My Spontaneous Pneumothorax & Hospital Admission

Adjusting to Lymphangioleiomyomatosis (LAM)

Join me and my friend and karaoke-fiend, Nina, for another episode of Let's Talk LAM. We talk about how we met, my initial thoughts/feelings when receiving the LAM diagnosis, my return to work, taking medication, and general changes and adjustments as I learn to live with LAM. In the episode, I also share my favourite poem. Tune in to find out how it relates to LAM and what Holland has to do with it! Please share, follow, and leave a comment to get the conversation started. GET IN TOUCH: I'd love to hear from you: letstalkLAM11@gmail.com [letstalkLAM11@gmail.com] Instagram: @letstalkLAM MORE INFORMATION ABOUT LAM: LAM Action UK: LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis [https://lamaction.org/] The LAM Foundation: Home - The LAM Foundation [https://www.thelamfoundation.org/] SUPPORT THE POD: Let's Talk LAM is entirely self-funded and costs money for equipment, editing and publishing software. If you enjoy my content, I'd appreciate any support to help me to keep the pod going: htttps://buymeacoffee.com/letstalklam [http://buymeacoffee.com/letstalklam]

My Lymphangioleiomyomatosis (LAM) Diagnosis Story

Join me and my sweet friend Beth for the third episode of Let's Talk LAM. We talk about how we met, receiving letters following my hospital discharge suggestive of cystic lung disease, and receiving some surprising news following my CT scan. We then talk about the day I got my diagnosis of lymphangioleiomyomatosis (LAM). Tune in to find out what Coldplay has to do with my story (Chris Martin - please feel free to get in touch!) Please share, follow, and leave a comment to get the conversation started. GET IN TOUCH: I'd love to hear from you: letstalkLAM11@gmail.com [letstalkLAM11@gmail.com] Instagram: @letstalkLAM MORE INFORMATION ABOUT LAM: LAM Action UK: LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis [https://lamaction.org/] The LAM Foundation: Home - The LAM Foundation [https://www.thelamfoundation.org/] SUPPORT THE POD: Let's Talk LAM is entirely self-funded and costs money for equipment, editing and publishing software. If you enjoy my content, I'd appreciate any support to help me to keep the pod going: htttps://buymeacoffee.com/letstalklam [http://buymeacoffee.com/letstalklam]

My Spontaneous Pneumothorax & Hospital Admission

Join me and my lovely friend Hilary for the second episode of Let's Talk LAM. We talk about how we met, my experience of going to A&E after a day of severe chest pain, and being told I had a spontaneous pneumothorax (lung collapse) requiring a chest drain insertion. We also discuss my two week hospital admission, ending up having thoracic (VATS) surgery; all before I even knew that I had lymphangioleiomyomatosis (LAM).   Please share, follow, and leave a comment to get the conversation started. GET IN TOUCH:  I'd love to hear from you: letstalklam11@gmail.com [letstalklam11@gmail.com]  Instagram: @letstalklam MORE INFORMATION ABOUT LAM: LAM Action UK: LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis [https://lamaction.org/] The LAM Foundation: Home - The LAM Foundation [https://www.thelamfoundation.org/] 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 [https://buymeacoffee.com/letstalklam]

Intro to the Pod & Lymphangioleiomyomatosis (LAM)

Join me and my wonderful friend Sian on the first ever episode of Let's Talk LAM.  We talk about how we met, my current understanding of lymphangioleiomyomatosis (LAM), how LAM is currently affecting my day-to-day life, and what I'd advise other women who are newly diagnosed with LAM.  We also discuss my plans for the Let's Talk LAM podcast, including topics I'd like to discuss in future episodes and my hopes and fears in sharing my LAM journey.   Please share, follow, and leave a comment to get the conversation started. GET IN TOUCH:  I'd love to hear from you: letstalklam11@gmail.com [letstalklam11@gmail.com]  Instagram: @letstalklam MORE INFORMATION ABOUT LAM: LAM Action UK: LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis [https://lamaction.org/] The LAM Foundation: Home - The LAM Foundation [https://www.thelamfoundation.org/] 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 [https://buymeacoffee.com/letstalklam]