Navigating Side Effects, Fear of Recurrence, and Life After Treatment

Felicia kent

A casual night watching sports, a quick self-exam, and a lump that did not belong there. Faced with no insurance and four months of not knowing what to do, Felicia Kent walked into a neighborhood clinic, received a referral to The Rose, and heard the three words that changed everything: you have cancer. In this episode, she talks about choosing a treatment center, using research and strict adherence to medication to blunt chemo side effects, and learning to live with radiation fatigue, lymphedema, neuropathy, and a body that will never be the same. She also shares how faith, a determined daughter, an emotional support dog, and a calling to serve other survivors led her to start a nonprofit, finish her psychology degree, and focus on practical support and early mammograms in the African American community.

On the Road for Early Detection

Shelly Kot

Some women clear their calendar for a mammogram. Others step onto a 40-foot pink coach in their office parking lot. As Director of Mobile Services at The Rose, Shelly Kot oversees a pink fleet of five mobile mammography coaches that deliver the same 3D breast cancer screening you’d get in a breast health center, to women across 45 Southeast Texas counties. During this conversation, she talks about the moving parts that keep those rolling clinics on the road, the disappointment when a failed generator or quality check shuts a mobile day down, and why she still puts on a badge and does mammograms herself. She also shares how being raised by her grandparents, working inside both nonprofit and for-profit systems, and parenting a daughter shapes the way she teaches women to push for answers when something feels wrong.

Access to Treatment Takes More Than a Pathology Report

Patient Navigation

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

Anonymous Donor - Question Mark

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

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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.

CPRIT, The Texas Cancer Plan, and You

Carlton

How does one man’s dedication to community health reshape cancer prevention efforts in Texas? Carlton Allen’s passion for public health and population health, sparked during his academic years, led him to an influential role at the Cancer Prevention and Research Institute of Texas (CPRIT). Through his guidance, CPRIT addresses significant cancer burdens and health disparities statewide. Meanwhile, Allen champions the Texas Cancer Plan as a comprehensive roadmap for continued progress in cancer prevention and care.

She Lost Her Job, Then Found a Lump In Her Breast

Ayanna Wilcher

Diagnosed with DCIS while underinsured and between jobs, Ayanna Wilcher found compassionate biopsy care at The Rose and chose her own path through mastectomy and multiple opinions. Now, she leads survivor work and Rising in Grace, delivering post mastectomy comfort kits and community.

Keeping Access and Compassion First In Every Board Decision

Shannon W

Board Chair Shannon Wiesedeppe carries a deep family history of breast cancer into every decision she helps make at The Rose. From hurricanes and COVID to a Co-Founder and CEO transition, she keeps The Rose focused on access, reimbursement realities, mobile coaches, and identical care for uninsured and insured women.