Our daughter, Cedar, has spent much of her young life fighting a rare autoimmune neurological disease called Opsoclonus-Myoclonus Syndrome (OMS), associated with ANNA-1 antibodies.

Since she was only two years old, Cedar has endured years of treatments, hospital stays, procedures, chemotherapy, and countless challenges that no child should have to face. Through it all, she has remained incredibly brave, resilient, and full of light.

After exhausting many treatment options, Cedar is now undergoing a stem cell transplant at Mayo Clinic. This treatment represents hope—a chance to stop the progression of her disease and give her the best opportunity for a healthier future.

As parents, our priority is being at Cedar's bedside throughout this process. The demands of her treatment and recovery have required significant time away from work. While we have applied for family leave benefits, we do not yet know when those benefits will begin or how long approval will take.

The financial uncertainty during this time has placed a tremendous strain on our family. Donations will help us cover everyday living expenses and provide stability while we focus on what matters most: helping Cedar heal.

Cedar has shown more courage in her few years than most people show in a lifetime. If you're able to donate, share her story, or simply keep her in your thoughts, we are deeply grateful.

Thank you for helping our family through one of the most difficult and hopeful chapters of our lives.

With gratitude,

Shannon, Larry, Willow and Cedar

"Watching your child fight a rare disease is heartbreaking. We would give anything to take this burden from Cedar, but for now, we are taking it one day at a time and holding onto hope."