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…
Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions. Childhood Rare Disease Advocacy.