Post 8: Tools for Recovery Against the Gene Therapy: Hyperbarics and Nutritional Retooling

I'm not a licensed physician (Ph.D. in Neuroscience/Toxicology), so this is not medical advice, just insights and suggestions that you need to assess for yourself.

We are now facing the reality that the mRNA gene therapies that were marketed as vaccines, are in actuality bioweapons. The work of Katherine Watt (paralegal and Constitutional expert) and Sasha Latypova (Biotech/Pharma consultant and regulatory expert) have both dug deep and give a great summary of what they have found regarding the Department of Defense (DoD). Their review via CD Media interview is jaw-dropping.

We have been told that the gene therapy mRNA technologies deliver the coding sequence for expressing the spike protein (Pfizer; P.17 and ModeRNA; P. 12), but it appears that the manufacturing practices are well below accepted standards of Current Good Manufacturing Practice [cGMP] (there were no requirements to follow cGMP under the Other Transactional Authority rule that was used to manufacture the jabs) and the DoD was not paying for “vaccines”, but for a manufacturing demonstration for countermeasures (against who?): (image from Bailiwick News, below)

Due to the rising and observable wave of neurological, cardiovascular and immune system disorders across all age groups (from all nations using these novel mRNA delivery technologies), PRIVATE CITIZEN LED groups began to track the injectable bioweapons by lot numbers. Craig Paardekooper and the folks that set up Howbadismybatch (HBiMB) need to be nominated for a Nobel Peace Prize for the incredible work they have accomplished on privately funded, small donations. HBiMB has shown conclusively that some batches of the injectables were more likely to kill/injure than other batches (about 5%). This is work that federal and state institutions should have carried out to protect consumers and the nation, but did they?

Not CDC.

Not FDA.

Not NIH.

Furthermore, we cannot even verify what is actually in the bioweapons. The DoD has control of the supply chain and the distribution. Legally, you cannot get a vial for analysis.

We can only assume that what was delivered via the lipid nanoparticles (LNPs) was the mRNA sequence that encoded the S-protein of the SARs-Cov-2 virus. For the most part, it seems to be the case.

The S-protein has been shown to induce clots, which can produce a series of embolism, strokes, mini-embolisms and organ damage due to blood loss or loss of oxygenation. A proportion of the neurological injuries and symptoms appear to be by-products of the clots. Spike protein also appears to impair neuronal function directly

At the same time, depending in where the S-protein is expressed, strong inflammatory signals can be induced, especially in the heart tissue (myocarditis), pulmonary inflammation, cytokine storm, encephalitis and spongiform-type neurological injuries.

Those are just the fun ones.

Stopping the Damage

If you are considering taking another jab, DON’T.

They are ALL RISK and NO BENEFIT (actually, negative benefit - which translates to HARM).

Mouse Study

Extended SARS-CoV-2 RBD booster vaccination induces humoral and cellular immune tolerance in mice (Science Direct, Volume 25, Issue 12, 22 December 2022, 105479, DOI: https://doi.org/10.1016/j.isci.2022.105479)

Extended immunizations impaired the serum neutralization activity

(Translation: Effective antibodies to stop infection where not produced).

Extended immunizations suppressed the formation of germinal center

(Translation: immune organs (spleen, lymph nodes) that activate the cells that produce antibodies are no longer forming) (FUCK ME -- THIS IS BAD)

Extended immunizations inhibited the activation of CD8+T cells

(Translation: T-cells (which are identified by the CD8+ receptor they express) are critical in SEARCH & DESTROY functions. They kill infected cells, AS WELL AS CANCER CELLS.) (REPORTS OF CANCERS EXPLODING IN THE POPULATION NOW BEGIN TO MAKE SENSE - - DOUBLE FUCK ME)

The detailed and long-term study in mice is corroborated from the clinical experience that was reported by the Cleveland Clinic.

Clinical Study

Effectiveness of the Coronavirus Disease 2019 (COVID-19) Bivalent Vaccine (MedRxiV, Dec 19, 2022, doi: https://doi.org/10.1101/2022.12.17.22283625)

“The association of increased risk of COVID-19 with higher numbers of prior vaccine doses in our study was unexpected.”

Now that that is out of the way, let’s begin.

Enough Good News…How Can You Recover from or Reduce the Damage?

The most significant thing you can do, if you have co-morbidities (diabetes, COPD, heart disease, kidney damage, etc…) or have suffered a recent injury, is to loop in your health practitioner and tell him or her (or zee or zer if you or they are into the pronoun derangement) that you will be attempting something new.

1. Bromelain is a supplement. You can start by taking regular doses, as is generally recognized as safe (GRAS) and is considered a digestive supplement (https://www.healthline.com/health/bromelain). Bromelain is measured in gelatin digesting units (GDUs) per gram. Doses range from 80–400 milligrams per serving, two to three times daily. Your doctor may recommend that you take bromelain with meals in order to aid digestion, or on an empty stomach to reduce inflammation.

2. Begin supplementing with oral N-acetylcysteine (NAC) powder or pills. NAC comes in prescription strength and in supplement form. It is an incredibly useful vitamin in hospitals, as it is used to treat Acetaminophen (Tylenol) poisoning or for lung collapse due to mucus blockage. It is also an incredible anti-inflammatory. The list of regular NAC supplementation is growing (https://www.healthline.com/nutrition/nac-benefits). I recently ordered Purple Powder, which is NAC and other essential vitamins.

3. Ivermectin - if you can get it, get a prescription. Otherwise, begin using quercitin as a supplement. Both have show excellent abilities to stop S-protein from damaging organs.

As if by kismet or morphogenic field (or divine providence, take you pick), at WMC Research, they reported on the computer model mechanisms-of-action of Bromelain.

Bromelain has the potential to dock-and-block the S-protein. This was confirmed in a cell-culture assay (DOI: 10.3390/v13030425; The Combination of Bromelain and Acetylcysteine (BromAc) Synergistically Inactivates SARS-CoV-2) in which the wild-type, mutant variants of SARs-Cov-2 (and recombinant spike and envelope SARS-CoV-2 proteins) were disrupted by the combined use of bromelain and acetylcysteine.

This combination can be used as a means to stop infection.

But there is no reason that it can be used during and after (or Long-COVID) to sweep up any remaining spike protein from the virus. Or, in this case, from the jabs that are causing long-term expression.

What is very interesting about the reported use of Bromelain and Acetylcysteine (AC) is the reported benefit of N-acetylcysteine (NAC) in treating/preventing SARS-Cov-2 infections ( N-Acetylcysteine as Adjuvant Therapy for COVID-19 - A Perspective on the Current State of the Evidence, DOI: 10.2147/JIR.S306849 ; N-Acetylcysteine to Combat COVID-19: An Evidence Review, DOI: 10.2147/TCRM.S273700 ; N-acetylcysteine for prevention and treatment of COVID-19: Current state of evidence and future directions, DOI: 10.1016/j.jiph.2022.11.009 ). NAC and AC are both pre-cursors for making glutathione in the body. Glutathione is an antioxidant that works to turbo-charge the immune system function, help with tissue building and repair, and is essential for making proteins in the body. NAC has also been used to treat Long-COVID symptoms (Science Alert).

Additionally, ivermectin has shown a similar ability to dock & block the S-protein ( The Journal of Antibiotics (2022) 75:60–71, The mechanisms of action of ivermectin against SARS-CoV-2—an extensive review, https://doi.org/10.1038/s41429-021-00491-6). For all the propaganda against ivermectin, the reliability and effectiveness of this drug remains incredibly high.

Now, the majority of the work has looked at blocking or limiting the infection by SARs-Cov-2 with supplements and drugs. Here, we are talking about recovering from the S-protein damage (SARs-Cov-2 or the gene therapy bioweapons), which is a slightly different beast. This will require a combination of treatments.

Since we are hypothesizing on methods to recover from the damage, we have to assume that the S-protein may still be circulating or is being expressed if you took the jab or are suffering from Long COVID.

The listed supplement are a good place to start to block the S-protein.

Rebuilding the Systems - Adding Hyperbaric Oxygen (HBO) to the Mix

So, as long as we are doing the supplement + effective drug treatments, we can add a powerful and general boost to the body. Doing HBO along with the supplementations has the benefit of reducing inflammation, rebuilding lost or blocked blood vessels, accelerating recovery of damaged cells and (in cases of neurological stroke or cardiomyopathy) restoring and protecting cells of the brain and the heart.

The effects of micro-clots produce zones of dead or “stunned” cells. By stunned, I mean cells can sometime enter into a state of suspended animation or low-metabolic activity. These cells are not technically dead, but they are not working at full power.

The landmark studies of Blackstone et al.¹, ² were the first to provide evidence for a mechanism that could induce a state of suspended animation in cells (neurons in particular). Blackstone et al. demonstrated the ability to down-regulate mitochondrial respiration by simultaneously exposing mice to gaseous H2S (hydrogen sulfide) and reducing oxygen levels. Not only did the mice survive periods of reduced oxygen tension of > 6 hour at 5% oxygen (mice die at those oxygen tensions), there was no measurable neurological or myocardial damage when they were restored to normal oxygen levels and metabolic function [1, 2]. The discovery of an H2S mechanism in neurons ³ suggests that this signaling gas is a conserved mechanism in mammals ⁴⁵ ⁶ ⁷ ⁸. From a mechanism perspective, enzymatic systems in mammalian neural tissues (and potentially other cell types) produce H2S locally and could induce a local hypometabolic state by direct regulation of mitochondrial activity ⁹ ¹⁰ ¹¹ ¹² ¹³.

HBO treatments have shown the ability to activate previously “dead” or inactive zones in the brain. This has been observed in Long COVID, brain injury and in stroke! So, when you have damage from clots, there is a good chance that HBO can recover the function of the affected organ or tissue.

By combining the use of HBO and the supplements, you can boost your chances at recovery. HBO is a force multiplier in treatment.

At the same time, the NIH has a far more complete set of protocols that they are NOT SHARING with those injured by the gene therapy bioweapons (see https://www.theepochtimes.com/brianne-dressen-gaslit-by-doctors-and-loved-ones-some-vaccine-injured-are-making-the-ultimate-choice-to-end-their-suffering_4994340.html).

The report of Brianne Dressen and her journey to recovery highlights the very real evidence that NIH knows of the many adverse and serious adverse events of the jabs. The thought and treatment leader for both SARs-Cov-2 and gene therapy bioweapon injuries is Dr. Avindar Nath at NINDS. Yet, there is no reporting or admission.

We are on our own (no surprise there).

Taking Control of Your Recovery

So, lets recap:

Supplement with NAC and Bromelain. They are potent anti-inflammatories and they destroy S-protein.

Add ivermectin or quercitin to your regular dosage either prophylactical or recovery.

Start doing HBO to accelerate recovery (if you can). HBO has many benefits other than COVID and jab recovery.

Get together with friends/family and ask for help.

Keep fighting. Keep learning.

Pray and meditate.

Every little bit helps.

Until next time.

1. Blackstone, E., M. Morrison, and M.B. Roth, H2S induces a suspended animation-like state in mice. Science, 2005. 308(5721): p. 518.

2. Blackstone, E. and M.B. Roth, Suspended animation-like state protects mice from lethal hypoxia. Shock,2007.27(4):p.370-2.

3. Eta, K., et al., Hydrogen sulfide is produced in response to neuronal excitation. J Neurosci, 2002. 22(9):p.3386-91

4. Chen, C.Q., H. Xin, and Y.Z. Zhu, Hydrogen sulfide: third gaseous transmitter, but with great pharmacological potential. Acta Pharmacol Sin, 2007. 28(11): p. 1709-16.

5. Qu, K., et al., Hydrogen sulfide: neurochemistry and neurobiology. Neurochem Int, 2008. 52(1-2): p. 155-65.

6. Baumgart, K., P. Radermacher, and F. Wagner, Applying gases for microcirculatory and cellular oxygenation in sepsis: effects of nitric oxide, carbon monoxide, and hydrogen sulfide. Curr Opin Anaesthesiol, 2009. 22(2): p. 168-76.

7. Wagner, F., et al., Bench-to-bedside review: Hydrogen sulfide--the third gaseous transmitter: applications for critical care. Crit Care, 2009. 13(3): p. 213.

8. Olson, K.R. and N.L. Whitfield, Hydrogen sulfide and oxygen sensing in the cardiovascular system. Antioxid Redox Signal, 2010. 12(10): p. 1219-34.

9. Pun, P.B., et al., Gases in the mitochondria. Mitochondrion, 2010. 10(2): p. 83-93.

10. Tay, A.S., et al., Hydrogen sulfide protects neurons against hypoxic injury via stimulation of ATP­ sensitive potassium channel/protein kinase Cfextracellular signal-regulated kinase/heat shock protein 90 pathway. Neuroscience, 2010. 167(2): p. 277-86.

11. Yong, Q.C., et al., Effect of hydrogen sulfide on intracellular calcium homeostasis in neuronal cells. Neurochem Int, 2010. 56(3): p. 508-15

12. Mikami, Y., et al., Hydrogen sulfide protects the retina from light-induced degeneration by the modulation of Ca2+ influx. J Biol Chem, 2011. 286(45): p. 39379-86.

13. Kimura, H., N. Shibuya, and Y. Kimura, Hydrogen sulfide is a signaling molecule and a cytoprotectant. Antioxid Redox Signal, 2012.