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 Summer 2018.
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.