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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
  • Get Help
    • Become a LMHF Family
    • Make-A-Wish Referrals
    • Resources
  • Get Involved
  • Contact us

Family Support Programs

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

*  Diagnosed with a rare, life-limiting disease with an average prognosis of less than 20 years of age
*  Currently placed in hospice care or is on palliative care due to an untreatable life-limiting condition
*  Undiagnosed with severe complex needs, considered medically fragile
* Diagnosed with a debilitating neurologic, metabolic, or genetic medical condition 

Click here to register for support

Family Support and Activities

We provide support for all members of the family by providing family-focused and sibling-focused groups and activities including tickets to free local Las Vegas shows and sporting events, attractions, and get-togethers.  Recent activities have included:

  • Vegas Golden Knights hockey games
  • Halloween party
  • Mom’s Night Out
  • Free movie screenings
  • Las Vegas 51s tickets
  • Jeff Civilico show at the Linq
  • Hospital PICU Care Bags
  • Rainbows in the Wind Festival

Rare and Undiagnosed Disease Support

Support and help to find the resources families need to help manage their child’s care.  This could be in the form of seeking out financial assistance (federal, local, or grant), research assistance (learning more about the disease process, future treatment possibilities, or researchers to contact), support groups (local workshops and groups, national/state foundations, etc.).  They will also be connected to other LMHF families so they may share experiences and references, vent their frustrations, and not feel alone in their journey.

 

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Our Upcoming Event!


Tee Up FORE Rare 2022
 

Featured Programs


Medical and Therapy Equipment Grant Program

Site Info

  • About Us
  • Our Mission
  • Latest News
  • Hannah’s Story
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Get Involved!

  • Become a LMHF Family
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  • Rare Disease Advocacy

Contact Us

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

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Copyright © 2023· Little Miss Hannah Foundation · Site By New Wave Media Design
Little Miss Hannah Foundation is a 501(c)(3) tax-exempt nonprofit corporation, EIN# 45-3993921