Post by Terry S. Singeltary Sr. on Jan 27, 2012 16:13:55 GMT -6
Greetings,
not sure how this might work out. so i thought i might _try_ it.
I thought there might be a few folks out there that would like to discuss these PrPSc Prion TSE mad cow type disease. there are many, in many species, and they are spreading in North America. sporadic Creutzfeldt Jakob disease CJD in humans have now been tied to atypical BSE in bovines, and atypical Nor-98 Scrapie in sheep and goats. Bovine Spongiform Encephalopathy aka BSE mad cow disease has now been documented in a goat, in the field. CWD in deer and elk has now mutated into a second strain. the scientific community is very concerned about the real potential for CWD being zoonotic. CWD is spreading rapidly from state to state. all of these TSE in different species have been documented in North America. the partial and voluntary mad cow feed ban of August 4, 1997, was nothing but ink on paper, it was never much enforced, with 10,000,000 million pounds of banned, blood laced MBM going into commerce one decade later, post August 4, 1997 mad cow feed ban in 2007. sporadic CJD is rising in North America, with a new strain of sCJD in humans, what they call 'pending classification sporadic creutzfeldt jakob disease'. as these different human and animal TSE prion disease mutate, they become more virulent, as with the atypical L-BSE, with a 50% shorter incubation period. we must not flounder with these TSE prion disease in North America any longer. you add all this human TSE exposure up, and you have the medical and surgical community awash with the TSE Prion PrPSc. human TSE prion disease of all strains and types should be made reportable with no age limits in every State and Internationally, ASAP. ...
CWD TSE prion disease survives ashing to 600 degrees celsius, that’s around 1112 degrees farenheit.
you cannot cook the CWD TSE prion disease out of meat.
you can take the ash and mix it with saline and inject that ash into a mouse, and the mouse will go down with TSE.
Prion Infected Meat-and-Bone Meal Is Still Infectious after Biodiesel Production as well.
the TSE prion agent also survives Simulated Wastewater Treatment Processes.
IN fact, you should also know that the CWD TSE Prion agent will survive in the environment for years, if not decades.
you can bury it and it will not go away.
CWD TSE agent is capable of infected your water table i.e. Detection of protease-resistant cervid prion protein in water from a CWD-endemic area.
it’s not your ordinary pathogen you can just cook it out and be done with.
that’s what’s so worrisome about Iatrogenic mode of transmission, a simple autoclave will not kill this TSE prion agent.
I lost my mom to the Heidenhain Variant of Creutzfeldt Jakob disease on December 14, 1997, and made a promise to her. ...
so, any kind questions, comments, or replies are welcome
this forum is to enhance the debate and knowledge of the PrPSc Prion TSE for the layperson.
for now, I am going to keep it closed for family members of PrPSc Prion TSE disease. this is subject to change. ...
full text with source references to video below ;
transmissiblespongiformencephalopathy.blogspot.com/2011/08/terry-singeltary-sr-on-creutzfeldt.html
kind regards,
terry
layperson
not sure how this might work out. so i thought i might _try_ it.
I thought there might be a few folks out there that would like to discuss these PrPSc Prion TSE mad cow type disease. there are many, in many species, and they are spreading in North America. sporadic Creutzfeldt Jakob disease CJD in humans have now been tied to atypical BSE in bovines, and atypical Nor-98 Scrapie in sheep and goats. Bovine Spongiform Encephalopathy aka BSE mad cow disease has now been documented in a goat, in the field. CWD in deer and elk has now mutated into a second strain. the scientific community is very concerned about the real potential for CWD being zoonotic. CWD is spreading rapidly from state to state. all of these TSE in different species have been documented in North America. the partial and voluntary mad cow feed ban of August 4, 1997, was nothing but ink on paper, it was never much enforced, with 10,000,000 million pounds of banned, blood laced MBM going into commerce one decade later, post August 4, 1997 mad cow feed ban in 2007. sporadic CJD is rising in North America, with a new strain of sCJD in humans, what they call 'pending classification sporadic creutzfeldt jakob disease'. as these different human and animal TSE prion disease mutate, they become more virulent, as with the atypical L-BSE, with a 50% shorter incubation period. we must not flounder with these TSE prion disease in North America any longer. you add all this human TSE exposure up, and you have the medical and surgical community awash with the TSE Prion PrPSc. human TSE prion disease of all strains and types should be made reportable with no age limits in every State and Internationally, ASAP. ...
CWD TSE prion disease survives ashing to 600 degrees celsius, that’s around 1112 degrees farenheit.
you cannot cook the CWD TSE prion disease out of meat.
you can take the ash and mix it with saline and inject that ash into a mouse, and the mouse will go down with TSE.
Prion Infected Meat-and-Bone Meal Is Still Infectious after Biodiesel Production as well.
the TSE prion agent also survives Simulated Wastewater Treatment Processes.
IN fact, you should also know that the CWD TSE Prion agent will survive in the environment for years, if not decades.
you can bury it and it will not go away.
CWD TSE agent is capable of infected your water table i.e. Detection of protease-resistant cervid prion protein in water from a CWD-endemic area.
it’s not your ordinary pathogen you can just cook it out and be done with.
that’s what’s so worrisome about Iatrogenic mode of transmission, a simple autoclave will not kill this TSE prion agent.
I lost my mom to the Heidenhain Variant of Creutzfeldt Jakob disease on December 14, 1997, and made a promise to her. ...
so, any kind questions, comments, or replies are welcome
this forum is to enhance the debate and knowledge of the PrPSc Prion TSE for the layperson.
for now, I am going to keep it closed for family members of PrPSc Prion TSE disease. this is subject to change. ...
full text with source references to video below ;
transmissiblespongiformencephalopathy.blogspot.com/2011/08/terry-singeltary-sr-on-creutzfeldt.html
kind regards,
terry
layperson