Archive for the ‘Lyme’ Category

43-Year-Old Man With Meningitis & Radiculitis Due to Lyme Disease

https://danielcameronmd.com/meningitis-and-radiculitis-lyme-disease/  Podcast Here

43-YEAR-OLD MAN WITH MENINGITIS AND RADICULITIS DUE TO LYME DISEASE

meningitis-lyme-disease

Hello, and welcome to another Inside Lyme Podcast. I am your host Dr. Daniel Cameron. In this episode, I will be discussing a unique case involving a 43-year-old man with neurological manifestations of Lyme disease including both meningitis and radiculitis.

The case was published in the journal Neurology International. [1] According to Dabiri and colleagues, the patient had a history of “scaly erythematous macular rash on his proximal medial upper and lower extremities.”

Within two weeks he presented with a broad range of symptoms “including cough, fever, anorexia, malaise, fatigue, myalgias, cervicalgia/neck stiffness with flexion and extension, mild photophobia, headache,”  the authors wrote.

The patient had extensive lab testing which revealed a mild abnormal liver function but no evidence of Lyme disease.  At the onset of symptoms, the patient refused to have a spinal tap.

Doctors presumed the man suffered from viral meningitis.

One month later, the patient developed progressive weakness, severe radicular lancinating pain, emotional lability along with depression and anxiety, an occasional action tremor in hands interfering with fine motor tasks, and tremor in his legs causing imbalance and instability.

Manifestations of the central nervous system (i.e, meningitis), as well as peripheral nervous system presentations (i.e., radiculitis) can occur in isolation or together.

Radiculitis or inflammation of the nerve root involving the peripheral nervous system (PNS) can lead to intractable pain, muscle denervation, and areflexia over one or a few adjacent dermatomes, wrote the authors.

At this point, results from a spinal tap were consistent with Lyme disease.  “A lumbar puncture was performed, and the patient’s cerebrospinal fluid (CSF) analysis showed lymphocytic pleocytosis with white blood cell count of 225 and elevated protein of 77 and decreased glucose 38,” the authors wrote.

The patient was treated with a 5-day course of doxycycline, followed by a month of intravenous ceftriaxone.

Approximately two weeks after starting treatment, the patient “noted his symptoms were significantly improved including resolution of the pain, weakness, constitutional and affective symptoms, while he still had some ambulatory difficulties.”

This podcast addresses the following questions:

  1. What is Lyme meningitis?
  2. What is Lyme radiculitis?
  3. Why is this case considered “unique”?
  4. CNS and PNS manifestations can occur in isolation or together?
  5. Can you discuss the patient’s symptoms of emotional lability, depression and anxiety?
  6. What is the significance of the rash?
  7. Initial testing for Lyme disease was inconclusive but follow-up tests were positive?
  8. Any significance to MRI and spinal tap results?
  9. What if the significance of a diagnosis of viral meningitis?
  10. What were the other symptoms that might have helped the diagnosis?
  11. Would clinical judgment to treat with antibiotics have been helpful?
  12. What are your thoughts regarding the course of treatment?
  13. Would it have been helpful to consider additional treatment for the remaining ambulatory difficulties?
    1. Thanks for listening to another Inside Lyme Podcast. You can read more about these cases in my show notes and on my website @DanielCameronMD.com. As always, it is your likes, comments, reviews, and shares that help spread the word about Lyme disease. Until next time on Inside Lyme.

Please remember that the advice given is general and not intended as specific advice as to any particular patient. If you require specific advice, then please seek that advice from an experienced professional.

Inside Lyme Podcast Series

This Inside Lyme case series will be discussed on my Facebook and made available on podcast and YouTube.  As always, it is your likes, comments, and shares that help spread the word about this series and our work. If you can, please leave a review on iTunes or wherever else you get your podcasts.

References:
  1. Dabiri I, Calvo N, Nauman F, Pahlavanzadeh M, Burakgazi AZ. Atypical presentation of Lyme neuroborreliosis related meningitis and radiculitis. Neurol Int. 2019 Dec 2;11(4):8318.
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https://madisonarealymesupportgroup.com/2019/03/17/first-case-of-b-corocidurae-in-native-european-presenting-as-meningitis-with-cranial-polyneuritis-cavernous-sinus-thrombosis/  European cases of B. crocidurae infection have been reported in travelers returning from endemic areas. We report the first autochthonous case in Europe of B. crocidurae infection, presenting as meningitis…..

Treatment Delays Increase Risk of Persistent Illness in Lyme Disease

https://www.hopkinslyme.org/news/treatment-delays-increase-risk-of-persistent-illness-in-lyme-disease/

Treatment Delays Increase Risk of Persistent Illness in Lyme Disease

Summary

In this retrospective study, one-third of Lyme disease patients report delayed treatment of greater than 30 days, and delayed treatment is associated with post-treatment Lyme disease (PTLD). Delays in treatment are shown to significantly impact patient outcomes and indicate that improved Lyme disease diagnosis and prevention strategies are needed.

Why was this study done?

The goals of the study were to analyze time-to-treatment in a sample of individuals treated for Lyme disease, including identifying risk factors for time to first medical contact and time under care. The study also evaluated associations between time-to-treatment and the development of post-treatment Lyme disease (PTLD). The study was done to determine if delays in treatment are significant to patient outcomes.

How was this study done?

A retrospective study was conducted of time-to-treatment among a general population sample of individuals treated for Lyme disease at Geisinger, a health system in Pennsylvania, the state with the most confirmed Lyme disease cases in the United States. Using electronic medical records and self-administered questionnaire data, respondents’ experiences were characterized by symptoms, care-seeking factors, diagnosis, and treatment. Associations between time-to-treatment and PTLD were examined, and risk factors were measured for delays in time to first medical contact and time under care.

Questionnaires were mailed to 5,314 adult patients who met previously described EHR-based criteria for Lyme disease between 2015 and 2017. Analyses focused on 778 respondents who reported that they were treated for Lyme disease within the past 5 years and reported a rash and/or a positive blood test for Lyme disease. Time-to-treatment was measured in days as the sum of two time windows: time to first medical contact and time under care. Logistic regression was used to evaluate factors associated with delayed time-to-treatment in each time window (>14 days vs. ≤14 days) and the association between total time-to-treatment (>30 days vs. ≤30 days) and PTLD.

What were the major findings?

In the sample of Lyme disease patients studied, delays in medical contact and care were identified in one-third of individuals and delays were associated with a higher risk for post-treatment Lyme disease. In the sample,

  • 25% had time to first medical contact greater than 14 days
  • 21% had time under care of a medical professional greater than 14 days
  • 31% had a total time-to-treatment greater than 30 days

Factors positively associated with delayed time to first medical contact included being uninsured and attributing initial symptoms to something other than Lyme disease. Diagnoses between November and April, and the absence of rash were positively associated with delays in contact and care. First medical contact in an emergency department or “other” setting showed delays in care.

Individuals whose treatment was delayed, defined as time-to treatment >30 days, had 2.26 times the odds of developing PTLD as those who were treated within 30 days of symptom onset.

What is the impact of this work?

Despite post-treatment Lyme disease occurring in an estimated 10-20% of Lyme disease cases, no peer-reviewed studies have evaluated the role of time-to-treatment in PTLD. This retrospective study indicates timely treatment may be important in preventing PTLD and other long-term consequences of Lyme disease.

Strategies to ensure more timely treatment of Lyme disease should include educational campaigns targeting patients and healthcare providers. Education could improve the recognition of the varied clinical presentations of Lyme disease and the erythema migrans rash and underscore the limitations of diagnostic tests. Although urgent care clinics can help patients be seen earlier, there is a clear need to improve disease recognition and diagnosis and reduce time-to-treatment in this setting. Another opportunity to reduce time-to-treatment is to build awareness among patients and medical providers of the risk of Lyme disease throughout the year in endemic regions.

Education, diagnostics, and prevention approaches are needed and should address the risk factors for treatment delays and aim to reduce both the time before and after contacting a medical professional.

This research was supported by:

funded by the Steven & Alexandra Cohen Foundation

Publication Information

Hirsch AG, Poulsen MN, Nordberg C, Moon KA, Rebman AW, Aucott JN, Heaney CD and Schwartz BS (2020) Risk Factors and Outcomes of Treatment Delays in Lyme Disease: A Population-Based Retrospective Cohort Study. Front. Med. 7:560018. doi: 10.3389/fmed.2020.560018

Johns Hopkins Lyme Disease Research Center

The Johns Hopkins Lyme Disease Research Center is focused on patient-based research in all manifestations of Lyme disease. Our goal is to translate our pioneering research into improved patient care, education, and health outcomes.

USE OF THIS SITE

All information contained within the Johns Hopkins Lyme Disease Research Center website is intended for educational purposes only. Physicians and other health care professionals are encouraged to consult other sources and confirm the information contained within this site. Consumers should never disregard medical advice or delay in seeking it because of something they may have read on this website.

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**Comment**

Although this study is helpful for demonstrating that delays in diagnosis and treatment are bad, there are a number of concerns:

  1. The continued use of outdated and stringent criteria such as the EM rash and blood serology testing. Reality has proven a huge subset of patients meet neither.
  2. Electronic medical records and self-administered questionnaire data are only as effective as the people are filling them out, the questions being asked, and the objectivity of the person compiling the data.
  3. The PTLD label is deceptive and assumes ongoing symptoms are not caused by persistent/chronic infections.

The major findings; however, were helpful in showing that more than half were not obtaining treatment until 14-30 days.  This is important in the light of this mouse study which demonstrated Bb in the brain within a week of infection.

The factors of being uninsured and uneducated on tick-borne illness led to delayed time to 1st medical contact as well as those being seen between Nov-April and the absence of rash (both of which really should be under the banner of being uneducated about tick-borne illness as you can be infected in any month and getting the rash is highly variable).

Study Finds Lyme in Mouse Brains Within a Week of Infection

https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1009256

A murine model of Lyme disease demonstrates that Borrelia burgdorferi colonizes the dura mater and induces inflammation in the central nervous system

journal.ppat.1009256.g003

Fig 3. B. burgdorferi in the dura mater are extravascular and motile.  Multiphoton image of ex vivo dura mater from C3H mouse after infection with GFP-Bb_297 for 7 days. B. burgdorferi is shown in green; collagen (second harmonics) shown in blue. Imaging parameters: Wavelength = 910 nm, pixel resolution = 135. See S1 Movie for image series movie showing spirochete motility.  https://doi.org/10.1371/journal.ppat.1009256.g003

Timothy Casselli, Ali Divan, Emilie E. Vomhof-DeKrey, Yvonne Tourand, Heidi L. Pecoraro, Catherine A. Brissette

Published: February 1, 2021

https://doi.org/10.1371/journal.ppat.1009256

 

Abstract

 

Lyme disease, which is caused by infection with Borrelia burgdorferi and related species, can lead to inflammatory pathologies affecting the joints, heart, and nervous systems including the central nervous system (CNS). Inbred laboratory mice have been used to define the kinetics of B. burgdorferi infection and host immune responses in joints and heart, however similar studies are lacking in the CNS of these animals. A tractable animal model for investigating host-Borrelia interactions in the CNS is key to understanding the mechanisms of CNS pathogenesis. Therefore, we characterized the kinetics of B. burgdorferi colonization and associated immune responses in the CNS of mice during early and subacute infection. Using fluorescence-immunohistochemistry, intravital microscopy, bacterial culture, and quantitative PCR, we found B. burgdorferi routinely colonized the dura mater of C3H mice, with peak spirochete burden at day 7 post-infection. Dura mater colonization was observed for several Lyme disease agents including B. burgdorferi, B. garinii, and B. mayonii. RNA-sequencing and quantitative RT-PCR showed that B. burgdorferi infection was associated with increased expression of inflammatory cytokines and a robust interferon (IFN) response in the dura mater. Histopathologic changes including leukocytic infiltrates and vascular changes were also observed in the meninges of infected animals. In contrast to the meninges, we did not detect B. burgdorferi, infiltrating leukocytes, or large-scale changes in cytokine profiles in the cerebral cortex or hippocampus during infection; however, both brain regions demonstrated similar changes in expression of IFN-stimulated genes as observed in peripheral tissues and meninges. Taken together, B. burgdorferi is capable of colonizing the meninges in laboratory mice, and induces localized inflammation similar to peripheral tissues. A sterile IFN response in the absence of B. burgdorferi or inflammatory cytokines is unique to the brain parenchyma, and provides insight into the potential mechanisms of CNS pathology associated with this important pathogen.

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**Comment**

Technically one could say this isn’t the brain.  It’s the outer layer called the meninges – of which, the dura mater is one layer.  Regardless, this inflammation caused by infections can cause swelling, pain, and so much more.  It’s also why some Lyme/MSIDS patients have been diagnosed with Chiari.

Important excerpts:

Overall, we report that B. burgdorferi routinely colonizes the meninges in laboratory mice during early and subacute infection, and induces similar localized inflammatory gene expression profiles as other peripheral tissues as well as histopathological changes.

Conclusion:

Overall, the findings reported in this study are significant, as the lack of a tractable animal model has hindered our understanding of host-pathogen interactions in the CNS during B. burgdorferi infection. Our results provide insight into potential mechanisms of CNS pathologies associated with Lyme disease, and describe a model system that will allow for future studies evaluating the bacterial, host, and environmental factors that can contribute to the severity of CNS involvement during B. burgdorferi infection. Such studies are critical for the development and implementation of novel prophylactic and therapeutic interventions for this important disease.

The discussion section mentioned something that’s always interested me: the location of the tick bite or injection site.  The authors state that although they were able to “readily culture spirochetes from the blood of all mice at day 7 post-infection, dura spirochetes were rarely detected in mice inoculated in the footpad, and spirochete burdens were dramatically reduced in mice inoculated in the dorsal lumbar skin compared to thoracic skin.”  Further, dissemination of Bb happens in more ways than via blood and that these other ways, such as through the lymphatic system, may contribute to increased early colonization of the dura mater in mice.  This was only true for early infection and by 28 days, Bb in the dura mater were comparable regardless of the inoculation site.

This article reveals what patients have been experiencing for decades: heads that feel as if they were going to explode.  I wondered if there would ever be a day without a headache.  I personally found that Minocycline was one of the most productive antibiotics for this.  

 

 

 

10 Top Causes of Symptoms in Chronic Lyme Disease

https://www.prohealth.com/library/ten-common-causes-of-symptoms-in-chronic-lyme-disease-8558

10 Top Causes Of Symptoms In Chronic Lyme Disease

(Please see link above for full article.  Excerpts below)

1) Mold toxicity

Real Time labs is among the most accurate of labs for mold testing. Effective mold toxin binders include the medication cholestyramine and activated charcoal.

2) Parasitic Infections

Parasitic infections are often not detectable on conventional lab tests, and may not even show up in sophisticated stool tests; therefore, using multiple forms of testing to detect parasites, such as electrodermal screening tools such as the Zyto or muscle testing, is important, along with lab testing with reputable labs such as Doctors’ Data.

3) Hormone and Neurotransmitter Imbalances

Replenishing the body’s stores of these chemicals can therefore profoundly support the healing process and Lyme doctors will commonly prescribe bio-identical hormones such as pregnenolone, DHEA and thyroid hormone to their patients, along with amino acids such as L-tyrosine, GABA and 5-HTP, which the body uses to make neurotransmitters. To make these amino acids work in the body, supplemental co-factors such as P5P, SAMe, and methyl B-12 are also sometimes important.

4) Vitamin and Mineral Deficiencies

Common deficiencies include magnesium, Vitamins D, C and B-vitamins; zinc and iron—among others. Supplementation with these nutrients can help to support the body during healing. (For more information on common nutritional deficiencies in Lyme disease and supplements that support the body, I encourage you to check out my 2012 book Beyond Lyme Disease).

5) Inflammation

Reducing inflammation involves mitigating all of its causes, such as removing pathogens and toxins from the body, and downregulating the immune response with nutrients and tools such as low-dose immunotherapy. High-quality, natural anti-inflammatory substances such as curcumin may also be helpful for supporting the body’s inflammatory response.

6) Mitochondrial Dysfunction

Supporting the mitochondria with supplements such as L-carnitine and CO Q-10 can help to mitigate fatigue and other symptoms related to mitochondrial dysfunction.

7) Emotional Trauma

Many studies have proven that trauma suppresses immune function and when prolonged, can open the door to chronic health challenges.

8) A Poor Diet

Removing allergenic foods and consuming fresh, organic “real” food, such as non-GMO, antibiotic, pesticide, and hormone-free meats, poultry, eggs, and other proteins; non-starchy veggies and low-glycemic fruits, along with healthy fats such as olive and coconut oil, can help to alleviate symptoms caused by food.

9) Poor Gastrointestinal Function

Supplementing with GI nutrients such as hydrochloric acid, digestive enzymes and probiotics may help to support gastrointestinal function in those with Lyme.

10) Environmental Toxicity

Sauna therapy, rebounding, coffee enemas, liver cleanses, and taking toxin binders such as zeolite, chlorella, EDTA, activated charcoal—among others, are just a few ways to remove toxins from the body.  Ideally, you’ll want to work with a practitioner who can test your body for toxins and prescribe a regimen in conjunction with Lyme disease treatment based on your needs. The same holds for the other causes of symptoms described here.

This article was first published on ProHealth.com on April 26, 2016 and was updated on September 22, 2020.


Connie Strasheim is the author of multiple wellness books, including three on Lyme disease. She is also a medical copywriter, editor and healing prayer minister. Her passion is to help people with complex chronic illnesses find freedom from disease and soul-spirit sickness using whole body medicine and prayer, and she collaborates with some of the world’s best integrative doctors to do this. In addition to Lyme disease, Connie’s books focus on cancer, nutrition, detoxification and spiritual healing. You can learn more about her work at: ConnieStrasheim.

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**Comment**

Not mentioned is Lyme itself, and the many other potential players.  While parasites apart from Lyme is mentioned, dealing with the infections is paramount.  Of course these infections are indirectly affected by the things listed in the helpful article, but never underestimate the infection(s) themselves.  Good, effective, savvy treatment is required.

For more:

The Problem with CDC Death Statistics

Recently, there’s been interest in the fact Lyme/MSIDS is horribly underreported, and with how deaths are recorded. This subject has resulted bill S.677A currently in the Assembly requiring coroners, pathologists, and medical examiners to report promptly to the local or superintending health department whether a deceased person at the time of death was afflicted with Lyme or any other tick-borne disease.

We’ve been told ad nauseam by our public ‘authorities’ that Lyme doesn’t kill people, yet it clearly does. A Wisconsin Lyme advocate keeps a memorial on her website of deaths linked to tick-borne illness. And, there’s a lot of them!

What is written on death certificates is very important as it directly affects how a disease is perceived.  A disease causing many deaths will be taken more seriously and will have more research funding allotted for it. We are seeing this play out with COVID-19 and the fact hospitals were paid to count deaths as COVID, even when there were confounding issues and many times COVID wasn’t even the direct cause. Then there’s the issue of faulty PCR testing for COVID which is positive for nearly everyone, which further casts doubt on the validity of COVID mortality statistics.  Yet, these inflated numbers are being used daily to drive a message that COVID is extremely deadly, despite the fact experts continue to say the mortality rate for COVID is nearly the same as the seasonal flu.

While all deaths are important, the CDC has inflated COVID deaths but has a long history of deflating Lyme/MSIDS deaths.

Recently, there’s been a call for an investigation into the CDC’s COVID ‘data disaster’:  https://madisonarealymesupportgroup.com/2021/02/15/data-disaster-call-for-a-cdc-investigation-free-online-event-feb-17-2021/  If you missed it but still want to view it, go here.

The following article sheds light on cause of death reporting:

https://healthimpactnews.com/2018/death-certificate-clerk-reveals-how-cause-of-death-reporting-is-subjective-and-cdc-statistics-not-reliable-when-making-public-health-decisions/

Death Certificate Clerk Reveals How Cause of Death Reporting is Subjective and CDC Statistics are Not Reliable When Making Public Health Decisions

This is a closeup view of the Death certificate

Comments by Brian Shilhavy
Editor, Health Impact News

Feb. 20, 2018

In our recently published article on Sudden Infant Death Syndrome (SIDS) we referenced how the Centers for Disease Control and Prevention (CDC) and the World Health Organization (WHO) list 130 official ways for an infant to die according to official categories of death, but adverse reactions to vaccines is not one of them.

Joy Fritz is a Death Certificate Clerk, and she recently published some of her observations in the field of death recording on Facebook.

Joy relates how she and her husband were concerned about the severity of the flu season as was being reported in the media, and that she “started reading the FDA package inserts for different flu immunization options to get informed on which immunizations might be safest for our <1 year old and 6 year old.”

She states that she wanted to make an informed decision for her family, and that

“What I ultimately wanted to compare was the risk of death.”

She learned that public records on influenza deaths stated that there were no deaths related to adverse reactions to flu medications or flu shots.

However, being in the field of death recording, she dug deeper, and has presented her research and experience to the public.

She writes:

Our current system for capturing mortality rates can and does provide a mostly uninvestigated and inaccurate picture of what causes a death. The process for creating and registering causes of death for public records is a complicated, convoluted, politicized, completely open to both ignorance and the manipulations of personal, professional, and governmental interests.

I’m the one creating these statistics and I offer you this: If you take one thing away from this, take away a healthier skepticism about even the most accepted mainstream, nationally reported, CDC or other ‘scientific’ statistics.

A Humbling Exposé into the Creation of Mortality Rates and its Impact on Our Public Health Beliefs and Choices

by Joy Fritz
Facebook

I work with doctors, coroners and the local county registrars everyday to create death records. It’s what I do for a living and wanted to share my thoughts on the mortality rates being thrown around on main stream and social media regarding the influenza epidemic. Please note: This information I am sharing is not limited to influenza reporting, but rather, serves as a case study of how the mortality rate recording system (mal)functions at large.

I am sorry to say that death rates are NOT as simple nor as valid as every news broadcaster with perfectly-trained vocal delivery makes them sound, and they are absolutely not the infallible pillar of medical history as the CDC purports.

Our current system for capturing mortality rates can and does provide a mostly uninvestigated and inaccurate picture of what causes a death. The process for creating and registering causes of death for public records is a complicated, convoluted, politicized, completely open to both ignorance and the manipulations of personal, professional, and governmental interests.

I have come to realize how greatly this reality becomes a public health issue during this past flu season when every major media outlet is providing us with live updates on the accruing death toll. Seeing these reports caused me concern for my family.

My husband and I discussed what preventative treatment we might consider. I started reading the FDA package inserts for different flu immunization options to get informed on which immunizations might be safest for our <1 year old and 6 year old. What I ultimately wanted to compare was the risk of death.

My kids getting sick is just part of life, other people getting sick is just part of life, lowering the risk of death to my family and the people around me is what I cared about when it came specifically to the seasonal flu.

I started researching mortality rates to find the line item in the CDC reports for deaths due to influenza vs adverse reaction to influenza medications and immunizations.

I found influenza rates, no problem.

Flu medications and shots? No deaths reported. Awesome. What a simple decision to make.

But, being in the mortuary industry and curious how they get these reports, I looked at the last full report for 2014 and dug deeper and found that they simply code and reorganize the data that they receive from death records. The death records that I am typing up and registering everyday.

So my head started exploding. And I felt, and still feel, sick. I have realized that without knowing it, I knew exactly how influenza deaths are recorded, and I know exactly why there is no line item in the CDC’s mortality rates for adverse reactions to common medical treatments.

Before I continue, please know that I will not be explaining all the ins and outs of my job, nor the incredibly rare reality that medication complications and adverse reactions do get captured (usually in box 112 of the death record, not as the primary underlying cause).

Those exceptions are made possible by exceptional, and likely, very principled people, choosing individually to go above and beyond the call of protocol, whether that be the family that is aware of the impact of the legal documentation that occurs after death and stays level-headed and involved mere hours after the death of their loved one, or an insanely humble and honest doctor, in conjunction with the coroner medical-legal officer that trusts and cooperates with the honest doctor and vigilant family to think outside the box of their standard procedures.

Almost 5 years and nearly 5,000 death certificates later, I can say with confidence that that kind of post-death communication concoction is at a statistical percentage point that even the CDC would consider insignificant.

So, in the spirit of very uncomfortable truthfulness I will share a snapshot of the core issues embedded in the daily procedures of creating the death statistics that we so desperately need to make prudent health decisions for ourselves and our families. I will also include some examples of how these core issues would manifest into faulty statistical analysis at the level of our public health and lead to the miscalculation of the benefits and risks surrounding our individual medical choices.

Core Issue A: Doctors that provide causes have not all been trained the same way, and therefore do not provide standardized responses.

This may at first glance seem minor, as it always has to me, but this directly affects the cause that the doctor lists on the death certificate.

Some doctors prefer providing the underlying cause of death as something that has happened immediately in the last days or weeks before death such as pneumonia or influenza, and leave out the more chronic illnesses. Other doctors decide they will provide the more long-standing health conditions as the cause of death such as diabetes, asthma and congenital abnormality while leaving out the more immediate illnesses.

Some doctors include both the short term and long term diagnoses. This has to do with many factors such as in what capacity the doctor saw the patient -hospital vs hospice care for example- or the immediate availability of the complete medical record within the time frame being impressed by the mortuary due to upcoming funeral or cremation services. Or, simply due to the way the doctor personally prioritizes information.

Again, way too many factors to go into here, but the basic issue of the lack of standardization in cause of death diagnosis and reporting remains.

In this case the same patient can have all these conditions: influenza, pneumonia, diabetes, asthma and congenital abnormality on his/her medical record simultaneously and any one of those conditions listed are correct and valid and could be entered as a stand alone cause and be registered by me and the local and state registrars offices without a query.

It’s the doctor’s preference and his medical opinionyet the national attention given, medical research dollars, and yearly health choices we all make are swayed by which ever cause this particular doctor, with his/her own particular training and personality decides to jot down on the worksheet and send back to me to enter into the official record.

CORE ISSUE B: What most people don’t know is that doctors are not allowed to attest to anything that is not a strictly NATURAL cause of death.

Falls, medication complications or overdoses, causes with the word ‘injury’ in it, anything that is considered an unnatural or external cause is outside the realm of their jurisdiction as far as the death record is concerned.

The Coroner would need to be contacted and agree to certify or co-certify a death record that has an unnatural or external cause listed.

This is a whole other, very complicated reporting issue that I will not get into in this post.

I will say, however, from perspective of a mortuary representative, that everyone involved (doctor, coroner, registrar and myself) understands that the delay caused by any coroner involvement is highly dreaded and avoided if at all possible due to the amplified grief it can cause the family if they do not want an autopsy or investigation done or have to suffer a delay in services and or an upset in their own personal closure process.

However, the majority of doctors are aware of their own limitation to certify only natural causes of death. And usually in the interest of serving the grieving family, will provide the simplest natural cause that they know will quickly pass the approval of the local registrar’s office, fulfill their duty as a signing physician, and enable the grieving family to move forward with their scheduled burial or cremation services.

It should be noted here that doctors are under an additional pressure since they have a limited time set out by their State Health and Safety Codes to provide causes of death to a funeral home.

In California it is within 15 hours of death, although that is rarely achieved. Delays of more than a few days after death would risk them getting their license reported to the the state medical board for lack of compliance.

What works about this system? The system is created in such a way that naturally occurring infectious disease (such as influenza) CAN and is being reported and recorded in national mortality rates. However, the lack of standardization in the way doctors report it creates an unreliable number to set as the threshold for what constitutes an epidemic.

What does NOT work about this system? It does not report on the true consequential timeline of the patient’s medical treatment, including unnatural and external complications and errors in their medical care and is therefore woefully inadequate to make ANY medical claims or recommendations.

The first example to illustrate the impact of this issue is as follows:

I read a post from a nurse the other day that shared her story of being hospitalized due to complications of the flu. Even though she had gotten the flu shot every year, she had only gotten influenza this year. Five days after experiencing flu symptoms she went into her medical provider and was prescribed Tamiflu.

She went through her course of medication. Her flu symptoms eased but she started getting a tightness in the chest, which further worsened until she needed to be hospitalized for pneumonia and a close call with sepsis.

The conclusion of her post -and her medical opinion as a nurse – was that this year’s flu was very dangerous and anyone less healthy than her could have easily died with her symptoms, so she urged everyone to please get the flu shot to prevent the flu from spreading.

The saddest part about reading her story was discovering that she must not have read the Tamiflu manufacturer’s insert, which states that:

“No influenza vaccine interaction study has been conducted” and “Efficacy of TAMIFLU in patients who begin treatment after 40 hours of symptoms has not been established” and furthermore, “Events reported more frequently in subjects receiving TAMIFLU compared to subjects receiving placebo in prophylaxis studies, and more commonly than in treatment studies, were aches and pains, rhinorrhea, dyspepsia and upper respiratory tract infections.”(emphasis added)

This would lead to an alternate, very feasible medical conclusion that her hospitalization and pneumonia was the result of using a medication that has not been tested on a population of her vaccination status and symptoms duration, which also has the adverse reaction of a URTI.

But what if it wasn’t her? What if someone less healthy than herself with her exact symptoms and medication course HAD died?

Her medical opinion, and many other medical care providers opinion would have been that it was influenza that had caused the death, instead of the complications of the medication.

In the medical provider’s mind, the likelihood of influenza causing the death is greater than the medication causing the death because of mortality rates – but they are the ones creating the mortality rates – so what is considered reasonable likelihood is being created in a closed loop. A regurgitating cycle.

So, whether the attending physician at the hospital was aware of this medical misstep by the other medical provider or not, in this case the hospital physician could simply put ‘Influenza’ on the causes of death worksheet and send it back to me. Influenza would be entered in the death record and be reported in the state and then national database as such with no question from me or the government registrars.

What this has created, then, is a serious public health reporting conundrum. Death due to complications of improperly prescribed medication are NOT being calculated into the national reporting agencies in a real-time setting.

Neither would they be communicated in real-time to the public. Instead the public would simply hear of the rising influenza death toll and run for more medication (and likely not be reading the manufacturer’s insert either to verify if they truly are a good candidate for that medication).

In this medication example, as you can imagine, even IF they realize that the medication was prescribed erroneously, it would not be in the professional best interest of the medical provider or medical facility to report this prescription error and it’s possibly fatal complications to the family or public health officials.

I have many friends and family in the medical industry and it is easily admitted that legal and personal liability is a factor in the considerations of proper reporting.

However, if and when this possibly fatal prescription misstep was ever reported it would be in some very passive EMR analysis many months or years later, with no urgency or real-time public health warning. The ability for government to cross-check and minutely examine nearly 3 million decedent medical records of varying electronic availability – annually – it’s just not there.

This failed mechanism in the mortality rate ‘generator,’ if you will, is the same for the hotly debated adverse vaccine reactions. This is the reason you see horrible adverse vaccine reactions and deaths being claimed by parents on social media, but no item line for them in national statistics.

It is not because they don’t exist or don’t happen. The real-time data reporting system of death recording is not set up to calculate these deaths.

For the families that become aware of the adverse reactions in time to request investigation (<24 hours after death), and are able to request any relevant pathological specimens to be procured before the burial or cremation of their loved one, would then need to have the time and resources to go through the lengthy reporting and court procedures through VAERS.

A very few families do, and if they can establish enough scientific evidence (like pathology reports), find and produce enough experts and professional support, they MIGHT eventually get the causes of death amended and compensation for their loss paid out by the allotted government fund. And after 5, 10, 15 or 20 years, this passive data capture system might accrue enough statistical information to be reported back to the medical community so that they adjust their recommendations.

So, just like in the medication example, any death due to an adverse reaction to the flu shot or for ANY regularly scheduled wellness immunization, would similarly not be captured in the standard process of death recording.

As before, the doctor can still provide either influenza or any other natural occurring immune response as the only cause of death. He would send it to me and I would enter it in, get the state to approve it, and ‘Viola!’ – a thoroughly inaccurate mortality rate reporting.

In Conclusion

One of the most difficult realities for me to recognize in examining the mortality rate reporting system that I am a part of, is that the medical community itself is suffering from the ignorance that this kind of circular mortality rate generating system creates. Doctors and coroners are limited by the already existing mortality rates to gauge the likelihood of what caused death.

That kind of system can only regurgitate the same causes of death over and over again by forcing its reporters to use the same types of ‘acceptable’ death diagnoses as what ALREADY exists.

And these are the statistics the medical community uses to educate themselves and provide informed consent to the patient on what the most prudent option is for medical care to safeguard health and prevent death.

And, yes, I will take the opportunity here to say that we can logically apply this critical analysis of the lack of proper data capture to those reluctant to vaccinate or use medications.

There is no current national data capture system that records the morbidity or mortality rates of those who chose less medical intervention or choose to not vaccinate themselves or their kids. We don’t know what their life expectancy, quality of life or mortality rate is in our modern day, with the advancements in hygiene, technology and post-disease-diagnosis medical care availability being considered. It could absolutely be worse, statistically, but we wouldn’t know.

For nationally reported statistics we are left then with bad data on one side, and no control group data on the other. Hardly the recipe for safe or settled scientifically guided medical care.

Now where does that leave you and me? Our highly subjective yet somehow infallible weaponry of mortality rates – whether from national statistics or the social media horror stories – has us and all our friends and family swinging the manic flag of ‘People are dying!’

This flu season for example, some of our friends are saying ‘People are dying from flu! Get vaccinated! Take medication!’ or other friends are saying ‘People are dying from adverse reactions to medications/shots! Don’t get vaccinated! Drink elderberry!’

And we are all running for the nearest remedies that we are sure will help us – why? Because of statistics – OR because we don’t see statistics reflecting our lived reality, so we do the best we can to discern our health without statistics.

But I’m the one creating these statistics and I offer you this: If you take one thing away from this, take away a healthier skepticism about even the most accepted mainstream, nationally reported, CDC or other ‘scientific’ statistics.

Humans who had no concept of their national impact made them. The numbers are not hard – they are very, very fluid. And conversely, have a healthier skepticism about all the alternative remedies we welcome as hopeful scientific-ish options. There is no unbiased, century long, data capture system set up for these choices either.

As a parent, the most painful part of taking a step back and looking at all this, is having to humbly admit – I don’t know what the right thing to do is.

I don’t have the unbiased data I need to make the safest decision for my children.

I don’t know what the right thing to do is for myself, or for my husband.

I don’t know what side of the fence to stand on in the vaccination and mainstream medicine battlefield, and I don’t want to stand on a side: I just want the unbiased, uncorrupted and standardized data needed to accurately assess the benefits vs. the ultimate risks for my family’s health.

In the face of this fallible data capture system, my own resolution that I am willing to publicly recommend – no matter what medical choices you decide is best – would be for us all to become self reporters. Keep a health journal for each family member complete with dates and times and severity of symptoms of illness and track dates and dosages of any medical treatment administered.

Track degree of fevers, severity of migraines, frequency of ear infections, changes of behavior, hospitalizations, medications dosages and immunization combinations etc.

Think critically and ask questions when you see inconsistencies in any health recommendations offered to you or your family. Request and encourage a satisfactory discussion of benefits and risks with your medical provider.

Download and thoroughly read the manufacturers insert provided on the FDA’s website for any medication or immunization you are considering and verify that you are a good candidate for that medication.

If you decide to use that medical treatment, record any minor reactions in the health journal and immediately report any somewhat severe reactions to your medical provider and ask for that information to be added to your electronic medical record so that it might inform any future medical provider on your individual contraindications you may have in other medication courses.

Remember that each of us is liable for our own health choices, you cannot expect a medical provider to be a perfect assessor of what’s best for you.

Follow up and make sure proper reporting was done on the medical provider’s part to the appropriate national databases, or report it yourself.

MedWatch reports for medications and VAERS reports for vaccines.

This recommendation is less for you and more for others and for the sake of having the appropriate authorities informed so they can eventually take medical treatments off the market and create the demand for safer ones.

Those kind of databases can only function well for the populations they serve if they are being used by everyone.

My Final Thought: Yes, people are dying. Everyday. I do their death records every flu season or surfing season.

And try as hard as we do – and no matter how absolutely shredded inside I am especially when I do an infant or child’s death certificate- we will never eradicate death.

We CAN work to slowly eradicate and reform bad systems and misinformation. And even though there is no immediate gratification in it, we will probably save more lives when we work intelligently, truthfully and ethically towards a better future. And that usually starts with a lot of humility and admitting that change is needed.

If anyone has ideas, would like to share their thoughts or their own expertise for consideration, or somehow otherwise contribute to unifying this polarized health battlefield, feel free to add a comment.

Original Source.

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**Comment**

Once again, you can’t count something you aren’t tracking.  If it doesn’t have a code, it doesn’t exist in the eyes of our public ‘authorities.’  It becomes circular reasoning – or an infinity loop containing only the data they perceive as important.

I agree with the author – be skeptical about anything coming from the CDC.  They tell you what they want you to know.

The reason autopsies aren’t performed on Lyme/MSIDS patients is because we’ve been told nobody’s dying from it, yet autopsies are precisely what we need.