• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar

Little Miss Hannah Foundation

Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions. Childhood Rare Disease Advocacy.

Make a Donation Volunteer Apply for Services
  • 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

Blog

March 3, 2015 by Carrie Ostrea

Girl Scout Troop 265 on Fox 5 for Little Miss Hannah Foundation

Claire and Kaitlynn from Girl Scout Troop 265 were on Fox 5 Las Vegas this morning to talk about their Silver Award Project – collecting items for our Little Miss Hannah Hospital PICU Care Bags! We are thrilled to partner with such ambitious and caring young women who are working so hard to help us fill…

Filed Under: Blog, front side, LMHF News

August 2, 2014 by Carrie Ostrea

Introducing Little Miss Hannah’s Hospital Care Bags Program

When you have a child in the PICU, you may spend days or weeks without ever leaving the hospital. We want to be able to help care for these families so they can concentrate on caring for their kids. We have launched our new program in honor of what would have been Little Miss Hannah’s…

Filed Under: Blog, LMHF News

August 1, 2014 by Carrie Ostrea

Third Annual Rainbows in the Wind Festival is a huge success!

On July 23, 2014, our 3rd Annual Little Miss Hannah’s “Rainbows in the Wind” event was held at Town Square, right in the heart of Las Vegas. (view photos) In celebration of what would have been our Little Miss Hannah’s 6th birthday, we invited the community to join us to bring your family down for a fun…

Filed Under: Blog, front side, LMHF News

July 22, 2014 by Carrie Ostrea

Our Visit to Morning Blend Vegas – July 17, 2014

On July 17, 2014, we were invited back to ABC News’ morning Show “Morning Blend” to talk with Shawn Tempesta and Dao Vu about our upcoming 3rd annual Rainbows in the Wind Festival. On the show with us was Bethany Lafferty, mom to one of our medical and therapy equipment grant recipients. She shared how the equipment we provided to…

Filed Under: Blog, front side, LMHF News

July 16, 2014 by Carrie Ostrea

Our new Little Miss Hannah Store!

"Be the Sunshine" Store - Little Miss Hannah Foundation

Thanks for your support of the Little Miss Hannah Foundation! All proceeds go towards providing support and services for local families of rare and medically complex kids. Click here to shop!

Filed Under: Blog, Featured, front side, LMHF News

  • « Go to Previous Page
  • Go to page 1
  • Interim pages omitted …
  • Go to page 6
  • Go to page 7
  • Go to page 8
  • Go to page 9
  • Go to page 10
  • Interim pages omitted …
  • Go to page 22
  • Go to Next Page »

Primary Sidebar

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
  • Programs

Get Involved!

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

Contact Us

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

Privacy Policy

Connect With Us

  • Email
  • Facebook
  • Instagram
  • Twitter

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