Access to Treatment Takes More Than a Pathology Report

Being uninsured, speaking a different language, or not understanding a 40-page form should never decide who lives or dies. In this episode, patient navigators Laura Tovar and Elizabeth Esparza walk us through what really happens after an uninsured woman hears “you have breast cancer” at The Rose. They explain how they review applications before diagnosis, sit in the room with the radiologist, and answer the first question they always hear: “How am I going to pay for this?” They also talk about the maze behind programs like Medicaid for Breast and Cervical Cancer and Harris Health, what it takes to keep coverage from lapsing in the middle of chemo, and the extreme steps some families take, from moving counties to divorcing, just to qualify. Along the way, Laura and Elizabeth share what it costs them emotionally to carry these stories, why they sometimes cry with husbands and children, and how quilts, gas cards, summer camps, and rent assistance become part of making sure no woman has to face breast cancer or the paperwork alone.
A Women’s Bakery, Orphaned Elephants, and Rural Breast Care: Giving With a Bigger Picture

Nonprofit leaders dream of someone walking in and saying, “I’m going to give you a million dollars.” Very few ever see it happen. In this episode, a longtime supporter explains why she chose to fund multiple mobile coaches, help open an East Texas hub, and seed The Rose’s Mammogram to Medical Home program instead of paying for brick and mortar. She talks about dividing her mother’s unrestricted giving fund among education, medical care, and conservation, and why she looks for small organizations whose work sends “tentacles” into whole communities and generations. From a women’s bakery in Africa that feeds thousands of children and sends girls to school, to knowledge mobiles, orphaned elephants, and seed grants for students, she returns over and over to one idea: food and health give people a chance at any future.
Dance, Culture, and Commitment to Breast Cancer Awareness

During this mashup episode, you’ll hear from supporters of Hats and Henna High Tea, a community driven event that celebrates survivors, supports patients, and raises critical funds for The Rose. These are supporters, caregivers, and champions. They talk about mothers and mothers in law facing breast cancer, the sacrifices families make, and the resilience that shows up in hospital rooms, small businesses, and dance floors. Hats and Henna Hight Tea brings culture, art, and local leadership together to focus on The Rose’s mission.
Early Screening, Genetic Testing, and Hope After Loss to Metastatic Breast Cancer

After losing her mother to de novo metastatic breast cancer, Elise turned grief into long term advocacy and board service at The Rose. She demystifies modern metastatic care, clinical trials, and lifelong treatment while urging women of every age to push for screenings and answers.
Meet the Interim CEO Guiding The Rose Through Change

Named interim CEO, Katherine Parsley brings decades of courtroom, nonprofit, and judicial experience to The Rose. As a longtime patient and daughter of a survivor, she centers early mammograms, steady leadership, and practical encouragement for a largely women led team in transition.
Julia Morales on Baseball, Motherhood, and Breast Cancer in the Family

Baseball built Julia’s career, but it’s the people behind the game who keep her in Houston. She traces her path from small‑town athlete to Astros broadcaster, then opens up about 2020, when pregnancy, COVID, and her mother’s breast cancer collided, pushing her to start mammograms early and speak candidly about family history and early detection.
Luncheon Lessons: Stories That Inspire Hope (and Change)

The Rose stands strong because of supporters who gather each year for the “Everything is Coming Up Roses Luncheon,” celebrating survivors, donors, and advocates who drive the mission forward.
God Winks, Ringing Bells, and The Rose: Nancy and Shelley’s Shared Journey as Honorees at the Everything’s Coming Up Roses Luncheon

Nancy and Shelley didn’t plan to share a breast cancer story, much less two very different diagnoses, eight years apart. One faced stage zero DCIS at 41 after pushing for a 3D mammogram; the other walked into an annual screening, felt no lump, and still heard “stage two HER2‑positive.” In this conversation, we talk about what happens when two pragmatic, organized women lean on faith, friendship, and their networks to move fast on treatment—then turn around and use their experience to champion The Rose and the women who rely on us for access to mammograms, diagnostics, and compassionate care.
From Plastics to Patient Advocate: Honoring Shelley Cooper at This Year’s Everything’s Coming Up Roses Luncheon

Shelley didn’t see herself as “an honoree.” She saw herself as a working mom in a male‑dominated industry who just wanted to stay ahead of breast cancer. In this conversation, she walks us through the mammogram she almost didn’t get, the stage zero DCIS diagnosis that still shook her, and the 10 years of follow‑up, skin checks, and colonoscopies that followed. Her story reminds us that early detection, asking questions, and having access to care—like the care The Rose offers uninsured and underinsured women—can change everything.
The Adventurer’s Guide to Surviving Breast Cancer

Trusting your instincts can change everything. Dorothy Gibbons and Jenny Fitzpatrick talk about early breast cancer diagnosis, persistent self-advocacy, and navigating treatment as a young mother. Jenny Fitzpatrick describes celebrating survivorship, building community, and creating new traditions. Stories connect lives. Experiences shape what comes next.