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…
Local Rare Kids
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
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…
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…
Meet Our Special LMHF Kids
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…