Five years ago, a friend I met through this blog let me know that Duke University had stem cell clinical trials for kids with cerebral palsy. She had a child with special needs, too, and she'd gone to an informational meeting at John Hopkins about stem cell therapy for children with disabilities. She thought I should know about what was happening at Duke. "I picked up an extra packet at the conference for you... It has a lot of info that may interest you!" she wrote.
I got in touch with the Duke University doctor in charge of the stem cell program, Joanne Kurtzberg, M.D. A few months later, Max got his stem cell infusion.
If it weren't for that reader, and her drive to look into anything and everything possible to help her son, I might have never known about the stem cell work being done at Duke.
That friend is Kate Leong of Chasing Rainbows. This week, it's a year since her son Gavin passed away—a year in which he's had an impact on countless lives, thanks to the do-good initiatives, organ donation awareness and charity initiatives Kate's launched in his honor, most recently Gavin's Playground Project. This week, I got an email from a mom to a 21-month-old girl with cerebral palsy. It read:
I just wanted to let you know that my daughter got a stem cell infusion at Duke University. I learned about it from your blog and wanted to thank you....
This is the circle of help and hope in our community. We inform, encourage and inspire each other. We know what it is like to be that mom of that child. While we don't always know exactly who we will help with our blog post or Facebook update or donation, we put it out there into the universe, powered by caring and compassion.
Sometimes, it comes back to you in the most amazing way.
What goes around comes around.
Image of hands: Shutterstock