Please join us for the Annual General Meeting on Tuesday 11 August 2020 at 18.00 AEST. Our AGM will be followed by a talk by Prof Allan Glanville, world clinical authority on the treatment of LAM. Our talk will be held on Zoom. If you have not received an email already about the AGM, pleased email us at firstname.lastname@example.org to register.
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.”