Australian Niemann-Pick Type C Disease Foundation

The Australian Niemann Pick Type C Disease Foundation was created by the now President Mandy Whitechurch after her two sons Matthew and Timmy Lloyd were diagnosed with this Rare Terminal Genetic Disease.
This has made it possible for other families in Australia to have somewhere to turn when they themselves or their children have been diagnosed with the disease.
There are approximately 25 known cases in Australia with only a hard full of families constantly fundraising for funds to go to research into a treatment / cure, which is being carried out at the Florey Institute in Melbourne.
The Foundation currently needs approximately $10,000 a month for this research to continue and we currently get no funding from the Government to assist with this, so if you are in anyway able to make a donation please note that we are a not for profit organisation so any donations over $2 are fully tax deductable.
No donation is to big or to small as it all adds up and is greatly appreciated.