Roots
Rooted in Hope. Growing Beyond Diagnosis.
“Every child deserves the opportunity to thrive beyond a neuroimmune diagnosis. ROOTS exists to provide resources, support, advocacy, and community that empower children and families to navigate the journey with confidence, resilience, and hope.”
INTRODUCTION OF ROOTS
Why I Started ROOTS
At eight years old, I was diagnosed with pediatric Multiple Sclerosis.
I know what it feels like to grow up navigating uncertainty, treatments, fear, and questions no child should have to answer alone.
ROOTS was created because every child deserves more than a diagnosis.
They deserve support, education, community, and the opportunity to flourish.
This is the emotional heart of the organization.
- Pediatric MS survivor.
- Mother.
- Advocate.
- Founder.
“I have MS, but MS does not have me.”
Our Programs
Family Navigation
Helping families understand diagnosis, treatment options, resources, and support systems.
Wellness & Quality of Life
Nutrition, movement, emotional wellness, and healthy lifestyle education.
“My name is Diana Saint Simon. I was diagnosed with pediatric MS at eight years old. For decades I searched for answers, hope, and quality of life. Today I’m launching ROOTS so children and families never have to walk that journey alone.”
I have known of MS! But never in this full extent! My heart for this author has me constantly reading what next… my reality on pediatric MS has my mind blown. So raw and graceful this book has been written. I’m honored to be in the presence of acknowledgment of what MS has stemmed from.
She let the reader understand the importance of a strong willingness to withstand and what a strong support system can provide
Very well written. It is a useful source for information about this autoimmune disease, and the benefits of being mitivated.