Podcasts about big pharm

Można Pięknie Żyć *---Witaj! "Można Pięknie Żyć*" to seria podcastów, w której odkrywamy, jak zmiany w stylu życia mogą poprawić nasze zdrowie metaboliczne. Skupiamy się na Terapeutycznym Ograniczaniu Węglowodanów i jego pozytywnym wpływie na metabolizm oraz ogólne samopoczucie. Pamiętaj, że zdrowie zaczyna się od wiedzy, a my jesteśmy tu, aby dostarczać Ci inspirację i praktyczne wskazówki na drodze do pięknego życia. Zaczynamy!

HE CAN RUN BUT HE CAN'T HIDE A report in the Wall Street Journal that quotes multiple government officials who witnessed Joe Biden's mental struggles during meetings with him should have people asking, not if he should run, but if he should be expected to be President four years from now.   Adam Andrzejewski, CEO/Founder of OpentheBooks.com has his usual amazing numbers. This time to show how much money Big Pharm paid in royalties for vaccines developed at Dr. Anthony Fauci's NIH.  Hans von Spakovsky of the Heritage Foundation says the Trump verdict means we're on the way to becoming  Venezuela.See omnystudio.com/listener for privacy information.

Do you truly understand the mRNA technology that is being used by the Big Pharm groups? Do we really want government to pretend to protect us from all things? A must hear discussion from a guy who has spent a career as a lobbyist.

Do you know who is actually fighting for your health? Do you think the insurance companies and BIG PHARM are really concerned about your health? You are going to meet one of the people who want people to be healthy. Dr. Robert Seik is on his grind to cuts costs and get Americans to a healthier state of life. www.twc.health/pbnGet your Medical Emergency Kit with 5 antibiotics, Ivermectin and much more! www.prepperbroadcasting.com

Sen Ed Markey submits a bill to revamp SCOTUS. Justice Alito's exposed as corrupt. Big Pharm consortium sues Biden for negotiating for lower drug prices. We pay for billionaires' submersible vacation. --- Send in a voice message: https://podcasters.spotify.com/pod/show/politicsdoneright/message Support this podcast: https://podcasters.spotify.com/pod/show/politicsdoneright/support

Author Stephen Steele continues the epic adventures of botanist and broke rancher Cyd Seeley and her partner, recovering drug addict Dr. Alex Farmer, in The Organ Grinder Factor, Book two in Steele's action suspense thriller trilogy, The Trouble with Miracles. Drawing upon real-world events, The Organ Grinder Factor takes readers from the unspeakable horrors of child slavery in Africa to today's turmoil in the Middle East. As the story begins, Alex and Cyd are in desperate search of a place to safely grow their Cannastar, a miracle cure for viruses that Big Pharm has made illegal. They shipwreck off the west coast of Africa and wash ashore in the drug and war-torn nation of Guinea-Bissau. Forced to flee for their lives, they arrive in Senegal where they become involved in the country's real-life child slavery problem and are nearly killed for their efforts. They find refuge in Israel where they meet the inventor of the Organ Grinder, a 3D printer that replaces damaged internal organs without the need for surgery. “This is not that far-fetched,” Steele said during an interview. “Scientists have already been able to replicate human tissue with a 3D printer.” In the book, the experimental research is funded by a ruthless billionaire with a secret past who becomes Cyd and Alex's investor in a vast new Cannastar plantation. But while living in Israel, Cyd is badly wounded in a rocket attack. Her only chance of survival is the Organ Grinder — which has never been tested on a human being. The Organ Grinder Factor is the action-filled follow-up to Steele's The Cannastar Factor, which introduced readers to Cyd and Alex and traced their desperate quest to grow Cannastar. Book Three in the series, The Trouble with Miracles, has just been released and tells the story of a desperate race to keep the discovery of the ancient secret to fusion energy out of the wrong hands in an adventure that ranges from Chile's high northern desert to the magic of Easter Island and its mysterious statues. About the Author Stephen Steele is a graduate of the University of North Texas with degrees in English literature and marketing. An avid sailor, swimmer and mountain biker, the author worked as a salesman, syndicator of television sports shows, builder and developer, ski instructor and cowboy. He lives in Montana in an 1800s Victorian home with his ruthless editor, Beverly. For more information, please visit www.stephensteelebooks.com, or follow the author on the following social media sites: Twitter: @StephenSteeleMT; Instagram: stephensteelebooks; Facebook: Stephen Steele – Author. The Organ Grinder Factor Publisher: Speaking Volumes ISBN-10: ‎ 1645405583 ISBN-13: ‎ 978-1645405580 Available from Amazon.com and Barnesandnoble.com About the show: Ash Brown is a gifted American producer, blogger, speaker, media personality and event emcee. The blog on AshSaidit.com showcases exclusive event invites, product reviews and so much more. Her motivational podcast "The Ash Said It Show" is available on major media platforms such as iTunes, Spotify, iHeart Radio & Google Podcasts. This program has over half a million streams worldwide. She uses these mediums to motivate & encourage her audience in the most powerful way. She keeps it real! ► Luxury Women Handbag Discounts: https://www.theofficialathena.... ► Become an Equus Coach®: https://equuscoach.com/?rfsn=7... ► For $5 in ride credit, download the Lyft app using my referral link: https://www.lyft.com/ici/ASH58... ► Review Us: https://itunes.apple.com/us/po... ► Subscribe: http://www.youtube.com/c/AshSa... ► Instagram: https://www.instagram.com/1lov... ► Facebook: https://www.facebook.com/ashsa... ► Twitter: https://twitter.com/1loveAsh ► Blog: http://www.ashsaidit.com/blog #atlanta #ashsaidit #theashsaiditshow #ashblogsit #ashsaidit®

Watch your head, it's about the hit the DEBT CEILING! We are 90 seconds to DOOMSDAY, according to a shame organization. Some Forest kooks are upset about a new Fun Squad training facility. People are smuggling food into the US. Big Pharm is trying to sell the first world vaccines for third world deseases. Trump and Desantis are looking to faceoff. and Russia must lose the war, OR ELSE! PLEASE CONSIDER DONATING ON PAYPAL! WE NEED YOUR SUPPORT TO KEEP GOING Huge Thanks to our Fiat Fun Coupon gifting Producers: D.O.F. (Canadian Dept. of Oceans and Fisheries) Hempress Emily M.   These fine folks found our donation link!We are also on Cashapp, $mmoshow, and Venmo @mmoshow. Thank you to all Boosters, both Live and Post: The Lovely Dame Boolysteed SirPaulieBravo Darren O'Neill The Booky Dame Trail Chicken Dirty Jersey Whore Darren O'Neill ChrisLAS SIRVO Don Mills MakeHeroism Mary Kate Ultra Lavish Phifer Boo-bury Billybon3s SeeDubs This Fed Free group sent in boosts, which are little bits of bitcoin donation, which allows for comments as well. These are read live on the show! For more information on boostagrams, Check out this post. Prove you're not a fed by donating to mmo.show/donate!   Thank you to providers of Content: Sirvo, helped code the Fed Buster Satoshi to USD python script! o7   Still listening on Apple Podcasts or Spotify? Gross. Get yourself a better and more masculine podcast app at NewPodcastApps.com Prove you're not a fed by donating to mmo.show/donate!   Runner Up Titles for Episode 55: Wet Mouth Guttural Noises Brand Safe Republicans Cop City Pig Pen Hen Cosplay Fun Squad   Cover your ears when you hear the Brown Note and Stay Frosty!   C U Next Tuesday!  

THE THESIS: If China stopped making drugs for America, this Nation would collapse in a Month or two. THE SCRIPTURE & SCRIPTURAL RESOURCES: Sometimes, God does not remove the thorn, He gives us His Grace and reminds us it is enough. That is so difficult when the pain is intense and so edifying when we learn to let God's Grace work.What Was Paul's Thorn in the Flesh? (2 Corinthians 12)THE NEWS & COMMENT:I fully believe Tony Fauci is a psychopath or sociopath, I know he is a spiritual captive. So much evil has been done through him. Now, the man who never once said in his thousands of TV interviews he had memory issues suddenly says he can't remember much . . . Fauci Could Not Recall Key Details During Deposition: Louisiana Attorney General. . . when he pretended his didn't pay attention to the Great Barrington Declaration, he was obviously lying under oath, but he's a career liar and left wiggle room he can slither through. How do I know he lied? Because he used our money to try to ruin the doctors and scientists who founded The Great Barrington Declaration. What does that say about who owns America?Speaking of our money:Biden's National Science Foundation Has Pumped Nearly $40 Million Into Social Media Censorship Grants and Contracts. . . The Party that gave your money to Big Pharma to make the mRNA clot shots, then spent at least $40 million to make sure Pharma got to lie with few challenges. Even as he retires in his blood money, Fauci keep letting himself be used for lies:[AUDIO] - Fauci: "When we're gathering at a family gathering for Thanksgiving, it makes sense that you might want to get a test before you come into a place where you could be infected and spread it."Who owns America? Is it the same groups that own Canada?[AUDIO] - “Unvaccinated patients have a mental problem and should be put on psychiatric medications.”PhD's in math, data analysis, systems analysis, people demonstrably gifted by God with intelligence to discern truth from lies are, to “doctor” Jha “random dudes on Twitter.” For whom is he speaking? [AUDIO] - “Dr”. Jha: "The real leaders of American medicine are out there telling you that you need to go get a vaccine. You can decide to trust America's physicians or you can trust some random dude on Twitter."I pray God will reveal to President Trump the truth about these injections. [AUDIO] - Trump STILL defends Big Pharma and the so-called Covid “vaccines …”This woman pretends lockdowns and masking just happened, no one is to blame. She also makes believe Mike Pompeo called all teachers filth. This is the same woman whose colleagues are installing Pharma outlets in schools. Who owns America?[AUDIO] - Boss/Head Capo of teacher's union Randi Weingarten: Teachers “have been dealing with all the anxieties & the aftershocks & aftereffects of Covid for children, including the mental health crises.”Who owns America? Well, what would happen if China, which makes most of these addictive drugs decided to stop?Steve writes:Hi Todd,I'm a long time radio fan who was very disappointed when they talked you into the FM Show. I want to disagree with you on something because I think you are falling for the Big Pharm's hype on it and not understanding how it actually works. I'm talking about the whole Serotonin controversy. When I became clinically depressed I actually didn't believe it was a real thing. I really thought it was most likely a bunch of whiners making excuses for never getting off of their backsides and doing anything. Not terribly compassionate on my part but I got my comeuppance. I started feeling down all of the time and became almost completely unable to sleep so I naturally turned to alcohol as a sleep aid. Two years of that took away my ability to stop drinking, so I had to quit that entirely which just left me not sleeping and feeling even worse. I went to a counselor and very sheepishly said that I might be kinda sorta possibly maybe a little depressed. He agreed and we had six months of therapy that hadn't budged my mood a half inch before he sent me to a psychiatrist for some “real help” as he called it. The white-haired veteran shrink that he sent me to was fabulous. He asked great questions and listened intently and we started on some medication. He told me right up front that prescribing anti-depressants is “pseudoscience” because there are no tests that will tell us what will help, only trial and error informed by his years of experience. You ramp up on each one slowly, and if it doesn't work you ramp back down and do it again with another one. It takes patience.What I think you're missing is that to this day I have no idea if serotonin had anything at all to do with the cause of my depression, but I do know that boosting it up had a lot to do with making it possible for me to live with it while I continued the “talk therapy” that was actually working on the root causes. It took eight years before I started to emerge from the fog, and I seriously doubt I would have let it go on anywhere near that long without the boost I got from the two anti-depressants that I ended up taking. Over the years we tried at least ten, but we didn't stick with most of them because there wasn't any significant benefit. Thanks to my years in sobriety groups I know lots of people who have experienced severe depression and I don't know a single one who would ever use the word “cure” in connection with any medication. They don't cure anything, they just lessen the worst of the horrible feelings so that you can tolerate them while you do the really long term part and get some help figuring out what part of your life is triggering the issue. I never became suicidal, and I don't believe in suicide at all, but I did worry about it because I could foresee that at some point the depression and insomnia would very likely break me.When you respond to the hype that drugs can cure depression, you're really falling for the marketing campaign. Also don't ever let anyone you know get meds from their general practitioner. There are hundreds of different, very narrowly focused medications with subtle differences and your average GP has experience with maybe a half dozen that he gives out like chiclets to any patient that might be somewhat depressed. You don't trust your GP to do brain surgery and you absolutely don't go to him for depression. “Ask your doctor about Symbalta” is pure marketing and nothing else. I'm sure it boosts sales right through the roof as a bunch of people in need of a subtle and accurate touch get something that they don't need prescribed by someone who really doesn't have any idea what they are doing.I do believe that there is an organic component of serious depression, something drops below the point where you have the ability to snap yourself out of it. You might ask if I ever prayed to be cured of it, and the answer to that would be no. The insidious part of depression is that there is nothing a depressed person likes to do more than review the times they have failed to live up to their own standards. The simple fact is that when we're in it we believe we deserve all of the misery.So, while I don't disagree that they are over-prescribed and very often mis-prescribed, I think you do a grave disservice to a lot of folks when you completely dismiss them.

Catherine Shanahan, M.D. and Jack Murphy Live. Dr. Cate and Jack discuss: - How big Ag, Big Pharm, and Big Education conspire to keep us fat, sick, and dumb - How food and environment effect your epigenetics and could be creating a separate nutritional class in America - The impact of your food choices on your children and DNA - Is Autism caused by seed oils? - Deep Nutrition - Fat Burn Fix Catherine Shanahan, M.D is a board-certified family physician. She trained in biochemistry and genetics at Cornell University before attending Robert Wood Johnson Medical School. She practiced medicine in Hawaii for a decade, where she studied ethnobotany, as well as the culinary habits of her healthiest patients. Her books include Deep Nutrition and The Fat Burn Fix. She currently runs a metabolic health clinic in Denver, Colorado and serves as the Director of the Los Angeles Lakers PRO Nutrition Program. Jack Murphy's Book, "Democrat To Deplorable," Now Available On Audiobook: https://adbl.co/3qXvlEY​​​​​​​​​​​​​​​​​​​​​​​​ Liminal Order: https://www.liminal-order.com Follow Jack Murphy: Twitter: https://twitter.com/jackmurphylive Instagram: https://www.instagram.com/jackmurphylive/ Minds: https://www.minds.com/jackmurphylive/  

Speaking with the astute Dr Sarah Myhill whose experience as a British medical doctor led her to what works in chronic illness: naturopathic medicine.  And no vaccines to poison us. Getting to the root of the problem. Her belief in the power of naturopathic medicine led her to deregister from the UK's General Medical Council and register with the Association of Naturopathic Practitioners.Medical Director of UK Medical Freedom AlliancePatron of ANP (Association of Naturopathic Practitioners)  Clinical Director of the College of Naturopathic Medicine https://www.drmyhill.co.uk/  - over 20 million hits to date.  BIO: Dr Myhill qualified from the Middlesex Hospital Medical School, London, Honours viva, 1981. She worked for 20 years as an NHS GP before moving to Independent Medical Practice with a special interest in CFS/ME. She practices Ecological Medicine – diagnosing mechanisms if disease which have obvious implications for management. She has been an active member of the BSEM since 1986 Hon Meetings Secretary (1993–1998) including  5 day International Conference “Sustainable Medicine” at Christ Church College Oxford, Hon Secretary 1999 -2007.  Lectures regularly to doctors and health professionals who are interested in Ecological Medicine.  Author of award winning books: “Chronic Fatigue Syndrome - it's mitochondria not hypochondria” BMA Prize Highly Commended 2014. Second edition 2017 (5 reprints)“Sustainable Medicine” (Beryl Bainbridge Prize 2016).“Diabetes” (Beryl Bainbridge Prize 2017)“The PK Cookbook” 2017, now updated to “Paleo-ketogenic - the why and the how – just what this doctor ordered”“The Infection Game” 2018, updated 2018“Ecological Medicine – the antidote to Big Pharm and fast food” 202) https://drmyhill.co.uk/wiki/My_book_Ecological_Medicine_-_The_Antidote_to_Big_Pharma_and_Fast_Foods“The Energy Equation – From the Naked Ape to the Knackered Ape” “Green Mother – Families Fit for the Future”  In the pipeline “The Underactive Thyroid – do it yourself because your doctor won't” She has made media appearances in Newsnight (silicone implants), Dispatches (BSE and organophosphate poisoning), Woman's hour (silicone breast implants, allergies), Esther Rantzen show (Chronic Fatigue Syndrome), Watchdog Healthcheck (silicone implants) as well as many Welsh TV programmes and local radio in UK and abroad.Lecturer to What Doctors Don't Tell You, BANT (British Association of Nutritional Therapists), BSEM,  ANP (Association of Naturopathic Practitioners)  and othersCo-author of three papers on CFS and mitochondrial function:·      http://www.ijcem.com/files/IJCEM812001.pdf ·     www.ijcem.com/files/IJCEM1204005.pdf  ·     http://www.ijcem.com/files/IJCEM1207003.pdf Everyone should know Dr Myhill, one of the good ones, one of the best.Counting down to weeks away to the publication of Transforming Trauma, a drugless and creative path to healing PTS and ACE.  I am again seeing patients and planning groups and retreats. Please email drheatherh@icloud.com for more info. Website: drheatherherington.com Support the show

"Welp This Is It!" Welcome back!! As always we start this pod off with a mental and spiritual check in then, we get in to Lil Meech's jail time plus his $1.4 million bail. We discuss red flags before going on a date, after a women was told to walk home from a date after she refused to go back to the guy's house. We talk this heat and musty people, the Pharmaceutical industry and you already know so much more to unpack! So lets't unpack it. Look for new episodes every Tuesday til then we'll holla! Thanks for tuning in to this week's episode we hope you enjoy! *Follow Us On The Socials* Tik-Tok - WelpThisIsItPod Instagram - thisisitpod *Follow Lahi* Twitter - NinawitTheNina --- Send in a voice message: https://anchor.fm/wwwwelpthisisitcom/message

Discussion of big pharmaceutical companies/medications vs our own mental health. "Taking Control" of your body & your mind for a better version of yourself. Listening to yourself & finding the best options for your mind, body & soul in a world pushing medications. (with special guest Brandi)Sponsor: The Healing Haus Co. (www.thehealinghausco.org)Discount Code: LITTLEBIT for 10% offThe Healing Haus Co: hand crafted wellness products, specifically their best selling Liquid Zanny, which helps with stress & anxiety relief during the day without making you sleepy. Liquid Zanny can be used on the bottom of your right big toe (Reflexology).

Vegetarians have 14% lower cancer risk than meat-eaters, study finds   Oxford University, February 24, 2022   Vegetarians have a 14% lower chance of developing cancer than carnivores, according to a large study that links meat-eating to a heightened risk of the disease. A team of researchers from Oxford University analysed data on more than 470,000 Britons and found that pescatarians had a 10% reduced risk. Compared with people who eat meat regularly – defined as more than five times a week – those who consumed small amounts had a 2% lower risk of developing cancer, the study found.   (NEXT)   Dietary Lutein Modulates Growth and Survival Genes in Prostate Cancer Cells   Indiana University School of Medicine, February 26, 2022   Reports from Indiana University School of Medicine Provide New Insights that Dietary Lutein Modulates Growth and Survival Genes in Prostate Cancer Cells) According to news originating from Indianapolis, Indiana, research stated, "Lutein is a carotenoid pigment present in fruits and vegetables that has anti-inflammatory and antitumor properties. In this study, we examined the effect of lutein on proliferation and survival-associated genes in prostate cancer (PC-3) cells." Our news journalists obtained a quote from the research from the Indiana University School of Medicine, "We found that in vitro culture of PC-3 cells with lutein induced mild decrease in proliferation that improved in combination treatment with peroxisome proliferator-activated receptor gamma (PPAR gamma) agonists and other chemotherapeutic agents. Flow cytometry analyses showed that lutein improved drug-induced cell cycle arrest and apoptosis in prostate cancer. Gene array and quantitative reverse transcription-polymerase chain reaction analyses showed that lutein altered the expression of growth and apoptosis-associated biomarker genes in PC-3 cells."   (NEXT)   Walnuts may support sperm health, according to new animal research   University of Delaware, Feb. 28, 2022    New animal research suggests eating a walnut-enriched diet may improve sperm quality by reducing lipid peroxidation, a process that can damage sperm cells. This form of cell damage harms sperm membranes, which are primarily made up of polyunsaturated fatty acids (PUFAs). Walnuts are the only tree nut that are predominantly comprised of PUFAs (one ounce contains 13 grams of PUFAs out of 18 grams of total fat). Research on the health benefits of PUFAs has advanced and most recently the 2015-2020 Dietary Guidelines for Americans has emphasized this type of fat as a replacement for saturated fats. As this is an animal study, there is no direct correlation to processes that occur in the human body. However, the findings support previous research suggesting that walnuts provide key nutrients that may be essential for sperm function.   (NEXT)   Broccoli and kale microgreens pack a nutritional punch that varies with growing conditions   American Chemical Society, February 15, 2022   Although microgreens were initially gourmet ingredients for upscale restaurants, they've become popular among gardeners and home cooks. Despite their “superfood” label, the levels of healthful compounds, such as phytonutrients, in most varieties of microgreens are unknown. Researchers in ACS Food Science & Technology now report that kale and broccoli microgreens grown in either windowsills or under commercial growing conditions are rich in phytonutrients, though the levels of some compounds varied considerably between the two environments.   (NEXT)   Sugar's molecular link to Alzheimer's: Study   University of Bath (UK), February 25, 2022   A "tipping point" molecular link between the blood sugar glucose and Alzheimer's disease has been established by scientists for the first time, who have shown that excess glucose damages a vital enzyme involved with inflammation response to the early stages of Alzheimer's. Abnormally high blood sugar levels, or hyperglycaemia, is well-known as a characteristic of diabetes and obesity, but its link to Alzheimer's disease is less familiar. Scientists already knew that glucose and its break-down products can damage proteins in cells via a reaction called glycation but the specific molecular link between glucose and Alzheimer's was not understood. But now scientists from the University of Bath Departments of Biology and Biochemistry, Chemistry and Pharmacy and Pharmacology, have unraveled that link.   (RFK)   Adam Nagourney's recent effort to cancel and condemn Robert Kennedy Jr. has registered another low in the New York Times' registry of crank tabloid journalism.  Americans' trust in our media is already at an all time low, down to 21 percent last year, and the lowest in the world. The Times' propensity for fake reporting undoubtedly has contributed to American journalism's steady decline. So if a journalist is clueless about the individual he is writing about, what better weapon to employ than Robert's own family members and friends?  Fortunately Nagourney's article is just a rambling, incoherent diatribe recycling earlier Times hit pieces by Roni Rabin and Robert's niece Dr. Kerry Kennedy Meltzer. Its message is that Robert has turned his life away from being a conscientious advocate for the environment and jumped on the conspiratorial bandwagon. However, there are glaring flaws in Nagourney's reasoning that his apparent ignorance about the subject matter would account for. Nowhere does Nagourney mention Robert's international bestselling book The Real Anthony Fauci, which has caused such a stir worldwide. Did the author bother to read the book?  Highly doubtful. Nagourney's writing seemingly focuses on Hollywood and LBGT issues.  Evidently he is not the ideal journalist for the Times' editorial management to assign an article that otherwise requires many years of research into our nation's federal health system and reams of legal documents and peer-reviewed studies about vaccine efficacy and safety. Robert is publicly on record inviting anyone who wishes to debate and challenge his book's content and the over 2,100 references supporting its claims. Would any of the Times' journalists, who hide behind their quills, have the courage to accept his invitation? To our knowledge nobody from the mainstream media has taken up Robert's offer. We might challenge the Times' editorial management to unearth a single instant where Robert has stated he was not pro-vaccine.  If the Times is so worried about Kennedy being on the wrong side of history and science, then why not review The Real Anthony Fauci with reliable, independent fact checkers to debunk any misstatements and untruths? The fact that the Times and the mainstream media have in unison ignored the book entirely, hoping it will fade away into obscurity, is itself gross negligence. Even Fauci and Bill Gates have failed to satisfactorily make a concerted effort to exonerate themselves from the book's damning evidence. If the Times' fraudulent charge is guilt by association, then yes indeed Robert has a fan base among tens of thousands of anti-vaccination parents across the nation with vaccine-damaged children. But this follows the kind of illogic that Bill Clinton, Bill Gates and Allen Dershowitz should be behind bars for their fellowship with Jeffrey Epstein. Repeatedly, Robert is very succinct about being pro-vaccine and he has reason to be very worried about the credibility of vaccine makers' clinical trial data and the deep conflicts of interest between the drug industry and federal regulators who are too willing and eager to give their Big Pharm masters a green light to licensure. That Nagnourney would resurrect the old vaccine-autism chestnut is to be expected of any hit person assigned to target an anti-vaxxer. Yet there is very sound evidence to support Robert's stance on the vaccine-autism debate. We may recall that it was Robert who filed the Freedom of Information request to uncover the smoking gun behind a CDC study showing that there was indeed a relationship between earlier thimerosal (mercury)-laced vaccines and neurological disorders, including autism. The evidence is clearly outlined in the transcript of a 2000 secret meeting held at the Simpsonwood retreat facility outside CDC headquarters in Atlanta.  During the meeting, the study's chief scientist, Dr. Thomas Verstraeten, stated, “This analysis suggests that in our study population, the risks of tics, ADD, language and speech delays, and developmental delays in general may be increased by exposures to mercury from thimerosal-containing vaccines during the first six months of life.”  The clandestine Simpsonwood gathering decided to withhold its findings from the public and, instead, proceed with a recalculation of the same data by employing confounders, or biased criteria selection in order to confirm the CDC's desired results. Later a House Committee on Government Reform's three-year review of the CDC's and FDA's handling of the exponential rise in autism concluded that “It appears that many who participated in the thimerosal debates allowed their standards to be dictated by their desire to disprove an unpleasant theory.” Dr Roger Bernier confirmed a deep concern Robert has been sounding for years to the mainstream media's plugged ears. During the Committee hearings, Dr. Bernier, who was then the CDC's associate director of science, stated, “It [removing thimerosal from vaccines] could entail financial losses of inventory if current vaccine inventory is wasted. It could harm one or more manufacturers and may then decrease the number of suppliers… The evidence justifying this kind of abrupt policy change [immediate removal of mercury from all vaccines] does not appear to exist, and it could entail financial losses for all existing stocks of vaccines that contain thimerosal.” In other words, for the CDC, then as now, protecting pharmaceutical interests and money trump public health and well-being. The Real Anthony Fauci is riddled with similar examples of financial incentives driving health policies directly under Fauci's control. Finally, the Commission recommended that “studies be conducted that pool the results of independent research that has been done thus far, and a comprehensive approach should be developed to rid humans, animals and the environment from this dangerous toxin.” Yet unsurprisingly a subsequent CDC study, after several attempts to massage the original data, was published to deny any relationship between vaccination and autism. This remains the position of the CDC, FDA and HHS despite a large body of independent research, with no conflict of interests with governmental and private industry interests, continues to mount against our policy makers' reliance on tabloid science. Separate from Robert, cases have been adjudicated through the Justice Department to award monetary compensation to victims of vaccine-related autism and encephalitis. However, most dramatic is the whistleblower case of Dr. William Thompson, a senior CDC epidemiologist. Dr. Thompson released thousands of documents to Prof. Brian Hooker, a biologist at Simpson University, providing evidence that the CDC under Julie Gerberding's watch, withheld and later destroyed research data proving the MMR vaccine contributed to higher autism rates in African American boys The documents also proved the CDC has known for years that the influenza vaccines, which still contain mercury, contributed to neurological tics and disorders. If we can easily find these references, certainly it is within the Times' capability to do so also. We should lend an attentive ear to Robert's Covid vaccine warnings because on many occasions in the past he has been on the correct side of history. Perhaps Nagourney's conflating the safety profiles between the experimental mRNA and adenovirus vector Covid injections from traditional pre-Covid vaccines. For example, Robert was a lead attorney in the historic ruling against Monsanto and its carcinogenic glyphosate herbicide or Roundup. The latest legal update is that Monsanto has settled nearly 100,000 lawsuits and paid out $11 billion. Another 26,000 cases remain pending. Throughout his law career Robert has been involved in hundreds of legal cases to protect the environment such as New York City's watershed; enforcement of the Clean Water Act; protecting poor minority, indigenous communities, and military personnel from corporate and federal toxic pollution; and legal victories against the oil, hydrofracking, pipeline and nuclear power industries. Last year, Robert's Children's Health Defense (CHD) won a US Court of Appeals case against the Federal Communications Commission for the agency's failure to review the health and safety guidelines on 5G and other wireless technology. In 2019, 26,000 scientists submitted a petition to the UN, World Health Organization, European Union and world governments demanding a halt to a 5G rollout. There are over 10,000 peer-reviewed studies now warranting global caution about radio frequency radiation's adverse effects to the environment and human DNA, the endocrine system and various organs. Undoubtedly the CHD case unsettled the New York Times; it may be a reason among others for the newspaper to print vindictive articles against Robert. Following the Times' partnership with the telecom giant Verizon to launch a 5G Journalism Lab, the paper's 5G coverage has consistently parroted the telecom industry's talking points. The Verizon collaboration will provide the newspaper with a jump start ahead of other mainstream media to gain “early access the 5G network.” Nor should we forget that the Times' top shareholder is Mexican billionaire and mobile phone magnate Carlos Slim, who is positioned to rake in billions from 5G's rollout south of the border. We might ask why Robert would risk tarnishing the Kennedy legacy, which his siblings seem determined to keep pristine? Quite simply, like his father and uncle, Bobby is a rebel at heart who seeks the truth rather than to preserve a family legacy or bureaucratic ideology. As for the New York Times, on matters of critical domestic and international importance, it has repeatedly proven to be unreliable. This is the same Times, despite its enormous resources and government contacts that has gotten its stories wrong at the cost of countless lives. It got the story of Iraq's weapons of mass destruction reprehensibly wrong, which led to one of the greatest debacles in foreign policy in this century. It got Libya, Venezuela, and Syria wrong. It was wrong about the Obama-Clinton backed coup spearheaded by Hillary sidekick Victoria Nuland.  And to this day the Times has failed to hold the US's co-responsibility for prolonging the Saudis' genocide in Yemen. And the Gray Lady refuses to cover other nations' success stories in their handling the pandemic, including prescribing repurposed inexpensive drugs such as ivermectin which has reduced SARS-2 infections and deaths dramatically. Had Nagourney, Rabin and Robert's siblings and friends spent thousands of hours doing meticulous research to uncover the truth, it would be less likely they would have proceeded in advancing their shared conspiratorial delusions. In the absence of any observable scientific background, to denigrate Robert with personal biases and dogmatic assumptions is disingenuous. Certainly he has spent more time investigating the corruption endemic in our federal health system than anyone in the history of the New York Times. So at what point do the Fed's junk science, misdemeanors, and perjury before Congress pile up to a tipping point whereby nothing coming our health agencies can be taken at their word?  Robert evidently passed that threshold long before the rest of us. As we witness our federal health officials back pedaling or abandoning their own health advice, rewrite scientific analyses, rapidly fund compromised research institutes in order to debunk the next damning study about the inefficacy of masks, social distancing and the Covid vaccines' adverse effects and mandates, we are observing a health system in dismal disarray. Improvising on a meditation by the Trappist monk Thomas Merton, who had carried on a correspondence with Robert's mother Ethel, Times' journalists such as Nagourney and Rabin are like people who wander the countryside painting billboards that say “The CDC Saves” or “Prepare to Meet God (Anthony Fauci).”  Oddly, these biased opinion essays should not make us think about the CDC nor Fauci. Rather we should wonder what goes on in these writers' minds. Absent any journalist integrity, we should wonder what their motives are to force THEIR CDC and Fauci upon us by way of condemning the critics of the government's failed Covid pandemic policies. Or rather should we pity these journalists' scorn and vitriol as simply pathetic projections of themselves?

This episode is about Nicki Minaj's and Drake Beef with Big Pharm right now. Nicki just shot back taking a stand against the vaccine. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/war/support

A certain Friendo decides to do this episode in the nude as they discuss what it would take to sell their souls to Joe Biden and Big Pharm. They also get ready for the NBA Playoffs and discuss YOUR MIAMI HEAT's chances at repeating as Eastern Conference Champions. Also, we are introduced to a series of riveting new games, one of them being, This Or That. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

The FDA, Shock Troops for the Pharmaceutical Industrial Complex   Richard Gale and Gary Null PhD Progressive Radio Network, May 17, 2021     As of this week, over 194 million doses of the Covid-19 vaccines have been administered in the US. Consequently, a growing majority of Americans are delighted that life may return to normal because most believe they are now protected from infection. Clearly that is not the case. Bill Maher tested positive for Covid last week and had to cancel his television show for his first time since 1993. This was despite Maher having been fully vaccinated. Moreover the vaccines’ serious adverse effects are being downplayed by health officials and the media. Who will experience an adverse effect appears to be arbitrary; therefore, it is a game of Russian Roulette as to whether a person will be critically injured or be protected from the virus. One of the world’s most accomplished rock guitar musicians Eric Clapton received both doses of AstraZeneca’s Covid vaccine and had such severe reactions he feared he might never play the guitar again.  Clapton posted a message:   “About six weeks later [after receiving the first shot] I was offered and took the second AZ shot, but with a little more knowledge of the dangers. Needless to say the reactions were disastrous, my hands and feet were either frozen, numb or burning, and pretty much useless for two weeks, I feared I would never play again, (I suffer with peripheral neuropathy and should never have gone near the needle.) But the propaganda said the vaccine was safe for everyone.”   However it is not simply a miniscule few who are suffering undesirable Covid-vaccine events such as blood clots and other cardiovascular complications, anaphylaxis, severe allergic reactions, various neuropathies, abnormal menstrual bleeding and suspected miscarriages, extreme muscle weakness, fatigue, etc.  If this were the case, an argument could be made for siding with benefits over risks. Covid vaccines have only been administered for less than six months, and it is becoming increasingly clear that the risks may outweigh the benefits. Suspected numbers of miscarriages following Covid vaccines is especially worrisome. A government study published in the New England Journal of Medicine attempted to analyze and downplay the risk. Yet at the same time, the study observed a trend of 11.6% of spontaneous abortions occurring less than 13 weeks after the mRNA vaccination.  It is becoming increasingly obvious that these vaccines’ safety profiles is far less than Anthony Fauci, the FDA and the CDC are touting   More younger adults are experiencing adverse vaccine symptoms than from the risks due to acquiring a wild coronavirus. Worldwide reported adverse effects and deaths are escalating dramatically. In the CDC’s Vaccine Adverse Events Reporting System (VAERS), reported Covid-19 vaccine deaths have now reached 4.434 as of May 13th 2021 which is more vaccine-related deaths from conventional vaccines recorded in VAERS during the past 21 years.  Since VAERS is a passive reporting system, the actual serious adverse effect rate may be as high as 1in 10 shots. No other vaccine on the CDC’s vaccination schedule has such a poor record of safety.   As with Bill Maher, fully vaccinated people are still being infected and testing positive. Younger healthy adults, who earlier had an insignificant chance of becoming sick or dying from the SARS-CoV-2 virus, are now being injured and in some cases dying from the vaccines.    A recent study published in JAMA observed delayed hypersensitivity vaccine reactions well after injections. The University of Pennsylvania estimates that between 5 to 10 percent of recipients of the mRNA vaccines have “severe adverse reactions” – an inordinately high percent compared to every other non-Covid vaccine. And a group of medical institutions including the University of Greifswald School of Medicine, and the Medical University of Vienna are proposing a new medical condition, “vaccine-induced prothrombotic immune thrombocytopenia,” now be associated with the AstraZeneca and Johnson and Johnson vaccines. A recent paper warns about the dangers of vaccine-induced prion disease. The list of adverse effects continues to mount.  Pfizer document refers to the possibility of Covid vaccine shedding to the unvaccinated.  Doctors are coming forward and accusing the CDC of scrubbing the statistics of actual vaccine-related deaths. The risks were quite obvious in the vaccine makers’ own clinical trial documents before the FDA awarded Covid vaccines with emergency use approval to launch a nation-wide vaccination program. Whether or not health officials at the CDC or FDA thoroughly deliberated on the many warnings or simply ignored them is open to debate.  But the evidence strongly leans towards the latter.   Earlier, we presented the historical evidence of widespread corruption at the CDC; however, the FDA is far more influential because it is the final watchdog that determines a drug’s efficacy and safety profile. In the most perverse scenario, the FDA relies upon outside experts to sit on its advisory committees to review a drug’s or a vaccine’s safety. Many of these experts have a gross conflict of interests with the pharmaceutical industry.  This institutional dilemma is steeped into the FDA’s very DNA. As far back as 2006, Public Citizen discovered that 1 out of 3 of outside consultants and advisory members to the FDA had financial conflicts. The situation has only worsened over the years.   A Pogo investigation in October last year, uncovered several advisers on the FDA’s Vaccines and Related Biological Products Advisory Committee who had direct ties with the Covid-vaccine companies, including direct payments for consulting fees. Dr. Archana Chatterjee, for example, has received over $200,000 from agreements with these companies. The same is true for the Committee’s chairman, University of Michigan Dr. Arnold Monto who received fees from the largest vaccine firms including  Pfizer, Sanofi, GlaxoSmithKline and Novartis. The previous chair, Dr. Hana El Sahly from Baylor University, had to recuse herself due to her role in supervising Moderna’s Covid-19 vaccine clinical trials. Earlier, Monto was the principal investigator for Sanofi’s influenza vaccine. Another is the president of Meharry Medical College where coronavirus clinical trials were conducted. Three other Committee members likewise held close conflict-of-interest relationships with vaccine makers.  Shortly before issuing emergency use approval, a second Pogo analysis concluded that the FDA Committee whitewashed the warnings indicated by the Covid-19 vaccine trials. The meeting was adjourned by the FDA director for the Office of Vaccines Research and Review in favor of green-lighting the vaccines before Committee members suspicious of the clinical results could weigh-in. Prof. Carl Elliott, a medical ethicist at the University of Minnesota, summarized the problem of corporate bias now plaguing the FDA. “You do something positive for a company that you feel confident is going to pay you back for it later on,” Elliot stated. “And they do.”  The FDA‘s current rules regarding conflict of interest is strictly limited to the honor system.  In Europe, on the other hand, the European Medicines Agency strictly prohibits experts with ties to private industry from sitting on its advisory committees.    Even with FDA efforts to crack down on conflicts of interests due to Congressional pressure, the industry has found other means to get their representatives onto advisory panels. And the heads of the agency willingly turn a blind eye.  A Science exposé reported on the growing strategy of “pay after” conflicts of interests. Outside advisors will declare no conflicts but then rule in favor of a drug or vaccine only to be reimbursed afterwards. The journal’s review of compensation records uncovered “pay after” schemes for the approval of 28 psychopharmacologic, arthritis, cardiac and renal drugs.” The investigation also uncovered:   “Of the more than $24 million in personal payments or research support from industry to the 16 top-earning advisers—who received more than $300,000 each—93% came from the makers of drugs those advisers previously reviewed or from competitors.”   Probing still deeper, the Pacific Legal Foundation released an analytical review of 2,952 rules issued by the Department of Health and Human Services over a 17-year period. The Foundation determined that 75 percent of these rules were unconstitutional and “issued by low-level officials and employees with no authority to issue rules.” With respect to the FDA dozens had no democratic controls and involved tens of millions of dollars ruled over by career bureaucrats.     Every American who is prescribed a drug by a physician has the belief that the pill has undergone rigorous trials to scrutinize its safety and will be effective. And when there are known potential adverse effects, we blindly assume the attending physician knows these dangers. However, this is a myth perpetuated not only by drug makers but also by our own federal health agencies.   As we have reported on many occasions, iatrogenic deaths, deaths caused by medical error and prescribed medications is now the third leading cause of mortality in the US. The Institute of Medicine has warned about “the nation’s epidemic of medical errors.” A large percent of these errors are related to adverse drug events (ADEs). The FDA states, “ADRs are one of the leading causes of morbidity and mortality in healthcare.” Dr. Curt Furburg published an article in the Archives of Internal Medicine proposing sweeping changes throughout the FDA.  Furburg and his colleagues wrote, “We see eight major problems with the current system of assessment and assurance of drug safety at the FDA.” A fundamental problem is the FDA’s initial review for drug approval that often fails to detect serious ADRs: “A study by the US General Accountability Office (GAO) concluded that 51% of all approved drugs had at least one serious ADR that was not recognized during the approval process.”   A 2003 investigation published in The Independent in the UK reported “under pressure from the pharmaceutical industry, the FDA routinely conceals information it considers commercially sensitive, leaving medical specialists unable to assess the true risks [of approved drugs].” One case involved a very popular over-the-counter drug, the painkiller ibuprofen. The investigators’ search uncovered concealed data showing that ibuprofen increased heart attack risks by 25 percent. Even Freedom of Information (FOI) filings to the FDA do not produce all the information being requested. For example, a group of Swiss investigators filed an FOI to procure trial data about the musculoskeletal pain drug Celecoxib and received back only 16 of the 27 trials conducted on it. A separate FOI concerning a similar drug, Valdecoxib, had pages and paragraphs deleted because sections of the document were marked as “trade secrets.” An even worse case involving a leaked report concerning internal memos and secret FDA reports provided detailed evidence that the FDA approved 9 different antidepressants, representing a total of 22 studies enrolling 4,250 children, while knowing full well that the risk of “suicide-related events” was twice as high as children taking a placebo. These are just several examples among numerous others, which may best be summarized by a Forbes article entitled “The FDA is Basically Approving Everything.”   Isn't it time for real truth telling? The FDA, which was budgeted for $5.9 billion in FY 2019, is ruled and governed by a small group of political scientists who have abdicated their ethical responsibilities as physicians and medical professionals. With all the controversy and debate over the efficacy and safety of new mRNA vaccines and the aggressive emergency approval of the ineffective anti-Covid drug remdesivir, we may consider a Harvard University article published in the Journal of Law, Medicine and Ethics entitled “Institutional Corruption of Pharmaceuticals and the Myth of Safe and Effective Drugs.”  For the past four decades, the paper states,    “patients have suffered from a largely hidden epidemic of side effects from drugs that usually have few offsetting benefits. The pharmaceutical industry has corrupted the practice of medicine through its influence over what drugs are developed, how they are tested, and how medical knowledge is created. Since 1906, heavy commercial influence has compromised Congressional legislation to protect the public from unsafe drugs. The authorization of user fees in 1992 has turned drug companies into the FDA’s prime clients, deepening the regulatory and cultural capture of the agency.”     We are witnessing the pharmaceutical industry increasing its demands for shorter than average times for the FDA to review new drug submissions; alternatively they have an option to pay the FDA costly fees to have these drugs fast-tracked under its Accelerated Approval Program, thereby jumping over many regulatory hurdles to bring their products to market more quickly. According to a 2019 review of the Program, conducted by the University of Nebraska’s Institute for Operations Research, “from 1992 to 2008, 36% of post-market studies had not been completed, and 50% of the uncompleted studies took on average of 5 years to even begin.”  Yet throughout the duration of years, these drugs continued to be prescribed and reap enormous profits for the companies benefiting from the FDA’s loopholes.    As a consequence, the FDA’s entire regulatory protocol has consistently deteriorated with each passing year. From a system originally mandated to function as a guardian to protect patients from dubious industry commercial interests, it has been transformed into an anti-preventative pipeline favoring drug companies’ bottom line and their shareholders.    In 2013, the Union of Concerned Scientists released its investigative report, four years after the Obama administration launched a process to increase transparency in the federal sciences agencies --- another well-meaning Obama initiative that failed to make any fundamental change. The Union concluded that the  FDA had created a culture lacking scientific integrity, including no formal procedures for investigating scientific misconduct.    The FDA’s serious failures to carry out its duties to monitor and regulate drug companies are well exemplified in the case of the North Carolina outsourcing firm Cetero.  After several years of gross negligence to thoroughly review pharmaceutical drugs, mostly generic knock-offs submitted for licensure, the agency finally uncovered Cetero’s five-year history of faking documents and data or early clinical trials and bioanalytics.  While we expect contractors who carry out clinical trials for large drug companies to be busy at work conducting research on the recorded trial data, on over 1,900 occasions there were no personnel in the Cetero facilities. Approximately 1,400 trials for roughly 100 drugs were faked. Whereas the FDA did little to conduct a thorough investigation, the European Medicines Agency on the other hand discovered that Cetero and its Big Pharm partners, including Roche and Genentech, failed to submit 80,000 reports on American approved drugs that killed over 15,000 Europeans. We need to consider that the Mayo Clinic is on record stating that the last ten years of cancer research are utterly useless due to systemic fraud,    To understand the systemic rot eating away the FDA, we may take note of the research of Dr. Charles Seife and his students at New York University. Seife and his team undertook the task to investigate and analyze the extent to which the FDA covers up evidence of fraud and corruption in medical drug trials. They reviewed FDA documents for about 600 clinical trials. One of Seife’s primary questions was the frequency that FDA officials discover flagrant and intentional misconduct and subsequently decide to bury the evidence and prevent it from becoming public to the medical community.  He discovered such actions to be an official pattern within the agency. Given the high rate of content deleted or blacked out from the documents the FDA provided, the investigators could only determine which pharmaceutical company or drug was involved in 1 of 6 of the reviewed trials. For one trial alone, where FDA inspectors found significant fraud and misconduct, 78 different medical publications printed articles based upon that single study.  In an article for Slate, Seife writes,    "Nobody ever finds out which data is bogus, which experiments are tainted, and which drugs might be on the market under false pretenses. The FDA has repeatedly hidden evidence of scientific fraud not just from the public, but also from its most trusted scientific advisers, even as they were deciding whether or not a new drug should be allowed on the market. Even a congressional panel investigating a case of fraud regarding a dangerous drug couldn't get forthright answers."   In one case, a new anti-blood clotting drug, rivaroxaban, involved four large trials recruiting thousands of patients in clinical sites in over a dozen countries. According to Seife, one of the trials "was a fiasco."  In half of the sixteen clinical sites, the FDA discovered "misconduct, fraud, fishy behavior or other practices so objectionable that the data had to be thrown out." One Colorado site falsified data. At the Mexican site, there was "systematic discarding of medical records." Despite these overwhelming problems, the drug trial was published favorably in the prestigious British journal The Lancet. The FDA found similar problems in the three other trials; in one the data was ruled "worthless." The FDA advisory committee of "expert" reviewers were only informed that inspectors discovered only "significant issues" at two sites in one of the trials. Rivaroxaban was nevertheless approved in 2011. Since then lawsuits for wrongful death from the drug continue to increase.    One of the deeper flaws within the FDA’s mode of operations is that it solely relies on the studies and clinical trials conducted by drug makers without conducting any studies of its own. Consequently these private firms have complete control over the clinical data and can provide such data or not at their own discretion. For example, if a company conducts 20 clinical trials on a potential new drug and15 trials conclude it is absolutely useless or results in serious reactions and deaths, the company is only required to submit documentation for the 5 trials that are favorable.    Over the years, Congressional subcommittees have voiced warnings to FDA officials to clean up their act. A House Government Reform Committee reported that both the CDC’s and FDA’s advisory committees for vaccines were thoroughly compromised with pharmaceutical conflicts of interest.     One of the most glaring examples of FDA misconduct, deceit and cover-up to protect pharmaceutical interests in the agency’s history was the federal case against Merck and its anti-inflammatory drug Vioxx. Dr. David Graham, a former Associate Director for Science and Medicine in the FDA’s Office of Drug Safety, testified before the US Senate. Dr. Graham has impeccable credentials qualifying him as an expert on the failures of pharmaceutical drugs. He graduated from the Johns Hopkins University School of Medicine, and trained in Internal Medicine at Yale and in adult Neurology at the University of Pennsylvania.    Dr. Graham told the Senate:   “During my career, I believe I have made a real difference for the cause of patient safety. My research and efforts within the FDA led to the withdrawal from the US market of Omniflox, an antibiotic that caused hemolytic anemia; Rezulin, a diabetes drug that caused acute liver failure; Fen-Phen and Redux, weight loss drugs that caused heart valve injury; and PPA (phenylpropanolamine), an over- the-counter decongestant and weight loss product that caused hemorrhagic stroke in young women.   “My research also led to the withdrawal from outpatient use of Trovan, an antibiotic that caused acute liver failure and death. I also contributed to the team effort that led to the withdrawal of Lotronex, a drug for irritable bowel syndrome that causes ischemic colitis; Baycol, a cholesterol-lowering drug that caused severe muscle injury, kidney failure and death; Seldane, an antihistamine that caused heart arrhythmias and death; and Propulsid, a drug for night-time heartburn that caused heart arrhythmias and death. . . .   “I have done extensive work concerning the issue of pregnancy exposure to Accutane, a drug that is used to treat acne but can cause birth defects in some children who are exposed in utero if their mothers take the drug during the first trimester. During my career, I have recommended the market withdrawal of twelve drugs. Only two of these remain on the market today—Accutane and Arava, a drug for the treatment of rheumatoid arthritis that I and a co-worker believe causes an unacceptably high risk of acute liver failure and death.”   The Los Angeles Times reported that witnesses told the Senate panel that Merck and the FDA knowingly had data well before the approval and licensure of Merck’s Vioxx painkiller that proved the drug’s serious cardiovascular health risks. Nevertheless, the FDA granted it approval without resolving the risks, and Vioxx was aggressively marketed.   Testifying about Merck’s Vioxx, Dr. Graham states:   "Today . . . you, we, are faced with what may be the single greatest drug safety catastrophe in the history of this country or the history of the world. We are talking about a catastrophe that I strongly believe could have, should have been largely or completely avoided. But it wasn’t, and over 100,000 Americans have paid dearly for this failure. In my opinion, the FDA has let the American people down, and sadly, betrayed a public trust."   According to Dr. Graham. “Not only did the FDA ignore known risks from Vioxx and related drugs but . . . it tried to prevent Graham and others from publicizing their own research that proved the extent of these risks.”   Members of Congress have echoed Graham’s concerns. Charles Grassley (R–Iowa) said he was concerned that the FDA “has a relationship with drug companies that is too cozy.”  Sen. Jeff Bingaman (D–New Mexico) said the problem was within the FDA’s own culture.“ This culture is one whereby the pharmaceutical industry, which the FDA is mandated to regulate, is the FDA’s most favored and lucrative client.   Sixteen years have passed since Dr. Graham’s public statements exposing the life-threatening policies and corruption that infest the FDA. It’s difficult to comprehend why the agency has been unable to clean up its act. Instead the FDA’s culture of deceit has only worsened. Nevertheless, the evidence clearly shows that our government health officials would rather support pharmaceutical profiteering than the health and safety and American citizens. In fact, 45 percent or $2.7 billion of its budget derives from private pharmaceutical “user fees.”   The disturbing data suggest that the FDA’s evaluation of pharmaceuticals for safety and efficacy may be so flawed that only 4% of all trial results are identified as such. As a result, FDA scientists and officials responsible for approving drugs to the market are kept largely uninformed about the egregious scientific misconduct involved in obtaining study data. Further, these erroneous and fraudulent studies are published in peer-reviewed scientific literature and accepted as valid science. The American public is ‘virtually defenseless’ if another medication proves to be unsafe after it is approved.   But it gets worse.  The agency has been warning against highly effective off-patent drugs to treat early SARS-CoV-2 infections such as hydroxychloroquine (HCQ) and ivermectin.  Shortly after the pandemic was formally announced, and with no promising treatment in sight, the FDA recommended HCQ but then reversed its decision in June after Anthony Fauci publicly announced the coming arrival of Gilead’s novel drug remdesivir. The FDA’s approval of remdesivir baffled many scientists, according to the journal Science, who were keeping a close watch on the drug’s clinical reports, which showed a “disproportionally high number of reports of liver and kidney problems”Nor did remdesivir lessen hospital stays or lower mortality rates.   Two months ago the agency issued a warning statement against the use of ivermectin. “The very next day,” reported the Alliance for Natural Health, “Merck announced positive results from a clinical trial on a new drug called molnupiravir in eliminating the virus in infected patients.”  Again, the FDA had been working in concert with the pharmaceutical industry to advance expensive experimental drugs rather than cheaper and proven drugs with decades of research to back their safety records.    In addition, the FDA has waged a war against alternative medical systems for many decades, including natural supplements. Last September, the agency attempted to ban N-acetylcysteine (NAC) after it showed promise to reduce cytokine storms associated with SARS-CoV-2 infection. The supplement had already been shown to improve lung problems due to respiratory infections such as pneumonia and acute respiratory distress symptom. Three years ago, an FDA advisory committee met to consider banning five supplements made by specialized compounding pharmacies: alpha lipoic acid, CoQ10, pyridoxal-5-phosphate, creatine monohydrate  and quercetin dehydrate. Earlier the FDA had banned curcumin, boswellia and aloe vera from pharmacologic compounding. One of the key executors of the agency’s revitalized assault against supplements and the natural health industry was Trump’s appointment of Scott Gottlieb as FDA Commissioner. Following his two years at the FDA’s helm, Gottlieb quit and joined Pfizer’s Board of Directors.   The FDA’s argument is rather straightforward, albeit dubious; since supplements, including Vitamin C and D, Omega-3 fatty acids, and even minerals such as magnesium and zinc have not been formally submitted to the FDA for evaluation to be registered as “approved drugs,” it is against the law to make any health claims about their health benefits.  This is despite the thousands of peer-reviewed studies in the National Library of Medicine to support their efficacy. The average median cost to conduct clinical trials to meet FDA standards for approval, according to a Johns Hopkins University evaluation, is $19 million and upwards to $2-3 billion. In other words to get Vitamin D officially recommended as a viable preventative defense against Covid-19 would require a minimum of $19 million in addition to numerous fees and other legal costs prior to and after submission. And that doesn’t even address the problem of ownership since Vitamin D is a natural substance and excluded from patenting. In the meantime, supplement manufacturers are prohibited from stating the vitamin’s benefit to the public thereby contributing to a gross disservice.    “Clearly these are the actions of an agency looking to restrict the supplement market,” according to the Alliance for Natural Health, “and remove as many products as possible in as many ways as possible.”  One reason is that if a vitamin or supplement were to go through the FDA licensure treadmill, the agency could potentially require a supplement’s access by prescription only. It would no longer be available over the counter. And this in turn would be another boon for the drug industry, which is already developing synthetic supplemental knock-offs that are patentable.    Much of the blame lies on the shoulders of politicians on both sides of the aisle and the mainstream media who have enabled the FDA and CDC to run amok and then propagate the pharmaceutical industry’s nonsense. A recent Harvard University and Robert Wood Johnson Foundation survey reported that public trust in America’s health care system has rapidly fallen during the pandemic to 34 percent. Only 37 percent stated they had much trust in the FDA.    This trend may very likely continue as a growing number of physicians and medical experts are sounding alarms over the flagrant incompetence of our federal officials leading the national efforts against Covid-19 and the approval vaccines with highly questionable safety records and expensive novel drugs that fail to warrant use. Worldwide, tens of thousands of otherwise orthodox medical professionals are charging Anthony Fauci, the CDC, FDA and the World Health Organization with gross mishandling of the pandemic.  Lawsuits are underway against national health ministries around the world for deceiving their populations with fraudulent PCR testing, fake mortality rates and unwarranted public health policies that have produced extreme harm and suffering.  As the situation deteriorates more suits will be anticipated.    Sadly there is no reason to expect the FDA to undergo a structural change. For decades Congressional committees have warned the agency about it’s ignoring the public health of Americans and its revolving door policies with drug makers. Yet matters continue to worsen. A complete overhaul by adopting policies similar to the European Medicines Agency such as independent leadership divorced from the pharmaceutical complex and full public funding, would be a decent start. Another  solution could be the creation of separate and independent National Drug Safety Board without ties to private industry or overlapping conflicts of interest with the existing health agencies in dire need of reform. However that tipping point has not been reached to expect any of our politicians to switch sides and for once serve the public’s health interests  

Are Big AG, Big Pharm, and Big Food profiting while making all of us sick? How much is our food system costing us? Listen in while Eleanor and Kristen start a conversation provoked by Mark Hyman’s book THE FOOD FIX.

Josep Borrell, kierujący służbą zagraniczną Unii Europejskiej, pojechał do Moskwy, "żeby rozmawiać", ale spotkał się tam z publicznie okazaną wrogością ze strony goszczącego go ministra Sergieja Ławrowa. W cotygodniowym podcaście "O świecie w Onecie", Michał Broniatowski i Adam Jasser ostro spierają się o sens wizyty Borrella w Rosji. Zdaniem Jassera, kluczowa była możliwość zaprotestowania na miejscu w Moskwie w sprawie uwięzienia przez Kreml opozycjonisty Aleksieja Nawalnego oraz ustalenia priorytetów przyszłych stosunków Brukseli z Kremlem. Broniatowski uważa natomiast, że z powodu sprawy Nawalnego, konieczny był gest w postaci odłożenia "z dawna planowanej" wizyty, bo bieżące sprawy omówić można przez telefon. Dawno tak ostrego starcia między Unią, a Rosją nie było, a krytyka Borrella w Brukseli zbiegła się w czasie z wielkim poruszeniem w najwyższych instytucjach UE w sprawie rzekomych błędów przewodniczącej Komisji Europejskiej Ursuli von der Leyen przy organizowaniu dostaw szczepionki na COVID-19 dla krajów członkowskich. Panią von der Leyen najostrzej zaatakowały największe i najbogatsze kraje Unii, które zapewne dostałyby szczepionkę szybciej i sprawniej, gdyby samodzielnie negocjowały z Big Pharmą. Jednak solidarne przejęcie całości negocjacji przez Brukselę uchroniło słabszych członków Wspólnoty (w tym na przykład Polskę) przed zepchnięciem na dalszy plan w dostawach, nawet jeśli oznacza to opóźnienia szczepień w Unii w stosunku do np. USA czy Wielkiej Brytanii. W ubiegłym tygodniu rozpadł się rząd Włoch i prezydent kraju poprosił o sformowanie nowego gabinetu byłego prezesa Europejskiego Banku Centralnego, Mario Draghiego. Adam Jasser szczegółowo opowiada o zasługach tej postaci dla europejskiej polityki, zwłaszcza w okresie tzw. kryzysu greckiego, który groził rozpadem strefy euro. Za Atlantykiem natomiast, prezydent Joe Biden przedstawił priorytety swojej polityki zagranicznej, podkreślając powrót Ameryki do sprawowania "moralnego przywództwa" w świecie po czterech latach prezydentury Donalda Trumpa, kiedy to przywództwo mierzono jedynie jego ewentualnym pożytkiem dla Stanów Zjednoczonych i często przyświecały mu cele czysto merkantylne.

  Dr Myhill qualified from the Middlesex Hospital Medical School, London, Honours viva, 1981. She worked for 20 years as an NHS GP before moving to Independent Medical Practice with a special interest in CFS/ME. She practices Ecological Medicine – diagnosing mechanisms if disease which have obvious implications for management. She has been an active member of the BSEM since 1986 Hon Meetings Secretary (1993–1998) including 5 day International Conference “Sustainable Medicine” at Christ Church College Oxford, Hon Secretary 1999 -2007.   Co-author with Dr John McLaren Howard Acumen and Prof Norman Booth Mansfield College Oxford:   Chronic Fatigue Syndrome and mitochondrial dysfunction: Ref Int J Clin Exp Med (2009) 2, 1-16, http://www.ijcem.com/files/IJCEM812001.pdf   Mitochondrial dysfunction and the pathophysiology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). www.ijcem.com/files/IJCEM1204005.pdf   Targeting mitochondrial dysfunction in the treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) – a clinical audit. http://www.ijcem.com/files/IJCEM1207003.pdf   Author of award winning books vis:   “Chronic Fatigue Syndrome - it’s mitochondria not hypochondria” BMA Prize Highly Commended 2014. Second edition 2017 (5 reprints) “Sustainable Medicine” (Beryl Bainbridge Prize 2016). “Diabetes” (Beryl Bainbridge Prize 2017) “The PK Cookbook” 2017 “The Infection Game” 2018, updated 2018 “Ecological Medicine – the antidote to Big Pharm and fast food” 202ohttps://drmyhill.co.uk/wiki/My_book_Ecological_Medicine_-_The_Antidote_to_Big_Pharma_and_Fast_Foods Due out shortly “The Energy Equation” In the pipeline “Green Mother”   She has made media appearances in Newsnight (silicone implants), Dispatches (BSE and organophosphate poisoning), Woman’s hour (silicone breast implants, allergies), Esther Rantzen show (Chronic Fatigue Syndrome), Watchdog Healthcheck (silicone implants) as well as many Welsh TV programmes and local radio in UK and abroad. Lecturer to What Doctors Don’t Tell You, BANT (British Association of Nutritional Therapists), BSEM, ANP (Association of Naturopathic Practitioners) and others   1994 Diploma in Clinical Nutrition Patron of ANP (Association of Naturopathic Practitioners)   ____________     We Discuss:
   The differences between Chronic Fatigue Syndrome, ME & Fibromyalgia   Normal fatigue vs. Chronic fatigue   Conventional tests & treatments for fatigue   What are mitochondria and what are the influencing factors   Dr Myhill’s thoughts on graded exercise & post-exertional malaise   Gut health & key nutrients for mitochondrial function including chronic infections and how do they affect mitochondria   Dr Myhill’s thoughts on the ketogenic diet to support mitochondrial function     Mentioned:   Dr Sarah Myhill’s co-authored published papers on Chronic Fatigue Syndrome & Mitochondrial Dysfunction   http://www.ijcem.com/files/IJCEM812001.pdf   http://www.ijcem.com/files/IJCEM1204005.pdf   http://www.ijcem.com/files/IJCEM1207003.pdf   Books authored by Dr Myhill   https://www.salesatdrmyhill.co.uk/dr-myhills-books-10-c.asp   Additional resources and information can be found on Dr Myhill’s wesbite   https://www.drmyhill.co.uk     ————   MY LINKS:   Try my favourite ORGANO KING coffee - https://vivanaturalhealth.myorganogold.com/gb-en/   Grab my favourite BluBlox glasses - https://bit.ly/2UXkNqT   ______   Got a podcast question? Send you emails to hormonesinharmony@gmail.com   Enjoyed this episode? Leave me a rating and review so that I can share this podcast with more women     Want more from me? You can find me online...   Website www.vivanaturalhealth.co.uk 
   Instagram www.instagram.com/vivanaturalhealth
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     Tune in now on iTunes, Spotify, my website or watch on Youtube (Viva Natural Health)   If you are enjoying the podcast, please leave me a rating and review, as this helps me to reach more women and continue to interview awesome guests! 
 
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In this podcast, we will host guests discussing all aspects that address what health and medical freedoms are all about. From Big Tech to Big Ag, Big Pharm to immune function and the deepest depths of the human psyche and soul. Our platform is a place for all walks of life to finally relearn what it feels like to be human again. Heath Freedom for Humanity stands to protect and advance the most basic and inalienable of human rights, the right to medical freedom. We stand in opposition to any act, law, measure, or constraint that threatens this right. With an unwavering commitment to integrity, we stand for humanity.

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MGS #036: THE #1 HEALTH SECRET BIG PHARM DOESN'T WANT YOU TO KNOW! Trigger Warning What I share in this show is NOT something we have been taught in school, by the government, or anywhere else in Western Society. It has been dismissed as "fake science" for too long. I challenge you to open your mind and heart to what's possible How Big Pharm Works Western Diets #1 Health Secret Science Behind It Want to hop on a call with me and some friends and hangout once a week? Text GILLEN GANG to 833-222-2694 for Exclusive Zoom Calls and Private Events with Marshal LIVE! Attend Marshalpalooza: httphttps://l.facebook.com/l.php?u=https%3A%2F%2Fbit.ly%2F2CNz0AO%3Ffbclid%3DIwAR2rPErtLBmw4Prawp_jr2f77YrD6-Mgp03cDWLocRz7du4sl0kOfM1ulhQ&h=AT0etj_BVirDAIXWicP44VTLOW8He4o3b-05Z32W4T4Ca3jsLwSdLsfI7yxoJ8vNIg5H9JYzjWMqqkijW-4g7DIe208cOPCjQuuBX-CrC2ubUDM_zEutZcBW44Kwhy5D8nkkoRKxI4-Y9cX0oFKWenI&__tn__=-UK-R&c[0]=AT0dRGGhufI6_jud27GlwyP2VR9kUMgHP8394dTQrpANq3xY8xjmaGv-ha2hwFj3lKZ99c9OME19U6VS_UHV004RVXDIbHLbNdpckxO0AIqWSXX4Q2-00Yf6U83sSL1KGagJNoH8kxPhpVFYc0sKr7JyTItabvQK (s://bit.ly/2CNz0AO) Shop: https://marshalgillen.com

Dont let the Globalist and Big Pharm win! here are some little tips on food prep! Happy Thanksgiving --- Support this podcast: https://anchor.fm/nutritionwarsnow/support

This week we sat down with Pontiac resident Sammie Rodgers and discussed him opening the first canibus vocational school, gave some important marijuana facts and ended the show with some random football talk

One of the greatest challenges facing the United States is the opioid crisis. This crisis causes despair, suicide, and shreds the moral fabric of America. Yet at its simplest level, it’s a problem of supply, demand, and a solution that evades us. Many experts place the supply problem on the medical profession, the demand problem on Big Pharm for faulty research and greed, which masquerades the latest new opioid drug as safe. And the insurance complex which reimburses drugs that obtunds addicts but reduces lengthy hospital care that patients need.

Controversy and Clinical Insights into the Health Effects and Breast Cancer Today on Couch Talk I am talking with Dr. Edwin Lee. He is a past Couch Talk guest and one of the best physicians I know. And we're talking about one of my favorite topics, the use of bio-identical hormones in the treatment of menopausal symptoms in women. Dr. Lee believes that the best way to treat hormonal imbalance is by natural bio-identical hormone therapy. Natural hormones are the exact and identical hormones that are made in your body (versus synthetic hormones which are not chemically structured the same as in your body). He feels that the use of bioidentical hormones with estradiol, estriol, progesterone and or testosterone in women is essential, whereas the use of testosterone in men is crucial to prevent early mortality. Dr. Lee combines functional medicine to determine the root problem with the use of bioidentical hormones to help his patients achieve wellness – along with an emphasis on improving on diet, lifestyle, and nutrition. Listen to the interview: A Great Way to Kick off Breast Cancer Awareness Month! It's the start of Breast Cancer Awareness month, so this Couch Talk interview was very well timed! We talked a lot about our own patient and clinical outcomes over our decades of combined practices in using bio-identical hormones to treat hot flashes, depression, anxiety, mood swings, vaginal atrophy and other symptoms commonly seen in menopause. We also talked a lot about the confusion relating to breast cancer risk. In thisinterview, you will learn, Why Dr. Lee tells his menopausal patients that menopause itself is a dangerous disease with a higher rate of Alzheimer's or dementia, heart disease, and osteoporosis…and what he feels they can do to prevent all of this. The importance of both an individual patient's ability to detox and their current lifestyle (diet, exercise, sleep, etc.) in determining the right menopausal treatment plan for them. Why he doesn't recommend oral estrogen therapy (Premarin, Prempro) ever be used. Why bio-identical progesterone is truly the “wonder hormone” that helps with sleep, anxiety, irritability, PMS…and more…and how it is protective against breast cancer (and could save your marriage!) Why oral synthetic progesterone (Provera) is a bad choice, clearly linked to increasing the risk of strokes and heart disease. Why just taking a hormone is never enough (hint: you need to improve your lifestyle decisions)! What plant-based estrogen SERM (Selective Estrogen Receptor Modulator) Dr. Lee has recommended that helps with hot flashes (and is safe). And We Covered So Much More! Why is it that less than 1% of women who have taken HRT therapy in his clinical practice have developed breast cancer (compared to 11% of women developing breast cancer in the general population)? We discussed both of our clinical observations as to what the answer to this might be. Finally, we talked about our “polite disagreements” with the American Association of Clinical Endocrinologists (of which Dr. Lee is a member) recently stating in a position paper that they do not recommend the use of bio-identical hormone therapy in many cases… What? Well...we both feel that endocrinologists already use bio-identical hormone therapy all of the time for standard care with insulin, cortisol, thyroid, progesterone, testosterone, transdermal estradiol, etc.! So what is going on in this position paper? Is it the definition of what is “synthetic” versus “natural”? Is it a bit of bias from the Big Pharm companies? Such an interesting discussion with my favorite endocrinologist! Meet Dr. Edwin Lee A little bit about Dr. Edwin Lee, and I hope you'll listen to our interview in the audio posted above! He's board-certified in internal medicine, endocrinology, diabetes, and metabolism, and has completed special training in regenerative and functional medicine. He is an author and an international speaker and educator. Dr. Lee founded the Institute for Hormonal Balance in 2008. Currently, he is the Assistant Professor of Internal Medicine at the University of Central Florida College of Medicine. In addition to writing his books, including two awesome children's books, one called, Your Awesome Brain, and the other is Your Amazing Heart—I highly recommend these—he's written, for those of us that really want to get a better understanding on hormones, a couple of other books. One is called Feel Good, Look Younger: Reversing Tiredness Through Hormonal Balance, and the book, Your Best Investment: Secrets to a Healthy Body and Mind.  Dr. Lee has also published many articles on internal medicine and endocrinology. He is an author in the fourth edition of Textbook of Critical Care. He's an active member of the Age Management Medicine Group and the American Association of Clinical Endocrinology. Find out more about Dr. Lee at http://instituteofhormonalbalance.com/

Controversy and Clinical Insights into the Health Effects and Breast Cancer Today on Couch Talk I am talking with Dr. Edwin Lee. He is a past Couch Talk guest and one of the best physicians I know. And we’re talking about one of my favorite topics, the use of bio-identical hormones in the treatment of menopausal symptoms in women. Dr. Lee believes that the best way to treat hormonal imbalance is by natural bio-identical hormone therapy. Natural hormones are the exact and identical hormones that are made in your body (versus synthetic hormones which are not chemically structured the same as in your body). He feels that the use of bioidentical hormones with estradiol, estriol, progesterone and or testosterone in women is essential, whereas the use of testosterone in men is crucial to prevent early mortality. Dr. Lee combines functional medicine to determine the root problem with the use of bioidentical hormones to help his patients achieve wellness – along with an emphasis on improving on diet, lifestyle, and nutrition. Listen to the interview: A Great Way to Kick off Breast Cancer Awareness Month! It’s the start of Breast Cancer Awareness month, so this Couch Talk interview was very well timed! We talked a lot about our own patient and clinical outcomes over our decades of combined practices in using bio-identical hormones to treat hot flashes, depression, anxiety, mood swings, vaginal atrophy and other symptoms commonly seen in menopause. We also talked a lot about the confusion relating to breast cancer risk. In thisinterview, you will learn, Why Dr. Lee tells his menopausal patients that menopause itself is a dangerous disease with a higher rate of Alzheimer’s or dementia, heart disease, and osteoporosis…and what he feels they can do to prevent all of this. The importance of both an individual patient’s ability to detox and their current lifestyle (diet, exercise, sleep, etc.) in determining the right menopausal treatment plan for them. Why he doesn’t recommend oral estrogen therapy (Premarin, Prempro) ever be used. Why bio-identical progesterone is truly the “wonder hormone” that helps with sleep, anxiety, irritability, PMS…and more…and how it is protective against breast cancer (and could save your marriage!) Why oral synthetic progesterone (Provera) is a bad choice, clearly linked to increasing the risk of strokes and heart disease. Why just taking a hormone is never enough (hint: you need to improve your lifestyle decisions)! What plant-based estrogen SERM (Selective Estrogen Receptor Modulator) Dr. Lee has recommended that helps with hot flashes (and is safe). And We Covered So Much More! Why is it that less than 1% of women who have taken HRT therapy in his clinical practice have developed breast cancer (compared to 11% of women developing breast cancer in the general population)? We discussed both of our clinical observations as to what the answer to this might be. Finally, we talked about our “polite disagreements” with the American Association of Clinical Endocrinologists (of which Dr. Lee is a member) recently stating in a position paper that they do not recommend the use of bio-identical hormone therapy in many cases… What? Well...we both feel that endocrinologists already use bio-identical hormone therapy all of the time for standard care with insulin, cortisol, thyroid, progesterone, testosterone, transdermal estradiol, etc.! So what is going on in this position paper? Is it the definition of what is “synthetic” versus “natural”? Is it a bit of bias from the Big Pharm companies? Such an interesting discussion with my favorite endocrinologist! Meet Dr. Edwin Lee A little bit about Dr. Edwin Lee, and I hope you’ll listen to our interview in the audio posted above! He’s board-certified in internal medicine, endocrinology, diabetes, and metabolism, and has completed special training in regenerative and functional medicine. He is an author and an international speaker and educator. Dr. Lee founded the Institute for Hormonal Balance in 2008. Currently, he is the Assistant Professor of Internal Medicine at the University of Central Florida College of Medicine. In addition to writing his books, including two awesome children’s books, one called, Your Awesome Brain, and the other is Your Amazing Heart—I highly recommend these—he’s written, for those of us that really want to get a better understanding on hormones, a couple of other books. One is called Feel Good, Look Younger: Reversing Tiredness Through Hormonal Balance, and the book, Your Best Investment: Secrets to a Healthy Body and Mind.  Dr. Lee has also published many articles on internal medicine and endocrinology. He is an author in the fourth edition of Textbook of Critical Care. He’s an active member of the Age Management Medicine Group and the American Association of Clinical Endocrinology. Find out more about Dr. Lee at http://instituteofhormonalbalance.com/

Big Pharm, FDA, War on Drugs, and Cannabis...

Laura and Robin are still sick. Bad Patient's producer (and resident cat) make a cameo. Laura, it turns out, is an alien who experiences no food cravings. This week's health news: Alzheimers medications abandoned http://beta.latimes.com/science/sciencenow/la-sci-sn-alzheimers-drug-fail-20180109-story.html Does getting more sleep kill sugar cravings? (Does anything?) https://www.livescience.com/61381-sleep-more-eat-better.html A swallowable capsule checks digestive processes (read: farts, farts, farts) https://www.npr.org/sections/health-shots/2018/01/08/575944661/gut-check-gas-sniffing-capsule-charts-the-digestive-tract Middle age is the prime time to turn around couch potato habits with high-intensity workouts http://www.labmanager.com/news/2018/01/middle-aged-couch-potatoes-may-reverse-heart-effects-of-a-sedentary-life-with-exercise-training#.WlY0Ta6nEdU

Drs Ron Gerry and Dan with over 150 years of medical experience, not controlled by Big Pharm or outside interests, will give you their opinions on the latest guidlines for hypertension and some ofthe side effects of commonly used medicaions. We will also review the past year and where we are heading in 2018.   Email docronradio@gmail.com Facebook: Dr Ron Unfiltered Uncensored   Also on iTunes, Stitcher, Blubrry and Google Play   347-989-8899

Israel put a temproary ban on American Ketchup because it is falsely promoted as real tomato paste. Yet it contains only a 21% concentrate of any substance. Israel demands it relabel as "tomato seasoning" if expecting to be sold in their nation. Also it contains chemicals that cause health issues. What other foods are killing us? We will look at this and also how Big Pharm plays a role in this.Sources:https://www.healthnutnews.com/israel-bans-heinz-ketchup-because-its-linked-to-liver-pancreas-immune-system-and-brain-issues/http://www.naturalnews.com/032659_arsenic_chicken.htmlhttps://jonrappoport.wordpress.com/2017/06/07/exposed-the-nazi-roots-of-the-european-union-2/

Israel put a temproary ban on American Ketchup because it is falsely promoted as real tomato paste. Yet it contains only a 21% concentrate of any substance. Israel demands it relabel as "tomato seasoning" if expecting to be sold in their nation. Also it contains chemicals that cause health issues. What other foods are killing us? We will look at this and also how Big Pharm plays a role in this.Sources:https://www.healthnutnews.com/israel-bans-heinz-ketchup-because-its-linked-to-liver-pancreas-immune-system-and-brain-issues/http://www.naturalnews.com/032659_arsenic_chicken.htmlhttps://jonrappoport.wordpress.com/2017/06/07/exposed-the-nazi-roots-of-the-european-union-2/

Your favorite show(we assume)is back, and we want to give you all a collective , good natured smack on the ass. Bernie Sanders joins us in the Pillow Fort at the top of the show to rail against unchecked capitalism. Lincoln Chafee is bad, and he should feel bad. What's on Charles' list of favorite things this week? Big Pharm dickwad is told to kick rocks by Bernie Sanders. We treat Alaina like she's one of the boys. Shes... not a fan. A man has a very specific fetish, and we want to help him get off. A child was beaten to death at a church in upstate NY. We've heard of Bible-thumping, but this is ridiculous. Playboy will soon stop showing titties in the pages of their magazine. Evie's a real dime. Justin Bieber's pecker makes its first appearance. When is domestic violence, ok? It's not, but hear us out. Aaron brings us the Subreddit of the week. Will this be the week that the period report pays off? Online dating is the tits, and SOOOO MUCH MORE!!!!