HELP US TO MAKE A DIFFERENCE! DONATE TODAY!
'Click on Link' Direct Deposit - Donations over $2 Tax-Deductible. Receipt Provided.
'Click on Link' Other ways to Donate and Help.
SEGO LEBRASSE & KANASUK GROUP Globe to Globe World Music Festival
Monday, 26 January 2015
Monday, 26 January 2015
Join Lupus Foundation with an evening of entertainment with one of the Foundation’s booking groups, ‘Sego Lebrasse & Kanasuk Group’. Stick around for the spectacular fireworks display that will be on after ‘Public Opinion Afro Orchestra’ (at the end of the night).
Performance Time: 7:20 p.m.
Fireworks after 9:30 p.m.
Entry $2 per person or $5 for families.
Come Say Hi!
Sego Lebrasse and the Kanasuk Group are considered legends of the Séga culture with an extensive family history of Séga performers both here and in Mauritius; the land of origin.
Séga itself is a mix of Mauritian African Creole and colonial culture stemming from the 19th century French colonial rule. Séga music emerged as an expression of daily life from the slavery struggles of the people.
Nowadays, Séga is widely accepted from Mauritians of all background becoming a fundamental part of the culture and with the introduction of western musical instruments; Séga’s upbeat sounds will continue to grow in popularity.
CAN YOU HELP?
Looking for a male with lupus and another person with lupus combined with APS to tell their story for a lupus documentary. Must live in Melbourne (Vic).
Email: email@example.com OR call 8555 9295 after 12.
LUPUS PHOTO JOURNAL
Looking for volunteers in NSW Bathurst, Central West area to share their story and experiences that will be photographed for a lupus photo journal i.e. doctor’s appt, waiting rooms, medication, etc.
Lupus Awareness Walk
In ALL States (CBD), official date yet to be confirmed. It’s never too early to register your interest or to volunteer, email: firstname.lastname@example.org
AUSTRALIA DAY PARADE 2016
Walk for Lupus Awareness!
REGISTER YOUR INTEREST NOW! Email OR Call.
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
SPARTAN SUPER RACE
Donate Now and Let's Conquer LUPUS!
Please help and support Jeda Cacioli and Team Lupus to raise funds for our lupus research.
Support ‘Team Lupus’ in their quest as they sacrifice their bodies to conquer lupus. This endurance race is designed to push them to their limits. Hills, trails, mud and custom-built ball breaking tests. No expense spared, no stone unturned.
To donate, Click on ‘Donate Now’ button 'above'.
WEGO HEALTH ACTIVIST AWARDS 2014/2015
Once again we are proud to partner with WEGO Health in the Annual WEGO Health Activist Awards representing the lupus community, world-wide.
WEGO Health is an American based online network comprised of Health Activists – leaders and influencers within the online health community – The Annual Health Activist Awards recognizes and rewards those who have made a difference.
“Bringing Awareness and Recognition
to Our Community”
MOOMBA BIRDMAN RALLY 2015
Sunday, 8 March
Who Will Fly and Who Will Flop! Where Man and Bird err Butterfly (sub)merge!
Looking for one or maybe two brave souls to jump for Lupus Awareness! And, a team OR creative individual to put together a lupus flying machine.
The Birdman Rally is a competition for home-made gliders, hand gliders, human-powered aircraft, fan-dangled flying machines and super heroes!
Birdman Rally is a Melbourne institution and is one of the main highlights of the Moomba Festival drawing huge crowds every year.
Let’s make our mark next year and take one big giant leap for Lupus Awareness! Feel free to download and share poster. Email interest to: firstname.lastname@example.org
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'.
'WIGS of LOVE' Challenge.....launching soon.
'WIGS of Love' 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 'WIGS of Love' Challenge for more information)