Activism

Voting Error Leads to 6-Year Prison Sentence for Black Woman in Tennessee

District Attorney Amy Weirich, a Republican, has been touting the success of her case, gaining nationwide attention by conservative pundits. “What we had proved, we presented to that jury, and they listened to the evidence. They listened to the facts. They applied their common sense, and they returned the verdict of guilty,” she said in a statement to WREG, a Memphis TV station.

Published

4 years ago

February 12, 2022

Oakland Post

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Pamela Moses journey began in 2019 to run for mayor of Memphis when she discovered she was not eligible because of a felony conviction. Facebook photo.

By Post Staff

Pamela Moses, a Black Lives Matter activist in Memphis, Tenn., was sentenced to six years in prison for attempting to register to vote.

Both her conviction last fall and her sentence on Feb. 4 have been met with furor by Black leaders and political progressives.

Janai Nelson, the associate director-counsel of the NAACP Legal Defense Fund, told NBC News it was another level of voter suppression aimed at breaking democracy in the U.S. today.

“Pamela Moses, a Black woman, has been sentenced to six years in prison because of a voting error,” Nelson’s tweet said. “Meanwhile, white individuals who are known to have committed blatant voter fraud have only received probation. There are two criminal justice systems in America.”

Referring to it as a ‘paper case,’ Josh Spickler, executive director of an advocacy group called Just City, wondered why it was prosecuted at all considering the spike in violent crime in Memphis.

“Elected officials have used incredible amounts of resources in a time when there’s a backlog in this justice system unlike any we’ve seen before. They use resources to try …(to) convict this woman for trying to vote,” he told the Memphis Commercial Appeal.

Moses, a former felon who wanted to run for mayor in 2019, tried to register to vote but was denied.

Believing that the denial was linked to miscalculating the terms of her sentence, Moses approached the department of corrections, where an official filled out the voter registration application for her, and then the county election commission signed off on her application.

What Moses didn’t know was, that under Tennessee law, her right to vote had been permanently revoked after her arrest in 2015 when she agreed to a felony plea deal because she couldn’t afford a $500,000 bond. “They never mentioned anything about not voting, being able to vote … none of that,” Moses said.

Moses would pay dearly for what she didn’t know because once the error on her voter registration application was discovered, the election commission, as was routine, notified the district attorney’s office.

What was not routine was that Moses would then face charges of perjury and falsifying an election document. This time, Moses refused to plead guilty because she didn’t believe she had done anything wrong.

In last November’s trial, Moses’ defense showed that the errors were made by government authorities, but the jury and the judge believed that Moses had knowingly attempted to subvert the law.

“I did not falsify anything,” Moses said at her sentencing hearing. “All I did was try to get my rights to vote back the way the people at the election commission told me and the way the clerk did.”

Judge Mark Ward wasn’t having it.

“You tricked the probation department into giving you documents saying you were off probation,” said Ward, who would consider granting her probation after she serves nine months.

Moses’ lawyer, Bede Anyanwu, told the Washington Post her client would appeal. “This case is one about the disparity in sentencing and punishment – and one that shouldn’t have happened.”

According to Sam Levine, an opinion writer for The Guardian, “The Republicans who actually cast illegal ballots in the name of relatives they definitely knew were dead each received light sentences. The Black woman who thought she was allowed to register to vote is set to spend the next 72 months in prison.”

At a press conference following her sentencing, Moses, 44, was joined by about a dozen supporters holding signs despite an ice storm “Trying to vote is not a crime” and “Justice for Pamela,” signs read.

In 2015, Moses pleaded guilty to two felonies and three misdemeanors, which led to her receiving probation for seven years. The felony convictions made her ineligible to vote in Tennessee permanently.

Depending on the offense, Tennessee is one of several states that disenfranchise former felons. California is one of 21 states where disenfranchisement ends after incarceration is complete. Maine, Vermont and Wash., D.C., allow prisoners to cast absentee ballots.

“I relied on the election commission because those are the people who are supposed to know what you’re supposed to do,” Moses told station WREG in Memphis. “And I found out that they didn’t know.”

Reports from The Memphis Commercial Appeal, The Guardian, The Washington Post, BET, WREG-TV and MSNBC were the sources for this report.

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Oakland Post: Week of July 8 – 14, 2026

The printed Weekly Edition of the Oakland Post: Week of July 8 – 14, 2026

Published

2 days ago

July 12, 2026

Oakland Post

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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.

Published

1 week ago

July 5, 2026

Oakland Post

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