LARA - LAM Australasia Research Alliance. Seeking a cure for LAM (Lymphangioleiomyomatosis)

Contact Us

Call +61 (0) 411 816 444

Address
PO Box 636 Bondi Junction
NSW 1355 Australia

Email: admin@lara.org.au

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

View all our Acknowledgements

Woolcock Institute
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Erin Dasczyk's Story

LYMPHANGIOLEIOMYOMATOSIS 24 letters that changed my life!

Erin Dasczyk (aged 26)
http://www.everydayhero.com.au/erin_dasczyk

As some of you know, I have recently been diagnosed with a terminal illness called Lymphangioleiomyomatosis. Otherwise known as LAM, it affects only women, usually in the prime of their life. It was pretty shocking news considering everything seemed to be going so perfectly. I had just bought a house with Rodgie and together with my beautiful dog, Bonnie, started a business. I am also working for the government. Naturally, I started 'googling' and have learnt a lot more about the disease. Ultimately I will require a double lung transplant. However, even with the transplant there is no cure for the disease.

Strangely, enough I do not feel angry, sorry for myself or sad that this has happened, I'm a lot more excited to LIVE and now really appreciate that I am still alive and realised just how much my friends really love me! :) In October 2011 I had a major operation to remove a large tumour in my stomach and was also filmed for the TV series RPA, which will be aired next year.

Last Thursday, I was lucky enough to attend the AGM of LARA, and have now become a committee member. I am focused on doing all I can to support the work of the organisation, which raises money for research into LAM and supports women like me with the disease. LARA is also working to educate doctors about LAM as so many women are misdiagnosed - sometimes for years. At the AGM I was able to meet a few other women with this devastating disease and researchers at the Woolcock Institute who are working to find a cure.

Over the past few years, there has been so many 'breakthroughs' in relation to research and I believe they are close to finding a cure, which is why I have set up this page. It's for all the women out there living with LAM and also dedicated to all the women who sadly lost the fight. If you feel like supporting this organisation to help them find a cure and help people like me to survive, please donate. Every donation is much appreciated and I thank you all in advance from the bottom of my heart, Erin xxx