The Pip.ilepsy Foundation has been established to assist the hospital systems within Australia to provide children suffering from epilepsy the highest level of care, treatment and support available.

The Pip.ilepsy Foundation was founded in November 2017 in response to a little girl named Piper (AKA Pip) being diagnosed with a rare and catastrophic form of epilepsy called PCDH19 epilepsy.

PCDH19 subjects Piper to huge clusters of life threatening seizures resulting in regular ICU admissions. 

Upon Piper's diagnosis it became evident that a higher level of support and services were required by her treating hospital to care for Pip and other children like her living with epilepsy.

With much hope, 

Sara and Heath Crawford
Piper's Mum and Dad.

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