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CENSUS CHAMPIONS – Jeri Green’s Life-Long Crusade to Reverse Historic Undercounts

CHARLESTON CHRONICLE — Jeri Green’s passion for the census is still sunrise bright. An outspoken champion of the concerns of African Africans and any people who have been diminished, marginalized or systemically undercounted, she is an enthusiastic and determined advocate for how participation in the census can contribute to healthier communities and a more equitable America.

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By Khalil Abdullah

(TriceEdneyWire.com) – WASHINGTON, D.C. – Jeri Green’s passion for the census is still sunrise bright. An outspoken champion of the concerns of African Africans and any people who have been diminished, marginalized or systemically undercounted, she is an enthusiastic and determined advocate for how participation in the census can contribute to healthier communities and a more equitable America.

“Let’s talk about the need for public education,” Green said. “We know African American children continue to be undercounted every census and likely will be so again in 2020. Same for Latino and Native American children. When we say, ‘Count every child in your household,’ it means just that. Grandchildren count, foster kids count, play cousins count. Unless this message is delivered and repeated over and over, families will miss receiving resources that are rightfully theirs.”

“And, quite frankly, why can’t we do a better job of counting formerly incarcerated Black men? We already know they are a disproportionate percentage of the over 650,000 individuals coming back to our communities from jails and prisons every year. They are returning citizens and we should be able to design ways to make sure they show up in the census as well.”

During her 20-year career at the Census Bureau, Green coordinated visits by congresspersons, the General Accounting Office and the Inspector General’s personnel, among others, to census field sites. “Individuals who have oversight responsibility or whose agencies conduct audits to make sure taxpayer dollars are being well spent, have a right to inspect and observe, but those visits have to be scheduled and conducted in a way that doesn’t interfere with the enumeration process or the public’s right to privacy.”

In 2017, she retired as Senior Advisor for Civic Engagement to former U.S. Census Bureau Director, John Thompson.

“He had left the Census Bureau and returned after a decade as a political appointee. He asked me to help him get reacquainted with the issues and concerns of the Civil Rights community, to establish some outreach.”

Green’s experience made her ideally suited for the task.

“When I started full-time, I was working on the advisory committee level,” she recalled. “In addition to serving as the liaison to the technical advisory committee, I was responsible for the five ethnic stand-alone advisory committees: Black; Hispanic; Native American and Alaskan; Asian; Hawaiians and Pacific Islanders.

“Back then, each committee had its own chair and vice chair. My job was to understand their needs, engage with them and get to know and understand their issues. I just thought I could automatically do this, that it was just a natural fit for me because – I’m Black! And I know all these issues. Wrong, wrong, and more wrong,” she said laughing.

“You cannot just assume, because you’re a person of color, that you understand another culture. It took time to talk to Native Americans, to understand the road they traveled and their customs. It was the same for each of those committees. It was a very humbling experience that made me a stronger employee and a stronger translator for the Census Bureau. I had to develop a level of trust that the Bureau didn’t have with these communities.”

Regarding her decision to resign, she said when Director Thompson opted to leave in 2017, “I followed him out the door. It was time.”

Her 10 years of prior employment in the District of Columbia government counted toward federal retirement eligibility. Reasons for leaving were personal and professional. For one, the politicization of the Census Bureau, under the Department of Commerce’s then new Secretary Wilbur Ross, carried some weight.

Green opposes Ross’s efforts to add a question on citizenship to the 2020 form. She concurs with other experts that doing so would likely reduce the number of survey respondents and thus undermine the government’s constitutional mandate to count all residents. But, the citizenship dispute, soon to be decided by the Supreme Court, was just one factor in her decision.

Despite the Census Bureau’s growing emphasis and reliance on technology for the 2020 count, “we are still going to need human capital and the funds won’t be there,” Green said. During the Obama administration, the Republican-controlled Congress mandated that 2020 Census costs be held to the life-cycle costs of the 2010 Census. “Who in the world can buy 2020 groceries on a 2010 budget?” she asks. In her opinion, already, and as a direct result of insufficient funding, there have been other consequences that may negatively impact census accuracy.

Between imagining how her daily work might be constrained and what she would do with more time to herself – continue practicing and performing with D.C.’s own KanKouran West African Dance Troupe or devoting longer hours to genealogical research – the idea of retirement began to fit like a favorite garment. She didn’t see the phone call coming, but she heard the message loud and clear.

“Marc Morial dialed me up on my cell phone right after I retired from the Census Bureau and said, ‘We need you,’” Green recalled. As president of the National Urban League (NUL) for over 15 years, a two-term mayor of New Orleans, and a former Louisiana state legislator, Morial knows and understands how census-derived revenue pours into county and city coffers to fund infrastructure projects and social service programs.

Morial chaired the 2010 Census Advisory Committee, an entity not reconstituted by the Trump administration for the 2020 Census. The committee focused on Hard-To-Count communities and had become part of Green’s portfolio during Morial’s tenure. Green now serves as senior advisor to the NUL on the 2020 Census and is a key participant in the NUL’s Census 2020 Black Roundtable, but her path to the NUL began long before.

Just as the Morial family can trace part of its lineage to the Whitney Plantation in Louisiana, Green’s folk, on her mother’s side, are descendants from formerly enslaved laborers on the Worsley Plantation near Rocky Mount in Edgecombe County, North Carolina.

Green was born in Washington, D.C., a descendant of part of the African American Worsley migration that eventually settled here. “My grandfather used to make me and my little sister hoe-cakes. He couldn’t read or write, nor could his mother, who was a formerly enslaved woman.”

After Eastern High School, Green pursued her undergraduate degree in Afro-American studies at the University of Maryland, College Park. At the time, there was no rapid public transportation linking her Washington neighborhood to the College Park campus as the D.C. Metrorail system had not been built. Without a car, the bus ride stretched out interminably. Travel time proved less a barrier than the social climate she encountered.

“Yes, it was only 15 miles, but it was like going to the Deep South, culturally and otherwise,” Green explained. “It was a real eye-opener for me. The whole blackface thing with Gov. Northam in Virginia? That was nothing. We saw blackface all the time at College Park in the 70s, a land-grant university built by formerly enslaved people.”

At College Park, she also encountered the Pan Africanism of Kwame Turé, the former Stokely Carmichael. “He made regular visits out there and would encourage us to be active and to fight injustice. We were the ones who fought for tenure for Black professors, for African American studies programs, and for the establishment of the Nyumburu Cultural Center, which provides a physical space for meetings and activities and is still there today.”

“African Americans are struggling to deal with police brutality, voter suppression, gentrification, and access to health care … so getting them to turn their attention to the census takes time and commitment.”

While earning her master’s degree in Urban Planning and Urban Affairs at Washington University in St. Louis, Green had her first prolonged encounter with “reams and reams of census data.” Job opportunities brought her back home where she worked for a few organizations before being hired by the D.C. Department of Public Works. It was a sprawling agency that Green recalls “was responsible for almost anything in the city with wheels, from public transportation to trash collection” before its duties were parceled out in a city government reorganization. Most of her time was spent working out of the mayor’s executive office. She served under Mayors Marion Barry and Sharon Pratt Kelly.

A mentor encouraged her to apply for openings at the Department of Commerce during its recruitment drive to staff the 2000 Census.

“I left a full-time job at the District government to join the Census Bureau as a temporary employee in 1997,” Green said.

The practice of bringing former temporary workers aboard after a decennial year is not unusual, those workers’ skills and performance having been subject to evaluation by Census Bureau staff who can then make full-time job offers to the best prospects.

Green is a veteran of three censuses. “I worked on the run-up to the 2000 Census; through the 2010 Census; and for the run-up for the 2020 Census when I left the Bureau in 2017, and I’m still working on 2020 issues with the National Urban League.”

“African Americans are struggling to deal with police brutality, voter suppression, gentrification, and access to health care,” she observed, “so getting them to turn their attention to the census takes time and commitment. But when you look at the issue of Black men being counted where they are incarcerated instead of where they reside, and how that affects political representation and the electoral process, what we at the National Urban League call prison-based gerrymandering, and then you also count the per-person census dollars lost to their communities because, again, that money stays within the communities not their own where they are imprisoned, we cannot remain silent.”

Green still bristles as she talks about the first census in 1790 when African Americans were not counted as full human beings – Native Americans not counted at all. And she has found, within an analysis of the 1860 Census data – and, due to the Civil War, the last census that recorded a captive population – names and information on some of her forebears in North Carolina. She knows full well, however, that most Africans Americans won’t be as fortunate in their quest for family, kinship, and identity.

“Instead of being defiant and not participating in the census, be defiant and let America know we’re still here,” Green inveighed.

Looking to the other side of the 2020 Census, Green envisions more time with children, grandchildren, and, she said, quite frankly, “I’m trying to be on somebody’s beach.”

This article originally appeared in the Charleston Chronicle

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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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