• (702) 608-2488
  • families@littlemisshannah.org

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Programs

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

Programs Are Now Closed

After 13 unforgettable years, the Little Miss Hannah Foundation’s programs have officially concluded. While our equipment grants, advocacy initiatives, and family activities are no longer active, the impact they made — and the community they built — will continue to be felt for years to come as part of Hannah’s enduring legacy.

Our programs were 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 I nformation 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

Medical and Therapy Equipment Grant Program

Through our Medical and Therapy Equipment Grant Program, LMHF provided vital tools such as communication devices, adaptive mobility equipment, and therapy aids that were often denied by insurance. By helping children with rare and medically complex conditions access the equipment they needed, we improved their independence, comfort, and overall quality of life, fulfilling every eligible grant request since 2016.

Childhood Rare Disease Advocacy

Advocacy was at the core of LMHF’s mission, working to raise awareness about the unique challenges faced by children living with rare and medically complex conditions. Through storytelling, public education, and community outreach, we gave families a stronger voice and helped foster understanding and compassion within our Southern Nevada community.

Family Activities

Recognizing the importance of connection and joy, LMHF hosted family-centered activities designed to bring rare disease families together in welcoming, accessible environments. From museum nights to holiday parties and sibling meetups, these events created opportunities for families to bond, share experiences, and build lasting friendships with others who truly understood their journey.