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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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February 28, 2017 by Carrie Ostrea

Today is Rare Disease Day

Today is World Rare Disease Day celebrating our Little Miss Hannah who was diagnosed with Gaucher Disease Type 2/3.  Please take a few minutes to learn why this day is so important to our rare disease  community. 

 

Filed Under: Blog, LMHF News Tagged With: Gaucher Disease, Hannah Ostrea, World Rare Disease Day

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