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On the show
Recent episodes
Breaking Cultural Taboos: A Breast Cancer Survivor’s Story in the South Asian Community
Jun 11, 2026
55m 14s
Más Allá del Miedo: Cómo El Cáncer de Mama Transformó a Maribel
Jun 10, 2026
29m 44s
Attorney, CPA, Philanthropist, and Breast Cancer Survivor: Marilyn Sims
Jun 9, 2026
33m 51s
“Dying was not an Option,” a Survivor’s Story
Jun 4, 2026
25m 40s
Peace, Love, and The Rose - A Sneak Peek at Shrimp Boil 2026
Jun 2, 2026
24m 49s
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 6/11/26 | ![]() Breaking Cultural Taboos: A Breast Cancer Survivor’s Story in the South Asian Community | How do you talk about breast cancer when it’s something your community rarely discusses, sometimes because of culture, sometimes because of faith, and sometimes just because it’s hard? Salima Hirani faced breast cancer not just as a patient, but as a mother, a daughter, and someone who knew the taboos around speaking up. In this episode: - You’ll hear how Salima found her own voice in a world that often keeps silent. - You’ll learn how faith and culture shape conversations about cancer in the family. - You’ll find out how sharing your story can help break stigma and help someone else feel less alone. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How did Salima first discover her breast cancer and when was she diagnosed? 2. What was Salima’s initial reaction upon being told she had breast cancer? 3.How did Salima share her diagnosis with her children and what were their reactions? 4. What was Salima’s treatment journey for breast cancer? 5. How did Salima’s children support her during her cancer journey? 6. What taboos or social challenges did Salima encounter in her community regarding breast cancer? 7. Why do some women in Salima’s community avoid breast cancer screening or mammograms? 8. How does Salima recommend supporting other women facing a breast cancer diagnosis? 9. What advice does Salima offer to her community about breast cancer awareness and prevention? 10. How does Salima view the importance of forming support groups and community awareness initiatives? Timestamped Overview 00:00 "Breaking Taboos on Breast Cancer" 06:05 Cancer Chart Reviewer Experience 07:59 Quick Errand Across Street 10:19 Single Parent's Concerns for Kids 13:26 Sibling Misunderstanding Spurs Emotions 17:48 "Nurse Overcomes MRI Anxiety" 21:06 "Personal Choice for Peace" 26:10 Private Strength Amid Diagnosis 29:23 "Prioritize Health Screenings Now" 31:12 Silent Support Network 34:41 Engaging Older Generations in Health Conversations 38:38 Addressing Health Concerns Early 39:51 Silent Struggle: Family's Cancer Journey 43:42 Breast Cancer: Treatable at Any Stage 49:08 Empowering Dialogue for Women's Health 52:58 Breast Cancer Warriors UniteSee omnystudio.com/listener for privacy information. | 55m 14s | ||||||
| 6/10/26 | ![]() Más Allá del Miedo: Cómo El Cáncer de Mama Transformó a Maribel | En este episodio, hablamos con Maribel, sobreviviente de cáncer de mama diagnosticada en The Rose. Maribel comparte cómo el cáncer de su hermana menor fue una señal de alerta que la motivó a realizarse una mamografía sin seguro médico. Gracias a la ayuda de The Rose, pudo recibir un diagnóstico a tiempo, lo que fue crucial para su tratamiento. Maribel nos cuenta sobre los desafíos emocionales, la pérdida de cabello, y su decisión de someterse a una mastectomía, destacando el apoyo de su familia y la transformación que vivió. Hoy, nos deja un mensaje de esperanza y nos recuerda la importancia de la prevención, especialmente para las mujeres latinas. Escucha este episodio y conoce la historia de Maribel, una inspiración para tomar acción con su salud. Preguntas clave respondidas en el episodio: ¿Cómo descubrió Maribel que tenía cáncer de mama y cuál fue el papel de The Rose en su diagnóstico? ¿Qué papel jugó el cáncer de su hermana en su decisión de realizarse la mamografía a pesar de no tener seguro médico? ¿Cuáles fueron los mayores desafíos emocionales y físicos durante el tratamiento, incluyendo la pérdida de cabello y la mastectomía? ¿Cómo impactó el diagnóstico de cáncer en la relación de Maribel con sus hijos y esposo? ¿Cómo se transformó Maribel a través de su experiencia con el cancer? ¿Cuál es su mensaje para otras mujeres latinas que aún no se hacen sus chequeos? See omnystudio.com/listener for privacy information. | 29m 44s | ||||||
| 6/9/26 | ![]() Attorney, CPA, Philanthropist, and Breast Cancer Survivor: Marilyn Sims | Marilyn is an attorney, CPA, and president of the Bill and Helen Crowder Foundation, the private foundation whose generosity helped build The Rose's podcast studio. She has been a Rose patient since the late 1970s, when she came in for her very first mammogram after moving to Houston. Decades later, she found herself in a very different role, as a Stage III HER2 positive breast cancer patient. Her advice is simple and direct: check yourself between mammograms, get second opinions, take care of yourself first, and know that The Rose and organizations like it exist so that every woman, insured or not, has a path to care. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How can a woman with a clean mammogram and ultrasound develop stage three breast cancer within eight months? 2. What does HER2 positive breast cancer mean and how does it affect treatment options? 3. What does a full 18-month breast cancer treatment plan look like, from the Red Devil through post-op chemo? 4. What are the visible side effects of aggressive chemo, including hair, nail, and eyebrow loss, and how do women manage them while working? 5. How did Marilyn continue working through 18 months of treatment and what did that decision do for her mentally? 6. What is the cold cap and why do some patients choose not to use it? 7. What are the stakes of declining post-op treatment, and how should a woman weigh a 45 percent recurrence risk? 8. How does a very private, high-achieving career woman learn to accept help, say no, and make herself the priority? 9. What role does the Bill and Helen Crowder Foundation play in supporting The Rose's mission, including the podcast studio? 10. How does self-exam between annual mammograms save lives, and why does Marilyn emphasize it so strongly? 11. What practical advice does Marilyn offer to women facing a breast cancer diagnosis for the first time? Timestamped Overview 00:00 Dorothy introduces Marilyn Sims: attorney, CPA, president of the Bill and Helen Crowder Foundation, and the donor behind the podcast studio. She previews Marilyn's stage three HER2 positive diagnosis, 18 months of treatment, and her evolution from private person to open advocate. 00:52 Dorothy describes Marilyn's treatment arc and the shift in her willingness to talk publicly. Episode CTA delivered. 01:49 Dorothy welcomes Marilyn on air and thanks the Crowder Foundation for the studio gift. 02:22 Marilyn gives the history of the Bill and Helen Crowder Foundation: established in 1998 under Bill's will, started with $3.5 million, has given away $6 million over 28 years, and still has millions remaining. 03:36 Marilyn explains Bill's passion for children's charities throughout his life, how the foundation was structured to give in perpetuity, and why Helen carried on that mission after his passing. 04:46 Marilyn explains why The Rose, while not a children's charity, fit the foundation's values. Children are affected by breast cancer, and the studio would carry Bill and Helen's legacy forward. 05:36 Dorothy reflects on the studio's impact, including young mothers sharing stories that reach other young women who don't know they could be at risk. 06:25 Marilyn shares that she first came to The Rose for her very first mammogram after moving to Houston in the late 1970s. 06:55 Dorothy asks about Marilyn's background. Marilyn traces her path from a small town to Pasadena, through night school, a business associate's degree at San Jacinto College, an accounting degree at UH Clear Lake, and ultimately to the University of Houston Law Center. 08:30 Marilyn explains how she chose estate planning over bankruptcy and litigation, combining her CPA credentials with her law degree at Ernst and Young before joining her current firm in 1993. 10:43 Dorothy moves to Marilyn's breast cancer story. Marilyn says she was shocked. She ate right, exercised, had no family history, and never anticipated a diagnosis. 11:24 Marilyn describes her screening history: annual mammograms, ultrasounds in recent years, and a clean scan in October 2023. 11:47 In August 2024, she felt a lump just before Labor Day. She made an appointment immediately. On September 13, 2024, she received her confirmed diagnosis. 12:47 Dorothy notes the cancer was particularly aggressive. Marilyn explains: HER2 positive, stage three, with lymph node involvement under the arm and in the neck, within eight months of her last clean scan. 13:30 Marilyn describes her treatment sequence: eight aggressive Red Devil chemo infusions every two weeks starting October 2nd, then mastectomy with same-day reconstruction on the right side, then 30 rounds of daily radiation. 14:58 Marilyn describes the post-op decision point. Scans came back clear, but declining the 14 lower-grade post-op chemo treatments carried a 45 percent recurrence risk. She chose to continue. She finished February 15th of this year. 15:50 Dorothy congratulates her. Marilyn reflects on the predictable rhythm of the later treatments: okay on day one, fine on day two, flu-like on day three, and cumulative fatigue over time. 16:56 Marilyn describes how she emailed her fellow shareholders the day she was diagnosed, asked to keep her routine, and worked through the full 18 months. Her colleagues' support gave her stamina and purpose. 18:00 Dorothy asks how many organizations Marilyn stays active in. Marilyn says staying busy and giving back, particularly to young women and girls, kept her mind off how serious things were. 18:55 Marilyn shares that she has no biological children but has long mentored young women. Her motivation for philanthropy is giving others the opportunity and role models she had access to. 19:35 Dorothy asks about Marilyn's support system. Marilyn credits her husband, who attended every single treatment, sometimes napping in the chair beside her, and her fully supportive office colleagues. 20:37 Marilyn describes the physical side effects of the Red Devil: hair loss, eyebrow and eyelash loss, fingernail and toenail loss, and varying neuropathy. She notes no two patients react the same way. 21:43 Marilyn explains the cold cap option, its time commitment of five to seven hours per treatment session, and the lack of guarantees. She chose wigs instead. 22:29 Dorothy notes that Marilyn's wig was convincing throughout treatment. Marilyn explains she had a custom wig made to match her hair before it fell out, then transitioned out of the wig after 18 months. Her hair grew back curly for the first time in her life. 23:41 Marilyn acknowledges the ongoing anxiety about recurrence and scans. She manages it with a deliberately positive mindset and a carry bag someone gave her early in treatment that reads "You Got This." 24:23 Marilyn describes how talking with other patients, even those with different symptoms and reactions, helped relieve anxiety and provided perspective. 24:59 Dorothy notes that Marilyn was once extremely private. Marilyn reflects on how treatment gradually opened her up, partly because of the sheer volume of medical appointments and people involved in her care. 26:41 Dorothy recalls watching the shift happen in real time. Marilyn explains the difference between being at the beginning of the tunnel versus the end, and how the inability to plan ahead was one of the hardest parts of treatment. 28:08 Dorothy observes that treatment forced Marilyn to stop being Superwoman. Marilyn agrees and names the lesson directly: career women push themselves to be everything to everyone, but you have to make yourself the priority first. 29:34 Dorothy asks if Marilyn sees herself as stronger now. Marilyn says not stronger exactly, but with a clearer sense of priorities, especially the importance of time and quality over constant activity. 30:09 Marilyn delivers her most direct advice: check yourself between mammograms. A year is a long time, and her cancer went from undetectable to stage three in eight months. 30:55 Marilyn advises listeners to explore all treatment options, get second opinions, and be clear with their care team about whether the goal is cure or minimal intervention. 32:20 Marilyn reflects on her insurance advantage and acknowledges how many women raising families and working jobs do not have the same options. She names The Rose's mobile units and reach across Texas as a critical resource. 33:04 Dorothy thanks Marilyn for the foundation's support and for coming on the show. Marilyn expresses genuine relief at being finished with treatment.See omnystudio.com/listener for privacy information. | 33m 51s | ||||||
| 6/4/26 | ![]() “Dying was not an Option,” a Survivor’s Story | Linda Petticrew is one determined woman. She’s worked hard and many long hours to build a stunning career as an Executive Assistant to some of the top CEO’s in the city. But her real strength tenacity was when she faced breast cancer, not once but twice. Diagnosed at a young age, she fought and won her battle and then twenty years later had to fight it again. During this episode, Linda talks about her experience. And she gets candid about her treatment in the workplace and the difference an employer can make in the life of someone dealing with treatment. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1.) How does maintaining a positive attitude and having a strong support system help in coping with a cancer diagnosis? 2.) Why are regular check-ups and screenings important for early detection and treatment of cancer? 3.) How can genetic testing provide valuable information for making informed decisions about preventive measures? 4.) What is the impact of cancer, beyond the individual and their entire family? Chapters 00:00 Introduction and Linda's Background 01:27 The Power of Executive Assistants and Supportive Work Environments 08:14 Maintaining a Positive Attitude and Overcoming Challenges 12:29 Genetic Testing and Preventive Measures 16:13 The Impact of Cancer on Family and Relationships 21:28 Prioritizing Family and Looking Towards the Future 23:17 Hope for a Cancer-Free FutureSee omnystudio.com/listener for privacy information. | 25m 40s | ||||||
| 6/2/26 | ![]() Peace, Love, and The Rose - A Sneak Peek at Shrimp Boil 2026 | Special Events Manager Shannon McNair takes us behind the scenes of The Rose’s annual Shrimp Boil, a nearly 40‑year tradition where fresh Gulf shrimp, auctions, raffles, and desserts turn a casual Saturday with 800 of your closest friends and family into a lifeline for breast health for women in our 45-county service area. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. What is The Rose’s Shrimp Boil and how did it begin?2. Why does the event feel more like a family reunion than a formal gala?3. How do silent and live auctions, raffles, and kids’ activities all contribute to fundraising?4. What food is served besides shrimp, and how do desserts and kid‑friendly options fit in?5. How does the mobile bidding system make it easy to participate in the auction from anywhere?6. What roles do volunteers, committee members, and staff play in making the event a success?7. How can local businesses, families, and individuals donate items for the auction or dessert table?8. How are tickets, tables, sponsorships, and underwriting structured so both families and companies can join?9. Why are unrestricted dollars from this event so important for covering unexpected needs throughout the year?10. What is new this year in terms of date, theme, and logistics, and how can people get involved? Timestamped overview 00:00 Dorothy opens the show with the standard introduction to Let’s Talk About Your Breasts and The Rose’s mission. 00:49 Roxann welcomes Shannon and asks her to describe her role as special events manager. 01:01 Shannon explains overseeing signature events and third‑party fundraisers that support The Rose’s mission. 01:34 They introduce the Shrimp Boil as The Rose’s longest‑running and largest event, approaching its 40th year. 01:41 Shannon shares the origin story of a community‑driven boat raffle that evolved into a major annual fundraiser. 02:41 She describes the atmosphere as casual, indoors at the Pasadena Convention Center, with a family reunion feel and 600 or more attendees. 02:59 Roxann notes there is more than food involved; Shannon adds details about DJ, emcee, and auction. 03:08 Shannon outlines the silent auction: dozens of items ranging from small baskets to big experiences like trips and electric bikes. 03:48 She describes the live auction and the energy brought by the auctioneer, as well as a cash bar supported by beverage sponsors. 04:16 They detail photo booths, popcorn, kids’ games, and adult games like the liquor toss, emphasizing fun for all ages. 05:23 Shannon highlights that survivors, their families, staff, and supporters all mingle, creating generational participation. 05:36 They discuss past themes and introduce this year’s 60s‑inspired Peace, Love and The Rose theme. 05:50 Shannon encourages attendees to dress up as much or as little as they like, from flower crowns to full costumes. 06:42 Roxann asks about donating auction items; Shannon explains that anyone can contribute goods, services, or gift cards. 08:06 Shannon explains the mobile bidding system, how guests register, receive outbid alerts, and check out without long lines. 11:20 They talk about 50/50 raffles staffed by roller‑derby volunteers who sell tickets throughout the room. 12:20 Shannon describes the volunteer and committee structure behind the event, with different leaders owning specific areas like desserts, bar, and kids’ zone. 14:16 They dig into desserts: long tables of homemade and bakery‑donated treats, from sheet cakes to famous pineapple upside‑down cakes. 17:01 Shannon notes that hot dogs and kids’ meals are available for those who do not or cannot eat shrimp. 17:48 Roxann notes the date change; Shannon explains moving to August 8 this year and mentions fresh Gulf shrimp as a highlight. 18:49 Shannon outlines pricing for individual tickets, tables, and sponsorship levels, plus underwriting options for specific elements like the photo booth. 19:56 They discuss buying tickets in advance versus at the door, as well as curbside pickup and why reserved tables work best for groups. 21:41 Roxann asks how the money is used; Shannon emphasizes the importance of unrestricted funds that help ensure no woman is turned away from care. 22:21 They recap the essential details and invite listeners to attend, volunteer, or donate to support the mission.See omnystudio.com/listener for privacy information. | 24m 49s | ||||||
| 5/28/26 | ![]() The Entrepreneur Who's Changing the Way the Black Community Talks About Breast Cancer | Her chance of dying from breast cancer is 50% higher than other women. She has a family history and she’s Black. But that’s not stopping Kim Roxie from changing the odds. Kim is a staunch supporter of The Rose and founder of LAMIK Beauty, a makeup line for women of color made with vegan, natural and organic ingredients. During this conversation, Dorothy talks with Kim about her mother, who lost her fight with breast cancer, and how she’s rallying the Black community to join the battle against cancer. Help us grow the show by subscribing to the show and sharing with your family and friends. And please consider supporting our mission at therose.org. Your donation could help save the life of an uninsured woman.See omnystudio.com/listener for privacy information. | 37m 47s | ||||||
| 5/26/26 | ![]() Navigating Side Effects, Fear of Recurrence, and Life After Treatment | A casual night watching sports, a quick breast 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How did Felicia find her lump and what kept her from seeking help immediately? 2. How does someone without insurance get from a neighborhood clinic to The Rose for diagnostic care? 3. What does it feel like to hear “you have cancer,” and how did Felicia share that news with her family? 4. How did she choose a treatment center and manage chemo, surgery, and radiation side effects day to day? 5. What practical strategies helped her reduce chemo side effects like nausea, mouth sores, and nosebleeds? 6. How is she now supporting other patients through a nonprofit, church outreach, and peer-to-peer work? 7. Why are mindset, faith, and social support so critical during and after breast cancer treatment? 8. How is she raising awareness about mammograms and access within the African American community? 9. What long-term issues like lymphedema, neuropathy, and fear of recurrence does she still live with? 10. How does an emotional support dog, movement, and counseling help manage post-treatment anxiety? Timestamped Overview 00:00 Episode opens, Felicia’s story as an uninsured survivor who reached The Rose through a neighborhood clinic is introduced.01:20 Guest host Shannon McNair welcomes Felicia and asks how she discovered her lump and used self-exams.01:40 Felicia describes finding the lump by chance, lacking insurance, and remembering The Rose from boutique work.02:40 She visits a nearby clinic, receives an immediate referral to The Rose, and later credits the team with saving her life.04:30 Telling her sister, leaning on prayer, and deciding early to be a testimony for others facing cancer.06:20 What she wishes she had known about treatment, side effects, and why she followed medication instructions exactly.07:40 Lesser-discussed chemo and radiation side effects like mouth sores, nosebleeds, and fluid issues, and how she managed them.08:40 Birth of her nonprofit work, finishing a psychology degree during treatment, and pursuing community health worker training.09:50 Current advocacy: blogs, peer-to-peer conversations, holiday outreach, and small gifts to patients during treatment.10:40 Common questions she hears about insurance, alternatives, and staying positive through harsh treatments.12:10 How to support someone with cancer when you do not know what to say, including quiet presence and simple statements of love.13:40 Encouraging friends and family to show up with meals, learning, and practical help, while survivors learn to express what they need.16:30 Holiday and year-round programs for patients, including Christmas deliveries, Valentine outreach, and church-based change collections for donations to The Rose.19:10 Focus on education and early detection in the African American community, especially for younger women and those wary of treatment.20:30 Balancing chemo, lumpectomy, graduation, radiation, and then managing fluid buildup and other late effects.23:50 How an emotional support dog, daily walks, and therapy help manage anxiety and fear of recurrence after treatment.26:00 Decision to delay reconstruction, experiences losing a young niece and a church member to breast cancer, and why that fuels her advocacy.27:20 She reflects on cancer as an ongoing learning experience, the importance of mental health care, and continuing in support groups.See omnystudio.com/listener for privacy information. | 29m 14s | ||||||
| 5/21/26 | ![]() Holistic Care for Breast Cancer Survivors | Marcella Herrera from the Canopy Cancer Survivorship Center at Memorial Hermann The Woodlands Medical Center joins the show to talk about the ways their all-volunteer staff helps survivors thrive after fighting the battle of their lives. During this episode, you'll learn about the wide array of programs offered, as well as the importance of having an empathetic shoulder to lean on (that's not a relative). And finally, Marcella tells Dorothy why providing support for survivors and their families could be the most important medicine. Learn more about the Canopy Cancer Survivorship Center at Memorial Hermann The Woodlands Medical Center here. Help us grow the show by leaving a review on your podcast platform and sharing with your family and friends. And please consider supporting our mission at therose.org. Your help could help save the life of an uninsured woman.See omnystudio.com/listener for privacy information. | 29m 39s | ||||||
| 5/19/26 | ![]() How The Rose's Mobile Mammograms Bring Screening to 45 Counties | 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 five-coach fleet that delivers the same 3D screening you’d get in a center to women across 45 counties in Southeast Texas. During this conversation, she talks about the moving parts that keep those rolling clinics on the road, the sick feeling when a generator or quality check shuts a 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How does The Rose’s mobile mammography program work for workplaces, churches, and schools? 2. What is the difference between screening on a coach and services at a breast center? 3. How far do The Rose’s five mobile coaches travel across Southeast Texas? 4. What happens when a mobile coach or critical equipment breaks down on screening day? 5. How do quality checks on the road protect patients and keep standards high? 6. Why did Shelly choose radiology and then specialize in mammography? 7. What did she learn working in both nonprofit and for-profit breast centers? 8. How does she support fearful patients during mammograms and biopsies? 9. What life lessons from her grandmother guide how she works and leads? 10. What does it mean for women to advocate for themselves when something feels wrong in their bodies? Timestamped Overview 00:00 Episode begins, mobile mammography program introduced.02:00 Role overseeing five mobile coaches and 45 counties.03:00 How workplaces, schools, and partners schedule a mobile coach.03:30 Same 3D technology on coaches as in The Rose’s centers.05:00 Breakdowns, generators, and failed quality checks that can cancel a full day.06:00 Daily quality control on moving coaches and why it matters.07:30 Choosing radiology, then focusing on mammography and caring for women.11:00 Seeing the difference between nonprofit and for-profit breast centers.13:00 A typical mobile day, early starts, and full screening schedules.14:00 Why she still performs mammograms as a director to stay close to patients.17:30 The Rose’s mission to serve insured and uninsured women alike.19:30 Life with a police officer husband and their “no work talk” rule.20:30 Being raised by her grandparents and lessons from her grandmother.23:00 Hopes for her daughter’s health and self-advocacy.24:30 Core life lesson about kindness and the lasting impact of words.See omnystudio.com/listener for privacy information. | 27m 19s | ||||||
| 5/14/26 | ![]() Blindness, Breast Cancer, and Bold Choices: One Woman’s Unyielding Spirit | Jennifer Parrish, Manager of Business Services at the Lighthouse of Houston, joins Dorothy to share her story. Parrish talks about managing work at the Lighthouse of Houston, overcoming transportation issues for treatments, and addressing misconceptions around breast cancer. Despite facing breast cancer, legal blindness, and personal loss, Jennifer's resilience and positive attitude shine. She emphasizes the importance of self-care and seeks to inspire others through The Lighthouse’s podcast, Sightless Voices, Unleashing Potential. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1.) What was Jennifer Parrish's oncotype score, and what did it imply? 2.) Why did Jennifer Parrish opt for surgery to remove her ovaries and fallopian tubes? 3.) How did Jennifer Parrish rate the difficulty of her breast cancer journey? 4.) Did Jennifer Parrish have time to grieve her father's passing? 5.) What challenges did Jennifer Parrish face in navigating healthcare facilities and appointments? 6.) What actions did Jennifer Parrish take to make her cancer experience more enjoyable? 7.) How did Jennifer Parrish manage her work during radiation therapy and her cancer treatments? Timestamped Overview 00:00 Jennifer Parrish: Inspiring journey overcoming challenges, inspiring empowerment. 03:40 Moved for better opportunities, settled in Houston. 06:41 Navigating challenges delays mammogram for blind patient. 09:46 Family support and friendships during cancer treatment. 15:11 Podcast helps raise awareness about cancer support services. 15:56 Used Google Maps, brushed up on Spanish. 22:11 Blindness intertwined with breast cancer challenge, manageable. 25:35 Need to relax more during recovery time. 27:00 Overheating scare during daily afternoon walk. 31:01 Understanding real issues fosters connection and empathy.See omnystudio.com/listener for privacy information. | 32m 37s | ||||||
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| 5/13/26 | ![]() El miedo a la mamografía: Lo que necesitas saber para estar tranquila | En este episodio, conversamos con la Dra. Cotes, radióloga experta en salud mamaria, para aclarar muchos de los mitos y preocupaciones comunes que existen sobre la mamografía. Desde la temida radiación hasta los diferentes tipos de exámenes disponibles, la Dra. Cotes nos explica de manera sencilla cómo la mamografía es una herramienta segura y crucial para detectar el cáncer de mama en etapas tempranas. Además, hablamos sobre el impacto de la densidad mamaria y la importancia de los exámenes anuales, así como las últimas innovaciones tecnológicas, como la resonancia magnética y los ultrasonidos, que ayudan a mejorar los diagnósticos. Si tiene duda sobre su salud mamaria o la mamografía, este episodio es para usted.See omnystudio.com/listener for privacy information. | 27m 35s | ||||||
| 5/12/26 | ![]() 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 assistance programs for uninsured patients, what it takes to keep coverage from lapsing in the middle of chemo, and the impossible choices some families face during their breast cancer journey. 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. What does “patient navigation to treatment” mean at The Rose, and how is it different from scheduling or basic navigation? 2. How do Laura and Elizabeth first learn about a woman, and what happens between her initial mammogram and a positive diagnosis? 3. What are the main treatment access programs for uninsured women in this episode (Harris Health/Gold Card and Medicaid for Breast and Cervical Cancer)? 4. Who qualifies for Medicaid for Breast and Cervical Cancer, and how do income, age, citizenship, and “working quarters” factor in? 5. Why do many newly diagnosed women worry more about cost and payment than about the cancer itself? 6. How do navigators match patients with facilities and oncology practices that actually accept their specific Medicaid HMO plan? 7. What happens when Medicaid coverage lapses during chemo, and how do Laura and Elizabeth intervene to get treatment restarted? 8. How do they explain a breast cancer diagnosis differently to small children, teenagers, and spouses, and why are husbands often the most visibly shaken? 9. What are some of the hardest situations they see, including women moving counties or divorcing to meet eligibility rules, or being asked for large deposits to start chemo? 10. How do Laura and Elizabeth support patients with complex applications, missing documents, language barriers, and repeated denials from eligibility offices? 11. What other practical resources do they connect families to, such as food assistance, utility and rent support, camps for kids, gas cards, wigs, bras, and comfort items? 12. How do they cope with the emotional toll of this work while trying to remain steady for patients and their families? Timestamped Overview 00:00 Dorothy opens with how insurance status, language, and paperwork can determine who lives or dies, and introduces patient navigators Laura Tovar and Elizabeth Esparza.01:45 Laura and Elizabeth share how long they have been at The Rose and the roles they held before moving into patient navigation to treatment.02:35 Dorothy explains “sponsorship” as intake for assistance programs and why The Rose avoids the word “charity.”03:10 Elizabeth defines patient navigation to treatment as helping mostly uninsured, newly diagnosed women find a path into actual cancer care.03:50 Elizabeth describes reviewing applications a day or two before diagnosis to anticipate which treatment program might fit.04:25 Laura walks through what happens on the day a woman learns she has breast cancer and how navigators stay with her after the radiologist leaves.05:30 Elizabeth outlines key treatment programs: Harris Health (Gold Card) for county residents and Medicaid for Breast and Cervical Cancer (MBCC).06:00 Laura and Elizabeth explain MBCC eligibility, including age limits, income guidelines, citizenship, legal residency, five-year residency rules, and working quarters.08:20 They describe the questions women ask first after diagnosis, centered on cost, payment, and whether existing coverage at The Rose will extend to treatment.09:20 Laura explains why The Rose refers many MBCC patients to Texas Oncology and how they choose facilities that accept specific Medicaid HMO plans.10:30 They discuss how confusing HMO choices and insurance concepts are for women who have never had coverage and fear they will have to “pay it back.”11:20 Dorothy notes that many major cancer hospitals do not accept these plans, increasing reliance on a smaller network of providers.12:00 Laura and Elizabeth talk about the need to renew Medicaid every 12 months, how patients can forget during treatment, and what happens when coverage expires mid-chemo.12:35 They describe calling Medicaid, troubleshooting reasons for termination, and sometimes getting coverage reinstated within days.13:40 Dorothy asks how much information patients actually absorb at diagnosis; Laura and Elizabeth estimate many do not hear most of what is said.14:10 Laura explains follow-up calls, longer consultations, and sometimes separate visits to help spouses and children understand the diagnosis and plan.15:10 They share that husbands often cry more than patients because they feel helpless and unable to “fix” the situation or pay for care.16:30 Elizabeth describes how they tailor explanations for children by age, avoiding the word “cancer” with very young kids and framing treatment as strong medicine.17:10 They talk about the emotional toll of this work, the difficulty of holding in tears, and moments when they cry alongside patients.18:20 Dorothy raises the growing number of women who do not meet changing criteria for key programs and need entirely different solutions.18:55 Elizabeth describes families uprooting their lives to move into Harris County so they can qualify for Harris Health coverage.19:40 Dorothy notes some women feel forced to divorce to reduce household income enough to meet eligibility rules.20:20 They mention stopgap strategies like GoFundMe campaigns, cash-pay arrangements, and sliding-scale clinics that still remain expensive for women living paycheck to paycheck.21:20 Laura and Elizabeth share examples of women being asked for large deposits, including a $15,000 payment to begin chemotherapy.22:10 They discuss the complexity and length of application packets like the Harris Health form and why careful completion matters.22:40 Laura explains how nerves cause patients to make simple errors—wrong dates, missing boxes—that delay approval for months.23:30 They describe helping women who were diagnosed elsewhere but come to The Rose for help with Gold Card or other eligibility obstacles.24:10 Laura outlines how they review documents, join three-way calls with agencies, and clarify what paperwork is actually missing.24:50 Elizabeth explains why they personally deliver applications to eligibility centers instead of relying on patients who lack transportation or time.25:35 Dorothy reflects on her earlier belief that a diagnosis and pathology report would be enough, and how language and bureaucracy proved otherwise.26:20 She recalls that the realization of repeated denials and confusion led directly to creating the Patient Navigation to Treatment program.27:15 Elizabeth shares work with Rice University and Camp Kesem to connect children of cancer patients with supportive summer programs.28:10 Laura and Elizabeth list other resources they connect families to, including food banks, rent and utility help, medication support, gas cards, wigs, bras, prostheses, and comfort bags.29:20 Dorothy highlights the impact of donated quilts, heart pillows, and small items that remind women someone cares about them.30:00 Laura and Elizabeth admit that the work is overwhelming at times, especially when they cannot find a path to treatment for a particular woman.30:30 Dorothy closes by emphasizing that, for most uninsured patients, Laura and Elizabeth are the bridge to treatment and invites listeners to recognize and support this work.See omnystudio.com/listener for privacy information. | 31m 19s | ||||||
| 5/7/26 | ![]() Following Mom’s Lead by Paying it Forward to The Rose | Jennifer Pareya's support for The Rose spans more than twenty years and it all started with her mom’s breast cancer experience. Jennifer’s mom, Judy, was diagnosed at The Rose and after beating breast cancer, she insisted on the family giving back. And they’ve done so tenfold. From fundraisers at the Lighthouse Pub to Bikers Against Breast Cancer, they’ve spent many years advocating on behalf of uninsured women in Texas. Now, she champions the adult beverage stand at the iconic Shrimp Boil. But it’s more than that. Jennifer understands the life-saving importance of mammograms and encourages insured women to schedule their mammograms at The Rose so that uninsured women can be seen as well. It's a simple act that makes a big impact. Learn more at therose.org/shrimpboil. Key Questions Answered 1.) How has Jennifer Pareya and her family supported The Rose for over two decades? 2.) Why is it important for Jennifer to bring two insured women with her to her mammogram appointments? 3.) What are Jennifer’s favorite moments from past Shrimp Boils? Chapters 00:00 Jennifer's Fundraising Journey 02:44 The Shrimp Bowl: A Fun and Successful Fundraiser 03:40 Giving Back to the Rose 07:06 Jennifer's Strategy for Fundraising 09:29 The Impact of the Rose and Paying It Forward 10:53 Special Memories at the Shrimp BoilSee omnystudio.com/listener for privacy information. | 15m 05s | ||||||
| 5/5/26 | ![]() 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 Regional Service Center, 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. Why did this donor decide to fund mobile mammography coaches instead of buildings or equipment alone? 2. What led her to support The Rose’s Mammogram to Medical Home program for uninsured women without a doctor? 3. How does she evaluate nonprofits and decide where her giving can reach the most people? 4. What impact has her support had on The Rose’s reach across rural counties in Texas? 5. How does the women’s bakery in Africa change entire families and communities over time? 6. Why is conservation, especially in Africa, a core part of her philanthropy? 7. How have personal family health issues shaped her interest in medical research and smaller organizations? Time-stamped Overview 00:00 Episode begins, Dorothy welcomes a returning donor and recaps her support for coaches, machines, and the East Texas hub.01:00 Dorothy remembers the first meeting, meant to discuss Hispanic outreach, that turned into a million-plus-dollar commitment.03:00 Donor explains why she dislikes brick-and-mortar projects and pushed instead for funding a mobile coach.04:00 She shares why serving uninsured and Hispanic communities and multiple rural counties made the coach gift feel right.05:00 She describes hearing from a friend whose East Side clinics routinely send women to The Rose.06:40 Background on the unrestricted giving fund her mother left, and how she divided it among education, medical care, and conservation.07:30 Story of the women’s bakery in Africa, where uneducated women become bakers, feed thousands of children, and send girls to school.09:30 Benny’s journey from hungry child to baker and first in his family to pursue higher education.12:00 Why she prefers projects with “tentacles” that ripple across generations rather than one-time efforts.13:15 Family roots in geological conservation and how that grew into wildlife and environmental work in Africa.14:30 Description of funding “knowledge mobiles” in Botswana that teach children and teachers about animals and conservation.15:30 Support for vehicles and projects in Madagascar and elsewhere that combine conservation, education, and livelihoods.16:45 How a first trip to Kenya and later bird-watching deepened her awareness of poverty and need.18:00 Why she values organizations where 100 percent of donations flow directly to field partners.19:00 How she vets small organizations through trusted partners and prefers to give seed money.21:00 Dorothy recalls how the donor also seeded the Mammogram to Medical Home program after a declined grant.22:00 Structure of the Mammogram to Medical Home model and why it is unusual in mammography.23:30 Donor shares why reducing fear and complexity for uninsured women matters so much to her.24:20 She reflects on being raised to help people regardless of background and to treat everyone with respect.24:50 Dorothy describes how the coaches and the Lufkin hub expanded The Rose’s reach far beyond Houston.26:00 Dorothy notes the donor’s humility and curiosity, always learning servers’ stories and quietly backing new programs.27:30 Donor shares her introverted childhood and how marriage nudged her into connection and a wide circle of friends.28:20 She considers future giving priorities, including food security on Native reservations and broader food and health efforts.30:30 Examples of seed grants for arts and music students at universities who lack funds for travel, internships, and competitions.31:30 Final reflection that food and health give people a foundation for any future, followed by closing thanks and call to support The Rose.See omnystudio.com/listener for privacy information. | 33m 41s | ||||||
| 4/30/26 | ![]() How 3D Mammography and MRI are Transforming Care | Dorothy sits down with Dr. Wei Yang, a renowned professor and breast radiologist. Dr. Yang emphasizes the significance of mammography, recommending annual screening starting at age 40 for women at average risk. During this conversation, you’ll hear about the benefits of digital breast tomosynthesis (3D mammography) and breast MRI for women at elevated risk, highlighting the positive outcomes associated with early-stage breast cancer diagnosis. Dr. Yang underscores the importance of early detection and the role of emerging technologies, such as contrast-enhanced mammograms and artificial intelligence, in improving breast imaging, and more. Her personal story is as interesting as the work she is doing to level the playing field for all women, insured or uninsured. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. What is the importance of breast cancer screening, and what are Dr. Yang's recommendations for mammography screening? 2. How do digital breast tomosynthesis (3D mammography) and breast MRI benefit women at elevated risk of breast cancer? 3. What are the positive outcomes associated with early-stage breast cancer diagnosis, and why is early detection so crucial? 4. What new technologies, such as contrast-enhanced mammograms and artificial intelligence, are emerging to improve breast imaging? Chapters 00:00 Introduction and Background 03:16 Choosing Radiology and Specializing in Breast Imaging 05:40 Different Screening Modalities in Breast Cancer 07:00 Understanding Digital Breast Tomosynthesis 09:55 The Role of Breast MRI in High-Risk Women 14:11 Diagnostic Workup for Abnormal Mammograms 18:50 Exploring New Technologies in Breast Imaging 20:42 Embracing Artificial Intelligence in Medicine 21:09 Navigating Gender Asymmetry in Medicine 22:36 Supporting Patients and Delivering Clear Communication 25:31 The Importance of Forgiving Self and Taking One Step at a Time 28:23 Hopes for the Future and the Importance of Passion 30:14 Encouraging Women to Prioritize Their HealthSee omnystudio.com/listener for privacy information. | 31m 50s | ||||||
| 4/28/26 | ![]() 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. Who helps bring Hats and Henna to life and why this event matters so deeply to them. 2. How Lin Lin connects restaurant ownership and radio work with advocating for women’s health and mammograms. 3. How breast cancer in the family shaped Iman’s decision to start her own jewelry business and live with more courage. 4. What lessons a young person can carry for life after watching a loved one go through breast cancer treatment. 5. Why Sami believes The Rose stands out among charities working in breast cancer and community health. 6. How Hats and Henna helps raise both awareness and funds for mammograms and navigation services. 7. How Parita used dance to cope with her mother’s diagnosis and to create a supportive community around performance. 8. What it means for children and teens to give up activities and relocate in order to support a parent in treatment. 9. How loss shaped Somya’s commitment to working with The Rose and reaching more families earlier. 10. Why every story at Hats and Henna comes back to the message that self care and early diagnosis can change outcomes. Timestamped Overview 00:00 Episode and event introduction, focus on community stories00:40 Lin Lin on women’s self care, mammograms, and partnership02:00 Iman on Ashma’s journey, family resilience, and starting a business04:20 Sami on why he supports The Rose and Hats and Henna05:40 Parita on leaving Chicago, dancing through her mom’s chemo06:50 Somya on losing her mother in law and finding purpose with The Rose08:00 Closing reflections, gratitude, and reminder that self care is essentialSee omnystudio.com/listener for privacy information. | 8m 55s | ||||||
| 4/23/26 | ![]() Yoga Therapy and Breast Cancer: Insights from a Survivor | Diagnosed with breast cancer while living a health-conscious lifestyle, Nancy Martch aggressively battled her Stage 3B diagnosis head-on. Now, leveraging her yoga expertise, Nancy empowers others through personalized yoga therapy, blending acceptance and self-awareness into her healing approach. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How did Nancy discover her breast cancer? 2. What kind of lifestyle was Nancy leading when she was diagnosed with cancer? 3. How has yoga helped Nancy cope with her cancer diagnosis and treatments? 4. Which specific yoga poses does Nancy find beneficial for relaxation and stress reduction? 5. What is the importance of self-assessment in yoga according to Nancy? 6. What is the role of non-competitive self-acceptance in Nancy's yoga practice? Timestamped Overview 00:00 Yoga therapy is personalized; classes are generalized. 05:04 Yoga integrates body awareness and lifelong practice. 07:37 Advocate for yourself; misdiagnosis taught me. 12:50 Acceptance and awareness: adapting self-care through challenges. 13:57 Breathing techniques helped manage panic effectively. 20:03 Teaching relaxation and breath exercises for self-use. 22:33 Yoga is adaptable and tailored to individual needs. 26:12 Diagnosis doesn't define us; posture can improve. 28:22 Self-love empowers us to support ourselves.See omnystudio.com/listener for privacy information. | 30m 59s | ||||||
| 4/21/26 | ![]() 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. 10 Key Questions Answered 1. How Elise became involved with The Rose board and metastatic breast cancer advocacy. 2. What happened during her mother’s initial breast cancer diagnosis and why it was classified as de novo metastatic. 3. How metastatic breast cancer treatment looked in the early 1990s, including bone marrow transplant approaches. 4. What key advances have changed metastatic breast cancer care since her mother’s time, such as genetic testing and subtype specific treatments. 5. How clinical trials for metastatic breast cancer usually work today and why they rarely involve placebo without treatment. 6. Why metastatic patients often need lifelong treatment and careful monitoring to stay on effective therapy as long as possible. 7. How advocacy groups and steering committees at MD Anderson direct research funds toward metastatic specific projects. 8. Why self advocacy and persistence with providers can be critical, especially for younger women seeking mammograms or additional testing. 9. How Elise balances her volunteer work, legal background, and family life while staying active on multiple boards and committees. 10. What message she wants women and families to remember about screening, self care, and not putting their own health last. Timestamped Overview 00:00 Board recruitment and early connection to The Rose02:30 High risk programs, navigation, and genetic testing03:45 Mother’s de novo metastatic diagnosis and treatment in the 1990s08:30 Limited options then versus today’s targeted therapies10:00 Role of subtyping, genetics, and clinical trials now11:30 How trials work, ongoing treatment, and progression13:00 Starting early mammograms and self advocacy in her 30s17:30 Younger women, “too young” barriers, and trusting your body21:30 Advanced breast cancer steering committee and research funding24:30 Boot Walk fundraising and metastatic specific projects28:00 Broader volunteer work and intensity of patient needs31:00 Navigation, uninsured women, and final call to advocateSee omnystudio.com/listener for privacy information. | 35m 23s | ||||||
| 4/16/26 | ![]() CPRIT, The Texas Cancer Plan, and You | 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 in 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. Key Questions Answered 1. How did Carlton Allen get into public health? 2. What differentiates public health from direct patient care according to Carlton? 3. Where did Carlton Allen complete his education? 4. How did Carlton Allen integrate community health workers (CHWs) into clinical operations? 5. What are the challenges in obtaining funding for community health workers? 6. What is the Cancer Prevention Research Institute of Texas (CPRIT) and what roles does it play? 7. How does CPRIT impact cancer prevention and research in Texas? 8. What frustrations does Carlton Allen face in his role at CPRIT? 9. What was Carlton Allen’s role in the Texas Cancer Plan? 10. What values does Carlton hope to instill in his children based on his community work? Timestamped Overview 00:00 Community Health Workers' Impact 03:42 Healthcare Worker Reimbursement Challenge 07:46 Expanding Healthcare Outreach with Grants 10:07 Visiting Texas Prevention Grantees 13:27 Advancements in Cancer Prevention 16:51 Cancer Secrecy in Males 21:14 Inclusive Cancer Care Guidelines 25:57 Community Engagement and Volunteerism 27:56 Raising Hardworking, Community-Minded Children Learn more about CPRIT here. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts.See omnystudio.com/listener for privacy information. | 31m 59s | ||||||
| 4/15/26 | ![]() De Colombia a Houston: La Historia Personal que Impulsó la Carrera de la Radióloga Cotes | En este episodio, la Dra. Cotes, profesora asistente y jefa de la división de imágenes mamarias en UT Health en Houston, comparte su inspiradora historia, desde su Colombia natal hasta convertirse en una destacada radióloga mamaria en los EE.UU., su misión de servir a la comunidad hispana y su transición de The Rose a UT Health.See omnystudio.com/listener for privacy information. | 23m 14s | ||||||
| 4/14/26 | ![]() She Lost Her Job, Then Found a Lump In Her Breast | 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How Ayanna’s life and work shifted in the year leading up to her diagnosis, including job loss and a move back into higher education. 2. How she first felt a lump, what her recent mammogram history was, and which steps her doctor friend urged her to take. 3. What it was like to be underinsured when a biopsy was recommended and how she was referred to The Rose for care. 4. How Ayanna experienced her biopsy at The Rose, including the provider’s communication, pain control, and overall respect. 5. What happened the day she received her cancer diagnosis while traveling, and how she coped emotionally during her conference responsibilities. 6. Why she and her team named the cancer “Beulah” and how humor and mindset helped her face decisions about surgery. 7. How insurance battles over imaging, multiple oncology opinions, and differing chemo recommendations led her to choose a non chemo maintenance path with Texas Oncology. 8. How her husband’s decision to take a lower paying out of state job for health insurance, and her children’s responses, shaped the family’s experience of her cancer. 9. What specific challenges women face after mastectomy, from drains and lack of rest to the cost of pillows, bras, and other comfort items. 10. How Rising in Grace and Ayanna’s work with Angels Surviving Cancer and patient navigation training aim to make post mastectomy life less isolating and more supported. Timestamped Overview 00:00 Introduction, background, and 2026 as a rebuild year02:00 Clean mammogram, new lump, and fast follow up03:30 Job loss, underinsurance, and biopsy denial03:45 Referral to The Rose and compassionate biopsy experience05:00 DCIS diagnosis on a flight and initial shock06:30 Humor, naming “Beulah,” and building a care plan07:50 Meeting oncology team and facing mastectomy decision09:30 Moomoo mastectomy party and surgery day12:30 Pathology results, nine invasive sites, and chemo debate13:40 Second and third opinions, choosing no chemo, “bet on yourself”15:15 Impact on husband, children, and mother; caregiver burden20:00 Angels Surviving Cancer, patient navigator training, leadership21:30 Launching Rising in Grace and creating post mastectomy kits23:30 Realities of drains, rest, and the cost of comfort items26:00 Body image, bras, and emotional recovery after mastectomy29:00 Final message: act early, seek support, and remember it is not the endSee omnystudio.com/listener for privacy information. | 34m 11s | ||||||
| 4/9/26 | ![]() Keeping Access and Compassion First in Every Board Decision | 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How Shannon was recruited to The Rose board through Junior League connections and early exposure to the mission. 2. What roles she has held within the Junior League and how that prepared her for board leadership. 3. How her family’s multi generational breast cancer history shapes her personal vigilance and advocacy. 4. What major events The Rose has weathered during her board tenure, including hurricanes, COVID, and large anonymous gifts. 5. How the board and staff worked together creatively to keep services going when many nonprofits closed. 6. Why the board chair role is central to managing CEO transitions and aligning leadership with the strategic plan. 7. How collaboration and partnerships can extend The Rose’s services and why those relationships take patience and persistence. 8. What Shannon learned about insurance, government funding, and reimbursement and how these dynamics affect breast imaging access. 9. Why awareness and education remain urgent even after forty years, especially for women reaching screening age for the first time. 10. What single message she wants women to hear about The Rose’s role as a partner in making mammograms and next steps less stressful. Timestamped Overview00:00 Board service, crises, and change01:20 Joining The Rose board through Junior League connections03:00 Family breast cancer history and personal vigilance04:30 Surviving hurricanes, COVID, and funding shocks06:00 Staff grit, creative problem solving, and board support09:00 CEO oversight and navigating a founder transition11:00 Strategic plan, partnerships, and collaborations21:00 Learning reimbursement, funding, and insurance realities24:00 Awareness, myths, and reaching each new generation27:00 Why The Rose matters, access, and mobile mammography29:00 Core message: The Rose as a partner through stressful careSee omnystudio.com/listener for privacy information. | 33m 20s | ||||||
| 4/7/26 | ![]() Meet the Interim CEO Guiding The Rose Through Change | 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. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How did a legal and nonprofit career lead to serving as interim CEO at The Rose? 2. What lessons come from moving from the courtroom to Crime Stoppers and other mission-driven organizations? 3. How does being both a Rose patient and the daughter of a breast cancer survivor shape one’s perspective on early detection? 4. What are the primary responsibilities of an interim CEO in a healthcare nonprofit? 5. How can an interim leader best support the team during the search for permanent leadership? 6. Why does women’s tendency to put themselves last make breast health messaging especially important? 7. How can prioritizing relationships, travel, and downtime with family contribute to personal wellbeing? 8. What does it take to lead a workplace of more than 100 employees, most of whom are women? 9. How do deep Houston roots and an extended family network influence a commitment to local service? 10. How can a career of service leave a lasting impact, and what legacy can leaders aim to build in each role? Timestamped Overview 02:00 Legal and nonprofit background, prosecutor to judge to CEO04:00 Personal breast cancer connection and being a Rose patient08:00 Family life, Houston roots, and love of community10:00 Women’s self neglect, modeling consistent healthcare, self care14:00 Leading as an interim, stabilizing the team and mission17:00 Open door leadership style and message to staff19:00 Legacy, impact, and making a difference through each roleSee omnystudio.com/listener for privacy information. | 27m 46s | ||||||
| 4/2/26 | ![]() How One Woman’s Breast Cancer Battle Led to the Self-Care Movement | As the Executive Director of The Jung Center, Dr. Fitzpatrick's not only given the Rose community hope in the darkest of times, such as during the pandemic, but he’s also done so for countless others in the Houston area. During this conversation, Dorothy and Dr. Fitzpatrick talk about past challenges and how they’ve impacted the breast cancer community. He also discusses the need for caregivers to embrace self-care and encourages breast cancer patients to engage in self-acceptance. Additionally, we get a brief history lesson when Dr. Fitzpatrick discusses Audre Lorde, who was faced with the difficult decision of either living out what life she had left serving her values, helping women’s groups that were forming in the 1970s and the 1980s, or if she was going to take the step back to seek treatment for breast cancer. Learn more about Dr. Fitzpatrick's work and The Jung Center at www.junghouston.com. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. Why is must we nurture our well-being, especially in the face of adversity? as the isolation brought on by the pandemic. 2. How is breast cancer tied to the origin of self-care? 3. What can we do to foster better support networks in our community? 4. What are Dr. Fitzpatrick’s tips for managing self-care? Timestamped Overview 00:00 Self-care in pandemic: simplified approach for all. 03:51 Infants have instinct to notice surroundings instinctively. 07:47 Paying attention to body signals for calm. 12:55 Well being defined as happiness and contentment. 15:04 Well-being through relationships, including self and community. 18:38 Commute time transformed during pandemic, newfound appreciation. 23:46 Audrey Lord, influential writer, faced cancer decision. 24:48 Self-care as political act for black woman. 28:11 Recognize interdependence, create spaces for connection.See omnystudio.com/listener for privacy information. | 32m 47s | ||||||
| 3/31/26 | ![]() Saying Goodbye: Dorothy’s Farewell After 40 Years at The Rose | Forty years at The Rose taught our co-founder and CEO Dorothy Gibbons this: you don’t walk away from women, even when the system does. In this farewell episode, Dorothy share the stories that shaped her, why she's stepping back, and why your support and your stories still matter. Support The Rose HERE. Subscribe to Let’s Talk About Your Breasts on Apple Podcasts, Spotify, iHeart, and wherever you get your podcasts. Key Questions Answered 1. How were Dorothy and Dr. Dixie received as two women creating a new breast health nonprofit in the mid‑1980s? 2. What kind of resistance did Dorothy encounter from male‑dominated leadership when she pushed for mammograms and a place for uninsured women? 3. Who were early patients and volunteers like Annabelle and Diana, and how did they shape The Rose’s culture? 4. Why does Dorothy believe patient stories—and hearing “someone else has been there”—still matter just as much as technology? 5. What does it mean for The Rose to be a Breast Imaging Center of Excellence, and why was that accreditation such a milestone? 6. Which values at The Rose are non‑negotiable for Dorothy, especially around how women and working mothers are treated? 7. What has truly improved in breast cancer imaging, awareness, and treatment in 40 years—and what has barely changed for uninsured and low‑income women? 8. How did gifts ranging from one dollar at a gas station to a surprise million‑dollar donation keep The Rose going? 9. After four decades, how does Dorothy keep her passion for women’s health, and what unfinished business does she believe belongs to the next generation? 10. What advice does she give anyone starting a nonprofit today—and why does she insist real change requires policy change, not just good programs? Timestamped Overview 1:00 Dorothy reflects on starting The Rose and how little the world understood mammograms and uninsured women in the mid‑1980s. 02:00 Stories of early skepticism, male‑dominated rooms, and how Dr. Dixie’s trailblazing surgical career gave them cover to push forward. 05:30 Remembering first patients and volunteers like Annabelle and Diana, their opposite personalities, and how they taught Dorothy there’s no one “right” way to live with cancer. 08:30 Why sharing patient stories on the podcast still matters: faith, courage, and the power of hearing your own experience in someone else’s words. 10:20 What becoming a Breast Imaging Center of Excellence required from staff, physicians, and equipment—and why that recognition mattered. 12:40 Dorothy’s non‑negotiables: valuing women, backing employees as whole people, and the day a tone‑deaf salesman lost a contract with one sexist comment. 15:40 What has improved in imaging, awareness, and treatment over 40 years—and what remains broken for uninsured and low‑income women. 18:00 The emotional toll of fundraising shortfalls, policy stagnation, and why closing the doors never felt like an option. 19:30 How advocacy and policy wins like Texas’s Cancer Prevention and Research Institute funding changed the landscape for prevention and research. 21:30 The unforgettable million‑dollar donor in overalls and the equally powerful one‑dollar gift at a gas station in El Paso. 24:00 Sponsored patients who gave back, like the woman who saved for years to fund another biopsy, and how those gifts shaped Dorothy’s view of generosity. 25:30 Keeping passion after four decades, why 40 years went by in a blink, and the stories that still fuel Dorothy’s work. 26:30 Letting The Rose “grow up,” what kind of energy Dorothy hopes to leave behind, and why she believes in the quiet power of “you can do it.” 28:00 Life after pink: how Dorothy imagines her next chapter and her advice for anyone bold enough to launch a nonprofit today.See omnystudio.com/listener for privacy information. | 30m 29s | ||||||
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4 placements across 4 markets.
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4 placements across 4 markets.

