‘It’s Killing the Women You Represent’: Texas Widower’s Plea to Lawmakers to End Abortion Ban

After his 35-year-old wife bled to death from a miscarriage in a Houston-area hospital, a Texas father is suing—and taking her story to Capitol Hill.

“Choosing to bring new life into the world shouldn’t be a death sentence,” insisted Michelle Maloney, the San Antonio attorney working to bring justice to Texas widower Hope Ngumezi and his two young sons.

Three years ago, in June 2023, Hope’s beloved wife Porsha was happily expecting the couple’s third child until she began to miscarry at 11 weeks pregnant. The healthy 35-year-old finance manager for a charter school went to the emergency room at Houston Methodist Sugar Land Hospital, just 10 minutes from her home in suburban Houston.

Both she and Hope were certain that she would receive the safe and critical medical care that she needed as she passed fetal tissue and blood clots the size of grapefruits at the hospital. An ultrasound confirmed that she had partially miscarried and that her fetus no longer had a heartbeat. But the heavy bleeding didn’t stop.

Still, the hospital’s OB-GYN, who examined her just once, moved Porsha from the ER—where staff were equipped to respond to emergencies—to a regular floor, where she received less monitoring. Porsha arrived at the hospital at 3:37 p.m. By 2 a.m., she began gasping for air and within minutes, she had died of hemorrhage.

A dozen doctors who reviewed her medical records for ProPublica, which broke the story about her death, said that Porsha should have urgently received a very simple and standard procedure for a miscarriage—a D&C (dilation and curettage). The 10-15 minute D&C would have removed all remaining fetal tissue in her womb, which her uterus was trying to expel with heavy contractions and bleeding. The procedure would have stopped the bleeding.

“The poor thing bled to death for lack of a D&C. It’s atrocious,” Austin OB-GYN Nancy Binford told Courier Texas.

My Hysterectomy Was a Gift. Dr. Kemi Doll Shows Why Women Need to Share Our ‘Womb Stories’

Determined to prevent uterine cancer deaths, Dr. Doll published A Terrible Strength: The Hidden Crisis of the Black Womb and Your Survival Guide to Healing in May. Both comprehensive and compassionate, the book focuses on individuals of African descent, showing how everyone will benefit.

Upon finishing A Terrible Strength, I took its message to heart: One need not have a womb to prioritize womb health. We can all join Kemi Doll’s Womb Sisterhood through the “deliberate telling and sharing” of “womb stories” with “our true friends.” 

Fortunately, women have already started talking. Personal testimonies changed health outcomes in the 1970s and ’80s—and they’re doing the same now. Earlier generations suffered through perimenopause in silence, but today, women in their 20s, 30s and 40s hear about not only hot flashes but also itchy ears and frozen shoulders. And, as a woman in my early 50s, I’m not completely in the dark about hormone replacement therapy (HRT).

Nevertheless, deadly silence remains.

I am childfree by choice, so pregnancy never fueled my concerns, but I became preoccupied with gynecology in 2017. Fibroids were wreaking havoc in my life, and I pursued a hysterectomy to end my suffering. As Doll puts it, this “definitive treatment” is “welcomed by some and mourned by others.” Though I very much welcomed a hysterectomy, I couldn’t secure one until May 2021, despite my best efforts. 

From now on, I will participate in the “deliberate telling and sharing” of “womb stories.” Doing so is difficult but necessary. As Doll explains, sharing our experience requires us to “shift away from a strength that withstands suffering, silence and pain.” It requires, in her words, “a strength that embraces our vulnerability and can demand better care from the larger world.”

The Feminist Case for Loving ‘Charlie’s Angels’

I don’t remember how old I was when I first heard the term “jiggle TV,” but I know it was decades after I was a devoted, starry-eyed fangirl of the genre. And I do mean “girl”—Wonder Woman came into the world just a year after I did, Charlie’s Angels two years after, Three’s Company the year after that. I watched them all—first in weekly nighttime installments, later in endlessly imbibable reruns—as I was learning to walk, talk, dress, eat, interact with other girls and other boys, and understand how the world saw me and where I fit into it.

The term “jiggle TV” was coined in the mid-1970s by NBC exec Paul Klein to describe and deride rival network ABC’s successful lineup of shows starring women who wore excessively revealing clothing, with Charlie’s Angels as its prime example. Whatever age I was when I first heard the term, I was old enough to immediately grasp its demeaning, objectifying implications. I remember it hitting me like a ton of bricks: The fictional world I’d been gazing at with such awe and reverence was, in the eyes of others, somewhere between a turn-on and a joke.

Without making a big thing about it, I tucked my childhood obsession away in a remote-storage corner of my brain and, for decades, lived an Angels-free life.

Until this year, when Charlie’s Angels turned the big 5-0.

I decided to attempt a full-series rewatch. I wanted to see if immersing myself in the series again after all these years would pull my memories out of remote storage and give me a more detailed picture of how the show’s storylines and messages had affected my pliable young mind.

What had I picked up and taken away from the show besides starry-eyed fangirl devotion?

The answer was: plenty.

On the Voting Rights Act’s Anniversary, Short Film ‘Selma Sisters March On’ Captures 1965’s Fight for the Right to Vote

Aug. 6, 2026, marks the 61st anniversary of the Voting Rights Act. Signed into law by President Lyndon B. Johnson in 1965, the VRA sought to end Jim Crow-era voter disenfranchisement. Particularly in Southern states, voting officials routinely required Black voters to jump through hoops such as “literacy tests” or arbitrary rules such as having to name every county in the state before voting. Even if a Black voter managed to make it this far, election administrators sometimes intentionally sent them to the wrong location to vote, ensuring their vote never actually got counted.

The Voting Rights Act made it illegal for states to discriminate against voters by race, color or language-minority status, thereby reaffirming all U.S. citizens’ constitutional right to vote. The VRA also introduced additional changes to make voting more widely accessible, such as ballots in languages other than English and protections for blind, disabled and illiterate voters.

However, the VRA only became law after decades of struggle and widespread civil rights protests, including the famous marches from Selma to Montgomery, Ala., in March 1965. Protesters, many of whom were young students, faced violent attacks from law enforcement, from tear gas to imprisonment, as they fought for their right to vote.

Sisters Alice and Denise Thomas were only 16 and 14 when they joined the Selma to Montgomery marches and other protests in their home state of Alabama before the VRA became law. In the new short documentary Selma Sisters March On, the Thomas sisters describe in their own words the fateful events of 1965 as they experienced them as high school-aged civil-rights activists.

The Voting Rights Act Turns 61 as New Threats to the Ballot Box Mount

This year’s midterm elections have the power to dramatically alter representation in the current Republican-leaning Congress: All 435 congressional seats in the U.S. House are up for grabs, as is two-thirds of the Senate. Public health, women’s health, abortion access, the cost of living, healthcare affordability, immigration justice and a host of other issues hang in the balance.

However, the Trump administration is working to quietly disrupt voting this November, from firing the remaining U.S. Election Assistance Commission (EAC) members, to continuing to challenge the legality of mail-in ballots and lobby the Supreme Court to do Trump’s bidding—part of an ongoing effort to expand federal control over election administration ahead of the midterms.

“There’s just this onslaught that’s coming from the administration itself, and then the judiciary,” Celina Stewart, CEO of the League of Women Voters, told Ms. “I don’t think it gives people a lot of confidence that [the Supreme Court justices] understand how important voting rights are … You can see the erosion on the Court as they move toward supporting the administration more and moving away from public discourse and public opinion.”

Thursday, Aug. 6, will mark the 61st anniversary of the Voting Rights Act, first passed in 1965 under President Lyndon B. Johnson to prohibit racial discrimination in voting. Congress passed the VRA in order to end post-Civil War and Jim Crow-era voter disenfranchisement, especially in southern states, by prohibiting “literacy tests,” mass voter challenges and other techniques states were using to stop Black Americans from voting.

On Saturday, Aug. 8, the League of Women Voters is leading a nationwide “Unite and Rise for Voting Rights” Day of Action to commemorate the VRA’s anniversary and call attention to SCOTUS’ attempt to decimate it. The Day of Action will also bring together League of Women Voters chapters and partner organizations across the country to lead hundreds of events with the goal of mobilizing voters before November’s midterms.

The Day of Action is part of the League’s Unite and Rise 8.5 initiative, started in 2025, which hopes to engage 8.5 million U.S. voters before November’s midterms—10 percent of the 89.2 million who did not vote in the 2024 presidential election.

And on the VRA’s anniversary on Thursday, Aug. 6, the League will host a virtual rally.

Who’s Paying the Price for Trump’s Medicaid Cuts? Communities of Color and People Living With HIV.

President Trump and his Republican backers have been determined to gut the Affordable Care Act (ACA) and expanded Medicaid coverage ever since his first term in office. This year he is finally getting his way, putting the health of tens of millions of Americans at risk.

It is racial minorities and the chronically ill who will be the most harmed.

A year ago, Congress passed the so-called One Big Beautiful Bill Act, putting in place onerous new eligibility requirements for Medicaid coverage, including work requirements. Medicaid enrollees ages 19 to 64 must complete at least 80 hours a month of work, community service, job training or education to maintain coverage, unless they qualify for an exemption. All states must comply with the new rule by Jan. 1, 2027.

The combination of ACA cuts and new barriers to Medicaid enrollment will likely cause historic coverage losses across the United States for years to come, according to new research: Nearly 16 million people stand to lose coverage by 2034.

A Jim Crow-Era Voter Suppression Tool Is Back: Mass Voter Challenges

In March 2025, two members of the DOGE team communicated with a political advocacy group that was seeking to “find evidence of voter fraud and to overturn election results in certain States.” The group was trying to match Social Security records with copies of voter files that it had acquired. One of the DOGE team members even signed a “Voter Data Agreement” with the group. While it’s still unclear whether DOGE members shared any personal Social Security data, the revelation raised a scary prospect: The federal government might collaborate with election deniers seeking to block American voters from the ballot box.

Most states have laws that allow voters to challenge other voters’ eligibility. Baseless mass challenges to hundreds or thousands of voters at a time are a growing problem. They threaten voters. They swamp overburdened election officials with unnecessary work. And they fuel mistrust in our elections.

Inspired by the Greek Myth, Independent Film Series ‘The Cassandra Project’ Asks Viewers to Believe Women

Even in the wake of the #MeToo movement and heighteend awareness around sexual vioelnce, sexual assault is still one of the most underreported crimes. Although one in four women will experience sexual violence in her lifetime, fewer than 5 percent of these cases ever get reported to the police. In many situations, women fear that the police won’t believe them.

Unfortunately, this fear is well founded. Even though so few reports of sexual assault make it to the police in the first place, data shows that law enforcement will determine that one in five reported cases is “unfounded” and dismiss it.

There are dire consequences to not believing women. The Cassandra Project, a new trilogy of independent short films spearheaded by filmmaker Barclay DeVeau, hopes to illustrate “the profound consequences that arise when women are not believed and their voices are disregarded and dismissed.”

The Myth of the ‘Perfect Birth’: What America Gets Wrong About Pregnancy, Birth and Maternal Care

Project 2026’s pronatalist vision insists that America needs more babies—but largely ignores the conditions that make pregnancy and childbirth unnecessarily dangerous in the first place. In this interview with Ms., The Perfect Birth Myth co-authors Avital Norman Nathman and Deborah Wage argue that improving maternal health requires more than rhetoric about “family values.” It demands investments in midwives, doulas, paid family leave, prenatal and postpartum care, and policies that address the racial and economic inequities driving the nation’s maternal mortality crisis.

Drawing on surveys of nearly 3,000 parents and healthcare providers, Nathman and Wage dismantle persistent myths about birth while exposing the structural failures of the U.S. maternity care system—from hospital closures and Medicaid cuts to the medical establishment’s resistance to alternative models of care. They explain why Black women continue to face disproportionately poor outcomes regardless of income or education, why conservative pronatalist policies fall short, and what it would take to build a maternal healthcare system that truly supports families.

What Happens When a Dancer Is Forced to Become a Refugee? ‘Born to Dance, Forced to Run’ Captures Life Under the Shadow of Deportation

Born to Dance, Forced to Run is a powerful new documentary that follows Steeven Labady, a queer Haitian dancer whose relentless pursuit of his artistic dreams is continually upended by displacement, asylum battles and the constant threat of deportation. Through his extraordinary journey, filmmaker and Haitian feminist activist Pascale Solages reveals the human cost of migration policies, transforming an abstract political debate into an intimate story of resilience, survival and hope.

At a moment when the Trump administration is dismantling Temporary Protected Status for Haitians and escalating immigration enforcement, the film’s message could not be more urgent. It’s a deeply human portrait of what it means to live undocumented under the shadow of deportation.

Born to Dance, Forced to Run premieres in New York on Saturday, July 25, at 6 p.m. at the Brooklyn Children’s Museum, where audiences will have an opportunity to experience this moving documentary on the big screen, followed by a Q&A.