After Amy Farber learned she had the rare and fatal disease called LAM in 2005, she became determined to increase and speed up research into her illness with the hope of finding a cure in her lifetime.
Please donate today
ALL DONATIONS TO LAM AUSTRALIA RESEARCH ALLIANCE ARE FULLY TAX DEDUCTIBLE
Your contribution to LAM Australia Research Alliance will directly fund research to find a cure for LAM
LAM educational symposium
If you are living with LAM, or are close to or treating someone who has this rare disease, we hope you will join us for the LAM educational symposium. For more details and to register
Kate Wingrave’s Story
“November 2010 is a month I will never forget. This was the month when I was rushed to hospital with severe back pain and came home diagnosed with lymphangioleiomyomatosis, a disease I'd never heard of before.”