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 @letstalkLAMMORE INFORMATION ABOUT LAM:LAM Action UK: LAM Action | LAM Action is the UK charity for those with LymphangioleiomyomatosisThe LAM Foundation: Home - The LAM FoundationSUPPORT WOMEN LIKE ME WITH LAM: Donate | LAM ActionWays to Give - The LAM FoundationSUPPORT 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 goinghttps://buymeacoffee.com/letstalklamGET IN TOUCH:Email: : @letstalklamI'd love to hear from you!