Building Equity in the Breast Cancer Community, feat. Jasmine Souers of the Missing Pink Breast Cancer Alliance

Wait, How Do You Spell That? A Rare Disease Podcast

For Breast Cancer Awareness month, in this episode we're speaking with Jasmine Souers, the president and CEO of the Missing Pink Breast Cancer Alliance about some topics that aren't often covered in mainstream oncology. We discuss the individual genotypes, treatment factors and other considerations that make each case of breast cancer a "rare" experience. We also talk about the experiences of people of color, the "spectrum of need" in patients, and how to build equity in the breast cancer community.

If you'd like to learn more about the Missing Pink Breast Cancer Alliance and the work they're doing in the community, you can check out their website at TheMissingPink.org.

Also be sure to pick up a copy of their newly-launched More Life Magazine for breast cancer patient stories, perspectives, resources and more! Get your copy today at MoreLifeMag.com.

###

Chronic conditions and rare diseases don't discriminate. Patient Worthy and its partners are interested in amplifying the voices of those from all identities and backgrounds. If you have a breast cancer journey to share, reach out to learn more about how your voice can help spread awareness and inspire individuals from all walks of life.