Bay Area

It’s Filipino American History Month a Note from an Asian American Israeli

As a pacifist, I find that the news from the Middle East is depressing. The death tolls will rise higher before any talks can begin between the sides. So, I pray for people I know there, an estimated 35,000 Filipinos in Israel, a small part of the 2-3 million Filipinos in the Middle East. But one friend is unique. A Filipino American born in the U.S., he married the Israeli sweetheart of his youth and moved to Israel nearly a decade ago. He is essentially an Asian American Filipino Israeli.

Published

3 years ago

October 15, 2023

Oakland Post

OPINION

By Emil Guillermo

It’s my birthday this week. I am 118.

No lie.

Prior to this week, I figured age was just a number, and stopped counting.

But now I’m into counting each and every year. With honor.

It hit me as I prepared for talks commemorating October as Filipino American History Month.

My father would have been 118 this year. And only now have I realized that his life has been my life; History is my story.

He was born in the Philippines under the American flag in 1905.

That’s seven years after the U.S. bought the country from Spain after the Spanish American War in 1898. The Treaty of Paris sealed the deal 125 years ago. The U.S. paid $20 million mostly for the Catholic artifacts. Note, that’s less than the Golden State Warriors pay some of their star players.

Through the treaty, my father became more than a Filipino. He was a colonized American national, and able to come to America without papers.

He was legally undocumented.

But when my father came to California in 1928, he was not lucky enough to immediately start a family. Not in 1928, ’38, ’48, but in the ’50s.

What happened? Was he a bumbler in loud, unappealing clothes? Or was he just caught in Filipino American history, a racist one where Filipinos were plugged up, stopped up, dammed up.

Or maybe just damned.

Men like my father were brought in to replace excluded Chinese and Japanese labor, which made the male-to-female ratio among Filipinos around 14-1. You couldn’t find a Filipino wife. Anti-miscegenation laws were also in play. Filipinos were shot or lynched just for looking at a white woman. That often caused riots where angry whites protested the “peaceful penetration” of Filipinos.

My father was only able to start a family well after World War II when Filipino women were allowed to come more easily to America. But my father didn’t take part in the segregated U.S. Army. His health and age prevented him from enlisting. But that meant he couldn’t get the biggest boost into the American middle class and generational wealth—the GI Bill.

We never owned a home, never owned a car, and lived paycheck to paycheck.

If you didn’t serve in the military, you relived the ’20s, the ’30s, and the ’40s in the ’50s, ’60s, and ’70s.

But he did meet my mother. Though not a traditional Filipina “war bride,” she had survived the Japanese occupation of Manila. She hid under sewing machines at a seamstress shop to avoid being forced to become a Filipina ‘comfort’ woman to Japanese soldiers.

She was saved by a Spanish citizen who took her under her wing and brought her to San Francisco.

When she met my father in the early 1950s, it was well after the war. But then, the delayed second generation of Filipino Americans began.

As part of the second generation, I was born in the U.S. But I was always treated like the first, my father’s generation.

Filipino American history has always controlled my life. Even when I break glass ceilings, I am wounded by the shards.

During Filipino American History Month, it only makes sense to honor my father. My story begins with his on the day he was born under the American flag in the Philippines. A colonized American national who was too often treated as less than in America.

So today, this week, is my birthday. I am 118. I will always gladly explain how. It’s in the history of our treatment in America.

A Note from An Asian American Israeli

As a pacifist, I find that the news from the Middle East is depressing. The death tolls will rise higher before any talks can begin between the sides.

So, I pray for people I know there, an estimated 35,000 Filipinos in Israel, a small part of the 2-3 million Filipinos in the Middle East.

But one friend is unique. A Filipino American born in the U.S., he married the Israeli sweetheart of his youth and moved to Israel nearly a decade ago.

He is essentially an Asian American Filipino Israeli.

When Israel was attacked, I contacted him to make sure he and his family were fine.

“We are fine, away from the southern conflict areas,” he wrote to me. “A major intelligence and operational failure by the IDF [Israeli Defense Forces]. The watchmen were sleeping. Israel’s 9/11.”

I was relieved to hear he was safe.

“There should have been a trigger with troops rushing in if there was a breach of the high-tech security fence. A quick reaction force. Failure of intel component,” he continued.

But he knew on Sunday something bigger and more deadly was brewing.

“The West Bank is ringed with troops. The northern border is on high alert. And Hezbollah leader Hassan Nazrullah learned his lesson in 2006,” he said. “A big ground war is coming. Two months tops on the fighting. But it is going to be bloody.”

I asked him if he was leaving for safety.

He said he’d canceled a planned trip to the U.S. and was sure he would volunteer for security duties once things were organized.

But he sounded clear and determined as you’d expect an Asian American Filipino Israeli.

“We aren’t leaving.”

He said it with a fearless defiance, full of pride and the willingness to endure whatever it takes in the fight for the right to exist.

It’s the reason the deaths will keep rising, until someone says enough. And then talks will begin.

That’s too late. For me, it’s enough already.

Emil Guillermo is a journalist and commentator. He does a micro-talk show on www.amok.com

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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.

Published

3 days 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

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Oakland Post: Week of July 1 – 7, 2026

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

Published

3 days ago

July 5, 2026

Oakland Post

To enlarge your view of this issue, use the slider, magnifying glass icon or full page icon in the lower right corner of the browser window.

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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.

Published

2 weeks ago

June 26, 2026

Oakland Post

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

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.