Little Miss Hannah Foundation

Support for Parents and Siblings of Terminally Ill Children & Childhood Rare Disease Advocates

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3rd Annual Jeans for Genes Day School Awareness Event was a great success!

Jeans for Genes Day - School Awareness Event 2013

Join us this summer!

Little Miss Hannah Foundation's "Rainbows to the Sky" Event

New Medical Equipment Grant Program

Medical-Therapy Equipment Grant Program

LMHF Night with the Las Vegas 51s

Little Miss Hannah Night at the Las Vegas 51s Baseball Game

Join us on June 15th at Cashman Field for the Little Miss Hannah Foundation night with the Las Vegas 51s Triple-AAA baseball team! Saturday June 15th at 7:05pm   Tickets:  $10 each  (click to buy) Price includes: * Reserved seating ticket ($11 value) * 51s baseball hat ($18 value) * Admission to the Kid’s Carnival  … [Continue Reading]

Abigail’s Angels Sibling Program

Big Sister, Little sister

One of the most heart-breaking side effects of dealing a sick child’s critical needs, is that time, attention, energy and funds are often taken away from the sick child’s siblings. Abigail's Angels, named after Hannah's big sister, Abigail, is our program created to … [More...]

Featured Articles

Starting our day at the Washington Club

Getting Ready to “Storm the Congressional Hill”

This morning, we will all meet as a group at The Washington Club to be briefed on our visit to Capitol Hill and then we will head to Congress to deliver our messages. Our … [Read More...]

Little MIss Hannah Foundation Executive Director Carrie Ostrea

Rare Disease Legislative Conference

The Rare Disease Legislative Advocates (RDLA) organized a fantastic conference today, held at the historic National Press Club in Washington, D.C., designed to empower patient … [Read More...]

Here.Us.Now. Rare Disease Documentary

World Rare Disease Day Washington Kickoff Event – Here.Us.Now.

Monday night’s screening of Here.Us.Now., hosted by the Rare Disease Legislative Associates, launched a weeklong schedule of events in Washington, D.C. for rare disease … [Read More...]

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Latest LMHF News

Rainbows to the Sky Event Update!

Today is Nevada Big Give Day!

Little Miss Hannah Continues to Impact the Rare Disease Community

Join us for Little Miss Hannah Night at the Las Vegas 51s Baseball Game

Medical and Therapy Equipment Grant Recipients Chosen

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Little Miss Hannah Foundation is a 501c3 tax-exempt nonprofit corporation                   © 2013 ~ Serenity Studiopress

Site Info

  • About LMHF
  • Blog
  • Hannah's Story
  • Programs
  • Resources

Get Involved!

  • Become a LMHF Family
  • Upcoming Events
  • Donate
  • Volunteer
  • Rare Disease Advocacy

Contact Us!

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