He saw something he couldn't ignore. They asked for the evidence. He provided it. They took his license...The story that needs to be heard and shared with EVERYONE, ESPECIALLY parents...
Ever wonder why the tyrannical stooges at big pharma never do any studies like this? It would show their poison vaccines are far more harmful to children and humans than doing nothing at all. GUARANTEED!
Apply to all political measures and ask yourself: which ones are humanistic?
If one point fails, it is proven beyond doubt the thing undermines the remnants of democracy.
I could not find ANY measure NOT being inhumane or undemocratic on this simple 5-point scale.
Back to our trial:
Communicate directly via mesh from client to client, everyone storing redundantly a part of the trial and communications. No server.
Develop simple website based trials for interrogation, some may be needed to be done at a humanistic physicians practice, choose someone with the heart on the right spot shortly before retirement. They saved us all along in the pandemic.
Ask: what would you do to prevent CoV or Flu from becoming nasty in me? If he mentions “early”, “determined” and mumti-drug multi-target (we call it multi-modal therapy), you can stay. If he is honest and says: look, I do not know, dependa on your system, di what granny has told you, this is nearly as good. If not, go to next. I estimate you have to polish the door handle of at least 100 physicians’ sites.
Cheap detection of eg IgA based Antibodjes whatever:
Just produce the tests you need by fablab / biolab bio hacker space based on RTLAMP (bead-LAMP eg) or di detective‘s work to protect a handfull of labs against (structural) corruption ir blackmail or attacks.
Do ask the right QUESTION.
Prof. John Ioannides tried to hint on this problem.
- possibility of shedding from relatives (breastfeeding, close skin contact to kids, i timate persons) during “transfectious” period (probably 1-2 weeks for most, if no plasmide infection took place, then 1/2 year or more, the Post-Vax victims will hide some of these, see Ananamide’s deep sequencing revealing antiviotic resistant infectious plasmides doing mRNA copies indefinetely, explaining a part of long term spike shedding as well).
Install measurement of number if activated monocytes.
Measure before/after events like severe infections or vaccination.
Then we will find that the more distance to PEG2k and wuhan spike and generally deep infection (blood, then organs; making b-cell based antibodies necessary) we have due to reduced nK / innate antibody response strenghts, the worse the health situation.
Then we can ask for vaccines that are yeRs back, like hepatitis combo.
Lastly, when having established a measurement possibility for the perfection of training of innate antibodies to some antigen, we can proof the self-vaccination therory (which is already proofed):
When you shed droplets or aerosol that is not infecting others, it still trains their innate antibodies, and every pre-immunity vastly decreases chance of severe cause even if vulnerable.
Intermezzo:
(VULNERABLE: symptoms not treated properly in the sense of basic law.
Working thesis: having free ACE2 in blood.
Mostly hidden, ie undetected symptoms lurk like a pitfall upon crisis, everything inflammation and irritable mast cells,
MCAS, or monocytes (too many H1 activated ones, MAS), or the AI prevalent ones, not able to efficiently kill memory cells against auto-antibodies any deep infection brings along. )
First we MEASURE the efficacy of ONE round of training (1-2 weeks) by a family member (not viral any more, but still coughing uninfectious droplets with broken pathogens while LHCS/ recovery phase of flu etc..
Then we go heretical:
Propose DIY vaccines ANY private person or physician or small lab can do:
- take some infected’s snot (blow into little bowl, keep 3m+ distance, wait 40sec for droplets to sink down, better do droplet things sneezing coughing NOSE BLOWING : OUTSIDES ;)
- sterilise and filtrate
- put into nasal spray (having sterile filters and at least back-drip stop vent in tip)
- add some stabiliser (non-soothing antiseptic, problem: all inorganic antiseptics soothe the immune system. Low but sufficient dose. Use the best: eg 50ppm CIO2 (aq) (ie diluted CDS) in a nasal spray enabled with backdrip-vent so keeping it sterile, will evaporate when cycling pressure a bit (temperature). (One can measure by color extinctometry the use-up of Oxidans CIO2 by the mucus/antigens for 3€ color led, photo transistor, Wlan microcontroller).
For a lab, if known what type of pathogen we have, RNA, DNA, bacterial, …, one can of course eg replicate just the RNA purified a bit from a sample. Special
Surface magnetic micro-beads normally do the job.
Look, this method takes 5 mins. (if you want only one spray) to one day (if you replicate antigens) till you can start spraying vulnerable people wanting to have some protection (elderly peoples homes) to train their innate antibodies, like 5x/day for one week, spray breathing in to nose eg. , depending on primary infection site.
I do not think one needs some adjuvans; in the past, these made only problems. A possible path is plant-based, a bit irritating saponines. (Not chestnut, it soothes.)
Thesis:
We just need time, the week is just my working thesis.
Also, this method only passively immunises, so no sterilising immunity is to be expected from the first round of training. Could need three.
I would wait for the next wave to have different variants as antigens. Our unit antibodies will pick the common denominator and be more variant independent. Eg..
We have to design reporting on reduction of severe cases in average. Objectively.
The test fails if someone produces b-cell based antibodies (be aware vaccinated having wuhan based will mostly fall to antigenic sin, always only producing Abs to wuhan spike or whatever is in, so one can not detect eg NC Abs though suffering deep infection, but will observe rise to wuhan spike Abs: the body produces Abs of “first contact” preferably, so new contact will give rise to thi, if defense by nK fails;
Antigenic sin thus being detrimental, as ALL CoV can now do ADE-I as of Delta as prokfed vy many paths of retrograde evolution away from and shortly after back to delta, dicumented in cities sequencing every PCR, and as of May 2022, BA.4, we observe ADE-D, as substantially more vaccinated with comparable health populate ICU _due_ to CoV than their share in population, but we have to objectively measure this and not fall prey to many confoundors).
Only by making innate antibodies’ binding strengths to some antigen measurable by the 5-point rule, “democratic-humanistic”, especially available and cheap, we will be able to document the paths to endemic and the CAUSAL influence of natural immunity and nK strengths.
My feeling: it is a wonder we did not broke up completely DUE to “measures”.
Making decreased nK visible, offers opportunity to SEE this hidden symptom, and as in all crisis: compensate risks, do prevention like I-PREVENT, please including one inorganic antiseptic (CIO2, NaHCIO, H2O2, SaNOtize, PVP-I) applied to “where it starts”:
- saliva glands (1/5ths) and
- throat RING (4/5ths of infections starting site);
* search for nK boosting food and herbs (many do) and mushrooms, and
* mental practices (all prayers and meditation).
* And laughing with people, smiling in their faces, watching their mouth mimic we need to empathise. Zrain back amygdala (no fluorine, no spike in brain, I-RECOVER, DMSO, micellarly solved progesterone, short-chained hyalurone, chromolynium acid, before night 1st Gen. H1-blocker, etc.)
As ALL measures decrease exposure to broken-up antigens, like masks by FACTOR 100 ca. (while NOT offering protection against droplet infection; that’s why they were so important:), or outright decrease nK as the base for innate antibodies (like lockdowns, fear porn in legacy news, existential sorrows due to deliberately installed economic tsunamis, splitting up families by divide-et-impera mass formation psychosis, and mainly nK reduction by reprogramming epigenetics (also reducing CD4/8/34+). Search for mRNA .. reduce .. “in an inheritable fashion”.
Ever wonder why the tyrannical stooges at big pharma never do any studies like this? It would show their poison vaccines are far more harmful to children and humans than doing nothing at all. GUARANTEED!
QUARANTEENED!
(I misread it first this way, had to laugh and share.)
Yes - we can.
Skip WHOever is doing harm to people. And DIY.
Care for others. Proof. Investigate. Research.
Organisation and precision is key.
Use interventions (in this case distributed decentralised trial) that fulfill humanistic conditions 5/5 (logical AND linked):
- safe
- effective
- cheap
- available
- TRANSPARENT (protected agains - structural - corruption visibly and stealth mode.
Apply to all political measures and ask yourself: which ones are humanistic?
If one point fails, it is proven beyond doubt the thing undermines the remnants of democracy.
I could not find ANY measure NOT being inhumane or undemocratic on this simple 5-point scale.
Back to our trial:
Communicate directly via mesh from client to client, everyone storing redundantly a part of the trial and communications. No server.
Develop simple website based trials for interrogation, some may be needed to be done at a humanistic physicians practice, choose someone with the heart on the right spot shortly before retirement. They saved us all along in the pandemic.
Ask: what would you do to prevent CoV or Flu from becoming nasty in me? If he mentions “early”, “determined” and mumti-drug multi-target (we call it multi-modal therapy), you can stay. If he is honest and says: look, I do not know, dependa on your system, di what granny has told you, this is nearly as good. If not, go to next. I estimate you have to polish the door handle of at least 100 physicians’ sites.
Cheap detection of eg IgA based Antibodjes whatever:
Just produce the tests you need by fablab / biolab bio hacker space based on RTLAMP (bead-LAMP eg) or di detective‘s work to protect a handfull of labs against (structural) corruption ir blackmail or attacks.
Do ask the right QUESTION.
Prof. John Ioannides tried to hint on this problem.
“Why most researched findings are false”:
https://journals.plos.org/plosmedicine/article/file?id=10.1371/journal.pmed.0020124&type=printable
1. Evaluate natural immunity depending on
- vaccination status
- possibility of shedding from relatives (breastfeeding, close skin contact to kids, i timate persons) during “transfectious” period (probably 1-2 weeks for most, if no plasmide infection took place, then 1/2 year or more, the Post-Vax victims will hide some of these, see Ananamide’s deep sequencing revealing antiviotic resistant infectious plasmides doing mRNA copies indefinetely, explaining a part of long term spike shedding as well).
Install measurement of number if activated monocytes.
Measure before/after events like severe infections or vaccination.
Then we will find that the more distance to PEG2k and wuhan spike and generally deep infection (blood, then organs; making b-cell based antibodies necessary) we have due to reduced nK / innate antibody response strenghts, the worse the health situation.
Then we can ask for vaccines that are yeRs back, like hepatitis combo.
Lastly, when having established a measurement possibility for the perfection of training of innate antibodies to some antigen, we can proof the self-vaccination therory (which is already proofed):
When you shed droplets or aerosol that is not infecting others, it still trains their innate antibodies, and every pre-immunity vastly decreases chance of severe cause even if vulnerable.
Intermezzo:
(VULNERABLE: symptoms not treated properly in the sense of basic law.
Working thesis: having free ACE2 in blood.
Mostly hidden, ie undetected symptoms lurk like a pitfall upon crisis, everything inflammation and irritable mast cells,
MCAS, or monocytes (too many H1 activated ones, MAS), or the AI prevalent ones, not able to efficiently kill memory cells against auto-antibodies any deep infection brings along. )
First we MEASURE the efficacy of ONE round of training (1-2 weeks) by a family member (not viral any more, but still coughing uninfectious droplets with broken pathogens while LHCS/ recovery phase of flu etc..
Then we go heretical:
Propose DIY vaccines ANY private person or physician or small lab can do:
- take some infected’s snot (blow into little bowl, keep 3m+ distance, wait 40sec for droplets to sink down, better do droplet things sneezing coughing NOSE BLOWING : OUTSIDES ;)
- sterilise and filtrate
- put into nasal spray (having sterile filters and at least back-drip stop vent in tip)
- add some stabiliser (non-soothing antiseptic, problem: all inorganic antiseptics soothe the immune system. Low but sufficient dose. Use the best: eg 50ppm CIO2 (aq) (ie diluted CDS) in a nasal spray enabled with backdrip-vent so keeping it sterile, will evaporate when cycling pressure a bit (temperature). (One can measure by color extinctometry the use-up of Oxidans CIO2 by the mucus/antigens for 3€ color led, photo transistor, Wlan microcontroller).
For a lab, if known what type of pathogen we have, RNA, DNA, bacterial, …, one can of course eg replicate just the RNA purified a bit from a sample. Special
Surface magnetic micro-beads normally do the job.
Look, this method takes 5 mins. (if you want only one spray) to one day (if you replicate antigens) till you can start spraying vulnerable people wanting to have some protection (elderly peoples homes) to train their innate antibodies, like 5x/day for one week, spray breathing in to nose eg. , depending on primary infection site.
I do not think one needs some adjuvans; in the past, these made only problems. A possible path is plant-based, a bit irritating saponines. (Not chestnut, it soothes.)
Thesis:
We just need time, the week is just my working thesis.
Also, this method only passively immunises, so no sterilising immunity is to be expected from the first round of training. Could need three.
I would wait for the next wave to have different variants as antigens. Our unit antibodies will pick the common denominator and be more variant independent. Eg..
We have to design reporting on reduction of severe cases in average. Objectively.
The test fails if someone produces b-cell based antibodies (be aware vaccinated having wuhan based will mostly fall to antigenic sin, always only producing Abs to wuhan spike or whatever is in, so one can not detect eg NC Abs though suffering deep infection, but will observe rise to wuhan spike Abs: the body produces Abs of “first contact” preferably, so new contact will give rise to thi, if defense by nK fails;
Antigenic sin thus being detrimental, as ALL CoV can now do ADE-I as of Delta as prokfed vy many paths of retrograde evolution away from and shortly after back to delta, dicumented in cities sequencing every PCR, and as of May 2022, BA.4, we observe ADE-D, as substantially more vaccinated with comparable health populate ICU _due_ to CoV than their share in population, but we have to objectively measure this and not fall prey to many confoundors).
Only by making innate antibodies’ binding strengths to some antigen measurable by the 5-point rule, “democratic-humanistic”, especially available and cheap, we will be able to document the paths to endemic and the CAUSAL influence of natural immunity and nK strengths.
My feeling: it is a wonder we did not broke up completely DUE to “measures”.
Making decreased nK visible, offers opportunity to SEE this hidden symptom, and as in all crisis: compensate risks, do prevention like I-PREVENT, please including one inorganic antiseptic (CIO2, NaHCIO, H2O2, SaNOtize, PVP-I) applied to “where it starts”:
- saliva glands (1/5ths) and
- throat RING (4/5ths of infections starting site);
* search for nK boosting food and herbs (many do) and mushrooms, and
* mental practices (all prayers and meditation).
* And laughing with people, smiling in their faces, watching their mouth mimic we need to empathise. Zrain back amygdala (no fluorine, no spike in brain, I-RECOVER, DMSO, micellarly solved progesterone, short-chained hyalurone, chromolynium acid, before night 1st Gen. H1-blocker, etc.)
As ALL measures decrease exposure to broken-up antigens, like masks by FACTOR 100 ca. (while NOT offering protection against droplet infection; that’s why they were so important:), or outright decrease nK as the base for innate antibodies (like lockdowns, fear porn in legacy news, existential sorrows due to deliberately installed economic tsunamis, splitting up families by divide-et-impera mass formation psychosis, and mainly nK reduction by reprogramming epigenetics (also reducing CD4/8/34+). Search for mRNA .. reduce .. “in an inheritable fashion”.
https://www.biorxiv.org/content/10.1101/2022.03.16.484616v2
And “teprograms both the adaptive and innate immune system”:
https://www.medrxiv.org/content/10.1101/2021.05.03.21256520v1#disqus_thread
And the genius paper on exosomes:
https://pubmed.ncbi.nlm.nih.gov/35436552/
All pointing to disrupted epigenetics, sometimes with hidden symptoms only, for the share vaccinated by PEG2k medical _device_ based mRNA vaccines.
Which we’ll have to heal:
Physiology: Herbs&Mushrooms.
Heal Soul&spirit.
Heal Information exchange amongst cells and to world.
Let us wish ourselves boldness, courage and love for the fellow human in “interesting times”.