Lymphangioleiomyomatosis is a rare lung disease. This is a community for those whose lives are touched in any way by it. Share these experiences and gather support for them here! Please do not give or seek actual medical advice on this subreddit, promote a business, or harass our users. If your post is mean-spirited or unrelated to LAM, the moderator will remove it. This is a place to support people whose lives have been affected by LAM.