While all of this sounds plausible, it also sounds like industrial sabotage. Not a J&J stan, but I seem to remember some shenanigans in 2021 where pfizer was pushing the blood clot stories against j&j and we now see what their own document drops are showing. I am so ready for the whole medical/pharma industrial complex to be glassed.
I'm with you on that last one. Unfortunately, with Cabal stranglehold on Medicine, Media, Pharma, Academia, Government, and Science in general, serious inquiry is severely hampered. First step to their demise is the loss of trust from one-time believers and advocates. I think we are there. We've seen the slam pig without her makeup, and that can never be unseen.
Wouldn’t there be a massive outbreak in everyone, not just kids? If it’s aerosolized all over the place, wouldn’t everyone person who got the j&j be spreading?
Adenoviral infections are common in kids since they have typically not encountered them before. Not common in adults as we have residual resistance from our own encounters as children. This type of cross resistance is also common with coronaviruses which include several of the common cold viruses.
A key aspect of the cited hypothesis is host taking the Gilead pre-exposure HIV med, which may have caused the replication of the Adenoviral vector.
Moral of the story, careful when you fuck with nature because nature knows how to fuck too.
This seems like a good time to remind people not to get rid of dandelions but grow them, use the young small leaves in salads, or buy dandelion liquid supplement to make a tea or cold drink out of. Dandelion is highly liver protective.
Found it - edit formatting sucks I’ll see if I can fix it from my pc later)
Here is the US recipe (Canuck here with litres and silliness)
Dandelion flowers - 3/4 gallon
Lemon - 1
Orange - 1
Ginger root - 1 piece (thumb size)
Sugar - 3lbs
Citric acid - 1/4oz
Tannins - 1/16oz
Yeast - all purpose but I’ve used champagne yeast and ec-1118 and anything else I have on hand all were good
Yeast nutrient - follow the instructions on whichever you use. I sometimes use tomato paste (1 tablespoon)
Pectin destroying enzymes follow the instructions it comes with.
Wash the flowers and drain
Put them in a pail and cover with 1 gallon of boiling water (4.5l so imperial gallon not US)
Cover the pail and let it sit 3 days stirring every day.
Pare the zest from the orange and lemon and squeeze out the juices in a large pot
Bruise the ginger put it in the pot
Squeeze the flowers to get the juices out and discard.
Add the liquid to your pot along with the sugar, Citrix acid, tannins stir to dissolve the sugar boil 30mins and pour into your primary fermenter
When cool add your pectin destroying enzymes cover and let stand in a warm place
After 24 hours pitch your test and add yeast nutrient
After a week rack into your secondary fermenter and seal it with an airlock
When fermentation is done rack to a clean container add a crushed Camden tablet or whatever sulfite you like to stop fermentation (cold crash it even, whatever works for you)
Seal with airlock rack every 2 months for 6 months the. Rack one final time let any sediment settle and bottle it.
Tastes great with shrimp/seafood etc
I have a great chokecherry wine recipe too if you need :)
I use to brew a lot of hooch back in the day, grandpa had quite a collection, everything from dew berry wine to kumquat liquor.
Now days I tincture most everything for my apothecary.
Soft leaves and flowers in 20-40% grain alcohol.
Nuts, seeds, roots, bark and even heart wood and stems in 40-80% grain alcohol.
It last forever, it's super easy, you can get a lot of medicine on a small shelf.
Essential oils also pack a punch, and last forever. Distillation isn't hard but the yield is so low. I'm glad I know how to do it, but I bought a collection of EOs that will probably last my lifetime.
Now while all that's fine and dandy, none of it would impress a date over a fine meal of seafood.
That coupled with the fact that inflation plus the sin tax on booze is outrageous ridiculous, it just might make it worth my while to start brewing, fermenting and distilling once again, it would make grandpa proud.
I'm always grateful and happy to have a good recipe, tks.fren
Recently heard someone, can't recall who, stating that the majority of increased child/hep cases were in America and UK. UK used the AstraZenenca (Oxford) jab on many people for 1st two doses. For third jab and beyond UK used mainly Pfizer, public narrative was also AZ/rare bloodclots. AZ purportedly used chimpanzee adenovirus not human. One question I have would be: how is hep only happening now in UK when AZ stopped being used in the UK in 2021? Does it take time for hep to develop? https://www.nature.com/articles/srep16756/
My interpretation of this gentleman's post is that lag time is related to the time it takes for a new virus to develop, mutate and replicate again and begin to circulate in the population. interesting that they specifically mention the Gilead HIV drug as initiator. As you can imagine, it would take some time for all of these variables to coalesce.
Now we have a new hepatis inducing Adenovirus circulating in the wild if the hypothesis is correct, and it's spread will be independent of any other actions.
Not going to bet the farm on any particular scenario at this point. We need real investigation and real science. Only thing we know for sure is that if the medical establishment and big pharma are the cause, they will hide and bury the fuck out of it.
While adenovirus are common, keep in mind that this particular adenovirus (ad26) is engineered to defeat the human immune response.
While ((supposedly)) non replicating, life has once again found a way around man's stupidity. Or it's simply doing what it's been design to do, self replicating viral vector.
While it is evident this strain is rather virulent, it doesn't necessarily have to be a ether/or adeno vs. mRNA question. It could very well be the disastrous duo.
We know the spike and sub particles are sheding from the mRNA jabies, and the spikes further degrade the immunity, plus alter the liver dna.
We also now know this Ad26 is transmissible from person to person and, since it's known to effect GI, urinary, liver, and respiratory, that mode of transmission may be many.
The unfortunate soul that is exposed to both, jab of one and social contact of the other, or social contact by both, may be experiencing an assault on multiple fronts the human immunity cannot overcome.
Misdirection, distraction?
Or just another layer of complication to unravel, before we can undo, what has been unleashed upon us.
Good points all. Barring substantive actions by whistleblowers, definitive understanding will remain elusive until control is wrested from the malign forces.
My sense is none of these gene therapy-based vaccine approaches are viable. Observed (significantly suppressed) safety profiles so abhorrent, they seem intentional and poor efficacy are ample justification for rejection, IMO.
Add to that the potential (seemingly realized) for mutagenesis, metabolic pathway corruption, and inhibition there is just too much that can go wrong, even if intentions were benign.
Our bodies do not like foreign genetic material in them, nor should they. Gene therapies can only "work" if there is immune suppression. It appears our adversaries have developed considerable expertise in this area.
While all of this sounds plausible, it also sounds like industrial sabotage. Not a J&J stan, but I seem to remember some shenanigans in 2021 where pfizer was pushing the blood clot stories against j&j and we now see what their own document drops are showing. I am so ready for the whole medical/pharma industrial complex to be glassed.
I'm with you on that last one. Unfortunately, with Cabal stranglehold on Medicine, Media, Pharma, Academia, Government, and Science in general, serious inquiry is severely hampered. First step to their demise is the loss of trust from one-time believers and advocates. I think we are there. We've seen the slam pig without her makeup, and that can never be unseen.
Wouldn’t there be a massive outbreak in everyone, not just kids? If it’s aerosolized all over the place, wouldn’t everyone person who got the j&j be spreading?
This needs an answer b/c I have close people who took the J&J.
Adenoviral infections are common in kids since they have typically not encountered them before. Not common in adults as we have residual resistance from our own encounters as children. This type of cross resistance is also common with coronaviruses which include several of the common cold viruses.
A key aspect of the cited hypothesis is host taking the Gilead pre-exposure HIV med, which may have caused the replication of the Adenoviral vector.
Moral of the story, careful when you fuck with nature because nature knows how to fuck too.
This seems like a good time to remind people not to get rid of dandelions but grow them, use the young small leaves in salads, or buy dandelion liquid supplement to make a tea or cold drink out of. Dandelion is highly liver protective.
TY, good info. I pondered the fate of the dandelions in my back yard just today.
***Seems we have a Ghey, Satanist Lurker about.
Mine always turn into wine. I’m sure I loose whatever benefit is in them though :D
Not at all, some constituents are only solvent in alcohol, medicinal wines have been used for 1000s of years.
It's hard to argue against tintures but wine's the next best thing, when low alcohol percentages are called for.
How do you brew your dandelion hooch?
I make my kids slave labour and pick just the flowers then I’ll dig up the recipe for you and post it because I don’t remember it by heart :)
Found it - edit formatting sucks I’ll see if I can fix it from my pc later)
Here is the US recipe (Canuck here with litres and silliness)
Dandelion flowers - 3/4 gallon Lemon - 1 Orange - 1 Ginger root - 1 piece (thumb size) Sugar - 3lbs Citric acid - 1/4oz Tannins - 1/16oz Yeast - all purpose but I’ve used champagne yeast and ec-1118 and anything else I have on hand all were good
Yeast nutrient - follow the instructions on whichever you use. I sometimes use tomato paste (1 tablespoon)
Pectin destroying enzymes follow the instructions it comes with.
Wash the flowers and drain Put them in a pail and cover with 1 gallon of boiling water (4.5l so imperial gallon not US) Cover the pail and let it sit 3 days stirring every day. Pare the zest from the orange and lemon and squeeze out the juices in a large pot Bruise the ginger put it in the pot Squeeze the flowers to get the juices out and discard.
Add the liquid to your pot along with the sugar, Citrix acid, tannins stir to dissolve the sugar boil 30mins and pour into your primary fermenter
When cool add your pectin destroying enzymes cover and let stand in a warm place After 24 hours pitch your test and add yeast nutrient
After a week rack into your secondary fermenter and seal it with an airlock
When fermentation is done rack to a clean container add a crushed Camden tablet or whatever sulfite you like to stop fermentation (cold crash it even, whatever works for you)
Seal with airlock rack every 2 months for 6 months the. Rack one final time let any sediment settle and bottle it.
Tastes great with shrimp/seafood etc
I have a great chokecherry wine recipe too if you need :)
Sweet,
I use to brew a lot of hooch back in the day, grandpa had quite a collection, everything from dew berry wine to kumquat liquor.
Now days I tincture most everything for my apothecary. Soft leaves and flowers in 20-40% grain alcohol.
Nuts, seeds, roots, bark and even heart wood and stems in 40-80% grain alcohol.
It last forever, it's super easy, you can get a lot of medicine on a small shelf.
Essential oils also pack a punch, and last forever. Distillation isn't hard but the yield is so low. I'm glad I know how to do it, but I bought a collection of EOs that will probably last my lifetime.
Now while all that's fine and dandy, none of it would impress a date over a fine meal of seafood.
That coupled with the fact that inflation plus the sin tax on booze is outrageous ridiculous, it just might make it worth my while to start brewing, fermenting and distilling once again, it would make grandpa proud.
I'm always grateful and happy to have a good recipe, tks.fren
So is milk thistle.
Recently heard someone, can't recall who, stating that the majority of increased child/hep cases were in America and UK. UK used the AstraZenenca (Oxford) jab on many people for 1st two doses. For third jab and beyond UK used mainly Pfizer, public narrative was also AZ/rare bloodclots. AZ purportedly used chimpanzee adenovirus not human. One question I have would be: how is hep only happening now in UK when AZ stopped being used in the UK in 2021? Does it take time for hep to develop? https://www.nature.com/articles/srep16756/
Thanks for link, will study.
My interpretation of this gentleman's post is that lag time is related to the time it takes for a new virus to develop, mutate and replicate again and begin to circulate in the population. interesting that they specifically mention the Gilead HIV drug as initiator. As you can imagine, it would take some time for all of these variables to coalesce.
Now we have a new hepatis inducing Adenovirus circulating in the wild if the hypothesis is correct, and it's spread will be independent of any other actions.
Not going to bet the farm on any particular scenario at this point. We need real investigation and real science. Only thing we know for sure is that if the medical establishment and big pharma are the cause, they will hide and bury the fuck out of it.
While adenovirus are common, keep in mind that this particular adenovirus (ad26) is engineered to defeat the human immune response.
While ((supposedly)) non replicating, life has once again found a way around man's stupidity. Or it's simply doing what it's been design to do, self replicating viral vector.
While it is evident this strain is rather virulent, it doesn't necessarily have to be a ether/or adeno vs. mRNA question. It could very well be the disastrous duo.
We know the spike and sub particles are sheding from the mRNA jabies, and the spikes further degrade the immunity, plus alter the liver dna.
We also now know this Ad26 is transmissible from person to person and, since it's known to effect GI, urinary, liver, and respiratory, that mode of transmission may be many.
The unfortunate soul that is exposed to both, jab of one and social contact of the other, or social contact by both, may be experiencing an assault on multiple fronts the human immunity cannot overcome.
Misdirection, distraction?
Or just another layer of complication to unravel, before we can undo, what has been unleashed upon us.
Good points all. Barring substantive actions by whistleblowers, definitive understanding will remain elusive until control is wrested from the malign forces.
My sense is none of these gene therapy-based vaccine approaches are viable. Observed (significantly suppressed) safety profiles so abhorrent, they seem intentional and poor efficacy are ample justification for rejection, IMO.
Add to that the potential (seemingly realized) for mutagenesis, metabolic pathway corruption, and inhibition there is just too much that can go wrong, even if intentions were benign.
Our bodies do not like foreign genetic material in them, nor should they. Gene therapies can only "work" if there is immune suppression. It appears our adversaries have developed considerable expertise in this area.
And into "the wild" all certainty is lost, regardless of intention.
But, I think this is;
Targeted,
Intentional and
Consequential...
It appears (obvious) our adversaries have developed considerable expertise in this area.
We speak the same language.
Good post OP
Perhaps. Assertion here is still "vaccine" caused, just not the mRNA vaccines, but rather the J&J Viral Vector DNA vaccine.
Many types of harm clearly done by mRNA shots is not refuted.