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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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brian garcia

May 5, 2018 by Carrie Ostrea

2018 Scholarship Winner Essay – Jasmin Garcia

Written by Jasmin Garcia, 2018 Awardee of the Hannah Ostrea Memorial College Scholarship for siblings affected by childhood rare disease. To this day, I cannot remember a time in my life that our lives did not revolve around my brother Brian. I was only three years old when he was born so I can’t say that I…

Filed Under: Blog, LMHF News Tagged With: 2018 Scholarship Recipient, advocate, brian garcia, Jasmin Garcia, Lennox Gastaut Syndrome

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

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