ICWA Weekly News 8-7-24
Early election results; If vaccines were the most highly studied products ever, why so many adverse reactions? Notice of Liability served to Chelan-Douglas BoH; Announcing VAXXED III in Lakewood
In this issue:
WA Primary Election BLUF - Some hope
Vaccine Adverse Reactions in Washington Children
Seven Citizens Serve Notice of Liability to Chelan-Douglas Board of Health
Radio Show Links
Upcoming Events:
Watch VAXXED III - Announcing new screening location in Lakewood (near Tacoma) – Sept. 18
Pandemic Response Harms 2.0 in Wenatchee - Sept. 21
On Hiatus: 🐓 The Guano 💩 Report 🐄; Tune in next week when we update you again on all the crap going on.
WA Primary BLUF
The bottom-line-up-front (BLUF) appraisal of early election returns show some hope, but still no Red Wave. Since the Republican party is increasingly aligned with the concept of health freedom and the Democrat party has an insane love affair with public health policies to the point of overreach, ICWA members have hoped for a Red Wave for many elections now.
There is some hope and some forward momentum on the candidates that Stand for Health Freedom endorsed. Keep in mind that the following analysis is only based on the early ballot counting from August 6.
Congressional District 3: this district shifted to Democrat Marie Perez in 2022 when the plan to oust Trump-impeacher Jamie Herrera-Buetler (R) backfired. Now, if all Republican votes consolidate in the General election, then second-place Joe Kent could get into office. Expect a huge battleground race in the General election for this seat.
Congressional district 4: after Dan Newhouse was able to keep the seat in 2022, even after voting to impeach Trump, Jerrod Sessler (R) has a four-point lead over him. If this district pools all Republican votes in November, the seat will remain in Republican hands, but it remains to be seen where Tiffany Smiley‘s 20% of the early vote will be portioned out across the two Republican finalists
All other congressional districts are likely to remain held by incumbent parties.
The governor race looks very likely to pit Bob Ferguson against Dave Reichert. The best health freedom candidate Semi Bird has not tallied many votes - only 10%, so a horrible outlook coming out of the 2024 election gates.
Attorney General: Pete Serrano has a commanding lead in the primary, but if all Democrat votes join up, it will end up in another 60/40 vote with Nick Brown getting elected to the office.
An interesting race is forming up for the Commissioner of Public Lands with Jamie Herrera Beutler (ex-long-time Congressman and a Trump impeacher), gathering the most votes at this stage at 22 1/2% with Sue Kuehle Pederson at 20 1/4 percent and Dave Upthegrove at almost 20%.
In the very important Superintendent of Public Instruction (OSPI) position incumbent Chris Reykdal has the most votes in this supposedly non-partisan office, with David Olson, a strong second. It will remain to be seen how the other two candidate’s votes will spread across the two finalists
Presumptively. Insurance Commissioner will likely come down to Patty Kuderer versus Phil Fortunato.
With low turnouts expected, low-information voters will carry the day in the General election as they are swayed by mainstream advertising using false information. Brace yourself and maybe consider reminding all those around you to do a little research and vote. WA state is not heading down a path that respects individual rights.
Vaccine Adverse Reactions in Washington Children
Last week, the Informed Consent Action Network (ICAN) recirculated a data table with the explanatory title: “None of the vaccine doses the CDC recommends for routine injection into children were licensed by the FDA based on a long-term placebo-controlled trial.” We look at three of those common, yet understudied, childhood vaccines.
The most notorious for this lack of safety data in children has been the Measles-Mumps-Rubella (MMR) shots. For example, eight minutes into a January 24, 2024 congressional briefing, Representative Dr. Kim Schrier from Washington’s eighth congressional district picked on Dr. Andrew Wakefield for his questioning of the safety of the MMR shots:
However, despite generations of celebrating the opportunity to be vaccinated, I saw in my own practice a steady increase in vaccine hesitancy and even in some cases outright refusal. Now much of this began with the fraudster Dr. Wakefield’s claim that the MMR vaccine was a cause of autism, which understandably scared parents. He has since lost his medical license and has been completely discredited.
The ICWA Weekly News sets the record straight in regards to Schrier’s claim:
It’s clear Schrier is merely repeating what the drug industry spoon-fed to the media and the public health infrastructure years ago. Her comment reveals she knows nothing about Dr. Andrew Wakefield, the case series paper that was attacked six years after publication, the thirteen authors, the twelve children studied, or the paper’s conclusion: “We did not prove an association between measles, mumps, and rubella vaccine and the syndrome [autism] described. Virological studies are underway that may help to resolve this issue.” See this ICWA post for more information: The BMJ Correction.
The ICAN table shows that no placebo control was used when testing MMR II. No long term safety studies were done, either. The “safety review after injection” went for only forty-two days. ICAN noted the following regarding Merck’s MMR II (approved in 1978) and GlaxoSmithKline Biological’s Priorix (approved in 2022):
M-M-R-II trials totaled only 834 children and a third developed gastrointestinal issues and a third respiratory issues. In Priorix trial, both vaccine groups had high rate of serious adverse events, emergency room visits, and new chronic diseases (e.g., autoimmune disorders, asthma, type I diabetes, celiac, and allergies).
VAERS is essentially the only record of adverse events that the public can access and it shows 91,284 adverse reactions from MMR shots, with 481 of those shots resulting in death.
It also important to keep in mind the 2011 Harvard Pilgrim Health Care study estimated that one percent of adverse events from vaccinations are reported to VAERS.
Washingtonians have reported 2,053 adverse events following the MMR shots.
Four of those adverse events in Washington resulted in death.
VAERS ID: 56638
12-year-old male’s onset began one day after taking the Merck MMR shot on August 20, 1993. He died two days later. Submitted write-up: deep sleep/unconscious, t102.8, admitted to hospital cerebral edema, papilledema/infarctions, brain death/cardio respiratory failure;
VAERS ID: 338821
This one-year-old female died the day after taking the MMR shot on January 21, 2009. Submitted write-up: His case was reported by a healthcare professional and described the occurrence of death nos in a 12-month-old female subject who was vaccinated with HAVRIX (GlaxoSmithKline), MMR II (strain not specified), VARIVAX and PREVNAR. On 21 January 2009 at 07:43, the subject received unspecified dose of HAVRIX (.5 ml, unknown, right thigh), unspecified dose of MMR II (unknown), unspecified dose of VARIVAX (unknown), and unspecified dose of PREVNAR (unknown). On 22 January 2009, 1 day after vaccination with HAVRIX, after vaccination with MMR II, PREVNAR, and VARIVAX, the subject experienced death nos. The healthcare professional considered the event was disabling, life threatening and clinically significant (or requiring intervention). The subject died on 22 January 2009 from death nos. It was unknown whether an autopsy was performed. It was reported the subject had "no history of illness or medical problems. Not on medications at time of death. Medical examiner stated undetermined cause of death on death certificate". 3/5/09 Autopsy report received with COD: Undetermined. Manner of Death: Undetermined. Child had presented to PCP earlier on the DOD with fever and URI sx. 4 vax given that day. Child remained cranky and put down to nap. Approximately 1 hour later found face down without pulse or respirations. Resuscitation unsuccessful.
VAERS ID: 664201
The onset for this 6-year-old male began sixteen days after taking the Merck MMR shot on September 30, 2016. He died fourteen days later on October 30, 2016. Submitted write-up: Parents report intermittent illness since vaccination: fever(101) every other day x7 days, nausea, vomiting, diarrhea, headache, fatigue, somnolence, dizziness, cough, Left leg pain.
VAERS ID: 862890
The onset for this one-year-old boy began one day after taking the Merck MMR shot on January 29,2021. He died on February 22, 2020. Submitted write-up: Patient is a previously healthy 13 month old boy who presented with respiratory failure, then developed ARDS and multiorgan dysfunction on VA ECMO, requiring vasoactive support and CRRT. Subsequently found to have multiple disseminated viral infections, including HSV, adenovirus, and low level positive CMV and EBV. Suspected immunodeficiency, workup pending. In setting of recent MMR and varicella vaccinations, critical illness, and suspected immunodeficiency, workup for disseminated vaccine strain measles sent at CDC. Positive for vaccine-strain measles from nasopharynx and urine. Patient initially presented with an otitis media on 1/30 and then re-presented with stridor and rapid respiratory failure. Evidence of epiglottic inflammation with "white dots" noted during intubation and cervical & retropharyngeal lymphadenitis. He had a respiratory PCR positive for adenovirus and RSV and serum positive for adenovirus, though not remarkably high level. EBV PCR in serum also low-level positive but serology from OSH suggestive of past infection. I&D of L neck lymphadenitis performed; cultures from lymph node I&D are negative. CT with evidence of developing retropharyngeal phlegmon. Subsequently developed knee lesion which was positive for HSV, HSV PCR from serum shows disseminated HSV at high viral levels. EBV and CMV positive at low levels, also HHV6 positive, likely represent reactivation in setting of severe illness. Based on multiple viral infections, immunology team involved and on DDX are immunodeficiencies such as TLR defects. HLH/MAS was considered and he met some criteria for this; was on anakinra and received intermittent steroid dosing. BAL cytology from 2/14 showed multinucleated giant cells. ETT quantitative RSV level pending. When measles results from NP/urine returned on 2/21, started on oral ribavirin (while pursuing IV ribavirin), high dose vitamin A, and redosed IVIG. HSV level continuing to fall. Unclear of contribution of measles vaccine strain to respiratory presentation; felt to be unclear whether represented prolonged shedding versus true pneumonia/pneumonitis. Further testing at CDC pending including measles IgM and measles PCR on deep respiratory sample.
Representative Shrier’s aforementioned congressional briefing was a six minute presentation on the need for passing H.R. 3633, which would create a taxpayer-funded marketing campaign for HPV vaccination to the tune of $5 million annually for the next four years and increase funding for breast and cervical cancer testing to $300 Million annually through 2028. This looks like a sweetheart deal for pharmaceutical and cancer test developers . . . we have to ask why. Why are taxpayers funding marketing campaigns for Merck? And while early detection of any medical issue is, of course, prudent, why are taxpayers funding cancer screening tests, isn’t testing covered by all insurance plans? Shouldn’t such tests be affordable for most-of-pocket? It’s not new science.
Anybody care to do a Freedom of Information Act (FOIA) request on Rep. Shrier and see what she and Merck have been talking about?
The corruption and dangers of the Gardasil shots for HPV have been widely exposed by Mary Holland in her book The HPV Vaccine on Trial. Also, lawsuits against Merck are in progress. Evidence shows they “concealed the risks of autoimmune diseases and other long term side effects of Gardasil while falsely promoting the vaccine as a safe and effective treatment to prevent cervical cancer”.
The ICAN table shows that no placebo-controlled trial was used for the Gardasil shots used for preventing HPV. The “safety review after injection” for the Gardasil 9 shots went for one month in five trials, six months in one trial, and four years in another trial. ICAN noted the following:
Gardasil 9 trial gave 306 people placebo after full series of Gardasil 4. In Gardasil 4’s trial, controls received aluminum adjuvant, AAHS, except 320 people labeled “Saline Placebo” that actually received all vaccine ingredients except antigens and AAHS. Across trials, 2-3% receiving vaccine or aluminum adjuvant (used to induce autoimmunity) had a suspected autoimmune disorder.
VAERS shows 22,502 adverse reactions from Gardasil 9 shots, with fifty-six of those events resulting in death.
VAERS shows 363 adverse events in Washington following Gardasil 9, and no deaths. However, remember that follow-up reports to initial VAERS reports are not public-facing. Did all of the 363 recover? Did symptoms worsen? Are any experiencing long-term medical issues? The final outcome of the 363 are unknown.
Now, let’s cast our view to the top of the ICAN table and the three doses that supposedly prevent hepatitis B. No placebo-controlled studies or long-term safety studies have been performed. For the Recombivax HB vaccine, the safety review period was performed for just five days. For the Engerix B product, the safety review period was just four days long.
ICAN summarized the underlying problems:
Note that to license a vaccine for children, the FDA relies upon the clinical trial conducted with children, not adults, because as the FDA explains, “It’s important that the public recognize that, because young children are still growing and developing, it’s critical that thorough and robust clinical trials of adequate size are completed to evaluate the safety and the immune response to a … vaccine in this population. Children are not small adults[.]”
The fact that a baby’s immune and neurological systems — which are interrelated — are not yet mature when these shots are given make the practice unethical. Dr. Christina Parks explains that the practice increases risk of asthma, allergy, autoimmune disease, and more. And a close reading of the package inserts of vaccine products shows that infants have minimal protective immune response to the first series of injections. This makes them all risk and no benefit. The world of animal medicine is more ethical regarding vaccination timing. For an interesting read on cows, see “Vaccination Strategies to Maximize Preventive Health and to Minimize Adverse Effects on Market Quality.” The Merck Manual says “Newborn animals cannot be successfully vaccinated because of the presence of antibodies derived from their mother. Effective vaccination must wait until maternal immunity has waned.” This is true in human mammals, too.
A search on www.medalerts.org leads to a link for researching the adverse events for the Hepatitis B vaccine.
The results from the above entry show 76,241 adverse reactions following the hepatitis B shots in which 1,408 of those events resulted in death, and 748 of those deaths were to those under six months of age.
Washington has reported 1,532 adverse reactions following the hepatitis B shots with 238 of them occurring for those under six months of age.
In Washington, twenty have died following the hepatitis B shots, including thirteen under six months of age. Below are writeups of the eighteen reports on those under one year of age who perished.
VAERS ID: 80138
Listed as a 0.2 old male. Submitted write-up: Patient came into hospital ER the morning of 01DEC95 DOA; probable SIDS; autopsy performed 1DEC95
VAERS ID: 91557
Listed as a 0.1 female. Submitted write-up: pt was given vax @ approx 1PM & died @ approx 8PM:pt went into coma in afternoon & was rushed to hospital.
VAERS ID: 100174
Listed as a 0.2 female: Submitted write-up: death 11FEB97 6PM;autopsy result SIDS: autopsy report given pathological dx SIDS w/intrathoracic visceral petechiae, visceral congestion & minute foci of early bronchopenumonia;
VAERS ID: 114917
Listed as a 0.1 female. Submitted write-up: pt recv vax 16SEP97 - SIDS on 21SEP97;parents requested VAERS on 22SEP98-1yr anniversary of pt death;
VAERS ID: 118636
Listed as 0.17 male. Submitted write-up: pt started getting a fever @ 1PM the same day as vax;pt had swelling @ the site of DTP as well as soreness;pt was very cranky & was sore for 3 days following vax;3rd day pt died;
VAERS ID: 197618
Listed as a 0.3 male. Submitted write-up: A nurse reported that a male infant received a dose of Prevnar along with DTaP, IPOL and hep B vaccines on 9/5/02 at 4 months of age. On 9/26/02 at 5 months of age, the infant died. SIDS was the reported cause of death. No further info was available at the date of this report. This report of a serious, labeled event is being submitted in a 15-day time frame as requested. Info regarding this event has been forwarded to manufacturer of IPOL vaccine. From initial information received at manufacturer on 03/03/2003 from another manufacturer regarding an event that happened in the U.S. concerning a 4-month-old male patient who received IPOL on 02/05/2002. The lot number and site/route for the vaccination was not reported. The patient died on 09/26/2002 from SUDDEN INFANT DEATH SYNDROME. From additional information received at manufacturer on 04/24/2003, it was reported that the patient also received Prevnar, DTaP and Hepatitis B Vaccine on 09/05/2002. The manufacturer, lot number and route/site were all not reported for Hepatitis B Vaccine and DTaP. Prevnar was given intra-muscular. Autopsy results showed Sudden Infant Death Syndrome (LLT, SIDS) as reported cause of death. From additional information received on 05/13/2003 from manufacturer, it was reported that their manufacturer number be added to WAES 0305USA00241.
VAERS ID: 199646
Listed as a 0.6 male. Submitted write-up: Patient previously healthy. Six days after 6 mo WCC and vaccines x 3 (hep B, DTaP, HIB), patient presented with vomiting and jaundice. Transferred to hospital on 12/20/02. Developed fulminant liver failure of unknown etiology and died 1/22/03. Principal diagnosis: idiopathic liver failure. Secondary diagnoses: hypoglycemia. Coagulopathy. Citrobacter freundii bacteremia and line infection. Multiorgan system failure.
VAERS ID: 206350
The listed 0.17 males died two days after taking a second Merck Hepatitis B shot as part of six shots. The only thing said in the submitted write-up was, “Coroner ruled SIDS.”
VAERS ID: 265462
Listed as a 0.13 female. Submitted write-up: After administering vaccines child became very fussy and over tired, would not wake to eat and passed away a little over a day later. Autopsy could not say that vaccines did not play role in death.
VAERS ID: 335226
Listed as 0.3 female. Mother’s account as part of the long submitted write-up: I would like some help to find out if my daughter’s death was caused by a Vaccine Induced Reaction. This all started on November 13 2008. This is the day the I took my daughter to the clinic. She was supposed to be seen for her 2 month well child exam which she was not. The primary doctor had only seen her once and this was on her 2 week well child exam. When we went in for her 2 month checkup we had seen a nurse practitioner. The doctor never came into see her not even once on this day nor did the nurse weigh her do any of the measurements of check to make sure that everything was growing normally. She had me sign for 2 vaccines when after all this i found out that she was given for 2 that i didn’t know about. We were sent home right after the vaccines were given and told to come back in 4 weeks for more and to expect drowsiness, fussiness, low appetite, not sleeping, irritability, that’s what had happened Thursday night. She slept most that afternoon and evening with very little to eat. Friday morning she was a little fussier then usual. Later on into the day we had noticed her to be warm to the touch but i had checked and it was normal a few more hours into the night. She developed a fairly high pitched cry and it seemed like she had a belly ache but yet eating very much. She was up about every 30 min during that Friday night and she usually was a really good sleeper through the night. On Saturday morning, I had gotten up to feed her I made a 6 oz bottle she still had about 2 oz left. When she was finished I burped her changed her she was still really fussy so i laid her down on a u shaped pillow and put her on her belly and i laid down beside her and patted her on her bottom and I fell back asleep next to her and was woke up by her father that had just gotten out of bed and told me to make sure the baby is breathing. I grabbed her and her body was limp but still warm to touch. I held her close to my body and ran across the street to the police station where the ambulance had responded and took us to the hospital. They were able to resuscitate her but she could not breath on her own nor did she have any brain function. They then air lifted us to the hospital. After being there for 24 hours the doctor had told us that our baby was not going to live and they see retinal hemorrhaging in the back of the eyes and the only 2 ways were a car wreck or some body had to of shaken her. Well, I know that that is not what happened and i have research about these vaccines and all the signs start the day she was vaccinated. Thank you for your time.
VAERS ID: 356473
Listed as a 0.7 female. She had taken three doses each of the Hepatitis B (Engerix-B), Pentacel, and Prevnar vaccines. Submitted write-up: Death. 9/11/09 Autopsy received DOD 07/09/2009. Sudden Unexplained Death in Infancy (SUIDI or SIDS). The manner of death is natural. Additional information abstracted: Infant was found dead in crib, positioned supine. No evidence of injury.
VAERS ID: 362090
Listed as a 0.17 female with the write-up only saying “Infant was found dead.” The data sheet shows that the death occurred after taking the vaccine on October 14, 2009.
VAERS ID: 402744
Listed as a 0.18 male. Submitted write-up: Per police report, pt was found deceased in parents bed, in prone position. Vaccines were given 4 days prior to death. No complications occurred in the Doctor’s office on that day.
VAERS ID: 456170
Listed as a 0.82 female. The death occurred one day after taking a third dose of the Hepatitis B vaccine (Engerix-B) on May 9, 2012.
VAERS ID: 744185
Listed as 0.0 male. Submitted write-up: Extreme congestion (runny nose, etc) starting about a week after birth/vaccination and up until his death on 10/28/17. The only vaccine listed on the data sheet is the Engerix-B shot for Hepatitis B.
VAERS ID: 779618
Listed as a 0.17 female. Submitted write-up: Child found unresponsive at 0450 am on 9/26/18 and EMS called immediately. CPR was initiated. Child was last seen breathing at midnight. Child taken to the emergency department at hospital. Child pronounced dead at 5:44 am.
VAERS ID: 959237
Submitted write-up [says it all]: My daughter was given 2 vaccines in her first 24 hours of life. We were released from the hospital at hour 28 of life, and she died at home at hour 39, due to "unknown causes" which they later diagnosed as SUIDS.
Comirnaty for treating COVID-19 is only one of two shots in the ICAN table that used a placebo control study. True to form, however, that saline-placebo arm of the study lasted for just six months and then was ‘unblinded,’ where data collection stopped and participants were encouraged to get the Emergency Use Authorized shot, thereby ending any chance to study long-term effects. Later on in 2021, Pfizer became the first manufacturer to navigate the shortened approval process when the FDA “approved” Comirnaty, giving public health agencies and providers a talking point that some kind of product was approved. Yet today, the mystery grows around whether the Comirnaty shots have ever been distributed to the public. A June 3, 2022 article in The Dossier, a Substack written by Jordan Schachtel, called Comirnaty a “ghost shot.” The headline stated, “Pfizer quietly admits it will never manufacture original FDA approved COVID vaccines.”
Explaining this ghost shot, they write:
In May, Pfizer updated its statement to mention a December 2021 licensed Comirnaty product, which was granted a license four months after the highly-publicized August FDA press release.
And just last week, Pfizer finally acknowledged that its original licensed product will never be distributed. In an unreported update on the CDC website, Pfizer told the agency:
“Pfizer received initial FDA BLA license on 8/23/2021 for its COVID-19 vaccine for use in individuals 16 and older (COMIRNATY). At that time, the FDA published a BLA package insert that included the approved new COVID-19 vaccine tradename COMIRNATY and listed 2 new NDCs (0069-1000-03, 0069-1000-02) and images of labels with the new tradename. These NDCs will not be manufactured. Only NDCs for the subsequently BLA approved tris-sucrose formulation will be produced.”
Seven Citizens Serve Notice of Liability to Chelan-Douglas Board of Health
At the July 15 Chelan-Douglas Board of Health meeting, seven public commenters eyed the board members with righteous indignation while reading 3-minute portions of a Notice of Liability for the board’s “actions and omissions” that caused much harm and suffering during the declared COVID-19 emergency. We hope they post to the Board of Health site the audio recording of the meeting some day soon.
The first speaker started with the following introduction to the Notice of Liability:
On behalf of the people of Chelan and Douglas Counties, in the State of Washington, we hereby place the Chelan-Douglas Board of Health (Board of Health), supervising the Chelan-Douglas Health District, as a corporation and as individual directors, on notice that:
The speaker then read the following four Roman numeral points in their allotted three minutes:
I. Your actions and omissions, both during and following the Covid-19 public health ‘emergency’ declared in 2020 contributed to mass harm and human suffering, including psychological and emotional distress, financial loss and/or monetary damage, loss of learning, loss of freedom to gather to worship, physical harm, and even loss of life upon the people of Chelan and Douglas Counties.
II. Said actions and omissions include administering tens of thousands of insufficiently tested SARS-CoV-2 gene therapies, falsely termed ‘vaccines,’ denying proper informed consent to those receiving the ‘vaccines,’ recommending against implementation of proven safe and effective interventions, recommending and enforcing unscientific masking protocols and inhumane and anti-scientific ‘social distancing’ measures, distributing and administering ineffective and fraudulent PCR tests that incited unwarranted fears and were subsequently used to grossly exaggerate impacts of the ‘pandemic’ and create false ‘casedemics’ in order to justify unlawful and unwarranted ‘lockdowns,’ business closures, school closures, and restrictions on religious gatherings and other social and personal interactions;
III. Said actions and omissions were undertaken, and some continued for over 4 years despite this board being presented credible scientific and medical findings and other information documenting significant concerns regarding the safety and efficacy of the ‘vaccines’, efficacy of the testing and treatment protocols, and the adverse social, educational, and economic consequences of your pronouncements and enactments. This information was accompanied and supported by additional information and pleas from the public to investigate, reevaluate, and rescind your chosen course of action.
IV. By this Notice, we demand that, with immediate effect, you, the Chelan-Douglas Board of Health, cease and desist from taking further actions involving unscientific, medically unsupported, and any and all other deceptive, false/or fraudulent communication to the people of Chelan and Douglas Counties, thereby causing or resulting in the type of physical, social, and economic outcomes enumerated in this Notice. The conclusion of this Notice contains a full list of our demands.
The second speaker then read the main body of the Notice of Personal Liability section:
We also put you on notice that failure to cease and desist from continued or repeated involvement or implication in the above actions or omissions and resulting harms may render you liable both in your personal and corporate capacity. As individuals, you may be investigated for criminal conspiracy to inflict harm upon the public by commission of your actions or through your negligence, or other violations of criminal law as well as liability under civil law. As a corporation, you may be investigated for gross negligence, misconduct in public office, corporate fraud, and potential criminal or civil liability for the deaths, personal injuries, and monetary and other damages resulting from your misconduct.
Further to the above Notices, and to clarify our position, may we respectfully remind you of your legal responsibilities as members of this board.
Duties of a Local Board of Health (RCW 70.05.060):
“Each local board of health shall have supervision of all matters pertaining to the preservation of the life and health of the people within its jurisdiction.” And from Chelan-Douglas Health District’s own website: “The Board sets county-wide policies and regulations to protect and promote the health of residents of Chelan and Douglas Counties.”
When carrying out your duties as a local board of health, you are obligated to consult with a diversity of experts, including those who might disagree with your recommendations on health, to ensure that best practice is ethically and objectively demonstrated in your efforts to uphold the life and health of the public. Relying solely on information and recommendations provided by Centers for Disease Control and Prevention (CDC) and the Washington Department of Health when making decisions affecting the people within your jurisdiction is not adequate and does not meet the standard for best practices for upholding life and health of the public.
As early as 2020, international experts were cautioning against the novel Covid strategies recommended by the Board of Health, especially, but not limited to the experimental modRNA medical technologies developed to function purportedly as vaccines. This information was provided to the Board of Health on numerous occasions.
The third speaker began with the end of the Notice of Liability section:
By your recommendation and implementation of harmful Covid practices, the community, represented by the Board of Health, does not believe that you have acted in good faith and in accordance with your duties under RCW 70.05.060. If your actions are found to be in contravention of your duties or violated the rights of the people you are assigned to protect, you will not be covered by established liability immunities. In other words, you may be personally liable for any deaths and suffering caused on account of your role in the unlawful and harmful implementation of recommendations or omission of information when you knew or should have known they would result in harm.
The third speaker then read the following from the “Consequences of the Board of Health Covid Policies, Mandates, Recommendations, Advice, and Omissions” section.
A. Immeasurable suffering and death In the past four years, many people who trusted and complied with Chelan-Douglas Health District’s public health advice have experienced ongoing physical and mental suffering, illness, disability, loss of income, poverty, loss of opportunity, loss of learning, child abuse and other violence, adverse reactions, and even death as a result.
B. Human rights violations Local governments, businesses, schools, health care facilities, and senior care facilities implemented severe emergency measures based on the Chelan-Douglas Health District’s recommendations resulting in flagrant violations of fundamental human rights. Businesses were shuttered and their employees laid off. Employees were fired or were coerced to leave the workplace for non-compliance. People died alone in the sterility of a hospital. Elders were denied access to their families. Many children were forced to endure abusive situations at home without the respite of going to school. All were denied their freedom to gather for worship. Boys, girls, and babies were masked and injected with experimental drugs. During all of this, the Board of Health did nothing to address or even investigate reports of the harm its policies caused despite numerous warnings from the public and subject matter experts.
C. Failure to recommend inexpensive, safe, and effective treatments and remedies for Covid-19. It is well established through numerous peer reviewed studies that Covid-19 can be effectively treated with safe and established multi-purpose generic medicines, including ivermectin and hydroxychloroquine, in combination with zinc, vitamin D, vitamin C, and other immune boosting, health-promoting and anti-coagulant treatments. Failure to disclose and raise public awareness of these studies and the efficacy of off-label use of these drugs resulted in unnecessary suffering and in many instances the deaths of people who could have otherwise gone on to live long and productive lives.
The fourth speaker read the rest of the “C” section as well as part of the “D” section in the “Consequences of the Board of Health Covid Policies, Mandates, Recommendations, Advice, and Omissions” section.
The Chelan-Douglas Health District’s recommendations against the use of ivermectin to treat Covid-19 and omissions of expert medical advice on how to attain the highest level of health during the Covid-19 scare using minimally intrusive interventions contributed to area medical practitioners withholding ivermectin and other effective treatments. Furthermore, many patients with valid prescriptions were denied at local pharmacies in favor of expensive experimental drugs with little regard for safety of their use. Amazingly and inexplicably, as of the date of this notice, Chelan-Douglas Health District is recommending against use of ivermectin to treat Covid-19. Thus, the people of Chelan and Douglas Counties may hold you responsible for the consequences of serious omissions related to minimally intrusive safe and effective treatments for Covid-19.
D. Dangerous experimental gene therapies deployed under the guise of vaccines. You may also be personally liable for death, personal injury, pain, suffering, and consequential financial damage in relation to the SARS-CoV-2 ‘vaccines’ as you have authorized the administration of the ‘vaccines’ and have not advised people of the following:
1. The long-term material risks of these ‘vaccines’ are unknown. In fact, these are not vaccines, but something else altogether. The LNP-modRNA platform fulfills US legal definition for a genetically modified organism (GMO), and a gene therapy, where material risks are identified as potentially prenatal and up to 15 years postnatal. People were not advised as required by law that the so-called ‘vaccines’ are, in fact, GMOs.
2. Pfizer used one process to manufacture the products that they submitted for approval but a different process to manufacture the product supplied for injection into the world’s population. The latter product was manufactured using E.coli bacteria and plasmid DNA, which has resulted in excessive synthetic DNA contamination confirmed as able to integrate with the human genome. Moderna’s use of plasmid DNA in manufacture has also led to excessive synthetic DNA contamination.
3. Pfizer products include an SV40 virus-derived enhancer gene sequence. This gene sequence is known to facilitate the transport of the synthetic DNA into cell nuclei, posing a real risk of chromosomal integration. This threatens permanent genetic modification of inoculated people without their knowledge or consent and can only be harmful.
4. The contents of these genetic injections do not stay in the arm muscle.
5. Spike proteins are produced for a prolonged and unknown period of time, possibly indefinitely.
6. These spike proteins have been proven to trigger extensive microvascular blood clotting as well as large vessel blood clots.
7. Spike proteins are deposited in many tissues and organs including the heart, brain, testis, ovaries, liver and spleen, causing tissue degeneration and disease.
The fifth speaker read the remaining points raised in the “D” section as well as the first two paragraphs of the “E” section:
8. The large quantity of spike proteins may overwhelm the immune system, causing immune system dysfunction and worsening risk of all infections and cancers.
9. The spike protein is toxic in itself, but this foreign antigen also marks the victims’ own tissues as non-self, triggering autoimmune disease within these tissues.
10. The antibodies generated are non-neutralizing and worsen Covid disease; this is “antibody dependent enhancement” of infection.
11. Undeclared plasmid DNA in these products carries further dangers, especially in the case of Pfizer and the concealed SV40 enhancer and promotor sequences. This includes the disruption of tumor suppressor genes and adds to the list of mechanisms by which these products increase cancer risk.
12. The artificial modRNA in these products is hyper-persistent due to the substitution of N1-methylpseudouridine in place of uracil. This prolongs the production of the toxic spike proteins, but also causes ribosome frame shifting, such that a variety of unpredictable proteins and polypeptides are also generated. These pose serious risk for triggering a large spectrum of autoimmune diseases.
13. Additionally, the pegylated lipid nanoparticles, which deliver the genetic payload into the victims’ cells, are toxic in and of themselves.
E. Violation of informed consent
Based on your authority as the Board of Health, the majority of people in Chelan and Douglas Counties trusted your words when you stated that Covid-19 GMOs and gene therapies were “safe and effective.” This claim cannot be substantiated and is further disproved by numerous peer reviewed studies and the manufacturers’ own documents. As such, the right to free and informed consent was violated for every human being who was injected with the experimental Covid-19 GMO gene therapy that you promote as ‘vaccines.’
We can find no evidence you informed people of the risks associated with these experimental GMO injections, nor have you shared the mounting vaccine injury reports with the public. The Vaccine Adverse Events Reporting System, VAERS -- the national vaccine safety clearing house database -- holds the records of over 2.6 million people suspected of having been harmed by the Covid-19 genetic ‘vaccines’ including reports of over 37,000 deaths. Yet you have failed to even investigate reported safety signals and warnings of these data presented to the Board of Health. On more than one occasion, the Board of Health refused to investigate the adequacy of its own informed consent documents despite warnings that they may not be adequate.
The sixth speaker finished the “E” section:
This is in direct contravention of the Nuremberg Code, which was internationally agreed to in 1948, including in the United States of America, to prevent non-consensual medical experimentation on human beings, following gross human rights violations during the Second World War. Your failure to offer, advise on, recommend, promote and ensure free and informed consent for these Covid-19 GMO gene therapies can be prosecuted for both breach of your duty of care as well as for battery.
The sixth speaker then read to the board the rest of the Notice of Liability:
Our Invitation
Clearly, the health of the people of Chelan and Douglas Counties is much poorer for the actions taken by the Chelan-Douglas Board of Health both during and following the declared public health ‘emergency.’ As such, we are morally obligated to invite you to defend your actions or apologize publicly with a corrective plan.
We Demand
In light of the now clearly established negligence on the part of the Chelan-Douglas Board of Health, and its responsibility to the community as codified in law, and in the interest of public health and safety, we demand that you:
1. Cease and desist from recommending and administering the Covid-19 GMO gene therapy products with immediate effect.
2. Prepare and deliver to every member of the community who received the ‘vaccines,’ whether administered under the Chelan-Douglas Health District or other party within your jurisdiction, a full disclosure statement regarding the potential benefits and risks to their well-being of having received the Covid ‘vaccines’ in compliance with the Nuremberg Code, Hippocratic medical ethics, and the law.
3. Cease and desist from making recommendations against the off-label use of ivermectin as a safe and effective treatment for Covid-19, as this decision should be between the patient and their doctor.
4. In the conduct of your duties as the Board of Health, refrain from further actions involving unscientific, medically unsupported, and any and all other deceptive, false/or fraudulent communication to the people of Chelan and Douglas Counties.
The seventh speaker listed the names of those from the Truth and Accountability Project Washington (TAPWA) who were signing onto this Notice of Liability. She told the board, “We seek to bring truth, awareness, and resources to those harmed by the COVID 19 ‘vaccines’ and the public health pandemic response in our community and beyond.”
TAPWA serves as a valuable resource for action, news, and references for combatting the injustices done by the COVID-19 policies.
The next Chelan-Douglas Board of Health meeting will be on Monday, August 19. Of interest for medical freedom lovers will be whether this Notice of Liability will be addressed by the board during this meeting. TAPWA hopes that this Notice of Liability can serve as a template for others to use against other local boards of health.
August 2 Episode of Informed Life Radio - - notes and links
Health Hour: Sunlight is Essential
Modern life and systemic inaccurate medical advice have undermined human health by reducing exposure to sunlight.
Guests Roman Shapoval and Bohdanna Diduch explain the importance of sunlight to health and positive steps we can all take to restore a healthy relationship with the sun.
Alexander Wunsch - LED WARNING MESSAGES - what you should know before using solid state lighting
Einstein's Legacy: The Photoelectric Effect | Scientific American
Liberty Hour: Securing Proper Nutrition
Guest: Dr. Dana Flavin discusses how we can and must ensure access to clean water and unadulterated food, the building blocks of life.
Upcoming Events
Sept. 18 Vaxxed III: Authorized to Kill
The nationwide premiere of VAXXED III will be on September 18, mainly in AMC theaters in the US. There are four locations in Washington where you can join the nation in witnessing people’s powerful testimonies of deadly protocols.
Reserve Tickets by August 18 and spread the word:
Save the Date: Sept. 21 in Wenatchee
Pandemic Response Harms 2.0 - Connecting the Dots - Forward Boldly
Many more speakers will confirm.
Capping things off with a current-event meme:
Great issue...thank you. Encouraging news...keep standing together.
Another fantastic jam-packed report. Thank you!
Kudos to TAPWA for its remarkable action. Let us hope that Chelan Douglas BOH complies with the reasonable demands so that some healing may occur and further suffering may be prevented. May a similar notice of liability be served on public health bodies across the land!