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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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    • Latest News
    • Our Impact Results
  • Hannah’s Story
  • Programs
    • Medical-Therapy Equipment Assistance Program
    • College Scholarship
    • Childhood Rare Disease Advocacy
    • Family Support and Activities
  • 2023 Tee Up FORE Rare
  • 2023 Vegas Rare 5K
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    • Become a LMHF Family
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Newborn Screening – Nevada

 
We are thrilled to share that our Little Miss Hannah Foundation has been chosen to represent our families on the Nevada state team of the Mountain States Regional Genetics Network.

We are looking forward to working more closely with their exceptional team in creating more access for newborn screening for all families in our state. More details coming soon.

For more information on newborn screening in Nevada, please visit Baby’s First Test.

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Our Upcoming Event!


Tee Up FORE Rare 2022
 

Featured Programs


Medical and Therapy Equipment Grant Program

Site Info

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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