I'm taking part in the Sit Up Challenge - and I need your support!
This May, I’m taking on the Sit-Up Challenge to celebrate 75 years of the Endeavour Foundation and raise funds for people with disability.
Every sit-up I do and every dollar raised isn’t just about fitness, it’s about continuing a legacy. For 75 years, the Endeavour Foundation has been creating opportunities, breaking down barriers, and helping people with disability live their best lives.
Your support will help fund vital services, technology, and programs that help people with disability to be seen today and for the next 75 years.
Please join me in keeping this legacy strong. Every contribution, big or small, makes a real difference.
Thank you for helping me make every sit-up count, and for supporting a movement that has changed lives for decades.
My Achievements
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Received 5 Donations
Raised $50
Raised $175
Raised $500
Raised $1000
My Updates
More Than Just a Workout - 75 Reps for a Future Without Limits
Friday 24th AprI’ve always known movement is medicine. Over the last year it has become how I regulate my intuition (nervous) system and find my ground. But this month, my daily movement has a very specific, very personal heartbeat behind it.
I’m committing to 75 sit-ups every day for the Endeavour Foundation, and for me, this isn’t just another fitness challenge.
Why This Hits Close to Home
As a mother to a son with Angelman Syndrome and an intellectual disability, the "disability space" isn't a concept to me—it’s my life. It’s my morning, my noon, and my night. It’s navigating a world that often feels like it wasn't built for us, and constantly advocating for the visibility and support my son deserves.
The Endeavour Foundation focuses on things that keep me up at night: Where will he work? How can he live independently? Who will support his goals when I can’t? By funding employment, housing, and lifestyle support, they are building the infrastructure for the future I want for my son.
The Grit and the Grace
I’m going to be honest—some days, 75 sit-ups will feel like a breeze. Other days, when the sleep is low and the "carer" load is high, it’s going to feel like a mountain. But I’m leaning into that. I’m doing this to show up for the caregivers, the parents, and most importantly, for the individuals who face hurdles every single day just by existing in a neurotypical world.
Whether you donate five dollars or share this post, you are helping to create a more inclusive Australia for people like my son.
I’ll be posting my progress—the good, the bad, and the sweaty. Thank you for being in my corner.
