
Darla Clayton's Fundraiser

Help us find Better Treatments and a Cure for CCM.
You can make an impact—one donation at a time.
Through Our Eyes: Why We Stride
Living with cavernous malformation isn’t just a diagnosis—it’s a daily journey filled with uncertainty, resilience, and hope. For my family, it started with Trent when he was just a baby and he wasn't using his right hand. It wasn't long after that Trent was having his first brain surgery. Then we discovered that he has a genetic variant, which I also have and so does Ama. Since then, every step forward has mattered. We are in a race to find a cure before more irreversible brain damage occurs.
If you’re able, please consider joining us or making a donation. Together, we can take steps that lead to something greater—a cure.