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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Services, Providers, Locations. Welcome to Cure 4 The Kids! Cure 4 The Kids Foundation was organized in April 2007 solely for charitable, educational, and scientific purposes to address the specialized health care needs of children in Nevada and the surrounding region. Make a donation to Cure 4 The Kids Foundation. News for Patients and Parents.
Information on Oils I use on Hailey. Find us on Google Plus. Saturday, March 24, 2018. This years Hugs for Hailey fundraising shirts are available NOW! We now have our new Hugs for Hailey Heartbeat shirts available! This is our biggest fundraising item! Just those two trips alone cost more then we can afford. We also have Hats available as well! Have you w.
Protocol Collaboration at the NIH. Protocol Collaboration with the NIH. NGLY1org eliminates the challenges of N-glycanase deficiency. Through research, awareness, and support. Treatments and cures are Positively Possible. Learn more about this rare genetic disorder.
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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.DESCRIPTION
The Little Miss Hannah Foundations mission to work with Nevada families who have young children with life-limiting rare diseases, undiagnosed complex medical needs, and terminally diagnosed children who have been placed in hospice or palliative care. LMHF is a strong advocate for the childhood rare disease community. LMHF will host workshops on medical record management, media awareness opportunities, using social media to reach out for support, and finding the right information about your childs condPARSED CONTENT
The website littlemisshannah.org had the following in the web page, "Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions." I analyzed that the webpage stated " One Child at a Time." They also stated " One Child at a Time. Our Mission Enhance the quality of life for children diagnosed with rare and complex medical conditions in Southern Nevada." The meta header had advocacy as the first search term. This keyword was followed by rare disease, terminally ill child, and sibling which isn't as important as advocacy. The other words they used was bereavement parents. children support groups is also included but could not be understood by search engines.ANALYZE OTHER WEB SITES
December 30, 2008 by Overloaded Mama. Subscribe to Little Miss Hannah by Email. December 27, 2008 by Overloaded Mama. If you have us on your blogroll or links list, please update our information.
Monday, February 16, 2015. Sunday, June 2, 2013. Much has changed in my life since I started writing here so, so long ago. Where did the time go? Thank you for the last 4 years.
Future wedding planner, author and inspiration. Rain, rain, go away, come again another day! September 2, 2013. Hi to everyone who reads this,. I love to dream, all day, everyday.
Sharing ME moments, with YOU! About Me Me Me . LittleMissHazey! On May 2, 2013. lets see if i can make it through to the end. On April 19, 2013. My beautiful little Baby Boy, KYROS KASH. X HAPPY VALENTINES DAY X. On February 14, 2011. On December 13, 2010. On November 24, 2010. On November 4, 2010.