• 24 Allan Street, Altona North, Melbourne, Victoria, Australia.
  • (0400) 333339 - Deanne / (0400) 914 277 Tab
  • hello@brodiekellyfund.org.au

The Fund

The Fund

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Welcome to the Brodie Kelly Fund, a place where you can make a significant difference in the lives of children with specific neurological conditions.

The Brodie Kelly Fund is expected to be a Charitable Tax Deductible Trust endorsed by the Australian Tax Office.  We are just waiting on our application to register with the Australian Charities and Not-for-profits Commission.

ABN: 989 068 018 91

The Brodie Kelly Fund is a registered not for profit charity in Australia, committed to helping children from birth to 18 years of age with neurological conditions in the tubulin mutation class.  Tubulin mutations are rarest of rare disorders.  Some of these children (including Brodie) are part of a worldwide research program about identifying genes in rare disorders.  Subsequently funding and support is limited because of falling between the gaps of government support.  This is the fund’s role.

Children with tubulin mutations require extensive equipment for both mobility and monitoring purposes.

Typical symptoms that present in children affected by this disorder are:

– Intellectual disability
– Physical disability
– Neurological symptoms and deficits
– Encephalopathy (disorder or disease of the brain)
– Seizures
– Movement disorders
– Temperature instability
– Feeding difficulties

The Brodie Kelly Fund raises desperately needed funds to support children like Brodie by assisting family’s through general support (see our ‘Parents’ knowledge Centre) as well as funding to enable the purchase of vital equipment and therapy.

Please donate and support children with neurological conditions in the tubulin mutation class and help provide the quality of life that every child should be entitled to.