• 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

Get Involved

donate_button_1volunteer_button_1

The Little Miss Hannah Foundation provides support to families of young children diagnosed rare, ife-limiting, undiagnosed complex medical needs, and children who have been placed in hospice or palliative care.

A child living with a rare or undiagnosed life-threatening medical condition faces countless doctor’s visits, blood draws, lab tests, hospitalizations, medications, a lot of medical equipment (wheelchairs, feeding tubes, breathing tubes, pulse oximeters…) and more.  These measures, along with the symptoms of their disease, are hard on the child, the parents, and especially the brothers and sisters. The emotional, physical, and financial burdens are heavy.

Maximizing the child’s happiness and enabling families to enjoy the best quality of life available with their child is impossible without support. Friends and community members can provide this essential support by lifting the emotional and financial burdens, as easily as one dollar, card, or hug at a time.

A rare or life-limiting diagnosis does not have to mean isolation. The Little Miss Hannah Foundation connects.  By working closely with families who are faced with possibly losing their child due to a medical condition, we will strive to empower, educate, and support these families during this emotionally-charged time of their lives.

Your donation will help us set up activities, support groups, and other resources for our LMHF families as well as by providing the families, especially the siblings, with gifts, meals, and activities to help bring some moments of happiness.   

donate_button_1volunteer_button_1

Primary Sidebar

Our Upcoming Event!


Tee Up FORE Rare 2022
 

Featured Programs

Medical and Therapy Equipment Grant Program

Rare Disease Facts

Rare diseases are responsible for 35% of deaths in the first year of life
Little Miss Hannah Foundation
2016-11-18T20:30:03+00:00
Rare diseases are responsible for 35% of deaths in the first year of life
https://littlemisshannah.org/testimonials/3941/
0
0
Little Miss Hannah Foundation

Like Us on Facebook!

Little Miss Hannah Foundation

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