Monday, July 21, 2008

Officials await tests on man for human Mad Cow Disease (Texas)

Officials await tests on man for human Mad Cow Disease

By Mary Ann Cavazos (Contact) Originally published 05:30 p.m., July 21, 2008 Updated 05:30 p.m., July 21, 2008

CORPUS CHRISTI — Local health officials are awaiting test results to determine whether a Corpus Christi man who died earlier this month had the human form of mad cow disease.
Annette Rodriguez, interim director of the Corpus Christi-Nueces County Health District, said the district was notified by officials from a local hospital that a patient may have had Creutzfeldt-Jakob disease.

A brain biopsy is needed to confirm if the man had the disease and whether it is the variant linked to mad cow. Those results will come from out-of-state and will be available in about two months, Rodriguez said.

According to the Centers for Disease Control and Prevention’s Web site, variant Creutzfeldt-Jakob disease is a rare but fatal brain disorder in humans.

It is believed that humans can become infected by consuming contaminated meat or through a blood transfusion from a person who already has the disease.

The man, whose identity and age were not released, traveled extensively and it is unclear where he may have been exposed to the disease, Rodriguez said.

“He traveled all over the world,” she said

CJD TEXAS (cjd clusters)

don't these dummies know by now that the USA does not have any mad cow disease and or any human cjd ramifications from a mad cow, cause the USDA says so... NOT

there has been a decade old, systematic cover-up of corporate homicide just because of trade, futures and commodities. the elderly demented, your grandma and grandpa, mom and dad, sisters and brothers, are all expendable, due to the fact the American joe-cue-public is just to damn lazy to care. the elderly and demented are expendable. but mark my word here and now, it's here, and has been, call it what you like.....

10 people killed by new CJD-like disease

Public release date: 9-Jul-2008

Since Gambetti's team wrote a paper describing an initial 11 cases referred to his centre between 2002 and 2006 (Annals of Neurology, vol 63, p 697), another five have come to light. "So it is possible that it could be just the tip of the iceberg," Gambetti says.


sporadic CJD, the big lie

Thursday, July 10, 2008 A Novel Human Disease with Abnormal Prion Protein Sensitive to Protease update July 10, 2008

Thursday, July 10, 2008 A New Prionopathy update July 10, 2008

MAD COW DISEASE terminology UK c-BSE (typical), atypical BSE H or L, and or Italian L-BASE

Saturday, June 21, 2008 HUMAN and ANIMAL TSE Classifications i.e. mad cow disease and the UKBSEnvCJD only theory JUNE 2008

if you will notice on the forms page on the cjd foundation site, there is not cjd questionnaire ??? strange...

vCJD questionnaire


why is a cjd questionnaire not listed on the cjd foundation 'forms' site with the rest of their forms ???

i thought they had one now going out to all families of victims of a human TSE???

this is very important that a _written_ cjd questionnaire, asking extensive questions pertaining to any potential route and source of the TSE agent be submitted to every family of a victim of a human TSE. this is key to finding cause. so why is this still so difficult? are the families of CJD victims getting these written cjd questionnaires??? i hope so....

The statistical incidence of CJD cases in the United States has been revised to reflect that there is

_one case per 9000 in adults age 55 and older_.

Eighty-five percent of the cases are sporadic, meaning there is no known cause at present.



Sunday, July 20, 2008 Red Cross told to fix blood collection or face charges 15 years after warnings issued, few changes made to ensure safety

we know how clusters are handled in NJ too. as long as the infamous UKBSEnvCJD only theory is in play, the CDC et al will play it out to the T. no other science will exist, and it does not matter that the last two mad cows in the USA were atypical BSE. as old stan said, nothing else matters, just the beef crossing the borders. just because science is now pointing to not only BSE to nvCJD, but atypical BSE looking like some sub types of sporadic CJD, atypical scrapie looking also like some sub types of sporadic CJD. CWD to humans as ? come on folks, how long can this same sad masquerade keep on playing out$$$

An Evaluation of a Suspected Cluster of Creutzfeldt-Jakob Disease (CJD) in New Jersey May 2004 Division of Epidemiology, Environmental and Occupational Health


If consumption of BSE contaminated beef at the GSRT between 1988 and 1992 caused sporadic CJD, the data should show increases in the numbers of case-patients by now, assuming the same lag (incubation) period as vCJD.


The Case of the Cherry Hill Cluster By D.T. MAX

Published: March 28, 2004

-- the scientists who say it exists; the heartbroken family members who doubt it. Early, deep in his grief, he would sign his e-mail messages to scientists, ''I am the madson of a deadmom who died of madcow.'' Singeltary turned out to be helpful for Skarbek. He pointed her to a paper that was published in 2002 in the journal of the European Molecular Biology Organization by John Collinge, the premier prion researcher in England. Collinge argued that experiments conducted in mice suggest that infections with mad cow can sometimes look like sporadic C.J.D. Collinge accepted the implications: he recommended that ''serious consideration should be given'' to the idea that some of the more recent sporadic C.J.D. cases in Europe were in fact related to mad cow disease.

i hate to inform them, but sporadic CJD has increased. sporadic CJD in the USA went from 28 cases _documented_ in 1997, to 170 cases of sporadic CJD _documented_ in 2007. i'm not a math wiz, but looks like an increase to me. ...

6 Includes 55 cases with type determination pending in which the diagnosis of vCJD has been excluded.

hmmm, they can exclude vCJD, but yet include them as a prion disease, but yet not know what the hell it is, and at the same time, keep telling everyone i.e. media, that ;

>>>Further tests will be conducted to determine the cause of the Cape patient's illness, but state disease trackers said there is nothing to suggest that the patient's case is associated with mad cow disease. Instead, like virtually all cases in the United States, it is almost certainly not linked to any obvious external cause.<<<

stupid is, as stupid does, and joe-q-public continues to believe this garbage. ...TSS
He added that because the CDC only provide information on diseases, they have no plans
to make a separate press release on the issue including the result of the investigation.
and that is the way they plan to keep it, all spontaneous, sporadic, no route, no source $$$

DEEP THROAT TO TSS 2000-2001 (take these old snips of emails with how ever many grains of salt you wish. ...tss)

The most frightening thing I have read all day is the report of Gambetti's finding of a new strain of sporadic cjd in young people...

Dear God, what in the name of all that is holy is that!!! If the US has different strains of scrapie.....why????than the UK...

then would the same mechanisms that make different strains of scrapie here make different strains of BSE...if the patterns are different in sheep and mice for scrapie.....could not the BSE be different in the cattle, in the mink, in the humans.......I really think the slides or tissues and everything from these young people with the new strain of sporadic cjd should be put up to be analyzed by many, many experts in cjd........bse.....scrapie Scrape the damn slide and put it into mice.....wait.....chop up the mouse brain and and spinal cord........put into some more mice.....dammit amplify the thing and start the damned research.....This is NOT rocket science...we need to use what we know and get off our butts and move....the whining about how long everything takes.....well it takes a whole lot longer if you whine for a year and then start the research!!!

Not sure where I read this but it was a recent press release or something like that: I thought I would fall out of my chair when I read about how there was no worry about infectivity from a histopath slide or tissues because they are preserved in formic acid, or formalin or formaldehyde.....for God's sake........ Ask any pathologist in the UK what the brain tissues in the formalin looks like after a is a big fat sponge...the agent continues to eat the brain can't make slides anymore because the agent has never stopped........and the old slides that are stained with Hemolysin and Eosin......they get holier and holier and degenerate and continue...what you looked at 6 months ago is not there........Gambetti better be photographing every damned thing he is looking at.....

Okay, you need to know. You don't need to pass it on as nothing will come of it and there is not a damned thing anyone can do about it. Don't even hint at it as it will be denied and laughed at.......... USDA is gonna do as little as possible until there is actually a human case in the USA of the nvcjd........if you want to move this thing along and shake the earth....then we gotta get the victims families to make sure whoever is doing the autopsy is credible, trustworthy, and a saint with the courage of Joan of Arc........I am not kidding!!!! so, unless we get a human death from EXACTLY the same form with EXACTLY the same histopath lesions as seen in the UK nvcjd........forget any is ALL gonna be sporadic!!!

And, if there is a case.......there is gonna be every effort to link it to international travel, international food, etc. etc. etc. etc. etc. They will go so far as to find out if a sex partner had ever traveled to the UK/europe, etc. etc. .... It is gonna be a long, lonely, dangerous twisted journey to the truth. They have all the cards, all the money, and are willing to threaten and carry out those threats....and this may be their biggest downfall...

Thanks as always for your help. (Recently had a very startling revelation from a rather senior person in government here..........knocked me out of my must keep pushing. If I was a power person....I would be demanding that there be a least a million bovine tested as soon as possible and agressively seeking this disease. The big players are coming out of the woodwork as there is money to be made!!! In short: "FIRE AT WILL"!!! for the very dumb....who's "will"! "Will be the burden to bare if there is any coverup!"

again it was said years ago and it should be taken seriously....BSE will NEVER be found in the US! As for the BSE conference call...I think you did a great service to freedom of information and making some people feign integrity...I find it scary to see that most of the "experts" are employed by the federal government or are supported on the "teat" of federal funds. A scary picture! I hope there is a confidential panel organized by the new government to really investigate this thing.

You need to watch your back........but keep picking at a buzzard to the just may get to the truth!!! (You probably have more support than you know. Too many people are afraid to show you or let anyone else know. I have heard a few things myself... you ask the questions that everyone else is too afraid to ask.)



1 comment:

Terry S. Singeltary Sr. said...

Biopsy on brain indicates man free of mad cow By Elaine Marsilio (Contact)

Originally published 10:15 a.m., November 12, 2008 Updated 11:43 p.m., November 12, 2008

CORPUS CHRISTI — Brain biopsy results on a Corpus Christi man who died in July and who officials thought may have had a form of mad cow disease determined he didn't have the illness, officials said Wednesday.

The Corpus Christi-Nueces County Health District announced that results confirmed the man had prion disease with characteristics of a fatal brain disorder. But in this case the man, who was older than 60, contracted a form of the disease called Creutzfeldt-Jakob Disease that isn't linked to mad cow disease, said Mike Hacker, health district acting assistant director.

Officials would not release the man's name, citing privacy laws.

Prion disease, a family of rare neurodegenerative disorders, affects both humans and animals, according to the Centers for Disease Control and Prevention Web site. Certain types of prion disease only occur in humans. The CDC defines Creutzfeldt-Jakob Disease as a neurodegnerative disease that infects the brain with "sponge-like lesions" and typically results in death within a year of the disease's early stages.

A local physician who treated the man ordered a brain biopsy of the man to determine what disease he had, Hacker said, noting he didn't think the man's cause of death had been determined.

The Creutzfeldt-Jakob Disease Foundation Inc. Web site defines the sporadic form of the disease as not having a definite cause. The disease tends to cause conditions like mental deterioration or blindness.

Hacker agreed the disease is rare, but always fatal once contracted.

"It's not like a disease you can catch from someone else," he said.

Contact Elaine Marsilio at 886-3794 or

Tuesday, November 11, 2008

Transmission of atypical bovine prions to mice transgenic for human prion protein
DOI: 10.3201/eid1412.080941