Building Trust in HPV Cancer Prevention — One Conversation at a Time

By Cervivor Communications Director Sara Lyle-Ingersoll

Twenty years ago, the HPV vaccine changed the future of cancer prevention. It now protects against six HPV-related cancers: cervical, anal, vulvar, vaginal, penile, and oropharyngeal (throat) cancers.

Yet scientific progress alone isn’t enough.

While the nation’s Healthy People 2030 initiative has set a goal of 80% of adolescents completing the HPV vaccine series, only about 62% of U.S. teens are currently up to date. Coverage varies widely across the country, with some states reporting fewer than half of adolescents completing the series.   

As National Immunization Awareness Month (NIAM) highlights the lifesaving impact of vaccines, public confidence in immunization is being tested by misinformation, growing distrust, and legal challenges to evidence-based vaccine recommendations.

Portrait of Tamika Felder, a 25-year cervical cancer survivor, founder of Cervivor, and advocate for HPV vaccination and cervical cancer prevention.
Tamika Felder

For 25-year cervical cancer survivor and Cervivor Founder and Chief Visionary Tamika Felder, safeguarding the next generation is personal.

“When I was diagnosed with cervical cancer, there wasn’t a vaccine that could have prevented what happened to me,” she says. “Today’s young people have that opportunity. Protecting that progress means making sure families have access to accurate information, trusted guidance, and the confidence to choose prevention.”

That commitment extends to public policy. Last month, Cervivor joined dozens of leading medical, public health, and patient advocacy organizations in signing an amicus brief in the federal lawsuit American Academy of Pediatrics v. Kennedy, supporting evidence-based vaccine recommendations and the scientific integrity of the nation’s immunization policies.

For National Immunization Awareness Month, we asked HPV cancer survivors, physicians, and public health leaders a simple but urgent question: How do we build trust in the HPV vaccine?

The Evidence Has Never Been Stronger

In countries with high HPV vaccination rates, the impact is unmistakable. A landmark 2026 study from England found that cervical cancer deaths among young women offered the HPV vaccine at ages 12 to 13 had fallen close to zero.

Here in the U.S., researchers continue to document declines in cervical precancers and HPV infections among vaccinated generations. A recent June 2026 clinical trial of adults treated for anal or vulvar precancer reinforced what scientists already know: Early vaccination is one of our strongest tools for preventing HPV-related cancers.  

However, despite decades of compelling evidence, misinformation continues to circulate online. A 2024 study found that HPV vaccine misinformation tends to cluster around four themes:

  • Safety concerns
  • Claims that the vaccine is unnecessary or that “natural” approaches are sufficient
  • Conspiracy theories
  • Distrust of medical authorities

Dr. Michelle Fiscus, MD, FAAP, Chief Medical Officer of the Association of Immunization Managers, has heard them all.

Dr. Michelle Fiscus

“We have been using the HPV vaccine to prevent HPV-related cancers for more than 20 years,” she says. “Vaccines undergo more safety monitoring than any other medical product in the United States, and the HPV vaccine has been used in more than 80 countries. Our safety monitoring systems continue to watch for even rare safety signals, and the HPV vaccine has proven to be extremely safe.”

When people argue that natural immunity is better than vaccination, she offers a perspective that’s difficult to forget.

“The immune response the vaccine creates is natural. The vaccine teaches our immune system to recognize the virus and eliminate it before it can go on to cause cancer,” she says. “What isn’t natural is the surgery, chemotherapy, and radiation needed to treat these cancers after they become established.”

Trust is the Missing Ingredient

If the evidence supporting HPV vaccination is stronger than ever, why do misinformation and misconceptions continue to gain traction?

No one understands that challenge better than physician, healthcare technology leader, and best-selling author Dr. Geeta Nayyar, MD, MBA. In her book, Dead Wrong: Diagnosing and Treating Healthcare’s Misinformation Illness, she examines why misinformation spreads.

Portrait of Dr. Geeta Nayyar, physician, healthcare technology leader, and bestselling author who studies healthcare misinformation and trust.
Dr. Geeta Nayyar

“Facts matter enormously,” she says. “But facts alone do not create trust. When someone is frightened or feels dismissed, presenting more data can sometimes make them feel as though we are arguing with them rather than listening to them.”

According to Dr. Nayyar, people don’t evaluate health information in a vacuum. Their experiences, beliefs, and trust in the messenger shape how they receive new information.

Part of the reason misinformation spreads so easily, she says, is that it rarely looks like misinformation.

“It is often packaged as protection: ‘I’m just asking questions,’ ‘Do your own research,’ or ‘They aren’t telling you the whole story,'” she explains. “That language can be compelling because it offers people a sense of agency while suggesting that trusted institutions are withholding the truth.”

The HPV vaccine presents an additional challenge because it touches on three deeply emotional subjects at once: children, sexuality, and cancer. “We cannot dismiss a parent’s instinct to protect their child,” Dr. Nayyar says. “We have to honor it while helping parents understand that vaccination is itself an act of protection against future cancers.”

From Information to Conversation

For immunization leader Dr. Fiscus, that starts with listening.

“When someone has genuine questions or hesitations about vaccines, I find it’s helpful to ask about the concern and the source of that information,” she says. “If it’s something I’ve heard before, I ask permission to share what I know. If it’s new information, I’ll tell them I understand why it would cause concern and offer to look into it and circle back.”

Dr. Nayyar agrees that people are far more likely to reconsider a belief when they feel respected.

“The goal of every conversation does not have to be immediate agreement. Sometimes the most meaningful outcome is simply leaving the door open. Trust is built through connection, humility, and consistency — not through winning an argument.”

When Survivors Lead, Conversations Change

Statistics tell us what the HPV vaccine can prevent. Survivor stories remind us why prevention matters.

“Survivors and organizations like Cervivor can share compelling stories and facts about the success of the HPV vaccine, not only in the U.S., but around the world,” says Dr. Fiscus. “They can share how much easier it is to prevent HPV-related cancers than to treat them after they have been established.”

Calvin Nokes

For HPV cancer survivor Calvin Nokes, the lesson came the hard way. “For years, whenever HPV was mentioned, it was almost always connected to women and cervical cancer,” he says. “I honestly believed it was something only women had to worry about. No one ever told me men could get HPV.”

Everything changed when he was diagnosed with anal cancer in 2009. 

“That’s why I say everywhere I go, ‘Men get HPV, too. Men get HPV-related cancers, too,'” he says. “HPV doesn’t care whether you’re male or female. Boys grow up to become men, and they should be vaccinated, too. We have the opportunity to protect today’s children before they ever face that risk.”

Cervical cancer survivor Athena Porter knows that building trust starts with understanding your audience. 

A Cervivor Ambassador, rural Iowa resident, and woman of faith, Athena leads Cervivor’s virtual Bible study. When questions arise about the persistent myth that the HPV vaccine somehow encourages promiscuity, she doesn’t argue. Instead, she gently reframes the conversation. 

“A person can be cautious and not engage in sexual relations until they get married,” she says, “but there is no guarantee that their future spouse did the same.”

For Athena, emphasizing that the vaccine is about cancer prevention — not sexual activity — helps families see the issue through a different lens. Since graduating from Cervivor School in 2025, she’s continued bringing that message to her community, including in a recent television interview about the importance of HPV vaccination.

Athena Porter, with her husband and their two daughters, who live in rural Iowa.

Protecting Progress Starts with Us

The HPV vaccine has already changed the future of cancer prevention. Protecting that progress, however, will require more than scientific breakthroughs. It will take trusted conversations, compassionate listening, and people willing to share their stories. 

As Tamika puts it, “Advocacy isn’t about having all the answers. It’s about being willing to listen, share your story, and help someone make an informed decision. If one conversation leads to one family choosing cancer prevention, that’s how real change happens.” 

Dr. Nayyar offers similar advice for anyone who wants to help build trust: “Begin with curiosity rather than correction. Ask, ‘What concerns you most about the vaccine?’ Then listen without interrupting or judging.”

Here’s how you can help protect progress:

  • If you’re a parent or caregiver: Talk with your child’s healthcare provider about the HPV vaccine. It’s routinely recommended for girls and boys at ages 11 to 12 and can begin as early as age 9.
  • If you’re an HPV-related cancer survivor: Your experience has the power to build trust in ways statistics alone cannot. Sharing your story may be the conversation that helps another family choose prevention.
  • If you’re ready to advocate: Register for Cervivor’s upcoming Gynecological Cancer Survivors Retreat and Advocacy Training (September 24 to 27) to strengthen your skills, connect with fellow survivors, and help advance HPV vaccination, early detection, and equitable care.
  • Wherever you are: Share credible information, lead with empathy, and keep the conversation going. Every respectful discussion is an opportunity to protect someone from an HPV-related cancer.

Because that’s how progress is protected — one conversation, one informed decision, and one less cancer diagnosis at a time.

About the Author

SARA LYLE-INGERSOLL is a content and communications expert dedicated to transforming lived experiences into impactful stories. Her award-winning magazine feature about a close friend who died from cervical cancer in their twenties led her to Cervivor, and solidified her commitment to cervical cancer awareness and prevention. Now, as Cervivor’s Communications Director, Sara brings this mission full circle.

Finding Your Own Summer: Navigating Cervical Cancer Survivorship When the World Feels “On Vacation”

By the Cervivor Communications Team

“Just relax.”

It’s easy advice to give during the summer.

After all, this is supposed to be the season of vacations, sunshine, and making memories. Social media fills with beach trips, backyard barbecues, family reunions, and weekends by the water.

But for many cervical cancer survivors, summer can bring a complicated mix of emotions. While the world seems to lean into rest and normalcy, survivorship doesn’t take the summer off.

For some, this season brings milestones worth celebrating. For others, it’s marked by treatment cycles, scan anxiety, grief, or the lingering effects of cancer that don’t fade when the weather warms. Many experience all of it.

In a recent letter published in CURE, Cervivor Founder and Chief Visionary Tamika Felder reflected on this disconnect from personal experience. Just days before her 26th birthday, she underwent a radical hysterectomy — and even planning a simple vacation felt different. Packing meant extra toiletries, a “barf bag” close by, and mapping every restroom along the route.

Realities like these inspired Tamika to create Cervivor 21 years ago: a community where no one has to pretend they’re “fine” just because treatment has ended or the sun is shining.

That message continues to resonate across the Cervivor community.

Healing Isn’t Always What We Expect

“Anything by the water is my happy place,” says Tiera. But after finishing treatment, the scars from cancer and other surgeries almost kept her from taking a beach vacation.

For Cervivor Community Outreach and Partnership Director Tiera Wade, one of the first summers after treatment was supposed to be a celebration. She and her best friend had planned a beach getaway, and she couldn’t wait to spend time by the water.

Then she looked in the mirror. After multiple surgeries, more than 10 scars crossed her abdomen. For a moment, excitement gave way to self-consciousness. “I can’t go to the beach like this,” she remembered thinking.

But instead of staying behind, Tiera chose something different. She showed up anyway — scars and all.

Today, after even more surgeries, including a hip replacement that changed one of her favorite tattoos, she sees those scars differently. They tell the story of everything she’s endured and everything she’s overcome.

“This summer,” she says, “I’m showing out proudly — by the water, in the sun, scars and all — still showing up, still celebrating, and still busy living.”

Her experience is one many survivors recognize: Learning that healing isn’t about returning to the person you were before cancer. It’s about making peace with the person you’ve become.

The Invisible Weight of Survivorship

This summer marks an incredible milestone for Cervivor Program Coordinator Lauren Lastauskas: 10 years cancer-free.

“It’s a huge milestone,” she says.

Yet survivorship has taught her that milestones and mixed emotions can exist side by side.

Lauren was diagnosed with cervical cancer at 23. In the summer of 2017, she joined a weeklong whitewater kayaking trip with First Descents in Montana. “I absolutely loved the adventure,” she says, “but it was so hard to see how much my physical abilities had changed since cancer.”

A day at the beach or on the boat still means thinking about where the nearest restroom is because of long-term side effects. Hiking can aggravate nerve damage. Compression socks are a daily necessity because of lymphedema.

Then, every fall, another reminder arrives. As social media fills with back-to-school photos, Lauren is reminded of one of cancer’s lasting losses: the children she’ll never have.

“Ten years later,” she reflects, “summer is just a constant reminder that my body isn’t what it used to be.”

Summer, Through the Eyes of Cervical Cancer Survivors

We recently asked members of the Cervivor community how summer feels after cervical cancer. Their answers revealed that while every journey is different, many survivors carry invisible burdens that others never see.

“Summer is when it all started for me. I knew something was wrong, but I didn’t know what it was. Now, every summer feels like a blessing because I’m still here to experience it.” — Lindsay Gullatte-Lee, North Carolina, three-year survivor

“I was diagnosed in the summer of 2022. I call it ‘The Summer That Never Was.’ I spent those months in treatment and fighting blood clots. Was it worth it? Absolutely. I’d gladly give up another summer to still be here.” Ann Marie McHale Hartung, Massachusetts, 3.5-year survivor

“I am existing from scan to scan right now. I try to live life fully, but every three weeks, immunotherapy is a reminder. The fear of recurrence is always there.” Stephenie Milita Jacobs, Virginia, recent survivor

“Cancer changed the way I travel. I can’t book a vacation months in advance without wondering if I’ll still be in treatment. We always buy trip insurance, and I travel with a medical bag full of supplies. Vacation isn’t carefree anymore—but I still want to make memories with my family.” Sara Dennin Johney, Virginia, currently in treatment

“Summer used to be my favorite season. Now, with dual nephrostomy tubes, the heat and everything that comes with treatment, I often feel left out. I miss swimming, biking, and volleyball. Some days it’s easier to stay home, but I try to join in when I can.” Nancy Long, Michigan, currently in treatment

“Bilateral nephrostomies, compression stockings, medications that make me burn more easily—there are so many impediments to easy summer fun. I can’t swim with my kids, but I can still take them swimming. I’ve learned to adapt instead of giving up.” Lauren, Washington, 9-year survivor (6-year metastatic)

“I’m proud of my scars and my ostomy, but summer can still be hard. I’m constantly navigating weight changes from thyroid cancer and hormone imbalances, and I don’t always feel as comfortable in a bathing suit or summer dress as I once did. I remind myself I’m there to relax, but the anxiety sometimes gets to me.” — Karla Chavez Aplicano, Honduras, cervical and thyroid cancer survivor

“Being diagnosed just before Memorial Day, I spent my summers in treatment, and later my recurrences affected them, too. Even if all I could do was sit on my back porch with the sun on my face, I felt transformed. Find the little things that give you summer joy. It may not be the summer you planned, but it doesn’t have to dictate how you find your happiness.” Carol Lacey, California, 15-year survivor

Finding Your Own Summer — Together 

There isn’t one right way to navigate summer after cervical cancer.

Finding your own summer doesn’t mean pretending cancer never happened. It means making room for both gratitude and grief, healing and hard days, celebration and uncertainty. Most importantly, it means remembering that you don’t have to figure it all out by yourself.

If this season feels more complicated than carefree, here are a few ways to care for yourself and stay connected:

  • Redefine what a “good” summer looks like. Maybe it’s a weekend getaway — or maybe it’s an evening on the porch watching the sunset. Both count.
  • Stay connected instead of isolating. Request to join Cervivor’s private Facebook community, where thousands of people affected by cervical cancer share encouragement, practical advice, and honest conversations about survivorship.
  • Join us for Creating Connections. Our next virtual meetup is Tuesday, August 11, offering a welcoming space to connect with others who understand the realities of cervical cancer survivorship. You can also join one of our tailored community meetups, Cervivor Noir for Black survivors, or Café Con Leche for members of Cervivor Español. Each gathering offers support, conversation, and connection tailored to your lived experience.
  • Practice self-care in ways that truly serve you. Listen to your body, set boundaries, ask for help, rest when you need to, and celebrate what your body has carried you through. Self-care isn’t about perfection — it’s about giving yourself the compassion you’d offer a friend.
  • Remember that every survivor’s journey is different. However you’re spending this summer, your experience is valid.

Summer may remind you of what cervical cancer changed. But it can also remind you of your resilience, your capacity to adapt, and the community standing beside you every step of the way.

Even when the rest of the world feels “on vacation,” you never have to navigate cervical cancer survivorship alone.