<![CDATA[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!

]]>https://www.instagram.com/letstalklamRiverside.fm (https://riverside.com)Tue, 07 Apr 2026 12:16:50 GMTSat, 07 Feb 2026 11:05:42 GMT60Emwills<p>If you live with LAM or know someone who does, “Let’s Talk LAM” is the podcast for you.</p><p>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. </p><p>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.</p><p>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. </p><p>Please share, follow, and comment get the conversation started. To go behind the scenes of the pod, find Let's Talk LAM on Instagram <a rel="noopener noreferrer nofollow" href="https://www.instagram.com/letstalklam" target="_blank">@letstalkLAM</a></p><p></p><p>MORE INFORMATION ABOUT LAM:</p><p>LAM Action UK: <a rel="noopener noreferrer nofollow" href="https://lamaction.org/" target="_blank">LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis</a></p><p>The LAM Foundation: <a rel="noopener noreferrer nofollow" href="https://www.thelamfoundation.org/" target="_blank">Home - The LAM Foundation</a></p><p></p><p>SUPPORT WOMEN LIKE ME WITH LAM: </p><p><a rel="noopener noreferrer nofollow" href="https://lamaction.org/donate/" target="_blank">Donate | LAM Action</a></p><p><a rel="noopener noreferrer nofollow" href="https://www.thelamfoundation.org/donate/ways-to-give/#online" target="_blank">Ways to Give - The LAM Foundation</a></p><p></p><p>SUPPORT THE POD:</p><p>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</p><p>https://buymeacoffee.com/letstalklam</p><p></p><p>GET IN TOUCH:</p><p>Email: <a rel="noopener noreferrer nofollow" href="mailto:letstalklam11@gmail.com" target="_blank">letstalklam11@gmail.com</a></p><p>Instagram: <a rel="noopener noreferrer nofollow" href="https://www.instagram.com/letstalklam" target="_blank">@letstalklam</a></p><p>I'd love to hear from you!</p>episodicEmwillse.willmott11@gmail.comno<![CDATA[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

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 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

]]>e82d2fb1-dd88-45bf-9ff7-cf5ffc2ad037Sun, 22 Mar 2026 06:00:00 GMT<p>Join me and my sweet friend Beth for the third episode of Let's Talk LAM.</p><p></p><p>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.</p><p></p><p>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!)</p><p></p><p>Please share, follow, and leave a comment to get the conversation started.</p><p></p><p>GET IN TOUCH:</p><p>I'd love to hear from you: <a rel="noopener noreferrer nofollow" href="mailto:letstalkLAM11@gmail.com" target="_blank">letstalkLAM11@gmail.com</a></p><p></p><p>Instagram: @letstalkLAM</p><p></p><p>MORE INFORMATION ABOUT LAM:</p><p></p><p>LAM Action UK: <a rel="noopener noreferrer nofollow" href="https://lamaction.org/" target="_blank">LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis</a></p><p></p><p>The LAM Foundation: <a rel="noopener noreferrer nofollow" href="https://www.thelamfoundation.org/" target="_blank">Home - The LAM Foundation</a></p><p></p><p>SUPPORT THE POD:</p><p></p><p>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:</p><p></p><p>htttps://<a rel="noopener noreferrer nofollow" href="http://buymeacoffee.com/letstalklam" target="_blank">buymeacoffee.com/letstalklam</a></p>no00:44:42My Lymphangioleiomyomatosis (LAM) Diagnosis Storyfull<![CDATA[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 

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 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

]]>998fbafa-671b-4660-b7fa-eb6754249592Sun, 22 Feb 2026 06:00:00 GMT<p>Join me and my lovely friend Hilary for the second episode of Let's Talk LAM.</p><p></p><p>We talk about how we met, my experience of going to A&amp;E after a day of severe chest pain, and being told I had a spontaneous pneumothorax (lung collapse) requiring a chest drain insertion.</p><p></p><p>We also discuss my two week hospital admission, ending up having thoracic (VATS) surgery; all before I even knew that I had lymphangioleiomyomatosis (LAM).</p><p> </p><p>Please share, follow, and leave a comment to get the conversation started.</p><p></p><p>GET IN TOUCH: </p><p>I'd love to hear from you: <a rel="noopener noreferrer nofollow" href="mailto:letstalklam11@gmail.com" target="_blank">letstalklam11@gmail.com</a> </p><p>Instagram: @letstalklam</p><p></p><p>MORE INFORMATION ABOUT LAM:</p><p>LAM Action UK: <a rel="noopener noreferrer nofollow" href="https://lamaction.org/" target="_blank">LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis</a></p><p>The LAM Foundation: <a rel="noopener noreferrer nofollow" href="https://www.thelamfoundation.org/" target="_blank">Home - The LAM Foundation</a></p><p></p><p>SUPPORT THE POD:</p><p>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:</p><p><a rel="noopener noreferrer nofollow" href="https://buymeacoffee.com/letstalklam" target="_blank">https://buymeacoffee.com/letstalklam</a></p>no00:54:02My Spontaneous Pneumothorax & Hospital Admissionfull<![CDATA[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 

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 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

]]>Buzzsprout-18561976Sun, 25 Jan 2026 20:00:00 GMT<p>Join me and my wonderful friend Sian on the first ever episode of Let's Talk LAM. </p><p></p><p>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. </p><p></p><p>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.</p><p> </p><p>Please share, follow, and leave a comment to get the conversation started.</p><p></p><p>GET IN TOUCH: </p><p>I'd love to hear from you: <a rel="noopener noreferrer nofollow" href="mailto:letstalklam11@gmail.com" target="_blank">letstalklam11@gmail.com</a> </p><p>Instagram: @letstalklam</p><p></p><p>MORE INFORMATION ABOUT LAM:</p><p>LAM Action UK: <a rel="noopener noreferrer nofollow" href="https://lamaction.org/" target="_blank">LAM Action | LAM Action is the UK charity for those with Lymphangioleiomyomatosis</a></p><p>The LAM Foundation: <a rel="noopener noreferrer nofollow" href="https://www.thelamfoundation.org/" target="_blank">Home - The LAM Foundation</a></p><p></p><p>SUPPORT THE POD:</p><p>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</p><p><a rel="noopener noreferrer nofollow" href="https://buymeacoffee.com/letstalklam" target="_blank">https://buymeacoffee.com/letstalklam</a></p><p></p>no00:45:35Intro to the Pod & Lymphangioleiomyomatosis (LAM)full