Our daughter Emsley is eight years old and lives with spastic quadriplegic cerebral palsy. She is the sweetest girl and brings joy to everyone who meets her. But every day she faces challenges most children never have to think about.

Over the past year, Emsley’s dystonia, painful, involuntary muscle contractions, has significantly increased. We have worked closely with her medical team and have exhausted the traditional treatment options available through standard medical care. Despite medications and therapies, her dystonia continues to make everyday life harder for her.

We are now pursuing a new option that gives us hope: Muse stem cell therapy. These stem cells have shown promising results in helping reduce dystonia and improving motor function in some patients. The treatment is currently not FDA-approved in the United States, which means we must travel to Mexico for Emsley to receive it.

Our hope is that these treatments could help reduce Emsley’s dystonia and potentially give her new abilities—such as improved head control, better hand function, and possibly even the ability to speak. Even small gains could dramatically improve her comfort, independence, and quality of life.

Our goal is for Emsley to receive 4–6 treatments. Each treatment costs approximately $14,000, and with travel expenses, our estimated total is about $20,000 per treatment.

We are hoping to take Emsley for her first treatment on July 13, but we need $10,000 down soon to secure her appointment.

Right now, our immediate goal is simply to get her through the first treatment, and then we will continue to take the journey one step at a time.

If you feel led to support Emsley, whether through donating, sharing this page, or keeping her in your prayers we are incredibly grateful. Every share helps spread her story, and every prayer means the world to our family.

Thank you for loving our girl and believing in hope for her future.

— The Alexander Family