When Kathryn was diagnosed with MS in 2000, it marked the beginning of a series of challenges that are hard to comprehend. She was with her husband, Greg, when the first symptoms showed, in 1999. “I remember him asking how many drinks I’d had. I told him ‘only one’, and he said it must have been a strong one!’” she said. Living in Miles, Queensland at the time, Kathryn needed ...
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It’s good to know I can get what I need, not being told when my therapies are, or where I’m going. In the past, that’s how it’s been. As I see it, the NDIS is the only way to go.
Giovanni, NDIS participant