cofe4cf.blogspot.com
The Great COFE for Cystic Fibrosis: Time flies...
http://cofe4cf.blogspot.com/2008/09/time-flies.html
The Great COFE for Cystic Fibrosis. THE OFFICIAL COUGHING THE DISTANCE WEBSITE IS HERE. This website was the blog we kept. The official website is here:. Also, my latest adventures are here: www.coughing4cf.com. Friday, September 05, 2008. Subscribe to: Post Comments (Atom). People with CF need lung transplants! YOUR HELP IS NEEDED. If you think your company can help us distribute, sell or promote our books or documentary please contact. Read All About It! The ride was partly sponsored by The Mad Bomber.
cofe4cf.blogspot.com
The Great COFE for Cystic Fibrosis: The Advocate 19 August 08
http://cofe4cf.blogspot.com/2008/08/advocate-19-august-08.html
The Great COFE for Cystic Fibrosis. THE OFFICIAL COUGHING THE DISTANCE WEBSITE IS HERE. This website was the blog we kept. The official website is here:. Also, my latest adventures are here: www.coughing4cf.com. Sunday, August 24, 2008. The Advocate 19 August 08. My fav. local journo Sarah Webb wrote this great article in the Advocate for Tuesday August 19. Subscribe to: Post Comments (Atom). People with CF need lung transplants! YOUR HELP IS NEEDED. Read All About It! Throughout the 72 day ride film mak...
cofe4cf.blogspot.com
The Great COFE for Cystic Fibrosis: ACT CF Association
http://cofe4cf.blogspot.com/2008/08/act-cf-association.html
The Great COFE for Cystic Fibrosis. THE OFFICIAL COUGHING THE DISTANCE WEBSITE IS HERE. This website was the blog we kept. The official website is here:. Also, my latest adventures are here: www.coughing4cf.com. Thursday, August 21, 2008. Wow, I found this at my mother's home, the July 2008 newsletter of the ACT CF Association. I was in it with a beautiful photo of me consuming a German Ale and a story I had written for them in the past. Subscribe to: Post Comments (Atom). YOUR HELP IS NEEDED. Throughout...
madbomber.wordpress.com
The Mad Bomber Chronicles | Because it's cool out there! | Page 2
https://madbomber.wordpress.com/page/2
The Mad Bomber Chronicles. Because it's cool out there! Adventures of a Mad Bomber. April 1, 2012 by. Here at Mad Bomber we pay attention to our fans. It looks like you seek out cool adventures. So here we go, starting with a new character, Walter, and his Mad Bomber hat. Of course we will feature a Mad Bomber steal with each email. Read on and enjoy. Northpole Alaska, here we come! Mad Bomber Wrist Warmers. January 6, 2012 by. Order your favorite Team Bomber. Check them out at www.madbomber.com. I know ...
coughing4cf.com
Coughing for Cystic Fibrosis: Dwellingup to Chadora and Mount Wells
http://www.coughing4cf.com/2015/05/dwellingup-to-chadora-and-mount-wells.html
Walter van Praag has Cystic Fibrosis and does inspirational adventures to raise awareness and funds for CF and encourage people to become Organ Donors. This timne walter is teaming up with people with other disabilities to cycle from Lake Eyre to Mount Kosciuszko! DONATE DIRECTLY TO THE TEAM:. Wednesday, May 20, 2015. Dwellingup to Chadora and Mount Wells. Whilst in Dwellingup we had casually looked for trail markers but never saw any, and I wasn't about to ask anyone of course as we have a GPS! Due to e...
coughing4cf.com
Coughing for Cystic Fibrosis: February 2015
http://www.coughing4cf.com/2015_02_01_archive.html
Walter van Praag has Cystic Fibrosis and does inspirational adventures to raise awareness and funds for CF and encourage people to become Organ Donors. This timne walter is teaming up with people with other disabilities to cycle from Lake Eyre to Mount Kosciuszko! DONATE DIRECTLY TO THE TEAM:. Saturday, February 28, 2015. Welcome on board to PowerCom Solar. And we are also starting to collect for Cystic Fibrosis now that we are getting on the road: give.everydayhero.com/au/coughing4cf-1. Getting the cara...
coughing4cf.com
Coughing for Cystic Fibrosis: January 2015
http://www.coughing4cf.com/2015_01_01_archive.html
Walter van Praag has Cystic Fibrosis and does inspirational adventures to raise awareness and funds for CF and encourage people to become Organ Donors. This timne walter is teaming up with people with other disabilities to cycle from Lake Eyre to Mount Kosciuszko! DONATE DIRECTLY TO THE TEAM:. Saturday, January 31, 2015. Look, we have an image. It will look fetching with our matching new team T-shirts! We now also have a Spot 3Gen. It does cost over $200 to operate, another important team expense. Please...
cofe4cf.blogspot.com
The Great COFE for Cystic Fibrosis: Next Adventure!!
http://cofe4cf.blogspot.com/2010/06/next-adventure.html
The Great COFE for Cystic Fibrosis. THE OFFICIAL COUGHING THE DISTANCE WEBSITE IS HERE. This website was the blog we kept. The official website is here:. Also, my latest adventures are here: www.coughing4cf.com. Thursday, June 10, 2010. STOP PRESS Read all about it! The next adventure: www.coughing4cf.com. 卡爾桑得柏:「除非先有夢,否則一切皆不成。」共勉! . You two make a lovely couple! It takes all kinds to make a world. . Keep in contact. Good Luck . 死亡是悲哀的,但活得不快樂更悲哀。 . Poverty tries friends . Tell me what do you think. Peopl...
cofe4cf.blogspot.com
The Great COFE for Cystic Fibrosis: Still getting recognition
http://cofe4cf.blogspot.com/2010/10/still-getting-recognition.html
The Great COFE for Cystic Fibrosis. THE OFFICIAL COUGHING THE DISTANCE WEBSITE IS HERE. This website was the blog we kept. The official website is here:. Also, my latest adventures are here: www.coughing4cf.com. Sunday, October 10, 2010. Amazing how I made the top 120 list. Of most inspirational people on the coast! Wait till they hear about www.coughing4cf.com. And see me ride my dutch bike from Sydney to Melbourne. Walter - Thank You! Subscribe to: Post Comments (Atom). YOUR HELP IS NEEDED. 2007 For in...
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