Fm1 Member
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    A new very alarming signal in UK : https://www.youtube.com/watch?v=Zoso8Um9P2M


    atrial fibrillation .... But the data is still hidden...

    I agree that AF has spiked during Covid and the virus as well as the vax has contributed but the main culprit is more likely air quality. AF has been rising for decades in the UK, the number of undiagnosed is staggering

    Atrial Fibrillation Cases Skyrocket in the UK—1 in 45 Now Live with Condition

    Atrial Fibrillation Cases Skyrocket in the UK—1 in 45 Now Live with Condition
    Why is the number of persons in the UK diagnosed with atrial fibrillation surging 50% in just a decade, totaling 1.5 million today? This means that 1 in 45…
    www.trialsitenews.com


    High Air Pollution Days Increases Risk of Premature Death in Heart Failure Patients

    High Air Pollution Days Increases Risk of Premature Death in Heart Failure Patients
    Patients with heart failure have an increased risk of dying from their condition on days with a high level of air pollution and up to two days afterwards,…
    www.trialsitenews.com


    Long-Term Exposure to Air Pollution Associated with Increased Risk for Severe COVID-19

    Long-Term Exposure to Air Pollution Associated with Increased Risk for Severe COVID-19
    People with a long history of exposure to air pollution have a higher risk of developing severe disease, admission to hospital or an intensive care unit (ICU)…
    www.trialsitenews.com

    Tommy, if you believe this crap, I've got a bridge you might be interested in

    German COVID-19 Vax Injured All But Abandoned by the State

    German COVID-19 Vax Injured All But Abandoned by the State
    In 2023, Germany has become more active in activism supporting COVID-19 vaccine-injured persons. Europe’s economic and physical center, the German nation…
    www.trialsitenews.com


    In 2023, Germany has become more active in activism supporting COVID-19 vaccine-injured persons. Europe’s economic and physical center, the German nation commenced COVID-19 vaccination on December 26, 2020, and vaccinated much of the population of 83.2 million. By April of this year, in Germany 76.4% of the population received a basic COVID-19 immunization; 62.6% received at least one dose and over 192 million doses were administered. The government spent over 13.1 billion euros on vaccination by January 2023. As TrialSite reported German Health Minister Karl Lauterbach expressed earlier in the year a desire to help the population who suffered adverse side effects from the COVID-19 jabs. The mainstream media of Germany has carefully moved into the dialogue, such as DW, a public broadcaster focusing on international matters, funded by the German taxpayer.


    In March, Oliver Pieper, writing for DW, suggested any help for the COVID-19 vaccine injured would be a “long overdue step.” This is significant media coverage—on par with PBS doing a similar story in America.


    Pieper starts his piece by introducing case examples of the COVID-19 vaccine injured— using both examples involving the AstraZeneca vaccine as well as the Pfizer-BioNTech mRNA vaccine product. Then, the DW writer introduced the “knowledge gap” after the first surge of vaccinations. For example, the person used as the story's center could not find an immunologist to help him for six months. The vaccine injured, much like in America in Germany were continuously gaslighted by doctor after doctor—being told it was psychosomatic and that it cannot be from a safe vaccine. But how did they know?


    One patient, Sascha Schwartz, calls himself a post-vac victim. He isn’t alone. According to Paul Ehrlich Institute, the German Federal Institute for Vaccines and Biomedical Drugs, by March of this year, 333,492 cases of suspected harmful COVID-19 vaccine side effects were registered, equaling a rate of 1.78 per 1,000 COVID vaccine doses, reports DW.


    Post-Vaccine outpatient unit

    The Marburg University Hospital set up a post-COVID-19 vaccine outpatient unit, something not easy to find in the far bigger America. Sascha Schwartz was ultimately diagnosed there with hyperinflammation of the immune system due to the COVID-19 vaccine. By March of this year, DW reports unfortunately, nothing has worked to help this patient.


    Abandoned by the State

    Like so many other injured Germans and their European and American counterparts, governments have just abandoned them, leaving them for death in some cases. Sascha Schwartz has not received any compensation to date from the state. This is in spite of the fact that his health insurer rejected applications for a blood purification treatment with a $16,000 price tag. He is on his way to living off unemployment while accumulating growing debt. The situation for many is far worse.


    Tobias Ulbrich---taking on COVID vax cases




    Teutonic COVID vax lawsuits

    Lawsuits are filed and may proceed in 2023. For example, a law firm in Dusseldorf owned by Tobias Ulbrich has opened up a practice at the firm Rogert & Ulbrich specializing in COVID-19 vaccine injuries. Now representing 750 persons he has filed 130 lawsuits in German against both BioNTech and Moderna.


    DW reports that the lawyer went on the record that the lack of informed consent was devastating to some people. The German government failed to offer even the basic information about risk telling Oliver Pieper at DW, “We have a federal minister who for quite some time has dubbed vaccination as free of side effects.” Here, he refers to Lauterbach, who now has supposedly seen the light and wants to help those more unfortunate—but will he? Talk is cheap.


    Court hearing

    Last month, the first civil case against BioNTech was heard in a Frankfurt court. This case involves a 57-year-old woman who has alleged the COVID-19 mRNA jab led to heart damage. Proceedings in Frankenthaler, Dusseldorf and Munich will follow.


    Waivers a matter of degree

    Apparently, unlike in the U.S. where under the PREP Act manufacturers like Pfizer-BioNTech and Moderna enjoy near-universal liability waivers, German lawyers appear to have a little more wiggle room to sue the vaccine makers. But in actuality, any victories would simply be covered by the government. The drug companies negotiated pretty much the same waiver of liability in Europe.


    Attorney Ulrich told DW, “In our case, civil claims are always against the manufacturer. And ultimately it is then the manufacturer who can again demand exemption from liability, i.e., repayment by the federal government. So, from a purely economic point of view, we have the Federal Republic of Germany as an opponent and only on paper, the vaccine manufacturer.”


    Will Lauterbach make good on his talk? Not likely, given the stakes in the COVID-19 era.


    TrialSite reached out to Tobias Ulbrich to answer some questions. We will update this article upon a response.


    Post-vac syndrome — the forgotten COVID victims – DW – 03/21/2023
    German Health Minister Karl Lauterbach wants to help those who suffer from serious side-effects from COVID-19 vaccines. For those affected, this is a long…
    www.dw.com

    A Plague Upon Our House” By Special White House Advisor Dr. Scott Atlas

    White House Preoccupation with Testing, Contact Tracing, Masks, and Lockdowns Reveals Blindspot for Sick Americans with Acute COVID-19

    “A Plague Upon Our House” By Special White House Advisor Dr. Scott Atlas
    White House Preoccupation with Testing, Contact Tracing, Masks, and Lockdowns Reveals Blindspot for Sick Americans with Acute COVID-19
    petermcculloughmd.substack.com


    By Peter A. McCullough, MD, MPH


    I have had a chance to get to know Dr. Scott Atlas, former academic neuroradiologist and health policy scholar at the Hoover Institute, Stanford University. I have great respect for his intellectual honesty and courage challenging others inside the White House during his tenure as Special White House Coronavirus Advisor from July to December, 2020. However, I read his account of what happened titled “A Plague Upon Our House” with particular attention to what I saw in community medicine and with millions of Americans falling sick with COVID-19 during that time period. I was actively publishing on medical advancements alongside Atlas in The Hill and in peer-reviewed manuscripts. Here are two OPEDs within a month of each other—Atlas as well as the entire White House were oblivious to the important issue I raise—saving American lives with early treatment

    Vitamin D is the key to a long healthy life!!!


    High Dose Vitamin D3 Could Protect Neuropsychiatric Problems in Children

    High Dose Vitamin D3 Could Protect Neuropsychiatric Problems in Children
    Supplementing high-dose vitamin D3 (VD3) in infancy could decrease mental health problems in children, shows new study data.  Among the many health…
    www.trialsitenews.com


    Supplementing high-dose vitamin D3 (VD3) in infancy could decrease mental health problems in children, shows new study data.


    Among the many health benefits of vitamin D, research suggests it may be critical for healthy brain development. For instance, both children with attention deficit hyperactivity disorder (ADHD) and autism are more likely to have VD3 deficiency than those without the condition. In addition, low blood 25(OH)D – a soluble form of VD3 passed from mothers into fetuses – has also been associated with ADHD and autism, as well as depressive symptoms in children.


    In light of this evidence, a Finnish-based research team investigated the preventive impact of VD3 on childhood neuropsychiatric symptoms. Their results found children who took high VD3 doses as infants were less likely to develop emotional problems compared with controls.


    The study, published in Jama Network Open on May 19th, is a continuation of the University of Helsinki's Vitamin D Intervention in Infants (VIDI) clinical trial. The VIDI study compared neuropsychiatric symptoms between infants aged two weeks and two years old who supplemented either a 1000 IU or a 400 IU of VD3 daily. The high dose is above recommended guidelines of 400-800 IU per day.


    Vitamin D’s Crucial Role in Dopamine Function and Schizophrenia

    Vitamin D's Crucial Role in Dopamine Function and Schizophrenia - Neuroscience News
    Neuroscientists discovered how vitamin D deficiency impacts the development of neurons, contributing to disorders such as schizophrenia.
    neurosciencenews.com


    Summary: Neuroscientists discovered how vitamin D deficiency impacts the development of neurons, contributing to disorders such as schizophrenia.


    Using innovative technology, they were able to observe that a lack of vitamin D not only changes neuron growth but also affects the brain’s dopamine release mechanism. They found dopamine release was enhanced in cells grown in the presence of vitamin D, compared to a control.


    This study underscores the importance of vitamin D in the structural differentiation of dopaminergic neurons and suggests that maternal vitamin D deficiency might alter how early dopaminergic circuits form.


    Key Facts:


    The research team showed that vitamin D deficiency affects the growth and dopamine release mechanisms in dopaminergic neurons.

    They found that dopamine release was enhanced in cells grown in the presence of the vitamin D hormone compared to a control.

    The study posits that early alterations to dopamine neuron differentiation due to vitamin D deficiency may be the neurodevelopmental origin of dopamine dysfunction in adults who develop schizophrenia.

    In the first round of VIDI results, published in 2021, the research team found no significant effect of high-dose VD3 on the infants, explaining "behavioral and psychiatric problems may not be fully manifested during the early years but may become more evident when environmental demands increase."


    At ages six to eight, 346 infants from the original study had their symptoms reassessed.


    Through analyzing parent responses on the Childhood Behaviour Checklist (CBCL), the researchers showed more children in the 400 IU group (11.8%) had internalizing problems – emotional states characterized by depression, withdrawal, and anxiety – compared to the 1200 IU group (5.6%).


    "Our results suggest that a higher dose of vitamin D3 supplementation during the first years of life may reduce the risk of internalizing psychiatric symptoms in late preschool and early school age," said Samuel Sandboge, Lead Study Author and Postdoctoral Research Fellow at Tampere University.


    The study authors described several limitations to their results, writing, "the results and their potential implications are interesting, but further research is needed." For instance, they noted how CBCL responses were recorded throughout the pandemic, possibly influencing the children's behaviors, and drew light to potential inaccuracies of having parents judge their child's behavior.


    Nonetheless, with estimates revealing one-tenth of the global population as vitamin D deficient, and mental disorders in one-eighth of children in developed countries, the study results warrant further investigation into vitamin D3, neurodevelopmental risk and the protective potential of supplements.


    Effect of Vitamin D3 Supplementation in First 2 Years of Life on Psychiatric Symptoms at Ages 6-8 Years
    This secondary analysis of a randomized clinical trial investigates the effect of increased vitamin D supplementation up to age 2 years on the risk of…
    jamanetwork.com

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    Can Bivalent mRNA COVID-19 Vaccine Trigger Leukemia? Taiwanese Clinicians Find a Likely Rare Case

    Can Bivalent mRNA COVID-19 Vaccine Trigger Leukemia? Taiwanese Clinicians Find a Likely Rare Case
    A case series involving a generally, healthy 43-year-old woman in Taiwan represents one of the rare and highly disturbing cases of COVID-19 vaccinations linked…
    www.trialsitenews.com


    A case series involving a generally, healthy 43-year-old woman in Taiwan represents one of the rare and highly disturbing cases of COVID-19 vaccinations linked to sporadic hematopoietic adverse events. Although, the physician-scientists do point out there currently isn’t sufficient evidence to correlate anti-spike protein immune responses and hematopoietic adverse events of vaccinations. Nonetheless, Dr. Chung-Ta Chang, an emergency physician and orthopedic surgeon at Far Eastern Memorial Hospital in New Taipei City, and colleagues apparently had such a case—diagnosing a Ph-positive B-cell acute lymphoblastic leukemia (ALL) occurring directly after the patient received Moderna’s mRNA COVID-19 bivalent (Omicron BA.4/BA.5) booster vaccine on January 3, 2023. It turns out that the 43-year-old had a total of six spike antigen exposures over the past 1.5 years (two doses of AstraZeneca, and half dose of Moderna’s monovalent mRNA vaccine and Novavax) on June 4, 2021, August 31, 2021, January 15, 2022, and July 15, 2020, respectively. While Dr. Chung-Ta Chang and colleagues acknowledge the challenges in declaring a causal relationship between the bivalent mRNA vaccination and Ph-positive B-cell ALL, the Taiwanese doctors clearly are concerned, proposing “that anti-spike protein immune responses could be a trigger for leukemia.” The doctors have a message for both clinicians and researchers--carefully investigate hematopoietic adverse events closely after COVID-19 vaccinations and launch preclinical studies to investigate the safety of bivalent mRNA COVID-19 vaccines.


    Taiwanese researchers affiliated with multiple academic medical centers author a case report with disturbing implications involving a 43-year-old woman with no problematic health record receiving her bivalent Omicron BA.4/BA.5) mRNA-1273 COVID-19 vaccine on January 3, 2023. Immediately after the injection, the patient immediately felt off—with a few concerning side effects from dizziness, mild dyspnea (breathing difficulty) to an overall general malaise. Five days after the booster dose was administered, the patient’s general malaise continued, along with worsening breathing problems, so she made it to Far Eastern Memorial Hospital Emergency Department in New Taipei City. Physicians at the emergency department observed no fever or respiratory symptoms, and she tested negative for COVID-19. Doctors reported tachycardia (119 beats/min) with normal blood pressure, and no abnormal bleeding, petechia or ecchymosis detected. A series of other blood tests led to the identification of ALL symptoms.


    As part of the case series, the Taiwanese physicians researched the incidence of hematologic malignancy occurrence after mRNA COVID-19 vaccinations. A disturbing topic, that is, the highly rare connection between mRNA vaccination and ALL. The disease itself, ALL—is rare with a poor prognosis. The 5-year overall survival equals 35% in patients aged between 18 to 60 years. The cause of adult ALL includes old age (>70 years), recent viral infection, chemotherapy or radiation exposure and genetic disorders.


    What follows is a brief TrialSite breakdown of their findings published in MDPI.


    Far Eastern Memorial Hospital




    How many other cases of hematologic malignancy occurring after mRNA vaccination have occurred to date?

    Seven (7). All cases received monovalent BNT162b2 (Pfizer-BioNTech) vaccination. TrialSite notes that these are the only cases documented and that there could be more. Four of the seven cases were identified as acute myeloid leukemia. Onset of symptoms varies but on average, was four to five weeks after vaccination.


    In the current Taiwanese case, how fast was the onset of BCR-ABL1 Ph–positive (p190 form) B-cell acute lymphoblastic leukemia?

    Five (5) days.


    Was there any previous incident that could be a cause?

    Not likely. The Taiwanese team reported that the patient was otherwise healthy with no risk factors for ALL. While she did have COVID-19 on August 19, 2022, none of her tests at the time revealed any abnormalities or cause for concern. This is why Dr. Chung-Ta Chang and colleagues write, “Therefore, this case report might present a possible correlation between the development of Ph–positive B-cell acute lymphoblastic leukemia and bivalent mRNA vaccinations.”


    Are immune-pathological features “frequently” noticed and described after SARS-CoV-2 infection or COVID-19 vaccination?

    Yes. The doctors acknowledge this and provide examples in the case series.


    What’s a key premise involved in this case series that will likely not make its way into mainstream media anytime soon?

    That “repeated spike antigen exposures involved with COVID-19 vaccination amplify the immune cell response in a condensed period of time, thereby potentially increasing incidence of B-cell acute lymphoblastic leukemia.


    Even though important pre-vaccine test results and comprehensive bone marrow studies were provided, can the team definitively conclude the causal relationship between the mRNA bivalent vaccination and occurrence of ALL?

    No.


    What do the case report authors recommend is needed?

    Robust population-level studies investigation if there is an increased incidence of hematolymphoid neoplasms post COVID-19 vaccination. Also, they argue it’s “imperative to keep monitoring the hematopoietic adverse events after these new technology bivalent mRNA COVID-19 vaccinations, especially for patients with multiple spike antigen exposures in a relatively short-term period.” Finally, the authors suggest more pre-clinical studies evaluating the safety of the COVID-19 vaccines.


    Lead Research/Investigators

    Chung-Ta Chang, M.D., Ph.D. Far Eastern Memorial Hospital, Emergency Department, Taipei Medical University, College of Oral Medicine, Yuan Ze University, Graduate Institute of Medicine; Corresponding Author


    Shy-Yau Ang, Far Eastern Memorial Hospital, Emergency Department


    Yi-Fang Huang, Chang Gung Memorial Hospital; Taipei Medical University, College of Oral Medicine; Yuan Ze University, Graduate Institute of Medicine


    Ph-Positive B-Cell Acute Lymphoblastic Leukemia Occurring after Receipt of Bivalent SARS-CoV-2 mRNA Vaccine Booster: A Case Report
    The coronavirus disease 2019 (COVID-19) pandemic is a universal emergency public health issue. A large proportion of the world’s population has had…
    www.mdpi.com

    Feds Fall Woefully Short with COVID-19 Vax Injury Compensation: CICP Director: No Computer Systems!

    Feds Fall Woefully Short with COVID-19 Vax Injury Compensation: CICP Director: No Computer Systems!
    With almost 12,000 people having filed claims with the Countermeasures Injury Compensation Program (CICP), the vaccine injury compensation scheme established…
    www.trialsitenews.com


    With almost 12,000 people having filed claims with the Countermeasures Injury Compensation Program (CICP), the vaccine injury compensation scheme established with the national public health emergency, just a few of these injured persons have secured any payment, and those compensated are done so on average at $1,500 per claimant. Mainstream media inches its way into coverage, discussion and commentary. It is a tragic situation for those injured by vaccines that were often mandated to take. The government, while overreaching in many respects during the pandemic, did little to nothing to anticipate the tens of thousands that would claim injuries. The program is understaffed, and now, a director from the Countermeasure Injury Compensation Program (CICP) told a Georgia-based Congressperson that they had no technology to support the scale up of the program. Also, the CICP program is severely understaffed. Who in the federal government is responsible for this reality?


    Most recently, WXIA-TV (11Alive) television station in Atlanta, Georgia, United States, affiliated with NBC covered this disturbing problem. Owned by Tegna Inc. alongside MyNetworkTV affiliate WAT, the piece reveals that only 706 claims have been processed to date, with the vast majority denied.


    Enter one case study on the waiting game: Allen Storey. Still recovering after receiving the COVID-19 vaccine two years ago, bills have mounted. Waiting in limbo, 11Alive investigated, discovering that Mike Collins, representing the 10th District of Georgia, demanded to discuss the growing crisis with CICP leadership.


    The CICP’s leadership now claims that technology is the core of the problem, writes Rebecca Lindstrom for 11Alive. For example, Collins reports the CICP director program laments the lack of technology to support the scale out of the program:


    “They did not even have a computer system in place, a software system to handle people making requests or even inquiring about what their status was, which was what you were talking about in y'all's reporting.”


    Although CICP recently launched a claims portal to track claims, they are purportedly requesting $15 million from Congress to “enhance communication” as well as “substantially increase its capacity to review at least 2,000 claims.”


    Crisis scenario

    This is clearly not enough. While CICP hopes to access technology that can help the federal group scale up to 2,000 claims, this is nowhere near enough. At the current case load rate of claimed COVID-19 vaccine-related injuries, the CICP director informed Congressman Collins that it would take five years to get to them.


    In addition to the lack of technology which represents a complete lack of planning on the part of the federal government, Collins reports to 11Alive that “a third of the federal employees have been working from home. And that just doesn't work very well.”


    Last year, the CICP funded only 34 positions to deal with over 11,000 claims and now the federal group proposes a budget for an additional 42 full-time employees. But will this be enough?


    “You're asking the same questions that we ask,” Collins said. “They don't know how many people they employ; the federal government, these departments, they don't know. And so that's one of the big issues that we have. You're right. Do you have enough people who are inefficient, or do you not have enough people?”


    COVID-19 vaccine injured struggling

    The plight of the Storey family was featured in this latest piece from 11Alive. With an average payout to date of $1,500 (and just a few persons compensated), Allen Storey’s bills accumulate to what will likely be in the tens of thousands.


    What are people injured by the COVID-19 vaccines supposed to do? In many cases they were mandated to get the shots, and that same government compelling the procedure waived all liability of the vaccine manufacturers.


    Groups such as React19 have been launched in the private sector to support persons injured by the COVID-19 vaccines. While that nonprofit has recruited a network of now over 20,000 vaccine injured people and over 200 doctors supporting this class of care, this is nowhere near enough to deal with the accumulating demand.


    Rebecca Lindstrom reports that likely, most persons injured by the COVID-19 vaccines are not even aware of the CICP program. According to Allen Storey, “I don’t think most people know this program exists. You can probably walk down and 10 out of 10 people don’t know about it. I don’t know how they would find out about it if they weren’t specifically looking for this program. Most doctors don’t even know about it.”


    This lack of awareness also represents a problem for persons injured by the vaccines seeking help from the private sector. React19 has often been censored by Facebook, traditionally, the number one social network for patient groups. Why the censorship? A confluence of government, media and social tech companies have collaborated during the pandemic to censor key information including stories about COVID-19 vaccine injuries, even if the information is truthful.


    Clearly, the federal government has on the one hand, completely overstepped its boundaries during the pandemic while at the same time, when it comes to caring for the nation’s population damaged by the mass vaccination program they stepped back, doing not nearly enough.


    Call to Action: Need help and support for COVID-19 vaccine injury? Contact React19. For more information on the CICP program—follow the link.


    Note aggregate data on CICP can be found here.

    Countermeasures Injury Compensation Program (CICP) Data | HRSA


    https://www.11alive.com/article/news/local/program-pay-covid-vaccine-injuries-15-million-fix-problems/85-4947974e-ecb4-483a-b8cf-bada7a6db47d

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    Vitamin d is the key!!!!!


    Estimation of Vitamin D Levels in Patients With Retinal Vein Occlusions and a Comparison With Age-Matched Control Groups

    Estimation of Vitamin D Levels in Patients With Retinal Vein Occlusions and a Comparison With Age-Matched Control Groups
    Background In the older population, retinal vein occlusion (RVO) is a major contributor to vision loss and blindness. RVO is the second most common form of…
    www.cureus.com


    Abstract

    Background

    In the older population, retinal vein occlusion (RVO) is a major contributor to vision loss and blindness. RVO is the second most common form of retinal vascular disease, following diabetic retinopathy. On the other hand, there is a paucity of studies on vitamin D insufficiency and its influence on the causation of RVOs. The goal of this study is to demonstrate a link between vitamin D levels of individuals in rural India who have RVOs.


    Methods

    This study is a hospital-based prospective case-control study. All patients aged 18 years and above with RVO visiting the ophthalmology outpatient department at a tertiary care facility in central India and all controls in the same age group were chosen for the study after taking into consideration inclusion and exclusion criteria. Fasting for 12 hours prior to blood sample collection was required of all participants. The total vitamin D concentration in the serum was determined using tandem mass spectrometry after it had been frozen at 20°C. For this study, vitamin D levels were collected from 70 participants.


    Results

    The average age is 60, with a standard variation of 10 for both cases and controls. There is a 49% prevalence of central RVO (CRVO), 34% prevalence of inferotemporal branched RVO (IT BRVO), and 17% prevalence of superotemporal BRVO (ST BRVO). Twenty percent of the 35 patients were deficient in vitamin D, and 80% had insufficient levels. No case patient had vitamin D levels within the normal range. No one with vitamin D insufficiency was found among the 35 controls. Twenty-five percent of the patients had adequate vitamin D levels, but only 28.6% of the controls did. The p-value of 0.01 indicates a remarkable difference in vitamin D levels between the diagnosed cases and controls. Cases had mean vitamin D levels of 21.408 +/− 4.947 ng/dl, while controls had mean levels of 37.808 +/− 11.799 ng/dl. Vitamin D levels did not differ significantly across RVO subtypes. The study also shows the association of RVO with hypertension (HTN) and dyslipidemia as the p-value was noted to be significant (p = 0.0147 < p = 0.05) for HTN with an odds ratio of 3.43 (CI, 1.25-9.4) and was significant (p = 0.0404 < p = 0.05) for dyslipidemia with an odds ratio of 4.87 (CI, 0.96-24.97). Diabetes, smoking, hyperhomocysteinemia, dyslipidemia, cardiovascular disease, and cerebrovascular accident are all well-known risk factors, but we found no evidence associating them together.


    Conclusion

    Vitamin D proved to be an important risk factor in the causation of RVOs. Other risk factors like HTN and dyslipidemia also showed significant relation in the study. Vitamin D levels should be advised as a routine investigation in patients who are diagnosed with RVOs along with screening for other risk factors. Vitamin D supplementation should be given as prophylaxis in cases of deficiency.

    Daily Vitamin D Intake Could Significantly Reduce Overall Cancer Mortality

    Daily Vitamin D Intake Could Significantly Reduce Overall Cancer Mortality
    A meta-analysis conducted at the German Cancer Research Center shows daily vitamin D intake could reduce cancer mortality in the population by 12%. The…
    www.trialsitenews.com


    A meta-analysis conducted at the German Cancer Research Center shows daily vitamin D intake could reduce cancer mortality in the population by 12%. The results from the analysis were published in Ageing Research Reviews.


    Vitamin D deficiency is prevalent worldwide and more common in cancer patients during cancer therapy than in the general population. The potential effects of vitamin D supplementation and the development or prognosis of cancer have been investigated in numerous prior studies. However, evidence regarding vitamin D3 and cancer mortality from these studies is conflicting.


    For the current study, researchers sought to evaluate the effect of vitamin D3 supplementation on cancer mortality in the general population and on prognosis in cancer patients.


    The investigative team conducted a systematic literature search that identified 14 studies with a total of nearly 105,000 participants. The researchers considered only studies whose participants had been randomly assigned to the vitamin D3 arm or the placebo arm.


    When all 14 studies were pooled, no statistically significant results emerged. The main meta-analysis yielded a reduction in cancer mortality of only 6%.


    However, when the studies were divided according to whether vitamin D3 was taken daily in a low dose (400 to 4000 IU per day) or in higher doses administered at longer intervals, (60,000 to 120,000 IU once per month or less) a large difference was seen.


    In the four studies with the infrequent higher doses, there was no effect on cancer mortality. In contrast, in the summary of the ten studies with daily dosing, the researchers determined a statistically significant twelve percent reduction in cancer mortality.


    "We observed this twelve percent reduction in cancer mortality after untargeted vitamin D3 administration to individuals with and without vitamin D deficiency. We can therefore assume that the effect is significantly higher for those people who are actually vitamin D deficient," said Ben Schöttker, an epidemiologist at the German Cancer Research Center.


    The better efficacy outcome with daily doses of vitamin D3 can be explained by the more regular bioavailability of the active agent, the hormone 1,25-dihydroxyvitamin D, which is only produced by reactions of vitamin D in the body and can presumably inhibit tumor growth, said Schöttker.


    Upon further analysis of the studies with daily intake, people aged 70 and older benefited most from vitamin D3 therapy. In addition, the effect was most evident when vitamin D intake was started before the cancer diagnosis.


    References

    Reduced cancer mortality with daily vitamin D intake

    Is Pfizer’s mRNA COVID-19 Vaccine Linked to a Surge of Potentially Deadly RSV Cases?

    Is Pfizer’s mRNA COVID-19 Vaccine Linked to a Surge of Potentially Deadly RSV Cases?
    Recently, a concerned citizen and post-graduate student studying at the University of California tipped TrialSite to a possible injury concern with…
    www.trialsitenews.com


    Recently, a concerned citizen and post-graduate student studying at the University of California tipped TrialSite to a possible injury concern with Pfizer’s vaccine development initiatives. In fact, according to this source, the Pfizer COVID-19 vaccine promoted aggressively by the Biden administration nearly killed this university student’s young sister. The claim: “Pfizer's vaccine caused Respiratory Syncytial Virus (RSV) spreading among kids and seniors.” And big surprise, of course, Pfizer is working to get its RSV vaccine approved by the U.S. Food and Drug Administration (FDA). Could Pfizer be on track to “double down” on profits from vaccines? While the linkages are tenuous at best, some research digs up relevant information.


    James Lopez, the postgraduate studying in University of California, nearly lost his beloved eight-year-old sister, Carolyn, just weeks ago. According to Lopez after his sister received the mRNA COVID-19 Pfizer-BioNTech vaccine (BNT162b2) she rapidly developed a fever and coughing that night. Their parents and James initially thought that the results were just standard side effects, or at worse, adverse events. But according to Lopez, “We were wrong.” Little Carolyn’s coughing became so severe that she couldn't breathe. The family called 911 in a panic. She was diagnosed with Respiratory syncytial virus (RSV) bronchitis at the hospital. Thanks to timely treatment, Carolyn continues to slowly recover.


    While James Lopez articulated to TrialSite that the Pfizer mRNA vaccine triggered the RSV incident, we at TrialSite cannot be certain, as there is no formal medical confirmation or access to records. But family members are convinced that the two are causally related.


    “Why should my sister experience those sufferings just for taking the Pfizer COVID vaccine?” asks the university student.


    Since the incident (and again, we at TrialSite cannot declare that Carolyn’s Pfizer jab led to the bout of RSV), Lopez investigated COVID-19 vaccines promoted aggressively by the Biden administration. Lopez communicated with TrialSite “Something appalling came out.”


    According to an adverse event of special interest (AESI) analysis report from Pfizer exposed in April 2021, Respiratory syncytial virus bronchiolitis and Respiratory syncytial virus bronchitis were clearly listed as Pfizer Covid-19 vaccine's adverse event in APPENDIX 1!




    Interestingly, in May 2018, Pfizer initiated a Phase 1/2 study to evaluate a respiratory syncytial virus vaccine but had no progress to report later. However, with the onset of the pandemic, by April 2020, Pfizer had inked a deal with BioNTech to co-develop the mRNA-based COVID-19 vaccine, as reported by the German company to investors.


    The document Lopez cites as evidence that RSV is a potential side effect of the Pfizer-BioNTech COVID-19 vaccine is titled “5.3.6 Cumulative Analysis of Post -Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received through 28-Feb-2021.” Sure enough, RSV is listed under Appendix 1: List of Adverse Events of Special Interest marked page 30.


    While we don’t have a total listing from this document, RSV was observed as an AESI in association with BNT162b2 as noted in Appendix 1.


    React19 co-founder Brianne Dressen was asked about incidence of respiratory problems after COVID-19 vaccination. Her organization represents over 20,000 COVID-19 vaccine injured persons. She told this author “We have heard reports of many people after vaccination report extensive coughs—it’s called a cough covid.” Ms. Dressen said that after her confirmed COVID-19 vaccine injury she also experienced a lengthy cough and respiratory problems. She told this author “I was tested for COVID-19 12 times as well as a spinal tap and never once was COVID-19 confirmed.” Could RSV have been at play? The prospect intrigued her, but she didn’t know if it could be the case, nor do we.


    Back to James Lopez and the question he posed for TrialSite: As soon as Pfizer launched the BNT162b2 COVID-19 vaccine clinical program with BioNTech in April 2020, why and how did in parallel crank out the RSV vaccine research just two months later? James Lopez speculates that this large pharmaceutical company knew one of the adverse events of the COVID-19 vaccine would be fatal RSV, and that the market need of RSV vaccine would certainly surge. Undoubtedly, the opportunity for profits was there. But could they have known at such an early stage? It’s unlikely, given Pfizer would not even know at the time if their COVID-19 vaccine would make it to the regulatory finish line.


    What’s the status of RSV side effects?

    Sonia Elijah has authored a handful of critical analyses covering Pfizer COVID-19 vaccine documentation released due to court ordered freedom of information act (FOIA) rulings. For example, in part 1 the England-based author reviewed thousands of Case Report Forms in relation to the FDA’s latest release of Pfizer-BioNTech COVID-19 vaccine clinical trial documents. This analysis by Elijah uncovered numerous errors and anomalies, raising critical questions as to the overall integrity of the clinical trial data. In Part 2, Elijah probed in depth at the confidential ‘Nonclinical Overview’ document.


    Of course, Biden took office in the first month of 2021, just as the COVID-19 vaccines were being rolled out. But Lopez is correct in that the Biden administration would have been aware of any material side effects, including RSV.


    However, any claim that Biden personally knew or would have the reason to know that the COVID-19 vaccines would possibly lead to a potentially lethal infection among children and seniors would be a stretch to say the least. Biden knows little of science and medical research and undoubtedly, would simply defer to the “experts” such as Dr. Anthony Fauci, who was still director of the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH).


    TrialSite is fully aware that some leaders within the NIH, as well as the FDA and the Centers for Disease Control and Prevention (CDC) were aware of serious side effects associated with the COVID-19 vaccines. In fact, Brianne Dressen, co-founder of React19 was injured by the AstraZeneca vaccine during the Phase 3 clinical trial. Ms. Dressen was part of a COVID-19 vaccine injured cohort that visited the NIH multiple times. During various phone and email communications other government officials were present—not only from the NIH, but also the FDA, CDC and even Pfizer (Albert Bourla, the CEO was actually cc’d in at least one set of emails involving COVID-19 vaccine injuries). TrialSite has reviewed some of these communications.


    James Lopez doesn’t want to let Biden off of his responsibility, however. According to the university student, “The truth is, Biden has openly supported and promoted Pfizer's Covid vaccine since his taking office, even though he KNEW it would cause lethal infectious diseases among kids and seniors.”


    Again, we at TrialSite disagree with this presumption (that Biden would be aware of the situation at that level, but most certainly, some of his inner health-focused leadership (e.g., Fauci, Marks, etc.) would have likely been aware of such a possibility, as rare and unlikely as it may be.


    From Feb 2021 to Dec 2022, the Biden admin purchased 905 million doses of the Pfizer vaccine. At the same time, hospitalization rates of RSV for seniors were about 10 times higher than the years before the COVID-19 pandemic according to some research Lopez conducted. According to the latest data from CDC, national hospitalization rates of RSV from 2022 to 2023 were nearly twice the rates from 2018 to 2019.




    Other studies confirm the surge of RSV cases in 2021, such as this report in The Lancet.


    This author must remind all that there have been no formal studies tying together the COVID-19 mRNA vaccine from Pfizer and RSV other than a listing in some of the regulatory documents reporting on at least some incidents as AESIs.


    Any claims for definitive linkages would be speculative and not citable as evidence. In fact, this is why this entry is falling under OPINION.


    The FDA has granted approval of RSV vaccine to GlaxoSmithKline Biologicals on May 3. And Pfizer's RSV vaccine is on the way. Some FDA experts were concerned not enough participants in Pfizer's trial got infected with RSV to adequately assess the vaccine's efficacy. The concern for regulatory capture is palpable with many people who interact with us around the country and beyond. Pfizer has cultivated lots of allies in Washington, or that’s the fear on the street.


    But this could be changing. After all, as recently reported by Reuters, Albert Bourla said of pending U.S. drug price plans that it was like “negotiating with a gun to your head.”


    The mood in Washington may turn sour against Big Pharma but that doesn’t necessarily mean that the estimated half-a-million to 2 million people who sustained material serious adverse events impacting daily life will be compensated or cared for anytime soon. I emphasize that this estimation is that of TrialSite and may be incorrect. Many in the anti-vax or medical freedoms community make claims for far more but their evidence is questionable. On the other hand, the government keeps any estimates awfully close to the chest—which raises suspicion.

    Low Vitamin D Levels Are Associated With Long COVID Syndrome in COVID-19 Survivors

    Low Vitamin D Levels Are Associated With Long COVID Syndrome in COVID-19 Survivors
    AbstractContext. Long COVID is an emerging syndrome affecting 50% to 70% of COVID-19 survivors that still lacks predicting factors.Objective. Due to the extrask
    academic.oup.com


    Abstract

    Context

    Long COVID is an emerging syndrome affecting 50% to 70% of COVID-19 survivors that still lacks predicting factors.


    Objective

    Due to the extraskeletal effects of vitamin D, we retrospectively assessed the association between 25(OH) vitamin D levels and long COVID in COVID-19 survivors 6 months after hospitalization.


    Methods

    Long COVID was defined according to NICE guidelines. Fifty long COVID and 50 non–long-COVID subjects matched on a 1:1 basis were enrolled from an outpatient clinic post-COVID cohort seen from August to November 2020. Therapies/comorbidities affecting calcium/vitamin D/bone metabolism, and/or admission to the intensive care unit during hospitalization were exclusion criteria. 25(OH) Vitamin D was measured at hospital admission and 6 months after discharge.


    Results

    We observed lower 25(OH) vitamin D levels, evaluated at follow-up, in subjects with long COVID than those without (20.1 vs 23.2 ng/mL, P = .03). Regarding the affected health areas evaluated in the entire cohort, we observed lower 25(OH) vitamin D levels in those with neurocognitive symptoms at follow-up (n = 7) than those without (n = 93) (14.6 vs 20.6 ng/mL, P = .042). In patients presenting vitamin D deficiency (<20 ng/mL), both at admission and at follow-up (n = 42), those affected by long COVID (n = 22) presented lower 25(OH) vitamin D levels at follow-up than those not affected (n = 20) (12.7 vs 15.2 ng/mL, P = .041). In multiple regression analyses, lower 25(OH) vitamin D levels at follow-up were the only variable significantly associated with long COVID in our cohort (P = .008, OR 1.09, CI 1.01-1.16).


    Conclusion

    COVID-19 survivors with long COVID have lower 25(OH) vitamin D levels than matched patients without long COVID. Our data suggest that vitamin D levels should be evaluated in COVID-19 patients after hospital discharge. The role of vitamin D supplementation as a preventive strategy of COVID-19 sequelae should be tested in randomized controlled trials.

    7.3M Patient Real World Study Bombshell—mRNA Vax Leads to Heightened Risk of Retinal Vascular Occlusion

    7.3M Patient Real World Study Bombshell—mRNA Vax Leads to Heightened Risk of Retinal Vascular Occlusion
    Taiwanese researchers from the Chung Shan Medical University Hospital and China Medical University School of Medicine and other colleagues recently had their…
    www.trialsitenews.com


    Taiwanese researchers from the Chung Shan Medical University Hospital and China Medical University School of Medicine and other colleagues recently had their large 7.3 million patient multi-site real-world study involving COVID-19 vaccine-related retinal vascular occlusion risk published in the journal npj Vaccines (Nature). The authors acknowledge “several documented possible complications” associated with the increased vaccination rates linked to the mass COVID-19 vaccination program. In this study, the Taiwan-based medical researchers investigated the risk of retinal vascular occlusion post-COVID-19 vaccination. Leveraging the real-world data associated with the TriNetX global network of federated medical centers, the study team included persons vaccinated with COVID-19 vaccines between the duration from January 2020, and December 2022. To ensure better quality data, the protocol excluded persons with any history of retinal vascular occlusion or those who used any systemic medication that could possibly affect blood coagulation before receiving the COVID-19 jab.


    What’s the condition under study?

    Retinal vein occlusion is a blockage of the small veins that carry blood away from the retina. The retina is the layer of tissue at the back of the inner eye that converts light images to nerve signals and sends them to the brain. Retinal vein occlusion is one of the most common blinding conditions in the United States; without treatment, central retinal vein occlusion (CRVO), the most severe type of retinal vein occlusion, often leads to significant or permanent vision loss, according to a National Institutes of Health report.


    Study analysis

    In analyzing the data associated with the risk of retinal vascular occlusion, the Taiwanese study team used multivariable-adjusted Cox proportional hazards models once they performed a 1:1 propensity score matching between both COVID-19 vaccinated and unvaccinated study groups.


    Findings

    The study authors find problems with the COVID-19 vaccinated cohort, writing:


    “Individuals with COVID-19 vaccination had a higher risk of all forms of retinal vascular occlusion in 2 years after vaccination, with an overall hazard ratio of 2.19 (95% confidence interval 2.00–2.39). The cumulative incidence of retinal vascular occlusion was significantly higher in the vaccinated cohort compared to the unvaccinated cohort, 2 years and 12 weeks after vaccination.”


    Furthermore, corresponding authors James Cheng-Chung Wei and Chun-Ju Lin and co-authors report that during the first two weeks post COVID-19 vaccination and onward for another 12 weeks the risk of retinal vascular occlusion was significantly higher.


    This risk, report the study authors, remains higher with the mRNA-based COVID-19 vaccines. For example, they summarize in the peer reviewed journal that persons “with first and second dose of BNT162b2 and mRNA-1273 had significantly increased risk of retinal vascular occlusion 2 years following vaccination.”


    No distinct differences were found between the various brand and vaccine dose.


    Conclusion must be taken seriously

    The authors report the findings in stronger language than TrialSite typically observes coming out of mainstream journals. Their results strike a note of concern:


    “This large multicenter study strengthens the findings of previous cases. Retinal vascular occlusion may not be a coincidental finding after COVID-19 vaccination.


    Lead Research/Investigator

    James Cheng-Chung Wei, M.D., Ph.D. Department of Medical Research, Chung Shan Medical University Hospital; Institute of Medicine, Chung Shan Medical University; Institute of Integrated Medicine, China Medical University

    Chun-Ju Lin; School of Medicine, College of Medicine, China Medical University; Department of Ophthalmology, China Medical University Hospital; Department of Optometry, Asia University

    Greed of Elsevier Drives 40 Scientific Editors of NeuroImage to Quit En Mass—Launch a Competitive Journal

    Greed of Elsevier Drives 40 Scientific Editors of NeuroImage to Quit En Mass—Launch a Competitive Journal
    The corporate greed at a major scientific journal has become too great to bear anymore for a collection of 40 leading scientists serving on an editorial board.…
    www.trialsitenews.com


    The corporate greed at a major scientific journal has become too great to bear anymore for a collection of 40 leading scientists serving on an editorial board. The group, including tenured professors from Oxford University, King’s College London and Cardiff University resigned collectively from the editorial board of the journal Neuroimage protest wanton greed at the publishing giant of Elsevier in what academics around the world hope is a rebellion against corporate capture and associated greed. The move was recently announced Tweet / Twitter on Twitter by Professor Chris Chambers, head of brain stimulation at Cardiff University, and one of the resigning team members, and in a piece for The Guardian authored by Anna Fazackerley. These intensified chatter across the scientific academic community lamenting of profit margins in academic publishing that are purportedly richer than big tech such as Apple, Google and Amazon. Recently covered as well by Katharine Sanderson writing for the journal Nature, a movement builds against open access charges. The collective issued a statement on April 17, declaring their new direction.


    The context

    Professor Chris Chambers, head of brain stimulation at Cardiff University, and one of the resigning academics on the editorial board tweeted the unfolding drama, declaring at one point, “Elsevier preys on the academic community, claiming huge profits while adding little value to science.”


    A Mega-Corp controlling much of the journal business

    A Dutch-based publishing giant, Elsevier specializes in scientific, technical and medical content. Some of the top medical and scientific journals are owned by this multinational corporation, from The Lancet and Cell to ScienceDirect and a collection of electronic journals from Trends and the Current Opinion to online citation databases such as Scopus, the SciVal tool for measuring research performance, the ClinicalKey search engine and the CriticalPath evidence-based cancer care service. As described on the company’s Wikipedia page, they offer a range of products and services covering digital tools for data management, instruction, research analytics and assessment.


    Publicly traded, by 2021, Elsevier reported over 600,000 articles annually across over 2,700 journals containing over 17 million documents and 40,000 e-books. Over a billion downloads occur with their content per year.


    Called RELX, the company is traded on the New York Stock Exchange with a $58.53 market capitalization on $8.55 billion in annual turnover, and $1.63 billion in net income.


    These healthy numbers anger growing numbers of academic authors given that a lot of the research Elsevier publishes is in fact publicly funded. With mounting costs, critics charge “rent-seeking,” calling for boycotts and alternative publications to disseminate scientific information such as preprint servers and shadow libraries. Aggressive copyright practices also had fuel to the rebellious academic-driven fire.


    Greed drives serious collective resignation, move to launch a competitor

    Anna Fazackerley reports in The Guardian that while Neuroimage, a leading journal focused on brain-imaging research has gone “open access,” meaning the content is not solely accessible via a subscription-based paywall, authors must now pay over £2,700 ($,3,414) to get their paper published. What’s behind the steep price? As The Guardian notes, it is the journal’s “prestige.” Former editors are outraged, declaring the move “unethical.” They point out the cost increase has nothing to do with the underlying cost structure to produce the content.


    Now, academics are increasingly turning to submitting papers to a nonprofit open-access journal which a team is setting up instead.


    Professor Chambers told The Guardian that “all Elsevier cares about is money and this will cost them a lot of money. They just got too greedy. The academic community can withdraw our consent to be exploited at any time. That time is now.”


    Importantly, while costs are often borne on the academic, often through various grants typically either the public sector through universities or via private grants or at times industry grants, the author(s) can spend inordinate amounts of their own time to produce scientific pieces.


    Elsevier capitalizes on this model, continuously raising the fees they charge authors to access their journals, meaning the company is maximizing their profits.


    Movement for alternatives

    An Oxford University biomedical engineering professor told The Guardian for the recent piece while many authors have felt “powerless” given the leverage and size of Elsevier, Stephen Smith however declared, “Enough is enough. By taking the entire set of editors across to start the new journal, we are taking the reputation with us.”


    As reported by Nature, the new journal launched by the breakaway editors at Neuroimage will be hosted by MIT Press.


    Call to Action: See the breakaway editors' announcement.


    The breakaway editors include: Stephen Smith (Oxford, UK), Til Ole Bergmann (Johannes Gutenberg, Mainz, Germany), Birte Forstmann (Amsterdam, Netherlands), Alain Dagher (McGill, Montreal, Canada), Shella Keilholz (Emory / Georgia Tech, USA), Kristen Kennedy (UT Dallas, USA), Sonja Kotz (Maastricht, Netherlands), Cindy Lustig (University of Michigan, USA), Bruce Pike (University of Calgary, Canada), Marc Tittgemeyer (Cologne, Germany), Mark Woolrich (Oxford, UK), Thomas Yeo (NUS, Singapore), Andrew Alexander (Madison, Wisconsin, USA), Janine Bijsterbosch (Wash U, St Louis, USA), Tjeerd Boonstra (Maastricht, Netherlands), Mallar Chakravarty (Quebec, Canada), Chris Chambers (Cardiff, UK), Catie Chang (Vanderbilt, USA), Bradley Christian (Madison, Wisconsin, USA), Sarang Dalal (Aarhus, Denmark), Nai Ding (Zhejiang, Hangzhou, China), Audrey Duarte (UT Austin, USA), Audrey Fan (UC Davis, USA), Alexandre Gramfort (Paris-Saclay, France), Gesa Hartwigsen (University of Leipzig and MPI-CBS Leipzig, Germany), Mbemba Jabbi (UT Austin, USA), Ulrike Krämer (Lübeck, Germany), Martin Lindquist (Johns Hopkins, USA), Jean-Francois Mangin (NeuroSpin, France), Kevin Murphy (Cardiff, UK), Jonathan Polimeni (Harvard, USA), Emma Robinson (KCL, UK), Monica Rosenberg (University of Chicago, USA), Sepideh Sadaghiani (UIUC, Illinois, USA), Mohamed Seghier (Khalifa University, UAE), Yen-Yu Ian Shih (UNC Chapel Hill, USA), Axel Thielscher (TU Denmark, Denmark), Lucina Uddin (UCLA, USA), Dimitri Van De Ville (EPFL and UNIGE, Switzerland), Wim Vanduffel (KU Leuven, Belgium), Chao-Gan Yan (CAS, Beijing, China), Anastasia Yendiki (Harvard, USA).

    SARS-CoV-2 Spike Protein Accumulation in the Skull-Meninges-Brain Axis: Potential Implications for Long-Term Neurological Complications in post-COVID-19


    SARS-CoV-2 Spike Protein Accumulation in the Skull-Meninges-Brain Axis: Potential Implications for Long-Term Neurological Complications in post-COVID-19
    Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), has been associated mainly with a range…
    www.biorxiv.org


    Brand New Study: Spike Protein Accumulates in Brain and Skull and Causes Damage
    Brand New Study: Spike Protein Accumulates in Brain and Skull and Causes DamageIf you like this content and want more, I am doing a special lifetime membersh...
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    I wonder if there's anyone left still waiting for evidence to say if the bat soup hypothesis-fantasy was ever true.

    Some times it takes time


    Lab leak is the biggest suspect in 1977 flu pandemic. But it took 3 decades to gain currency

    The 1977 pandemic — called the 'Russian Flu' — was caused by the Human influenza H1N1 virus. It came to be known as such because it was first reported by the erstwhile Soviet Union.

    Lab leak is the biggest suspect in 1977 flu pandemic. But it took 3 decades to gain currency
    The 1977 pandemic — called the 'Russian Flu' — was caused by the Human influenza H1N1 virus. It came to be known as such because it was first reported by the…
    theprint.in