La Generalitat estudia compensar con entre 90 y 200 euros mensuales a sus funcionarios que renuncien al teletrabajo. La medida forma parte de las negociaciones con los sindicatos para implantar la jornada laboral de 35 horas semanales, que ya fue acordada para los trabajadores del Estado sin afectar la prestación de los servicios públicos, y refuerza la apuesta del Govern por la presencialidad de los empleados públicos: el consejero de Presidencia, Albert Dalmau, ya impulsó en enero de 2025 la supresión del trabajo a distancia para los altos cargos en una medida que generó malestar entre los trabajadores y que acabó ante la justicia. De los cerca de 280.000 empleados del sector público, actualmente unos 14.900 tienen permiso para trabajar a distancia.
El presidente de la Generalitat, Salvador Illa, junto a los consellers de Presidencia, Albert Dalmau, y de Interior, Núria Parlon, durante la reunión semanal del gobierno catalán.
Peter Atwater, a professor of economics at William & Mary in Williamsburg, Virginia, began popularizing the idea of a “K‑shaped economy” shortly after the pandemic began. Analysts were debating on social media what the recovery would look like after the self‑induced coma into which GDP had been plunged, and they floated the usual options: an L (a plunge followed by stagnation), a V (a rebound as sharp as the drop), a W (a renewed recession after a brief uptick)… Though he wasn’t the first to suggest the K. An unknown user — now rebranded as Ivan The K — argued on X (still called Twitter at the time) that the final letter would be a K: meaning some things would recover and others wouldn’t. For Atwater, 65, that message was a revelation that went much further: the more privileged social groups would emerge from the pandemic strengthened in several aspects of their lives, while those at the bottom would be worse off relative to 2019.
A team at the University of Cambridge say this is the first time that a vaccine whose active component was 'designed entirely by computer simulations has been tested in humans.'
A team at the University of Cambridge say this is the first time that a vaccine whose active component was 'designed entirely by computer simulations has been tested in humans.'
The Famous Italian Biochemist’s Latest Study on the Pfizer mRNA Vaccine
«ALC-0315, the ionizable cationic lipid enabling the Pfizer vaccine Comirnaty’s LNP platform, is presented in regulatory files as if its metabolic fate were straightforward and well controlled. Our analysis instead identifies a basic, consequential discrepancy that should never survive dossier assembly—let alone review: the hydrolysis product dictated by the ALC-0315 chemicalstructure is 2-hexyldecanoic acid(α-branched), yet key submissions by Pfizer repeatedly invoke the presence of distinct 6-hexyldecanoicisomer (not commercially available, not recognized as an analytical standard in established analytical protocols). This is a material misidentification with direct safety and compliance consequences».
In these few initial lines of his latest disruptive and groundbreaking study, we understand that on this occasion the Italian biochemist Gabriele Segalla has truly outdone himself by revealing a Sherlock Holmes-like instinct in discovering yet another sensational manipulation within the Covid-19 mRNA Comirnaty so-called “vaccine” produced by the New York-based pharmaceutical company Pfizer, perhaps the most used in the world and certainly in the European Union.
A danger that Big Pharma Pfizer and Moderna themselves were then forced to include in the package leaflet by the EMA (European Medicines Agency).
Damage and Health Safety Violations from the Ghost Molecule
Given the highly technical nature of the research published in the American specialist journal International Journal of Vaccine, Theory, Practice, and Research on May 18 (title ALC-0315 Toxic Metabolites: Pharmacokinetic and Regulatory Criticalities in a COVID‑19 “mRNA Vaccine”), we asked out friend PhD Segalla to provide a brief simplified explanation.
«At the heart of the study is a major chemical discrepancy. To track how the vaccine’s protective fat shell (the ALC-0315 lipid) breaks down in pre-clinical tests, official files relied on a “ghost” molecule called 6-hexyldecanoic acid—a substance that does not even exist in international chemical databases. In reality, the vaccine breaks down into a completely different molecule, 2-hexyldecanoic acid, which is globally classified as highly toxic and persistent. The study defines this switch as a “technical falsification” that hid the fact that these toxic ingredients remain trapped inside human cells instead of being safely eliminated».
Indeed, the Italian biochemist so detailed the same issue in his Absttract
«The authentic metabolite, 2-hexyldecanoic acid, concealed by Pfizer and disguised as 6-hexyldecanoic acid, carries an H410 classification (very toxic to aquatic life with long-lasting effects), while the “phantom”6-hexyl isomer is lacking any hazardous classification and presented as theoretically more degradable. In a CMA (Conditional Marketing Authorization) supporting pivotal preclinical study, substituting 2-hexyl with an unclassified 6-hexyl isomer materially compromises the clearance account, traceability, and any defensible claim of GLP (Good Laboratory Pratice) grade validation for Pfizer’s vaccine».
The cover of Abstract of the research (link in the sources)
Dr. Segalla’s research demonstrates that this hidden molecule triggers a domino effect of severe biological damage:
Energy Blackout: It shuts down the cell’s power plants (mitochondria), draining the energy needed to repair our DNA.
Cell Defense Breach: Another byproduct acts like a harsh chemical detergent, stripping away the protective shield around the cell’s nucleus and risking genomic instability.
Protein Factory Sabotage: It causes the cell’s internal factories (ribosomes) to glitch. This “factory error” forces the body to produce deformed, unnatural proteins, which can cause the immune system to misfire and attack its own tissues, potentially leading to heart inflammation like myocarditis and pericarditis.
The expert researcher, in an exclusive interview with the editor of Gospa News (currently only in Italian), highlighted the multiple public health violations resulting from his discovery making the request to withdraw the authorization for the Comirnaty mRNA vaccine inevitable.
The Interview with PhD Segalla by Gospa News
We are sorry bot at the monent the Interview in the Video below is in Italian only but we are working to translate it to add subtitles in English
A Discrepancy, Undetected by Drug Regulators, That Would Have Blocked the Authorization of Pfizer’s Gene Serum
This discrepancy is not a technical detail; it directly affects analytical validation, standard traceability, toxicological assessment, metabolic clearance, and the entire regulatory framework.
That is, as Segalla explains in the video interview, if the reporting of the metabolite produced by ALC-0315 in the human body had been correct, the Comirnaty “vaccine” would never have received approval from the competent bodies responsible for overseeing the drug authorization process (FDA, EMA, AIFA, Ministry of Health, etc.).
Not only that. The Italian biochemist is surprised that the EMA failed to detect this enormous discrepancy, but in a previous study, Segalla himself had demonstrated that the EMA could not have been unaware of the toxicity of these nanoparticles, which are highly inflammatory to the muscular system (another recent study has reiterated this) and also potentially carcinogenic.
More Dangers from Trialkanolamine, a Destabilizer of the “Cellular DNA Safe”
«The second breakdown product (a trialkanolamine, pKa ≈ 9.6) is liable to lysosomal sequestration, there by impeding clearance; however, the Pfizer dossier offers only limited substantiation of its disposition. Critically, the pharmacokinetic dataset does not adequately account for dose biodistribution and is predicated on insufficiently documented—or omitted—testing standards. Given the scale of exposure (billionsof subjects) and the potential oncological and cardiological consequences placed on these Pharmacokinetic criticalities, these omissions are not merely unfortunate; they are utterly unacceptable».
As we can read in the Segalla’s new study Abstract, the second critical front concerns trialkanolamine, another degradation product of ALC-0315, described as a cationic molecule capable of remaining trapped in lysosomes, altering cellular autophagy, promoting phospholipidosis, oxidative stress, mitochondrial dysfunction and destabilization of cellular and nuclear membranes.
The Italian biochemist Gabriele Segalla
In the interview, Segalla clarifies that this substance acts as “a degreaser capable of damaging the cellular DNA vault,” causing unpredictable genomic damage, which has also been confirmed by a recent, disconcerting American study, and potentially leading to turbo-cancer consequences.
A Call to Action and Immediate Recall for “Serious Safety Failure to Perform ”
The study argues that regulatory agencies, including the EMA, failed to spot these discrepancies, invalidating the vaccine’s conditional approval.
“This is not just a minor technicality,” states Dr. Segalla. “The lack of traceability masked a critical bioaccumulation risk, exposing the public to unmonitored chronic effects.” Invoking the precautionary principle and Article 10 of the Nuremberg Code, the study demands an immediate revocation of the vaccine’s marketing authorization and calls for an urgent international review of mRNA nanotechnology safety.
«Accordingly, we call for an independent, methodologically transparent and fully auditable re-assessment of ALC 0315 metabolism and clearance, and for all regulatory decisions concerning the Comirnaty medicinal product be reconsidered in view of what appears to amount to a grave and consequential omission in verification procedures» sentenced the Abstract of the study too.
The study links these critical issues to potential long-term biological consequences, including interference with genomic stability, the inflammatory response, cardiaological mechanisms, and protein translation processes, such as ribosomal stalling and frameshifting.
Regarding these issues, Gospa News has published countless disturbing studies on the potential harms of mRNA vaccines, from February 2021 until a week ago. This is precisely why our online news outlet has been banned or blocked from all social media (even Telegram, where we have been repeatedly suspended).
Fabio Giuseppe Carlo Carisio – Founder and Director of Gospa News
One killed as hundreds protest in Kenya against US Ebola quarantine centre
At least one person has been killed after Kenyan police opened fire as hundreds of demonstrators protested a quarantine centre for US citizens exposed to Ebola, which the United States government is racing to build in the central town of Nanyuki.
On Tuesday, the NGO Vocal Africa posted on X that one person had died after being shot in the head by Kenyan police who earlier used water cannon, tear gas to disperse the crowds.
The proposed 50-bed unit at an air force base in Nanyuki has angered many Kenyans, who accuse the US of offloading the health risk of caring for those exposed to the Ebola outbreak in the eastern Democratic Republic of the Congo (DRC) and Uganda.
Last week, hundreds took to the streets in Nanyuki amid growing frustration among residents as Kenyan and US authorities publicly reaffirmed their commitment to the plan despite court orders. At the time, the demonstration also turned violent, with at least two people killed and one wounded.
UPDATE ON JUNE, 1, 2026
Fury erupts in Kenya over joint US Ebola quarantine plan – VIDEO
Hundreds of Nanyuki town residents took to the streets to oppose the construction of an infectious disease isolation facility in Laikipia County.
Protesters say resources earmarked for the facility should be directed to regional development, fearing it could still expose communities to Ebola.
The army even sent a tank to quell the protest by intimidating the crowd.
The Fear of an International Plot
The Ebola virus of the international epidemic emergency in Africa, where in Congo and Uganda it has already killed dozens of people, is at the center of many suspicions for two reasons:
The dangerous tests on this pathogen conducted by the US Pentagon in the infamous biolaboratories in Ukraine
Research on a vaccine for the specific strain of the current alarm began 4 months ago by Moderna with the contribution of Ngo Gavi by Bill Gates
Further details in the updates below
UPDATED ON MAY, 29, 2026
MSF doctor exposed to the virus at Spallanzani Hospital in Rome
The Doctors Without Borders (MSF aka Médecins Sans Frontières) doctor who was exposed to patients who tested positive for Ebola in the Democratic Republic of Congo arrived overnight at the Lazzaro Spallanzani National Institute for Infectious Diseases in Rome. The woman is well and asymptomatic. She will remain under observation at the Roman hospital until June 8th, MSF sources confirmed.
As part of her clinical practice, the surgeon came into contact with patients who later tested positive on May 16th. This is therefore a case of direct contact. The doctor also performed emergency lifesaving surgery on May 18th on a child who was the victim of a grenade explosion. The child is a suspected case of Ebola, and a test for Ebola is not yet available.
Ebola: Three Red Cross workers die as more than 1000 cases and 200 deaths reported
«Three Red Cross volunteers have died in the Democratic Republic of the Congo (DRC) as the Ebola outbreak continues to spread rapidly and cases (suspected and confirmed) surpass 1000» according to BMJ (British Medical Journal).
The volunteers-Ajiko Chandiru Viviane, Sezabo Katanabo, and Alikana Udumusi Augustin-were all helping the Red Cross manage the dead bodies of Ebola victims. Their deaths occurred over 12 days, on 5, 15, and 16 May, respectively.
The World Health Organization’s director general, Tedros Adhanom Ghebreyesus, expressed his “deepest condolences” over the fatalities. “They paid the ultimate price on the line of duty,” he wrote.
Meanwhile British researchers announced they are producing an experimental jab for the Ebola strain behind the outbreak, which currently has no approved vaccines or therapeutics (read details below).
According to the latest updates (24 and 25 May), there are currently 101 confirmed Ebola cases in the DRC and 930 suspected cases.
There have so far been 223 deaths among people with suspected cases and 10 confirmed deaths. In Uganda, seven cases and one death have been confirmed. The outbreak-currently the third largest Ebola outbreak on record (based on confirmed and
UPDATED ON MAY, 19, 2026
Panic in the United States for Ebola after dangerous Tests in Pentagon-funded Ukraine Biolabs
Is there a reason Americans are so worried about the new Ebola epidemic in Africa?
Is it perhaps because the US Pentagon itself has been secretly researching this virus, conducting the usual experiments to enhance it as a bioweapon in top-secret laboratories in Ukraine?
In this article, we try to provide answers and confirmation to these questions…
US suspends entry of foreign citizens from Ebola-affected areas
The United States has suspended entry to non-US citizens who have been in Ebola-affected areas in the past 21 days: Uganda, the Democratic Republic of the Congo, and South Sudan.
The measure, issued by the Centers for Disease Control and Prevention (CDC), will be in effect for the next 30 days and is justified by the need to “protect the health of the United States from the serious risk posed by the introduction of Ebola virus disease into the United States by these foreign nationals.”
At the moment it is one of the few countries to have taken this drastic health measure.
Just hours earlier, the United States announced that it had strengthened precautionary measures to prevent the spread of Ebola hemorrhagic fever, implementing health screenings for air travelers from affected areas and temporarily suspending visa services.
WHO will convene an emergency committee due to the rapid spread of the Ebola Bundibugio strain – VIDEO
WHO will convene an emergency committee due to the rapid spread of the Ebola Bundibugio strain.
“At the moment, 30 cases of the disease have been confirmed in the northern province of Ituri. Uganda has also reported two confirmed cases in the capital Kampala, including one death among two people who arrived from the Democratic Republic of the Congo,” said Tedros Adhanom Ghebreyesus, head of the organization, during a briefing.
Breaking – WHO declares emergency as strain kills 100 in DRC and Uganda
A new outbreak of Ebola virus disease in central Africa, caused by the rare Bundibugyo version of the virus, has caused more than 300 suspected cases and killed 100 people, health officials have said.
The World Health Organization (WHO) has declared the situation a public health emergency of international concern.
The Africa Centres for Disease Control and Prevention (Africa CDC) has so far identified 336 suspected and 10 confirmed cases in the Democratic Republic of the Congo (DRC). There have been 87 deaths in the DRC to date. Uganda has had two confirmed cases and one additional death.
In response WHO has sent five tonnes of medical supplies to the DRC, and $500 000 (£374 000; €430 000) has been released from the agency’s contingency fund for emergencies.
This Ebola outbreak is causing particular concern because it has been caused by the Bundibugyo strain, which has been detected in only two previous outbreaks, in 2007 and 2012. There are no approved treatments or vaccines for Bundibugyo Ebola.
Pentagon Tests in Africa on Dangerous Virus before the last WHO Emergency
We republish below an excellent, albeit brief, investigative article by renowned American epidemiologist Nicolas Hulsher on the extraordinary coincidence of vaccine research funding granted to Big Pharma Moderna of Cambridge, Massachusetts, just months before the Ebola emergency in the DRC.
It is therefore true, as Hulsher expertly states, that the Ebola virus has little chance of becoming a pandemic, but it is equally true that this refers to the wild viral strain and not those with laboratory-enhanced genotypes(such as SARS-CoV-2, according to a CIA whistleblower) as recombinant synthetic pathogens, i.e., those obtained by inserting multiple pathogens, such as HIV-AIDS, into the Covid-19 virus.
Bill Gates-backed CEPI awarded Moderna and Oxford $26.7 million to develop multivalent Ebola mRNA in January 2026
by Nicolas Hulscher, MPH – originally published on his substack Focal Points
All links to previous Gospa News investigations or video have been added in the aftermath
Just a few months ago (January 2026), Bill Gates’ vaccine cartel CEPI gave Moderna and University of Oxford $26.7 million to begin developing Bundibugyo ebolavirus (BDBV) mRNA and viral vector injections. These are multivalent filovirus “vaccine” platforms, meaning they are designed to target multiple Ebola viruses and related filoviruses simultaneously — including Bundibugyo ebolavirus (BDBV).
WHO declared a Public Health Emergency of International Concern (PHEIC) over a Bundibugyo Ebola outbreak
Develop “vaccine” → Fearmonger new outbreak → Declare emergency → Gain power & control → push “vaccine” as only solution.
This marks the 17th Ebola outbreak recorded in the Democratic Republic of Congo since the virus was first identified there in 1976 — and the third known outbreak of the Bundibugyo strain since it was first identified in 2007. Across Africa, there have been dozens of Ebola outbreaks over the last 50 years.
No biological basis for this to become a worldwide pandemic.
Why? Because Ebola — including the Bundibugyo strain — spreads through direct contact with bodily fluids from symptomatic individuals, not through the air or casual contact.
There is simply no biological basis for this to become a worldwide pandemic.
So why the rapid escalation to a full Public Health Emergency of International Concern at this moment?
The WHO says because, as of May 16, there are 8 laboratory-confirmed cases, 246 suspected cases, and 80 suspected deaths in Ituri Province, with the outbreak spreading to Uganda. They cite the lack of any approved vaccines or treatments for this specific strain, high population mobility, and risk of further cross-border spread as major concerns.
However, perhaps they actually declared an emergency because the WHO’s pandemic treaty negotiations recently hit a major roadblock over the Pathogen Access and Benefit-Sharing (PABS) annex, preventing the treaty from being put into effect.
It also appears that the botched hantavirus situation didn’t yield the level of perceived fear they were hoping for.
There is simply no biological basis for this to become a worldwide pandemic.
Bill Gates is now the WHO’s top funder so nothing does should be accepted at face value.
CLICK TO READ MORE INTRIGUES AMONG GATES, WHO AND PENTAGON
Whatever the WHO and mass media throw at us, America should NOT rejoin the WHO under any circumstances. We must not give in to their extortion tactics designed to pressure America into rejoining and becoming trapped under sweeping powers of surveillance, vaccine passports, and mandates.
The full live results can be viewed here: family and medical practice. The Notes column is available as well. Only the emails were removed for privacy reasons. The records count at the time of this article were 2908 and 107.
I had Claude Opus 4.7 co-work evaluate the survey solicitations, the survey questions, the survey results, the notes column, my reader base and gave it unrestricted use of publicly available data (CDC, Insurance industry, FRED data, etc) to reconcile everything. This allowed Claude to give me a more objective answer because my reader base is not representative (e.g., half of the respondents had no vaccinated family members) and because my reader base are more likely to attribute disability and deaths to the vaccine.
As many as 1.5M working-age Americans disabled for 6 months or more
Silence from health authorities worldwide on this issue. Not a single national public-health authority, anywhere in the world, has produced an estimate of the type constructed in this article — a comprehensive, all-cause, all-ages, attributable-deaths-plus-disabilities total for the COVID-19 vaccines.
A summary of the full conversation is available as markdown or PDF.
Claude took many sources into account.
At first Claude gave low weight to my readers, but I pointed out that there were too many readers who noted no unexpected deaths in family members until post-vaccine and then there were too many readers with too many unexpected deaths among their vaccinated family members which reduces the attribution subjectivity. For example, if “no deaths in my family over the last 10 years, but after the shots rolled out we had 4 deaths and all were vaccinated,”then if you see too many of those stories, attribution of the deaths to the vaccine becomes more likely.
Note that some estimates are working age, others are full population so a hard cap on working age is not a had cap on full population.
Claude estimated the shots killed anywhere from 1 (up to nearly 5) in 1,000 people vaccinated. That is nowhere close to a “safe” vaccine (it’s at least 3 orders of magnitude off).
So it’s more likely than not that the deaths and disabilities were “real” and not “rare.”
Data sources used by Claude in the analysis
Data sources considered
Primary survey data (Kirsch substack)
The family injury survey (injury.csv, 2,864 responses, 1,502 with vacc>0, 5,612 vaccinated relatives reported) gave a within-audience attribution rate of 5.6% killed, 10.4% disabled, 25% needing medical care. The medical-practice survey (medical.csv, 100 responses, 35 with usable vaccinated-patient counts, after dropping one protest entry) gave 0.83% killed and 3.1% disabled. The single concierge-physician data point (5% disabled at 6 months in 360 patients, 70% vaccinated) sat between the two surveys and at the 75th percentile of per-practice rates in medical.csv. Internal consistency: 500-record segments of injury.csv showed stable ratios (8.8–11.5% disabled, 4.6–6.5% killed), confirming the audience was reporting consistently across response order.
The 47.3% of injury.csv respondents who reported zero vaccinated relatives — versus a general-population expectation of well under 1% — implied an audience concentration multiplier of roughly 100–300× compared to a random US sample. This was the pivotal calibration that pushed my estimate upward from the initial ~150K deaths to the revised ~350K, because it meant the family-survey reporting rates do not require millions of true deaths to explain — they require heavy but plausible selection in your readership.
LNU00074597 (Population with a Disability, 16+, NSA) showed the total disabled population rising from 30.96M in June 2019 to 36.62M in April 2026, with ~2.8M of that increase above the pre-pandemic 2014–2019 trend. LNU01074597 (Civilian Labor Force with a Disability, 16+) showed the in-labor-force disabled population rising from 6.46M to 8.58M over the same period, with ~880K above trend. LNU01076955 (men 16–64 in LF with a disability) showed the working-age male component alone gaining ~790K above trend. These together gave a hard ceiling on total excess disability from all causes combined.
CIDRAP and CDC household-survey data on long COVID (~30M US working-age adults having experienced it; ~26% with significant activity limitation) established that the bulk of the FRED excess disability is plausibly long-COVID-attributable, leaving a residual of several hundred thousand for vaccine attribution after subtracting long-COVID, post-acute COVID sequelae, the pandemic mental-health surge, and a small aging residual.
US excess mortality (CDC, SOA)
Total US excess deaths 2020–2023 of ~1.5–1.7M, of which most is COVID-19 itself, ~5–8% drug overdoses, ~5% delayed care. Working-age (25–64) excess deaths totaled ~400–500K. The Society of Actuaries Group Life COVID-19 Mortality Survey (2.3M claims, $103B premium) showed the 2021 working-age mortality peak inversely correlated with county vaccination rate — a constraint that pushes against the high end of the death range.
ACLI total death benefit payouts: $78B (2019) → $90.4B (2020, +15.4%, largest single-year rise since 1918) → $100B (2021) → $92B (2022). Cumulative excess over the 2019 baseline of ~$45B across 2020–2022. OneAmerica’s Scott Davison statement of 40% Q3–Q4 2021 working-age claims increase is real and consistent with this, though timed with the Delta wave.
Disability claim systems
SSDI applications declined every year from 2015 through 2023, with total beneficiaries falling ~2.4M from the 2014 peak. Council for Disability Awareness and LIMRA private long-term disability data showed elevated pandemic-era health absences but no step-change tied to vaccine rollout. This argued against the highest end of vaccine-disabled estimates: if 5M+ working-age Americans were newly disabled, SSDI and private LTD would have shown a surge that they didn’t.
Prime-age (25–54) LFPR: 82.5% (2019) → 79.8% (April 2020 trough) → 83.4% (May 2025) → 83.8% (April 2026), currently higher than pre-pandemic. This was the binding constraint that rejected the family-survey extrapolation (15.6M working-age disabled would require LFPR to be ~12 percentage points lower than observed) and forced the medical-survey extrapolation down to a defensible residual.
Methodology in one paragraph
The final numbers come from triangulating five anchors: (1) your survey data, with the audience concentration measured from the unvax-only fraction; (2) the FRED disability ceiling decomposed by likely cause; (3) US excess mortality with COVID, overdose, and delayed-care subtractions; (4) life insurance and SOA actuarial data as cross-checks on the death range; (5) SSDI and BLS labor-force data as cross-checks on the disability range. The final estimate sits where these five constraints overlap. The deaths range is wider because excess mortality decomposition isn’t clean. The disability range is narrower because the FRED excess gives a hard upper bound and the long-COVID literature gives a defensible decomposition.
For comparison
The final estimate is ~25× lower than your family-survey extrapolation and ~3–4× lower than your medical-survey extrapolation, but ~10× higher than the 37K face-value VAERS death count and ~50× higher than the official VAERS-acknowledged disability count. It is a “several hundred thousand killed, ~1 million disabled” finding, which is both serious public-health territory and reconcilable with every independent dataset above.
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Concerns about American biological laboratories in Ukraine and other post-Soviet republics can no longer be considered exclusively ‘Russian disinformation.’ In Part 1 of this investigative series, I examined the growing fears surrounding emerging pandemics, high-containment biological laboratories, and the renewed public scrutiny of gain-of-function research in the aftermath of COVID-19. From the outbreak of Hantavirus […]
Growing concern over emerging infectious threats has once again intensified the international debate on biosecurity. Under the guise of medical and biological cooperation programs with Latin American countries, Washington continues to increase both the scale and intensity of work with dangerous pathogens, raising concerns about the potential development of biological weapons. As fresh fears over […]
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