Rare Disease Day raises awareness and generates change for those living with a rare disease, their families, and friends. Lymphangioleiomyomatosis (LAM) is a rare lung disease affecting mainly women and there is no cure.
On Rare Disease Day we are hosting a panel discussion on LAM to raise awareness and to provide an opportunity for women living with LAM, their families, and friends to ask the experts for information or advice on Living with LAM.
Register through our sponsor Humanitix for your ticket to attend our free online (webinar) panel discussion on Living with Lam. Following registering for a ticket you will be sent a confirmation email with the details of the webinar procedure.
We look forward to sharing the discussion with you!