Living in the Public Eye with MBC: An Interview with Kelly Crump
MBC Patients, Living with MBC, Challenges and Barriers, Making Our Best MBC Life Our MBClife MBC Patients, Living with MBC, Challenges and Barriers, Making Our Best MBC Life Our MBClife

Living in the Public Eye with MBC: An Interview with Kelly Crump

Anne Woodward sits down with a special guest to discuss the in’s and outs of having MBC while living in the public eye. Get ready folks, pull up a chair you are not going to want to miss hearing from Kelly Crump, the first ever sports illustrated swimsuit model photographed while posing on a picturesque beach in a gorgeous swimsuit with a mastectomy scar for all the world to see. In this incredible interview Kelly explains how she embraced social media to live out loud and in doing so harnessed all the attention to be an inspiration and help her 30,000 + followers.

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Living with a de novo MBC diagnosis
Living with MBC, MBC Allies, MBC Patients, Making Our Best MBC Life, Relationships and Communication Our MBClife Living with MBC, MBC Allies, MBC Patients, Making Our Best MBC Life, Relationships and Communication Our MBClife

Living with a de novo MBC diagnosis

The Our MBC Life podcast hosts a panel to discuss what it’s really like to be diagnosed stage 4 from the beginning or de novo MBC. Those of us diagnosed de novo don’t get an introduction to breast cancer at earlier stages and that presents some unique issues.

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The Magic of Palliative Care: Our Stories
Living with MBC, MBC Patients, Medical Community, Paliative Care, Long Term Adverse Effects, MBC Stories, Making Our Best MBC Life, Relationships and Communication, Challenges and Barriers, Health Disparities, Advocacy, Obstacles to Better Outcomes, Quality of Life Our MBClife Living with MBC, MBC Patients, Medical Community, Paliative Care, Long Term Adverse Effects, MBC Stories, Making Our Best MBC Life, Relationships and Communication, Challenges and Barriers, Health Disparities, Advocacy, Obstacles to Better Outcomes, Quality of Life Our MBClife

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.

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Policy and the Power of Patient Advocacy
Advocacy, MBC Allies, Patient Advocates, Legacy, Challenges and Barriers, Access to Care and Drugs, BC Policies and Legislation, Health Disparities, Living with MBC, Making Our Best MBC Life Our MBClife Advocacy, MBC Allies, Patient Advocates, Legacy, Challenges and Barriers, Access to Care and Drugs, BC Policies and Legislation, Health Disparities, Living with MBC, Making Our Best MBC Life Our MBClife

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.

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Working while Living with MBC
MBC Patients, Living with MBC, Making Our Best MBC Life, Difficult Life Choices, Working with MBC, MBC Stories, Relationships and Communication, Challenges and Barriers, Financial Toxicity, Quality of Life Our MBClife MBC Patients, Living with MBC, Making Our Best MBC Life, Difficult Life Choices, Working with MBC, MBC Stories, Relationships and Communication, Challenges and Barriers, Financial Toxicity, Quality of Life Our MBClife

Working while Living with MBC

Working while Living with MBC. A panel of MBC patients share their experiences working while living with MBC and we talk to an Alison Greenberg, an employment lawyer about what’s important when communicating your diagnosis at work.
Carol Evans, CEO and Executive Director, joins us to talk about her vision for SHARE’s future, how the metastatic community has changed how she thinks about breast cancer and her trailblazing career in media. We also talk about coping with COVID and cancer in the workplace.

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The Cancer Couch
Advocacy, Caregivers, In Memoriam, Patient Advocates, Grief and Loss and End of Life, MBC Research Funding, Legacy, MBC Stories, Relationships and Communication Our MBClife Advocacy, Caregivers, In Memoriam, Patient Advocates, Grief and Loss and End of Life, MBC Research Funding, Legacy, MBC Stories, Relationships and Communication Our MBClife

The Cancer Couch

Tom Scalera talks about what motivates him to carry on the work his wife, Rebecca Timlin-Scalera, started at The Cancer Couch Foundation. He joins Lisa in this episode to talk about the need for research, new treatments, and how Covid has impacted the grief process.

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