Mandy Whitechurch

We sometimes wonder when Mandy (better known as “Mandy Mum” to Benalla locals) finds time to sleep. The mum-of-two founded the Australian Niemann-Pick Disease Foundation after her sons, Timmy and Matthew, were diagnosed with the degenerative condition.

Mandy’s first-hand experience of the NDIS gives her a unique insight that our clients and families find invaluable. One of her many superpowers is translating complex jargon and processes into plain English. Mandy grew up on a dairy farm, collects cows (living and ornamental) and cherishes time with family and friends.

Connect with Mandy on LinkedIn