Testimonials

Hear From Jodie

Hear From Jodie

How did you hear about Max Family?

I heard about the Max Family Program through friends who had done the program previously, and they asked me if I’d was interested and then forwarded my name

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Hear From Emily

Hear From Emily

How did you find out about Max Family?

I found out about the Max Family Program thru a friend that did the program last time. She posted a link on Facebook about the celebration evening and we’ve came along.

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Hear From Terry

Hear From Terry

What was your intention for Max Family?

My intention was about providing support to families that I knew around me who simply were not equipped to be able to handle the challenges of lifelong care.

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Hear From Karen

Hear From Karen

How did you hear about the Max Family program?

I’ve recently moved to the area, and talking to other parents of the school saying I’ve receive letters in the mail about the NDIS and not really understanding at all and having a bit of confusion.

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Hear From Lauren

Hear From Lauren

How did you hear about the Max Family program?
 
I heard about the Max family program through one of my friends, who has the same – who has a daughter with the same syndrome as mine. And she said it has been a really good impact for her, in her life and her family and so she said that we need to give it a go. So, yeah.

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Hear from Nicole

Hear from Nicole

What condition does your child have?

Our little girl is 23 months now, she has Russell-Silver syndrome. It’s a genetic condition that happens one in every 100,000. Russell-Silver syndrome has deformities, so it can be internal. She has Clinodactyly fingers which are turned in. She has a large head, pixie like ears, a small triangular face.

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Hear from Brooke

Hear from Brooke

What condition does your son have?

Brooke: My son Cody has a very rare syndrome. The condition he has is called CFC which is that’s for short Cardiofaciocutaneous Syndrome and there’s only 17 cases in Australia, 17 kids in Australia with that condition.

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