Showing posts with label APHIS-2008-0010-0008 RIN:0579-AC68 BSE BOVINE SPONGIFORM ENCEPHALOPATHY CJD TSE PRION ATYPICAL. Show all posts
Showing posts with label APHIS-2008-0010-0008 RIN:0579-AC68 BSE BOVINE SPONGIFORM ENCEPHALOPATHY CJD TSE PRION ATYPICAL. Show all posts

Wednesday, April 4, 2012

Bovine Spongiform Encephalopathy; Importation of Bovines and Bovine Products APHIS-2008-0010-0008 RIN:0579-AC68







Family friend of John Gummer is killed by CJD aged 23 By ANDREW LEVY

Last updated at 19:16 11 October 2007

Elizabeth Smith: She learned on her 21st birthday that she had vCJD

A family friend of former Tory agriculture minister John Gummer has died from the human form of mad cow disease.

Elizabeth Smith died last week, more than two years after learning on her 21st birthday that she had new variant Creutzfeldt-Jakob disease.

Her father, retired vicar Roger Smith, is a friend of Mr Gummer, a former parishioner who famously attempted to allay fears about BSE in 1990 when he publicly fed a burger to his four-year-old daughter, Cordelia.

At the time, Mr Gummer said: "I can assure the public there is no cause for concern.

"The Government has taken all the advice it can from the experts. Their conclusion is that beef is perfectly safe."

University student Miss Smith quit her course days after the diagnosis in March 2005 and soon became so ill she needed round-the-clock treatment.

She was 23 when she died at her parents' home. Yesterday, they paid tribute to their "active and intelligent" daughter.

Mr Smith, of St Margaret South Elmham in Suffolk, said: "By the time she came home she had trouble swallowing and then couldn't swallow at all, so for the last two-and-a-half years she was fitted with a gastro-tube.

"After that the disease was remorseless in the way that it killed her off. She was unable to walk for the last two years of her life and couldn't speak or smile.

"Elizabeth had to be cared for 24 hours a day, seven days a week.

It's safe: John Gummer feeds his daughter Cordelia a burger

"She was more helpless for those last two years than when she was born - at least then she could move her arms and cry but by the end she couldn't even do that."

Describing her daughter's 21st birthday, Molly Smith said: "That was the worst time because we all had to cope with the fact that she was going to die.

"Elizabeth was clever, bright and intelligent. If she had been able to do her final exams she would have got a very good degree.

"She wanted to do primary school teaching and had a place on a postgraduate training course."

Miss Smith, who had a brother, Andrew, 39, passed four A-levels before going to Birmingham University in 2002 to read geography.

She first became ill in August 2004 but it was not until seven months later that she was told by doctors she had vCJD.

Mr Smith said yesterday that he was "99.9 per cent certain" that his daughter's illness had been caused by contaminated beef.

But he refused to blame Mr Gummer, saying the episode with the burger had not changed the way he viewed meat.

He added: "One of the few comforting thoughts is that almost certainly Elizabeth's degree of awareness in the last two years of her life was minimal. Some doctors would say that vCJD is far more painful to watch than suffer."

Miss Smith was the 162nd person to die from new variant CJD, which was first identified in 1996 after being linked to an outbreak of BSE (bovine spongiform encephalopathy) in cattle. vCJD slowly destroys the brain, giving it a sponge-like appearance.

It is thought to be caused by the build up in the brain of an abnormal form of the naturally occurring prion protein.

Most cases have developed as a result of eating infected meat, although five victims have been vegetarians. The disease has also been transmitted by blood transfusion and infected surgical equipment.

Mr Gummer was not available for comment yesterday.

http://www.dailymail.co.uk/health/article-487074/Family-friend-John-Gummer-killed-CJD-aged-23.html
 
 GOVERNOR RICK PERRY TEXAS PHOTO OP



https://ichef.bbci.co.uk/news/304/media/images/59522000/jpg/_59522150_perry.jpg

Subject: Bovine Spongiform Encephalopathy; Importation of Bovines and Bovine Products APHIS-2008-0010-0008 RIN:0579-AC68

Comment from Terry Singeltary

Document ID: APHIS-2008-0010-0008 Document Type: Public Submission

This is comment on Proposed Rule: Bovine Spongiform Encephalopathy; Importation of Bovines and Bovine Products

Docket ID: APHIS-2008-0010 RIN:0579-AC68

Topics: No Topics associated with this document
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Document Subtype: Public Comment

Status: Posted

Received Date: March 22 2012, at 12:00 AM Eastern Daylight Time

Date Posted: March 22 2012, at 12:00 AM Eastern Daylight Time

Comment Start Date: March 16 2012, at 12:00 AM Eastern Daylight Time

Comment Due Date: May 15 2012, at 11:59 PM Eastern Daylight Time

Tracking Number: 80fdd617

First Name: Terry

Middle Name: S.

Last Name: Singeltary

City: Bacliff

Country: United States

State or Province: TX

Organization Name: CJD TSE PRION

Submitter's Representative: CONSUMERS

Comment:

comment submission

Document ID APHIS-2008-0010-0001

Greetings USDA, OIE et al,

what a difference it makes with science, from one day to the next. i.e. that mad cow gold card the USA once held. up until that fateful day in December of 2003, the science of BSE was NO IMPORTS TO USA FROM BSE COUNTRY. what a difference a day makes$ now that the shoe is on the other foot, the USDA via the OIE, wants to change science again, just for trade $ I implore the OIE decision and policy makers, for the sake of the world, to refuse any status quo of the USA BSE risk assessment. if at al, the USA BSE GBR should be raise to BSE GBR IV, for the following reasons. North America is awash with many different TSE Prion strains, in many different species, and they are mutating and spreading. IF the OIE, and whatever policy makers, do anything but raise the risk factor for BSE in North America, they I would regard that to be highly suspicious. IN fact, it would be criminal in my opinion, because the OIE knows this, and to knowingly expose the rest of the world to this dangerous pathogen, would be ‘knowingly’ and ‘willfully’, just for the almighty dollar, once again. I warned the OIE about all this, including the risk factors for CWD, and the fact that the zoonosis potential was great, way back in 2002. THE OIE in collaboration with the USDA, made the legal trading of the atypical Nor-98 Scrapie a legal global commodity. yes, thanks to the OIE and the USDA et al, it’s now legal to trade the atypical Nor-98 Scrapie strain all around the globe. IF you let them, they will do the same thing with atypical BSE and CWD (both strains to date). This with science showing that indeed these TSE prion strains are transmissible. I strenuously urge the OIE et al to refuse any weakening to the USA trade protocols for the BSE TSE prion disease (all strains), and urge them to reclassify the USA with BSE GBR IV risk factor.


SEE REFERENCE SOURCES IN ATTACHMENTS


SEE Terry S. Singeltary Sr. Attachment WORD FILE ;


http://www.regulations.gov/#!documentDetail;D=APHIS-2008-0010-0008


http://www.regulations.gov/#!docketDetail;D=APHIS-2008-0010


Sunday, March 11, 2012


APHIS Proposes New Bovine Spongiform Encephalopathy Import Regulations in Line with International Animal Health Standards Proposal Aims to Ensure Health of the U.S. Beef Herd, Assist in Negotiations


http://transmissiblespongiformencephalopathy.blogspot.com/2012/03/aphis-proposes-new-bovine-spongiform.html


L-BSE, TME, AND SPORADIC CJD aka mad cow disease in North America


Moreover, transmission experiments to non-human primates suggest that some TSE agents in addition to Classical BSE prions in cattle (namely L-type Atypical BSE, Classical BSE in sheep, transmissible mink encephalopathy (TME) and chronic wasting disease (CWD) agents) might have zoonotic potential.

snip...


http://www.efsa.europa.eu/en/efsajournal/pub/e991.htm?emt=1


http://www.efsa.europa.eu/en/efsajournal/doc/e991.pdf


Thursday, August 12, 2010

Seven main threats for the future linked to prions

First threat

The TSE road map defining the evolution of European policy for protection against prion diseases is based on a certain numbers of hypotheses some of which may turn out to be erroneous. In particular, a form of BSE (called atypical Bovine Spongiform Encephalopathy), recently identified by systematic testing in aged cattle without clinical signs, may be the origin of classical BSE and thus potentially constitute a reservoir, which may be impossible to eradicate if a sporadic origin is confirmed.

***Also, a link is suspected between atypical BSE and some apparently sporadic cases of Creutzfeldt-Jakob disease in humans. These atypical BSE cases constitute an unforeseen first threat that could sharply modify the European approach to prion diseases.

Second threat

snip...


http://www.neuroprion.org/en/np-neuroprion.html


Saturday, June 25, 2011


Transmissibility of BSE-L and Cattle-Adapted TME Prion Strain to Cynomolgus Macaque


Emmanuel Comoy,1,† Valérie Durand,1 Evelyne Correia,1 Sophie Freire,1 Jürgen Richt,2 Justin Greenlee,3 Juan-Maria Torres,4 Paul Brown,1 Bob Hills5 and Jean-Philippe Deslys1

1Atomic Energy Commission; Fontenay-aux-Roses, France; 2Kansas State University; Manhattan, KS USA; 3USDA; Ames, IA USA; 4INIA; Madrid, Spain; 5Health Canada; Ottawa, ON Canada†Presenting author; Email: emmanuel.comoy@cea.fr

The epidemiology of Transmissible mink encephalopathy (TME) indicates an alimentary origin. Several inter-species transmission experiments have not succeeded in establishing with certainty any natural reservoir of this prion strain, although both ovine and bovine sources have been suspected. Cattle exposed to TME develop a spongiform encephalopathy that is distinct from classical Bovine Spongiform Encephalopathy (c-BSE).

Inoculation of c-BSE to cynomolgus macaque provided early evidence of a possible risk to humans, and remains an important model to define the risk of both primary (oral transmission from cattle to primate) and secondary (intravenous intra-species transmission) exposures. We have also evaluated the transmissibility of other cattle prion strains to macaques, including L- and H- atypical forms of BSE, namely BSE-L and BSE-H, and cattle-adapted TME.

BSE-L induced a neurological disease distinct from c-BSE. Peripheral exposures demonstrate the transmissibility of BSE-L by oral, intravenous, and intra-cerebral routes, with incubation periods similar to c-BSE. Cattle-adapted TME also induced a rapid disease in cynomolgus macaque. The clinical features, lesion profile, and biochemical signature of the induced disease was similar to the features observed in animals exposed to BSE-L, suggesting a link between the two prion strains. Secondary transmissions to a common host (transgenic mouse overexpressing bovine PrP) of cattle-TME and BSE-L before or after passage in primates induced diseases with similar incubation periods: like the c-BSE strain, these cattle strains maintained their distinctive features regardless of the donor species and passages.

If the link between TME and BSE-L is confirmed, our results would suggest that BSE-L in North America may have existed for decades, and highlight a possible preferential transmission of animal prion strains to primates after passage in cattle.

=====================end...tss====================

link url not available, please see PRION 2011 ;

http://www.prion2011.ca/files/PRION_2011_-_Posters_(May_5-11).pdf


Volume 13, Number 12–December 2007
Research

Phenotypic Similarity of Transmissible Mink Encephalopathy in Cattle and L-type Bovine Spongiform Encephalopathy in a Mouse Model

Thierry Baron,* Anna Bencsik,* Anne-Gaëlle Biacabe,* Eric Morignat,* andRichard A. Bessen†*Agence Française de Sécurité Sanitaire des Aliments–Lyon, Lyon, France; and†Montana State University, Bozeman, Montana, USA

Abstract

Transmissible mink encepholapathy (TME) is a foodborne transmissible spongiform encephalopathy (TSE) of ranch-raised mink; infection with a ruminant TSE has been proposed as the cause, but the precise origin of TME is unknown. To compare the phenotypes of each TSE, bovine-passaged TME isolate and 3 distinct natural bovine spongiform encephalopathy (BSE) agents (typical BSE, H-type BSE, and L-type BSE) were inoculated into an ovine transgenic mouse line (TgOvPrP4). Transgenic mice were susceptible to infection with bovine-passaged TME, typical BSE, and L-type BSE but not to H-type BSE. Based on survival periods, brain lesions profiles, disease-associated prion protein brain distribution, and biochemical properties of protease-resistant prion protein, typical BSE had a distint phenotype in ovine transgenic mice compared to L-type BSE and bovine TME.The similar phenotypic properties of L-type BSE and bovine TME in TgOvPrP4 mice suggest that L-type BSE is a much more likely candidate for the origin of TME than is typical BSE.

snip...

Conclusion

These studies provide experimental evidence that the Stetsonville TME agent is distinct from typical BSE but has phenotypic similarities to L-type BSE in TgOvPrP4 mice. Our conclusion is that L-type BSE is a more likely candidate for a bovine source of TME infection than typical BSE. In the scenario that a ruminant TSE is the source for TME infection in mink, this would be a second example of transmission of a TSE from ruminants to non-ruminants under natural conditions or farming practices in addition to transmission of typical BSE to humans, domestic cats, and exotic zoo animals(37). The potential importance of this finding is relevant to L-type BSE, which based on experimental transmission into humanized PrP transgenic mice and macaques, suggests that L-type BSE is more pathogenic for humans than typical BSE (24,38).

http://www.cdc.gov/eid/content/13/12/1887.htm?s_cid=eid1887_e


PLEASE NOTE *

Over the next 8-10 weeks, approximately 40% of all the adult mink on the farm died from TME.

snip...

The rancher was a ''dead stock'' feeder using mostly (>95%) downer or dead dairy cattle...


http://web.archive.org/web/20030516051623/http://www.bseinquiry.gov.uk/files/mb/m09/tab05.pdf

PLoS One. 2012; 7(2): e31449.

Published online 2012 February 21. doi: 10.1371/journal.pone.0031449

PMCID: PMC3283643


Infectivity in Skeletal Muscle of Cattle with Atypical Bovine Spongiform Encephalopathy

The present data offer novel information on the tropism of the BASE agent and highlight relevant public health issues. While the transmission barrier for classical BSE is high in most species, BASE prions are readily transmissible to a variety of mammals including non-human primates [11]–[13], [35]. Accordingly, the possibility of spreading of BASE prions through skeletal muscle to other species should be taken into account and evaluated in risk analysis studies.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283643/?tool=pubmed

Thursday, March 29, 2012

atypical Nor-98 Scrapie has spread from coast to coast in the USA 2012

NIAA Annual Conference April 11-14, 2011San Antonio, Texas

http://nor-98.blogspot.com/2012/03/atypical-nor-98-scrapie-has-spread-from.html


WHICH CAME FIRST, THE CART OR THE HORSE ???

Minnesota

CAPTIVE CWD CONFIRMED 2002

FREE RANGING CWD CONFIRMED 2011

http://wwwnc.cdc.gov/eid/article/18/3/11-0685-f1.htm

Colorado

Captive CWD discovered 1967

Free ranging CWD discovered 1981

PLEASE STUDY THIS MAP !

SEE CWD MAP, RELATE TO DATES OF GAME FARM INFECTION, TO DATE OF INFECTION RATE IN WILD, SURROUNDING SAID INFECTED GAME FARMS. ...TSS

http://wwwnc.cdc.gov/eid/article/18/3/11-0685-f1.htm


*** Chronic Wasting Disease CWD CDC REPORT MARCH 2012 ***

Saturday, February 18, 2012

Occurrence, Transmission, and Zoonotic Potential of Chronic Wasting Disease

CDC Volume 18, Number 3—March 2012

SNIP...

Long-term effects of CWD on cervid populations and ecosystems remain unclear as the disease continues to spread and prevalence increases. In captive herds, CWD might persist at high levels and lead to complete herd destruction in the absence of human culling. Epidemiologic modeling suggests the disease could have severe effects on free-ranging deer populations, depending on hunting policies and environmental persistence (8,9). CWD has been associated with large decreases in free-ranging mule deer populations in an area of high CWD prevalence (Boulder, Colorado, USA) (5).

SNIP...

Reasons for Caution There are several reasons for caution with respect to zoonotic and interspecies CWD transmission. First, there is strong evidence that distinct CWD strains exist (36). Prion strains are distinguished by varied incubation periods, clinical symptoms, PrPSc conformations, and CNS PrPSc depositions (3,32). Strains have been identified in other natural prion diseases, including scrapie, BSE, and CJD (3). Intraspecies and interspecies transmission of prions from CWD-positive deer and elk isolates resulted in identification of >2 strains of CWD in rodent models (36), indicating that CWD strains likely exist in cervids. However, nothing is currently known about natural distribution and prevalence of CWD strains. Currently, host range and pathogenicity vary with prion strain (28,37). Therefore, zoonotic potential of CWD may also vary with CWD strain. In addition, diversity in host (cervid) and target (e.g., human) genotypes further complicates definitive findings of zoonotic and interspecies transmission potentials of CWD. Intraspecies and interspecies passage of the CWD agent may also increase the risk for zoonotic CWD transmission. The CWD prion agent is undergoing serial passage naturally as the disease continues to emerge. In vitro and in vivo intraspecies transmission of the CWD agent yields PrPSc with an increased capacity to convert human PrPc to PrPSc (30). Interspecies prion transmission can alter CWD host range (38) and yield multiple novel prion strains (3,28). The potential for interspecies CWD transmission (by cohabitating mammals) will only increase as the disease spreads and CWD prions continue to be shed into the environment. This environmental passage itself may alter CWD prions or exert selective pressures on CWD strain mixtures by interactions with soil, which are known to vary with prion strain (25), or exposure to environmental or gut degradation. Given that prion disease in humans can be difficult to diagnose and the asymptomatic incubation period can last decades, continued research, epidemiologic surveillance, and caution in handling risky material remain prudent as CWD continues to spread and the opportunity for interspecies transmission increases. Otherwise, similar to what occurred in the United Kingdom after detection of variant CJD and its subsequent link to BSE, years of prevention could be lost if zoonotic transmission of CWD is subsequently identified, SNIP...SEE FULL TEXT ;


*** Chronic Wasting Disease CWD CDC REPORT MARCH 2012 ***

Saturday, February 18, 2012

Occurrence, Transmission, and Zoonotic Potential of Chronic Wasting Disease

CDC Volume 18, Number 3—March 2012

http://wwwnc.cdc.gov/eid/article/18/3/11-0685_article.htm

see much more here ;

http://chronic-wasting-disease.blogspot.com/2012/02/occurrence-transmission-and-zoonotic.html

Sunday, January 22, 2012

Chronic Wasting Disease CWD cervids interspecies transmission

http://chronic-wasting-disease.blogspot.com/2012/01/chronic-wasting-disease-cwd-cervids.html

Thursday, January 26, 2012

The Risk of Prion Zoonoses

Science 27 January 2012: Vol. 335 no. 6067 pp. 411-413 DOI: 10.1126/science.1218167

http://transmissiblespongiformencephalopathy.blogspot.com/2012/01/risk-of-prion-zoonoses.html

Thursday, January 26, 2012

Facilitated Cross-Species Transmission of Prions in Extraneural Tissue

Science 27 January 2012: Vol. 335 no. 6067 pp. 472-475 DOI: 10.1126/science.1215659

http://transmissiblespongiformencephalopathy.blogspot.com/2012/01/facilitated-cross-species-transmission.html

CJD9/10022

October 1994

Mr R.N. Elmhirst Chairman British Deer Farmers Association Holly Lodge Spencers Lane BerksWell Coventry CV7 7BZ

Dear Mr Elmhirst,

CREUTZFELDT-JAKOB DISEASE (CJD) SURVEILLANCE UNIT REPORT

Thank you for your recent letter concerning the publication of the third annual report from the CJD Surveillance Unit. I am sorry that you are dissatisfied with the way in which this report was published.

The Surveillance Unit is a completely independant outside body and the Department of Health is committed to publishing their reports as soon as they become available. In the circumstances it is not the practice to circulate the report for comment since the findings of the report would not be amended. In future we can ensure that the British Deer Farmers Association receives a copy of the report in advance of publication.

The Chief Medical Officer has undertaken to keep the public fully informed of the results of any research in respect of CJD. This report was entirely the work of the unit and was produced completely independantly of the the Department.

The statistical results reqarding the consumption of venison was put into perspective in the body of the report and was not mentioned at all in the press release. Media attention regarding this report was low key but gave a realistic presentation of the statistical findings of the Unit. This approach to publication was successful in that consumption of venison was highlighted only once by the media ie. in the News at one television proqramme.

I believe that a further statement about the report, or indeed statistical links between CJD and consumption of venison, would increase, and quite possibly give damaging credence, to the whole issue. From the low key media reports of which I am aware it seems unlikely that venison consumption will suffer adversely, if at all.


http://web.archive.org/web/20030511010117/http://www.bseinquiry.gov.uk/files/yb/1994/10/00003001.pdf


THIRD CJD REPORT UK 1994

snip...

Consumption of venison and veal was much less widespread among both cases and controls. For both of these meats, there was evidence of a trend with increasing frequency of consumption being associated with increasing risk of CJD. These associations were largely unchanged when attention was restricted to pairs with data obtained from relatives. ...


http://www.cjd.ed.ac.uk/Archive%20reports/report3.pdf


Saturday, March 10, 2012

Enhanced Surveillance Strategies for Detecting and Monitoring Chronic Wasting Disease in Free-Ranging Cervids Open-File Report 2012–1036 National Wildlife Health Center

Open-File Report 2012–1036

http://chronic-wasting-disease.blogspot.com/2012/03/enhanced-surveillance-strategies-for.html


a few things to consider please. one, CWD has already been transmitted to many cattle in the lab (86% in one study). the oral route would have a much longer incubation period, but we already know that CWD will transmit back to cervids via the oral route, very efficiently. the threat of spreading CWD via close contact, like at feeding grounds is great. every bit of science to date shows this. so to congregate deer together by unnatural means is not smart in my opinion. another fear has come to pass as well, another strain of CWD, yes a second strain. and just recently science has shown that a natural case of BSE has been transmitted to a GOAT. These findings demonstrate that when CWD is directly inoculated into the brain of cattle, 86% of inoculated cattle develop clinical signs of the disease.

http://www.ars.usda.gov/research/publications/publications.htm?seq_no_115=194089

Thursday, February 09, 2012

50 GAME FARMS IN USA INFECTED WITH CHRONIC WASTING DISEASE

http://chronic-wasting-disease.blogspot.com/2012/02/50-game-farms-to-date-in-usa-infected.html


and when these game farms claim they are testing, and everything is o.k., think again...


Saturday, February 04, 2012

Wisconsin 16 age limit on testing dead deer Game Farm CWD Testing Protocol Needs To Be Revised

http://chronic-wasting-disease.blogspot.com/2012/02/wisconsin-16-age-limit-on-testing-dead.html


Saturday, November 6, 2010


TAFS1 Position Paper on Position Paper on Relaxation of the Feed Ban in the EU


Berne, 2010 TAFS INTERNATIONAL FORUM FOR TRANSMISSIBLE ANIMAL DISEASES AND FOOD SAFETY a non-profit Swiss Foundation

http://madcowfeed.blogspot.com/2010/11/tafs1-position-paper-on-position-paper.html


Archive Number 20101206.4364 Published Date 06-DEC-2010 Subject PRO/AH/EDR>


Prion disease update 2010 (11) PRION DISEASE UPDATE 2010 (11)


http://www.promedmail.org/direct.php?id=20101206.4364


> > > Ackerman says downed cattle are 50 times more likely to have mad cow disease (also known as Bovine Spongiform Encephalopathy, or BSE) than ambulatory cattle that are suspected of having BSE. Of the 20 confirmed cases of mad cow disease in North America since 1993, at least 16 have involved downer cattle, he said. < < <

don’t forget the children...


PLEASE be aware, for 4 years, the USDA fed our children all across the Nation (including TEXAS) dead stock downer cows, the most high risk cattle for BSE aka mad cow disease and other dangerous pathogens.


who will watch our children for CJD for the next 5+ decades ???


WAS your child exposed to mad cow disease via the NSLP ???


SCHOOL LUNCH PROGRAM FROM DOWNER CATTLE UPDATE


http://downercattle.blogspot.com/2009/05/who-will-watch-children.html


http://downercattle.blogspot.com/


DID YOUR CHILD CONSUME SOME OF THESE DEAD STOCK DOWNER COWS, THE MOST HIGH RISK FOR MAD COW DISEASE ???


you can check and see here ;


http://www.fns.usda.gov/fns/safety/pdf/Hallmark-Westland_byState.pdf


Saturday, March 5, 2011

MAD COW ATYPICAL CJD PRION TSE CASES WITH CLASSIFICATIONS PENDING ON THE RISE IN NORTH AMERICA

http://transmissiblespongiformencephalopathy.blogspot.com/2011/03/mad-cow-atypical-cjd-prion-tse-cases.html


Sunday, February 12, 2012

National Prion Disease Pathology Surveillance Center Cases Examined1 (August 19, 2011) including Texas

http://transmissiblespongiformencephalopathy.blogspot.com/2012/02/national-prion-disease-pathology.html


pink slime and a ship of fools, with Governor Rick Perry at the helm.


john gummer of England, force fed his daughter mad cow beef. a few years later, a young friend of theirs (23) died from mad cow disease. NOW, Governor Rick Perry, shows he is as big a fool as John Gummer.

http://media.kansascity.com/smedia/2012/03/29/21/01/MiPpi.SlMa.81.jpg


http://i.dailymail.co.uk/i/pix/2009/12/30/article-0-01F258B0000004B0-450_468x286.jpg


see more on this sad sad saga here ;


Wednesday, March 14, 2012


PINK SLIME, MRM’s, BSE AKA MAD COW DISEASE, AND THE USDA NSLP


http://madcowusda.blogspot.com/2012/03/pink-slime-mrms-bse-aka-mad-cow-disease.html


Sunday, August 28, 2011


Rick Perry, Texas, BSE aka mad cow disease, CJD, and 12 years of lies there from


http://sciencebushwhacked.blogspot.com/2011/08/rick-perry-texas-bse-aka-mad-cow.html


BY the way, ammonia treated beef DOES NOT KILL MAD COW DISEASE !!!


MOM DOD 12-14-97 Heidenhain Variant Creutzfeldt Jakob Disease ‘confirmed’ TEXAS, YEARS OF RICK PERRY BEING TEXAS AGRICULTURE COMMISSIONER, THEN ON TO GOVERNOR OF TEXAS, WHERE TWO MAD COWS WERE COVERED UP under Perry’s watch, ONE SUCCESSFULLY, AND ONE THAT TOOK AN ACT OF CONGRESS and 7 MONTHS TO FINALLY CONFIRM via WEYBRIDGE ENGLAND.

layperson


Terry S. Singeltary Sr.
Bacliff, Texas USA 77518
flounder9@verizon.net