Story

TOFS has been nothing short of a lifeline for our Aria — and for us as a completely overwhelmed family trying to navigate the wild world of TOF/OA amoung other things

When Aria was born, we were suddenly thrown into a maze of surgeries, medical jargon, and Google searches we definitely should have avoided. In the middle of all that chaos, TOFS was the one place that made us feel understood, supported, and a little less alone.

They’ve given us guidance when we didn’t even know what questions to ask, reassurance on the days when everything felt too much, and a community of families who truly understand what this journey is like. Their support has carried us through some of our hardest moments, and we honestly can’t imagine doing this without them🩷

And if you can spare anything at all, we’d be so grateful. We’re taking on this challenge together for Aria and for TOFS (even though we are wildly unfit🤣). Expect us to be out of breath, red-faced, and questioning all our choices… but every shaky step is for a charity that has carried us through so much. Your support means the world to families with children like Aria, to us, and to our very unprepared legs 🏃‍♀️💨💗.

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Supporting

TOFS

Live life unlimited

Our vision is for anyone born with OA/TOF to be able to live life unlimited.

We are working towards a world in which those born with OA/TOF live long and healthy lives, unconstrained by the impact of being born with these conditions.

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