Little Miss Hannah Foundation

Empowerment, education, and support for parents and siblings of terminally ill children

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    Helping Kids with a Terminally Ill Sibling

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    Pediatric Hospice

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    World Rare Disease Day 2012

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    Our Mission and Goals

    Cooper Knight

    Empowerment.  Education.   Support. The LMHF’s mission is to work with families who have young children with life-limiting rare diseases, undiagnosed complex medical needs, and children who have been placed in hospice or palliative care. The foundation … [More...]

    Shades of Grey

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    By the time Texas residents Nicole and Bill Morris celebrated the birth of their fourth son, they were no strangers to childhood illnesses. Their careers – Bill as a pediatric nurse and Nicole as a special education teacher – taught them about health issues that affect … [More...]

    About the LMHF

    Abigail, Hannah, and Ethan Ostrea

    The Little Miss Hannah Foundation was created in December 2011 in memory of Hannah Ostrea, a beautiful 3-year-old girl who lost her battle against Neuronopathic Gaucher's Disease, an extremely rare and life-limiting genetic metabolic disorder.   The foundation also honors her older brother and sister, Ethan and Abigail - siblings who were playmates, best friends, and the light's of this little girl's life. When … [More...]

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    Copyright © 2012 ~ Serenity Studiopress

    Site Info

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

    Get Involved!

    • Become a LMHF Family
    • Upcoming Events
    • Donate
    • Volunteer
    • Adopt-A-Family

    Contact Us!

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