Breaking the Bonds of Race and Genomics

Posted in Articles, Health/Medicine/Genetics, Media Archive, Politics/Public Policy on 2012-05-07 19:41Z by Steven

Breaking the Bonds of Race and Genomics

GeneWatch
Volume 25, Issue 1 (January-February, 2012): Genetics in 20 Years

Dorothy Roberts, George A. Weiss University Professor of Law and Sociology; Raymond Pace and Sadie Tanner Mossell Alexander Professor of Civil Rights
University of Pennsylvania

Twenty years ago it appeared that mainstream science finally was abandoning the concept of biological human races. From 18th century typologists to 20th century eugenicists, scientists have always been instrumental in justifying the myth that the human species is naturally divided by race. But the rejection of eugenics after World War II and discoveries by human evolutionary biologists in subsequent decades brought hope that a new science of human genetic diversity would replace the old racial science. In 2000, the Human Genome Project, which mapped the entire human genetic code, confirmed the genetic unity of the human species and the futility of identifying discrete racial groups in the remaining genetic difference. Biologically, there is only one human race. Race applied to human beings is a social grouping; it is a system originally devised in the 1700s to support slavery and colonialism that classifies people into a social hierarchy based on invented biological, cultural, and legal demarcations.

But instead of hammering the last nail in the coffin of an obsolete system, the science that emerged from sequencing the human genome has been shaped by a resurgence of interest in race-based genetic variation. Some scientists claim that clusters of genetic similarity detected with novel genomic theories and computer technologies correspond to antiquated racial classifications and prove that human racial differences are real and significant. Others are searching for genetic differences between races that could explain staggering inequalities in health and disease as well as variations in drug response, with the biotechnology and pharmaceutical industries poised to convert the new racial science into race-specific products. As we wait for the promise of gene-tailored medicine to materialize, race has become an avenue for turning the vision of tomorrow’s personalized medicines into today’s profit making commodities. While uncritically importing antiquated racial categories into research, the emerging racial science has a new twist—it claims to measure biological distinctions across races and “admixed” populations with more accurate precision, and without social bias

Read the entire article here.

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A race-based detour to personalized medicine

Posted in Articles, Health/Medicine/Genetics, Media Archive, Politics/Public Policy on 2012-05-07 16:46Z by Steven

A race-based detour to personalized medicine

Canadian Medical Association Journal
Volume 184, Number 7 (2012-03-12)
DOI: 10.1503/cmaj.109-4133

Roger Collier, News Staff

Few experts in medical genetics would argue that June 23, 2005 wasn’t an important day. Consensus on whether it was a good or bad day is another matter. Some claim a major step on the long road to personalized medical care was taken. Others are far less convinced, suggesting it was the day the United States government decided, unwisely, to push the field of medical genetics into the heated realm of racial politics.

On that date, the US Food and Drug Administration (FDA) approved, for the first time, a drug for a specific race, to wit, the fixed-dose combination drug isosorbide dinitrate and hydralazine (BiDil) for use as a heart disease medication within the black population, who have a much higher risk of heart failure than whites…

…The licensing of isosorbide dinitrate/hydralazine thus became a turning point in discussions on the merits of race-based medicine, a debate that continues to rage. Critics of race-specific therapies argue that focusing on genetics rather than on social and economic inequalities will not reduce disparities in health outcomes and access to care among different ethnic groups. Furthermore, they say, race is a social, rather than a biological, construct.

Using race is a bad proxy for genetic ancestry,” says Althea Grant, chief of the Epidemiology and Surveillance Branch, Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, at the US Centers for Disease Control and Prevention.

This opinion is shared by one of the world’s most famous geneticists: Craig Venter, the genetics pioneer who led the team that first sequenced the human genome in 2001. He has referred to the use of race and ethnicity in medical genetics as a crude tool and a personal pet peeve, suggesting that it will no longer be necessary once the price of sequencing genomes falls to an amount that would make it reasonable to sequence everybody’s genome, a figure he pegged at US$1000…

…The first problem with using race in medical genetics is determining which races constitute a part of someone’s background. Few people have extensive knowledge of their ancestral lineage, and skin colour and other external markers don’t tell the full story. Even people who are aware of their mixed heritage often place themselves in one camp — or are put there by others. Prominent examples include US President Barack Obama and professional golfer Tiger Woods, who are often referred to as black even though the former has a white mother and the latter’s mother hails from Thailand.

“People tend to self-identify with a particular race more than another even if there is a mix,” says Grant. “They might not even know all the ancestries that are in the mix.”

In some areas of medicine, using race as a screening tool has already been shown to create problems, both practical and ethical. That’s why states abandoned the practice of screening only black newborns for hemoglobinopathies, such as sickle cell disease, Grant and colleagues concluded (Ethn Health 2011;16:377–88). The state of Georgia, the last holdout for ethnicity-based newborn screening, discontinued its use in 1998…

“If we go back to its origins, we find that BiDil did not begin as an ethnic drug. Rather it became ethnic over time and through a complex array of legal, commercial, and medical interventions, that transformed the drug’s identity,” wrote Jonathan Kahn, a law professor at Hamline University in Saint Paul, Minnesota (www.councilforresponsiblegenetics.org/pageDocuments/PLMVM6FTAO.pdf). Unlike “racialized medicine, which treats race as genetic, the use of race in medical practice has many legitimate and important places. Collecting broad-based epidemiological data is perhaps foremost among these. Only by using social categories of race is it possible to identify and track racial disparities in health, health care access and outcomes.”

Read the entire article here.

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A 30 Percent of Mixed Race Component in Argentina’s Population

Posted in Anthropology, Articles, Caribbean/Latin America, Health/Medicine/Genetics, History, Media Archive, Social Science on 2012-05-05 02:07Z by Steven

A 30 Percent of Mixed Race Component in Argentina’s Population

Agentina Investiga: Divulgación y Noticas Universitarias
Universidad Maimónides
Facultad de Ciencias Médicas
2012-04-09

Adrián Giacchino
Departamento de Prensa
Universidad Maimónides

The research of a team formed by anthropologists, biologists, biochemists and archeologists proves that the autochthonous contribution in Argentina’s population might be of a 30%. The results of the work, emerged from an analysis of blood donors in diverse regions of our country, indicate that there is a 65% of European component, a 30% Amerindian and a 5% African. Amerindian lineage is mainly maternal, decreases as we come close to the city of Buenos Aires and increases towards the north and the south.

How many times we have heard that in Argentina “we come from the ships…” and that we are “a melting pot”. This is believed by many people and it was written many times and even legitimated as valid knowledge. But, do we really come from the ships and are we a real melting pot?

“What exists is the mythology that we are white and European –indicates to InfoUniversidades Dr. Francisco Raúl Carnese, who is in charge of the laboratory of Biological Anthropology of the University-. However, our population is mixed. The native composition is very striking, especially in maternal ancestry, which increases towards the north and the south and it is also very important in the metropolitan area of Buenos Aires, particularly in the suburbs. We have the need to “bleach” populations, but the concept of “melting pot” is questioned. The populations’ genetics showed that there is no continuity between human populations, that the biological variations are of continuous nature. Races do not reflect biological reality, but are social constructions…

Read the entire article here.

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Cultural Inversion and the One-Drop Rule: An Essay on Biology, Racial Classification, and the Rhetoric of Racial Transcendence

Posted in Articles, Barack Obama, Health/Medicine/Genetics, Law, Media Archive, Politics/Public Policy, Social Science, United States on 2012-05-03 02:58Z by Steven

Cultural Inversion and the One-Drop Rule: An Essay on Biology, Racial Classification, and the Rhetoric of Racial Transcendence

Albany Law Review
Volume 72, Issue 4 (2009)
Pages 909-928

Deborah W. Post, Professor Emeritus of Law
Touro College, Jacob D. Fuchsberg School of Law
Central Islip, New York

The great paradox in contemporary race politics is exemplified in the narrative constructed by and about President Barack Obama. This narrative is all about race even as it makes various claims about the diminished significance of race: the prospect of racial healing, the ability of a new generation of Americans to transcend race or to choose their own identity, and the emergence of a postracial society. While I do not subscribe to the post-racial theories that have been floated in the press and other media, I do believe that something of great cultural significance occurred which made the candidacy and the election of Barack Obama possible. This essay is an attempt on my part to consider what that change might have been by examining the relationship between science and social change, language and cultural categories, and the role law has played, if any, in dismantling the structures of racism.

What I have to say has very little to do with biology, except to the extent that racial classification is a cultural practice that sometimes deploys biological arguments strategically. Early in the Twentieth century sociologists and anthropologists noted that in the United States, race was more a matter of caste than class and that, unlike other caste systems, it is not cultural, but “biological.” In a racial caste, one sociologist argued, “the criterion is primarily physiognomic, usually chromatic, with socio-economic differences implied.”  Another noted that “American caste is pinned not to cultural but to biological features—to color, features, hair form, and the like.” Biology was used in this early sociological literature on race in a way that made it synonymous with physical appearance or physical characteristics. In politics and legal discourse at the time, racial purity was about “blood” and rules of descent…

…In this article, my thesis is simple. If racial caste has been upended by changes in legal rules that created a hierarchical racial structure, its demise also has been hastened by the use of symbols, a strategy of cultural inversion with respect to the meaning of race.  The operative terms of a centuries-old debate have been inverted. Instead of policing racial purity with arguments about blood and biology or the modern version of them, DNA and genes, these instruments of exclusion, the tools of white supremacists and segregationists, have been used effectively, most recently by Barack Obama, to demonstrate the physical connection between groups that are still treated discursively, politically and socially, as racially distinct…

…The movement to escape the one-drop rule, the rule that examines blood lines as far back as five generations or more, if that is what the multiracial movement is all about, is not, as far as I know, a movement that began in the black community. A major proponent is a white woman, Susan Graham, founder of “Project RACE,” which is the acronym for Reclassify All Children Equally.  What Susan Graham demands is that the children of parents who come from different races be acknowledged as the product of both groups. In other words, this white mother of a child or children whose father is a black man demands that the public, the discourse, the political  instrumentalities, the private institutions, acknowledge the status of her child as white as well as black…

…The demand for multiracial identity for the children of interracial marriage, however, may be explained in terms of a desire for status as long as we live in a society in which there is still a clear racial hierarchy. The demand that multiracial children be recognized as partly white did not come from blacks.  Nor is it surprising that Susan Graham, a major advocate for the multiracial category on the United States Census found an ally in Newt Gingrich, who opined that such a category might “‘be an important step toward transcending racial division.’” The enthusiasm for such alternative classifications leads skeptics to believe that this system of reclassification and the rhetoric of transcendence will make it easy to ignore the reality and the structure of racism.

It may be that the promotion of a multiracial identity provides some white parents with the assurance that they have not been rejected by their own children. Their children are part of them and, therefore, partly white. People who cross racial lines to marry do not leave behind all of their attitudes towards race; their internalized assumptions about racial characteristics and racial hierarchy can be a source of misunderstanding, a vulnerability that at the very worst can injure or divide family members…

Read the entire article here.

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Dorothy Roberts Debunks Race as Biological in “Fatal Invention”

Posted in Articles, Health/Medicine/Genetics, Interviews, Media Archive, Politics/Public Policy, Social Science, United States on 2012-04-26 23:03Z by Steven

Dorothy Roberts Debunks Race as Biological in “Fatal Invention”

Institute for Ethics & Emerging Technologies
2012-01-15

Ytasha L. Womack, Contributor

Dorothy Roberts is author of the book Fatal Invention: How Science, Politics, and Big Business Re-create Race in the Twenty-First Century (New Press, 2011). She is also the Kirkland & Ellis Professor at Northwestern University School of Law and a faculty fellow at the Institute for Policy Research, with appointments in the departments of Sociology and African American Studies. Here she discusses the rise in identifying race as biological among some scientists.

Ytasha L Womack: Why did you write Fatal Invention?

Dorothy Roberts: I decided to write it because I have noticed resurgence in the use of the term race as a biological category. And also [I noticed] a growing acceptance among colleagues and speakers that race really is biological and somehow genomic science will soon discover the biological truths about race. The more I looked into it, I saw there were more scientists that said they discovered race in the genes, more products coming out showing that race is a natural division.

YLW: But race is not biological, it’s purely a political creation.

DR: I thought this trend [of race as biological] was supporting a false concept of race. But also, I was alarmed that knowing history; the biological construct of race has been used to obscure the political origin of racial inequality, to make it seem as if the reason people of color are disadvantaged in society is natural, as opposed to political and institutional.
It’s a very frightening development. We would accomplish so much more, if all the money that was going into race based genes were going into cleaning up the toxins in black neighborhoods that cause black people to get cancer and die, cleaning up education or basic health care for everybody.

YLW: Many people have a hard time accepting that race is a political creation and not biological, despite the years of proving otherwise…

…DR: There are studies to explain racial divisions in health that are actually caused by social inequalities. Yet you have researchers studying high blood pressure, asthma among blacks, etc. and looking for a genetic cause. However, research shows these [illnesses] are the effects of racial inequality and the stress of racial inequality.

YLW: So race based medicines, like a heart medicine for African Americans, are illogical, because since race isn’t biological, you can’t have a medicine targeting this group?

DR: Correct. Of those who say [race is biological], they usually point to sickle cell anemia, as proof that illnesses are race-based. Even if you look at these genetic diseases that seem to run along with race, it’s actually caused by environment. Sickle cell is an adaptation in areas with high rates of malaria. You find it in some areas of Africa, Asia and Europe. It’s not about race at all.

DR: To me it’s so obvious that race is a political category. Who is considered black, Asian, Indian, all these things changes depending on political circumstances and are determined by political markers. Yet people hold on to this idea that if scientist keep searching and searching they will find the divisions of a human species, and we’ve found it is a false pursuit…

Read the entire interview here.

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Segregation’s Science: Eugenics and Society in Virginia

Posted in Books, Health/Medicine/Genetics, History, Law, Media Archive, Monographs, Politics/Public Policy, Social Science, United States, Virginia on 2012-04-26 03:57Z by Steven

Segregation’s Science: Eugenics and Society in Virginia

University of Virginia Press
November 2008
312 pages
6.125 x 9.25
Cloth ISBN: 9780813927558
Ebook ISBN: 9780813930343

Gregory Michael Dorr, Visiting Assistant Professor in Law, Jurisprudence, and Social Thought
Amherst College

Blending social, intellectual, legal, medical, gender, and cultural history, Segregation’s Science: Eugenics and Society in Virginia examines how eugenic theory and practice bolstered Virginia’s various cultures of segregation—rich from poor, sick from well, able from disabled, male from female, and black from white and Native American. Famously articulated by Thomas Jefferson, ideas about biological inequalities among groups evolved throughout the nineteenth century. By the early twentieth century, proponents of eugenics—the “science” of racial improvement–melded evolutionary biology and incipient genetics with long-standing cultural racism. The resulting theories, taught to generations of Virginia high school, college, and medical students, became social policy as Virginia legislators passed eugenic marriage and sterilization statutes. The enforcement of these laws victimized men and women labeled “feebleminded,” African Americans, and Native Americans for over forty years. However, this is much more than the story of majority agents dominating minority subjects. Although white elites were the first to champion eugenics, by the 1910s African American Virginians were advancing their own hereditarian ideas, creating an effective counter-narrative to white scientific racism. Ultimately, segregation’s science contained the seeds of biological determinism’s undoing, realized through the civil, women’s, Native American, and welfare rights movements. Of interest to historians, educators, biologists, physicians, and social workers, this study reminds readers that science is socially constructed; the syllogism “Science is objective; objective things are moral; therefore science is moral” remains as potentially dangerous and misleading today as it was in the past.

Contents

  • Acknowledgments
  • Introduction: “You Are Your Brother’s Keeper!”
  • 1. “The Sacrifice of a Race” Virginia’s Proto-eugenicists Survey Humanity
  • 2. “Rearing the Human Thoroughbred” Progressive Era Eugenics in Virginia
  • 3. “Defending the Thin Red Line” Academics and Eugenics
  • 4. “Sterilize the Misfits Promptly” Virginia Controls the Feebleminded
  • 5. “Mongrel Virginians” Eugenics and the “Race Question”
  • 6. “A Healthier and Happier America” Persistent Eugenics in Virginia
  • 7. “They Saw Black All Over” Eugenics, Massive Resistance, and Punitive Sterilization
  • Conclusion: “I Never Knew What They’d Done with Me”
  • Notes
  • Bibliography
  • Index
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Dispensing of Heart Drug Not ‘Black and White’

Posted in Articles, Health/Medicine/Genetics, Media Archive, Politics/Public Policy, United States on 2012-04-26 03:45Z by Steven

Dispensing of Heart Drug Not ‘Black and White’

University of Alabama Research Magazine
2005-10-10

Chris Bryant

Think we’ve advanced too far in Civil Rights issues and medical care to resort to making health judgments based on skin color? Don’t be so sure, says Dr. Gregory Dorr, an assistant professor of history at The University of Alabama, who has joined scholars at the Massachusetts Institute of Technology researching so-called “designer medicines” and the possibilities they could lead to racial medicine.

When a recent study of a heart medicine claimed to show the drug reduced the mortality rate of blacks with severe cardiac disease by 43 percent, but had no effect on whites, controversy erupted.

“According to the study, BiDil (the cardiac disease drug) gave a marked increase in lowering the morbidity rates among black patients with end-stage heart disease,” Dorr said. “White people didn’t show any benefit from it. There were problems with the way the study was done that seemed to suggest that it may not be so clear cut.”…

…“In order to understand pharmacogenetics, you have to understand the longer history of race and medicine in America and how they interacted over time,” Dorr said. “I think there is a lot of potential good in genetic medicine. But, when people conflate race and genetics, we get into a very dangerous and murky area.”

Read the entire article here.

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The short life of a race drug

Posted in Articles, Health/Medicine/Genetics, Media Archive, Politics/Public Policy, United States on 2012-04-23 23:44Z by Steven

The short life of a race drug

The Lancet
Volume 379, Issue 9811 (2012-01-14 through 2012-01-20)
pages 114-115
DOI: 10.1016/S0140-6736(12)60052-X

Sheldon Krimsky, Professor of Urban & Environmental Policy & Planning; Adjunct Professor of Public Health and Family Medicine
Tufts School of Medicine
Tufts University, Medford, Massachusetts

The headlines back in June, 2005, read “FDA approves a heart drug for African Americans”. The decision that gave the company NitroMed approval for its drug BiDil exclusively to a “racial group” represented a milestone in US drug policy. The decision ignited a debate that polarised the African American community, confounded proponents of personalised medicine, and dismayed groups opposed to reinscribing racial categories into science. Ever since Ashley Montagu published Man’s Most Dangerous Myth: The Fallacy of Race in 1964 [1942?], scientists have reached a broad consensus that “race” applied to human populations has no standing in science…

…In a historical context too, the use of such racial classification is shown to be a subjective process. The concept of “race” in the USA grew out of slavery when state laws dictated racial identity by percentage admixture. A person who self-identifies as African American could have one great-grandfather (or about one-eighth of his or her genome) as the exclusive source of that identity. Homer Plessy was the plaintiff in an 1896 US Supreme Court decision (Plessy v. Ferguson) that established the “separate but equal” foundations of segregation in the USA. Plessy, who was escorted off a train for whites only, was considered black based on the infamous “one drop rule”, even though he considered himself seven-eighths white. By contrast, Jean Toomer, author of the 1923 book Cane, which chronicled the lives of black Americans, sometimes identified himself as black and sometimes as white. Thus, two individuals, both with one-eighth African ancestry, might either be defined by others as black or self-identify as white or black. Why should the drug’s approval for a differentiated group be based upon such quixotic criteria? Despite all the reasons why “race” has no role in science, it was a science-based agency that approved BiDil for a racial group…

…While many commentators who supported the approval of BiDil for black patients state that “race” is not a scientifically precise term for identifying relevant genomic or physiological characteristics that differentiate population groups, nevertheless, they argue that “self-identified race” is a useful proxy for those characteristics. However, what is the evidence that the proxy “self-identified race” is a reliable surrogate? The best evidence derives from the fact that genetic variation conferring disease susceptibility is not equally distributed among ancestral populations. For example, sickle cell anaemia is more prevalent in populations whose ancestry can be traced to sub-Saharan Africa. However, “self-identified race” is a subjective term, influenced by cultural factors, and not even grounded in the ancestral genomics of, for example, the International HapMap Project. For the purpose of the clinical trials, “self-identified race” is interpreted as a dichotomous variable (black or non-black). If race were used as a proxy for ancestral African genomics it should be a continuous function (10%, 30%, 70%, etc). It makes no scientific sense to map a continuous function onto a dichotomous variable…

Read the entire article here or here.

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Making Race: Biology and the Evolution of the Race Concept in 20 Century American Thought

Posted in Dissertations, Health/Medicine/Genetics, Media Archive, Politics/Public Policy, Social Science, United States on 2012-04-23 20:41Z by Steven

Making Race: Biology and the Evolution of the Race Concept in 20 Century American Thought

Columbia University
December 2008
309 pages

Michael Yudell

Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy under the Executive Committee of the Graduate School of Arts and Sciences

At the dawn of the 21st century the idea of race—the belief that the peoples of the world can be organized into biologically distinctive groups, each with its own discrete physical, social and intellectual characteristics—is seen by most natural and social scientists as unsound and unscientific. Race and racism, while drawn from the visual cues of human diversity, are ideas with a measurable past, identifiable present, and uncertain future. They are concepts that change with time and place; the changes themselves products of a range of variables including time, place, geography, politics, science, and economics. As much as scientists once thought that race and racism were reflections of physical or biological differences, today social scientists, with help from colleagues in the natural sciences, have shown that the once scientific concept of race is in fact a product of history with an unmistakable impact on the American story. This dissertation examines the history of the biological race concept during the 20th century, studying how the biological sciences helped to shape thinking about human difference. This work argues that in the 20th century biology and genetics became the arbiter of the meaning of race. This work also brings the story of the evolution of the race concept to the present by examining the early impact of the genomic sciences on race, and by placing it in a contemporary public health context.

Table of Contents

  • Acknowledgements
  • Dedication
  • Preface
  • Introduction: The Permanence of Race
  • Chapter 1: A Eugenic Foundation
  • Chapter 2: Making Race A Biological Difference
  • Chapter 3: Race Problems for Biology
  • Chapter 4: Consolidating the Biological Race Concept
  • Chapter 5: Race in the Molecular Age
  • Conclusion: Race, Genomics, and the Public’s Health
  • Bibliography

Read the entire dissertation here.

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Canada’s famous first black doctor

Posted in Articles, Canada, Health/Medicine/Genetics, History, Media Archive, Passing on 2012-04-16 04:18Z by Steven

Canada’s famous first black doctor

National Review of Medicine
Montreal, Quebec, Canada
Volume 1, Number 4 (2004-02-28)

Marvin Ross

Born in Toronto in 1837, Dr Anderson Abbott was a close friend of Abe Lincoln but refused to serve in the US Colored Troops

Not only was Anderson Ruffin Abbott the first black man to graduate from medical school in Canada (University of Toronto, 1861), he is described in a US history textbook as “probably the most famous British North American-born surgeon to serve coloured soldiers during the Civil War.” He was also a close friend of Abraham Lincoln, whose widow presented him with the shawl Lincoln wore to his first inauguration.

Dr Abbott’s father, Wilson, was born in Richmond, Virginia in 1801 to free parents but he eventually moved to Canada in 1835 to escape prejudice in the US. Wilson prospered in Toronto where he became an influential real estate dealer and city alderman. Anderson, who was born in 1837, studied medicine at the University of Toronto and graduated in 1861. While working as an intern, or medical licentiate as it was then known, in 1863 he petitioned President Lincoln to be allowed to join the Union Army.

He became one of only eight black surgeons serving, which brought him to the president’s attention and led to their friendship. Dr Abbott, however, refused to serve in the United States Colored Troops—a segregated unit. Instead, he opted to work as a contract surgeon. He explained why in a 1907 letter, writing that he felt equal to operating on any man and that having been born in a land where all men are free, he was not going to submit to government-endorsed segregation. His heroic act had a negative side effect, though: because of his refusal to serve in the segregated regiment, his widow was denied a Civil War Widow’s Pension…

…His son, Wilson R. Abbott, also became a doctor and practised as a lung and heart surgeon in Chicago. But unlike his father, he wasn’t relegated to a segregated black hospital—not because the laws had changed, but because he worked at a white hospital by passing. Anderson Abbott had married a woman from St Catharines, Ontario who was of mixed racial background. His son, Wilson, married a white woman and they and their descendents began to live as whites. Ms Slaney only learned that she was part black in 1975 at age 24 when she was approached by the Ontario Black History Society to ask about her great-great grandfather. No one had ever told her that half her family was black and, as she pointed out that at the time, “I didn’t even know any black people.” Her story and that of her black ancestor is the subject of her book Family Secrets: Crossing the Colour Line.

Read the entire article here.

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