Can the mRNA vaccine alter my DNA or cause death? Yes, definitely, and here is the proof (investigational article)

Photo Credit: National Cancer Institute – 10min read

RNA and DNA can be hybridised, and scientists have known this for almost a century. It’s been done in labs around the world, in vitro and in vivo. This is why Remdesivir (the intravenous medication given to Covid-19 declared patients is deadly – it inhibits RNA and DNA). Death after vaccine might not occur shortly, but on the longterm it is increasingly closer than before due to the repercussions of the therapy.

Keep in mind that more than 50% of the patients that died with the new Wuhan virus could have been saved in record time with steam baths with antiseptic oils (based on real science from doctors and nurses working across London, and personal experience), steroids, antibiotics, and other highly potent medication for cold and flu. The other 30% let’s say, with more severe underlying conditions like the immunocompromised, could have been treated using plasma therapies and immunotherapies like specific immunoglobulin vaccines (remember that I used to produce immunoglobulin vaccines). You never infect the immunocompromised with RNA, mRNA, or anything else! Their immune system cannot cope with the infection, and most probably they will experience sudden death. The rest of 20% were probably in such a poor shape that even the slightest cold virus they’ve even had in the past could’ve taken them down. They can be considered negligible due to their poor state. Bringing a coronavirus vaccine for everybody, despite having highly effective therapies already, is bio-terrorism by any definition, madness, and proof that science in the wrong hands is an act of war.

The components of mRNA vaccines:

1. Incompetent (cannot infect cells on its own) adenovirus vector (original RNA has been removed) from chimpanzees;
2. Lab synthesised Sars-Cov-2 RNA sequence responsible for the infamous spike protein;
3. They are using recombinant DNA technology (used to add sequences to the animal genome, including humans), cultures of human embryo cells;
4. Proprietary information (you will never find out what it is as it’s protected by patents);
5. Untested chemicals that form the suspension;
6. Lipid nanoparticles encapsulating the GMO;
7. Other ingredients depending on company.

Side effects:

1. Blood cloths anywhere in the body;
2. Low platelets count (those cells dealing with blood coagulation when you have a cut); this is itself is a type of haemophilia and on the longterm might need coagulation medication (also produced by the lab I used to work for);
3. Anaphylactic shock (this can cause death in minutes);
4. Severe infection of the blood with spike protein (making you incompatible with blood donation – worldwide shortage of blood);
5. Severe damage of the nervous system (neurones do not replicate – when you lose them they’re gone forever);
6. Damage of the placenta in pregnant women;
7. Shedding of dangerous particles for the ones around you for unknown lengths of time through stool, breath, saliva, skin, pee;
8. Headaches;
9. Low count of white blood cells (the mRNA nanoparticles infect white cells too);
10. Acquired immunodeficiency as your body will try to take out your own spike-producing cells;
11. Increased enzymes in the liver (can make liver collapse);
12. Infection of important organs and the brain.
13. Infertility by destroying the eggs in a woman’s ovaries (roughly 500-600 eggs)/infecting the testicles – causing mutated sperm; the vaccine contains millions of mRNA nanoparticles that can target any area of the body; in the specialty literature you’ll find that “there is no data about infertility caused by the mRNA technology”, but that does not eliminate the risk – if you don’t look at something it doesn’t mean it will not happen; shedding of viral particles in the ovaries and testicles has been reported;
14. Change in the natural expression of your cells by producing dangerous proteins capable of overloading your immune system;
15. The RNA becoming double stranded through Reverse Transcriptase inside the cell, and then possibly being introduced into the cell’s nucleus.
16. Producing dangerous new mutations when getting infected with the real virus or even other coronaviruses, exponentially increasing the number of novel coronaviruses in nature; this can potentially be fatal for all humans, especially the vaccinated as they don’t have antibodies for the real main virus and they live with an overloaded immune system;
17. Last but not least, NO antibodies are being produced against the real virus;
18. It will change the expression of your cells for a long time, as most cells have an extended lifespan.

Proof of the above is the following

ZOLGENSMA is a child company of Novartis, dealing with Gene Therapies. In 2019 Zolgensma have created a vaccine that can deliver a new working gene to the nucleus of the cells of children with SMA (Spinal Muscular Atrophy). In its study, the company declares that this therapy does not modify the child’s DNA, but that the working SMN gene does get delivered to the nucleus of the cell. This therapy has caused deaths and they admitted it. The purpose of this treatment is to make the cells produce the SMN protein, which is essential to motor neurone cell survival – the cells that will get the genes (the delivery method is able to break through the protective barrier of the central nervous system).

Contents of ZOLGENSMA:

1. Incompetent adenovirus vector (host for the SMN working gene – DNA sequence);
2. Untested chemicals that form the suspension;
3. Recombinant DNA technology in human embryonic cells;
4. Proprietary information;
5. Reverse transcriptase;
6. Lipid nanoparticles containing the vectors.

ZOLGENSMA have not mentioned anywhere in their documentation submitted to the FDA and the European Union about the delivery method, which is messenger technology (mRNA/DNA). Upon contacting them about this delivery method they refused to comment or give details and they sent me to contact the mother company, Novartis. If they would’ve mentioned that this delivery method can deliver the gene to the nucleus, word would’ve got out into the mainstream and gone would’ve been the uptake of the mRNA vaccine by the population. To answer your unspoken worry, YES, it is the exact technology as the killer mRNA vaccines promoted in 2021. As I’m writing this article, tens of thousands of people worldwide have died because of the mRNA vaccines. Over 10,000 in the US alone. There are more deaths in developed countries because they have vaccinated most of their population compared to poorer countries. The new perks of living in a developed country…

Now the interesting part: Side effects of ZOLGENSMA therapy

1. Increased enzymes in the liver/liver collapse.
2. Low platelets count.
3. High protein expression in female ovaries after week 12.
4. The risk for transfer of a non-integrative, non-replicative vector to offspring via spermatocytes is low. The risk is low but still there. They are arguing that because the patients are six months of age when they receive the therapy, the risk of them transmitting the gene by the time they reach the reproductive age is negligible. Now think that the mRNA vaccines (the same technology) are being given to full grown adults!
5. Change in the natural expression of the cells for a long time (in this case it can be argued that it is a good thing, since these childrens’ life is already highly damaged without the SMN protein); still, the risk of dying and developing other serious conditions is extreme.
6. High viral DNA in the brain and the spinal cord.
7. Risk for humans from shedding, especially of wildtype viruses with mutated genes if the patient gets infected with a live virus.
8. Thrombotic Microangiopathy (TMA) caused by blood clots about one week after vaccination. Thrombotic microangiopathies (TMA) are clinical syndromes defined by the presence of hemolytic anemia (destruction of red blood cells), low platelets, and organ damage due to the formation of microscopic blood clots in capillaries and small arteries.
9. Infection of other organs and the brain.
10. Anaphylactic shock (this can cause death in minutes);

In the case of SMA condition you could say that the benefits outweigh the dangers (admittedly the condition stops spreading), although they are quite close to each other. In the case of the mRNA vaccines the risk of getting permanent damage or death is almost 1/1, whereas the risk of dying or getting permanently damaged from the real coronavirus is 1/1,000,000 approximately. If you think these details make it ok to introduce a known deadly technology into healthcare, then by all mean have the vaccine. And yes, this is proof that the mRNA particle can deliver the RNA sequence to your nucleus. Though, this isn’t the only thing you should worry about…