https://defeatthemandatesdc.com/  Info & Registration Here

The Plan

We will start the march at 11:30am at the Washington Monument and we’ll walk together to the steps of the Lincoln Memorial (approximately 1 mile).

At the Lincoln Memorial, a wide range of featured guests will be waiting.

Recording artists, prominent doctors, journalists, pro athletes, actors and premier thought leaders will give a series of inspiring talks and musical performances. 

Stay tuned here for updates on our list of special guests!

Join us live in Washington, DC!

Sunday, January 23, 2022 @ 11:30am EST 

Starting at the Washington Monument 

Get directions

Contact info: https://defeatthemandatesdc.com/pages/contact-us

Steve Kirsh wrote on his Substack,

“We are not marching against the COVID vaccines, we’re marching against the government forcing these vaccines onto Americans. It’s something I hope we can all agree on.”

He further explained:

  1. We don’t even know what is inside these vials and we are being forced to take it.
  2. The VAERS data shows the vaccines kill more people than they save (by 15X).
  3. The vaccines suppress your immune system making you more likely to be infected.
  4. There is no stopping condition. If 1M people are killed by the vaccines, they won’t stop them.

Speaking with The New American in December, Kirsch said that according to his calculations, the COVID shots have killed more people than they saved. That disproportion is even worse when it comes to children: for every 1 child saved from COVID, 117 will die because of the vaccine-associated adverse events.

https://www.treatlyme.net/guide/recovery-timeline-for-lyme-bartonella-babesia  Video Here

When You Might Start to Feel Better: The Lyme, Bartonella, and Babesia Timelines

In this video article, Marty Ross MD describes when you should start to feel better in your treatment. As Dr. Ross describes, it all depends on the which infections you are treating.

Resources

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**Comment**

This topic paramount, as patients desperately want their lives back.  At least I did.

I remember finding a man who was infected but had achieved his health back.  In a vast pool of sick people, he appeared to be a lone survivor.  Frantically, I emailed him for answers.  Per usual, he got right back to me with encouragement.  (This has been my experience time and time again.  Infected people “get it,” and immediately help those looking for it).

To be honest, I only remember one thing he said: “Don’t be depressed about feeling depressed.”  You may laugh, but that simple statement probably helped me more than any other advice, because this complex illness will truly sift you like wheat making you question your very sanity and your desire to continue with life.

I would compare having Lyme/MSIDS to being dropped behind enemy lines in an Arctic climate where you are given nothing but a toothpick and a shovel for survival.

I would love to say that I completely agree with Dr. Ross but it just wasn’t our experience.  Since both my husband and I are infected and have both waged this battle (and continue to wage it), I have two narratives I am quite intimate with – plus many other patients who tell me their stories.

Tracking improvement is like catching a greased pig.  Very hard to do.  Nothing about this is linear.  There are forward steps, stalls, and backward steps – sometimes within the same day!

I advise patients to keep a monthly calendar close by with lines on it for writing.  Write down your major symptoms every day.  This will really help if you are tracking others in your family as well.  If you don’t do this you will likely forget much of what you experience.

If possible, then take these notes and write or type up an executive summary noting the main symptoms.  This will help your Lyme literate doctor more than anything.  They are versed in the various symptoms and your documentation will show what infections are dominant at the time (and this varies from time to time.)

It is true that if you are not experiencing change (improvement or worsening) you are likely in a plateau which should indicate you need to change your treatment.  Be honest about this and talk with your LLMD about this so you are in agreement.  This is NOT an illness that you can just ‘trust the experts’ with.  You NEED to be a part of this unique partnership.  Admittedly, in the beginning you won’t know much and won’t be able to be much help, but in time you will become a quasi-expert.  I tell patients that doctors are experts in THE human body but you are the expert with YOUR body.  Your intel is indispensable to your physician.  If they don’t want your intel, it’s time to find a new doctor!

For more:

https://danielcameronmd.com/clinicians-difficulty-identifying-ticks/

Clinicians have difficulty identifying ticks

identifying-ticks

Welcome to another Inside Lyme Podcast with your host Dr. Daniel Cameron. In this episode, Dr. Cameron discusses findings from a recent study which examined the proficiency of clinicians at identifying ticks in the northeastern region of the United States.

The study by Laga and colleagues entitled “Proficiency at Tick Identification by Pathologists and Clinicians Is Poor” was published in The American Journal of Dermatopathology.¹

Using high-resolution photographs of ticks, the authors surveyed 115 health care providers, which included primarily medical students, medical residents, and physicians.

CLICK HERE TO WATCH A VIDEO DISCUSSING TICK IDENTIFICATION WITH DR. CAMERON

The survey was simple. Each health care provider was asked to look at high-resolution color pictures of ticks provided by the University of Rhode Island Tick Encounter Resource Center.  (The dimensions of each image were 1 5/8 inches by 2 inches.)

The participants were asked to select one of 5 possible answers for each photograph:

  1. American dog tick
  2. Deer/ blacklegged tick
  3. Lone Star tick
  4. Brown dog tick
  5. “I do not know”

Only 1 in 3 ticks were correctly identified.

The survey participants correctly identified 60% of the non-engorged black-legged ticks but only 34% correctly identified a partially engorged black-legged tick.

“Likely explanations are that texts and media rarely show partially engorged ticks,” the authors explain.

Additionally, “the color contrast seen between the scutum and abdomen in the blacklegged tick, for example, is lost after 2.5–3 days of engorgement.”

Participants had more difficulty identifying the other tick species:

  • 1 in 2 participants identified a non-engorged Lone Star tick;
  • 1 in 3 identified a non-engorged American dog tick;
  • 1 in 4 identified a non-engorged adult Brown dog tick.

The number of ticks correctly identified was worse for partially engorged ticks.

Medical students and non-physician health care providers (i.e., nurses, physician assistants) fared the worse with only about 1 in 4 correctly identifying the ticks.

In everyday practice, health care providers do not view high-resolution photographs of ticks. Their experience, instead, is with actual ticks which appear much smaller.

“In addition to choosing the easier-to-identify female ticks for our test, we also chose adult rather than nymphal ticks for the quiz,” the authors explain.

“Nymphal ticks, in addition to be being smaller, tend to have more muted colors and less distinctive markings on their scutums.”

In actual practice, it’s important that health care providers can identify engorged ticks. Yet, the survey shows that engorged ticks were more difficult for providers to identify.

The following questions are addressed in this podcast episode:

  1. How often is the tick seen?
  2. Have you found it difficult to identify a tick?
  3. What are a few tips to identifying ticks?
  4. What diseases does each tick carry?
  5. Why is it important to be able to identify an engorged tick?
  6. What is the risk of an engorged tick?
  7. What educational information should clinicians receive?
  8. What do Lyme disease patients know?
  9. What are treatment options for a tick bite?
  10. What are the risks and benefits of a single 200 mg dose of doxycycline for a tick bite?
  11. How effective is testing of ticks for diseases?

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. Laga AC, Granter SR, Mather TN. Proficiency at Tick Identification by Pathologists and Clinicians Is Poor. Am J Dermatopathol. May 11 2021.

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**Comment**

As they say, “There’s no such thing as a good tick.”

That said, doctors are woefully educated on ticks, the diseases they spread, how to diagnose, treat, and recognize not just various ticks but the wide variety of symptoms patients struggle with.

This study partially reveals the many problems in Lyme-land.

Yesterday, I posted an article proposing guidelines by supposed ‘experts’ that call themselves the ‘Wilderness Medical Society.’  In the comment section I break down the various continually regurgitated myths used as talking points and the basis for all research and clinical guidelines. One of the things discussed is how the “wait and see” approach has been dooming patients for decades. This essentially means that rather than quickly treating known tick bites prophylactically, they simply wait and see if the person develops symptoms.

They also continue to push the one-dose doxy prophylactic treatment which doesn’t work. Neither does two pills. Unfortunately, researchers still believe the EM rash is some magical symbol.  The EM rash comes and goes at will and should never be a marker for effectiveness of treatment.

The catch with all of this is doctors can’t identify the ticks involved.

Ironically, if the doctor can’t identify the tick, or if attachment time is unknown, they still recommend the “wait and see” approach, even though that particular refrain has caused untold damage.

**UPDATE May, 2022**

Please see this article which includes the update at the beginning on how frequently adverse events were reported as “unrelated” to the ‘vaccine.’

Recently, a judge ruled in favor of a group of experts who sued the FDA over lack of access to Pfizer COVID injection data.  Instead of the FDA’s request of 75 years to slow drip the data, the judge ordered them to release 55,000 pages per month – which would take approximately 8 months for completion. Unfortunately, the FDA will redact information that it decides is not for public consumption, which might make the data meaningless. For instance, if the FDA redacts batch numbers it will be difficult to identify which participants were harmed by which batches. If they redact ID numbers, it will be difficult to track adverse events.

https://maryannedemasi.com/publications/f/experts-weigh-in-after-suing-fda-for-access-to-pfizer-trial-data

Experts weigh in after suing FDA for access to Pfizer trial data

20 December 2021|COVID-19
COVID-19, mRNA, vaccine, Pfizer, transparency, trial data, FDA, DOJ, Aaron Siri, Aaron Kheriaty, Tom Jefferson

By Maryanne Demasi, PhD

In Dec 2020, the US drug regulator (FDA) granted emergency use authorisation to Pfizer’s Covid-19 mRNA vaccine with limited data from phase III trials.

Amid the urgency of the pandemic, the review of the trial data was conducted faster than usual. What would normally take an average of 10 months to review, only took the FDA 108 days.

Immediately, it raised doubts about the speed with which the agency made its decision.

Fast forward to Aug 2021 and the FDA granted full approval to Pfizer’s (Comirnaty) mRNA vaccine, without releasing the full data set to the public for independent scrutiny. 

Experts became concerned that all the publicly available information on a fully licensed product, was limited to journal articles, press releases, and assessments by drug regulators – all of which are subject to conflicts of interest and bias.  (See link for article)

________________

Highlights:

  • 80 public health officers and researchers formed an alliance to get the data.
  • The group filed a FOIA lawsuit in September due to lack of public disclosure of FDA data.
  • The placebo & therefore the control group was eliminated because the shot was offered to all.
  • The group argues that due to insufficient and hurried testing & a culture of secrecy, the idea of informed consent is arguable.
  • There has been under-reporting adverse events, falsification of data, and a lack of efficacy  regarding the Pfizer injections.
  • DOJ lawyers wanted to drip feed Pfizer data over decades (75 years in fact, which is laughable).
  • The FDA claims it is insufficiently staffed.  They have 18,000 employees and $6.5 billion in funding.

Important quote:

“It is dystopian for the government to give Pfizer billions, mandate Americans to take its product, prohibit Americans from suing for harm, but yet refuse to let Americans see the data underlying its licensure.” ~ Aaron Siri, US attorney acting on behalf of PHMPT

  • The first round of Pfizer’s documents has already been released by the FDA.
  • It showed 1,223 people died from the shot within the first 90 days of the rollout, but much of the document is redacted and it is unknown how many doses had been shipped out, i.e. how many total doses were given.
  • Please see top link for a telling graph of 10 months of the COVID shots vs 20 years of flu vaccines.  Shocking would be an understatement.
  • https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf  Starting on page 30, there are nearly 9 pages of single spaced adverse reactions.

**UPDATE Jan. 11, 2022**

A recent article showed a video presentation where International trial lawyer Dr. Reiner Fuellmich and Dr. Wolfgang Wodarg discuss the findings of researcher Craig Paardekooper of Kingston University London.  Paardekooper states “about 1 in 200 of the batches are highly toxic.” VAERS data shows “vaccine” batches are sequentially marked by varying toxicity which has been statistically graphed and proves manufacturers purpose and intent to maim people.  The injections have different ingredients, are shaped differently, and have different effects.  Excerpt:

“If you look at the totality of the evidence, there’s more than enough evidence. A very recent presentation done by [former Pfizer vice president] Dr. Mike Yeadon shows precisely how they use these different batches in order to have an experiment within an experiment in order to try out what kind of dosage is needed in order to kill people and maim people,” said Fuellmich, who has successfully indicted big companies like Volkswagen and Deutsche Bank.

“And it is inescapable evidence of premeditation and once you have premeditation, there is no immunity for anyone anymore. Not even in the United States.”

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https://www.brighteon.com/cc47526e-aadb-46db-adc7-7372f2dcdc1f  Video Here (Approx. 14 Min)

Targeted Genocide: Deadly Vax Lot Numbers Identified

The Stew Peters Show

Jan. 3, 2022

The video above states that the most dangerous lots are the following:

  • Children: Pfizer EW, FA, FC
  • Adults: Pfizer EN, ER
  • All Ages Moderna ends in 20A
  • Moderna supertoxic: J, K, L, M

* The deadliest doses are being distributed in America.
* The most injurious doses are distributed in Europe.

Right now, humans getting these injections are actively enrolled in an ongoing study.  Data is being collected.  Numerous arms exist in this ongoing study where various doses are used including a placebo, but most importantly the three COVID injection manufacturers are conducting lethal dose studies.  This goes against informed consent and all ethical, and regulatory rule.

For more:  https://howbad.info/

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https://www.brighteon.com/d68b1f37-fb03-4abd-bdc7-54b1cf19ae76  Video Here (Approx. 6 min)

Vax-Injured Being Gaslit Much Like Lyme/MSIDS Patients

Doctors are labeling those injured from the COVID injections with Functional Neurological Disorders (FND) and a psychosomatic or ‘it’s all in your head’ label.  Further, in Soviet Canada, the doctor who exposed the stillbirth explosion in COVID “vaccinated” moms was just thrown into the psych-ward with a convenient diagnosis of “frontal-lobe dementia.”

Does this ring any bells?
This same, exact tactic has been utilized for over 40 years in Lyme-land. Just simply label & discount problem people.
  • Lyme denialist Dr. Shapiro has used the MUS label to discount severely ill Lyme/MSIDS patients and urges the medical community to develop ways to prevent “healthcare-seeking behaviors” by parents who believed their children may have Lyme disease.
  • Many Lyme/MSIDS patients are dismissed with an ‘it’s all in your head’ diagnosis. In fact, it appears this diagnosis has become medicine’s silent epidemic.
  • Lyme/MSIDS patients are also plagued with involuntary body movement that has been falsely diagnosed as psychosomatic. (I may involuntarily hit a doctor for this lazy, self-serving diagnosis)
  • Of course, the injured who are attempting to warn others on social media are quickly labeled as either having ADE or partaking in “hate speech” or “misinformation.”  The ‘powers that be’ will use this to further crack down and censor those who are simply trying to warn others.

If you don’t believe there’s a distinct possibility that those injured by the COVID shots could be force-medicated with psych drugs, it’s been done before.

Already, there’s been a loud public cry for the “vaccine” injured to be heard.  Wisconsin Senator Ron Johnson has been outspoken about the lack of “vaccine” safety and has given a forum for the injured to speak. Further, he’s held an expert panel to dispel the accepted narrative that these injections are ‘safe and effective,’ and that the unvaccinated are causing the pandemic. Of course, this has brought him nothing but ridicule and a smear campaign from mainstream media, medicine, and corrupt public health agencies who are all in the back pocket of Big Pharma.

Please see this collection of over 1,000 studies showing the COVID injections are dangerous.