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Olivia Lamosa

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Join me in my efforts to support Diabetes Research Institute Foundation!

I will never forget August 1, 2011. This is when the ER Doctor confirmed Olivia's diagnose, Type1 Diabetes and there is a NO CURE. Her life line, insulin. Like the rest of the world, I didn't know what that meant. Impossible there is NO CURE. My only HOPE, the DRI where scientist are working around the clock for a CURE.

5 years it has meant waking up in the middle of the night to make sure she is alive, addressing if she has a low blood sugar by giving her carbs to bring her up or injecting her because she is too high. It means being a robot every hour every day. No piece of mind, no freedom and our lives revolves around this disease.

It means multitudes of finger prinks, insulin injections and changing her CGM site as if she was a living pin cushion. It means no one really understands what our lives is like unless you walk in our shoes.

Olivia is our HERO because she fights the strongest enemy everyday (over 2,000 days already). It's name is T1D. Yet she is a happy, beautiful, strong, smart and confident 8 year old.

Please help us fight with Olivia because fighting alone is not an option. No amount is too small and no amount is too large. Every dollar will only get us closer to a biological cure.

Thank you for fighting with us!
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