Emwills
Let's Talk LAM
If you live with LAM or know someone who does, “Let’s Talk LAM” is the podcast for you. I’m Emma, I’m in my 30s, I live in London, and I’m learning to live with lymphangioleiomyomatosis, or LAM for short. I was diagnosed aged 32 following a spontaneous pneumothorax. Each episode I’ll be talking about living with LAM alongside people that are important and inspirational to me, including my friends, family, and other women with LAM. I aim to delve into topics such as diagnosis, managing symptoms, medications, hospital stays, navigating procedures and surgeries, and mostly just day to day living, laughing, and loving when you have a chronic, invisible, and very rare disease. Please share, follow, comment to start a conversation. MORE INFORMATION ABOUT LAM: LAM Action UK: LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis The LAM Foundation: Home - The LAM Foundation SUPPORT WOMEN LIKE ME WITH LAM: Donate | LAM Action Ways to Give - The LAM Foundation SUPPORT THE POD: Let's Talk LAM is entirely self-funded and costs money for equipment, editing software, and publishing software. If you enjoy my content, I'd appreciate any support me to help me to keep the pod going https://buymeacoffee.com/letstalklam CONTACT EMMA: Please get in touch, I'd love to hear from you! letstalklam11@gmail.com
© 2026 Let's Talk LAM
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