Sarah is travelling the world to raise awareness of the condition and to connect the global LAM community
Sarah, who was diagnosed with lymphangioleiomyomatosis (LAM) in 2010, is working on behalf of the LAM Foundation by travelling the world for a year to raise awareness of the condition and help connect the global LAM community.
Sarah, and her husband Justin, have visited 47 countries to date and met with patients, doctors, researchers and individuals from other global organisations.
Read more about this exciting venture on their website where you can find out more about the countries they have visited (the photo shows Sarah in Edinburgh, Scotland, UK) and the inspiring people they have met.
You can also link up with Sarah via Facebook, Twitter and through the travel blog.