US 100% fatal brain disease strikes 3 people in Oregon - Hood River County in Oregon reported three cases of Creutzfeldt-Jakob disease, a rare human brain disease very similar to "mad cow."

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Source: https://www.livescience.com/health/...atal-brain-disease-strikes-3-people-in-oregon
Archive: https://archive.is/OgsZ6
Original mention - @Otterly

100% fatal brain disease strikes 3 people in Oregon​

By Nicoletta Lanese published yesterday
Hood River County in Oregon reported three cases of Creutzfeldt-Jakob disease, a rare human brain disease very similar to "mad cow."

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Three cases of a mad cow-like disease with a 100% fatality rate have been reported in a single county in Oregon.

Within the last eight months, health officials have confirmed one case and identified two probable cases of the rare brain disease, according to a statement released by the Hood River County Health Department on April 14. Hood River County is located south of the Columbia River on the Washington-Oregon border. Two of the people with the condition have died, the department reported.

One case was confirmed by autopsy, while the other two are presumptive, The Oregonian reported. Trish Elliott, director of the health department, told The Oregonian that the presumptive cases can only be confirmed after death by examining brain tissue and cerebrospinal fluid — the clear fluid that surrounds the brain and spinal cord — and she said this process can take months.

"At this time, there is no identifiable link between these three cases," the health department added.

The mad cow-like disease reported in Oregon is called Creutzfeldt-Jakob disease (CJD), named for two German doctors who first described the condition in the 1920s. The disease impacts around 1 to 2 people per million worldwide, and the United States sees roughly 350 cases a year. About 23,000 to 24,000 people live in Hood River County, according to census data, so seeing three CJD cases crop up is statistically unusual.

Like mad cow, CJD is a prion disease, meaning it's caused by abnormally folded proteins that damage brain tissue; in CJD, this causes sponge-like holes to form in the brain. The prions also cause normal proteins in the brain to turncoat, transforming into prions that then inflict further damage.

The disease can cause a slew of symptoms, including confusion, disorientation, hallucinations, lack of coordination and muscle stiffness, along with personality changes, new-onset psychological problems, and seizures. The symptoms progress quickly, leaving people with the disease unaware of their surroundings and unable to communicate. The disease is always fatal, with about 70% of those affected dying within a year of diagnosis.

The most common type of CJD is "sporadic," meaning normal proteins in the brain spontaneously transform into prions for unknown reasons. The next most common type is genetic, triggered by inherited mutations in a gene called PRNP. The gene carries instructions to make prion protein (PrP), which is known to be active in the brain but whose normal functions aren't fully understood. Some studies suggest the normal version of PrP may help protect neurons from injury and form connections between neurons.

Perhaps the most famous form of CJD is the rarest, however, accounting for less than 1% of cases. It involves prions entering the body from external sources. For instance, this can occur if a person eats beef from cows that have bovine spongiform encephalopathy (BSE), better known as "mad cow disease;" only seven cases of BSE have ever been detected among cows in the U.S. Another potential source of prions is through medical exposures, such as a person getting a transplant or blood transfusion from a donor with CJD.

To prevent cases of "acquired" CJD, the U.S. has had strict agricultural regulations in place since the 1990s to keep mad cow-affected beef out of the food supply. There are also infection control guidelines to prevent the transmission of CJD through medical procedures.

The Hood River County Health Department has not announced which type of CJD is likely implicated in the recent cases, but Elliott told The Oregonian that they don't think infected cattle are the cause. And again, it appears that the three cases aren't linked to one another, the department noted.

"The risk of getting CJD is extremely low," the department's statement emphasized. "It does not spread through the air, touch, social contact, or water."

The department is conducting an "active and ongoing investigation" of the cases and has partnered with Oregon Health Authority and the Centers for Disease Control and Prevention. "The health department will continue to monitor the situation and keep you informed of any risk to public health."
 
Population ~25,000. Odds of this just sort of happening for no particular reason at the base rate are extremely low. Not impossible of course!
What's worse, prions can't be sterilized, they just lie around forever waiting to infect someone. They're not viruses, like rabies, or even bacteria; they're just misfolded proteins. They can't be killed, because they aren't alive. Fucking terrifying.
Lol, it's not that bad. Viruses aren't "alive" either. But a protein is just a molecule, it can be denatured (or even just destroyed through chemical processes). If you cremate a person's remains, I'm pretty sure the prions would not survive. Excuse me, "survive".
 
Population ~25,000. Odds of this just sort of happening for no particular reason at the base rate are extremely low. Not impossible of course!

Lol, it's not that bad. Viruses aren't "alive" either. But a protein is just a molecule, it can be denatured (or even just destroyed through chemical processes). If you cremate a person's remains, I'm pretty sure the prions would not survive. Excuse me, "survive".
Temperatures need to be between 1,100F to 1,800F to neutralize them. The average temperature in retorts (for humans) is between 1,400 to 1,800F, so cremation should do the job.
 
I think there is also a surgery/tissue link in a hospital, once due to improper cleaning of surgical tools regarding eye surgery for elderly patients, where five or so people caught it all in the same city.
Skin grafts from infected tissue will also give you CJD. There were 132 known cases in Japan up to 2008 because the disease actually can incubate for years, and these grafts had happened between 1978 and 1993.

So this was either very fast-acting, or they had gotten the same surgery some years ago.
 
I think there is also a surgery/tissue link in a hospital, once due to improper cleaning of surgical tools regarding eye surgery for elderly patients, where five or so people caught it all in the same city.
Imagine going blind from old age so you get an implant to stop it but instead you get a brain disease that's Alzheimer's on crack.

What a horrible way to go.
 
given my experience with Oregon it's probably this
Hood River is close enough to Portland that it's entirely shitlib dominated. If there are medical problems, it's from DEI hires and not funding at least.
 
Oh boy, something I know an autistic amount about! I love these kinds of threads!
Three cases is neither "sporadic" nor "genetic". Motherfuckers are eating brains.
Or spinal cord tissue. Prions are also known to hang out in neurological tissue afaik

I say again: Prion diseases are pure fucking nightmare fuel. They are untreatable and fatal. Period.

What's worse, prions can't be sterilized, they just lie around forever waiting to infect someone. They're not viruses, like rabies, or even bacteria; they're just misfolded proteins. They can't be killed, because they aren't alive. Fucking terrifying.
They're literally a fucked up building block of cellular growth. Also sometimes they can just appear out of fucking nowhere. CJD isn't even the only prion related disease in humans either.
Skin grafts from infected tissue will also give you CJD. There were 132 known cases in Japan up to 2008 because the disease actually can incubate for years, and these grafts had happened between 1978 and 1993.

So this was either very fast-acting, or they had gotten the same surgery some years ago.
I know there was a series of infections from improperly treated dura mater grafts as well.

I really do think there is a link between these three cases and it's not food-related (unless they're hunting deer with Chronic Wasting Disease, which is like the deer equivalent, and there's an epidemic in that area that local biologists aren't aware of.)

My guess? Check neurology specialty suites in the region.
 
It's not very similar to mad cow disease it is mad cow disease which you other countries definitely didn't lie about getting last time...

At least that town will be banned from donating blood like us Brits in America now right.
Right?
That ban has now been lifted. Which figures,letting faggots donate blood is far riskier and they're allowed to as well.
 
Either they ate infected deer meet, or zombies, one of the two
We are overdue for CWD to jump from infected deer populations to humans i recall New Brunswick, Canada having a large occurrence of CJD like cases that didn't register on tests. Deer are kinda the perfect vector you have high population density due to a lack of natural predators near human mixed with an animal that will readily scavenge carrion when its can.
 
Can't this also spread from cannibalism?
Yes, in PNG it is called Kuru.
But transmission from eating cow meat is also from (indirect) caniballism.

When this got famous in the 80s/90s it was because Brittish farmers would grind down the remains of cows, including the brain, after slaughter and all human edible pieces were removed, and then feed these remains as a protein-rich food to the other cows.

So, you got it either directly from human canniballism or you could get it indirectly from cow-canniballism.
There are also non-cannibal-related ways to get it but that is very boring so I pretend those vectors do not exist.
 
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Skin grafts from infected tissue will also give you CJD. There were 132 known cases in Japan up to 2008 because the disease actually can incubate for years, and these grafts had happened between 1978 and 1993.

So this was either very fast-acting, or they had gotten the same surgery some years ago.
That means there is hope that Amhole autist Kevin Gibes gets a Creutzfeldt–Jakob-stinkditch,
 
Population ~25,000. Odds of this just sort of happening for no particular reason at the base rate are extremely low. Not impossible of course!

Lol, it's not that bad. Viruses aren't "alive" either. But a protein is just a molecule, it can be denatured (or even just destroyed through chemical processes). If you cremate a person's remains, I'm pretty sure the prions would not survive. Excuse me, "survive".
Although viruses aren’t “alive” they nonetheless replicate in a nucleic acid dependent manner such that damaging enough of the given’s DNA/RNA would render them innocuous. With these prion diseases the proteins do not need a proper sequence to retain virality, rather it is maintenance of a particular 3d structure which induces changes in healthy proteins. This prion-structure is usually a minimum in the folding landscape such that “denaturing” wouldn’t be possible beyond total destruction of the protein (presumably through thermic, chemical, or protease means). Renaturing is possible through chaperone proteins/RNA, which is how such misfolded proteins are handled endogenously, but the success of such efforts depends on the protein. Such matters come to roost in food safety as the temperatures needed to sterilize most pathogens are generally insufficient at destroying these prions (chemical/protease methods would likely fare better, but they aren’t exactly applicable for foodstuffs), hence the outbreaks of mad cow disease. The reasons prion diseases are rare is because cannibalism is rare (for both humans and their livestock), but if some schmucks start feeding their cattle eachother (or other such animals which can spontaneously develop prions post mortem) it could become quite the scary problem. I guess we’ll have to wait and see what was the cause in this case, it very well may have been the more common, non-prionic, CJD arising in proximity by mere happenstance.
 
Such matters come to roost in food safety as the temperatures needed to sterilize most pathogens are generally insufficient at destroying these prions (chemical/protease methods would likely fare better, but they aren’t exactly applicable for foodstuffs)
Ha, yeah unless you like eating plain carbon you're probably not going to be destroying them in food with temperature. Thanks for the info on folding landscape. Prions present some unique and unfortunate challenges for sterilization, kill you in horrifying ways, and to top it off they're linked to cannibalism; but often when people are describing them, they make them sound like an eldritch abomination, which is...well, maybe partially appropriate. I actually remember Michael Moore describing them that way, including the whole "they're not alive so you can't kill them" thing, in one of his books.
 
Hood River is close enough to Portland that it's entirely shitlib dominated. If there are medical problems, it's from DEI hires and not funding at least.

DEI hires in Oregon are very, very high level, see my ranting on the Albany sex offender enrolling in high school thread for an example

Oregon manages melinated levels of dysfunction with no melanin whatsoever, just commies no darkies
 
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