This Charlotte boy was born in Miami and moved to North Carolina when he was 3-months old. He is non-verbal, has developmental delays, and lives with seizures.
Still no hot water (Day Three), but heat is working and we’re feeling like campers on in our own home on this break. It’s kinda fun. Enjoying this time and logging on now specifically to relay one story that needs sharing.
The Hearts and Hope Foundation, Inc. is organizing a first-time pajama drive, to help parents who are stuck in the hospital this holiday season with their sick children.
Hartley Plyler is a longtime one of our #MollysKids who is no longer a kid herself. She has graduated from ClemsonLIFE and though still in treatments, doing great.
Update on this vibrant 10-year-old in Monroe—she might be battling a nasty brain tumor, but this past weekend, appeared on the Carolina Panthers field at halftime as a part of the Junior TopCats.
YES! A happy update on the unique story about Silas Patterson, the Mooresville boy who is the only child in the world living with a specific type of his rare genetic condition.
Christine Patterson said she worked on sending the letter below for six months. So much happened in the course of that time, her words had to keep getting updated.
Surprise mail.If you’ve been following here awhile you might remember Margaret Hayes. She lived in the Charlotte-area. Like many of you, she followed #MollysKids.