Scientific racism's long history mandates caution

PUBLIC RELEASE DATE:

14-Feb-2014

Contact: A'ndrea Elyse Messer aem1@psu.edu 814-865-9481 Penn State

Racism as a social and scientific concept is reshaped and reborn periodically through the ages and according to a Penn State anthropologist, both medical and scientific researchers need to be careful that the growth of genomics does not bring about another resurgence of scientific racism.

"What we are facing is a time when genomic knowledge widens and gene engineering will be possible and widespread," said Nina Jablonski, Distinguished Professor of Anthropology. "We must constantly monitor how this information on human gene diversity is used and interpreted. Any belief system that seeks to separate people on the basis of genetic endowment or different physical or intellectual features is simply inadmissible in human society."

What worries Jablonski and the sociologists, psychologists and evolutionary biologists in her session at the annual meeting of the American Association for the Advancement of Science, today (Feb. 14) in Chicago, are people who believe that they can use genetic traits to describe races and to develop race-specific interventions for each group. One particularly disturbing approach, although currently suggested as beneficial, is application of genetics to create special approaches to education. The idea that certain individuals and groups learn differently due to their genetic makeup, and so need specialized educational programs could be the first step in a slippery slope to recreating a new brand of "separate but equal."

Similar approaches in medicine that are based not on personal genetics but on racial generalizations can be just as incorrect and troubling, especially because human genetic admixture is so prevalent.

"Our species is defined by regular admixture of peoples and ideas over millennia," said Jablonski. "To come up with new reasons for segregating people is hideous."

Classification of humans began innocently enough with Carl Linnaeus and Johann Friedrich Blumenbach, who simply classified humans into races in the same way they classified dogs or cats -- by their physical characteristics. These were scientists classifying the world around them and realizing that the classifications were not immutable but had a great deal of diversity and overlap. However, in the last quarter of the 18th century, philosophers, especially Immanuel Kant, looked to classify people by behavior and culture as well as genetics. Kant suggested that there were four groups of people, three of which because they existed under conditions not conducive to great intellect or achievement were inferior. Only the European race was capable of self-improvement and highest level of civilization.

Kant's ideas, widely accepted during his lifetime, set up the idea of European superiority in the future. Coupled with the great rise and profitability of slavery at the time, his views were adopted and morphed to legitimize the slave trade.

Visit link:

Scientific racism's long history mandates caution

European Parliamentarian Vows to "Fight to the End" Child Euthanasia Law

Luca Volonte Says Measure is a Step Backwards For Society Rome, February 14, 2014 (Zenit.org) | 102 hits

A prominent member of the Council of Europe criticized yesterdays decision in Belgium that extended the countrys euthanasia law to children under the age of 18.

In an interview with Avvenire, Luca Volonte, Italian member of the Parliamentary Assembly of the Council of Europe, has been one of many opponents of the new law, calling it a step in the wrong direction.

We are at a point of no return, the law in favor of euthanasia for children is a step backwards to the beginning of the 20th century, when the culture of statewide eugenics provoked the appalling tragedies that we all know, Volonte said.

The Italian politician, who participated in prayer vigils against the law, has now thrown his support behind a petition carried out by CitizenGo that will be presented to King Philippe of Belgium, urging him to not sign the controversial measure.

Volonte said the law invents an alleged consensus by children from 4-5 years old, while suggesting that such a consensus was only made by pressure from a commission of experts examining the request for euthanasia.

Everyone knows that before 10 years old, children havent even grasped the concept of death, many pediatricians and child psychologists have said so; many of whom, and not by chance, have opposed the law, he said.

Despite the overwhelming support for the law in Parliament, Volonte expressed his hope that the voice of the Belgian people will overcome. The Italian politician said that recent polls indicated that 55% of the Belgian population is against the law. In short, Belgian society has reawakened, he said.

Regarding the petition campaign that will be sent to the king, Volonte said that King Philippe can send the measure back to parliament. This shameful law, he said, was imposed by a majority that, above all, in a few months, will not be there any more. If the measure is sent back, the Belgian Parliament will most likely be unable to pass a new measure prior to elections.

Volonte, who is also chairman of the Dignitatis Humanae Institute, also raised the possibility of international pressure against the law, which he said, goes against the eugenics practices that have been banned by the United Nations.

Go here to read the rest:

European Parliamentarian Vows to "Fight to the End" Child Euthanasia Law

Black History Month talk to focus on story of Joshua Glover

RACINE One of the leaders of Americas Black Holocaust Museum will be at the Racine Public Library, 75 7th St., for a pair of events during Black History Month.

Reggie Jacksons first talk will be Wednesday night about Joshua Glover, a runaway slave who sought asylum in Racine. The free event is scheduled to begin at 6 p.m.

Glover escaped from St. Louis and lived in Racine for about two years before he was captured and jailed. Jackson said his speech will focus on how local residents helped free Glover from jail and move him to Canada through the Underground Railroad.

Its really a fascinating story of how the Underground Railroad was a part of Wisconsin, Jackson said.

His Feb. 26 speech, which also begins at 6 p.m., will focus on eugenics, a practice prevalent in the late 1800s and early 1900s that sought to improve genetics, in part by sterilizing people in the bottom rungs of society.

Jackson will discuss the ramifications of that practice and laws in place at the time that still make an impact today.

Jackson is no stranger to the Racine library. He appeared multiple times last year, facilitating a movie series on civil rights and a presentation on Americas Black Holocaust Museum founder, Dr. James Cameron.

Hes planning more speeches on race later this year, he said. Jackson has gotten a great response each time and the library is eager to have him back, Librarian Nick Demske said.

Jackson regularly gives talks in Wisconsin and around the Midwest on aspects of history related to blacks. By day, hes a special education teacher in Milwaukee.

Hes been involved with Americas Black Holocaust Museum since 2002. While the museum closed in 2008, Jackson helped establish an online presence for the museum and is part of an ongoing effort to re-establish a physical presence.

Continue reading here:

Black History Month talk to focus on story of Joshua Glover

PETA Combats Dog Breeding With Hitler Mustache

PETA has a message to share, and it's going to share it whether it has to depict a dog with a Hitler mustache or not. (It does though.)

In anticipation of the upcoming Westminster Kennel Club dog show, PETA's latest ad campaign equates dog breeding to eugenics with the catchy tagline "Master Race? Wrong for People. Wrong for Dogs. Ban Breeding." A black comb partially obscures the upper lip of a...what is that? A poodle?...giving it the appearance of a Furry Fhrer. It's unclear what the animal's baby pink ribbon and small side ponytail are meant to represent, but, if we had to guess, we'd say the Khmer Rouge and...Mean Girls? Respectively? Maybe the other way?

"A fetish for 'pure bloodlines' and a disdain for 'mixed breeds' is a despicable attitude to have toward any living being," PETA Senior VP Daphna Nachminovitch said in a statement. "As millions of animals die in animal shelters every year for lack of good homes, it's criminal to celebrate the breeders who contribute to this deadly overpopulation crisis."

A rally will be held outside Madison Square Garden on February 10the first day of the dog showat 5 p.m.

Link:

PETA Combats Dog Breeding With Hitler Mustache

To Catch a Killer Gene: Sisters Race to Stop Mystery Disease

Days before she ended her pregnancy, Joselin Linder was thrilled to imagine herself as a parent. She was 37, newly-married, and though her baby-to-be wasnt planned, it was soon deeply desired. Maybe its that I played with dolls until I was so old I had to play with them in my closet, she says. But it seemed inevitable that I would one day be a mother.

Linder is not a mother today, more than a year later, because she had an abortion at 10 weeks. She still wanted the childwanted to call it George, perhapsbut she feared she would pass along the disease that killed her father in mid-life, practically fusing his organs and ballooning his body. She and her sister Hilary inherited the same unnamed illness, but as with most of the thousands of inheritable diseases known to science, there is no cureexcept for stopping the affected bloodline.

Its an agonizing form of prevention the Linder sisters have turned to four times combined. Theyve had three abortions, and in 2009, Hilary and her husband paid $20,000 out of pocket for a round of in vitro fertilization aimed at creating an unaffected embryo. The gene has killed five people in the Linder family, and it now threatens the sisters themselves. But if they have their way, it will die out in their generation.

I think thats a big deal, says Joselin, who lives in Brooklyn, N.Y. I think weve done something amazing with this particular gene.

The Linders story is personal, of course, but its also a public milestone. Its the first known example of genetic medicine not only identifying a deadly new mutationakin to the next Huntingtons or Cystic Fibrosisbut of a family banding together to stop a disease before it cuts a path through society itself. It illustrates the promise of genomic medicine, which may one day stop disease as we know it, but also the soul-troubling questions that arise when people have a hand in their own evolution.

America is experiencing a boom in biological fortune-telling. Doctors can now scan the genes of a fetus using only a drop of the mothers blood, testing for hundreds of known mutations, including Down syndrome. Soon theyll be able to detect a growing list of rare mutationsalmost none of them treatableand predict an embryos risk of more common ailments like diabetes, cancer, and heart disease. By that point, millions of pregnant women will be offered a God-like view of their child-to-be and a decision much like the Linders, a decision as miraculous as it is unnerving: When is a life worth living?

The family gene, as Joselin calls it, surfaced in the late 1980s, when her father William came home from a family trip complaining of swollen legs and strange fatigue. He waved it off as jet lag, but the swelling spread and the fatigue deepened. He was 40, vibrant and fit, a busy doctor in Columbus, Ohio. But within a couple years he was forced into semi-retirement, hardly able to take the stairs.

Im very, very sick, he told Joselin, who was then 17, and surprised to see her father start to cry. In the years that followed, his body filled with a creamy white fluid, which doctors pumped out by the liter. He got rounder, but lighter, his muscles withering even as something in his belly grew.

He moved into Brigham and Womens Hospital, a Harvard-affiliated facility in Boston, where he confounded some of the countrys best doctors. In his records, which Joselin shared with NBC News, a series of gobsmacked specialists noted puzzling resultsan occult malignancysomething brewing. None could come up with a diagnosis, however, let alone a cure.

William Linder died a medical mystery in September of 1996, his autopsy revealing a body both starved and bloated. The cause of death was officially unknown. His daughters visited him often, right to the end, shuffling ICU visits into their college schedules. They never suspected that they were getting a preview of their own genetic destiny.

Read the original here:

To Catch a Killer Gene: Sisters Race to Stop Mystery Disease

Alan Watt: The President’s Council on Bioethics Camouflages Eugenics (Part 2) – Video


Alan Watt: The President #39;s Council on Bioethics Camouflages Eugenics (Part 2)
See Us @SagaciousNewsNetwork.com http://sagaciousnewsnetwork.com/ Beyond Therapy: Biotechnology and the Pursuit of Happiness http://biotech.law.lsu.edu/resea...

By: SagaciousNewsNetwork

Read the original here:

Alan Watt: The President's Council on Bioethics Camouflages Eugenics (Part 2) - Video

Alan Watt: The President’s Council on Bioethics Camouflages Eugenics (Part 1) – Video


Alan Watt: The President #39;s Council on Bioethics Camouflages Eugenics (Part 1)
See Us @SagaciousNewsNetwork.com http://sagaciousnewsnetwork.com/ Beyond Therapy: Biotechnology and the Pursuit of Happiness http://biotech.law.lsu.edu/resea...

By: SagaciousNewsNetwork

Read more from the original source:

Alan Watt: The President's Council on Bioethics Camouflages Eugenics (Part 1) - Video

Alan Watt: The President’s Council on Bioethics Camouflages Eugenics (Part 3) – Video


Alan Watt: The President #39;s Council on Bioethics Camouflages Eugenics (Part 3)
See Us @SagaciousNewsNetwork.com http://sagaciousnewsnetwork.com/ Beyond Therapy: Biotechnology and the Pursuit of Happiness http://biotech.law.lsu.edu/resea...

By: SagaciousNewsNetwork

More:

Alan Watt: The President's Council on Bioethics Camouflages Eugenics (Part 3) - Video