Hello and welcome!
Just over 6 years ago I was diagnosed with a rare lung disease called lymphangioleiomyomatosis (LAM). This is my blog about my journey so far. You can call me Mary.
As a LAM patient I wanted to create a place where I could share my story, personal observations, new experiences as well as medical resources I’ve discovered and other things I think might be worth sharing while living with LAM.
That being said, this is my first blog and right now I’m working full time. I welcome feedback and conversation but I can’t say for certain how much time I will have after work and self-care to get back to you.
My hope is that by sharing my journey here I can contribute to a greater understanding of what it’s like to live with LAM.
Thanks for stopping by.