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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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July 16, 2014 by Carrie Ostrea

Our visit on Fox 5 Las Vegas – July 14, 2014

On July 14, 2014, we were invited back to Fox 5 Las Vegas to talk with Monica Jackson about our upcoming 3rd annual Rainbows in the Wind Festival.   We are touched that Monica remembers meeting Hannah in 2011, and even reminisced about how Hannah gave her such a big hug when they met.

On the show with us was Lori Johnson, mom to one of our medical and therapy equipment grant recipients.  Lori is an amazing advocate for not only her daughter but for the entire Rett syndrome community.

 

Filed Under: Blog, front side, LMHF News

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