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Little Miss Hannah Foundation

Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions. Childhood Rare Disease Advocacy.

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August 1, 2014 by Carrie Ostrea

Third Annual Rainbows in the Wind Festival is a huge success!

Jeff Civillico Las Vegas

Special guest performance by Jeff Civillico!

On July 23, 2014, our 3rd Annual Little Miss Hannah’s “Rainbows in the Wind” event was held at Town Square, right in the heart of Las Vegas.

(view photos)

In celebration of what would have been our Little Miss Hannah’s 6th birthday, we invited the community to join us to bring your family down for a fun evening of music, activities, dancing, and raffles, while raising over $12,000 to help support Las Vegas families of children diagnosed with rare, life-limiting, and complex medical conditions.

Over 1000 guests were treated to great games, activities, and live entertainment including a special performance by Jeff Civillico – Comedy in Action!

Thank you to our incredible sponsors for this year’s 3rd annual Rainbows in the Wind Festival. This is our largest fundraiser for the year, and because of their incredible generosity and support, we will be able to provide support and equipment for even more families than we were able to this previous year.

Filed Under: Blog, front side, LMHF News

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Little Miss Hannah Foundation is a 501(c)(3) tax-exempt nonprofit corporation, EIN# 45-3993921