We are closed until Feb 2018. Online support via FB will continue.
HELP US TO MAKE A DIFFERENCE in 2017!
Click on the blue button to make a direct deposit OR
set up a page on 'GoFundraise'.
You can create your own page and fundraise for an event such as ‘Colour Fun Run’ and Marathon Fun Runs (in all states), In Memory of a Loved One or as a Personal Challenge on the ‘Making a Difference’ page OR you can set up a personal ‘Seasons Giving Appeal’ and ask people to donate instead of getting useless presents that you will probably have to recycle. Why not help us instead to achieve bigger goals.
Making a Difference starts with YOU!
Organise your own Fundraiser at GoFundraise.
We are always in need of celebrities to support the cause. You don't have to have lupus to show your support.
LUPUS DOCUMENTARY "BUT YOU DON'T LOOK SICK!"
Raising Awareness for Lupus.
As many of you know, Jeda Cacioli has produced a documentary in conjunction with Lupus Foundation.
The Foundation wishes to acknowledge Jeda for her tremendous effort and express our deep sadness of the passing of one of the contributors, John Haigh.
A massive congratulations to Jeda for winning Best Human Relationship Documentary at Star Doc International Film Festival in LA, USA.
WALTER & ELIZA HALL INSITITUTE of MEDICAL RESEARCH TOUR
Lupus Foundation are organizing a tour of the premises of the ‘Walter & Eliza Hall Institute of Medical Research’. There are a number of researchers working towards solutions for lupus. This is an opportunity to meet with the researchers and witness first-hand what it is they do.
Looking for people with lupus willing to attend medical lectures to provide an insight from a patient’s prospective to medical students about their condition.
Lectures will be held at The Alfred Centre - 99 Commercial Rd, Melbourne. (The Alfred Hospital).
If you are interested email: email@example.com
ABC Radio Lupus Interview
Thank you Caroline Salisbury and Alex Sloan (presenter) for the 30 min segment on lupus. Lupus Interview with our medical advisor Prof. Matthew Cook lupus researcher/Immunologist and Keren Dando. Click on link to listen: alex-sloan-chats-with-Prof. Matthew Cook and Keren Dando
LUPUS 'WIGS for KIDS' Challenge
Please grow out your hair, for those whose hair remains bare."
Lupus 'Wigs for Kids' Challenge is a permanent ongoing lupus fundraiser. Participation is open to anyone world-wide.
Participants are asked to sponsor and grow their locks to a minimum length of 30 cm and then donate their hair to make medical wigs for the ‘Wigs for Kids’ program supporting kids with lupus, cancer, alopecia areata and other illnesses. As part of the program, the kids are given a voucher to the total amount of $400 to use at selected wig makers.
AND, if you don’t have hair to give, you can still fundraise and we will still provide you with your own fundraising page AND if that seems like too much hard work, you can also donate funds, products for auctions and items for our gift bags for our functions and events.
So, there’s plenty of ways to show your support.
(refer to Lupus 'Wigs for Kids' Challenge for more information)
BIRTH of LIFE
Encouraging pregnant women to donate their umbilical cord and placenta!
Lupus Foundation will embark on its most ambitious project to date,
‘Increasing Cord Blood Stem Cells in Australia.’ for Lupus Stem Cell Treatment & Research.
This is a major project that will benefit ALL illnesses. Read more under 'Our Services'.
Thank You ALL SPORTS AUCTIONS
Thank you to Brae Lukav
All Sports Auctions for helping us to promote lupus awareness at his functions. We truly appreciate it.
Click on poster to go to their website.