Latest KD News
We are now registered with Go Fundraise which allows out supporters an increased range of options to fundraise.
These can be direct donations or in the form of:
- Personal Challenge
- In Memory
- Special Occasion
- Making a Difference
- Event Specific
fundraising pages where funds raised directly benefit the Foundation.
Another way to make a donation is through PayPal
Make a Paypal Donation...
All donations over $2 are tax deductible.
N.S.W Visit by State Coordinators
On a recent visit to N.S.W we organised get togethers for KD families at Newcastle, Gosford and Sydney. These get togethers allowed parents the opportunity to discuss their KD experience and the children to realise they were not the only ones to have had Kawasaki Disease.
Click here to view photos.
We have parents in each of these areas willing to meet, email or talk with other KD families and maybe a local catch up can be organised. Please email us if you are interested and we'll pass on your details.
Latest published article in Australia
Dr David Burgner and Dr Katherine Chen discussing their latest research study.
Dr. Burgner, and Dr. Michael Cheung conducted a study in conjunction with the Princess Margaret Hospital for Children (W.A). looking at the incidence of Kawasaki Disease. Their results found the number of cases is on the rise and over the last 30 years has increased markedly and was also three times higher than previously thought.
The study has just been published in the leading child health journal Pediatrics. To read this study click here: Study Paper
Our medical advisor Dr. Burgner, who is based at the Murdoch Children's Research Institute and Dr. Michael Cheung, who is Director of Cardiology at the Royal Children's Hospital Melbourne, has also had an article on Kawasaki Disease in the Australian Family Physician which is published by the Royal Australian College of General Practitioners.
This article stresses the importance of prompt recognition and early referral. It is very easy to read and an excellent resource for any medical professionals. To read this article - click here.
The KD Foundation Co-ordinators recently addressed the Maternal Health Nurses at the Geelong Regional meeting. We presented them with an awareness package including a copy of this article.
To see a photo of this presentation - click here.
KD Foundation is now on Facebook. 'Like and share our page'.
Run/Walk to support us
For the last few years we have had supporters compete in the Sydney Marathon as part of the Blackmores running festival and the Melbourne Marathon.
We would like to thank them for their efforts and to the many people who donated on their behalf to support our work.
Registrations are now open for this year.
Adelaide City to Bay Fun Run
Sunday 21st Sept. 12km, 6km and 3km running and walking events. Visit http://www.city-bay.org.au for details.
Alex Prichard, whose son had KD last year is competing in this year's event and has set up a personal donation page here.
She has also set up a general South Australian page here for anyone in South Australia who may like to compete or donate. Every donation will help fund our awareness campaign.
Last year Dr. Burgner and his son competed in the annual Melbourne "City to Sea" run held on Sunday 17 November.
Thanks to the generous sponsorship from our KD families and friends nearly $600 was raised for the Foundation.
The Blackmore Sydney Running Festival will be held on September 21st 2014.
Registrations are now open and if you 'run for a cause' you can run for free. Please let us know if you are interested in supporting us.
Melbourne Marathon - 12th October 2014
Join thousands of runners and walkers on Sunday 12th October to take part in Melbourne's premier event: 2013 was a huge success so why not get a team together, get involved and help raise even more. We can assist with creating a team page.
Visit Melbourne Marathon site here for event details.
for photos of the Melbourne Marathon and Quinn who had KD recently. He was the inspiration for his mum competing in her first marathon.
Very Exciting News
In the U.S on the 28th March, Grey's Anatomy (Medical T.V Show) featured a story "that's near and dear to many of us - the story of a mother's intuition and a child's fight for life before he was diagnosed with Kawasaki Disease.
The episode starred actress and KD parent Sarah Chalke, as she relived one of the worst nightmares parents can go through - fighting for a correct diagnoses for her sick child". (from U.S Foundation Website)
The little boy who played the role of Sarah's son on the show has also had KD.
Although it was only a minor story line it was a wonderful opportunity for the U.S Foundation to increase awareness and raise funds. Sarah has since been on several talk shows talking about KD.
The ABC program Catalyst on ABC1 in Melbourne ran a story on Kawasaki Disease on the 17th May 2012. This is the first time an extended program segment about KD has been shown on Australian television.
You can watch this story plus view extended interviews by clicking on the following link - Click here
Sydney Information Session
Following the success of our Information Session in Melbourne we held an Information Session at The Sydney Children's Hospital in September 2012. We are hoping to provide more of these sessions in the future.
Kawasaki Disease Awareness Day