The Mauli Ola Foundation (MOF) was organized to promote education, awareness of genetic diseases and to increase research for genetic disorders. They strive to provide a direct and immediate option for children with genetic disorders an enjoyable and healthy way of life through natural treatments.
This group of Hawaiian pro surfers is reaching out to help kids with genetic diseases such as Cystic Fibrosis so we thought their efforts were worth a mention!
They recently held a ‘Surf Experience Day’ in Hawaii 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.
Here’s a video from their recent Surf Experience Day:
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