Little Miss Hannah Foundation played Santa this year to 17 families (more than 25 kids). Gifts specifically chosen for each child based on what they wanted most – including 11 pairs of shoes, two dozen toys, clothes, and stuffed animals. It makes us feel so good knowing that because of our sweet Hannah these families…
LMHF News
Equipment Assistance
We are excited to announce one of our two new programs for 2013! * Medical Equipment Grant Program * Caring for a child with a debilitating neurologic, metabolic, or genetic condition, quality of life becomes one of the most important aspects of parenting. We also know first-hand how difficult this lifestyle is – emotionally, physically, and…
Little Miss Hannah Foundation receives Genzyme’s Patient Advocacy Leader award
The Little Miss Hannah Foundation was awarded the Genzyme Patient Advocacy Leader 2012 Award for our school-involved World Rare Disease Day program! We were only one of 9 organizations world-wide to receive this honor along with a grant to help us expand our program. We are very proud to receive this award for our Little…
Preparing for World Rare Disease Day 2013
On February 22nd, the Little Miss Hannah Foundation will be working with students in the Henderson area on our THIRD World Rare Disease Day awareness campaign – Jeans for Genes day! For the past two years, Vanderburg Elementary has led the way by hosting this wonderful event with their students and staff. This year,…
Rainbows to the Sky Event recap!
(click for event program) On July 25, 2012, the Little Miss Hannah Foundation launched ourselves into the Las Vegas community with our “Rainbows to the Sky” event, our first fundraiser and community event. DJ Miguel Guidos of Soli Concepts Entertainment kept the crowd going with great music, audience participation, raffles, and the highlight of the evening…three…