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Helping Women Win: Catching Up with LaPhonza Butler, First Black President of EMILY’s List 

When she was just 30 years old, more than 400,0000 members of California’s largest labor union, SEIU Local 2015, elected LaPhonza Butler to be their president. Known for her outspoken, straight-shooting style as well as her poise and even temper, Butler has a reputation for being a leader capable of building bridges and driving consensus.

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LaPhonza Butler/ Emily's List

When she was just 30 years old, more than 400,0000 members of California’s largest labor union, SEIU Local 2015, elected LaPhonza Butler to be their president. Known for her outspoken, straight-shooting style as well as her poise and even temper, Butler has a reputation for being a leader capable of building bridges and driving consensus.

As the head of the largest union of health care workers in the country, Butler led the campaign to raise the minimum wage to $15 in California.

A respected and trusted political strategist, prominent women in California politics have relied on her advice and understanding of the political ground game to get them elected. Among them are Vice President Kamala Harris, Los Angeles County Supervisor Holly Mitchell and state Assemblymember Wendy Carillo (D-Boyle Heights). 

Now, at 42, Butler was recently named the president of EMILY’s List, a move that will take her from Los Angeles to Wash., D.C., to head the organization that bills itself as “the country’s largest resource for women in politics.” 

She is the first African American CEO of the organization that says its mission is “to elect democratic, pro-choice women to office and to add diversity to our political leadership.” 

California Black Media spoke with Butler recently about her vision and top priorities for EMILY’s List, her thoughts on how to assist Black and other women of color who feel unsupported by their political parties, and more.  

CBM: Congrats. How does it feel taking over an organization that has done so much to move the needle for women involved in politics?

BUTLER: I’m very excited. I am only the third president of EMILY’s List in our organization’s 36-year history. It is a real point of pride for sure as well as an incredible responsibility.

When I think about my role at EMILY’s List, I think about my 7-year-old daughter and the kind of community she wants to be a part of, and I see this role as an opportunity to make that possible. 

CBM: What are some of your short-term goals? 

BUTLER: It’s still early. This is just day nine for me, but I can tell you conceptually what I want to accomplish.

I want to build power for women voters and women candidates, ensuring that we are first-in-class as it relates to creating an example of an organization with diversity at its center. I want us to win. 

Immediately, I am focused on making sure that we are able to win in Virginia in 2021.  

We must hold the Democratic majority and grow the number of Democratic pro-choice women that are in the Virginia statehouse. We have fantastic candidate for Lieutenant Governor in Hala Ayala. She will be the first Afro-Latina to hold that office if we are successful. 

Also, there is anti-abortion legislation moving forward in states across the country. We are doing the work to engage the electorate at the state and local levels. It is important for us to push back on restrictions on a woman’s right to make her own health care decisions. 

CBM: What’s your longer-term vision? 

BUTLER: Building partners. From working with unions in California, I realize the importance of partnerships, of forming coalitions.  

When we worked to raise the minimum wage, we included small business partners. We included workers. 

What I would like to do with EMILY’s List is to make sure that we are throwing the doors open for every woman – no matter what her financial background may be. If she wants to serve, she can find the resources, training and support that she needs at EMILY’s List.  I want to do that in partnership with organizations like Higher Heights, Emerge, Voto Latino and #VoteProChoice.

CBM: What do you want EMILY’s List to represent for women and girls across America?

BUTLER: I want it to mean that every woman can belong anywhere she chooses and at any decision-making table where she wants to be, assured that her voice will be heard. 

I also want the organization to be able to communicate clearly that whether you are a woman of color, or from a working-class background, or immigrant woman, your place in electoral politics is normal. You’re not a groundbreaker, not a celling breaker. You belong at those tables. 

CBM: What’s your message for men?

BUTLER: I want men to know that they, too, have a place and a role in ensuring that their wives, mothers, sisters, daughters and aunts are capable of being strong leaders, not just in their families, but in the halls of government. 

I want men to know that their resources are welcome in supporting organizations like EMILY’s list to help make the dreams their family members’ dreams come true. 

Black women overwhelmingly vote for Democratic candidates. They are leaders and grassroots organizers, and they are the most loyal voting bloc in the party. Yet, Black women candidates often point out that they are not always supported with the levels of enthusiasm, endorsements or funding they deserve. What are your thoughts about this problem?

They are legitimate concerns for Black women, specifically, and women of color, generally. Their voices are the last heard if heard at all. Their experiences are the least valued if valued at all. I can surely appreciate and attest to their leadership. 

As it relates to EMILYs list, I want to hear those concerns and I want to understand them. I want to continue to support Black woman, women of color and all women. 

At the same time, I would invite people to take a look at EMILY’s List and the work we have done to support Black women like U.S. Congresswomen Lucy McBath,  Lauren Underwood or Jahana Hayes. These Black women, who ran and won in majority white districts — white Republican districts.  They all had the support of EMILY’s List. 

The new mayor of St. Louis, Tishaura Jones, for example, has also benefitted from the work of EMILY’s List. 

EMILY’s list has a strong history of being an organization created to diversify women holding elected office. And we can do more to work inside a system that wasn’t built for us. A system that we forced our way into and want to continue to be a part of. 

I’ve heard you say in other interviews ‘when women win, we all win.’ What do you mean? 

What we know about women is that when they go to the ballot box, they carry their whole families. They carry their children, their husbands, their mothers, their fathers. They do not only carry those persons as individuals; they also carry their concerns. I made that statement and I believe that when women are in elected office, the choices that they make are representative of entire communities. That is the way that we lead our families. That is the way we lead our civic organizations and churches. 

CBM: Do you have any advice for women who are interested in running for elected office but don’t know how to get started?

BUTLER: I would say reach out to EMILY’s list if she is looking for a way to get started. We actually have an online community called Run to Win that is made up of tens of thousands of women who are contemplating this very question. Our staff gives them advice and I think the most powerful part is that they give advice to each other based on real-life experiences. 

Even if they have doubts, those women should run anyway. Our Congress and state legislatures are filled with women who didn’t win the first time. 

CBM: You went to an HBCU, Jackson State. Does that experience play a role in shaping who you are as an organizer, visionary and person?

BUTLER: I wouldn’t be who I am today or where I am today but for my experience at Jackson State. My fellow Tigers and the professors that I had who were SNCC or CORE organizers, who may have spent their young adulthoods going to jail fighting to expand the right to vote. They took those experiences and poured them into us in the classroom. They provided the intellectual rigor of higher education and combined it with the civic responsibility to continue to push for better, to fight when there is struggle and to lead when no one else will stand.

It is more than just an institution of higher learning. It is a space where you really do come into the fullness and beauty of all that it means to be a Black person in this nation.

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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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Activism

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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