By the way, how come the FDA didn't consider a pause after 1,233 deaths and over 40,000 adverse effects in the report I note. From: Retain Mike Sent: Sunday, November 19, 2023 11:14 AM To: Dana Haynes Subject: Letter to the Editor [#19844]
If you don’t like the backup I used in my letter, does this help?
Dr. Mark Trozzi: 1000 peer reviewed articles on “Vaccine” injuries
https://drtrozzi.org/2023/09/28/1000-peer-reviewed-articles-on-vaccine-injuries/
From:
Sent: Sunday, February 27, 2022 3:30 PM To: Dana Haynes Subject: RE: Feedback via the Letter to the Editor [#19844]
What nonsense. Try reading the supporting information.
From: Dana Haynes Sent: Saturday, February 26, 2022 3:54 PM To: rtn.sat.cong@outlook.com Subject: Fw: Feedback via the Letter to the Editor [#19844]
Please knock this off. Conspiracy theories are fun. Did Amelia Earhart work for FDR? Did the CIA kidnap Elvis? But this conspiracy theory is killing people. It’s not funny.
Dana Haynes, Editor in Chief, Portland Tribune Managing Editor, Pamplin Media Group dhaynes@pamplinmedia.com
971-204-7735
________________________________________ From: burst@emailmeform.com on behalf of EmailMeForm Sent: Friday, February 25, 2022 5:58 PM To: Kevin Harden ; Dana Haynes Subject: Feedback via the Letter to the Editor [#19844]
Letter to the editor*: FDA Approves Crippling and Lethal Vaccines
I visited websites listing the adverse effects of pneumonia, flu, and shingles vaccines as injection site soreness, fever and chills, fatigue, muscle aches, severe allergic reaction, decreased appetite, nasal congestion, chest pain, fast/irregular heartbeat, seizures, headache, stomach pain, and nausea.
However, those for COVID 19 vaccines are numerous and disturbing. The American Heart Association using the PLUS Cardiac Test generates a score predicting the 5 yr risk (percentage chance) of a new Acute Coronary Syndrome. They concluded that the mRNA vacs dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle and may account for observations of increased thrombosis, cardiomyopathy, and other vascular events following vaccination.
A federal judge ordered Food and Drug Administration (FDA) compliance with a Freedom of Information Act request to disclose Pfizer data that factored into FDA’s recent decision granting the experimental mRNA vaccine an Emergency Use Authorization. The first released data recorded over 800 adverse side effects. Most alarming were acute myocardial infarction, arrhythmia, cardiac failure, cardiogenic shock, coronary artery disease, myocardial infarction, postural orthostatic tachycardia syndrome, stress cardiomyopathy, tachycardia, liver injury, facial paralysis, immune mediated/autoimmune disorders, arthritis, chronic fatigue syndrome, polyarthritis, rheumatoid arthritis, Guillain-Barre syndrome, fibromyalgia/trigeminal neuralgia, amniotic cavity infection, congenital anomaly, death neonatal, eclampsia, and fetal distress syndrome.
Pfizer’s general overview of 42,086 cases of adverse effects in ninety days found 20,112 persons recovered, 1,233 died, and the balance pended resolution.
Considering those circumstances, Oregon parents refusing vaccinations for their children should not have access to public education obstructed by bureaucrats.
Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS
https://thegatewaypundit.com/2021/12/court-orders-fda-comply-foia-release-information-pfizer-eua-first-batch-documents-shows-1200-vaccine-deaths-within-first-90-days/
5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
Thank you.