Marshall’s Mountain: Pompe Disease Fundraising

Marshall’s Mountain was formed after our son was diagnosed with Pompe disease. We aim to uplift the Pompe community by funding research, providing education, and offering patient support. Our mission has grown to improve the quality of life of those affected by Pompe disease and other rare diseases and disabilities.

Moving Mountains Trackchair Program

Get ready to embark on a journey of accessibility and adventure like never before!

With no cure currently available, Marshall will climb this mountain his entire life.

Although the journey is difficult, we know it is inspiring, educating and impacting others each day.

When Marshall arrived in the world, he changed our lives in ways we never could have imagined. Shortly after birth, he was diagnosed with Pompe Disease. The more we learned about this rare genetic disorder, the more determined we became to move mountains—for our child, for others and for Pompe research.

Get to know our bright, beautiful boy.

See updates on our lives & family

See updates on
our lives & family.

Follow Our Climb

Learn more about advocacy efforts

Learn more about
advocacy efforts.

Our Affiliates

Help us move mountains for Pompe research

Help us move mountains
for Pompe research.

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