❤️ REPAIRING DAMAGED HEARTS: Anti-MMP Properties of Sub-Antimicrobial Doxycycline ❤️
WEEKEND FLASH SALE STARTS NOW!
In the early days of the PSYOP-19 scamdemic, Dr. Didier Raoult discovered that azithromycin used in combination with hydroxychloroquine and zinc was a superior late stage COVID treatment protocol than just hydroxychloroquine and zinc on its own.
Initially, it was assumed that the improved outcomes with azithromycin were due to the amelioration of secondary bacterial infections.
The late Dr. Zelenko improved on this protocol by adding Doxycycline to the above combo. The reason Doxycycline was added in addition to azithromycin was not for its traditional role as an antibacterial, but, rather, because Doxycycline down-regulates the matrix metalloproteinase (MMP) enzyme that is responsible for tissue injury and scarring.
When patients suffer a serious autoimmune reaction from either SARS‑CoV‑2, or, far more likely, the slow kill bioweapon “vaccines,” a cytokine storm is triggered which results in severe tissue injury and scarring to the lungs.
Doxycycline has shown to effectively resolve the lung injuries from cytokine storms.
Periodontists have known for many years that compounds with anti-MMP properties, especially Doxycycline, may help with resolving gum injuries.
As early as 2005, professor of dentistry at the University of Toronto Dr. Howard Tenenbaum was studying effects of anti-MMP compounds on animals with induced myocarditis. The results showed that the MMP were down-regulated by the anti-MMP compounds, resulting in repair of the heart tissue.
This research showed potentially transformative outcomes for those suffering from myocarditis — an exceedingly rare disease at that time.
Some key findings and conclusions in morphology and gene expression in a rat model:
Cardiac Function: The study validated the MI (myocardial infarction) model by demonstrating a significant decrease in ventricular function post-MI compared to sham-operated rats at day 35. Treatment with either MMP inhibitors or ACE inhibitors significantly improved ventricular function compared to non-treatment.
Morphological Changes: Drug administration, particularly with MMP inhibitors, appeared to promote the formation of smaller MI areas and reduced left ventricular circumference compared to non-treated groups. This suggests that these treatments helped preserve normal anatomical features of the heart.
Collagen Deposition: Decreased collagen deposition, observed especially in the MMP inhibitor-treated group, may have contributed to the maintenance of cardiac function, distensibility, and contractility. Non-treated MI hearts showed the highest levels of collagen content, fibrosis, and organization.
Gene Expression: The study analyzed changes in gene expression in response to different treatments. While there were only minor changes in the expression profiles for structural genes, the findings suggest that down-regulation of genes involved in apoptosis and up-regulation of genes producing anti-inflammatory proteins could support post-MI cardiomyocyte viability and reduce cell death and hypertrophy.
Renin-Angiotensin-Aldosterone System (RAAS): Decreased expression of RAAS components is likely responsible, at least in part, for improved function due to hemodynamic regulation in the treated groups.
Limitations of Microarray: The study acknowledges the limitations of microarray analysis, emphasizing the need for careful interpretation of gene expression data and the importance of confirming results with further research assays.
Overall, this research provides a comprehensive understanding of the complex mechanisms involved in post-MI cardiac remodeling and how different treatments can influence cardiac function, morphology, and gene expression. The findings support the potential therapeutic benefits of MMP inhibitors and ACE inhibitors in the context of myocardial infarction.
Fast forward to 2021 when the slow kill bioweapon “vaccines” were foisted on the world, and myocarditis became a common adverse event (NOT RARE AS PER THE CENTERS FOR DISEASE CRIMES [CDC]).
These injuries are a result of autoimmune attacks on the heart cells expressing proteins not recognized by the immune system. This condition is a direct result of the Modified mRNA injections, which induce the cellular machinery of heart cells to express unrecognized proteins.
Too many people that subjected themselves to these pernicious “vaccines” are now suffering from this once-rare condition.
And one of those unfortunate individuals that experienced massive heart damage from these “vaccines” happened to be my relative; to wit:
After the above article was written much fact-finding was performed on behalf of my relative. During that time Dr. Tenenbaum provided this Substack with an exclusive research paper that was instrumental in healing my relative:
EXCLUSIVE RESEARCH BOMBSHELL: Possible Treatment Approach for Management of Post-COVID Vaccination Myocarditis
This is perhaps the most important article in this Substack’s ongoing series exposing the Modified mRNA slow kill bioweapon, and the various associated “vaccine”-induced death and disease mitigation strategies incorporating inexpensive repurposed drugs that actually work.
To repair her heart, my relative initially started with a full Doxycycline dose of 100mg, as well as an Ivermectin dose of 24mg per day.
After a month of this protocol a followup article was published:
More SUBSCRIBER SUCCESS STORIES: DEATHVAX™-Induced Heart Damage & Cancer
In this Substack’s ongoing series of anecdotal repurposed drug cures come two more incredibly encouraging stories.
Now that my relative’s heart condition has stabilized, she is currently taking, as per the aforementioned research, a sub-antimicrobial Doxycycline dose of 25mg exclusively for its anti-MMP properties. She still takes 24mg of Ivermectin as an insurance policy, and because she claims to feel markedly worse whenever she stops administering it.
The WEEKEND FLASH SALE starts today!
Please use code HEART20 for 20% off on the Nobel Prize winning miracle compound Ivermectin, the no less miraculous Fenbendazole, Doxycycline, the full spectrum organic CBD oil containing 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG, the powerful immune support nutraceutical and spike support formula VIR-X, and the sugar craving reducing, blood sugar balancing and even anti-cancer allulose sugar substitute FLAV-X!
Please note that all of the amazing products that this Substack has been promoting for many years will now be offered exclusively by RESOLVX HEALTH.
This WEEKEND FLASH SALE ends Sunday, June 1st (midnight eastern time), 2025.
Upon adding products to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code HEART20 in the Use Coupon Code field.
Please contact the company directly with any product questions: info@resolvx.health
Do NOT comply.
2SGW thank you for reposting this. I note:
"To repair her heart, my relative initially started with a full Doxycycline dose of 100mg, as well as an Ivermectin dose of 24mg per day."
Am I correct in taking that as she was on 100mg Doxycycline per day?
In March of 2020, Americans learned about a potentially deadly virus that was traveling across continents, heading towards their communities.
What most didn’t know is that this event represented the materialization of nefarious plans in bioterrorism that had been in the making for not just months, but decades.
A criminal racketeering consortium between the Gates Foundation, the Wellcome Trust, NIAID, the NIH, CDC, FDA, and their co-conspirators across the WHO and Global Preparedness Monitoring Board executed a plan to terrorize the world, murder millions, and reap incalculable financial rewards.
And now, they’re at it again.
In 2019, the World Health Organization, Wellcome Trust, NIAID, and the Gates Foundation conducted a global experiment on the accidental (or intentional) release of a lethal respiratory pathogen on September 19, 2019.
In an online document still available today called “The World At Risk,” readers were told that the exercise was being performed to create a “universal vaccine that the world would accept by September of 2022."
The current threat was published in April of 2024, but is now being circulated after Dr. David E. Martin uncovered the document, researched the co-conspirators and their ties to gain-of-function research, and revealed his findings to the world.
Page 7 of “The National Blueprint for Biodefense Report of the Bipartisan Commission on Biodefense” states, “Inevitably, there will be some subsequent pandemics and other biological events that will be worse than COVID-19, and similar responses will not suffice if we hope to save lives, preserve our economic strength, and buttress national security.”
The Event 201-type scenario suggests bioterrorists “—attacked the Nation’s Capital and other US cities with biological weapons as we celebrated Independence Day. The infectious agent they used killed at least 280,000 Americans and infected at least 400,000 throughout the country in a single day, in addition to the 200,000 dead and 800,000 sickened animals. These numbers will increase as the disease spreads. Many of our own colleagues and staff here in Congress fell ill and died. Coordinated attacks in allied nations in the days that followed killed tens of thousands more.”
“Laboratory tests confirm that Nipah virus caused the disease, but we still do not know what methods our adversaries used to infect humans and spread the disease among livestock in rural communities.”
“The virus, which in nature does not spread easily among people, was genetically modified to increase its ability to spread from animalto-animal, animal-to-person, and person-to-person, while still retaining a mortality rate of over 40%.”
Americans, it is our responsibility to soberly inspect this potential threat. Your government is not coming to save you.
We only anticipate this threat being thwarted by SHARING this video with everybody you know. Darkness wants to hide in the shadows.
If we bring this threat to life, there is a chance we can save millions.
We know the playbook. Now, it’s time to let the conspirators know we have caught them.
I pray there is enough time to raise awareness and take action... before it's too late.
https://rumble.com/v6u3f51-preparing-for-the-next-plandemic-and-fighting-for-humanity-w-dr.-david-mart.html
https://www.canva.com/design/DAGo8_h7nnY/pWM-UQ-VS8b35ekhnn3OCQ/watch?utm_content=DAGo8_h7nnY&utm_campaign=designshare&utm_medium=link2&utm_source=uniquelinks&utlId=h015c7c0461