Bay Area

Gus Newport: A Soldier for Justice

One year ago, on June 12, 2023, my husband of 35 years was picked up by a van at our house in Oakland. It was the last time I saw him alive. The van was owned by Owl Transport, a company used by the Department of Veterans Affairs. It was to take my husband to the San Francisco VA Medical Center to see about getting a new hearing aid. Within a half hour of leaving the house, a San Francisco Fire Department ambulance was called to 8th and Harrison streets because Gus was unconscious. When they arrived at San Francisco General Hospital, Gus’s cell phone, wheelchair and tote bag had all gone missing. An enterprising social worker Googled Gus and found a phone number for his daughter in Atlanta; she called her brother in Oakland, and he immediately called me.

Published

2 years ago

June 13, 2024

Oakland Post

Kathryn Kasch and Gus Newport

By Kathryn Kasch

One year ago, on June 12, 2023, my husband of 35 years was picked up by a van at our house in Oakland. It was the last time I saw him alive.

The van was owned by Owl Transport, a company used by the Department of Veterans Affairs. It was to take my husband to the San Francisco VA Medical Center to see about getting a new hearing aid.

Eugene “Gus” Newport was 88 years old and wheelchair-bound because he had lost a leg in 2021, but my husband remained as active as I had always known him, forever engaged in civil rights and community development work, just as he had been as mayor of Berkeley from 1979 to 1986.

Gus had a busy week ahead of him: on June 16 he was going to be interviewed for a film about his friendship with Malcolm X; on the following day he was scheduled to fly to Atlanta for a weekend board meeting.

Within a half hour of leaving the house, a San Francisco Fire Department ambulance was called to 8^th and Harrison streets because Gus was unconscious. When they arrived at San Francisco General Hospital, Gus’s cell phone, wheelchair and tote bag had all gone missing. An enterprising social worker Googled Gus and found a phone number for his daughter in Atlanta; she called her brother in Oakland, and he immediately called me.

The next morning, I called Owl; they said they were investigating and had notified the VA, but the VA never called the family. I was able to reach Gus’s VA doctor, who works primarily at UCSF, and she told me to call the Patient Advocate number, but they never called me back.

The doctors at the hospital determined that Gus had suffered a severe neck and spinal injury and that if he ever regained consciousness, he would be a permanent quadriplegic. On June 17, we decided to let him go. The VA doctor helped me convince the San Francisco Medical Examiner to carry out an autopsy, which was finally done on June 30, and it confirmed that Gus’s injuries were the result of somehow falling backward in the van.

Three weeks after the accident, someone finally called me from the Veterans Transportation Service office in San Francisco — but he would not tell me anything about what they thought happened in the van, though he said they were working to make sure this never happens again. They had never looked for a second phone number to reach the family and continued to call Gus’s missing cell phone after he died.

In July 2023 the family filed a wrongful death lawsuit against Owl in San Francisco Superior Court, and we are waiting for a trial date to be set. In December 2023, the Chronicle ran an investigative article about the poor billing system for the SFFD ambulances, and sure enough, when I asked our lawyers if they had seen a bill, they showed me an invoice “addressed” to “Eugene Doe, Homeless, San Francisco, CA 94107” — adding insult to injury, even though the driver had Gus’s name and address on his log sheet since he had just picked him up.

Congresswoman Barbara Lee made some inquiries to the VA on our behalf, and in February, eight months after the accident, an undersecretary of the VA called me — but only to offer me his condolences. He still said nothing about what their investigation had revealed. After I asked him some questions, he said they are still using Owl because they have not been able to find another company to serve the Oakland area — more discouraging news.

And in September 2023 our attorney filed a claim for wrongful death with the VA, but when he called the Office of the General Counsel in February, he learned that the claim had been received but had never been downloaded into their system, let alone assigned to a claim agent!

Gus was drafted into the Army in 1956 and was sent from his hometown of Rochester, N.Y., to Fort Knox, KY, giving him his first exposure to racist Jim Crow rules in Indiana and Kentucky. From there he was stationed in Heidelberg, Germany, where he worked in intelligence and logistics and played football for the base team, injuring his right knee — “playing football for my country,” he said. He also uncovered corruption among American officers who were skimming money from payments to German civilian workers. He threatened to go to the Stars and Stripes newspaper and was abruptly discharged and put on a plane back to the U.S.

Gus was a civil rights and peace activist all his life, starting with protesting police violence against Blacks in Rochester in the 1960s. He came to Berkeley in the 1970s and in the spring of 1979 was drafted by Berkeley Citizens Action to run for mayor. He won that election and was re-elected in 1982 by the biggest plurality in Berkeley history. He challenged unnecessary wars and budget priorities that consistently fund excessive Pentagon spending instead of our domestic needs and security. He supported sanctuary for refugees from Central America, divested from apartheid South Africa, and pioneered in providing domestic benefits for unwed partners.

Countless times in his life, Gus stepped up when his voice was needed. On April 5, 1977, his birthday, a group of protestors in San Francisco began the longest occupation of a federal building in U.S. history, and Gus showed up to support the dozens of disabled activists who were demanding their civil rights. Specifically, they called for implementation of Section 504 of the 1973 Rehabilitation Act, which was designed to help returning Vietnam veterans and included language stipulating that no person should be discriminated against on the basis of disability in any program receiving federal assistance — from schools to transportation and public buildings. After 25 days the “504 occupation” succeeded.

When Gus was elected mayor, his administration created the Mayor’s Task Force on Persons with Disabilities, passed ordinances to ensure access to all public meetings and non-discrimination in City hiring and provided funding for programs serving people with disabilities.

Now we are still faced with the task of uncovering the truth of what happened to Gus in the Owl van and seeking justice for our loss. Unfortunately, except for the one doctor, the Veterans Administration has done nothing to answer our questions or help with our plight.

Years ago, I remember Gus’s granddaughter had just learned the Pledge of Allegiance in kindergarten. She was declaiming some of it in the back seat of our car — “with liberty and justice for all” — and she paused. She asked us, “What’s justice?”

Kathryn Kasch is a retired housing planner who was born and raised in Oakland. For more information, go to gusnewport.com.

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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