The Magic of Palliative Care: Our Stories
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 Magic of Palliative Care -Patients and Their Providers
This month we have focused on quality-of-life issues and this episode is part one of a two part series on the “Magic of Palliative Care”. At times the term “palliative care” is misunderstood and so we also use the newer term ‘supportive care’ to better explain how this care supports your quality of life as you go through MBC treatment. We first turn our focus to the medical providers who help us manage symptoms and treatment side effects and, by doing so, improve multiple aspects of our lives.
Policy and the Power of Patient Advocacy
“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.
A conversation with Carol Evans
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.
GRASP: Guiding Researchers and Advocates to Scientific Partnerships
Co-host Natalia Green finds out how Christine Hodgdon and Julia Maués, co-founders of GRASP (Guiding Researchers and Advocates to Scientific Partnerships) saw an opportunity last year to bridge the gap between researchers and MBC advocates in the pursuit of better research connections.
#TheRightDose
Anne Loeser and Dr. Aditya Bardia join the podcast to talk about the importance of getting The Right Dose.
Parenting while Living with MBC
We dedicate this podcast on Parenting while Living with MBC to Heidi Armitage Green. Heidi’s son Walker shares his experience before and after she died. We also hear from Natalia Green and others on how they talk with their children about their metastatic breast cancer diagnosis. Learn about resources you can use for your own converations.
Bonus - Kate Petrides
Kate Petrides joins Lisa and special guest host Emily Veach to share her story. From early stage diagnosis to her metastatic life she has been an advocate for MBC research. Kate shares how she has prepared for a lifespan that is shorter than what she expected. This is a very personal account of life with metastatic breast cancer.
Male Breast Cancer & Remembering Ryan Keith
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.
Mets Monday Advocate Spotlight on Katherine O’Brien
Kicking off Breast Cancer Awareness Month is Katherine O’Brien, a leading force in MBC advocacy. In her interview with Lisa Laudico she talks about the continuing lack of MBC awareness and the MBCA’s new Here ALL Year initiative launching this month.
Dept. of Defense Breast Cancer Research Program
Dr. Gayle Vaday, Program Manager of the Department of Defense Congressionally Directed Medical Research Programs focused on Breast Cancer (BCRP), joins co-hosts Sheila McGlown and Lisa Laudico for a conversation about MBC funding and research and how the funds are distributed. In addition, Sheila McGlown talks about her experience as a consumer reviewer at DoD and her special connection to this critical research funder.
Just Gotta Share
Hear from listeners and guests with their Just Gotta Share moments and meet the Our MBC Life team.