Melissa Grosboll of The Many Faces of Cancer Podcast interviews Erin Cummings, co-founder and executive director of Hodgkin’s International. 

Sheri Prentiss, MD, MPH, CPS/A, CPE, FACPE is both a clinician and a cancer survivor. She was diagnosed with breast cancer and has been living with one of the most difficult repercussions from her treatment – lymphedema. Dr. Prentiss poignantly describes her ongoing battle with this late effect.

The data indicates that there is, indeed, an increased risk for pulmonary issues, including pneumonia, for young adult survivors. The article does not specify what causes this outcome, but we do know that radiation to the chest area can be a major culprit. If you have been treated for cancer, especially with radiation, you may want to be followed by a pulmonologist in addition to your other providers. Many Hodgkin’s survivors have regular “pulmonary function tests,” or PFT’s, to help monitor our lung health.

Authored by Dr.Christina Poza-Kaderman and Saul Wisnia, this article offers some great advice for AYA’s who are challenged by a cancer diagnosis.

Survivorship follow-up care is currently a much debated topic. Questions such as, “Who is in charge of my care now that treatment is completed?” are commonly asked by survivors, and the answers are varied and often confusing. This article addresses many of those questions. It includes comments from Dr. Kevin Oeffinger, who has worked tirelessly to create quality care for survivors.

Hodgkin International’s Rachel Gingold reflects on 36 years of survivorship.

Young adulthood is full of challenges, but when a cancer diagnosis enters the picture, things get really intense, really fast. Fresh out of undergrad at 24, my life changed overnight when the symptoms I’d been having for nearly a year turned out to be Hodgkin lymphoma – cancer.

Jennifer Young, a melanoma survivor, reflects on what it meant to see her daughter reach age 19, the same age she was when she was first diagnosed. She shares how her cancer experience made her more resilient, more empathetic, and more grateful for everyday moments.

For survivors who have finished treatment and are in remission, the question “Am I cured?” is both natural and complicated. In this thoughtful patient handout, Dr. Wendy Harpham explores how the word “cure” is used in oncology, why some doctors avoid it, and what survivors truly need to focus on after treatment.

What should high-quality survivorship care look like? In this presentation, Dr. Michelle Mollica of the National Cancer Institute outlines new national standards that aim to ensure every survivor receives comprehensive, evidence-based support after treatment. From care coordination to managing long-term effects, these guidelines offer a roadmap for improving both patient outcomes and research.