“No More Eye Rolls” — How One Mom Simplified Her Care Journey with mejo

Caring for a child with rare disease and complex medical needs can feel like a full-time job. Endless forms, repeated questions, and scattered notes often leave families drained before the real work of caregiving even begins.

That’s the reality Jennifer Sills faced. Her daughter Juliet, now 16, was one of the first in the world diagnosed with the ultra-rare Okur-Chung Neurodevelopmental Syndrome. At one point, Juliet had 16 providers delivering 25–35 hours of therapy every week. Each one needed the same information like doctors, therapists, medications, and history over and over again.

For years, Jennifer joked that she had perfected the “eye roll” every time a new provider asked for details she had already shared countless times. But everything changed when she discovered mejo.

Watch Jennifer’s Story

Hear directly from Jennifer about how mejo transformed her family’s care journey:

How mejo Makes Care Easier

With mejo, Jennifer finally found the support she needed:

• One place for everything. Enter once, share everywhere. Providers, schools, and specialists get the information they need without repeated forms and questions.

• Track what matters most. Juliet requires regular weight checks due to failure-to-thrive. Instead of losing notes on scraps of paper, Jennifer logs them in mejo’s Tracker and securely shares updates with Juliet’s care team.

• Stay organized and in control. From therapy plans to lab reports, mejo keeps all documents safe and accessible — no binders or clutter required.

  
  

For Jennifer, mejo has been a lifeline. Instead of constant stress and wasted time, she has a simple, reliable way to keep Juliet’s care connected.

Every family deserves less chaos and more moments that matter. Join families like Jennifer’s and see how mejo can help lighten the load. Start today at mymejo.com.