MISSION STATEMENT >>>

The Mauli Ola Foundation exists to introduce surfing as a natural treatment to people with genetic disorders. Since 2007 we have concentrated on the amazing connection between Surfing and Cystic Fibrosis. We have taken nearly 400 CF Patients Surfing at over 40 MOF Surf Experience Days. In 2011 we look to expand our program to help patients affected with Cancer and Alpha 1 Antitypsin. We appreciate your interest and would love for you to join the Mauli Ola Foundation Ohana by becoming a member and help us with our mission to help people with genetic disorders through Surfing.

Aloha, James Dunlop

SURF EXPERIENCE DAYS FOR THE KIDS >>>

Surf Experience Days (MOF) were created to get kids who have cystic fibrosis out into the ocean water (which is high in saline) and experience what natural therapies can do for their lungs. The exercise and fun they get from these events is truly fantastic. What is even more amazing, kids who have cystic fibrosis respond very well to the salt water environment. The saline in the air and water breaks down the congestion that is in their lungs. This congestion is what causes them to go to hospitals constantly and leads them to have to take lots of medication on daily basis. With salt water treatments, their hospital visits are cut down in half, leading to a healthier and more fulfilling life with fun activities. Please see these articles that describe the saline treatments:

HISTORY >>>

The Mauli Ola Foundation (MOF) was organized to promote education, awareness of genetic diseases and to increase research for genetic disorders. The MOF raises funds to support programs for kids and adults with life-threatening illnesses and disabilities through social events such as music concerts, sports tournaments, galas, and other great events. We want to provide a direct and immediate option for children with genetic disorders an enjoyable and healthy way of life through natural treatments.