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First African-American Resident Physician at VUMC

THE TENNESSEE TRIBUNE — Harold Jordan, MD was the first African-American resident physician at Vanderbilt University Medical Center.

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By Tribune Staff

Dr. Harold Willoughby Jordan is the second grandson of Dr. John Henry Jordan and was born in the house in Newnan that John built. Harold was raised there in the shadow of his grandfather. He spent his childhood playing with John’s old medical bag, surrounded by his medical books and lasting legacy. From a young age, it was Harold’s desire to become a doctor, and he knew his parents expected it of him. 

Harold was educated in Newnan and finished high school there before relocating to Atlanta to attend Morehouse College. He graduated from Morehouse with a bachelor’s degree in Biology in 1958 and then followed in his grandfather’s and great-grandfather’s footsteps by enrolling as a student at Meharry Medical College. Harold graduated in 1962 and completed one year of a residency in internal medicine before deciding to pursue psychiatry instead. He was the first black medical resident on record at Vanderbilt University.

After completing his education, Harold became a faculty member at Meharry Medical College and served as Chairman of the Department of Psychiatry for 18 years as well as Acting Dean of the School of Medicine. He was loyal to Meharry and only left in the 1970’s to serve as the first black Commissioner of Mental Health for the State of Tennessee. A state building, the Harold W. Jordan Habilitation Center, is named in his honor. 

February 8, 2019 marked the launch of the newest of the named lectures in the Department of Psychiatry and Behavioral Sciences – the Dr. Harold Jordan Diversity and Inclusion Lecture.

Harold Jordan, MD was the first African-American resident physician at Vanderbilt University Medical Center, completing a general psychiatry residency between 1964 and 1967. Dr. Jordan’s history with the Department of Psychiatry and Vanderbilt University School of Medicine was outlined in the article “Hidden Figure” from the Summer 2017 issue of Vanderbilt Medicine Magazine.

 Harold Jordan, M.D., has had a distinguished medical career that includes many highlights, including being chair of Psychiatry at Meharry Medical College, his medical alma mater, and serving as acting dean of the School of Medicine at Meharry as well.

Besides his academic career, Jordan was devoted to improving mental health care for the public through governmental service. He was Assistant Commissioner for Psychiatric Services and, following that, Commissioner of Mental Health and Mental Retardation for the state of Tennessee, and performed those jobs with such distinction that the state named a building in his honor on the campus of Clover Bottom Developmental Center, the state facility for people with severe intellectual disabilities which closed in 2016.

But a lesser-known part of Jordan’s professional life is his role as a pioneer at Vanderbilt University Medical Center (VUMC). In 1964 he became the first African-American resident physician at VUMC.

It’s fair to say that he began that groundbreaking achievement with little fanfare, and it’s fair to say that the achievement has received little fanfare since.

Reached at his home in California, where he moved after retirement, Jordan recalled interviewing with William F. Orr Jr., M.D., who was chair of Psychiatry at Vanderbilt from 1947 to 1969.

“Dr. Lloyd Elam arranged for me to meet Dr. Orr,” he said. With bemused understatement, and the hint of a chuckle, he added, “Obviously, that was very good for me.”

Elam, who later served as President of Meharry, was on the Psychiatry faculty at that institution and recommended that Jordan, who had already done an internship year at Meharry in Internal Medicine, consider a slot at Vanderbilt because, at the time, Meharry did not offer a residency in Psychiatry.

The interview went well, and Orr offered Jordan one of the three residency slots in Psychiatry that year.

But, Jordan recalls, Orr did more than offer him a position.

“Dr. Orr was very encouraging, accepting and protective,” Jordan said, clearly recalling a time when not all institutions exhibited those attitudes toward African-Americans. “He made it clear that I would be accepted. I felt secure. I knew the path was clear for me.”

Jordan’s family roots in medicine are deep; both his great-grandfather and grandfather were physicians who trained at Meharry. When he was growing up in Newnan, Georgia, just south of Atlanta, he heard family tales of his medical forbears and was inspired to follow their footsteps.

“I had wanted to do that since I heard about them,” he said.

Despite the low-key nature with which Jordan’s residency was handled, the groundbreaking nature of what was going on would have been known to all of the participants.

Vanderbilt’s first African-American student, Joseph Johnson Jr., was admitted to the Divinity School in 1953, and in 1956 two black law students had been admitted as well. But despite the presence of a few black students on campus, at that time there were no African-American residents at Vanderbilt Hospital, and it would be two more years, 1966, before the Vanderbilt School of Medicine would admit its first African-American student, Levi Watkins Jr.

“He paved the way for everyone who came after him,” Churchwell said. “To be an African-American resident in a sea of white residents at a Southern medical institution, I would call him a true Robinson Crusoe.”

Just as Vanderbilt was changing in that era, so was the country. As it happened, the day after Jordan began his residency at VUMC, July 1, 1964, President Lyndon Johnson signed the Civil Rights Act of 1964, mandating an end to discrimination in public accommodations.

Jordan says the faculty and his fellow residents were encouraging and supportive—“My colleagues were fine—there were no problems in Psychiatry”—but the unusual sight for that time of an African-American physician at Vanderbilt sometimes made for awkward misunderstandings.

“I walked into the Emergency Room [for a consult] and somebody thought I was the janitor and said, ‘The trash is over there,’” he remembered.

From across the decades of an honored career in medicine, Jordan, who turned 80 this year, says he has no ill feeling about such slights. “I would laugh at them, like, ‘What are you talking about?’” he said.

After his three years of residency at VUMC, Jordan pursued his academic career at Meharry and his public service career with the State of Tennessee, but also maintained a clinical appointment on the faculty of the Vanderbilt University School of Medicine until 2016.

In a 1971 letter in support of Jordan’s faculty appointment at Vanderbilt, Robert M. Reed, M.D., a Psychiatry faculty member of that era, wrote that, since Jordan was the first black resident to train at Vanderbilt, “his original appointment and subsequent performance were watched and monitored by a great many people as constituting something of a ‘test case.’”

He adds, “If indeed it were a test, then Harold passed it with honors, in my opinion.”

Andre Churchwell, M.D., Chief Diversity Officer for Vanderbilt University Medical Center, senior associate dean for Diversity Affairs, and Levi Watkins Jr. M.D. Chair, professor of Medicine, Biomedical Engineering and Radiology and Radiological Sciences, said that Jordan’s contributions to VUMC are important to remember.

“He paved the way for everyone who came after him,” Churchwell said. “To be an African-American resident in a sea of white residents at a Southern medical institution, I would call him a true Robinson Crusoe.”

A 1967 Psychiatry departmental group photo makes Churchwell’s point. It shows 40 or so people lined up around the traditional entrance to the School of Medicine, and Jordan is indeed the only African-American in a sea of white faces.

Given the varieties of reactions to Jordan’s presence and his role at the Medical Center in the mid-1960s, Churchwell added, “The fact that he was studying psychiatry probably helped him.”

For his part, Jordan says his time at Vanderbilt was important to him, both personally and professionally.

“It was a very positive influence,” he said. “I just felt very supported at both Meharry and Vanderbilt. I felt blessed to have had that experience in Psychiatry.”

He is married to Geraldine Crawford Jordan, a Meharry Medical College nursing school graduate. Thy have four children: Harold, Vincent, Karen and Kristi, as well as four grandchildren.

This article originally appeared in The Tennessee Tribune

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Activism

Diabetes in Black California: Turning the Tide from Crisis to Control

According to the Centers for Disease Control and Prevention (CDC) Behavioral Risk Factor Surveillance System data, nearly 17.9% of Black adults in California have been diagnosed with diabetes — above the national Black adult average of 16.8%, and nearly five points higher than California’s overall adult rate of 12.6% across all races. California ranks 24th out of 39 states with available data for Black adult diabetes rates.

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Dr. Khadijah Lang is a family physician with a clinic in Los Angeles who specializes in several family medical practices, including prenatal care. Lang believes in family medicine. She says it is important to treat all members of a family. Thursday, June 5, 2026. Photo by Solomon O. Smith/California Black Media.
Dr. Khadijah Lang is a family physician with a clinic in Los Angeles who specializes in several family medical practices, including prenatal care. Lang believes in family medicine. She says it is important to treat all members of a family. Thursday, June 5, 2026. Photo by Solomon O. Smith/California Black Media.

By Charlene Muhammad, California Black Media

Crystal Lambert knew something was terribly wrong with her three-year-old granddaughter as she sped down the street trying to get her to the hospital.

“I thought she got a hold of some poison,” Lambert recalled.

Doctors found Lambert’s granddaughter had a blood sugar level over 800, diagnosing her with Diabetic Ketoacidosis(DKA), a state in which the body, starved of insulin, begins to shut down.

Lambert said she was born with a pancreas that was not fully functioning — it lacked the specialized cells required to produce insulin.

Her granddaughter survived and is five years old today.  Now, she gives herself insulin shots, asks endless questions about her condition, and runs like the spirited child she is. But the terror of that night transformed Lambert — and ultimately inspired her to launch the We Fight Back Organization, a mobile health and food access initiative serving underserved communities across California. Lambert is the executive director.

The Crisis by the Numbers

According to the Centers for Disease Control and Prevention (CDC) Behavioral Risk Factor Surveillance System data, nearly 17.9% of Black adults in California have been diagnosed with diabetes — above the national Black adult average of 16.8%, and nearly five points higher than California’s overall adult rate of 12.6% across all races. California ranks 24th out of 39 states with available data for Black adult diabetes rates.

Nationally, according to the U.S. Department of Health and Human Services, Black Americans were 24% more likely than the overall U.S. population to have diabetes in 2024. They also died from diabetes 78% more often than the general population in 2022. Black Americans are also more than twice as likely as the overall population to develop kidney failure caused by diabetes.

According to the California Health Care Foundation’s 2024 Health Disparities Almanac, Black Californians have the shortest life expectancy in the state at just 74.6 years — due in part to chronic conditions like diabetes and its devastating complications.

Leon Rock, co-founder of the African American Diabetes Association, believes statistics, though revealing, only tell part of the story.

“There are a whole bunch of Black folks that don’t tell you that they have diabetes — or don’t know,” he said.

And the disease itself, Rock is careful to note, is not what kills. “They die from the complications. That’s heart attack, that’s stroke, that’s amputations of legs, of feet. Going blind. All those complications are inherent in a system that has impacted Black folks with diabetes in California and across America.”

Crystal Lambert, creator and executive director of We Fight Back. She started the organization out of a need to learn more about diabetes on behalf of her granddaughter. Now she is looking to spread the impact of her organization to the valley. Friday, June 6, 2026. Photo by Solomon O. Smith/California Black Media.

Crystal Lambert, creator and executive director of the We Fight Back Organization, started out of a need to learn more about diabetes on behalf of her granddaughter. Now she is looking to spread her organization to the valley, on Friday, June 6, 2026 Photo by Solomon O. Smith/ California Black Media

An Information Gap Fuels the Crisis

For Rock, part of the solution is diagnosis. He says the medical and public health systems are failing Black Californians by the absence of information designed for them.

“That is the bottom line. We need good information. Information that is culturally specific,” said Rock.

Telling people to eat healthy or exercise, he added, falls short when culturally specific alternatives are not provided, and when many residents of urban communities do not feel safe exercising in some neighborhoods – or outside at night.

Dr. Khadijah Lang, a family medicine physician and president of the Golden State Medical Association, agrees that the roots of the crisis run deeper than individual behavior — and blaming patients misses the point.

“We are not genetically predisposed to diabetes,” Lang said. “But the system under which we live increases the likelihood that we will develop it.” 

What the Body Needs — What Communities Are Denied

Type 2 diabetes, which accounts for 90 to 95% of all diabetes cases, according to the CDC, develops when the body can no longer use insulin effectively to regulate blood sugar. Left unmanaged, it damages nerves, kidneys, eyes, and the cardiovascular system. The hemoglobin A1C test is a blood draw that reveals how the body has processed sugar over the previous three months — not just at the moment of the test. It is the standard tool for both diagnosis and ongoing monitoring.

That distinction matters, Lang emphasized, because patients cannot manipulate three months of blood sugar history the way they might fast for a day before a single blood draw.

“The pill is not meant to undo or control a sugar level that’s being constantly stressed,” Lang said. “It’s meant to work in conjunction with a low-carbohydrate diet and exercise.” She recommended at minimum 30 minutes of physical activity five days a week — breakable into 10-minute sessions for those who need it.

Lang stressed that education must be delivered in language people recognize and can relate to. The goal is to inform them of the choices that serve their health best, she said.

But for many Black Californians, even those informed choices remain out of reach, Lambert said.

“They need access to healthy foods and medication, too” she said.

California has made some critical policy advances. The state has expanded access to the Continuous Glucose Monitor (CGM), which has transformed diabetes care for state residents. Assembly Bill 365, introduced in 2024, proposed requiring Medi-Cal to cover the costs of CGM and other related medical equipment but it failed in the State Senate. Since then, the California Department of Health Care Services (DHCS) reports that the core Medi-Cal CGM benefit now available to eligible patients was solidified through previous budget actions and pharmacy policy updates.

These measures, while meaningful, have not closed the gap for the communities most at risk, according to advocates.

Control Through Community

Health care advocates conclude that the solution must be communal, culturally grounded, and sustained — not a fad, not a celebrity moment, not a single clinic visit. For example, observed Lang, lifestyle shaped by shared values and collective accountability can move the needle where individual prescriptions have not.

Rock is building infrastructure to match the urgency, establishing local chapters of the African American Diabetes Association across the country, with California next.

“We have to do for self, period,” he said. “Health is wealth. We have to eat to live.”

And Lambert, whose granddaughter unknowingly started all of this for her, keeps showing up.

“Diabetes advocacy is about dignity, education, prevention, and hope,” she said.

Video: Diabetes Disparity Exposed in California

This article is supported by the California Health Care Foundation 

(CHCF). Visit www.chcf.org 

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Activism

Oakland Post: Week of July 1 – 7, 2026

The printed Weekly Edition of the Oakland Post: Week of July 1 – 7, 2026

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Arts and Culture

Prescott Circus Theatre Presents Free Summer Performance Series

Now in its 41st year, the Prescott Circus Theatre is a nationally recognized performing arts education program for Oakland youth. The circus offers safe environments that challenge Oakland youth, through circus arts training, to develop the skills and confidence to thrive on stage, in school, and in life.

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Prescott Circus showcase pathways pyramid. Photo courtesy of Prescott Circus.
Prescott Circus showcase pathways pyramid. Photo courtesy of Prescott Circus.

By Post Staff

The Prescott Circus, Oakland’s longest-running youth circus, is returning this summer with its free shows. Join the Prescott Circus’s young stars as they share their joys and talents through stilt-dancing, tumbling, juggling, and more.

At the heart of this one-hour show, which demonstrates teamwork, pride, and joy, are Oakland Unified School District students ages 8 – 17 from more than 10 different schools

Now in its 41st year, the Prescott Circus Theatre is a nationally recognized performing arts education program for Oakland youth. The circus offers safe environments that challenge Oakland youth, through circus arts training, to develop the skills and confidence to thrive on stage, in school, and in life.

This is accomplished through no-cost school and community programs for more than 300 Oakland youth each year. Performing company members from Prescott, where the program began, perform and make appearances at as many as 40 Bay Area events each year.

The summer program is funded in part by Oakland Fund for Children and Youth, California Arts Council, Port of Oakland, and the West Davis & Bergard Foundation.

Performances will be held Tuesday, July 14, 11 a.m. and 1:30 p.m. (ASL interpreted) and Wednesday, July 15, 11 a.m., at the Malonga Casquelourd Center for the Arts, 1428 Alice St., Oakland. For free reservations go to

https://PrescottCircusSummerShows.eventbrite.com

For group reservations for camps, childcare centers, senior centers, go to www.prescottcircus.org

A community show will be held Saturday, July 18, 2 p.m. to 3 p.m., at DeFremery Park,1651 Adeline St., Oakland.

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