All together, the results from all of these analyses further calls into question whether this drug should still be on the over-the-counter market or at all.

Background Data:

Acetaminophen is the only remaining member of the class of drugs known as “aniline analgesics” that is still on the market, as the rest were discontinued long ago. Acetaminophen only blocks the feelings of pain and reduces fever, it exerts no significant anti-inflammatory or therapeutic action.

advertisement - learn more

It is well-known that acetaminophen is very hard on the liver. About 40% of regular acetaminophen users show signs of liver damage. Acetaminophen reduces the liver’s store of the important detoxifying aid and antioxidant glutathione. When acetaminophen is combined with alcoholic drinks or other compounds toxic to the liver including other medications, its negative effects on the liver are multiplied. It should definitely not be used in anyone with impaired liver function and given the stress the liver experiences during pregnancy, it appears unwise to use it while carrying a child for both mother and the developing fetus.

Acetaminophen is often the drug of choice in children to relieve fever. However, use for fever in the first year of life is associated with an increase in the incidence of asthma and other allergic symptoms later in childhood. Asthma appears to be another disease process that is influenced greatly by antioxidant mechanisms. Acetaminophen severely depletes glutathione levels not only in the liver, but presumably other tissues as well, and should definitely not be used in people with asthma.

Each year acetaminophen causes over 100,000 calls to poison control centers; 50,000 emergency room visits, 26,000 hospitalizations, and more than 450 deaths from liver failure. In addition, regular use of acetaminophen is linked to a higher likelihood of Alzheimer’s disease, infertility, and hearing loss (especially in men under 50 years of age). Acetaminophen use during pregnancy has also been linked to the development of ADHD confirming animal studies showing acetaminophen use in pregnancy can disrupt normal brain development.

New Data:

To more closely assess the associations between maternal prenatal acetaminophen use and behavioral issues in their children, researchers in the United Kingdom collected and analyzed data 7,796 mothers along with their children. The data included acetaminophen use and behavioral assessments of the children were 7 years old. From this data the estimated risk ratios for behavioral problems in children after prenatal exposure to acetaminophen was determined.

The results showed that prenatal acetaminophen use at 18 and 32 weeks of pregnancy was associated with a 42% increased risk of the child having conduct problems and hyperactivity symptoms, while maternal acetaminophen use at 32 weeks was also associated with a 29% increased risk of the child having emotional symptoms and a 46% increase in total behavioral difficulties.

Obviously, the researchers concluded “Children exposed to acetaminophen prenatally are at increased risk of multiple behavioral difficulties, and the associations do not appear to be explained by unmeasured behavioral or social factors linked to acetaminophen use.”

Comment:

The results from this study and others are clear. Stay away from acetaminophen. Most people consider acetaminophen (e.g., Tylenol) as being an extremely safe pain reliever for both children and adults. The reality is that it can be extremely dangerous and causes significant side effects. The FDA has done a poor job alerting the public to the dangers of acetaminophen. In my opinion, it is a drug that serves no real medical purpose in the 21stcentury. Bottom line, it is time to pull it from the market.

As far as alternatives to acetaminophen during pregnancy, I would recommend ginger. Historically, the majority of complaints for which ginger (Zingiber officinale) was used concerned the gastrointestinal system as well as pain and inflammation. Several double-blind studies have shown ginger to yield positive results in a variety of gastrointestinal issues, especially those related to nausea and vomiting including severe morning sickness. In regards to pain and inflammation, dozens of clinical studies have supported this use with positive results in various forms of arthritis, chronic low back pain, muscle pain, and painful menstruation.

Ginger powder, ginger tea or a shot of fresh ginger juice added to any fresh fruit or vegetable juice is certainly a much better option to acetaminophen anytime, but especially during pregnancy.

My overall interpretation of the study is that depletion of glutathione caused by acetaminophen leaves cells, especially brain cells, susceptible to damage. I believe that future studies will not only show more evidence of a link to ADHD, but also autism as well. Glutathione is absolutely critical in protecting cellular function. Any factor that depletes glutathione is obviously going to alter proper development. In addition to acetaminophen, the following factors can deplete glutathione:

To boost your glutathione level it is important to focus on a diet rich in colorful fruits and vegetables. Their rich source of antioxidant phytochemicals and nutrients spare the use of glutathione and help to keep cellular levels high.

For additional related research use the following links: 


If you want to learn more from Greenmedinfo, sign up for their newsletter here


Reference

Stergiakouli E, Thapar A, Smith GD. Association of Acetaminophen Use During Pregnancy with Behavioral Problems in Childhood. Evidence Against Confounding. JAMA Pediatrics. Published online August 15, 2016. doi:10.1001/jamapediatrics.2016.1775


Dr. Murray is one of the world’s leading authorities on natural medicine. He has published over 40 books featuring natural approaches to health. His research into the health benefits of proper nutrition is the foundation for a best-selling line of dietary supplements from Natural Factors, where he is Director of Product Development. He is a graduate, former faculty member, and serves on the Board of Regents of Bastyr University in Seattle, Washington. Please Click Here to receive a Free 5 Interview Collection from Dr Murray’s Natural Medicine Summit with the Top Leaders in the Field of Natural Medicine. Sign up for his newsletter and receive a free copy of his book on Stress, Anxiety and Insomnia.

Help Support Collective Evolution

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!

cards

Continue Reading
advertisement - learn more
advertisement - learn more

Video

CETV

 

The all-new CETV brings together the leading voices in the truth and consciousness realm to a single platform for the first time ever. 

Thanks, you're keeping conscious media alive.