PANEL DISCUSSION:

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.

Our expert panel:

A/Prof. Brian Oliver - LAM in the Lab

A/Prof. Deborah Yates - Medical Management of LAM

Ana Paula Ruiz Ochoa - Lung Transplant Journey

We look forward to sharing this session with you!

Contact the host of Living with LAM Rare Disease Day