Anyone who has ever surfed or swam in the ocean can tell you about the positive effects the calming ocean can have. It can make us feel soulful and put our lives into perspective. Years ago it was discovered that it can also help those with cystic fibrosis. Australian researchers found kids with CF who surfed and were exposed to the salt water had healthier lungs than those who didn’t. Soon, the Cystic Fibrosis Foundation helped develop a hypertonic saline treatment that allows CF patients around the world to capture the benefits of the ocean.
About Pipeline to a Cure
10 years ago Pipeline to a Cure was founded to celebrate the positive connection between the ocean and cystic fibrosis, and no other community understands this better than surfers. Legendary surfers and watermen Laird Hamilton, Dave Kalama, Kai Lenny and Jamie Mitchell have stepped up as honorary co-chairs of what has become one of the most popular and anticipated philanthropic events in Orange County CA. Now in its tenth year, Pipeline to a Cure has raised more than $3.5 million in net revenue to help find a cure for this inherited deadly disease. The ocean isn’t enough and more research and treatments are needed to ensure that everyone with cystic fibrosis can live a long and healthy life.
Event Date: July 21, 2018
Event Time: 4:30pm-11:30pm
Hyatt Regency Huntington Beach Resort and Spa: 21500 Pacific Coast Hwy, Huntington Beach, CA 92648
WHAT IS CYSTIC FIBROSIS?
Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. In people with CF, a defective gene causes a thick, buildup of mucus in the lungs, pancreas, and other organs. In the lungs, the mucus clogs the airways and traps bacteria leading to infections, extensive lung damage, and eventually, respiratory failure. In the pancreas, the mucus prevents the release of digestive enzymes that allow the body to break down food and absorb vital nutrients.
Emily Haager 1983 - 2010
Emily was such an inspiration to those who knew her or heard her tell her story at Pipeline to a Cure in prior years. We will never forget Emily’s smiling face and courageous spirit. And we will carry on our fight in her memory. One of Emily’s most endearing qualities was her enormous capacity for gratitude. She was so grateful for life, for her family and friends, and for the support of the many people who cared enough to help her and others with cystic fibrosis.
Shelby brought her love of all things Green Day to the Pipeline to a Cure family after attending the event with her parents. Shelby likes to say that CF stands for Chronically Fabulous! In 2016 Shelby candidly described her near-death respiratory failure that left her in a medically induced coma for weeks. Shelby required a double lung transplant, and after 84 days in the hospital went home in time for her 18th birthday. Despite missing the first semester of her senior year, Shelby completed two semesters of work in a few months and graduated on time with a 4.0. She achieved her goal of walking across the stage to accept her Orange Lutheran diploma. Shelby continues to inspire everyone she comes in contact with especially other people with CF.
Carly, a close friend of Emily has been involved with Pipeline to a Cure from early on and continues to speak at the VIP party each year. Carly grew up surfing with Emily and continues to seek the healing ocean waves whenever she is back in southern California. Carly is in her Junior year at Syracuse University and is on the second drug approved for cystic fibrosis, Orkambi. Carly has benefitted greatly from Orkambi and is excited to graduate with her degree in communication sciences and disorders with a speech pathology focus. Carly lives every day to its fullest and continues to advocate for people with CF and raise awareness through her company “65 Wooden Roses”