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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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  • About Us
    • Our Mission
    • Meet our Team
    • Photos/Videos
      • Photos
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  • Hannah’s Story
  • Programs
    • Medical-Therapy Equipment Assistance Program
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Video Gallery

Click here for more videos


2018 CBS 8 News Now Las Vegas segment on Little Miss Hannah Foundation

Thank you to the Vegas Golden Knights for our Little Miss Hannah Night 2019

Robert Ostrea hosting 2017 Rare Disease Day Conference.

 


Gaucher’s Disease Awareness Video (Hannah): http://www.littlemisshannah.com


NBC 3 News story on Hannah’s last days with us plus the importance of rare disease awareness.


Rainbows to the Sky Event
, July 25th (video 1)


Rainbows to the Sky Event
, July 25th (video 2)

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Our Upcoming Event!


Vegas Cares About Rare Kids 5K
February 28, 2021

Featured Programs

Medical and Therapy Equipment Grant Program

Rare Disease Facts

Rare diseases are responsible for 35% of deaths in the first year of life
Little Miss Hannah Foundation
2016-11-18T20:30:03+00:00
Rare diseases are responsible for 35% of deaths in the first year of life
http://littlemisshannah.org/testimonials/3941/
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Little Miss Hannah Foundation

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Little Miss Hannah Foundation

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Contact Us

10624 S. Eastern Avenue, Suite A-847
Henderson, NV 89052
Phone: (702) 608-2488
Fax: (702) 541-9957

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