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Electricity about to be cut-off for an EB Family
$755 raised
108% of $700 goal
26 contributors
4 Years running
Meet the O’Neills. The O’Neills have 3 children, their youngest, Shaelynn was born at 24 weeks weighing less than 2 lbs with a rare genetic skin disease – Epidermolysis Bullosa, or EB for short. Those with EB are missing a protein which causes ...

Meet the O’Neills. The O’Neills have 3 children, their youngest, Shaelynn was born at 24 weeks weighing less than 2 lbs with a rare genetic skin disease – Epidermolysis Bullosa, or EB for short. Those with EB are missing a protein which causes their skin to blister and sheer off with the slightest of touch. Currently there is no cure for EB. While their insurance covers Shaelynn’s bandage needs – it does not cover other medically necessary supplies.

Veronica is a stay at home to her 3 children, while her husband is the sole income earner. His hourly wage supporting a family of 5 has not been making ends meet, and they have fallen several months behind on their electric bill. The electric company does not offer financial assistance, they only offer extended time to pay the bill – and at this point, they are days away from cut-off due to non-payment. Please help the O’Neills get current on their electric bill so that their electricity does not get cut off!! EB is a very temperature sensitive disease and keeping a consistent temperature in the apartment is a must. Any amount is helpful and appreciated and every dollar gets them closer to getting current on their bill.

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