Cervical Cancer Prevention Starts Here: HPV Vaccine Facts You Can Trust

By Kyle Minnis, Cervivor Communications Assistant

The United States, along with much of the world, is at a pivotal moment in cancer prevention. Various studies show that use of the human papillomavirus (HPV) vaccine—which can prevent over 90% of HPV-related cancers, including cervical cancer—is falling. If the trend continues, more children and families will face potentially life-threatening cancer diagnoses that could be avoided. 

The numbers speak for themselves: According to the Centers for Disease Control’s (CDC) most recent National Immunization Survey, only 78% of U.S. adolescents aged 13 to 17 have received at least one dose of the HPV vaccine, and fewer than 63% are up to date on the full series. This is significantly below the national Healthy People 2030 goal of 80% two-dose completion among adolescents aged 13 to 15. Recent data suggests the pandemic has widened gaps in vaccine uptake and fueled vaccine hesitancy.

Globally, approximately 31% of eligible girls have received at least one dose, though the percentage fully completing the recommended series falls well short of the World Health Organization (WHO) cervical cancer elimination target of 90% completion by age 15. The disease still claims the lives of nearly 400,000 people with a cervix worldwide each year.

As vaccine misinformation floods social media, parents and young adults encounter more conflicting messages than ever. Meanwhile, research infrastructure is under threat. In March 2025, the National Institutes of Health (NIH) terminated all funded research on vaccine hesitancy and uptake, telling scientists: “This award no longer effectuates agency priorities.” 

“Watching the headlines and talking to experts in the field, we know this is a critical time,” says cervical cancer survivor Tamika Felder, Cervivor’s Founder and Chief Visionary and co-chair of the American Cancer Society’s National HPV Vaccination Roundtable. “Respected scientists are being dismissed. Research is being defunded. ‘Vaccine’ has become an even more loaded word. And decades of hard-earned progress are at risk.” 

Cervivor Founder Tamika (center) addresses the audience at the 2025 National HPV Conference, a key gathering for leaders in HPV prevention.

For Cervivor Ambassador Zuli Garcia, who will mark her second cancer-versary this November, the issue is deeply personal. As a 2024 Cervivor School graduate and founder of Knock and Drop Iowa, she advocates for underserved families who often face barriers to timely HPV cancer prevention. “I’m living proof of what happens when access comes too late,” says Zuli, who was diagnosed at age 47. “The HPV vaccine represents hope, protection, and equity.”

To cut through the noise and offer clear, trustworthy HPV vaccine facts during National Immunization Awareness Month (NIAM), we’ve gathered insights from survivors and leading experts. What follows is a breakdown of the most essential information about the HPV vaccine—and why it’s needed to protect future generations from preventable cancers.

Why HPV Vaccination Matters More Than Ever

Every major health authority agrees: The HPV vaccine saves lives from cervical cancer and five other HPV-related cancers—including anal, throat, penile, vaginal, and vulvar cancers. Among teen girls, infections with the HPV types that cause most cancers have dropped by 88%, while infections among young women have dropped by 81%, according to a 2024 CDC report. Additionally, among vaccinated women, cervical precancers caused by high-risk HPV types have declined by 40%, with some studies showing up to 80% reductions in high-grade lesions among those vaccinated early.

In countries like Australia and Sweden—thanks to widespread vaccination and strong screening programs—HPV is close to being eliminated as a cause of cervical cancer. 

Dr. Heather Brandt

Dr. Heather Brandt, director of the HPV Cancer Prevention Program at St. Jude Children’s Research Hospital, stresses both the progress made and the work still ahead. “Here we are after almost 20 years of the vaccination being available and still working to make sure people understand how HPV vaccination protects against these diseases,” she says. She recalls feeling “such excitement” at the 2002 International Papillomavirus Conference when early trial results showed the vaccine could prevent HPV-related diseases, pre-cancers, cancers, genital warts, and even recurrent respiratory papillomatosis.

Today, after more than 15 years and over 500 million doses given worldwide, the vaccine’s safety record remains excellent. Serious side effects are extremely rare, and most reactions are mild, such as temporary soreness or fever. Real-world studies confirm that protection lasts at least 12 years—and likely much longer.

Who Should Get the HPV Vaccine and When?

Everyone—regardless of gender—should get the HPV vaccine. Here are the latest immunization guidelines: 

  • The ideal time to start is between ages 11 and 12, though it can be given as early as age 9 for maximum protection. 
  • If the first dose is given before age 15, only two doses are needed. 
  • For those starting later or who are immunocompromised, a three-dose series is recommended. 
  • Catch-up vaccination is advised through age 26, and adults up to age 45 may still benefit based on individual risk and guidance from their healthcare provider.

The following infographic provides additional information on when and why the vaccine is so important for saving lives from preventable cancers.

While insurance coverage for older teens and adults varies, several states—including Washington D.C., Virginia, Rhode Island, and Hawaii, plus Puerto Rico—have implemented school-entry requirements for the HPV vaccine. These policies significantly boost community-wide protection.

“HPV affects everyone—men and women—and the vaccine is about cancer prevention, not lifestyle choices,” says a spokesperson from Vaccinate Your Family, an organization dedicated to raising awareness about timely immunizations. Its current #FirstDayVax campaign aligns with CDC recommendations to bundle the HPV vaccine with other routine back-to-school shots, like Tdap and meningitis. 

Common HPV Vaccine Myths—and How to Address Them

Across the U.S.—especially in rural and conservative communities—misinformation and stigma are stalling progress. Rising non-medical exemptions, often fueled by online disinformation, threaten decades of gains for all vaccines, not just HPV. Without research and infrastructure support, public health programs are left without the tools they need to respond.

Kellie DeFelice

As Vaccinate Your Family warns: “Parents are increasingly exposed to false vaccine claims online, where algorithms and bots amplify misleading content and make anti-vaccine rhetoric appear as credible as scientific consensus.” 

Even parents who support vaccines can be swayed. Kellie Defelice, a Cervivor Ambassador, shares: “I was very pro-vaccine. But after reading a story online, I hesitated and turned down the HPV vaccine for my daughter. I regretted that decision when I was diagnosed with cervical cancer.” Her hope for fellow moms: “They see that I’m the real face of what HPV does—it isn’t just an STI. I risked my daughter getting a cancer that has destroyed so much for me.”

Other common myths include:

  • “The HPV vaccine is just for girls.” In fact, HPV affects everyone. Anal cancer rates in both men and women have been rising, with new cases increasing by about 2.2% per year over the past decade, according to the American Cancer Society. While men may not get cervical cancer, they can still contract and spread high-risk HPV strains.
  • “The vaccine encourages promiscuity.” Zuli explains that some parents worry the vaccine is a “permission slip for sex.” But as Vaccinate Your Family counters, “Vaccination does not change behavior—it simply protects against cancer-causing infections.”
  • “The vaccine isn’t necessary until kids are sexually active.” In reality, the vaccine works best before HPV exposure, which is why health organizations now recommend it for children as young as 9 years old.

How to Get Back on Track with HPV Vaccination Targets

Survivors and experts are pushing back against misinformation with evidence, stories, and culturally relevant outreach. Zuli says: “As a survivor, I’ll keep raising my voice until every child, every family, and every community has access to this protection.”

A review of nearly 60 studies conducted between 2006 and 2019 found that strong provider recommendations are among the most important—if not the most important—drivers of vaccine uptake, underscoring the need to equip health professionals with confidence and clarity in vaccine conversations.

Community partnerships also make a difference. In Memphis, the St. Jude HPV Cancer Prevention Program helped boost county vaccination rates by 19%, outpacing national averages. In Iowa, Zuli’s team at Knock and Drop Iowa combines bilingual education with on-site vaccinations—reaching 23 people in a single afternoon, she reports. “Meeting people where they are is what works,” Zuli explains. “Education first, vaccines immediately after, in a trusted setting.”

Cervivor Ambassador Zuli Garcia hosts an HPV vaccine outreach event in her home state of Iowa.

Vaccinate Your Family echoes this approach: “Conversations about vaccines should always start with empathy, not judgment. Questions about safety, side effects, or the need for certain vaccines are natural—and families should look to trusted, science-based sources.”

St. Jude’s Dr. Brandt highlights new “compelling” research: “Through our work…we have been discussing the implications of possible changes to the dosing schedule with partners. I know all of us are incredibly excited about the prospect of moving to a single dose in the U.S.”

She also offers caution: “We previously leaned in on the rigor of the FDA-approval processes for childhood vaccinations and then review by the Advisory Committee on Immunization Practices. Key changes to these entities may call into question the science. Changes in dosing with any gaps in evidence become fodder for purveyors of misinformation.”

Ultimately, cancer prevention shouldn’t be controversial—it should be celebrated. By recommitting to science, survivor voices, and trusted outreach, we can ensure every person has the chance to thrive, free from preventable cancers.

If you found this blog post helpful, please share it with friends or family members of recommended vaccination age. You may just save a life. 

About the Author

The image is a portrait of a young man with dark skin and short, curly black hair. He is wearing a blue collared shirt and black-framed glasses, and is smiling at the camera.
The man has dark skin and short, curly black hair.
His hair is cut close to his head, with a slight fade at the sides.
His eyebrows are thick and well-groomed.
He is wearing a blue collared shirt.
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It has a relaxed fit and is buttoned up to the top.
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Kyle Minnis is a senior studying Strategic Communications at the University of Kansas. He is currently serving as Cervivor’s Communications Assistant.

Every Cervix Matters: LGBTQIA+ Voices in the Fight Against Cervical Cancer

For queer and trans people facing cervical cancer, the challenges go far beyond the diagnosis. They’re compounded by systemic bias, stigma, and a long history of being overlooked or mistreated in healthcare. These barriers are only growing amid ongoing threats to LGBTQIA+ health equity. (Learn more about these challenges—and the work to overcome them—in part two of our Pride Month series. Stay tuned for Monday).

As Dr. Scout, a trans man and Executive Director of the National LGBT Cancer Network, explains, “It’s getting more dangerous to be openly queer in this country right now.” For many, staying safe means staying silent, often at the cost of their health. 

That’s why this Pride Month, Cervivor is proud to uplift the voices of Karen North, Anjelica Butcher, Gilma Pereda, and Pixie Bruner—members of our community whose experiences reveal both the challenges and courage of queer cervical cancer survivors. Their stories remind us that behind every statistic is a person who deserves to be seen, heard, and cared for.

Challenging Assumptions: Karen’s Advocacy

Karen, a former nurse from Liberty, Missouri, lives with her longtime partner, who shares the same first name, Karen “Murph” Murphy. Their relationship grew gradually after Karen’s 10-year marriage ended in 2001—a union that brought her a son, Matthew, and helped her recognize her identity as a lesbian. But fear of judgment lingered. “When I was still dealing with custody issues,” she recalls, “I’d deny my relationship with Murph in public if I had to.”

Karen North

By the time she was diagnosed with breast cancer—and then cervical cancer 18 months later in January 2016—Karen had stopped worrying about court rulings or public opinion. Instead, she leaned on her medical background to stay focused on treatment, not judgment. “I didn’t care what anyone thought. If I felt judged, I’d call it out and find another provider,” she says, adding with a laugh, “I can be a KAREN, in all caps, if I need to be.”

Karen discovered Cervivor in 2017, but it was Cervivor School in 2019 that truly “lit a fire” in her. Today, she leads the Cervivor Pride group and is a vocal advocate for inclusive language. “One of my biggest pet peeves is when people assume everyone with a cervix identifies as a woman,” says Karen.

Conversations with her transgender friend Zeke—who navigates gynecological care as a male-identifying person—have shaped her approach. Karen now avoids euphemisms like “coochie cancer,” opting instead for medical terms or inclusive phrases like “below-the-belt cancer,” which more accurately encompass HPV-related cancers, including cervical, vaginal, vulvar, penile, and anal.

And she credits her Every Cervix Matters hoodie for sparking meaningful dialogue. “A woman came up to me at a restaurant and said, ‘That’s great. Every cervix does matter.’ I got goosebumps,” Karen recalls. “It doesn’t center gender—it centers anatomy and health.”

Transforming Trauma: Gilma’s Awakening

Cervivor Ambassador Gilma, a graphic designer in California, echoes Karen’s message: “It’s called the human papillomavirus—not the women’s papillomavirus,” she emphasizes. “It doesn’t matter your sexual orientation or your gender.” 

This perspective led her to vaccinate her then-12-year-old child—now a trans woman—shortly after her cervical cancer diagnosis in 2016. “At her annual checkup, the doctor mentioned the vaccine could prevent cervical cancer,” Gilma recalls. “I said, ‘I don’t care if it’s for girls or boys—whatever it is, my child needs it.’”

Gilma Pereda

Gilma’s cervical cancer journey unfolded alongside a profound personal awakening. Raised in a traditional Catholic household in 1970s Mexico, she followed expected norms—marrying and having a child—despite always feeling “different.” After divorcing at 36 and supporting her child through gender exploration, she began to reflect on her own identity. “Cervical cancer changes your sexual life—a lot. So I stopped worrying about that,” she says. “But it gave me the freedom to express my gender differently.”

A metastatic recurrence at 47, which led her to shave her head after a lifetime of long hair, marked a turning point. “I’ve seen so many women devastated by hair loss—hair carries so much of our identity,” she says. “But for me, I was so happy.” Soon after, she came out to her parents. “I was done trying to fit a mold. Now, I feel comfortable being androgynous.”

Gilma’s advocacy stems from a deeply traumatic experience. During a painful, anesthesia-free cryotherapy procedure to remove precancerous cervical cells, a doctor’s inappropriate touch triggered memories of childhood sexual abuse, causing her to delay treatment for a year. “By that time, it was cancer,” she states.

She credits Cervivor—and years of advocacy training and witnessing other survivors doing “very, very difficult things”—with helping her transform that pain into purpose. Gilma has since shared her story in Spanish-language publications and on a bilingual panel addressing sexual abuse in medical settings, an issue that disproportionately affects her community. “I don’t like the spotlight,” she confides. “But I’ll do it again and again to help prevent this from happening to others.”

Confronting Disparities: Anjelica’s Fight

Anjelica, a small business and nonprofit owner in Baltimore, faced her cervical cancer diagnosis already carrying the weight of multiple identities: Black, queer, caregiver—and often the only one like her in the room. “My cultural background gave me strength and resilience,” she says, “but it also came with silence around topics like sexuality and cancer.”

She quickly saw how deeply healthcare disparities run. “I thought I had great insurance—until I found out it didn’t qualify as catastrophic coverage,” she recalls. Denied care for over a month, she had to pay out-of-pocket to start treatment. “It broke my heart realizing the only reason I made it through was because I could afford to. What happens to the people who can’t?”

Anjelica Butcher

For Anjelica, who’s identified as queer since age 13, her cervical cancer diagnosis also brought a realization that “hit hard.” “I was never offered the HPV vaccine—likely because of assumptions about my sexuality,” she shares, referencing persistent stigma and misinformation that overlook how HPV is transmitted: through intimate skin-to-skin contact, not just penetrative sex.

While most of her care team was respectful, certain invasive treatments—like internal radiation—left her feeling unseen and violated. Although the plan was eventually adjusted, the damage had already been done. One provider, referred by her primary doctor, made a lasting difference. “They taught me how to advocate for myself as a Black woman. Most people don’t know how, and it shouldn’t fall solely on us.”

Her support system—her mom, dad, partner, and chosen family—kept her grounded. And with help from a “phenomenal” oncological therapist, she began processing the emotional toll that surfaced after remission. “I didn’t realize how badly I needed community until then.”

Now active in Cervivor and the Ulman Foundation, supporting young adults impacted by cancer, Anjelica shows up in survivor spaces not to seek answers, but to offer hope. “Healing is possible. Remission doesn’t mean going back—it can mean becoming someone even stronger.”

Poetic Resilience: Pixie’s Voice

Pixie, a poet and Cervivor Ambassador from Snellville, Georgia, knows firsthand how gaps in care impact LGBTQIA+ communities. At 26, she was treated for cervical dysplasia, but not tested for HPV. “I wish I had known then what I know now,” she says.

Living with Ehlers-Danlos syndrome and type 1 diabetes, Pixie had always been vigilant about her health. So when she was diagnosed with cervical cancer at 50—with no symptoms—it came as a shock. “I felt numb, contaminated,” she recalls, struggling with the stigma of an STI-related cancer. She underwent a radical hysterectomy and bilateral oophorectomy. “It was basically the ‘Everything must go! Going out of business sale’ surgery,” she’s described.

Pixie Bruner

Living in rural Georgia, Pixie chose not to disclose her sexual orientation. “When I asked a nurse, ‘What do you define as sex here?’ the answer didn’t reflect my lived experience,” she says. After treatment, a conservative therapist dismissed her concerns about sexuality and body image. “I was reduced to parts—told they were irrelevant because of chemopause and their loss. That I should be grateful to be single. But I was still a sexual being, still human,” she says. “I fired that therapist.” 

Cervivor became her lifeline—offering connection, care packages, and space to heal. Her “fairy godmothers,” a married couple, delivered warm meals and encouragement. “Friends are my chosen family and were with me during the long recovery,” she says.

Today, she advocates for inclusive HPV education through Cervivor’s LGBTQIA+ community, and her award-winning poetry—including “Her Kind” and “Medusa With Cancer”—explores how illness reshapes identity. “Cervical cancer took ‘femininity’ and gender away from me in some ways,” she writes. “But my words helped give something back.” 

A Call to Action for Equitable Care

While Karen, Gilma, Anjelica, and Pixie each have unique stories, they share a common goal: a more just and inclusive future.

“I want a world where cervical cancer isn’t common,” says Pixie. “Where HPV vaccination is standard, no one is judged for having the ‘wrong’ cancer, self-care is valued, and early detection is affordable and accessible.”

At Cervivor, that vision means making space for everyone. As Community Engagement Liaison Morgan Newman, MSW, shares: “We stand with our cervical cancer community to demand protection and empowerment through prevention. As someone who’s faced this disease, I know the power of vaccines and the importance of accessible healthcare.”

Cervivor Ambassadors, Ann Marie Hartung and Kellie Defelice, tabling at a Pride event in Massachusetts.

If you or someone you know is part of the LGBTQIA+ community and impacted by cervical cancer, join the Cervivor Pride group (for more information, contact Karen), attend Creating Connections virtual meetups, or take part in local or national outreach.

Support Cervivor’s mission to end cervical cancer by contributing to the ongoing Tell 20, Give 20 awareness and fundraising campaign—honoring 20 years of advocacy, education, and survivorship.