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, and comment get the conversation started. To go behind the scenes of the pod, find Let's Talk LAM on Instagram @letstalkLAM 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 GET IN TOUCH: Email: letstalklam11@gmail.com Instagram: @letstalklam I'd love to hear from you!