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Alameda County In-Home Caretakers Seek $20 Wage, More Accessible Health Care

According to Lupe Martinez, who is SEIU 2015’s chief negotiator, many caretakers work well over 80 hours a month, but don’t receive healthcare, because much of those hours are off the books. As a result, many caretakers are effectively working a full-time job with no healthcare benefits. To help with this problem, SEIU 2015 wants a contract that would lower the minimum hours caretakers would need to work per month to qualify for such benefits.

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Alameda County IHSS caretaker Allen Whitfield (left) sits next to his mother, Charlene Smith, who is also his caretaking client, in her apartment complex in Union City. Whitfield and other caretakers in the SEIU 2015 union are preparing to ask for a $20 wage and expanded access to health care in their new contract. Photo by Zack Haber on December 13.
Alameda County IHSS caretaker Allen Whitfield (left) sits next to his mother, Charlene Smith, who is also his caretaking client, in her apartment complex in Union City. Whitfield and other caretakers in the SEIU 2015 union are preparing to ask for a $20 wage and expanded access to health care in their new contract. Photo by Zack Haber on December 13.

By Zack Haber

SEIU 2015, the union that represents more than 21,000 caretakers who work for Alameda County’s In-Home Supportive Services (IHSS), will be starting negotiations for a new contract early next year that they hope will ensure a $20-an-hour wage and improved access to health care for its members.

“Alameda is one of the most expensive places to live in the Bay Area,” said Lupe Martinez, who is SEIU 2015’s chief negotiator. “In order to provide their essential services, our members need to be able to have the proper wages to live here.”

SEIU 2015 sees their proposed wage increase as a way of reducing the wage gap across gender and racial lines. Across California, 81% of IHSS caretakers are women and 74% are people of color.

IHSS caretakers support those who are disabled or over 65 years old, and who are also unable to live at home safely without help. Typical duties include cooking, cleaning, giving out medications, helping with grocery shopping and bathing, and taking clients to doctor’s appointments.

“People do in-home care work because they love the people,” said Allen Whitfield, a lifelong Oakland resident who’s now in his 60s and works as a caretaker for two clients. “It’s definitely not for the pay.

Currently, Alameda County IHSS caretakers make an hourly wage of $15.75. Starting next year, their wage will increase to $16.75. The union plans to ask for a contract that allows all its members to make at least $20 an hour by 2024, and they’ve been circulating a petition calling for all California caretakers to get this wage increase.

Whitfield likes his job and says he’s “all for being there for people who need help, especially the underdog.” With the current rate of pay though, he can’t afford to rent his own apartment. Even renting a room in a house with roommates is so expensive that he often has to do odd jobs over the weekend to pay his bills. He regularly gets opportunities for steady work in other places for a higher salary, but he doesn’t take the work for one key reason.

“The only reason I don’t take other work,” Whitfield said. “Is that it would get in the way of taking care of my mom.”

Like many, but not all, IHSS caretakers, Whitfield’s clients are family members. In addition to caring for his mother, one of his distant relatives is also a client. Although on paper Whitfield works a little under 30 hours a week, he says he spends well over 40 hours a week caring for his mother and his distant relative.

According to Lupe Martinez, Whitfield’s experience is common among IHSS workers. She says that many clients’ need for care often far exceeds the number of hours that the county allots them to hire a paid caretaker. As a result, many caretakers, and not just those who work for family members, work extra hours off the books because they want to be there for their clients who often have no one else to turn to.

“If you see someone badly in need of care services,” she said. “You’re going to want to help them.”

“It’s an endless job because most of the time [clients] need more care than the hours provided,” said Whitfield.

The extra, unpaid work sometimes makes the job unsustainable. In the mid-2010s, Whitfield had another client who was blind and needed a lot of extra care. But Whitfield couldn’t get enough on-the-book hours to afford to be able to keep him as a client. The blind man has a new caretaker now, and he keeps in touch with Whitfield as a friend by calling him occasionally. While looking back on the forced separation, Whitfield described it as “kind of heartbreaking.”

Partly due to the reality that caretakers work off-the-book hours, SEIU 2015 wants to change how the county provides them health care. The county currently requires that all IHSS caretakers have at least 80 on-the-book hours per month to qualify for health care benefits.

According to Martinez, many caretakers work well over 80 hours a month, but don’t receive healthcare, because much of those hours are off the books. As a result, many caretakers are effectively working a full-time job with no healthcare benefits. To help with this problem, SEIU 2015 wants a contract that would lower the minimum hours caretakers would need to work per month to qualify for such benefits.

The Oakland Post called the Alameda County’s administration office and e-mailed that office detailed questions about how IHSS hours are allocated to clients and if the county plans to expand health care coverage and/or provide a $20 wage in the new contract but was met with no response.

Although Whitfield is committed to taking care of his clients, he feels the wage he makes from the county as a caretaker as well as the lack of appropriate hours is unfair and that the low pay “keeps people in poverty.”

“We just don’t get paid enough for the job that we do and the care that’s needed,” he said. “I don’t think we’re valued at all.”

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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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NPRC Joins National Grand Jury Proceedings Seeking Accountability, Constitutional Restoration

Organizers state that testimony will explore historical and political developments that they believe have contributed to the expansion of corporate influence over public institutions and governmental decision-making. Participants are expected to discuss concerns regarding constitutional governance, individual liberties, property rights, and the protection of vulnerable populations, including seniors and persons with disabilities.

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Photo by Billie Powers.
Photo by Billie Powers.

Special to The Post

The National Probate Reform Coalition (NPRC) has joined Toll and Roll and a growing coalition of advocacy organizations, victims, whistleblowers, and citizen groups in support of a nationally broadcast People’s Grand Jury proceeding scheduled for July 1 and July 7.

Organizers describe the event as a public forum designed to examine allegations of government abuse, judicial misconduct, legislative failures, and the erosion of constitutional protections affecting millions of Americans.

The proceedings will feature testimony from victims, families, advocates, and organizations from across the country who contend they have experienced harm through government actions, institutional neglect, and failures of oversight.

According to organizers, the People’s Grand Jury will focus on concerns involving probate courts, guardianships, conservatorships, child welfare systems, property rights, civil liberties, and what participants view as a growing disconnect between government institutions and the constitutional rights of the people they are sworn to serve.

NPRC is participating because many of the issues being examined mirror the concerns raised by advocates, victims, and families who have participated in its monthly town halls. For years, families have reported cases involving exploitation of elders, questionable guardianships, estate depletion, denial of due process, and a lack of meaningful oversight within probate court systems.

“This proceeding gives victims and advocates an opportunity to place their experiences on the public record,” said Tanya Dennis, lead facilitator of NPRC. “For too long, families have struggled to have their voices heard regarding elder abuse, probate exploitation, and government inaction. This forum allows those stories to be shared before a national audience.”

Organizers state that testimony will explore historical and political developments that they believe have contributed to the expansion of corporate influence over public institutions and governmental decision-making. Participants are expected to discuss concerns regarding constitutional governance, individual liberties, property rights, and the protection of vulnerable populations, including seniors and persons with disabilities.

In keeping with principles of transparency and fairness, invitations have been extended to legislators, members of the judiciary, law enforcement representatives, and other public officials who may wish to respond to concerns raised during the proceedings or defend actions taken by their respective institutions.

One of the primary outcomes sought by organizers is public consideration and support for the People’s Remedy and Restoration Act, a proposed legislative framework that advocates believe would strengthen oversight, increase accountability, provide remedies for victims of governmental abuse, and restore constitutional protections.

The proceedings are expected to be broadcast nationally, providing citizens throughout the United States an opportunity to observe testimony, review evidence presented, and participate in an ongoing conversation regarding government accountability and the protection of individual rights.

Advocates hope the hearings will encourage meaningful dialogue, legislative reform, and renewed public engagement in the democratic process.

Individuals, organizations, public officials, and members of the media interested in attending or obtaining access information may contact the organizers at tollandroll2025@gmail.com.

As Americans continue to debate the future of constitutional governance, judicial accountability, and the protection of vulnerable citizens, the July proceedings are expected to serve as a significant forum for public testimony and civic engagement. For more information, go to https://tollandroll.com

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