Everyone’s cancer is different but what should not be different is our access to healthcare, treatments & trials that can maintain our quality of life and improve overall survival. In these episodes, we are use our platform to ask questions, challenge norms, & demand change to create racial equity in the MBC and BC communities.
Jumping hurdles to get the treatments you want is the reality for people living with MBC. Add systemic racism into the healthcare mix and it’s clear that more needs to happen, and soon, to create equity and greater diversity in one of the most important tools in the MBC toolbox: clinical trials. In this episode, we check in with Stephanie Walker, who led the BECOME project and spearheads the Black Wo(Men) Speak Symposium, patient advocate and clinical trial participant Rev. Dr. Tawana Davis, and Patient Navigator Valarie Worthy. How does systemic racism affect what Black patients learn about MBC clinical trials? And how can those who need it most break down barriers to the best care?
We believe that Black History Month should always be celebrated but let's agree that it should not be just for one month but every month and every day.
This is the sixth stop in our series Road to a Cure. From the start our goal for this series was not only to educate and give hope to every listener but also to ensure that each of these special interviews feels like an intimate conversation with our smartest friend who also happens to be an oncologist researcher. This episode will not disappoint., Co-hosts Victoria Goldberg and Lisa Laudico, sit down with the Director of the Breast Unit of the Champalimaud Clinical Center in Lisbon, Portugal, Dr. Fatima Cardoso.
How famous is Dr Hope Rugo? She belongs to a tiny elite group of oncologists who have their own Wikipedia page. Dr. Dennis Slamon is quite possibly the only other member. Enough said. No surprise that we can’t wait to hear what she has to say about a new class of drugs, known as ADCs and specifically, the first ADC for mTNBC that already has a nickname – Sassy (sacituzumab govitecan). Do you know what a SARM is? It is a special class of drugs for those who are Androgen Receptor (AR) positive. Listen and find out.
join us for our discussion about the LGBTQ2S+ community and MBC. Co-host Natalia Green moderates a panel with Bob DeVito and Rainy Orteca, two guests living with MBC, and who are part of the LGBTQ2S+ community along with the co-founder of Queering Cancer, Dr. Evan Taylor. We also sit down with Kimiko Tobimatsu , a Canadian human rights lawyer and an award-winning graphic novelist whose book, Kimiko Does Cancer, tells the story of her breast cancer diagnosis at the age of 25 and the challenges she faced as a queer person, living with breast cancer.
Want to know why we call it “magic?” Hear from people living with MBC about their experiences. While they all agree and encourage others to seek Palliative Care they also are aware of the barriers to access. Our guests cover it all. And it gets real.
The MBC Alliance asks the question “How can we ensure Black people are better represented in cancer research? Finding the answer starts with patient voices.” The BECOME Project is positioned to do just that. BECOME project lead Stephanie Walker and committee member Sheila Fuhs join Lisa Laudico to talk about the important initiative and how YOU can get involved.
Welcome to the Episode 2 of the Trailblazer series. Have you ever asked yourself if Wonder Woman was real? Ask no more. She lives and her name is Jamil Rivers. She is also our Trailblazer of the Month. Jamil was diagnosed with MBC at age 39. She is a mother of three, a caregiver, a full-time CEO of a non-profit organization , the board president of METAvivor and if that’s not enough, she has recently embarked on a new venture—The Chrysalis Initiative, a project dedicated to eliminating disparities in outcomes for Black women with breast cancer. Also in this episode is a Dash of Joy from Our MBC Life’s own Dar Finkelstein. Dar is committed to living a life of joy and she shows us all how to do it. An episode full or hope, inspiration and joy.
“I see so much in the metastatic community this idea of just paying it forward, this idea of, yeah, this might not actually help me right now, but I'm still going to bring it up and I'm still going to advocate for it because it will help somebody else.” This is the story about the power of advocacy. Meet some of the individuals and organizations who are advocating for metastatic breast cancer every day wherever the work takes them.
Our first season 2 trailblazer focuses on the patient - providing them with free services that enable them to focus on healing and time with their families. Through their Thriver Fund, 305 Pink Pack also provides dedicated to support to those living with metastatic breast cancer. Meet Rosemary Carrera of 305 Pink Pack and come south with us to Miami. Also in this episode is a Dash of Joy from Our MBC Life’s own Dar Finkelstein. Dar is committed to living a life of joy and she shows us all how to do it. An episode full or hope, inspiration and joy.
Meet our season 1 Trailblazers. These amazing women are making a difference in their communities. Finding inspiration from their own cancer experiences they have created organizations to support others, close gaps, and give back.
We are excited to share another Best of from Season One. 3 Black Docs know how to keep it real and laugh and have fun. Dr. Karen Winkfield, Dr. Zanetta Lamar, and Dr. Tiffany Avery bring their professional take on racial disparities in healthcare and addressing structural barriers that lead to disparities in treatments and outcomes.
On this bonus episode hear our entire conversation with Carol Evans, CEO and Exec Dir. at SHARE Cancer Support. Carol joined us on two episodes last season - Working while Living with MBC and our December episode on the #inclusionpledge. Our talk with her covered much more and we want to share that with all of you.
Join us for a conversation on biases and disparities, privilege and stigmas, allyship and inclusion. Maimah Karmo, Julia Maues, and Christine Hodgdon join Sheila McGlown and Lisa Laudico for an authentic and real conversation on these issues and more.
Join us as we revisit our inaugural episode with Maimah Karmo of the Tigerlily Foundation. Hear about how Jersi Baker raised her voice asking “where are the people who look like me?” How the #InclusionPledge began and an update on the first six months. We’ll have more on the pledge when we air a new podcast with Maimah later this month.
Kate Keith and Michael Singer share their experiences with male breast cancer. Kate shares personal stories about her husband Ryan who died earlier this year from metastatic breast cancer.
Ricki Fairley, founder of TOUCH, the Black Breast Cancer Alliance, shares her incredible story of how she upended and changed her life and ended her successful marketing career when she was diagnosed Stage 3A Triple Negative Breast Cancer . Ricki talks about the founding of her organization and her overall goal to address Black Breast Cancer as a unique and special disease state, with the overall goal of reducing the mortality rate for Black women.
Recent federal legislation about health insurance coverage will impact the breast cancer community. Monica Bryant of Triage Cancer talks to us about changes to private insurance (through the ACA healthcare exchange marketplace) and publicly funded insurance including Medicare and Medicaid. We also discuss some of the potential ripple effects, including on cancer screening programs, that may impact the ability of many in the cancer community to access healthcare.