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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.

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CuresNow

December 7, 2016 by Carrie Ostrea

#CuresNow has passed! 21st Century Cures Act

Happy Tears today following the overwhelmingly positive vote in the Senate today for 21st Century Cures! Our family has worked with hundreds of rare disease advocates all over the U.S. to create HOPE for our rare disease community. Thank you U.S. Senator Dean Heller and Senator Harry Reid for putting our Nevada rare children’s needs…

Filed Under: Blog, LMHF News Tagged With: 21st Century Cures, Advocacy, CuresNow, Legislation, rare disease

November 15, 2016 by Carrie Ostrea

#CuresNOW – United Rare Disease Day of Action

* ACTION ALERT * PICK UP THE PHONE TODAY!! Every single person reading this can help us provide HOPE for children diagnosed with life-limiting rare diseases! #CuresNOW Today, we are calling on patients across America to take action for a United Rare Disease Day of Action. Our goal is to ensure that Congress passes the…

Filed Under: Blog, LMHF News Tagged With: 21st Century Cures, Advocacy, CuresNow, Funding, Research

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

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Little Miss Hannah Foundation is a 501(c)(3) tax-exempt nonprofit corporation, EIN# 45-3993921