This Sunday, we find ourselves reflecting deeply on the journey we’ve been walking — one filled with both challenge and incredible hope. This week brought the most incredible, unexpected news: Ella has been offered an early spot for stem cell transplant — something we expected to be on a waitlist for over two years to receive. And now, in just three weeks, she has the opportunity to begin what could be the most transformative chapter in her journey.

But alongside our joy, we want to share a bit more about what life looks like for Ella — the daily challenges she faces that many never see.

Ella has cerebral palsy, along with dystonia and spasticity, which make even the simplest movements difficult. Spasticity causes her muscles to tighten involuntarily, leading to pain, stiffness, and fatigue. Dystonia adds another layer — unpredictable, twisting muscle contractions that can affect her arms, legs, and even her ability to hold herself up. These aren’t just physical symptoms; they affect every part of her childhood — from how she plays to how she learns to move, sit, and explore the world.

Every day, Ella works so hard for things most of us take for granted: sitting without support, picking up a toy, reaching for a book, keeping her balance. Her body is always fighting itself — and yet, she smiles through it with such resilience.

This is why the stem cell treatment means so much.

The science behind it is promising: using her own cells, the treatment aims to reduce inflammation in the brain and improve communication between the nervous system and muscles. In children with CP, especially when done early, this kind of therapy can lead to better muscle control, reduced spasticity and dystonia, increased strength, and even new milestones in mobility.

In short, this could give Ella more freedom in her body. More ease. More comfort. More life.

We never imagined this chance would come so soon — and now we’re in a race against time to raise the funds before her appointment in just a few weeks.

If you’ve already given, please know how deeply thankful we are. You’re part of Ella’s story forever. And if you feel moved today — whether by Ella’s strength, her smile, or the hope this treatment holds — we ask you to consider:

We believe in Ella’s potential. We believe in healing. And we believe in the power of community to do extraordinary things together.

Thank you for being here — for reading, for caring, and for standing with us in faith and hope.

With gratitude,

The Gutierrez Family