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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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Medical-Therapy Equipment Assistance Program

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Caring for a child with a debilitating neurologic, metabolic, or genetic condition, quality of life becomes one of the most important aspects of parenting. We also know first-hand how difficult this lifestyle is – emotionally, physically, and financially. The Little Miss Hannah Foundation provides grants and other financial support to offset costs of equipment and related costs to enhance the quality of life of medically fragile and special-needs children and their families throughout Southern Nevada.

Upcoming Grant Cycle Deadline – May 31, 2021

Meet some of our past grant recipients.

Medical Grant Program Information:

  • Types of items considered for this program are (but are not limited to):  seating, mobility, transport, comfort, positioning, bathing, therapy tools, feeding, etc.
  • $750 per grant maximum (total item requested must be less than $1400 for partial payment consideration)
  • Requires letter of medical necessity from a primary pediatric specialist, pediatrician, therapist, or social worker
  • Grants are provided for new equipment only and paid directly to the vendor.
  • Download application packet here 
  • IMPORTANT:  Photos of grant application will not be accepted. Must be a cleanly scanned PDF, fax, or original copy of the application.

Eligibility:

We work directly with the families of medically fragile or special needs children, under 18 years of age, who are diagnosed with debilitating neurologic, metabolic, or genetic conditions. Must live in Southern Nevada more than 50% of the time.

2021 Application Deadlines

Grants will be reviewed by the Board of Directors four times per year and grants will be awarded following these meetings.

Deadline

February 28, 2021
May 31, 2021
August 31, 2021
November 30, 2021

Recipients Contacted

March 21, 2021
June 21, 2021
September 21, 2021
December 21, 2021

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Vegas Cares About Rare Kids 5K
February 28, 2021

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
http://littlemisshannah.org/testimonials/3938/
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10624 S. Eastern Avenue, Suite A-847
Henderson, NV 89052
Phone: (702) 608-2488
Fax: (702) 541-9957

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Copyright © 2021· 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