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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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December 7, 2016 by Carrie Ostrea

#CuresNow has passed! 21st Century Cures Act

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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 first by voting Yea. When Obama signs it into law next week, it will be a time for us to celebrate! #CuresNow

Want to learn more about why this is such a great win our rare disease community? Go to http://www.raredr.com/news/senate-votes-94-4

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

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