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Various diseases associated with COVID-19 vaccines have been reported. A recent case study indicated that COVID-19 vaccination may trigger the development of anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis, potentially damaging multiple organs. Among 29 patients, five underwent plasmapheresis treatment (the separation and replacement of plasma from blood), and five relied on dialysis therapy.
ANCA-associated vasculitis can cause damage to small blood vessels. Since these are distributed throughout the body, any part of the body can be affected, with the most common areas being the lungs, kidneys, joints, ears, nose, and nerves.
Neutrophils are a type of white blood cell that aids the body in fighting infection and healing injuries. ANCA are harmful autoantibodies that bind to neutrophils in the blood, releasing toxic substances and damaging the walls of small blood vessels. This can also result in the migration of neutrophils through blood vessel walls, inducing inflammation in the surrounding tissues. Additionally, it releases signaling factors that attract even more neutrophils, perpetuating inflammation and further damaging small blood vessels.
Case Report of ANCA-Associated Vasculitis
A case report published in Case Reports in Nephrology in April 2023 detailed an 82-year-old woman with high blood pressure who, after receiving her third booster COVID-19 vaccine booster, developed myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA)-associated vasculitis. MPO-ANCA is one of the primary autoantibodies in ANCA-associated vasculitis.
The patient received two doses of the Pfizer vaccine in May and June 2021, followed by a Moderna booster shot in early February 2022. The next day after the booster shot, she experienced a headache, which subsided after three days. However, starting in early March, her body temperature began to rise, accompanied by general malaise.
Upon examination, no apparent bacterial infection was found, but blood tests revealed an inflammatory reaction. The C-reactive protein level was elevated, and her white blood cell count was 13,000/microliters (the normal range is between 4,000 and 10,000/microliters), suggesting a bacterial infection. The doctor prescribed antibiotics for seven consecutive days, but there was no improvement.
The patient was later admitted to the hospital. Physical examination and imaging tests did not reveal fever, and kidney size and structure appeared normal. However, microscopic analysis uncovered hematuria (blood in the urine) and urinary protein. Additionally, the MPO-ANCA level was notably high. A kidney biopsy revealed cellular crescents in six glomeruli—the tiny filters inside the kidneys—and mild inflammation.
Furthermore, immunofluorescence confirmed pauci-immune glomerulonephritis. This is a rare small vessel vasculitis associated with rapidly progressive glomeruli inflammation, clinically characterized by kidney issues such as urinary abnormalities (hematuria and proteinuria) and high blood pressure resulting in kidney failure within days or weeks. Based on the pathological findings, the patient was diagnosed with renal-limited MPO-ANCA-associated vasculitis.
The patient was put on a steroid medication, and symptoms such as fever, malaise, and inflammatory reaction improved, while both hematuria and urinary protein disappeared. The doctor gradually reduced the steroid dosage, cutting it in half, and the patient’s condition stabilized.
The researchers stated that blood and urine tests conducted on the patient before her third vaccine dose did not reveal kidney damage or abnormalities, suggesting an association between the COVID-19 vaccine and the onset of MPO-ANCA-associated vasculitis.
The researchers suggested that the possibility of MPO-ANCA-associated vasculitis should be considered for patients experiencing fever, prolonged general malaise, hematuria, or kidney impairment after receiving a COVID-19 mRNA vaccine, especially Moderna, as was the case with this patient.
5 COVID-19 Vaccines Related to ANCA-Associated Vasculitis
An increasing number of reports indicate that widespread vaccination has led to the development of vasculitis in some people, resulting in damage to multiple organs.
A case-based review reported five types of COVID-19 vaccines linked to ANCA-associated vasculitis.
The study included cases from 29 patients, with 22 receiving mRNA vaccines (Moderna and Pfizer), four receiving AstraZeneca, two receiving Covaxin, and one receiving Johnson & Johnson. They all exhibited symptoms of ANCA-associated vasculitis after receiving one of these COVID-19 vaccines.
Specifically, 22 patients exhibited kidney damage, manifested as new-onset or recurrent glomerulonephritis. At least 24 individuals presented with hematuria. Ten experienced lung damage, with five cases involving alveolar hemorrhage. One person developed optic neuritis, and another had auricular chondritis. These are manifestations of organ damage following vaccine administration.
Most patients received immunosuppressive treatment, including steroid medications. Additionally, five underwent plasma exchange, and at least five patients continued to rely on dialysis at the last follow-up.
The study mentioned that mRNA vaccines may stimulate myeloid and dendritic cells to varying degrees, activating downstream pathways to generate autoinflammation. Furthermore, mRNA vaccines generate antiviral-neutralizing antibodies and activate CD8+ and CD4+ T cells, triggering strong immune responses. Compared to natural infection, mRNA vaccines may enhance innate and acquired immunity stimulation. In some individuals with compromised immune systems, the ability to clear nucleic acids may decrease, potentially impacting neutrophils.
Vasculitis May Lead to Multiorgan Damage
There are different types of ANCA-associated vasculitis, including microscopic polyangiitis, where the frequency of MPO-ANCA positivity is notably high.
According to data from the Japan Intractable Diseases Information Center, approximately 70 percent of patients with microscopic polyangiitis experience systemic symptoms, including fever, weight loss, and fatigue. Additionally, symptoms such as hemorrhage, ischemia, or infarction in body tissues may occur.
Necrotizing glomerulonephritis is the most common, presenting with symptoms like hematuria, protein in urine, and elevated serum creatinine. Early diagnosis is crucial, as the condition often progresses rapidly to kidney failure within weeks to months. Other prevalent manifestations include rash, with livedo reticularis, purpura, skin ulcers, and subcutaneous nodules in approximately 60 percent of patients with necrotizing glomerulonephritis. Polyneuropathy is observed in about 60 percent, joint pain in around 50 percent, and muscle pain in roughly 50 percent of cases.
Additionally, interstitial pneumonia is seen in approximately 25 percent, and alveolar hemorrhage in about 10 percent. Both conditions are attributed to vasculitis affecting the pulmonary capillaries, leading to cough, shortness of breath, rapid breathing, coughing up blood, bloody sputum, and severely low blood oxygen levels. Gastrointestinal involvement occurs in around 20 percent of cases, and myocardial involvement resulting in heart failure occurs in approximately 18 percent.
ANCA-associated vasculitis can be life-threatening if not promptly treated. Early diagnosis and appropriate treatment lead to improvement in the majority of cases. However, delayed treatment or poor response to initial therapy may result in irreversible organ dysfunction, necessitating procedures such as blood dialysis for patients experiencing kidney failure. Moreover, due to the possibility of symptom recurrence, patients should undergo regular checkups with specialists.
Source: theepochtimes.com
Mass Murder on a Worldwide Basis the Year 2020 Has Passed. And for Those Who Promised to Keep Safe, Perform Your Duties, or HNewsWire Will Expose Your Evil Agenda.
Scotland Week 2 – All-Cause Mortality a review of the trends 2010-2024. How the government LIES with statistics to hide the bodies and cover up their ongoing crimes.
https://dksdata.com/ExcessDeaths
In Scotland alone, just by using the ‘post-pandemic’ years, the government has moved the baseline average for calculating Excess Deaths for the first two weeks of 2024 by; 398 deaths over the 10-year pre-pandemic average. 293 deaths over the 5-year pre-pandemic average. Even 140 deaths over the 5-year rolling average.
This shift in the baseline artificially changes the expectation of how many deaths are acceptable to society. If 2020 was such a horrific ‘outlier’ ‘pandemic’ year with a huge number of unexpected deaths, then anything greater than that since should be just as unacceptable. However, it was accepted in 2021, 2022, 2023 and now has become a new baseline for 2024.
In 2020 we shut down the world for fewer excess deaths than we are now so readily accepting as a ‘New Normal’. How is it that the world has so easily accepted ‘pandemic’ level deaths as the status quo?
As we have had NO correction to account for the avoidable deaths between 2020 and 2023, even the 10-year pre-pandemic average should be considered high. Therefore, ‘unexpected deaths’ really should be considered off the charts right now, not negative numbers as the current stats pretend.
In Scotland alone, we have at least 32K in cumulative excess deaths since 2019 without the expected ‘correction’ for the ongoing rise in deaths (or the artificial lag hiding more bodies).
Like the UK, when you look at Scotland over 10 years you see a sign wave pattern on cumulative deaths. 2020 should have been the start of the 5-year downward trend for excess deaths. Instead, deaths started to rise significantly right after the first lockdowns (not before).
The COVID response killed people, plain and simple.
In the chart below (using Scottish NRS data), you can even see the bad ILI (Influenza Like Illness) season in 2018 where not many people were sick, but there was an increase in excess deaths. This is typical as we have a couple of bad flu seasons for infections (but not as many deaths) then a year of lower infection rates for ILI’s but more deaths.
This is how respiratory diseases work. They are either highly infectious or deadly, not both.
Check the thread below for England and Wales to see how this pattern matches as expected in the 10 years before the world lost its collective mind.
Wash and repeat across the world where the COVID response has killed millions.
And for those preparing for ‘next time’ – THIS IS NOT OVER. All the restrictions and insanity that started in March of 2020 worldwide are still in place for Care Homes and Hospitals. And everything used to EXECUTE the COVID response remains worldwide. Governments didn’t need a WHO ‘contract’ to do what they did in 2020 and beyond. Why do you think they would need one moving forward?
You were never “protecting Grandma”. You were helping governments kill them. And this continues in ignorance under the lie that is “focused protection”.
The damage from the COVID response is people dying at accelerated rates in all ages, especially children.
There is no excuse to say you don’t know anymore. There never really was.
https://avoidabledeathawareness.com
This only ends when you stand up and truly act for those with no voice. Those with no choice.
TIME IS UP.
And for those who swore an oath to protect. DO YOUR JOB.
The document reveals that within just 90 days after the EUA release of Pfizer’s mRNA vaccine, the company was already aware of voluntary adverse reaction reports that revealed 1,223 deaths and over 42,000 adverse reports describing a total of 158,893 adverse reactions. The reports originated from numerous countries, including the United States, United Kingdom, Italy, Germany, France, Portugal, Spain, and other nations.
Aside from “general disorders,” the No. 1 most frequently reported category of mRNA vaccine adverse reactions was Nervous system disorders, clocking in at 25,957 reports.
Pfizer is Aware that Its Vaccine Can Cause “Enhanced Disease”
Report Reveals Women Suffer more Damage, Spontaneous Abortion
With more to come, the First Secret Document is Extremely Disturbing, you can download it and read some of the dirty stuff that the FDA knew about.
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