https://childrenshealthdefense.org/news/americans-can-handle-an-open-discussion-on-vaccines-rfk-jr-responds-to-criticism-from-his-family/

AUGUST 15, 2019

Americans Can Handle an Open Discussion on Vaccines—RFK, Jr. Responds to Criticism from His Family

CHD NOTE: In early May 2019, Politico Magazine published an article written by three of Robert F. Kennedy, Jr.’s relatives, criticizing his advocacy for safe vaccines. After numerous requests, Politico magazine has refused to publish his response. 

By Robert F. Kennedy, Jr.  

Three of my Kennedy relatives recently published an article criticizing my advocacy for safe vaccines. Our contentious family dispute highlights the fierce national donnybrook over vaccinations that has divided communities and raised doubts about the Democratic Party’s commitment to some of its defining values: abhorrence of censorship, wariness toward excessive corporate power, support for free speech, religious freedom, and personal sovereignty over our bodies, and the rights of citizens (codified in the Nuremberg Code and other treaties to which we are signatories) to decline unwanted government-mandated medical interventions. The debate has also raised questions about the independence of our press and its role as a champion of free speech, and First Amendment rights as a bulwark against overreaching by government and corporations.

I love my family and sympathize with their anxieties when I call out government officials for corruption. The Kennedys have a long, close, and continuing relationship with public health agencies so it is understandably difficult for us to believe that powerful regulators would lie about vaccines. “All issues are simple,” the saw goes, “until you study them.”

Those conflicts motivate them to recommend ever more vaccines with minimal support from evidence-based science.

My skepticism

I’ve arrived at my skepticism after 15 years spent researching and litigating this issue. I have watched financial conflicts and institutional self-interest transform key sectors of our public health bureaucracies into appendages of the very pharmaceutical companies that Congress charged them to regulate.

Multiple investigations by Congress and the HHS Inspector General have consistently found that an overwhelming majority of the FDA officials directly charged with licensing vaccines, and the CDC officials who effectively mandate them for children, have personal financial entanglements with vaccine manufacturers. These public servants are often shareholders in, grant recipients from, and paid consultants to vaccine manufacturers, and, occasionally, patent holders of the very vaccines they vote to approve. Those conflicts motivate them to recommend ever more vaccines with minimal support from evidence-based science.

HHS partners with vaccine makers to develop, approve, recommend, and pass mandates for new products and then shares profits from vaccine sales.

The pharmaceutical industry also enforces policy discipline through agency budgets. FDA receives 45% of its annual budget from industry. The World Health Organization (WHO) gets roughly half its budget from private sources, including Pharma and its allied foundations.  And CDC, frankly, is a vaccine company; it owns 56 vaccine patents  and buys and distributes $4.6 billion in vaccines annually through the Vaccines for Children program, which is over 40% of its total budget. Further, Pharma directly funds, populates and controls dozens of CDC programs through the CDC foundation.  A British Medical Journal editorial excoriates CDC’s sweetheart relationship with pharma quotes UCLA Professor of Medicine Jerome R. Hoffman “most of us were shocked to learn the CDC takes funding from industry… It is outrageous that industry is apparently allowed to punish the CDC if the agency conducts research that has potential to cut into profits.”

HHS partners with vaccine makers to develop, approve, recommend, and pass mandates for new products and then shares profits from vaccine sales. HHS employees can personally collect up to $150,000 annually in royalties for products they work on. For example, key HHS officials collect money on every sale of Merck’s controversial HPV vaccine Gardasil, which also yields tens of millions annually for the agency in patent royalties. Furthermore, under the 1986 Act that created the National Vaccine Injury Compensation Program, HHS is the defendant in Vaccine Court and is legally obligated to defend against any claim that a vaccine causes injury. Despite high hurdles for recovery, HHS pays out hundreds of millions of dollars annually (over $4 billion total) to Americans injured by vaccines. Hence, if HHS publishes any study acknowledging that a vaccine causes a harm, claimants can use that study against HHS in Vaccine Court. In June 2009, a high-level HHS official, Tom Insel, killed a $16 million-dollar budget item to study the relationship between vaccines and autism by the Interagency Autism Coordinating Committee. Insel argued that petitioners would use these studies against HHS in vaccine court.

Such conflicts are a formula for “agency capture” on steroids. “Instead of a regulator and a regulated industry, we now have a partnership,” says Dr. Michael Carome, a former HHS employee who is now the director of the advocacy group Public Citizen. Carome says that these financial entanglements have tilted HHS “away from a public health perspective to an industry-friendly perspective.”

In 1986, Congress—awash in Pharma money (the pharmaceutical industry is number one for both political contributions and lobbying spending over the past 20 years) enacted a law granting vaccine makers blanket immunity from liability for injuries caused by vaccines. If vaccines were as safe as my family members claim, would we need to give pharmaceutical companies immunity for the injuries they cause? The subsequent gold rush by pharmaceutical companies boosted the number of recommended inoculations from twelve shots of five vaccines in 1986 to 54 shots of 13 vaccines today. A billion-dollar sideline grew into the $50 billion vaccine industry behemoth.

Since vaccines are liability-free—and effectively compulsory to a captive market of 76 million children—there is meager market incentive for companies to make them safe. The public must rely on the moral scruples of Merck, GlaxoSmithKline, Sanofi, and Pfizer. But these companies have a long history of operating recklessly and dishonestly, even with products that they must market to the public and for which they can be sued for injuries. The four companies that make virtually all of the recommended vaccines are all convicted felons.  Collectively they have paid over $35 billion since 2009 for defrauding regulators, lying to and bribing government officials and physicians, falsifying science, and leaving a trail of injuries and deaths from products they knew to be dangerous and sold under pretense of safety and efficacy.

Doesn’t it require a kind of cognitive dissonance to believe that vaccines are untainted by the greed, negligence, and corruption that bedevil every other pharmaceutical product?

For American kids born in 1986, only 12.8% had chronic diseases. That number has grown to 54% among the vaccine generation (those born after 1986) in lockstep with the expanding schedule.

No safety testing

Such concerns only deepen when one considers that, besides freedom from liability, vaccine makers enjoy another little-known lucrative loophole; vaccines are the only pharmaceutical or medical products that do not need to be rigorously safety tested. To win an FDA license, companies must safety test virtually every other drug for years in randomized comparisons against an inert placebo. Yet, not a single vaccine currently on the CDC schedule was tested against an inert placebo. Without placebo testing, regulators have no capacity to assess a medicine’s risks. During a January 2018 deposition, Dr. Stanley Plotkin, the world’s most influential vaccinologist, acknowledged that researches who try to ascertain vaccine safety without a placebo are in “La La land”. According to Dr. Drummond Rennie, Deputy Editor of the Journal of the American Medical Association, “It is the marketing department, not the science, that is driving the research.”  It seems plain wrong to me that Democratic-controlled legislatures across the country are frantically passing coercive mandates for pharmaceutical products for which no one knows the risks.

Furthermore, safety testing, which typically requires five or more years for other medical products, often lasts only a few days with vaccines—not nearly long enough to spot cancers or chronic conditions like autoimmune disease (e.g., juvenile diabetes, rheumatoid arthritis, multiple sclerosis), allergic illnesses (e.g., food allergies, allergic rhinitis, eczema, asthma), or neurological and neurodevelopmental injuries (e.g., ADD, ADHD, narcolepsy, epilepsy, seizure disorders, and autism). Manufacturers’ inserts accompanying every vial of mandated vaccines include warnings about these and over 400 other injuries including many serious immune, neurological, and chronic illnesses for which FDA suspects that vaccines may be the cause. Federal law requires that the package insert for each vaccine include “only those adverse events for which there is some basis to believe that there is a causal relationship between the drug and the occurrence of the adverse event.”

Many of these illnesses became epidemic in American children after 1986, coterminous with the exploding vaccine schedule. For American kids born in 1986, only 12.8% had chronic diseases. That number has grown to 54% among the vaccine generation (those born after 1986) in lockstep with the expanding schedule.  Evidence including HHS’s own surveillance reports, manufacturers’ inserts, and peer-reviewed studies link all of these injuries to vaccines. However, the associations are not definitive because CDC has failed to conduct the necessary randomized studies to prove or disprove causation.

HHS has directed the Institute of Medicine (IOM, now the National Academy of Medicine) to oversee the CDC’s vaccine safety science. IOM has repeatedly rebuked the agency for failing to study whether vaccines are causing these epidemics. In my experience, vaccine proponents rarely cite specific peer-reviewed studies to support their assertions that all vaccines are safe, relying instead on appeals to authority; CDC, FDA, WHO, or the AAP. My relatives, for example, argue that vaccines are safe because WHO, HHS, CDC, and FDA say so. But HHS designated the IOM as the ultimate arbiter of vaccine safety. And IOM says that the existing scientific literature does not support these claims.  Despite requests by the IOM, CDC has steadfastly refused to perform safety studies.

In total, three IOM reports (1991, 1994, and 2011/2012) investigated 231 adverse events associated with vaccines. For 34 conditions, IOM found that the evidence supported a causal connection between the vaccine and the adverse event. But for 184 adverse events, fully 80% of the conditions reviewed, the IOM found that HHS’s evidence was inadequate to accept or reject vaccine causation. How can our public health officials claim safety when there is no follow-up research on reported adverse events?

… the  IOM [Institute of Medicine now the National Academy of Medicine] study and the follow-up HHS study in 2014 both say that CDC has never performed a study to support CDC’s claim that DTaP does not cause autism.

Autism and vaccines

Let’s drill down on bedrock dogma that science has thoroughly debunked any links between autism and vaccines. That assumption is so engrained that media ridicules anyone who questions this orthodoxy as a dangerous heretic. But, look for a moment, at the facts. In 1986, Congress specifically ordered CDC to determine if pertussis-containing vaccines (DTP, later DTaP) were causing autism.  Then, as today, many parents with autistic children were claiming that vaccines were a cause of their child’s autism and DTP/DTaP vaccines were/are a popular suspect.

On its website, CDC declares that, “Vaccines don’t cause autism,” citing IOM’s comprehensive 2011/2012 literature review of vaccination safety science. However, the IOM study and the follow-up HHS study in 2014 both say that CDC has never performed a study to support CDC’s claim that DTaP does not cause autism.  The same is true for Hep B, Hib, PCV 13, and IPV. The only vaccine actually studied with regard to autism is MMR, and a senior CDC scientist claims the CDC did find an increased rate of autism after MMR in the only MMR/autism study ever conducted by the CDC with American children. Moreover, HHS’s primary autism expert recently provided an affidavit to the DOJ explaining that vaccines can cause autism in some children.

Autism has grown from about 1 in 2,500 prior to 1986 to one in 36 among vaccine generation children today. Why are we content with the CDC’s claim that the exponential explosion of autism is a mystery? CDC spares no expense systematically tracking the source of 800 measles cases. But when asked about the cataclysmic epidemic of upwards of 68,000 new autism cases annually, CDC shrugs. Why are we not demanding answers? “CDC is paralyzed right now when it comes to anything to do with autism,” explains former senior vaccine safety scientist Dr. William Thompson, who is still a CDC employee. Thompson told Congressman Bill Posey under oath that CDC bigwigs ordered him to destroy data that showed a link between autism and vaccines and to publish a fraudulent study dismissing the link. Today, he is remorseful, “When I see a family with a child with autism, I feel great shame because I have been part of the problem.”

… there are a hundredfold more adverse vaccine events than are reported.

We are killing children

HHS has also ignored its statutory obligations to study vaccine injuries and improve vaccine safety. In 1986, Congress—recognizing that drug companies no longer had any incentive to make vaccines safe—ordered HHS to study vaccine injuries, work to improve vaccine safety, and report to Congress on its progress every two years. A year ago, I brought a lawsuit that forced HHS to admit that in 36 years it had never performed any of those critical studies.

Post-licensure vaccine safety surveillance is also in shambles. The CDC’s Vaccine Adverse Event Reporting System (VAERS), to which doctors and patients may voluntarily report adverse vaccine events, received 58,381 reports in 2018, including 412 deaths, 1,237 permanent disabilities, and 4,217 hospitalizations. An HHS-funded review of VAERS concluded that “fewer than 1% of vaccine adverse events are reported” to VAERS. This suggests that there are a hundredfold more adverse vaccine events than are reported. The CDC has nonetheless refused to mandate or automate VAERS reporting.

Dr. Aaby was one of five co-authors of a 2017 study of the diphtheria tetanus, and pertussis (DTP) vaccine, the most widely used vaccine on earth, which found that children who received DTP had ten times the risk of dying compared to DTP-unvaccinated children.

On March 9, 2019, Dr. Peter Aaby issued a scathing rebuke to the world’s public health agencies for continuing to allow pharmaceutical companies to sell vaccines without proper safety testing.  Dr. Aaby, who has authored over 300 peer-reviewed studies, is one of world’s foremost authorities on WHO’s African vaccine program and the winner of Denmark’s highest honor for health care research. Dr. Aaby was one of five co-authors of a 2017 study of the diphtheria tetanus, and pertussis (DTP) vaccine, the most widely used vaccine on earth, which found that children who received DTP had ten times the risk of dying compared to DTP-unvaccinated children. For thirty years, doctors, including Aaby, never noticed the danger because vaccinated children were succumbing to illnesses and infections apparently unrelated to the vaccine. It turns out that while the vaccine protected children from diphtheria, tetanus, and pertussis, it so badly weakened their immune systems that they were dying in droves from unrelated infections. The researchers concluded: “The DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus and pertussis.”  In March, an alarmed Aaby plead for a policy change, “Most of you think we know what our vaccines are doing. But we don’t…. We are killing children.”

The world’s most aggressive vaccine schedule has not given our country the world’s healthiest children. We now rank 35th in overall health outcomes—just behind Costa Rica, making the U.S., by most measures, including infant mortality, the sickest in the developed world. In addition to those 400 chronic diseases and injuries that FDA suspects may be vaccine related, the vaccine generation suffers unprecedented levels of anxiety and depression and behavioral disorders running the gamut from aggression to anorexia. Peer-reviewed animal and human studies have linked all these symptoms to vaccines. The present generation is the first in a century to lose I.Q., having suffered an extraordinary drop of seven points.  Researchers concluded that some environmental cause is the trigger. In the U.S., SAT and, more recently, bar exam scores are plummeting. Could these declines be the outcome of injecting virtually every child with multiple doses of two of the world’s most potent neurotoxins—mercury and aluminum—in bolus doses beginning on the day of birth? Shouldn’t we be doing the research to reject this hypothesis? The logical approach to doing so would be to compare health outcomes between vaccinated and unvaccinated children. For years, public health officials, including the IOM, have urged CDC to conduct such studies.

In 2013, the IOM found that, “No studies have compared the differences in health outcomes… between entirely unimmunized populations of children and fully immunized children…. Furthermore, studies designed to examine the long-term effects of the cumulative number of vaccines or other aspects of the immunization schedule have not been conducted.” In a 2008 interview, former NIH Director Bernadette Healy explained that HHS refuses to perform safety studies out of fear that they will expose dangers, “that would scare the public away” from vaccines.  Healy continued, “First of all, I think the public is smarter than that… I don’t think you should ever turn your back on any scientific hypothesis because you’re afraid of what it might show.”

… the absence of press scrutiny leaves industry no incentive to improve vaccine safety.

Media malpractice

The suppression of critical safety science documented by the IOM would not be possible without a mass epidemic of media malpractice. Mainstream and social media outlets which collectively received $9.6 billion in revenues from pharmaceutical companies in 2016 have convinced themselves they are protecting public health by aggressively censoring criticism of these coercively mandated, zero liability, and untested pharmaceutical products.  But, the absence of press scrutiny leaves industry no incentive to improve vaccine safety.  Muzzling discussions of government corruption and deficient safety science and abolishing vaccine injuries by fiat is not a strategy that will solve the growing chronic disease epidemic.

The children who comprise this badly injured generation are now aging out of schools that needed to build quiet rooms and autism wings, install wobble chairs, hire security guards and hike special ed spending to 25% to accommodate them. They are landing on the social safety net which they threaten to sink. As Democratic lawmakers vote to mandate more vaccines and call for censorship of safety concerns, Democratic Presidential candidates argue about how to fix America’s straining health care system. If we don’t address the chronic disease epidemic, such proposals are like rearranging the deck chairs on the Titanic. The good news for Pharma is that many of these children have lifelong dependencies on blockbuster products like Adderall, Epi-Pens, asthma inhalers, and diabetes, arthritis, and anti-seizure meds made by the same companies that made the vaccines.

My uncle and my father argued that in a free and open society, the response to difficult questions should never be to shut down debate.

My belief that all or some of these injuries might be vaccine related has been the catalyst that wrenched so much of my focus away from the environmental and energy work that I love, and prompted me to become an advocate for vaccine safety. I have sacrificed friendships, income, credibility, and family relationships in an often-lonely campaign to force these companies to perform the tests that will definitively answer these questions.

People will vaccinate when they have confidence in regulators and industry.  When public confidence fails, coercion and censorship became the final options.  Silencing critics and deploying police powers to force untested medicines upon an unwilling public is not an optimal strategy in a democracy.

My uncle and my father argued that in a free and open society, the response to difficult questions should never be to shut down debate. What we need is science, not censorship. I am not anti-vax. I am pro-safety and pro-science. I want robust, transparent safety studies and independent regulators. These do not seem like the kind of radical demands that should divide our party or our families. As Americans and Kennedys, we ought to be able to have a civil, science-based debate about these legitimate concerns.

© [Aug 15, 2019] Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

________________

For more:  https://madisonarealymesupportgroup.com/2019/03/22/vaccines-best-video-yet/

https://madisonarealymesupportgroup.com/2019/08/05/fully-vaccinated-vs-unvaccinated-a-summary-of-the-research/

https://madisonarealymesupportgroup.com/2018/09/08/acip-vote-yes-for-new-vaccine-despite-no-safety-studies-on-cumulative-effect-with-other-vaccines/

https://madisonarealymesupportgroup.com/2019/03/02/mic-drop-at-the-acip-cdc-meeting-vaccine-science-not-settled/

https://madisonarealymesupportgroup.com/2019/08/09/former-merck-scientist-explains-why-he-doesnt-vaccinate-his-children-due-to-lack-of-vaccine-safety-studies/

https://madisonarealymesupportgroup.com/2019/06/13/blast-from-the-past-cdc-vaccine-authors-destroy-evidence-of-vaccine-harm/

https://madisonarealymesupportgroup.com/2019/01/22/bill-gates-former-doctor-says-billionaire-refused-to-vaccinate-his-children/

 

https://rawlsmd.com/webinars/overcome-lyme-arthritis/?

How to Overcome Lyme Arthritis

Live Webinar with Dr. Bill Rawls

Joint and muscle swelling and discomfort are common in early Lyme disease, and the majority of chronic Lyme patients develop painful arthritis that tends to migrate around the body.

Why are Lyme sufferers so prone to arthritis symptoms, and what can you do to find fast and lasting relief?

Join a live webinar with best-selling author Dr. Bill Rawls, who knows firsthand what it’s like to live with chronic Lyme disease and related inflammation and pain, as he demystifies Lyme arthritis and shares insights on the best and worst natural and conventional remedies.

RESERVE MY SEAT »

In this webinar, Dr. Rawls will also discuss:

  • Why joint pain and inflammation are so common in Lyme patients
  • Mycoplasma, babesia, and other Lyme coinfections that cause tick-borne arthritis
  • Foods and other lifestyle factors that make symptoms worse
  • The best herbs, diet, and natural remedies for effective relief
  • Numerous insights during the live Q&A with Dr. Rawls

Presented by Dr. Bill Rawls and Tim Yarborough

  • Wed, August 21st
  • 8pm EDT
  • Webinar can be viewed on any device

https://www.cnn.com/2019/07/28/health/eastern-equine-encephalitis-mosquito-outbreak-chickens-florida-trnd/index.html

A deadly mosquito-borne virus that causes brain swelling in humans has been detected in Florida

(CNN) Florida health officials are warning of an uptick in a mosquito-borne virus known as Eastern equine encephalitis (EEE).
Several sentinel chickens tested positive for EEE, which can spread to humans via infected mosquitoes and cause brain infection and swelling, the Florida Department of Health in Orange County said in a Thursday statement. Sentinel chickens are fowl that are tested regularly for the West Nile virus and EEE. Their blood can show the presence of the diseases, but they don’t suffer from the effects of the viruses.
Following the positive tests for the sentinel chickens in Orange County, the health department said “the risk of transmission to humans has increased.”
Only about seven cases of the EEE virus in humans are reported in the US each year, the Centers for Disease Control and Prevention says.
However, the disease can be fatal: about 30% of people who contract it die, according to the CDC. Many survivors have ongoing neurologic problems.
People develop symptoms about 4 to 10 days after they are bitten by an infected mosquito, the CDC says. Signs include sudden onset of headache, high fever, chills and vomiting. More severe symptoms include disorientation, seizures and coma.
With summer in full swing, mosquitoes are buzzing around at peak populations. Officials warned people to avoid being bitten by draining standing water around their homes, covering skin with clothing or repellant, and using screens to cover doors and windows.
___________________

https://www.psychologytoday.com/us/blog/holistic-psychiatry/201907/mast-cell-activation-syndrome-alert-psychiatrists

Mast Cell Activation Syndrome: An Alert to Psychiatrists

Mast Cell Activation Syndrome can present as depression, anxiety, or brain fog

Posted Jul 23, 2019

Many patients who call requesting an initial psychiatric consultation are suffering from a common condition known as mast cell activation syndrome (MCAS). MCAS can present with extremely diverse fluctuating symptoms. Brain fog, anxiety, depression, and insomnia are among the most common symptoms. It is truly unfortunate that MCAS is not on the radar of most psychiatrists.

When a patient reports massive bloating accompanied by a 15-pound weight gain in a week, or that they can only eat a very restricted dietbecause they have instant horrible reactions to foods, or are experiencing weird neurological symptoms, or that they have become ultra-sensitive to a wide variety of stimuli, I immediately wonder if MCAS is at play. For some patients, the recognition and treatment of this condition have made a big difference in terms of quick symptom relief.

Neil Nathan, MD has written an excellent chapter in his new book titled Toxic about MCAS. (pages 99-114).

 Neil Nathan MD
“Toxic” Neil Nathan MD
Source: Neil Nathan MD
Symptoms Dr. Nathan lists that can be attributed to MCAS include:
  • Intense anxiety and depression
  • Severe pain that can localize to joints, muscles, tendons and/or bones
  • Unusual neurological symptoms like numbness and tingling in different parts of the body, paralysis, and pseudoseizures
  • Headaches
  • Ringing in the ears
  • Sensitivity to a wide array of stimuli, such as light, touch, sound, smells, foods, chemicals, and electromagnetic frequencies (EMF)
  • Sore throat
  • Swollen lymph glands
  • Indigestion, including diarrhea, constipation, bloating, gas and heartburn
  • Chronic debilitating fatigue
  • Insomnia
  • Cognitive difficulties, including brain fog and decreased focus, memoryand concentration
  • Pelvic pain
  • Interstitial cystitis (painful inflammation of the bladder)
  • Shortness of breath
  • Air hunger ( a feeling of being unable to take a deep breath)
  • Skin rashes
  • Difficulties with equilibrium and balance

When patients consult their primary care doctor with many seemingly random dramatic complaints affecting unrelated organ symptoms, which often feature prominent psychiatric symptoms, they are often thought to be suffering from a psychosomatic condition and told “its all in your head.” They may be sent home with a prescription for an antidepressant or anti-anxiety medication, which not only is experienced as invalidating but does not address the root cause of their symptoms.

Identifying MCAS as the source of symptoms has important treatment implications and can speed recovery.

Mast cells are white blood cells that are part of the immune system and function as a bridge between the immune and the nervous system, acting to coordinate the two. Their primary function is to defend against toxins and infectious agents.

Mast cells can be found in all tissues of the body, but the highest concentrations are located in those parts of the body that interface with the outside world and are thus exposed to infections and toxins. These include the sinuses, throat, gastrointestinal tract, respiratory tract, skin, and genitourinary tract.

Mast cells are filled with vesicles called granules that contain more than 200 different biochemical signalers.  When a toxin or infectious agent is introduced, an individual with a well-functioning immune system will mobilize their mast cells to orchestrate an appropriately measured response. The mast cells release their biochemical mediators, most prominently histamine, serotonin and tryptase, to neutralize the danger.

If a person’s immune system has become dysregulated and hyperaroused, the mast cells can become overreactive. Instead of releasing their biochemical mediators in an appropriately self-limited way, they become disorganized and degranulate chaotically, causing the wide array of symptoms listed above.

Treatment consists of stabilizing the membranes of the mast cells so that they do not degranulate and calming down the nervous system.

For some patients, conventional over-the-counter antihistamines can be useful. Improvement may be immediate or can take up to two months. Another mast cell stabilizer is quercetin, a member of the vitamin C family. Another medication that can be helpful is the histamine-2 blocker, famotidine.

There are natural substances that can be helpful as well as prescription medications.

Some patients with MCAS benefit from a low histamine diet.  It is important to determine whether such a diet does in fact make a difference because it is not healthful to restrict diet unnecessarily.

In terms of addressing the hyperarousal of the nervous system, I often recommend Dynamic Neural Retraining System (DNRS), an intensive experiential program that integrates components of cognitive behavioral therapy, mindfulness-based cognitive restructuring, emotional restructuring therapy, neural linguistic programming, incremental training (a form of neural shaping) and behavior modification therapy to rewire neural circuits in the limbic system, which calms the hyperactive stress response.

Although treating MCAS is helpful for affording symptom relief, there is a need to address the underlying root cause in order for a patient to heal.

An exhaustive resource about MCAS is Lawrence Afrin MD’s 2016 book, Never Bet Against Occam: Mast Cell Activation Disease and the Modern Epidemic of Chronic Illness and Medical Complexity.

References

Nathan, Neil (2018) Toxic Canada Victory Belt Publishing 

Afrin, Lawrence (2015) Never Bet Against Occam: Mast Cell Activation Disease and the Modern Epidemic of Chronic Illness and Medical Complexity Sisters Media LLC

Lysander Jim, Yvonne Berry, Ming Dooley, James Ryan, Scott McMahon (2018) Diagnostic Process for Chronic Inflammatory Response Syndrome (CIRS): A Consensus Statement Internal Medicine Review Volume 4 Issue 5

________________

**Comment**

One of the most prevalent topics at the ILADS convention was MCAS involvement with Lyme/MSIDS. Many LLMD’s are seeing this trend of having both in their patients. Dealing with the MCAS helps the overall symptom picture greatly in these patients.

https://madisonarealymesupportgroup.com/2018/12/29/mcas-lyme-msids-2018-ilads-convention/

https://madisonarealymesupportgroup.com/2018/12/29/mcas-triggers-symptoms-how-to-cope/

https://madisonarealymesupportgroup.com/2019/05/08/9-proven-treatments-for-mast-cell-activation-syndrome-plus-a-surprising-new-comer/

https://madisonarealymesupportgroup.com/2018/03/13/mcas-lyme-msids/

https://madisonarealymesupportgroup.com/2018/03/26/the-agony-of-mcas/

 

https://hwcdn.libsyn.com/p/1/8/6/186252aabfba10ca/LMS_-_08.14.19_-_Richard_Horowitz_MD.mp3?  MP3 Here:  Approx. 40 Min.

Dr. Horowitz interviewed by Lillian McDermott

safe_image.php

  • Great, practical information on ticks, the diseases they carry, and the need for prevention
  • Discusses advances in the treatment of Lyme Disease and associated co-infections
  • Discusses some of the present work using ‘persister’ drug regimens such as dapsone and disulfiram, and how these regimens are showing promise in improving patients’ lives
  • Topic will be ‘Advances in Washington DC’ and progress made during the first two years of the Tick-borne Disease Working Group.Disclaimer: The views expressed during this program will be those of Dr Richard Horowitz, and do not represent the views of the Tick-Borne Disease Working Group, HHS or the United States.