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Steve Beard

Steve Beard

Steve Beard knows that diverse health care is better health care. The belief drives his efforts as CEO of Adtalem Global Education, a corporation that operates institutions for higher learning including Chamberlain University, Walden University, and Ross University School of Medicine. 'Science shows the benefits of a diverse health care workforce, and no one makes a larger contribution to that goal than Adtalem's institutions,' Beard says.
Under his leadership, Adtalem has made large strides in addressing shortages of health care workers while increasing racial representation. With more than 90,000 students currently enrolled at its schools, Adtalem has become one of the leading suppliers of doctors, nurses, veterinarians, and social workers to the U.S. workforce. Adtalem's medical schools are major producers of Black physicians in the U.S.—and over the past year, 95% of its medical school graduates have successfully secured hospital residencies, helping to shore up critical areas like primary care and underserved communities.
Beard's institutions are at the forefront of technology. In 2024, Adtalem forged a new partnership with Hippocratic AI, developing curricula to train nursing students—and soon physicians—to use AI tools to monitor patients and improve follow-ups after treatment. 'Some of these innovations will relieve administrative burdens in ways that create better quality of life, on the hospital floor and at the bedside,' Beard says.Beard's path from first-generation college student to changemaker is a personal success story—and through Adtalem, it's become a model for building the next generation of health care professionals.

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Sickle Cell Awareness: Hampton Roads teen siblings diagnosed at birth
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Sickle Cell Awareness: Hampton Roads teen siblings diagnosed at birth

NORFOLK, Va. (WAVY) — Sickle Cell Disease is the most common inherited blood disorder in the United States, affecting the lives of 100,000 people, per the Centers for Disease Control and Prevention. Teen siblings, Morgan Tarrer, 15, and Olivia Tarrer, 19, of Virginia Beach represent that number. Data from the CDC also shows approximately 1 in 365 Black or African American newborns are born with SCD, which is the case for Morgan and Olivia, whose parents are carriers. The two were diagnosed at birth and are left with no choice but to embrace their condition as there is still no cure. 'So I have an abnormality of my Hemoglobin,' says Khristina Reid, Virginia Sickle Cell Network founder and mother of Morgan and Olivia. 'So I carry the C-gene, and Olivia and Morgan's dad, he carries the S-gene. Together our children have both genes. The S and C-gene. So they live with Hemoglobin S-C Disease. While there have been many advances in treating sickle cell disease, the reality for the siblings and others is reduced life expectancy and the probability of health complications. 'It's something that I've found is always on your mind,' says Olivia. 'I'm in college. I'm up in New York, so I'm very far from my family. And I've realized, especially living in dorms, being around with friends, that you have to be extra, extra careful. Because with sickle cell, you're very, immunocompromised.' CDC finding reveal, more than 90% of people diagnosed with sickle cell in the US are non-Hispanic black or African American. 'So the reason is, sickle cell disease was the body's kind of defense mechanism against malaria,' says Reid. 'So you will find the highest prevalence of sickle cell disease in your, locations that are near the equator. So Nigeria right now is the, largest country, with the largest population of people living with sickle cell disease.' Those diagnosed with SCD can range in symptoms from frequent infections, anemia, episodes of pain, problems with vision and tiredness. Olivia's says she experiences a great deal of fatigue. While she remains optimistic, there's always concern about her years ahead. 'That has been a problem in school for me,' she says. 'I remember last not last year, but my senior year of high school. All through high school, it was a struggle getting to school because we had it so early. I think the most challenging part is uncertainty about the future. I'm in film. I'm a NYU film, and it's a very physical job. It's also a very, You have to be up early, go to sleep late. And that's when I do that. When I am on set, it's very strenuous, and I worry that I won't be able to be at the same caliber, as my peers.' For information on the Virginia Sickle Cell Network, click here. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

Church hosts conference to address mental health in the Black community
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MEMPHIS, Tenn. — According to the Centers for Disease Control (CDC), in 2023, suicide was the third leading cause of death among African Americans ages 15 to 34 in the U.S. Pastor Dianne Young with the Healing Center says this is why her church gathered professionals from across the country to educate people about depression and break the silence surrounding suicide in the Black community. 'We want to be able to let people talk freely about their struggles. We mention that we have them, but we don't talk about it,' said Pastor Young. Her church hosted the National Suicide and Black Church Conference at Southwest Community College. 📡 for Memphis and the Mid-South. 📧 and have the latest top stories sent right to your inbox. 'There was a theory that it didn't happen to Black people or African-Americans, but we found out it did from our own personal experiences,' she said. Executive Director of the American Psychiatric Association Foundation, Rawle Andrews Jr., says the stigma surrounding depression among Black people stems from three things: fear, shame, and discrimination. 'We were already thought to be less than human or second class, and then when I tell you I'm struggling with a mental health condition, now I'm leaning into the perception that I'm less than. I'm less than human,' said Andrews Jr. The APA says some of the common warning signs include talking or writing about death, withdrawal from friends and family, dramatic mood changes, and increased alcohol or drug use. 'If you don't see that person for a couple of days and their body language changes, get interested. Get curious,' said a workshop speaker. 'This is teaching you all to recognize, not diagnose, because when you diagnose somebody inappropriately, that can feel like a judgment or a label. Don't do that.' If you or someone you know is experiencing a crisis, experts encourage you to call the National Suicide and Crisis Lifeline at 988. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

New paper sheds light on experience of Black prisoners in infamous Stateville prison malaria experiments
New paper sheds light on experience of Black prisoners in infamous Stateville prison malaria experiments

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New paper sheds light on experience of Black prisoners in infamous Stateville prison malaria experiments

Much has been said and written over the years about controversial malaria research conducted on inmates at Illinois' Stateville Penitentiary starting in the 1940s. But at least one part of that story has been largely ignored until now: the role of Black prisoners in that research, which helped lead to the modern practice of using genetic testing to understand how individual patients will react to certain medications, according to the authors of a newly published paper out of the University of Utah. 'We want to highlight the stories of Black prisoners that participated in this prison research in the 1950s onward and give them their due,' said Hannah Allen, a medical ethicist and assistant professor of philosophy at the University of Texas Rio Grande Valley, and first author of the paper, which was published as an opinion piece Wednesday in the Journal of the American Medical Association. 'They haven't been properly acknowledged in the past, and their participation in these studies was really foundational in launching the field of pharmacogenetics and, later on, precision medicine,' said Allen, who recently completed her doctorate at the University of Utah. Starting in the 1940s, researchers infected inmates at the Joliet-area prison with malaria to test the effectiveness of drugs to treat the illness as part of a U.S. military-funded effort to protect American troops overseas, according to the paper. A University of Chicago doctor was the principal investigator. The inmates consented to being part of the studies and were paid for their participation. At first, the research was greeted with enthusiasm. In 1945, Life magazine ran a spread about it, featuring a photo of a Stateville inmate with cups containing malaria-carrying mosquitoes pressed against his bare chest. The first line of the story reads, 'In three U.S. penitentiaries men who have been imprisoned as enemies of society are now helping science fight another enemy of society.' But as the years passed, attitudes began to shift. Questions arose about whether inmates could truly, freely consent to participate in medical experiments or whether they felt coerced into them because of their often dire circumstances. At the Nuremberg trials, defense attorneys for Nazi doctors introduced text and images from the Life article about Stateville prison, though an Illinois physician argued at the trials that the prisoners in Stateville consented to being part of medical research whereas Nazi prisoners did not, according to the JAMA paper. In the mid-1970s, news broke about a study at Tuskegee, in which Black men with syphilis went untreated for years — news that raised awareness of ethical problems in medical research. News outlets also began publishing more stories about prison research, according to the JAMA article. The Chicago Tribune published an article in 1973, in which an inmate participating in the Stateville malaria research said: 'I've been coerced into the project — for the money. Being here has nothing to do with 'doing good for mankind' … I didn't want to keep taking money from my family.' The experiments at Stateville came to a halt in the 1970s. A number of protections and regulations are now in place when it comes to research involving prisoners. Since the 1970s, the Stateville research has often been discussed and analyzed but little attention has been paid to its Black participants, said James Tabery, a medical ethicist and philosophy professor at the University of Utah who led the new research, which was funded by the federal National Institutes of Health. For a time, Black prisoners were excluded from the studies because of a myth that Black people were immune to malaria, Tabery said. Later on, once scientists had pinpointed the drug primaquine as an effective medication for malaria, they turned their attention to the question of why 5% to 10% of Black men experienced a violent reaction to the drug, according to the paper. Ultimately, the scientists were successful, finding that the adverse reaction was related to a specific genetic deficiency. 'There are people all over Chicago today that are getting tested, that clinicians are recommending they get a genetic test before they get prescribed a drug because they want to make sure that their patient isn't going to have an adverse reaction to the drug,' Tabery said. 'It's really sort of powerful and interesting that you can trace that approach to doing good clinical medicine right back to this particular moment and place and population.' But Tabery and Allen also found that the Black prisoners were not treated the same as the white prisoners who participated in research at Stateville. For one, they weren't paid as much as the white prisoners, the rationale being that the white prisoners were infected with malaria, whereas the Black prisoners were given the drug but not infected with the disease — though some of the Black prisoners got very ill after taking the medication, according to the paper. Also, researchers didn't protect the Black participants' privacy as well as they did for other participants. They published certain identifying information about the Black participants, such as initials, ages, heights and weights, whereas participants in the previous research were represented with case numbers, according to the paper. Researchers also recruited the Black prisoners' family members for the study, which they didn't do with earlier participants, according to the paper. 'You see them just doing things with the Black prisoners that they're not doing with the white prisoners,' Tabery said. Also, though scientists made an important discovery through the research on Black prisoners, the episode also highlights the difficulty that can occur in translating discoveries into real life help for patients. Though the World Health Organization now recommends genetic testing to protect people who are sensitive to antimalarials, many of the people who would benefit most from such testing still don't receive it because of financial barriers, supply chain issues and a lack of training, according to the paper. 'What we found is when you sort of shift to what was happening to the Black prisoners, these other lessons you hadn't thought of as being derivable from Stateville suddenly do become apparent,' Tabery said.

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