Showing posts with label DNA. Show all posts
Showing posts with label DNA. Show all posts

Sunday, August 30, 2020

Tales Of The New Crown: From DARPA To DHHS - Brett Giroir Has A Prolife Moderna Trafficking Tiny Humans Dilemma - Humanized Mice v. Tiny Human Lab Rat

The national rate of neonatal abstinence syndrome nearly tripled between 2008 and 2015 (Q1-Q3), according to data from AHRQ’s Healthcare Cost and Utilization Project. Graph of Neonatal Abstinence Syndrome Rates per 1,000 births: 2008 2.2, 2009 2.8, 2010 3.4, 2011 4.0, 2012 4.7, 2013 5.5, 2014 6.1, 2015(Q1-Q3) 6.4, Source: Healthcare Cost and Utilization Project, State Inpatient Databases, 43-47 States, 2008-2015 (Q1-Q3). Note: For 2015 calendar year, only the 1st three quarters of data were used.
"Hey Brett! We need more tiny human lab rats."
Brett Giroir from DARPA to DHHS has a modern day trafficking tiny humans dilemma on his hands.

Does he refer to his acquired goods as humanized mice or tiny human lab rats?

I prefer tiny human lab rats just because I have adopted the term over 25 years ago.

This is what the prolifers like to cloak with their religious fervor of demonizing mothers who are losing their children in miscarriages due to ills of poverty.

The entire abortion argument promulgated through the halls of congress, which was created in the invasion of the Michigan Republican National Committee, is nothing but a false claim generated to garner more Faith Based Funding to continue the trafficking tiny humans through the Child Welfare System.

Using "The Poors" (always said with clinched teeth) as human lab rats is nothing new because no one cares.

You can order, from any mobile device, sperm and eggs, and grow them in your very own Corporate Shape Shifting Host, because they own the final product for commercial use.

That is fancy legal speak for trafficking tiny humans because you can not just sell them, you can financially leverage them and use them for all types of cooties testing.

The opioid crises was intentionally manufactured to maximize revenues, by and through public office, which is nothing more than an emolument, ,but if you swear an oath to another foreign nation, like the Vatican, that indelible seal will follow you, unless the chain of fidelity is broken.

Meet The Perfidious Sister Dede Byrne & Her Trafficking Tiny Humans Lab Rat RNC Convention Speech - Of Parental Rights & The Archdiocese Of Detroit Indelible Seal Situation


Moderna, as well as just about every other big pharma uses zygotes, which they will involuntarily induce labor through more lab rat human experiments on mothers."

No one wants to talk about the gestating mother.

Researchers mostly use Africa and other poor nations of war because there is no such thing as parental consent or parental rights.

Starvation, born of an U.S. invasion into a foreign land, will typically cause miscarriages.

Miscarriage is a form of abortion, as, abortion is not even a medical term; it is a legal term.

There are christian missionaries that conduct research on behalf of the universities and pharmaceutical corporations, to see how old a host, the latest term for a mother, can procreate.

I know of girls as young as 12 years of age giving birth in Guatemala, then having the child ripped from her arms to be adopted by good, christian, American parents.

Praise the lord and the Vatican orpha.net.

I know of medical research institutions in Detroit and Ukraine that love to collect the involuntarily induced miscarriages (a.k.a. abortion) where there is a surge in building more neonatal units because a mother does not have to carry full term, for a fetus of 5 weeks will do just fine in children's medical research training facilities.

They like to do things like dope up the water, which is why Detroit is #1 in infant mortality, a fetal good to be cherished in a CRISPR research event.

They ran similar tiny human lab rat operations in Flint.

Unfortunately, in case of Moderna, I shall go out there as say, once again, that they use children as lab rats, but in this case, the term tiny human lab rats, is a term most appropriately applied.

This is nothing more than another tale of modern day trafficking of tiny humans because no one cares....or do they?

https://beverlytran.blogspot.com/search?q=zygote

Market Summary > Moderna Inc
NASDAQ: MRNA
67.49 USD −0.54 (0.79%)
Closed: Aug 28, 7:59 PM EDT · Disclaimer
After hours 67.47 −0.020 (0.030%)

#maytheheavensfall

Moderna's Patents Probed by U.S. Defense Department, FT Says

Moderna Inc.’s patents that were filed or awarded are being probed by the U.S. Department of Defense’s research arm, the Financial Times reported, saying the company failed to disclose government funding as required by federal law.

Knowledge Ecology International, a patient advocacy group, said in a report this week that researchers didn’t disclose in vaccine patents where they got about $25 million in grants from the department’s Defense Advanced Research Projects Agency, or Darpa, for its vaccine technology, the newspaper said.

“The company believes it has complied with applicable patent reporting requirements regarding patent filings, including as they relate to the Darpa program,” Ray Jordan, a spokesman for Moderna, said Saturday. The company estimates that Darpa funding was about $50 million, or 1% of its $5.1 billion total private funding.

The newspaper cited Darpa spokesman Jared Adams as saying that all awards to Moderna included the need to report the role of government funding, adding that “Darpa is actively researching agency awards to Moderna to identify which patents and pending patents, if any at all, may be associated with Darpa support.”

At least one Darpa-linked patent shows government support was disclosed.

The Cambridge, Massachusetts-based company said earlier this week it’s in talks with Japan’s Ministry of Health, Labor and Welfare to potentially supply the country with 40 million or more doses of its vaccine candidate against Covid-19. It also unveiled new findings relating to its trial.

Summary of Humanized Mouse Model Workshop

On December 18, 2018, NIAID, in coordination with the NIH Office of the Director and HHS, organized a workshop to assess recent advances and opportunities in the development and use of humanized immune system (HIS) mouse models, in which the immune system of the mouse is partially replaced with human immune cells and tissues. Participants included leading scientists in the fields of immune system development and function, transplant immunology, autoimmunity, and infectious disease research. Adm Brett Giroir, Assistant Secretary of HHS, welcomed the participants and described HHS interest in this area, including a clearer understanding of the limitations and adequacy of existing HIS models, and the possibility of developing scientifically validated alternatives to the use of human fetal tissue. Dr. Daniel Rotrosen, Director of the Division of Allergy, Immunology and Transplantation at NIAID, provided an overview of the workshop goals and expected outcomes, including: evaluation of the features, strengths and limitations of current HIS mouse models; procedures to compare HIS models made from fetal and non-fetal tissue sources; and studies that would be required to fully characterize and standardize these models. Dr. Lawrence Tabak, NIH Principal Deputy Director, provided brief introductory comments on behalf of NIH.

Dr. Leonard Shultz provided a comprehensive summary of HIS mouse model development and usage from 1988 to the present. In following breakout sessions, participants discussed the strengths and limitations of various HIS mouse models and provided opinions on ways to optimize HIS models for the development of vaccines and therapeutics for infectious and immune-mediated diseases and cancer. The meeting participants reconvened for reports from the two breakout groups and a final discussion, that resulted in the following summary points:

Major scientific advances have been made in understanding infectious disease pathogenesis and development of therapeutics using HIS mouse models made with human fetal tissues.
No single humanized immune system model is universally appropriate or optimal for all applications.
Various models can recapitulate key aspects of human T cell immunity; existing models are less able to recapitulate human innate immunity and antibody responses regardless of tissue source. Improvements in modeling antibody responses should be a focus of future work and may be particularly important for advances in vaccinology; and in modeling infectious, autoimmune, and allergic diseases.
Few direct comparisons have been conducted of HIS mice derived using fetal vs. non-fetal human tissue sources.
Meeting participants included investigators working on fetal tissue-derived and non-fetal tissue-derived HIS models. Considering published data and other information shared at this meeting, participants expressed the opinion that fetal tissue-derived HIS models remain the “gold standard” to which other model systems should be compared. This preference is based on the preponderance of data indicating superior engraftment, differentiation, survival and function of the adaptive immune cells (particularly T cells) in fetal tissue-derived models.
Following the breakout sessions, there was strong opinion that work should proceed on a variety of models derived with fetal tissues or from alternative sources.









https://www.ahrq.gov/data/infographics/babies-dependent-opioids.html?utm_source=ahrq&utm_medium=en-2&utm_term=NNA&utm_content=2&utm_campaign=ahrq_en12_4_2018









Voting is beautiful, be beautiful ~ vote.©

Saturday, July 25, 2020

Tales Of The New Crown: Ending The Secret Diasporic Trafficking Of Tiny Humans - Foster Care & Adoption Reunification Database

Upon the Termination of Parental Rights, the immoveable , the birth certificate, chattel of the child is then transferred, sold, leveraged to be entrusted to a private entity.

I have yet to find out the formal, legal process of amending the register of human deeds for the live births.

Upon Termination of Parental Rights, the moveable chattel of the child, the body corpus, is then transferred through Foster Care, sold through Adoption, and levered in Child Welfare Services cost reimbursements to Medicaid, where the possibility substantially exists that the child will be processed through the underground legal markets of doing nasty things....

The residuals of the peculiar institution has created a diasporic pandemic in the stealin' of children, land & vote, particularly in this day and age of the Public Private Partnership in the promulgation of human asset management databases in the destruction of the posterity of our legacies.

Sunlight does cure the cooties.
Long-lost sisters find each other in the pandemic
These long-lost sisters found each other because of the coronavirus pandemic, they said. https://www.wxyz.com/news/national/coronavirus/sisters-credit-covid-19-for-reuniting-them
Posted by WXYZ-TV Channel 7 on Friday, July 24, 2020
#maytheheavensfall

Voting is beautiful, be beautiful ~ vote.©

Sunday, May 10, 2020

Happy Corporate Maternal Rights Day! Meet James Cottrell - Daddy Of Medicaid Fraud In Child Welfare

Meet James Cottrell.

James Cotrell seems to be the progenitor for the creation of the Lockean conjugal production of what is known as the Public Private Partnership where the paternal right of the U.S. impregnates, through the consent of congress, the appropriational semen funding of research grants its maternal NGO host, to gestate and birth an offspring of a fake ass authority, to go around to those god-foresaken "Third Worlds" (said with a hint of disdain), training those para-medical salvific saviors, to anesthetize tiny humans for those biogenetic lab rat experiments, and other nasty stuff, for the purposes of funding political campaigns, in order to generate the third generation of fake ass Corporate Shape Shifters, so they can continue to procure and purvey the trafficking of tiny humans, better recognized as the complex fraud scheme of modern day gerrymandering, otherwise, more readily understood as stealin' the children, land & vote, in the name of the tax exempt god, to maintain revenue maximization levels by warehousing more tiny humans goods, produced either by more tiny human girls or a petri dish, because, as a legally recognized corporate parent, with pseudo-animated spiritual rights of a functioning belief system, you do not need consent for personal inurement of a non-profit or for-profit, because your oath of fealty is to the Vatican, a foreign nation state, under the Queen Mother.

Whew! That was a mouthful!

Working on my 30 second elevator pitch.

His son is Paul Cottrell, but I like to call him Mr. Wannabe Tiny Human Mad Scientist because it seems that is what he wants to be when he grows up and gets his MD sheepskin.

Mr. Wannabe Tiny Human Mad Scientist used to live in Cass Corridor going to Wayne State University, but is really from Belleville.

He used to live in Iceland.



Welcome to your first peek behind the Iron Curtain of Foster Care and Adoption.

Enjoy.



Maybe Mr. Wannabe Tiny Human Mad Scientist wants to grow up to own tiny human somatic cell nuclear transfer research companies like Peter Nygard

 I wonder if Mr. Wannabe Tiny Human Mad Scientist wants to be like James Taylor. 

Paul Cottrell is a researcher in chaos theory and has interests in modeling financial markets. Some have considered him a polymath of sorts. Born in Detroit, Michigan he has extensive professional experience in engineering and design. After retiring…See More

He went to Wayne State University where I went. He is a Predictive Modeling Crapper and it looks to me like it is Econometrics. He worked with Catholic Charities in New York, where my Pretty Preet has been all over for a long time.

SHIELD INVESTMENTS INC. | ICIJ Offshore Leaks Database

We must definitely add Mr. Wannabe Tiny Human Mad Scientist to the list! 

Will I find you or your daddy here, Mr. Wannabe Tiny Human Mad Scientist?




I found patents!

This is fun.

Well, lookie here, a Rothschild law firm. I wonder if they have any kin over there at Fox Rothschild, but I am quite sure there is no relation....ship.....with the Vatican. 

I bet they are stealin' patents.

Oh boy! Oh boy! More predictive modeling crapper databases! I feel like a pretty princess right about now! 

Please tell me these are not the same people

How cute, they made a second generation tiny human offspring fund.
Frederick Gardner Cottrell Foundation Frederick Gardner Cottrell Foundation Research Corporation Technologies established the Frederick Gardner Cottrell Foundation in December 1998 to provide financial support for scientific research and educational programs at qualified nonprofit organizations. RCT named the foundation in honor of the university professor and inventor who championed the transfer of academic innovation to public use. The Cottrell Foundation receives its support from donations made by RCT and is a private, non-operating entity. Since its formation, the foundation has provided nearly $13 million in support of selected scientific and educational programs throughout the United States. The Foundation does not accept unsolicited grant requests. For a copy of recent financial statements of the foundation, please contact Rebecca Buescher, Secretary, Frederick Gardner Cottrell Foundation, 6440 N. Swan Road, Suite 200, Tucson, AZ 85718.
This is what these people really mean when it comes to Families First!

He was adopted at 10, studied journalism then rocket fuel.

He researched the effects of anesthetics on lungs with humans.

Infant nuerosurgery, Belleview New York.

The architect of Medicaid fraud in child welfare.

Politicians and movie stars to come to his meetings in research. Tucker Carlson and Hillary Clinton, of whom I do so adoringly call "Skankels" (A merging of the concepts - a skank and an older woman with gravity expansive wine loaded ankles.)

"She sells transposable models."

Happy Corporate Maternal Rights Day!

Awards, the entire kit and caboodle in research, including Nobel Prize winners.

He was known as the Kosher Hot Dog President.

 It seems he conjured up what is known and the university box lunch consortia for recruitment.

Perinstsl Research Corporate Risk Mitigation hitmen for hire to identify irresponsible testimony to discredit expert witnesses in court by providing their own manufactured witnesses, verified with their own accreditation networks.

Africa research.

Pediatric with the whoops babies

Fake ass jack legged doctors human resource network.

Each time a prolifer screams bloody murder of a tiny human, another zygote is dissected to discover another children's trust fund mutational modern day human trafficking scheme, in the name of the lord.

Praise the lord and save the Queen, for this residual of the peculiar institution has been in full force for quite some time, and it started in Detroit


#maytheheavensfall.


https://www.c-span.org/video/?187996-2/house-session&event=187996&playEvent&show=0


BARTLETT: MR. SPEAKER, I WAS IN MY OFFICE LAST EVENING ABOUT 11:00, AS WAS ALL THE REST OF THE HOUSE OF REPRESENTATIVES WAITING FOR A RESOLUTION OF SOME OF THE CONCERNS ON THE TRANSPORTATION BILL SO THAT WE COULD VOTE ON IT, WHEN WE WERE LOOKING AT THE DRUDGE REPORT ON OUR SCREEN AND WE SAW THERE A HEADLINE THAT I COULD HARDLY BELIEVE.

THAT SENATOR FRIST HAD REVERSED HIS POSITION ON EMBRYONIC SELLS -- STEM CELLS. WAS NOW ADVOCATING THE PASSAGE OF THE SENATE VERSION OF H.R. 810. I THOUGHT IT WOULD BE APPROPRIATE TODAY WITH STEM CELLS, EMBRYONIC STEM CELLS BEING SO MUCH IN THE NEWS IF WE COULD SPEND A FEW MINUTES LOOKING AT WHAT STEM CELLS ARE AND WHAT THIS IS ALL ABOUT.

WHAT WAS SENATOR FRIST TALKING ABOUT AND WHAT IS THE ISSUE HERE?

I HAVE HERE ON THE EASEL A CHART THAT SHOWS THE DEVELOPMENT, NOT ALL OF THE STAGES, BUT IT SHOWS THE DEVELOPMENT THE HUMAN EMBRYO.

IT STARTS WITH A ZYGOTE. THE ZYGOTE IS THE FERTILIZED EGG THAT NOW HAS CHROMOSOMES, GENES FROM THE SPERM AND GENES FROM THE EGG, HAVING WHAT WE CALL THE DIPLOID NUMBER OF CHROMOSOMES.

THAT DEVELOPS THROUGH SEVERAL STAGES, THROUGH THE BLASTOCYST STAGE AND TO THE GASTRULA STAGE. BY THE TIME YOU GET TO THE GAST LA -- GAST RUE LA STAGE, THE EMBRYO HAS DEVELOPED INTO A LARGE NUMBER OF CELLS.

AND WHAT'S SHOWN HERE IS THE EMBRYO AND THE PART OF THE WALL OF THE UTERUS TO WHICH IT IS ATTACHED.

BY THIS STAGE IN ITS DEVELOPMENT, THE EMBRYO HAS ALREADY NOW DEVELOPED FOUR VERY SPECIFIC STEM CELLS THAT WILL GO ON TO PRODUCE A VARIETY OF TISSUES AND ORGANS IN THE BODY, ALL OF THE TISSUES AND THE ORGANS IN THE BODY.

WE SEE THOSE DOWN HERE AT THE BOTTOM. SOME OF THEM DEVELOPMENT INTO ECTODERM THE EXTERNAL LAYER.

THE ECTODERM BECOMES TWO THINGS IN THE DEVELOPING BABY AND THE ADULT.

IT BECOMES THE SKIN AND THE NERVOUS SYSTEM AND SOME OF THE PIGMENT CELLS.

MOST OF WHAT WE ARE IN TERMS OF MASS IS ALL DEVELOPED FROM THE MIDDLE LAYER OR FROM THE MESODERM, FROM THAT DEVELOPS ALL OF YOUR SKELETAL MUSCLE, ALL OF YOUR BONES, ALL OF YOUR HEART MUSCLE. THE RED BLOOD CELLS, THE SMOOTH MUSCLE IN YOUR SBESTENS AND STOMACH SBSHSBEST -- AND YOUR INTES TIRKS NES.

THE ENTODERM IS THE LINING OF THE LUNG, THE THYROID GLAND, PANCREATIC CELLS, NOWHERE NEAR THE PASS PRODUCED BY THE MESODERM, BUT VERY IMPORTANT TISSUES NEVERTHELESS. THERE ARE SOME VERY UNIQUE CELLS DIFFERENT IN THE MALE AND THE FEMALE. THE GERM CELLS.

IN THE MALE THEY PRODUCE THE SPERM AND IN THE FEMALE THEY PRODUCE THE EGG.

SOME OF THESE STEM CELLS PERSIST EVEN INTO THE ADULT. IN THE BONE MARROW OF EVERY ADULT ARE STEM CELLS WHICH WILL PRODUCE YOUR RED BLOOD CELLS AND SOME OF YOUR WHITE BLOOD CELLS, WILL PRODUCE THOSE CELLS IN CLOTTING, THE THROMBOCYTE.

THERE HAS BEEN A LOT OF RESEARCH FOR MORE THAN THREE DECADES NOW ON USING THESE STEM CELLS TO SEE IF WE CAN'T CURE -- HELP PATIENTS WITH A NUMBER OF DIFFERENT DISEASES. THERE HAVE BEEN A NUMBER OF GOOD APPLICATIONS OF ADULT STEM CELLS.

THEY HAVE PRODUCED IN SOME CATIONS WHAT LOOKS LIKE ACTUAL CURES. BUT THESE ZULT STEM CELLS ARE LIMITED IN THEIR -- BUT THESE ADULT STEM CELLS ARE LIMBED IN THEIR CAPABILITY.

THEY ARE DIFFERENTIATED. THEY HAVE SPLIT AND ARE NOW DESTENED TO PRODUCE ONLY CERTAIN KINDS OF CELLS.

WHAT THE RESEARCHER TRIES TO DO AT TIMES IS TO TAKE THESE ADULT STEM CELLS AND PUT THEM IN AN ENVIRONMENT THAT CONVINCES THEM THEY ARE NOT AN ADULT STELL -- STEM CELL BUT BACK TO AN EMBRYONIC STEM CELL.

THE ULTIMATE EMBRYONIC STEM CELL IS THE ZYGOTE, ONE CELL WHICH WILL DIVIDE AGAIN AND AGAIN AND AGAIN AND DIFFERENTIATE AND FINALLY PRODUCE ALL OF THE CELLS OF THE BODY.

BUT HERE IN THE BLASTULA STAGE THE CELLS ARE DIFFERENTIATED IN TWO CATEGORIES. THOSE CELLS THAT WILL PRODUCE THE EMBRYO SHOWN HERE IN THE INNER CELL MASS AND THOSE CELLS WHICH WILL PRODUCE THE DECIDUA, THE CELLS AROUND THIS WHICH WILL BECOME AMNION AND CORION, PARTS OF THE PLACENTA. IN THE STAGE JUST BEFORE THIS ARE THE CELLS THAT CAN PRODUCE THE FULL EMBRYO.

I WOULD LIKE NOW TO LOOK AT OUR NEXT CHART HERE BECAUSE THIS SHOWS THE DEVELOPMENT OF THE EMBRYO AND IT HAS ALL OF THE STAGES THERE.

IT STARTS WITH THE ZYGOTE. HERE WE HAVE THE FERTILIZED EGG OR THE ZYGOTE. OF COURSE, THIS ALL BEGINS WITH AN OVARY.

THIS IS ONLY HALF OF THE REPRODUCTION SYSTEM OF THE FEMALE. AN OVARY WHICH, EVERY MONTH, ROUTINELY DURING THE CHILD BEARING YEARS, WILL PRODUCE AN OVUM.

HERE IS IS THE FOLLICLE RUPTURING AND THE OVUM COMING OUT.

HERE IS THE OOCYTE.

IT MAKES ITS WAY INTO THE FLOPIAN TUBE.

SOMETIMES THEY GET INTO THE ABDOMINAL CAVITY.

SOMETIMES THIS EGG IS NOT PICKED UP BY THIS FUNNEL SHAPED END AND SOMETIMES THAT CELL DOESN'T GET OUT THERE AND GET PICKED UP BY THE FALLOPIAN TUBE AND CARRIED DOWN WITH THE BEATING OF A NUMBER OF CYLIA AND GOES INTO THE BODY CAVITY.

THE SPERM GET OUT THERE TO.

THEY CAN BE FERTILIZED AND WE CALL THAT AN ECTOPIC PREGNANCY.

THE BABY CAN'T DEVELOP THERE AND WILL CAUSE PROBLEMS FOR THE MOTHER. SO THIS ECTOPIC PREGNANCY NEEDS TO BE TERMINATED BECAUSE IT WILL RESULT IN THE DEATH OF THE MOTHER IF IT CONTINUES.

AFTER FERTILIZATION THE EGG BEGINS ITS JOURNEY, TAKING SEVERAL DAYS, MAYBE AS MANY AS EIGHT, NINE, 10 DAYS UNTIL IT FINALLY REACHES THE END OF THE JOURNEY AND IMPLANTED INTO THE WALL OF THE UTERUS.

IT DIVIDES, FIRST TWO CELLS, THEN FOUR CELLS, AND THEN EIGHT CELLS. I WOULD LIKE TO PAUSE FOR JUST A MOMENT AT THAT EIGHT-CELL STAGE AND IMAGINE NOW WE ARE NOT IN THE REPRODUCTIVE TRACT OF THE FEMALE BUT IN A PETRI DISH IN THE LABORATORY.

BECAUSE THAT IS WHAT IN VITRO FERTILIZATION MEANS. THEY HAVE TAKEN THE EGG FROM THE MOTHER AND SPERM FROM THE FATHER AND COMBINED THESE TWO AND PRODUCED THE ZYGOTE.

IT DIVIDES AND DIVIDES UNTIL IT COMES TO THE EIGHT-CELL STAGE. AT THIS STAGE MORE THAN 1,000 TIMES WORLDWIDE IN ONE CLINIC IN ENGLAND MORE THAN 600 TIMES, THEY'VE TAKEN IN THE LABORATORY UNDER THE MICROSCOPE, A CELL AND SOMETIMES THEY GET TWO FROM THAT EIGHT-CELL STAGE AND THEY'VE DONE WHAT THEY CALL A PREIMPLANTATION GENETIC DIAGNOSIS.

THEY LOOK AT THE GENES AND YOU CAN DO THAT.

WE NOW KNOW WHAT THEY OUGHT TO LOOK LIKE AND THEY CAN DETERMINE IF THERE IS ANY GENETIC DEFECT.

WINSTON CUP DEFECT IS CALLED TRISOMI 21, MONGOLISM. IF THERE IS AN EXTRA CHROMOSOME YOU GET MONGOLISM.

IF THERE IS NO DEFECT IN THE CELL THEY ANALYZE, WHICH WILL BE LIKE ALL THE OTHER CELLS, THEN THEY IMPLANT WHAT IS REMAINING, THAT IS THE SIX OR SEVEN CELLS THAT ARE REMAINING AND NOW MORE THAN 1,000 TIMES WORLDWIDE WE'VE HAD WHAT LOOKS LIKE A PERFECTLY NORMAL BABY BORN FROM THIS PROCESS.

THIS TECHNIQUE, WHICH HAS BEEN WIDELY USED IN ENGLAND, IS NOW USED IN THIS COUNTRY.

JUST OUTSIDE OF WASHINGTON IN VIRGINIA IS A CLINIC THAT IS DOING THIS. THEY HAVE DONE IT MORE THAN 300 TIMES.

SEVERAL WEEKS AGO I TALKED FOR PERHAPS A HALF-HOUR WITH TWO OF THEIR DOCTORS ABOUT THE PROCEDURE. LET'S NOW TAKE A LOOK AT HOW THEY GET EMBRYONIC STEM CELL LINES. THEY TAKE AN EMBRYO IN THE LABORATORY, WHICH HAS BEEN PRODUCED BY THE FERTILIZATION OF AN EGG, AND THEY LET IT DEVELOP, NOT TO THE EIGHT-CELL STAGE, THEY GO JUST A LITTLE BEYOND THAT.

THEY GO TO THE INNER CELL MASS AND THEN THEY DESTROY THE EMBRYO AND THERE ARE NOW A LOT OF CELLS, NOT JUST EIGHT.

AND THEY TAKE A NUMBER OF THE CELLS FROM THE INNER CELL MASS WHICH I INDICATED PREVIOUSLY HAVE ALL THE GENETIC POTENTIAL TO PRODUCE THE BODY OF THE BABY, BUT NONE OF THE GENETIC DETAIL TO PRODUCE THE DECIDUA. THE DECIDUA, THE FINGERS LIKE THAT ARE GROWING INTO THE LINING OF THE UTERUS.

WHAT THIS DEBATE IS ALL ABOUT, MR. SPEAKER, IS ABOUT THE MORALITY, REALLY, THE ETHICS OF TAKING THIS LITTLE EMBRYO, WHICH IS A BABY IN MINIATURE BECAUSE IF YOU SEE IF IT GOES ON JUST A COUPLE OF DAYS LATER AND IMPLANTS IN THE UTERUS, IT WILL BECOME A BABY.

IT IS NOW IN THE PETRI DISH, BUT IT CAN BE IMPLANTED INTO THE UTERUS. TO TAKE THIS EMBRYO AND DESTROY IT AND TAKE THE CELLS FROM TINNER CELL MASS TO PRODUCE A STEM CELL LINE.

UP TO THIS TIME, THAT'S BEEN THE ONLY TECHNIQUE THAT HAS BEEN AVAILABLE FOR DEVELOPING THESE STEM CELL LINES. AND THE PRESIDENT HAD A VERY DIFFICULT DECISION TO MAKE FOUR YEARS AGO WHEN THERE WAS AN INTEREST OF USING FEDERAL MONEY.

MAYBE WE SHOULD PAUSE TO SEE WHY WE ARE SO MUCH INTERESTED IN STEM CELL RESEARCH .

BECAUSE THESE STEM CELLS AS THE EARLIER SLIDE SHOWED, CAN PRODUCE ALL OF THE TISSUES IN THE BODY, THERE IS THE HOPE, THE PROMISE, AND, IN FACT, THE REALIZATION OF SOME OF THE WORK WE HAVE DONE WITH ADULT STEM CELLS THAT WE CAN USE THESE STEM CELLS TO REPLACE TISSUES WHICH HAVE BEEN DAMAGED BY DISEASE OR SOME OTHER TRAUMA IN THE BODY.

WE CAN REPLACE THOSE SO AS TO RESTORE HEALTH. NOW, WE HAVE A LOT OF APPLICATIONS FROM ADULT STEM CELLS AND NO APPLICATIONS FROM EMBRYONIC STEM CELLS.

WHY SHOULD WE HAVE THIS DEBATE ABOUT EMBRYONIC STEM CELLS WHEN ALL OF THE APPLICATIONS HAVE BEEN FROM ADULT STEM CELLS.

WE HAVE BEEN WORKING WITH ADULT STEM CELLS FOR MORE THAN THREE DECADES.

WE HAVE HAD A LOT OF OPPORTUNITY TO MAKE APPLICATIONS THERE.

WE HAVE BEEN WORKING WITH EMBRYONIC STEM CELLS FOR ONLY ABOUT SIX YEARS AND THERE JUST HASN'T BEEN THE OPPORTUNITY TO MAKE THE MEDICAL APPLICATION FROM EMBRYONIC STEM CELLS THAT WE HAVE BEEN ABLE TO MAKE FROM ADULT STEM CELLS. BUT BECAUSE OF WHAT EMBRYONIC STEM CELLS ARE, BECAUSE EMBRYONIC STEM CELLS STILL HAVE ALL OF THE CAPABILITY TO PRODUCE ANY AND EVERY TISSUE IN THE BODY, DOCTORS AND RESEARCHERS BELIEVE INTUITIVELY FROM WHAT THEY KNOW OF EMB RYOLOGY THERE OUGHT TO BE MORE AND BETTER APPLICATIONS FROM EMBRYONIC STEM CELLS THAN ADULT STEM CELLS.

WE DON'T KNOW.

IT MAY BE THESE EMBRYONIC STEM CELLS MAY BE LIKE UNRULEY TEENAGERS, VERY DIFFICULT TO CONTROL.

YOU SEE, THEIR DESTINY IN LIFE IS TO TWIDE AND DIVIDE AND DIVIDE. WE WANT THEM TO DO THAT, BUT WE WANT TO BE ABLE TO CONTROL HOW THEY DIVIDE AND WHAT THEY PRODUCE.

IF IT'S A LIVER THAT YOUR PATIENT NEEDS, YOU NEED NOW TO CONVINCE THE EMBRYONIC STEM CELLS THAT'S WHAT THEY OUGHT TO BE PRODUCING. WHEN THEY HAVE DONE ENOUGH, THEY HAVE DONE ENOUGH AND THEY NEED TO QUIT. IT MAY BE THAT THEY ARE GOING TO BE VERY DIFFICULT TO CONTROL, LIKE THE UNRULEY TEENAGER, THEY MAY KEEP ON DIVIDING, WHEN YOU PUT THEM IN THE BODY THEY MAY END UP FORMING TUMORS. WE WON'T KNOW UNTIL WE DO THAT RESEARCH.

BECAUSE OF WHAT EMBRYONIC STEM CELLS ARE AND BECAUSE THEY HAVE THE ABILITY TO PRODUCE ANY AND EVERY CELL IN THE BODY, MANY AMERICANS BELIEVE THAT THERE MAY BE REALLY IMPORTANT APPLICATIONS FROM EMBRYONIC STEM CELLS TO MEDICINE.

WE DESERVE TO PROVIDE THE OPPORTUNITIES SO THAT THAT CAN BE DONE WITHOUT HARMING THE EMBRYO.

UP TO THIS DATE THE ONLY WAY THAT WE HAVE GOTTEN THESE EMBRYONIC STEM CELL LINES STARTED IS BY TAKING SOME OF THE CELLS FROM THIS INNER CELL MASS AND -- WHICH DESTROYS THE EMBRYO.

IN 2001 THE PRESIDENT WAS FACED WITH A VERY DIFFICULT DECISION.

HE NEEDED TO DETERMINE WHETHER FEDERAL FUNDS COULD BE USED IN EMBRYONIC STEM CELL RESEARCH WHEN THE ONLY WAY TO GET EMBRYOS AT THAT TIME WAS BY DESTROYING THE EMBRYO.

WHEN THE PRESIDENT WAS DELIBERATING, MAKING THAT DIFFICULT DECISION, THE SCIENTISTS AT N.I.H. HAD AN OPEN HOUSE FOR MEMBERS OF THE STAFF HERE AND MEMBERS OF CONGRESS TO COME TO N.I.H. TO LEARN ABOUT BRETCH -- EMBRYONIC STEM CELL RESEARCH AND THE POTENTIALS, AND I WENT THERE, MR. SPEAKER, AND I LISTENED TO THEIR PRESENTATIONS AND BECAUSE IN A FORMER LIFE I WAS PRIVILEGED TO BE ABLE TO GET A PH.D. , A DOCTOR'S DEGREE IN HUMAN PHYSIOLOGY, BECAUSE I TAUGHT MEDICAL SCHOOL, BECAUSE I HAD A COURSE IN ADVANCED EMBRYOLOGY, I KNEW A LITTLE BIT ABOUT WHAT THEY WERE TALKING ABOUT.

AS THE NEXT CHART SHOWS.

THE SPEAKER PRO TEMPORE: WILL THE GENTLEMAN SUSPEND FOR A MOMENT. THE CHAIR WILL RECEIVE A MESSAGE.

THE MESSENGER: MR. SPEAKER A. MESSAGE FROM THE SENATE. THE SECRETARY: MR. SPEAKER. THE SPEAKER PRO TEMPORE: MADAM SECRETARY. THE SECRETARY: I HAVE BEEN DIRECTED BY THE SENATE TO INFORM THE HOUSE THAT THE SENATE HAS AGREED TO THE CONFERENCE REPORT ON H.R. 6, AN ACT TO ENSURE JOBS FOR OUR FUTURE WITH SECURE, AFFORDABLE, AND RELIABLE ENERGY.

THE SPEAKER PRO TEMPORE: THE GENTLEMAN MAY PROCEED.

MR. BARTLETT: THANK YOU, MR. SPEAKER. AS I MENTIONED WHEN I SAT THERE LISTENING TO THE RESEARCHERS AT N.I.H. EXPLAINING WHAT THEY WERE DOING AND THE DREAMS AND THE HOPES THAT THEY HAD FOR THE APPLICATIONS OF EMBRYONIC STEM CELL RESEARCH AND WHEN I THOUGHT OF THE DILEMMA THAT THE PRESIDENT WAS IN IN TRYING TO DECIDE WHETHER IT WAS OK TO DESTROY THESE EMBRYOS TO GET A STEM CELL LINE TO GET SOMETHING THAT WOULD COME UP WITH MIRACULOUS CURES, I THOUGHT BACK TO MY STUDIES AND TO A COURSE THAT I HAD IN ADVANCED EMBRYOLOGY -- YOU DON'T NEED TO HAVE THE COURSE TO UNDERSTAND THIS. EVERYBODY CAN UNDERSTAND THIS. IT OCCURRED TO ME THAT NATURE HAD BEEN DOING FOR A VERY LONG TIME WHAT WE NEEDED TO DO, AND THAT WAS TO TAKE CELLS FROM THE EARLY EMBRYO WITHOUT HURTING THE EMBRYO.

HOW DID NATURE DO THIS?

NATURE HAD BEEN DOING THIS FOR A LONG TIME BY PRODUCING IDENTICAL TWINS.

YOU SEE, AN IDENTICAL TWIN HALF OF THE CELLS ARE TAKEN AWAY FROM THE EMBRYO, AND EACH HALF GOES ON TO PRODUCE A PERFECTLY NORMAL BABY.

BY THE WAY, MR. SPEAKER, ONE OF THOSE IDENTICAL TWINS IS A CLONE.

YOU DECIDE WHICH ONE IT IS, AND YOU THINK ABOUT THAT, MR. SPEAKER, AND DEE DECIDE HOW THIS RELATES TO THE DIALOGUE THAT WE ARE HAVING ON CLONING.

THERE ARE TWO DIFFERENT TIMES DURING THE DEVELOPMENT OF THE EMBRYO, AT LEAST TWO, MAYBE MORE, BUT AT LEAST TWO DIFFERENT TIMES DURING THE DEVELOPMENT OF THE EMBRYO THAT IT CAN SPLIT TO PRODUCE IDENTICAL TWINS. ONE IS AT THE TWO-CELL STAGE WHEN, THERE ARE TWO CELLS THERE AND INSTEAD OF JUST DIVIDING TO MAKE FOUR CELLS, IT SPLITS SO THAT THERE IS NOW TWO ONE-CELL EMBRYOS, AND EACH GOES ON TO DIVIDE AGAIN AND AGAIN AND AGAIN, FINALLY TO PRODUCE A BABY.

OR IT CAN WAIT UNTIL THE INNER CELL MASS STAGE, AT WHICH TIME IN SOME EMBRYOS ONCE IN A WHILE THERE ARE TWO INNER CELL MASSES , AND THAT CAN NOW SPLIT TO PERFORM IDENTICAL TWINS.

AS YOU KNOW, MR. SPEAKER, SOMETIMES THIS ISN'T PERFECT.

AND THEY DON'T SPLIT TOTALLY.

WE HAVE WHAT WE CALL SIAMESE TWINS.

THIS IS THE ORIGIN OF SIAMESE TWINS WHEN THE SPLIT HAS OCCURRED PROBABLY AT THE INNER CELL MASS STAGE AND IT HASN'T BEEN COMPLETE AND THEY REMAIN CLOSE ENOUGH TOGETHER THAT SOME PARTS OF THE BODY GROW TOGETHER.

NOW, WE KNOW THAT THE EGGS ARE CAPABLE, THE EMBRYO IS CAPABLE OF SPLITTING AT THESE TWO DIFFERENT STAGES BECAUSE OF THE WAY THE BABIES PRESENT THEMSELVES AT BIRTH. IF THEY ARE BOTH INSIDE THE SAME EMANYONIC SACK, THEY ARE SPLIT AT THE TWO CELLS STAGE. IF THEY EACH HAVE THEIR OWN EMBRYO, THEY PROBABLY SPLIT LATER ON, PROBABLY AT THE INNER CELL MASS STAGE.

IT OCCURRED TO ME SINCE NATURE MANY TIMES TAKES HALF OF THE CELLS AWAY FROM THE EARLY EMBRYO, AND THEY GO ON TO PRODUCE TWO PERFECTLY NORMAL BABIES, THAT WE OUGHT TO BE ABLE TO TAKE A CELL OR TWO FROM AN EARLY EMBRYO WITHOUT HURTING THE EARLY EMBRYO, AND I ASKED THE SCIENTISTS AT N.I.H., SHOULDN'T WE BE ABLE TO DO THIS?

THEY SAID, WELL, NATURE'S BEEN DOING IT FOR A LONG TIME.

WE OUGHT TO BE ABLE TO DO IT.

WE HAVE NOT DONE IT.

BUT WE OUGHT TO BE ABLE TO DO IT.

A LITTLE BIT AFTER THAT I WAS AT AN EVENT WHEN THE PRESIDENT WAS THERE AND I MENTIONED THIS PONLT TO THE PRESIDENT, HE -- POSSIBILITY TO THE PRESIDENT, AND HE HADN'T COME OUT WITH THE EXECUTIVE ORDER.

HE ASKED KARL ROVE TO FOLLOW UP.

AND A FEW DAYS LATER I GOT A CALL SAYING THAT THE WHITE HOUSE TOLD HIM WHAT I WAS PROPOSING WASN'T DOABLE.

I SAID, KARL, EITHER THEY DIDN'T UNDERSTAND YOUR QUESTION OR THERE'S SOME CONFUSION BECAUSE THESE ARE THE SAME PEOPLE THAT CAN TAKE A SINGLE CELL AND TAKE THE NUCLEUS OUT OF THAT CELL AND PUT ANOTHER IN IT.

OF COURSE THEY CAN TAKE A CELL OUT OF AN EARLY EMBRYO.

SO WE WENT BACK AND ASKED HIM AGAIN HE CAME BACK AND SAID HE GOT THE SAME ANSWER FROM THEM.

THAT THEY COULDN'T DO THIS. SO THE PRESIDENT CAME DOWN WITH HIS EXECUTIVE ORDER. A COUPLE YEARS AFTER THAT, NOT VERY MANY MONTHS AGO, AS A MATTER OF FACT, THE PEOPLE AT N.I.H. WERE SITTING IN MY OFFICE AND I ASKED THEM HOW COULD THIS HAVE HAPPENED?

WHAT APPARENTLY HAPPENED, WHAT SO OFTEN HAPPENS IN COMMUNICATIONS, THERE IS A MISCOMMUNICATION. WHAT THEY HAD TOLD KARL ROVE WAS THAT THEY WEREN'T SURE THEY COULD PRODUCE AN EMBRYONIC STEM CELL LINE FROM AN EMBRYO THAT EARLY.

BECAUSE THEY HAD NEVER DONE IT. NOT THAT IT WASN'T DOABLE. JUST THEY HAD NEVER DONE IT. HE INTERPRETED THIS AS SAYING, GEE, THEY COULDN'T TAKE THIS CELL AND THEREFORE THE RESEARCH COULDN'T BE DONE.

I'D LIKE TO SPEND JUST A MOMENT, MR. SPEAKER, LOOKING AT SOME OF THE REASONS THAT PEOPLE ARE SO CONCERNED AND WHY THIS WAS SUCH AN IMPORTANT DECISION ON THE PART OF THE PARENT OF THE PRESIDENT -- OF THE PRESIDENT AND WHY SENATOR FRIST'S DECISION LAST NIGHT HAS STIRRED UP SO MUCH CONTROVERSY.

IT'S BECAUSE THERE ARE A VERY LARGE NUMBER OF DISEASES THAT HAVE THE POTENTIAL OF BEING CURED ULTIMATELY WITH APPLICATION OF STEM CELLS.

LET ME GIVE YOU ONE OF THOSE WHICH IS THE MOST EXPENSIVE DISEASE IN OUR WHOLE COUNTRY, AND THAT'S DIABETES.

AND I HAVE BEEN IN MY OFFICE SEVERAL TIMES WHEN THE CHILDREN COME THROUGH WITH JUVENILE DIABETES -- IF YOU WANT A HEARTRENDING EXPERIENCE, MR. SPEAKER, THIS IS IT.

THESE KIDS COME IN WITH THIS HOCKEY PUCK LIKE THING UNDER THEIR SKIN, WHICH IS AN INSULIN PUMP BECAUSE THEY ARE SO BRITTLE THEY HAVE TO BE BRICKING THEIR FINGER OR THEIR THUMB OR EAR LOBE OR SOMETHING A NUMBER OF TIMES A DAY TO GET A GLUCOSE LEVEL SO THEY CAN SET THE PUMP SO THEY ARE GETTING THE RIGHT AMOUNT OF INSULIN IN, THEY ARE SO BRITTLE THEY CAN'T DO IT A FEW TIMES A DAY, IT HAS TO BE PUMPED IN REGULARLY ALONG.

THIS IS THE MOST EXPENSIVE DISEASE IN OUR COUNTRY.

AND IT IS POTENTIALLY TOTALLY CURABLE WITH STEM CELL APPLICATIONS. ALL YOU NEED TO DO, MR. SPEAKER, IS TO PRODUCE SOME IDENTIFYLET OF LONGER HAN CELLS.

THESE ARE THE CELLS THAT JUST HAPPEN TO BE EMBEDDED IN THE PANCREAS. I HAVE NO REASON WHY THEY NEED TO BE IN THE PANCREAS, THEY HAVE NOTHING TO DO WITH THE FUNCTION OF THE PANCREAS BECAUSE THE PANCREAS IS A BIG DIE JESSIVE GLAND AT THE TOP OF THE INTESTINE THAT PRODUCE ENZYMES THAT DIE JESS FATS, AND CARBOHYDRATES.

EMBEDED IN THE ISSUE ARE WHAT LOOK LIKE THESE LITTLE ISLANDS, THE GERMAN, AS HE LOOKED UNDER THE MICROSCOPE, SO WE CALL THEM THE ILETS OF LONGERHAN. INSULIN DOESN'T CURE DIABETES.

AS ANY PERSON WHO HAS DIABETES KNOWS.

IT SIMPLY DELAYS THE COURSE OF THE DISEASE, STILL THERE MAY ULTIMATELY BE PROBLEMS WITH THE EYES, PROBLEMS WITH CIRCULATION.

YOU LOSE SOME TOES. GANG GREEN SETS IN. -- GANGRENE SETS IN.

IF WE COULD CREATISLET -- CREATE ILET OF LONGERHAHN CELLS. ANYWHERE THE BLOOD CAN GET TO THEM SOT SOW THE KIRK LATION CAN PICK UP THE HORMONE PRODUCED BY THIS, THIS SHOULD CURE THE DISEASE.

PARTICULARLY THE MANY AUTOIMMUNE DISEASES, THERE ARE 63 AUTOIMMUNE DISEASES.

THESE ARE DISEASES WHAT THE BODY GETS CONFUSED WHAT'S REALLY BODY.

WHAT'S INTERESTING WITH THESE EARLY EMBRYOS, OBVIOUSLIEE WEE NEED TO KNOW WHAT'S US SO WHAT'S FOREIGN TO US IS GOING TO BE REJECTED WHEN IT COMES IN.

WHEN YOU GET INSIDE YOUR BODY, THERE ARE NO BACTERIA IN THERE. THAT'S A PRISTINE WORLD. WE HAVE A BIG ARMY OF WHITE CELLS IN THERE THAT MAKE SURE THAT IT KEEPS IT PRISTINE.

THESE WHITE CELLS ARE TOLD BY WHAT WE CALL T CELLS AS TO WHAT'S YOU AND WHAT'S NOT YOU SO THAT THEY ATTACK WHAT'S NOT YOU.

SOMETIMES, AND IN MORE PEOPLE THAN WE'D LIKE TO HAVE IT OCCUR, SOMETIMES THE BODY GETS CONFUSED AS TO WHAT'S REALLY YOU.

I HAVE A LITTLE PROBLEM, RULE TORREY ARTRY TIES. THAT'S AN AUTO IMMUNE DISEASE WHERE THE BODY HAS -- IT'S CONFUSED SO IT STARTED ATTACKING IT SELF.

THERE ARE 63 OF THOSE DISEASES. POTENTIALLY ALL OF THEM COULD BE ADDRESSED WITH STEM CELL RESEARCH.

ALZHEIMER'S DISEASE, VERY TRAGIC DISEASE, CENTRAL NERVE INJURY, YOU INJURE YOUR SPINAL CORD THEY DON'T GROW BACK, THERE IS THE POTENTIAL YOU COULD PUT NEW CELLS IN THERE AND PEOPLE WHO ARE IN THE WHEELCHAIR COULD WALK NEN GWEN. THERE IS THAT POTENTIAL.

WHICH IS EIGHTY GREAT INTEREST IN EMBRYONIC AND IN GENERAL STEM CELL RESEARCH, PARTICULARLY IN EMBRYONIC STEM CELL RESEARCH BECAUSE OF THE ENORMOUS POTENTIAL THEY OUGHT TO HAVE BECAUSE THEY ARE SO TOTALLY UNDIFFERENTIATED BECAUSE THEY CAN PRODUCE ANY AND EVERY CELL IN THE BODY.

I HAVE BEEN WORKING WITH THE WHITE HOUSE, WITH THE NATIONAL INSTITUTES OF HEALTH, WITH THE OF CATHOLIC BISHOPS, WITH THE PRO-LIFE COMMUNITY IN DEVELOPING A BILL THAT IS H.R. 3144, WHICH WOULD PERMIT RESEARCH ON NOT JUST THE PROCEDURE WHICH I RECOMMENDED MORE THAN FOUR YEARS AGO NOW, BUT SEVERAL OTHER PROCEDURES THAT ARE OUTLINED IN A BILL LOOK WHICH I HAVE HERE, CALLED "ALTERNATIVE SOURCES OF HUMAN PLURIPOTENT STEM CELLS, A WHITE PAPER, PRODUCED BY THE PRESIDENT'S COUNCIL ON BIOETHICS. " THEY TALK HERE ABOUT FOUR DIFFERENT KINDS OF RESEARCH THAT -- FOUR DIFFERENT KINDS OF WAYS OF PROCURING EMBRYONIC STEM CELLS THAT MIGHT BE ETHICALLY ACCEPTABLE TO THE PRO-LIFE COMMUNITY.

THE FIRST OF THESE IS PLURIPOTENT, BY PLURIPOTENT THEY MEAN CELLS THAT HAVE THE CAPABILITY TO PRODUCE ALL OF THE TISSUES OF THE EMBRYO BUT NOT THE DECIDUA.

PLURIPOTENT SELLS DERIVE FROM EMBRYOS THAT ARE ESSENTIALLY MORIBUND, DEAD.

THE EQUIVALENT, IF YOU WILL, OF AN ADULT THAT IS BRAIN-DEAD.

IT'S PERFECTLY ETHICAL, MOST PEOPLE BELIEVE, TO TAKE ORGANS, THAT'S HOW WE GET ORGANS FOR TRANSPLANT, FROM ADULTS THAT ARE BRAIN-DEAD.

IF YOU HAVE AN EMBRYO WHICH IS OBVIOUSLY NOT GOING TO DEVELOP BUT IT STILL IS ALIVE ENOUGH YOU MIGHT TAKE CELLS FROM IT TO PRODUCE A STEM CELL LINE, IF YOU KNEW IT WAS DEAD, IT COULD NEVER PRODUCE A BABY, ETHICALLY IT WOULD APPEAR TO MANY PEOPLE TO BE OK TO TAKE THAT -- CELLS FROM THAT TO ESTABLISH THE STEM CELL LINE.

YOU MIGHT HAVE A LITTLE CONCERN THAT AN EMBRYO THAT SAT THERE A DAY OR TWO AND NEVER DIVIDED, BECAUSE IT WAS SOMETHING WRONG WITH IT, THAT THE CELL YOU TOOK FROM IT TO PRODUCE THE STEM CELL LINE MIGHT NOT PRODUCE JUST THE HIGH QUALITY STEM CELL LINE THAT YOU MIGHT LIKE FOR RESEARCH, BUT AT LEAST IT'S WORTH EXPLORING AND IT GETS BY THE ETHICAL ARGUMENTS.

THE SECOND ONE OF THEIR PROPOSALS, I'D LIKE TO LOOK AT THE NEXT CHART AS WE DO THAT, THE NEXT CHART BECAUSE LET ME LOOK AT THIS CHART FOR A MOMENT HERE WITH YOU, THIS COMES FROM A WHITE PAPER ON THE PRESIDENT'S COUNCIL ON BIO ETHICS, AND LET ME LOOK AT THE HIGHLIGHTED PORTION, IT MAY BE SOME TIME BEFORE STEM CELLS CAN BE RELIABLY DERESERVED FROM SINGLE CELLS EXTRACTED FROM EARLY EMBRYO, A PROCEDURE THAT I WAS TALKING ABOUT THAT OCCURRED TO ME WHEN I WAS AT N.I.H. TALKING TO THE INVESTIGATORS THERE. AND IN WAYS THAT DO NO HARM TO THE EMBRYO, THUS BIOPSIED. THE INITIAL SUCCESS OF THE VERLINSKY.

VERLINSKY SAYS HE HAS DONE WHAT N.I.H. HAS SAID THEY ARE NOT SURE THEY COULD CAN, SPRUCE AN EMBRYONIC STEM CELL STEM CELL LINE FROM ONE EMBRYO.

 RAISING THE POSSIBILITY THAT PLURIPOTENT STEM CELLS CAN BE TAKEN FROM A BLASTOMERE, REMOVED FROM EARLY HUMAN EMBRYOS WITHOUT HARMING THEM. THE ASTERISK THERE.

IF YOU LOOK DOWN AT THE BOTTOM OF THE PAGE A SIMILAR IDEA WAS PROPOSED BY REPRESENTATIVE ROSCOE BARTLETT OR MARYLAND AS FAR BACK AS 2001.

WHAT THEY ARE REFERRING TO IS THE RECOMMENDATION THAT I MADE TO THE PRESIDENT THAT RERELAYED ON TO KARL ROVE.

SO THIS IS RECOGNIZED IN THIS FAIRLY RECENTLY PUBLISHED WHITE PAPER. ALTERNIVE SOURCES OF PURRY POTENT STEM CELLS. -- PLURIPOTENT STEM CELLS.

THEY TAKE CELLS FROM AN EMBRYO THAT IS GOING TO DIE, LIKE THE PERSON IS BRAIN DEAD, WHY NOT GET SOME BENEFIT. WE DO THAT WITH ORGAN TRANSPLANTS ALL THE TIME. THE THIRD ONE IS VERY INTERESTING.

THAT IS TO PRODUCE PLURI POTENT STEM CELLS DERIVED FROM BIOLOGICAL ARTIFACTS.

ONE OF THOSE GOES BACK TO THIS LITTLE EMBRYO IN THE PETRI DISH. THEY WANT TO GO IN THE EARLY EMBRYO AND TURN OFF SOME OF THE GENES. SO THAT IT CAN NEVER PRODUCE A BABY.

IT CAN GO ON DIVIDING AND PRODUCING A MASS OF CELLS. THIS IS CALLED AN ARTIFACT.

IF IT IS NOT GOING TO BE A BABY, IT IS JUST A MASS OF CELLS, MAYBE IT IS OK TO TAKE A CELL TO PRODUCE AN EMBRYONIC STEM CELL LINE.

SOME PEOPLE MAY HAVE CONCERN, MR. SPEAKER, THAT YOU HAVE GONE IN EARLY AND MESSED UP WHAT COULD HAVE BEEN A NORMAL BABY.

NOW YOU HAVE CREATED KIND OF A FREAK THAT YOU CAN TAKE SOME CELLS FROM. IF IT IS NOT GOING TO BE A BABY, YOU CAN TAKE THE CELLS.

AT LEAST IT IS A WAY OF GETTING EMBRYONIC STEM CELLS WITHOUT DESTROYING WHAT, AT THAT POINT, IS A STEM CELL. THERE IS A UNION WITHOUT SEX CELLS.

THE FOURTH TECHNIQUE IS INTERESTING, TAKING PLURI POTENT. TAKE A BODY CELL FROM ANYWHERE IN THE BODY, SKIN, MUSCLE, LUNGS AND DIFFERENTIATE IT. TRYING TO PRODUCE A CELL IN AN ENVIRONMENT THAT IS CONFUSED AS TO WHAT IT IS.

IT THINKS AND BEHAVES LIKE AN EMBRYONIC STEM CELL.

IF WE CAN DO THIS, THAT IS GREAT BECAUSE ETHICALLY THERE SHOULDN'T BE ANY PROBLEM WITH DOING THIS. THIS HAS NOT BEEN DONE.

THERE ARE BIG TECHNICAL CHALLENGES TO DOING THIS. 

THIS WHITE PAPER GIVES A VERY GOOD DISCUSSION OF THE PROPOSAL THAT WE MADE. 

THAT IS OF GETTING CELLS VIA BLASTOMERE EXTRACTION.

SOMETIMES CALLED BIOPSY. YOU ARE TAKING A CELL OR TWO. THEY EVEN TALK ABOUT PRODUCING THE REPAIR IT CAN WHICH WOULD BE REALLIED A VAN TAI JOUSE FOR THE -- ADVANTAGEOUS. IF IT NEEDS A NEW LIVER, NEW ISLET OF LANGERHANS CELLS. HOPEFULLY QUESTION PRODUCE THIS FROM A REPAIR IT CAN. 

IT ALMOST LOOKS TO ME LIKE TWO DIFFERENT GROUPS WROTE THE BODY OF THIS TEXT WHERE THEY TALK ABOUT THIS TECHNIQUE AND WHERE THEY MAKE THE RECOMMENDATIONS. 

IN THE RECOMMENDATIONS THEY SAY THE SECOND PROPOSAL, WE FIND THIS PROPOSAL TO BE ETHICALLY UNACCEPTABLE IN HUMANS OWING TO THE REASONS GIVEN IN THE ETHICAL ANALYSIS, WE SHOULD NOT IMPOSE RISKS ON OLIVING EMBRYOS DESTENED TO BECOME CHILDREN FOR THE STAKE OF GETTING STEM CELLS. 

I AGREE. THAT IS NOT THE REASON STEM CELLS ARE TAKEN FROM THIS BABY. CELLS ARE TAKEN WITH NO THOUGHT THEY ARE STEM CELLS TSM CELLS ARE TAKEN BY THE PARENTS TO PRODUCE A REPAIR IT CAN FOR THE BABY. I THINK MOST AMERICANS DON'T HAVE AN ETHICAL PROBLEM, MR. SPEAKER, WITH IN VITRO FERTILIZATION. 

I THINK MOST AMERICANS DON'T HAVE AN ETHICAL PROBLEM WITH DECIDING YOUR BABY IS NOT GOING TO HAVE A GENETIC DEFECT. I DON'T THINK HARDLY ANY AMERICANS COULD EVER HAVE A PROBLEM WITH ESTABLISHING A REPAIR IT CAN FOR YOUR BABY. 

AND WHAT IS ENVISIONED IS THAT AT THE END OF THE DAY THE PARENTS WOULD HAVE MADE AT LEAST TWO ETHICAL DECISIONS, THAT IS, TO HAVE THEIR OWN BABY -- THE ONLY WAY THEY CAN DO IT IS IN VITRO, AND ESTABLISH A REPAIR IT CAN FOR THEIR BABY AND ALL THAT NEEDS TO BE DONE TO GET ANOTHER STEM CELL LINE IS TO ASK THEM, COULDN'T WE HAVE SURPLUS CELLS FROM THE REPAIR IT CAN YOU HAVE ESTABLISHED. 

THERE'S A BIG DISCUSSION GOING ON IN OUR COUNTRY NOW, MR. SPEAKER, ABOUT EMBRYONIC STEM CELLS. 

THEY VOTED HOW MANY BILLIONS OF DOLLARS IN CALIFORNIA TO PURSUE EMBRYONIC STEM CELL RESEARCH BECAUSE A BIG PERCENT OF OUR POPULATION BELIEVES THERE COULD BE MAJOR MEDICAL APPLICATION THERE, WHICH WOULD PROVIDE MIRACULOUS CURES FOR MANY OF OUR DISEASES. 

THEN WE HAVE A LARGE NUMBER OF PEOPLE THE PRO-LIFE COMMUNITY, THAT HAVE A BIG PROBLEM WITH TAKING THESE EMBRYOS, ANY ONE OF WHICH COULD BECOME A BABY. 

WE HAD MORE THAN 100 OF THEM CALLED THE SNOW FLAKE BABIES THAT HAVE BEEN ADOPTED AND PLANTED IN THE RECEPTIVE WOMB OF A MOTHER AND HAVE BECOME A BABY.

TO TAKE THIS HUMAN LIFE, AND IT IS A LIFE AND IT IS HUMAN, TO DESTROY IT TO PRODUCE A STEM CELL LINE. NOW, MOST OF THIS DEBATE IGNORES THE FACT, SIMPLY BECAUSE THE DEBATERS DON'T KNOW THAT IT IS POSSIBLE, MR. SPEAKER, TO GET EMBRYONIC STEM CELL LINES WITHOUT HARMING EMBRYOS. I'D LIKE TO GO BACK TO THE SECOND CHART I SHOWED, THE HALF OF THE REPRODUCTIVE TRACT OF A FEMALE SO WE CAN LOOK AT THIS AGAIN TOGETHER SO THAT WE UNDERSTAND CLEARLY WHAT WE ARE TALKING ABOUT HERE. 

AND WE'LL IMAGINE NOW THAT THIS IS HAPPENING IN THE LABORATORY AND IT IS IN A PETRI DISH, IN GLASS, IN VITRO IS WHAT WE CALL IT. BECAUSE THE PARENTS COULDN'T HAVE A BABY ANY OH WAY, THEY DECIDED TO HAVE -- IN ANY OTHER WAY, THEY DECIDED TO HAVE IN VITRO FERTILIZATION AND THEY WOULD LIKE TO DO ONE THING, THAT IS ESTABLISH A REPAIR IT CAN FOR THEIR BABY. THEY MIGHT WANT TO DO A PREIMPLANTATION GENETIC DIAGNOSIS.

SO NOW THE PHYSICIAN IN THE CLINIC WILL WAIT UNTIL THE CELLS DIVIDE AND PRODUCE SEVERAL EMBRYOS. AND BY THE WAY, THEY DON'T ALL PRODUCE GOOD-LOOKING EMBRYOS.

SO THEY FERTILIZE MORE THAN ONE EGG. THEY WILL TAKE THE BEST OF THEM.

GENERALLY MORE THAN ONE OF THEM, ONE OF MY COLLEAGUES, MR. ROHRABACHER OF CALIFORNIA, HIS WIFE HAS THREE BEAUTIFUL BABIES FROM IN VITRO FERTILIZATION. 

I DON'T KNOW HOW MANY THE DOCTOR IMPLANTED, BUT THREE GREW AND SHE HAD TRIPLETS. I SAW A RECENT PICTURE OF THEM IN THEIR LIFE VESTS OUT IN THE SURF IN CALIFORNIA. 

THERE IS A POTENTIAL ETHICAL ARGUMENT EVEN IF WE LET THE PARENTS MAKE THE DECISION WE ARE GOING TO DO THE IN VITRO FERTILIZATION.

IF THE PARENTS ESTABLISH THEY ARE GOING MAKE A REPAIR IT CAN AND ALL WE ASK FOR IS A FEW CELLS FROM THAT REPAIR IT CAN. 

YOU SEE, IF THE CELL IS TAKEN FROM THE EIGHT-CELL STAGE, THEN YOU COULD MAKE THE ARGUMENT THAT MAYBE THE CELL YOU TOOK COULD BECOME ANOTHER EMBRYO. SO THEN YOU START ALL OVER AGAIN WITH THE ETHICAL ARGUMENT. YOU NOW HAVE ANOTHER EMBRYO. 

AND SO YOU NOW, ETHICALLY, SHOULDN'T DESTROY THAT EMBRYO WITH THE HOPE THAT YOU'RE GOING TO HAVE SOME APPLICATIONS TO HEALTH CARE FOR SOMEBODY ELSE. THERE IS, MR. SPEAKER, ONE WAY TO AVOID THIS. IT IS ONE OF THE THINGS OUR RESEARCH, H.R. 3144, WOULD PURSUE, THAT IS WAITING A LITTLE LATER TO TAKE THIS CELL. I'M NOT SURE FOR ALL THE REASONS THAT THEY TAKE THE CELL AT THE EIGHT-CELL STAGE, BUT THAT IS THE CONVENTION.

 IF YOU WAITED TO TAKE THAT CELL FROM THE INNER CELL MASS STAGE, WHICH IS A LITTLE LATER, A FEW DAYS LATER, THEN THE DIFFERENTIATION IS HAS ALREADY OCCURRED TO THE POINT THAT THE CELLS IN THE INNER CELL MASS WHICH CAN PRODUCE THE WHOLE BABY, BUT THEY CAN'T PRODUCE A BABY BY IMPLANTATION BECAUSE THEY HAVE LOST THE ABILITY TO PRODUCE DECIDUA. 

SO YOU HAVE NOW REMOVED THAT POSSIBLE ETHICAL ARGUMENT. 

ALTHOUGH THOSE WHO WROTE THE WHITE PAPER ON THE ALTERNATIVE SOURCES OF HUMAN PLURIPOTENT STEM CELLS DON'T BELIEVE YOU CAN DO THIS. IF THERE IS ANY POSSIBILITY YOU CAN DO THIS, THOSE WHOSE SENSITIVITIES WOULD BE OFFENDED BY THIS, IF YOU COULD DEMONSTRATE YOU TAKE IT FROM THE INNER CELL MASS STAGE NOW YOU HAVE BYPASSED EVEN THAT. OUR BILL, H.R. 3144, IS A BILL THAT LOOKS, FOR THE MOMENT, ONLY AT ANIMAL EXPERMENTATION. 

WE BELIEVE BEFORE YOU GO TO HUMANS YOU OUGHT TO KNOW WHAT YOU ARE DOING IS GOING TO WORK AND THAT IT HAS WORKED AND THE BEST WAY TO DO THAT IS GO TO ANIMALS AND NONHUMAN PRIMATES, THE BIG APES, WHICH GENETICALLY, BY THE WAY, ARE REMARKABLY CLOSE TO HUMANS. IT MAY BE EMBARRASSING TO LOOK AT THE GENETIC COMPLEMENT OF THE GREAT APES. 

THERE ISN'T ALL THAT MUCH DIFFERENCE. ONCE WE DEMONSTRATE IT THERE WE COULD HAVE MORE CERTAINTY IT IS GOING TO WORK IN HUMANS. 

WHAT WE DON'T NEED, MR. SPEAKER, IS FOR MILLIONS OF AMERICANS FEEL THEIR LAST BEST HOPE FOR A CURE FOR A RELATIVE HAS BEEN REMOVED WHEN THE PRESIDENT VETOS H.R. 810 AND ITS SENATE COMPLEMENT WHICH HE HAS SAID HE WILL DO AND I HOPE HE DOES, IT IS THE ETHICAL THING TO DO. WE NEED HAVE THIS BILL ON THE PRESIDENT'S DESK SO THE MILLIONS OF PEOPLE WHO BELIEVE THERE IS A POTENTIALLY A LOT OF APPLICATIONS IN HEALTH CARE WILL KNOW THAT THE FEDERAL GOVERNMENT BELIEVES WITH THEM THAT THIS IS POSSIBLE, THAT WE ARE GOING TO SUPPORT RESPONSIBLE, ETHICAL, RESEARCH. USING CELLS TAKEN FROM EARLY EMBRYOS THAT DO NOT KILL THE EMBRYO, DON'T HARM THE EMBRYO. 

AS A MATTER OF FACT, IF, MR. SPEAKER, WE GET THOSE SURPLUS CELLS FROM THE REPAIR IT CAN, THE PARENTS HAVE MADE TWO DECISIONS WHICH I THINK AND I BELIEVE MOST AMERICANS WILL THINK ARE ETHICAL. 

ONE IS TO HAVE THEIR OWN BABY THE ONLY WAY TO DO IT IS IN VITRO. SECONDLY, TO ESTABLISH A REPAIR IT CAN SO ANY TIME DURING ITS LIFE THEIR CHILD IS GOING TO HAVE THE POTENTIAL FOR NEW TISSUES, NEW ORGANS, NEW CELLS. IT IS GOING TO BE THEM SO THERE WILL BE NO REJECTION. 

MR. SPEAKER, WHAT WE SAW LAST NIGHT I HOPE RESULTS IN A VERY POSITIVE EVENTUALITY. 

I HOPE H.R. 810 AND ITS SENATE COMPLEMENT GETS TO THE PRESIDENT'S DESK THAT ALSO ON HIS DESK IS H.R. 3144 SO THAT THE PRESIDENT CAN SAY, TODAY I PROUDLY SIGN A BILL WHICH PROVIDES FOR RESEARCH THAT HAS THE POTENTIAL OF PRODUCING EMBRYONIC STEM CELLS FOR ALL THE MIRACULOUS APPLICATIONS TO HEALTH CARE THAT CITIZENS ALL ACROSS THE COUNTRY BELIEVE. BECAUSE IN STATE AFTER STATE NOW THEY ARE VOTING IN REF RENDA, SOMETIMES IN THE LEGISLATURE, SOMETIMES WITH JUST THE PEOPLE TO PROVIDE LARGE AMOUNTS OF MONEY STATEWIDE BECAUSE THE FEDERAL GOVERNMENT IS NOT DOING IT AND THEY BELIEVE THERE IS BIG POTENTIAL THERE. I HOPE IN THE NOT TOO DISTANT FUTURE WE WILL BE USING FEDERAL FUNDS TO SUPPORT RESPONSIBLE, ETH COOL, EMBRYONIC STEM CELL RESEARCH. H.R. 3144 WILL DO IT. 

THANK YOU VERY MUCH, MR. SPEAKER. I YIELD BACK THE BALANCE OF MY

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Friday, May 8, 2020

Tales Of The New Crown: Medicaid Fraud In Child Welfare Through The Eyes Of Bill Gates

They test the vaccines on children of "The Poors" (always said with clinched teeth).

Gates Foundation Partners With The Clinton Foundation In Child Welfare Trust Fund Fraud

This is the direction of SCOTUS.

This is about the residuals of the peculiar institution, by procuring and purveying tiny humans, in the name of the lord, through their Public Private Partnerships, by stealin' the children, land & vote.

Gerrymandering.

Welcome to the world of Medicaid Fraud in Child Welfare.

And no one will speak upon it, yet.

SCOTUS: The Very First Live Broadcast Of The Very First Time The World Witnesses The Dark Residuals Of The Peculiar Institution On Stealin' The Children, Land & Vote - Parental Rights




Listen to him talk about using the children as lab rats, and they die.

They run these tiny human testing with Medicaid, federal tax dollars. They buy and sell these kids for testing. It is horror and all the corporations have funding through their children's trust funds in these operations under the Vatican.

They snatch children from their mothers.

They make these zygotes in the lab.

And they do it in the name of god.

They force these mothers and girls into prostitution to snatch the babies to sell. It is called adoption. 

Refugee children come out these systems.

Foster children come out this system.

This is about Parental Rights because you do not have to worry about that pesky legal thing called consent.


Yet, no one cares, or do they, and are just terrified?

#maytheheavensfall

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Friday, May 1, 2020

Tales Of The New Crown: A SWIFT Alternative Transposable Model To Contact Tracing - Follow The Money

I have a way better idea for contact tracing using a transposable model.

It is economically feasible and there is already an established model.

Instead of tracing people contact, how about we trace the financial transactions behind everything government officials and their government sanctioned activities are doing, in a SWIFT, and efficient manner of due process through law enforcement?

Follow the money.

Considering the fact that these are public expenditures, I am quite sure there will be no problems with a FOIA.

If that does not work, keeping in mind that these are Public Private Partnerships, I am quite sure a SIGTARP subpoena would also work, just as swiftly because this is gerrymandering.

Detroit already has a tracer tracking system to ensure everyone makes their date, because, before you are a man, you are a child.


First, this happened.....

MDHHS Launches Large-scale, Volunteer Contact Tracing Effort; Expands Testing Criteria to Include Any Worker Still Reporting in Person

LANSING, MICH. As part of efforts to continue expanding COVID-19 testing and contact tracing of potentially exposed Michiganders, the Michigan Department of Health and Human Services (MDHHS) again expanded its testing criteria to include all essential workers still reporting to work in person, whether they have symptoms or not, and launched a large-scale effort with more than 2,000 volunteers to expand contact tracing capacity.

“Contact tracing is an essential public health tool and will help determine and limit the spread of COVID-19 in our state,” said Dr. Joneigh Khaldun, chief medical executive and chief deputy for health. “This effort is also giving Michiganders an important way to contribute to crisis response and we appreciate their willingness to step up for their communities, pitching in selflessly for work that will help us all.”

Contact tracing is a proven public health strategy that involves identifying those affected by COVID-19 and interviewing friends, families and others near that person about their contacts and symptoms. MDHHS is contracting with Great Lakes Community Engagement, a firm that specializes in outreach campaigns to engage citizens, and Every Action VAN, a voter/individual contact platform used by non-profits, to provide software to help organize remote phone banking and track information and contacts.

More than 2,200 volunteers have completed MDHHS’ contact tracing training and are ready to begin aiding local health departments. This workforce will increase the speed and thoroughness of contact tracing statewide. These volunteers are in addition to more than 130 MDHHS staff who have been assisting local health departments with case investigation over the past couple weeks and have reached more than 12,000 COVID-positive individuals.

Dedicating additional resources to contact tracing is needed as testing criteria and testing locations are rapidly expanding. Last week, MDHHS announced the expansion of testing to all Michiganders experiencing symptoms. Starting April 21, testing eligibility criteria is being expanded again to include all essential workers still reporting to work in person with potential COVID-19 exposure, whether symptomatic or asymptomatic. This will help identify asymptomatic cases who may still be spreading the virus as they report to work.

“This means that anyone with symptoms can get a test as well as any individual regularly interacting with others outside their household, as long as the testing location has the supplies,” Khaldun said. “MDHHSis also working with local health departments to expand testing in group living facilities with potential exposure.”

To sign up to volunteer for public health efforts, visit Michigan.gov/fightcovid19. To locate a testing site near you, visit Michigan.gov/CoronavirusTest.

Information around this outbreak is changing rapidly. The latest information is available at Michigan.gov/Coronavirus and CDC.gov/Coronavirus.

Then, this happened....

Voting is beautiful, be beautiful ~ vote.©

Thursday, April 23, 2020

Tales Of The New Crown: Sunlight Kills The Cooties - Then MSNBC Lied

I know what the light is.

The light cleanses. Listen to him.

The reporters are losing their minds. Sunshine and hot weather kills the cooties. It is recommended by DHS top doctors to spend lots of time outside, barbequing, with your family and friends, in the community.

Oooooooo.... these people already spent the money.

These black souls do not want sunlight.

These allegories are going to be important.

We may not need testing when it gets hot and sunny

"And there shall be feast and merriment throughout the land."



Sunlight kills the cooties.

No photo description available.

We will be addressing certain democratic states. 

Illinois will be talked about for a while. 

Michigan cometh.

#perkinscoiesucks

and so does JonesDay.



Then, MSNBC lied, again.

#maytheheavensfall

Voting is beautiful, be beautiful ~ vote.©

Friday, April 10, 2020

Tales Of The New Crown: Good Friday Is The Day For The Prayer Of Reparations - May The Heavens Fall

Image
"MeToo", said the blashphemer.
Good Friday is the day of the Prayer of Reparations.

Reparations have nothing to do with slavery or the color of one's skin, but the heretics do not care as long as they make money.

It is part of the Second Amendment for the crime of blasphemy for those in heaven, otherwise known as the elected officials who have been improperly defrocked by lies, propaganda, in the violation of oaths of office.

The Second Amendment is the default mechanism of the First Amendment, when your voice in grievance of governance is ignored.

There is a separate set of laws for officials who have been granted the right to bear the arms of the state.

Reparations is the prayer for Jesus, Christ the King, to receive justice for the ethical crime of blasphemy, or rather propaganda in false claims, which led to his removal of office as to protect the children's trust, more readily understood as public trust, the posterity of the best interests of society, in a removal as a leader, figure head of society, by and through the voice of the people in consent, not fear, in the public record, in a court ordered death, by fraud.

Hence, the fall from the heavens, stripped of his crown, in a stained, amorial in legacy, heraldry, devoid of due process or the right to voice one's innocence.

The apostasy is when these public and private for profit and not for profit officeholders renounce the laws of the land, in ethics, or what I prefer to call stealin' the children, land & votes, by exiling the right of vote, by kicking due process off the edge of the democratic world.

Grand juries possess the right to vote, you know.

The Prayer of Reparations is for office holders, who dedicate their lives through the oath of protecting the future of a civil society by representing the people who believe in the content of character, through the transfer of their voice, in consent or grievance, in justice for all in the triggering of the Second Amendment, through courts of law, in ancient mechanisms such as the writ of quo warranto.

Reparations:

  • the act of making amends, offering expiation, or giving satisfaction for a wrong or injuries
  • something done or given as amends or satisfaction
  • the payment of damages : INDEMNIFICATION
  • specifically : compensation in money or materials payable by a defeated nation for damages to or expenditures sustained by another nation as a result of hostilities with the defeated nation —usually used in plural

This story is used to teach society about bearing false witness.

Propaganda, lies against one who holds office and was made to fall from the heavens, to the earth, to be tried by the laws of man.

This Passion Prayer is performed on Good Friday.

I performed thees acts of therugy in the art of perfection in words, my prayers to the court.

Justice is not always about getting a check.

There is higher value of settlement; love, the agape of society.

The love of man is supposed to be the land, but it is not, as the United States maintains the hierarchic laws of human property classifications, residuals of the peculiar institution.

This is the foundation of the Second Amendment, the right to keep and bear the arms of the nation in heraldry, another set of ecclesiastic law.
Prayer of reparation for insults and blasphemies
O Jesus, my Savior and Redeemer, Son of the living God, behold, we kneel before Thee and offer Thee our reparation; we would make amends for all the blasphemies uttered against Thy holy name, for all the injuries done to Thee in the Blessed Sacrament, for all the irreverence shown toward Thine Immaculate Virgin Mother, for all the calumnies and slanders spoken against Thy spouse, the holy Catholic and Roman Church. O Jesus, who hast said: "If you ask the Father anything in My name, He will give it to you", we pray and beseech Thee for all our brethren who are in danger of sin; shield them from every temptation to fall away from the true faith; save those who are even now standing on the brink of the abyss; to all of them give light and knowledge of the truth, courage and strength for the conflict with evil, perseverance in faith and active charity! For this do we pray, most merciful Jesus, in Thy name, unto God the Father, with whom Thou livest and reignest in the unity of the Holy Spirit world without end. Amen

Blasphemy is what no one wants to talk about because there are certain heretics who wish to repeal ancient moral code, from the annals of history.

This moral concept of reparations is Talmudic in origin, but many fail to understand the mechanisms to engage such legal mechanisms, as these are not laws of the land, but of the heavens, or more intuitively understood as attorneys, elected officials, for and not for profit office holders who bear the arms of the state, being the United States.

When an elected official is removed from office, without due process, and dies, however shall reparations be obtained, is the sacred mystery of atonement we, as a world, have yet to address because Trump keeps obstructing justice by keeping that IG Report in his backpocket.

Perhaps, Trump will be the Easter Bunny and bring justice for all, in the form of reparations, because slavery was never abolished, it is just called modern human trafficking, but I prefer the term trafficking tiny humans, because it always starts with the children because that is how this great nation was built.

Duty of reparation
In the encyclical Miserentissimus Redemptor Pope Pius XI said:
"The creature's love should be given in return for the love of the Creator, another thing follows from this at once, namely that to the same uncreated Love, if so be it has been neglected by forgetfulness or violated by offense, some sort of compensation must be rendered for the injury, and this debt is commonly called by the name of reparation".

The Archdiocese of Detroit is praying for themselves and their co-conspirators, as the U.S. administrator of the Vatican, for what they are doing through the Detroit Land Bank Authority and the bastardization of my Sweetie's legacy.

I am the Rood, the original source.

 #maytheheavensfall

Knights of Columbus support Vatican broadcasts during Holy Week

The Knights of Columbus announce their financial support of the Vatican’s Holy Week and Easter broadcasts, and a gift to the Vatican’s Pediatric hospital.
By Fr. Benedict Mayaki, SJ

Christians around the world are preparing to celebrate the Easter Triduum amid the coronavirus pandemic. In order to help as many people as possible participate in the liturgies from the Vatican, the Knights of Columbus will provide financial support for the global broadcast of the Way of the Cross on Good Friday, and the Easter Mass on Sunday.

In a statement released on 8 April, the Knights communicate that they will underwrite the cost of broadcasting both the Good Friday Stations of the Cross on 10 April led by Pope Francis, and the Pope’s Easter Sunday Mass and Urbi et orbi blessing on 12 April. The funding will cover costs related to the satellite transmission of these events.

On 27 March, the Knights of Columbus sponsored the broadcast of Pope Francis’ extraordinary Moment of Prayer and Urbi et orbi blessing (to the city of Rome and the rest of the world) which took place in St. Peter’s Square.

Donation to hospital
In a separate initiative, the Knights are donating $100,000 to the Vatican’s Bambino Gesù pediatric hospital in Rome. This donation will be used to transform a space in the hospital’s neonatology department into a treatment room for infants and newborns who are infected with the Covid-19 virus.

The unit will be named after the founder of the Knights of Columbus, the Venerable Servant of God Father Michael J. McGivney. It will feature ventilators and other specialized equipment associated with the treatment of coronavirus’ respiratory symptoms.

Timely support
The Supreme Knight, Carl Anderson, noted that “these projects are particularly timely given the global pandemic…With so many in Italy and around the world currently homebound, our support of Vatican broadcasts will allow our Holy Father to join in prayer with Catholics from every corner of the globe during this critical time.”

The Knights of Columbus have worked in Rome at the request of the Popes for 100 years. “Our support of Bambino Gesù hospital continues that tradition of service,” the Supreme Knight said.

The Knights of Columbus
The Knights of Columbus were founded by the Venerable Father Michael J. McGivney in Connecticut, USA in 1882. The organization established its presence in Rome in 1920 at the invitation of Pope Benedict XV. The Knights have been supporters of the telecommunications efforts of the Vatican. In 1965, the organization funded a shortwave transmitter for Vatican Radio. They have also sponsored Vatican satellite broadcasts since 1977.


Happy Passover

Happy Ramadan

Voting is beautiful, be beautiful ~ vote.©

Sunday, April 5, 2020

The Death Of James Taylor: The Industry Of Trafficking Tiny Humans Is Quite Complex & Extremely Lucrative

James Taylor was quite fond of the tiny humans.

The industry of trafficking tiny humans is quite complex and extremely lucrative.

This is yet another segment modern day human trafficking.

There are many, many more.

https://nekrut.github.io/lab_site/

This is about Corporate Parental Rights.

Who owns the zygotes?

Better yet, where did they get the zygotes?

https://beverlytran.blogspot.com/2019/09/biogenetic-legal-library-of-corporate.html

In Memoriam, Professor James Taylor

Featured image
James Taylor
It is with great sorrow that the Krieger School of Arts and Sciences shares that James Taylor, Ralph S. O’Connor Professor of Biology and Professor of Computer Science, died on Thursday, April 2, 2020. He was 40.

Professor Taylor was a trailblazer in computational biology and genomics research. He had an enormous impact as a scientist, teacher, and colleague, and his loss is devastating to many – both here in our Hopkins community and around the globe.

As one of the original developers of the Galaxy platform for data analysis, Professor Taylor and his lab group focused on extending the Galaxy platform as well as on understanding genomic and epigenomic regulation of gene transcription through integrated analysis of functional genomic data. The ultimate goal is to achieve a complete understanding of the structure and function of genomes.

The Galaxy platform serves as software for the entire genomics community worldwide, giving a powerful boost to researchers’ ability to process data and make groundbreaking connections across organisms. But Professor Taylor was also involved with many other projects; for example, he developed a strategy to support the health of the Chesapeake Bay by detecting microorganisms in the Baltimore Harbor and monitoring their levels continuously using newly developed, portable, and rapid DNA sequencing technologies.

Vince Hilser, chair of the biology department, describes Professor Taylor as a bedrock of the department. “He came in 2014, and it was transformational. He was this catalyst for change, with a huge positive impact.” His presence in the department opened up many areas for research, as he was able to help other faculty members uncover new insights by revealing similarities between the proteins they were studying and those in other organisms.

What Professor Taylor did for the department, he also did for the broader research community. In addition to his crucial involvement with Galaxy, he collaborated broadly, and was cited with great frequency.

A familiar figure on the Homewood campus, riding his skateboard, Professor Taylor was a beloved teacher and mentor who treated his students as equals. He approached his work with passion and energy, and was a friend and colleague to many in our community, who share in mourning his loss deeply.

Biology Assistant Professor Rajiv McCoy says he counted Professor Taylor as a mentor and friend. “He blazed a trail for computational research within the Department of Biology and is one of the main reasons that I came to Hopkins. James was a selfless advocate for trainees and junior faculty, working tirelessly in the background on our behalf. James was also an outspoken proponent of reproducibility in computational research. His work to highlight this issue and develop tools for addressing it has been invaluable to the scientific community. I am shocked and heartbroken by this loss and its impact on his family, friends, and colleagues.”

John Kim, associate professor in Biology, shared adjoining offices and labs with Professor Taylor in the UTL building. He wrote, “For the past five years, we had grown very close as colleagues with common scientific interests but more importantly, as friends. He was such a passionate advocate for collaborative research and his influence went well beyond the university to the broader scientific community. His is an incalculable loss. James was soft-spoken, kind, and compassionate. His office door was always wide open, inviting anyone to come in to talk. He furnished it sparsely, with just a small round table in the middle and speakers by the windows playing a broad and eclectic selection of music while he worked on his laptop. It was an open, inviting space where I and many others would stop in to talk about science or just to say hello. He was a great listener, so thoughtful and generous with his time. We have lost a brilliant scientist and a great friend to the many lives he touched and made better.”

anVIL
https://anvilproject.org/
Michael Schatz, Bloomberg Distinguished Associate Professor of Computer Science and Biology, spoke of Professor Taylor’s far-reaching scientific and personal impact. “James was an exceptional scientist, colleague, mentor, and community builder,” Professor Schatz wrote. “His life’s pursuit was to understand how genomic information is used in normal development and how changes in the genome can dysregulate this process in disease. Further, through co-leading the Galaxy project and the Anvil project, a major thrust of James’ career has been to support the work of other scientists, especially to empower those with limited resources. His impact is immeasurable, with thousands of scientists that have benefited from his leadership and contributions. On a personal level, James was always kind, friendly, and generous, and we will miss him dearly.”

Galaxy Community Hub
https://galaxyproject.org/galaxy-project/

Professor Taylor earned his BS in computer science from the University of Vermont in 2000, and his PhD in computer science in 2006 from Penn State University, where he was involved in several vertebrate genome projects and the ENCODE project. Before arriving at Johns Hopkins, he was an associate professor in the departments of biology and mathematics and computer science at Emory University from 2008 until 2013. At Hopkins, he also held an appointment in the Whiting School’s Department of Computer Science.

https://www.encodeproject.org/
"Who owns the zzygote?"
He was a member of the Science Gateways Institute Steering Committee, and had been a member of the National Center for Genome Analysis Scientific Advisory Board from 2014 to 2016; a member of the iPlant Scientific Advisory Board member from 2013 to 2016; a member of the XSEDE Project User Advisory Committee from 2012 to 2014; and co-chair of the International Arabadopsis Informatics Consortium: Engineering, Architecture and Infrastructure Working Group in 2011.

Professor Taylor is survived by his wife, Meredith Greif, assistant professor in the Department of Sociology. We send our deepest condolences to her as well as to his colleagues in the Department of Biology and far beyond.

Voting is beautiful, be beautiful ~ vote.©