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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
      • Videos
    • Latest News
    • Our Impact Results
  • Hannah’s Story
  • Programs
    • Medical-Therapy Equipment Assistance Program
    • College Scholarship
    • Childhood Rare Disease Advocacy
    • Family Support and Activities
  • 2022 Tee Up FORE Rare Golf
  • 2023 Vegas Rare 5K
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    • Become a LMHF Family
    • Make-A-Wish Referrals
    • Resources
  • Get Involved
  • Contact us

Programs

 

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Our programs are created to support families with a child under 18 years old, living at home or medical care facility, meeting at least one of the following criteria:

*  Diagnosed with a rare disorder as defined by the Genetic and Rare Disease Information Center
*  Diagnosed with a life-limiting disease with an average prognosis of less than 20 years of age
*  Currently placed in hospice care or is on palliative care 
*  Undiagnosed with medically complex or medically fragile needs
*  Diagnosed with a debilitating neurologic, metabolic, or genetic medical condition

We currently service the Las Vegas and Southern Nevada areas.  (Click here to register)

Medical and Therapy Equipment Grant Program

The Little Miss Hannah Foundation provides grants and other financial support to offset costs of medical and therapy equipment and related costs to enhance the quality of life of medically fragile and special-needs children and their families throughout Southern Nevada.  Learn more.

College Scholarship for Siblings of Rare Disease

Each year, two students from Southern Nevada will receive a $1000 college scholarship based on their submitted essay, scholastic achievement and community service.  Learn more.

Medical Travel Financial Assistance Program

Medical Travel Assistance Program is created to assist families seeking the best possible medical care for their children.  Assistance will be considered for families who travel outside of Nevada to seek medical care and/or treatment, but lack adequate financial resources for the cost of this travel.   Starting 2019.

Childhood Rare Disease Advocacy

We are partnering with Global Genes – Allies in Rare Disease, one of the leading rare and genetic disease patient advocacy organizations in the world, to bring awareness and promote legislation to find treatments for the thousands of rare diseases that affect children.   Learn more.

Family Support and Activities

Support and help to find the resources families need to help manage their child’s care and be connected to other LMHF families so they may share experiences and references, vent their frustrations, and not feel alone in their journey.  Learn more.

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Our Upcoming Event!


Tee Up FORE Rare 2022
 

Featured Programs

Medical and Therapy Equipment Grant Program

Rare Disease Facts

30% of children diagnosed with a rare disease do not live to see their 5th birthday
Little Miss Hannah Foundation
2016-11-18T20:27:14+00:00
30% of children diagnosed with a rare disease do not live to see their 5th birthday
https://littlemisshannah.org/testimonials/3938/
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Little Miss Hannah Foundation

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Site Info

  • About Us
  • Our Mission
  • Latest News
  • Hannah’s Story
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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