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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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Legislation

March 1, 2013 by Carrie Ostrea

Little Miss Hannah Foundation joins Rare Disease Lobby Day to Advocate for Childhood Rare Disease Awareness and Funding

Dean Heller meeting with Little Miss Hannah Foundation, Carrie and Robert Ostrea, Chris and Hugh Hempel

On Tuesday, February 27, 2013, our Little Miss Hannah Foundation joined a group of 150 patient and parent advocates of rare disease awareness marched on Capitol Hill to meet with legislators. The event was organized by the Rare Disease Legislative Advocates and meetings with representatives from 45 states were arranged.  Our first goal was to make…

Filed Under: Blog, front side, LMHF News Tagged With: Advocacy, Legislation

October 11, 2012 by Carrie Ostrea

“Sequestration” and its Drastic Effects for Rare Disease

Sequestration is a term to describe the massive across-the-board cuts that the federal government will impose on all non-defense spending starting in January 2013 if Congress does not act to stop it. This was a result of both parties not agreeing on a plan to cut the federal deficit. What does this mean for those of…

Filed Under: Blog, Front Tagged With: Legislation

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