Janet +61 411 816 444
PO Box 636 Bondi Junction NSW 1355
Australia
The LAM Australasia Research Alliance (LARA) is dedicated to improving the health prospects of women with LAM in Australia, New Zealand and throughout the region. A disease that affects only women, LAM is rare and often devastating.
ALL DONATIONS TO LARA ARE FULLY TAX DEDUCTIBLE
Your contribution to LARA will go 100% to funding vital medical research to find a cure for LAM.
You can donate to the LAM Australasia Research Alliance by sending us a cheque, using our PayPal facility, or by making a deposit directly to our ANZ Bank account: 012 055 4926 67193.
Please advise us of your donation by sending an email to admin@lara.org.au with your name, address and email address. We will respond with our thanks and a fully tax deductible receipt.
Major Donors
Macquarie Group Foundation
Roth Charitable Foundation
Mr Robert Gavshon
Hollick Wines
Acknowledgements
LARA thanks the professionals who work pro bono for this not-for-profit organisation. We highly recommend the services of:
Ben Higham, Webhead
Karen Riethmuller, KGR Design
Peter Hersh, Loggica Pty Ltd
Peter Kelso
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First European LAM Conference
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First European LAM ConferenceUdine, Italy. 1st, 2nd, 3rd October, 2010. LAM Italia is hosting the first European LAM conference in Udine, Italy on the 1st, 2nd and 3rd of October. Udine is 130k north east of Venice, not far from the Slovenian border. LAM Italia’s President, Iris Bassi, says many of the world’s top researchers and LAM clinicians will be speaking at the conference. Anyone with an interest in LAM is invited to attend, including clinicians, researchers, and patients. LAM Italia hopes that LAM patient organisations from all over the world will be represented. For more information please click here To learn more about LAM Italia, go to www.lam-italia.org and use Google’s translation tool to read the site in English. ObjectivesThe objective of the conference is to provide an update on current researches and clinical trials against lymphangio- leiomyomatosis, a rare and fatal disease for which at the moment there is no known cure. This uncommon condition affecting a number of organs requires a multi-disciplinary approach on an international level. At this event, a number of researchers, clinicians and experts on LAM from across the globe will meet to discuss and establish the best strategy to work towards an effective treatment for lymphangioleiomyomatosis. AudienceMember of the national and international scientific community, in particular clinicians, pneumologists, researchers from Italy, Europe and the rest of the world. In particular, professionals who are involved in rare diseases, cancer and regene- rative medicine. The speakers invited to present at the Conference have all thorough experience in LAM. ParticipantsLocal AuthoritiesBruno Bembi / Centro Regionale delle Malattie Rare Regione Friuli Venezia Giulia Clinicians and PneumologistsPaolo Casali / Istituto Tumori, Milano, Italy ResearchersJudy Black / University of Sydney, Australia Representatives from LAM AssociationsLAM Australia, LAM Austria, FLAM / LAM France, LAM Germany, LAM Italia, LAM New Zeland, LAM Spain, LAM Action / UK, LAM Foundation / USA, The LAM Treatment Alliance Expected resultsFurther develop knowledge and understanding of lymphangioleiomyomatosis through the exchange of information within the international scientific community. Define strategies and ways to apply them in the near future in order to find a treatment for this disease. Location: Udine. Further details on location will be provided |