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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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Local Rare Kids

March 25, 2017 by Carrie Ostrea

Remembering our LMHF child, Brian

Written by Isela Garcia, Brian’s mom Brian Salvador Garcia was born August 20th, 2001. At the age of 3 months he had his first seizure and his fight began from there. As he got older, he was diagnosed with Lennox Gastaut Syndrome. With time, we as parents constantly traveled with Brian in search of treatments to…

Filed Under: Blog, Local Rare Kids Tagged With: brian garcia, Grant Recipient, Lennox Gastaut Syndrome

December 20, 2016 by Carrie Ostrea

Meet Eva, LMHF Grant Recipient

Meet adorable 3-year-old Eva whose sweet smile and infectious personality just warmed our heart when we met her to deliver special needs tricycle. This bike will Eva an opportunity to be able to participate in more activities with her family! To help us provide kids like Eva the equipment they need, please go tohttps://www.littlemisshannah.org/donate

Filed Under: Blog, LMHF News, Local Rare Kids Tagged With: Grant Recipient, LMHF Child, Local Rare Kids

November 12, 2016 by Carrie Ostrea

Meet Cecily, LMHF Grant Recipient

When we first met Cecily at our 2015 Rainbows in the Wind Festival, she just captured our hearts! We were thrilled to give her family a professional grade blender earlier this year so she can have pureed real food in her g-tube, and we are excited to know that she has been gaining weight because…

Filed Under: Blog, LMHF News, Local Rare Kids Tagged With: Grant Recipient, LMHF Child

October 25, 2016 by Carrie Ostrea

Meet Conor – LMHF Grant Recipient

Meet Conor, a sweetheart of a little boy! He was all smiles when we met him to give him his new Upsee. We are thrilled that he has this new piece of equipment to help him learn how to walk better. To help us provide kids like Conor the equipment they need, please go to…

Filed Under: Blog, LMHF News, Local Rare Kids Tagged With: conor, Grant Recipient, LMHF Child, Local Rare Kids

July 6, 2013 by Carrie Ostrea

Meet Our Special LMHF Kids

Camilla Johnson

From Camilla’s mom, Lori Johnson: A few months ago while at speech therapy with our daughter Camilla, our speech therapist shared with us a flyer from the Little Miss Hannah Foundation. She explained to us that there was a medical equipment grant program that might help us get the swing we wanted for Camilla. It…

Filed Under: Blog, Featured Right, front side, LMHF News, Local Rare Kids Tagged With: Grant Recipient, Local Rare Kids

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10624 S. Eastern Avenue, Suite A-847
Henderson, NV 89052
Phone: (702) 608-2488
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Little Miss Hannah Foundation is a 501(c)(3) tax-exempt nonprofit corporation, EIN# 45-3993921