Normally I am pretty light-hearted on this blog, there is enough bad stuff in this world that I don’t need to add anything to it...but I wanted to let you guys know that we Southern California surfers just lost a good member of our “family.”
Emily Haager, an amazing member of the surf community, has lost her lifelong fight with Cystic Fibrosis. Emily was an inspiration to all that know her, had a zeal for life and was a great ambassador for the amazing therapeutic effect that surfing has on combating ravages of Cystic Fibrosis.
For those interesting in attending her memorial, it will be held this Saturday May 8th, 11am at First Christian Church-HB 1207 Main St Huntington Beach - www.fcchb.com and a paddle out will follow shortly after down at Blackies in Newport.
I have shared this with you before about a year ago…but if you have the time please take a moment to watch this video of Emily speaking about surfing and CF.
(if you are reading this as an email you can watch the video here)
http://socalforecast.blogspot.com/search/label/Cystic%20Fibrosis%20Foundation
Donations to the CFF can be made in Emily’s honor here…
https://www.cff.org/Chapters/sca/EventDonation/?idEvent=10968
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Showing posts with label Pipeline to a Cure. Show all posts
Showing posts with label Pipeline to a Cure. Show all posts
Tuesday, May 4, 2010
Thursday, April 24, 2008
Cystic Fibrosis Foundation's Pipeline to a Cure
Hey Gang,
My friends that are associated with the Cystic Fibrosis Foundation sent over some cool stuff about a Black-Tie and Flip-Flop benefit dinner for the CF Foundation.
Apparently they have put together a big Gala (faaabulous!) Event together that will be at the Hyatt in Huntington Beach this summer...it sounds like a good time for a good cause.
If you aren't that familiar with Cystic Fibrosis here is a video that can get you up to speed. It actually features a local SoCal surfer named Emily...
Here are the details on the event...press release from CF Foundation.
We are pleased to announce that plans are underway for PACSUN’S PIPELINE TO A CURE Dinner Gala benefiting the Cystic Fibrosis Foundation, scheduled for Saturday, July 19, 2008 at the Hyatt Regency Huntington Beach, California. This black tie and flip flop gala will be recognizing the positive effect that surfing has on the lung health of children with cystic fibrosis. We are thrilled to join with the Cystic Fibrosis Foundation, our title sponsor PACSUN, Honorary Co-Chairmen Laird Hamilton and David Kalama and the Kelly Slater Foundation in this inaugural event.
PIPELINE TO A CURE is a fundraising campaign which recognizes the remarkable connection between surfing and this deadly genetic disease. One of the serious effects of cystic fibrosis is the production of thick sticky mucus which clogs the lungs and leads to life threatening lung infections. In recent years, doctors in Australia identified surfers with cystic fibrosis having significantly healthier lungs than their non surfer patients. While many surfers have long known the positive health effects of saltwater on the sinuses, it is simply amazing that saltwater mist has a direct positive effect on the lungs of CF patients. Doctors have since developed a breathing treatment called Hypertonic Saline Solution which helps cystic fibrosis patients eliminate this bacteria laden mucus. This new therapy daily mimics a “surf session” for the lungs of those who suffer from cystic fibrosis.
We would like to extend to you an incredible opportunity to support this event by participating as a sponsor, attendee or donating an ITEM or CERTIFICATE to be auctioned off the evening of the gala. Attached is a Sponsor Packet and Donation Agreement, a recent press release and a You Tube video of a young surfer with cystic fibrosis. You will be glad to know that over 90 cents on the dollar raised goes directly towards finding a cure for those that suffer from cystic fibrosis.
Thank you so much for your time and consideration. We look forward to your participation. If you have any questions, please contact Monika Gilbert at the Cystic Fibrosis Foundation at mgilbert@cff.org or by phone at 714-938-1393.
If you are interested in the event make sure to contact Monika of you can visit the website for more information www.pipelinetoacure.com
My friends that are associated with the Cystic Fibrosis Foundation sent over some cool stuff about a Black-Tie and Flip-Flop benefit dinner for the CF Foundation.
Apparently they have put together a big Gala (faaabulous!) Event together that will be at the Hyatt in Huntington Beach this summer...it sounds like a good time for a good cause.
If you aren't that familiar with Cystic Fibrosis here is a video that can get you up to speed. It actually features a local SoCal surfer named Emily...
Here are the details on the event...press release from CF Foundation.
We are pleased to announce that plans are underway for PACSUN’S PIPELINE TO A CURE Dinner Gala benefiting the Cystic Fibrosis Foundation, scheduled for Saturday, July 19, 2008 at the Hyatt Regency Huntington Beach, California. This black tie and flip flop gala will be recognizing the positive effect that surfing has on the lung health of children with cystic fibrosis. We are thrilled to join with the Cystic Fibrosis Foundation, our title sponsor PACSUN, Honorary Co-Chairmen Laird Hamilton and David Kalama and the Kelly Slater Foundation in this inaugural event.
PIPELINE TO A CURE is a fundraising campaign which recognizes the remarkable connection between surfing and this deadly genetic disease. One of the serious effects of cystic fibrosis is the production of thick sticky mucus which clogs the lungs and leads to life threatening lung infections. In recent years, doctors in Australia identified surfers with cystic fibrosis having significantly healthier lungs than their non surfer patients. While many surfers have long known the positive health effects of saltwater on the sinuses, it is simply amazing that saltwater mist has a direct positive effect on the lungs of CF patients. Doctors have since developed a breathing treatment called Hypertonic Saline Solution which helps cystic fibrosis patients eliminate this bacteria laden mucus. This new therapy daily mimics a “surf session” for the lungs of those who suffer from cystic fibrosis.
We would like to extend to you an incredible opportunity to support this event by participating as a sponsor, attendee or donating an ITEM or CERTIFICATE to be auctioned off the evening of the gala. Attached is a Sponsor Packet and Donation Agreement, a recent press release and a You Tube video of a young surfer with cystic fibrosis. You will be glad to know that over 90 cents on the dollar raised goes directly towards finding a cure for those that suffer from cystic fibrosis.
Thank you so much for your time and consideration. We look forward to your participation. If you have any questions, please contact Monika Gilbert at the Cystic Fibrosis Foundation at mgilbert@cff.org or by phone at 714-938-1393.
If you are interested in the event make sure to contact Monika of you can visit the website for more information www.pipelinetoacure.com
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