My Story

In 2020, my daughter began experiencing severe symptoms that led to a five‑year journey through the healthcare system. She was eventually diagnosed with MALS linked to Ehlers‑Danlos Syndrome and underwent life‑changing surgery in 2025.

The journey was long, traumatic, and far more difficult than it should have been. I learned how vital clear communication, persistence, and advocacy are — and how easily people can be dismissed or misunderstood.

This is why I now support others: to help them achieve clarity, confidence, and compassionate care without the years of struggle we endured.