Living with Small Cell Lung Cancer
Learning of a small cell lung cancer (SCLC) diagnosis or cancer progression can have a lasting emotional impact on yourself, your friends and your loved ones. But you do not have to embark on this journey alone. Featured here are stories of SCLC survivors who have shared their experiences in order to provide inspiration to anyone living with SCLC, and to help cope with the emotional aspects that often accompany the disease.
SCLC Patient Montessa
Watch Montessa’s Story: “If I was giving other people advice about how to get your care team intact, I would go back to some of the training we do for our new teachers. And we show them a story about finding your marigold, about planting those marigolds in your garden and finding people who are around you to support you and support your growth.”
SCLC Patient Annette
Watch Annette’s Story: “I needed to know that there was someone there when I had questions about how I was feeling, about how my body was reacting, and I needed to know that I had a doctor that was going to give me positive reinforcement.”
SCLC Patient Kim
Watch Kim’s Story: “Be very open about your small cell with your friends and your family. Make sure you use them as a support system for you, because that is the most important thing.”
What to Expect with Small Cell Lung Cancer
Like many, Kim had complex emotions that accompanied her diagnosis, but she didn’t allow living with small cell lung cancer (SCLC) to impact her relationships with her friends and family. In this video, she describes some of the emotional, social and physical considerations of living with SCLC.
Advice for SCLC Patients
Living with small cell lung cancer can present a different challenge each day. Nina relies on counseling, group support and her passion for art to help cope and stay focused.
Your Small Cell Lung Cancer Community
Learn how Montessa has used several resources to form close relationships with other cancer survivors.
Tips for SCLC Patients
Explore a wide range of resources on small cell lung cancer from health organizations in the cancer community.
Equality In Care: A Patient’s Perspective
Listen to Mari reflect on how being bilingual helped her to connect with her provider to understand crucial information about her care.
This information is for educational purposes only and should not take the place of talking to your doctor or a healthcare professional. The content included on this page does not constitute medical advice and should not be used for diagnosing or treating a health problem or disease. Please be sure to always consult with a physician or medical professional for questions about your medical condition.