The Mauli Ola Foundation began as a group of surfers who banded together to introduce surfing as a natural treatment to people with cystic fibrosis. Since 2007, Mauli Ola has taken nearly 1,300 CF patients surfing at nearly 100 Surf Experience Days and has now expanded it’s reach with hospital visits and other activities that touch the lives of kids with cancer and a variety of other health challenges. In 2010, MOF was awarded The Agent of Change Award by SURFER Magazine for its positive contributions and example to the surfing community.

Surf Experience Days exist to get kids who have cystic fibrosis out into the ocean water (which is high in saline) and experience what natural ther apies can do for their lungs.

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Children’s Hospital Visits were created for all hospitalized patients that can’t make it to the beach.

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Mission Statement: The Mauli Ola Foundation was organized to promote education, awareness of genetic disease and to increase research for genetic disorders.

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Board of Directors:
James Dunlop
Jason Steris
Jeff Booth
Mark Itri
Mick O’Brien
Victor Garbarini


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