Why Lebanon doesn’t trust Israeli-American intentions — and why it shouldn’t
By Hussein Mousavi | Press TV | November 1, 2025
As Lebanon’s government, led by Prime Minister Nawaf Salam, inches closer to implementing its multi-phase plan to disarm Hezbollah, one question continues to divide the country:
What if Hezbollah lays down its arms… and the Israeli regime still doesn’t change its behavior?
The plan – drafted under the supervision of the Lebanese Armed Forces (LAF) and backed by the US, France, and several Arab states, including Saudi Arabia, Qatar, and the UAE – seeks to reassert the state’s monopoly on the use of force.
On paper, it sounds like a long-delayed step toward full “sovereignty.” That’s how the Lebanese premier and his allies – both inside and outside the country – try to present the issue.
Yet for many ordinary Lebanese, the proposal feels less like progress and more like exposure. And so, it raises a deeper fear.
Disarming the Hezbollah resistance movement, they fear, could strip Lebanon of its last line of deterrence, without changing anything about Israeli long-standing hostility.
Syrian precedent: Disarmament without security
Elsewhere in the region, Syria’s experience stands as a grim reminder. Even after the Jolani regime made public gestures toward normalization with the Israeli regime, the airstrikes on Syrian territory have never stopped. They continued unabated.
These attacks – justified by Israel as “preemptive” measures against so-called Iranian entrenchment (despite any evidence suggesting the same) have convinced many in Lebanon that military restraint does not necessarily guarantee security.
To many Lebanese, that says it all: even a weakened and cooperative neighbor hasn’t been spared unprovoked Israeli assault.
So, for the majority of Lebanese, the question resonates: If a disarmed, diplomatically compliant Syria was still bombed, why would a disarmed Lebanon be treated any differently?
That logic has sunk deep… even among communities once skeptical of the resistance. This isn’t about ideology anymore. It’s about survival, sovereignty and dignity.
People genuinely fear that weakness, not resistance, invites aggression.
Social undercurrents: A shift in perception
Hezbollah’s argument for keeping its weapons has always been rooted in resistance to Israeli military occupation and the defense of Lebanese sovereignty and territorial integrity.
For years, that claim was losing traction—chipped away by the US, Israeli regime (Hasbara), and Persian Gulf-funded campaigns that painted the resistance movement as a destabilizing force.
But the chaos next door changed the mood.
The violence in Syria, especially the relentless massacres committed by Al-Qaeda-linked groups in Suweida, jolted many Lebanese back to a hard truth: in a region defined by uncertainty and terrorism, some form of deterrence is still necessary.
Even among Christians and Druze, there’s a quiet shift. What was once a divisive argument is slowly becoming a reluctant consensus:
“Lebanon without a deterrent is Lebanon exposed. And now, no one in Beirut really believes the skies will stay quiet after disarmament. Not anymore.”
Washington’s back-out: The missing guarantees
Lebanese skepticism was further reinforced by Washington itself. If anyone still hoped for international reassurance, Washington’s recent message was clear.
During his visit to Beirut, US envoy Tom Barrack openly admitted that Washington could not provide any binding guarantees that the Israeli occupation forces would refrain from future military action, even if Hezbollah were to be fully disarmed.
It was a rare moment of honesty, and a devastating one. For many Lebanese, it confirmed what Hezbollah has been saying for years: Without credible security guarantees, disarmament amounts to a strategic suicide.
Barrack’s inflammatory statement spread quickly across social media platforms and prime-time talk shows. It fueled the perception that Western powers are happy to demand disarmament but will not lift a finger to protect Lebanon afterward.
So, for now, Hezbollah’s deterrent remains the only shield people trust in a region where promises evaporate, and treaties rarely hold.
A state caught between principle and survival
That leaves the Lebanese government trapped in a painful paradox and facing an impossible balance.
Internationally, disarmament is pitched as a prerequisite for reconstruction after the 2024 Israeli aggression. Domestically, it looks more like a setup, an attempt to squeeze out concessions that Washington and Tel Aviv couldn’t win through war.
PM Salam insists the Lebanese Army can fill the security gap once Hezbollah disarms. But everyone knows the LAF is overstretched, underfunded, and struggling to retain personnel amid an economic meltdown.
Even LAF Commander “Rodolph Haykal” has quietly admitted the limits.
And with UNIFIL’s mandate due to expire in 2026, the southern buffer zone that once helped keep the peace is fading fast.
Given these realities, Hezbollah’s arsenal (long portrayed by Israeli, American, and certain Arab media as “the problem”) is tied to something deeper: the complete absence of trust in Israel’s intentions, and the lack of any reliable security guarantees from its allies.
Trust, deterrence, and the price of “peace”
Trust can’t be declared in a press release. It’s earned through behavior, consistency, and respect. For Lebanon, disarmament cannot be separated from reciprocity.
Unless the Israeli regime demonstrates, through verifiable actions, that it will respect Lebanese sovereignty – and unless those commitments are backed by enforceable international guarantees – any talk of disarmament will remain politically impossible and socially toxic.
A peace built on parity
Lebanon’s real dilemma isn’t whether disarmament is good in theory. It’s whether peace can exist without parity, and whether Western powers are willing to enforce that parity with real guarantees, not vague assurances.
Until that happens, every call for disarmament will collide with the realities of regional mistrust… and also with the same hard truth: You can’t convince its citizens to give up their shield when the sky above them still burns.
And that’s why, for many in Lebanon today, neither the government nor the resistance has any reason to trust the Israeli regime.
Hussein Mousavi is a Lebanese journalist and commentator
Burevestnik and Poseidon: Russia’s New Double Deterrent Against First Strike Aggression
Sputnik – 01.11.2025
President Putin has announced the back-to-back successful testing of the Burevestnik nuclear-powered, nuclear-capable unlimited range cruise missile, and the Poseidon nuclear-powered, nuclear-capable unmanned underwater vehicle. Sputnik asked a seasoned US Army vet and military analyst to comment on Russia’s new twin deterrence potential.
“The Burevestnik and the Poseidon are very interesting weapons… pretty much designed as defensive in nature,” retired US Army Lt. Col. Earl Rasmussen told Sputnik, characterizing the pair of nuclear doomsday scenario strategic systems as an effective new “counter strike type of capability.”
Touting the twin systems’ miniaturized nuclear engines as their key standout capability, Rasmussen noted that nuclear power essentially means unlimited range and loitering.
The weapons fundamentally enhance Russia’s nuclear deterrence, according to the observer. “There are some crazy generals out there that think they can win, do a preemptive strike and win a nuclear war, which is insane, essentially,” Rasmussen recalled, alluding to ideas like the Prompt Global Strike (PGS). Burevestnik and Poseidon are designed to nullify them.
With a system like the Poseidon, “you don’t have to strike anything. You could detonate it, probably flood and wipe out the entire British Isles or the entire east coast of the United States. So the impact could be quite devastating,” and far beyond the ‘acceptable loss’ calculations of any PGS-style planners.
“Like I said, I don’t look at Russia using them as a pure offensive-type weapon. I look at them as more of a defensive weapon and as a counterstrike type of capability. But it really, really enhances that capability to counter an adversary’s offensive actions against Russia,” Rasmussen summed up.
Kupyansk and Krasnoarmeysk Encirclements Make Ukraine’s Defeat ‘Too Big to Hide’
By Ekaterina Blinova – Sputnik – 01.11.2025
Volodymyr Zelensky and his Commander-in-Chief Oleksandr Syrsky are infamous for sacrificing Ukrainian lives to prolong fighting, Mikael Valtersson, former officer of the Swedish Armed Forces and Air Defense, tells Sputnik, commenting on the Krasnoarmeysk (Pokrovsk) and Kupyansk encirclements.
“[Their] policy has left up to 20,000 Ukrainian soldiers in a very precarious position. They are left with two bad alternatives, either being eliminated defending hopeless positions or taking heavy losses during a very hard withdrawal. In both cases Ukraine will lose invaluable military units,” Valtersson notes.
There is a little, if any, chance that Zelensky could order a surrender, as “the worst thing that could happen from Kiev’s point of view would be thousands of retreating or surrendering Ukrainian soldiers,” according to the pundit.
Zelensky’s team has put on a brave face, insisting there are no encirclements, while barring foreign journalists from the area.
“Such journalists would only expose Kiev’s lies about the situation and crush Ukrainian credibility,” Valtersson says.
Meanwhile, Ukraine’s defeat is a thing too big to hide, the military expert notes, projecting that Russia’s advance in November and December would lead to Ukraine losing several cities.
“Large cities like the Slavyansk, Kramatorsk, Konstantynivka urban area, Zaporozhye, Dnepropetrovsk and Kharkov might be up for grabs,” the pundit suggests. “The worst is yet to come for Ukraine in 2025. We are now witnessing the final fall of Krasnoarmeysk and Kupyansk.”
The Evolving Lens on SIDS: From Mystery to Focus on CDC’s Schedule
By Jefferey Jaxen | November 1, 2025
In America, infants are dying at a rate of around 1,300 to 4,500 per year depending on the reporting source. Lives ended suddenly, unexplained with the greater medical system appearing to be okay with it as evidenced by their lack of deeper investigation into the ‘syndrome.’
Sudden Infant Death Syndrome (SIDS) has long-haunted parents and pediatricians alike. Defined traditionally as the sudden death of an apparently healthy infant under one year old for unknown reasons – scientific and legal momentum may be moving towards public understanding.
For decades, it was viewed as an enigmatic “diagnosis of exclusion,” often chalked up to environmental factors like prone sleeping, overheating and in extreme cases blaming the parents for abuse.
Yet, as of 2025, this static portrait is fracturing. Emerging research, landmark court rulings, and legislative reforms reveal SIDS not as a singular black box, but a tapestry of metabolic, genetic, and iatrogenic vulnerabilities—chiefly, immature detoxification pathways and post-vaccination inflammatory cascades.
Florida’s House Bill 188, filed for the 2026 legislative session, exemplifies this paradigm shift legislatively. The bill amends state statutes to mandate comprehensive autopsies for Sudden Unexpected Infant Deaths (SUID) and Sudden Death in the Young (SDY), explicitly requiring microscopic toxicology, full immunization records from the past 90 days, and reporting to the CDC’s national SUID/SDY Case Registry.
No longer optional, these protocols aim to unmask hidden contributors, such as vaccine excipients or genetic polymorphisms, that prior “undetermined” classifications obscured.
And the best part, the bill comes with penalties for noncompliance—fines up to $5,000 and potential license revocation—underscore a growing impatience with incomplete probes. By integrating immunization data with federal surveillance, HB 188 positions SIDS investigations as proactive risk-factor hunts, potentially reclassifying dozens of annual cases from “unexplained” to preventably-framed within the context of the largely untested infant CDC vaccine schedule.
This rigor finds stark validation in the 2023 U.S. Court of Federal Claims ruling on Sims v. Secretary of Health and Human Services (No. 15-1526V), a rare vaccine court triumph that dismantled SIDS as a default for post-vaccination fatalities.
An eleven-week-old infant succumbed just eight hours after receiving five routine shots after a well baby visit. Autopsy revealed cerebral edema [brain swelling] and pulmonary congestion.
The Special Master Christian Moran ruled the vaccines triggered a “Table” encephalopathy via cytokine storms breaching the blood-brain barrier, leading to herniation and arrest. Expert witnesses retained by the Sims family skillfully displayed and achieved the “preponderant evidence” standard under the National Vaccine Injury Compensation Program (NVICP) against all odds that the Department of Justice attornies and their expert witnesses fought to deny justice.
HHS Secretary Kennedy said during a 2025 interivew with Tucker Carlson:
“The lawyers in the Department of Justice, the leaders of it were corrupt. They saw their job as protecting the trust fund rather than taking care of people who made this national sacrifice.”
The Sims family vaccine court award of $300,000 has ignited momentum and advocacy. As detailed in Wayne Rohde’s June 2025 Substack analysis, the case—amid fewer than 5% NVICP death-claim successes—challenges the “coincidental” narrative, urging deeper scrutiny of ~100 pending infant petitions. With the appeal deadline passing without action, we may be witnessing a precedent-proof vaccine link in such cases, eroding SIDS’s explanatory monopoly.
Scientifically, the puzzle pieces align with revelations on cytochrome P450 (CYP450) enzymes, the liver’s metabolic gatekeepers. A 2025 paper by Dr. Gary Goldman has highlighted infants’ CYP450 immaturity: at birth, activity hovers at 30-60% adult levels, with preterm babies hit hardest by “poor metabolizer” genetics (15-40% prevalence).
These enzymes process vaccine adjuvants like aluminum (up to 3,350 mcg in year one) and polysorbate 80. A vicious circle appears as inflammation from shots further suppresses the detoxification ability prolonging toxin exposure.
VAERS data clusters 75% of SIDS-like reports within a week post-vaccination, peaking at day two—echoing the Sims timeline. In serotonin-deficient brains (flagged in 70% SIDS autopsies). In a node to Florida’s SB 188, Dr. Goldman’s study warns current toxicology protocols ignore these developmental gaps, fostering misclassifications.
Together, these threads weave a bolder SIDS narrative: less “syndrome,” more sentinel for systemic oversights. HB 188’s mandates, the Sims precedent, and CYP450 insights demand holistic federal and state-level probes—genetic screening, excipient dosing tiers, and inflammation biomarkers. As Rohde posits, transparency could halve misattributions, saving lives while honoring the unexplained’s gravity. In 2025, SIDS evolves from fatalism to fixable, urging science and policy to catch up before another crib goes silent.
Blanket Informed Consent for Biologics Could Be Deadly
What You Need to Know and Need to Do
By Dr. Sherri Tenpenny | November 1, 2025
There’s a linguistic shift happening inside the walls of hospitals, surgical centers, and outpatient clinics — one that most people won’t notice until it’s too late. The word “vaccine” is vanishing from medical consent forms. In its place is a far broader, far murkier term being used: biologics. Let’s clarify some definitions:
- Biologics refers specifically to a class of therapeutic drugs and medical products that are produced from living organisms or their components (e.g., made from proteins, organ cells, tissues, blood, tallow, gelatin, glycerol, etc.). Biologics are specifically regulated medical products that are made from or contain components of living organisms.
- Biogenics is a broader, more general term meaning produced by living organisms or biological processes. It could be anything made by a living organism — plants, animals, bacteria, fungi, etc.
Examples:- Tree resin (produced by plants)
- Coral or seashells (made by marine animals)
- Methane (from decaying organic matter)
- Alcohol (from yeast fermentation)
Therefore, all biological products are biogenic, but not all biogenic materials are biological products. That means many new, modern medicines labeled “cutting-edge” — from mRNA injections to bioengineered cells — fall into the category of medically regulated biogenic products.
The Redefinition of Medicine
At first glance, it may sound harmless. Buried in the word salad of admission paperwork is a seismic change you might be agreeing to without realizing it. As a patient in a hospital, you could be injected, infused, or implanted with a biologic product you never specifically discussed with your treating physician, simply because the consent form used a broad term like “biologics” or “biogenics” and you didn’t fully understand the scope of that word.
It’s not that the hospital is secretly adding products; rather, the way the consent forms are worded gives them legal permission to use FDA-approved biologics or biologic materials when they are deemed medically necessary, without first discussing the pros and cons of the product.
You can view the full list of biologics on the FDA’s website. Vaccines are listed among the “approved biologics.” If you blindly sign a consent to receive a biologic, you’ve opened the door to a sweeping range of interventions that go far beyond what most would knowingly authorize.
Informed Consent: A Myth in Modern Medicine
The purpose of requiring informed consent is to promote the autonomy of the individual in medical decision-making. It is a legal doctrine that supports many of our cherished American ideals about our rights as individuals.
For decades, medical care has been governed by the principle that patients must be fully informed, fully aware, and provide informed consent for every healthcare procedure. It was more than a legal requirement; it has long been an ethical cornerstone. But as PubMed’s 1996 article, Legal and Ethical Myths About Informed Consent reminds us, even the foundation of informed consent came from a murky beginning.
In attempting to ascertain the origins of the phrase “informed consent,” it was first in a 1957 California case; no antecedent cases could be unearthed. The entire informed consent paragraph (in the first informed consent case) was adopted verbatim, and without attribution, from the amicus curiae brief submitted by the American College of Surgeons. It is an ironic twist of history that informed consent was dreamed up by lawyers employed by physicians.
Over time, the standard for truly informed consent has quietly been eroded. In many hospitals and clinics, informed consent forms have become little more than a formality: a few checks in digital checkboxes and a scribbled signature on an iPad. These consent forms are often buried within pages of fine print drafted by attorneys, intentionally dense and difficult to read. Even patients who try to understand the language find it nearly impossible to decipher.
The forms no longer use plain language. Instead of saying “Do you consent to receive the influenza vaccine or a COVID jab?”, the consent form may now ask if you consent to the use of biologic agents. The assumption is that you, the patient, understand that vaccines are biological agents. This raises the question: Is the confusing change in language intentional?
“Medically Necessary Biologics” — The Next Frontier
There is a push to categorize biologics as medically necessary. Once that phrase becomes standard, it reframes these products as non-optional. That’s a linguistic shift that carries enormous implications. If something is medically necessary, then refusing it becomes extremely difficult.
Now imagine being prepped for surgery. You’re told you must sign standard consent for “biologic products as necessary during the procedure.” You sign, thinking it refers to anesthesia, sutures, IV fluids, perhaps antibiotics. Your body then becomes an open field for whatever the institution – or your doctor – regards as necessary: a flu shot, a pneumonia shot, a pertussis shot, a monoclonal antibody infusion, or plasma/blood (perhaps from a COVID-vaccinated donor). You may never know what went into your body unless you ask for the record.
The Problem with Blanket Consent
Let’s look closer at what biologics encompass, according to the FDA and Congressional Research Service documents: Vaccines, monoclonal antibodies, gene therapy, whole blood and plasma, stem cells and T-cells, recombinant proteins, and growth factors.
The side effects of biologics vary depending on the specific product and how it is administered. Because these therapies are derived from living systems and often target the immune system, they can produce a wide range of reactions — from mild and localized to serious or life-threatening.
Most biologic drugs carry a risk of allergic or hypersensitivity reactions, since the body often recognizes the biologic as foreign. Those used to treat autoimmune conditions such as rheumatoid arthritis or psoriasis work by suppressing immune activity, which can increase the risk of infections. When given by injection, biologics often cause redness, swelling, or pain at the injection site; those administered intravenously can trigger infusion reactions, such as flushing, shortness of breath, or a sudden drop in blood pressure.
Common side effects include allergic reactions, injection-site irritation, chills, weakness, diarrhea, nausea, vomiting, rash, itching, high blood sugar, cough, and constipation. Other frequently reported effects are shortness of breath, leg swelling (peripheral edema), headache, fever, muscle or joint pain, decreased appetite, elevated triglycerides, insomnia, abdominal or back pain, dizziness, and various infusion reactions.
More serious side effects have included low blood pressure, anaphylaxis, serious or opportunistic infections, cancer, serum sickness, autoimmune thyroiditis, blood clots, heart failure, bleeding disorders, interstitial lung disease, hepatitis, enterocolitis, gastrointestinal perforation, stomatitis, anemia, and low white blood cell counts.
Each biologic drug has its own safety profile, and not all patients will experience these reactions. But because biologics act deeply within the body’s immune and cellular systems, their side effects can be complex, unpredictable, and sometimes severe. These products are not something you should be given without knowing the risks!
The Anesthesia Loophole
Anesthetized patients cannot give or withdraw consent in real time. Hospitals know this — and legal teams have prepared for it. That’s why pre-operative consent forms now carry generalized clauses authorizing “treatment using biologic materials.”
The rationale sounds protective: “We need flexibility in case of complications.”
The reality is exploitative: “We can administer what we deem appropriate.”
Under this loophole, you could receive a biologic without your explicit approval. Once it’s in your body, it cannot be undone. While this remains only a theoretical concern at this time, as AI increasingly takes over healthcare and personal options continue to be reduced, it is distinctly possible.
I found court cases where a patient received a biologic without specific consent. (here) (here). I didn’t find a published U.S. case that squarely says: “Because of the single word biologics in a blanket consent, a sedated patient got a biologic they would have refused.” But these two cases demonstrate the core risk is real.
What You Must Do
We are living in a time when words have become deceptive, from politics to healthcare. To protect yourself, you must re-establish your authority over your own body. Here’s a place to start. Print this and keep it with your health insurance card:
- Read every word. Never sign a consent form that contains vague terms like “biologics,” “biogenics,” or “cell-based therapies” without a full explanation from your doctor(s).
- Ask direct questions. Ask out loud: “Does this include vaccines, gene therapies, or blood products?” Write their answers and whether you agree or disagree.
- Refuse in writing. On both digital and paper copies, clearly state: “I do not consent to the administration of vaccines, biologics, or other synthetic materials.”
- Get a copy. Always request a printed copy or photo of your signed form, especially if it was done on an iPad.
- Have an advocate. Assign a trusted person to reiterate your refusal verbally and in writing if you are incapacitated. If you don’t have a close friend or family member who can navigate this with you, hire someone from GraithCare.com. They are knowledgeable and worth every penny.
- Document everything. After discharge, review your medical record and confirm what was administered. Side effects or complications may not materialize for weeks or months.
This is not paranoia; this is precautionary and wise self-care. The same level of attention you’d give to a financial contract should apply even more importantly to your medical care.
Bodily Autonomy Is a Spiritual Battle
At its heart, this is about sovereignty. The right to decide what enters your body — what merges with your cells — is not just a medical decision, it’s a moral and spiritual obligation.
Scripture says our bodies are temples of the Holy Spirit, not laboratories for untested technologies. To surrender consent to vague, corporate-crafted terms like “biologics” is to give the keys away to your own temple. I believe every human being deserves the dignity of true informed consent, not coerced compliance through deceptive wording.
Closing Thoughts
We are a litigious society, and physicians are always concerned and on the defensive about avoiding lawsuits. The timeless advice from that 1996 article on how you can best be perceived and help your patient’s decision-making process:
The best advice we can give is to treat patients like people, act sensitively and compassionately, and most of all, talk to patients. Have a conversation, have several; remember that this is a process. In this process, you will gradually come to know your patient’s decision-making style. Furthermore, do not press patients to decide quickly. Do not make them think that you do not have time for them. Because if you do, regardless of how much information they are given, they are going to be angry, and another name for an angry patient is plaintiff.
So please, before you sign anything: stop. Read. Ask. Refuse if you must. Line out what you don’t agree with, initial it, and date it. Your signature implies permission.






