Pathways Program: Support for Families Newly Diagnosed with MPS or ML

You're not alone. Begin your journey with guidance, resources, and support.

What Is the Pathways Program?

The Pathways Program is a free resource for families who are newly diagnosed with MPS or ML. It provides helpful information, personal support, and practical tools to guide you through the first steps of your journey. You’ll find syndrome-specific details, questions to ask your care team, and ways to connect with others in the community — all created to help you feel informed and supported.

Here When You Need Us Most

From diagnosis and treatment to everyday challenges, the National MPS Society offers support programs tailored to meet your family’s needs. Services include:

You’re Joining a Community

Thousands of families have faced the moment you’re in now — and they’re here to walk beside you. Through Courage Pages and family stories, you can read about others’ experiences and see how they’ve found hope, strength, and support along the way.

Getting Started: Resources for Newly Diagnosed Families

Reach Out for Support

Connect with the National MPS Society’s Pathways Program for personalized guidance during your first year after diagnosis.

Learn About Your Syndrome

Get detailed information on MPS and ML syndromes, current treatments, and clinical trials.

Download Helpful Materials

Visit the MPS Library to access digital syndrome booklets, fact sheets, and educational resources.

Connect with Other Families

Want to meet families facing similar challenges? We can help you connect with others who share your syndrome journey.

会員になる

Join the National MPS Society — membership is free for families, patients, and friends.

Attend Local Events

Find an MPS event or fundraiser near you and meet others in the community.

Learn More About MPS

Understanding MPS is the first step toward finding answers and making empowered decisions. Explore in-depth information about the different types, symptoms, and treatment options.