Home CF Challenge Cystic Fibrosis Foundation Team CFC Ride Schedule Meet Keira Rae

CF Endurance Challenge

Ride toward a CF Cure

Team CFC is proud to support the Cystic Fibrosis Foundation by contributing the miles we ride in this year's Limited Distance and Endurance Ride Season to help find a cure for people like Keira who are suffering from this devastating disease. Team CFC is a group of equestrians who enjoy the sport of endurance riding. The sport involves travelling many miles on your horse, anywhere from 25 (LD) to 100 miles in one day. Because of the generosity of individual donors like you the CF Foundation can continue their life saving mission. Your support is critical to ensuring that vital CF research moves forward. Working together, we can give children and adults with CF the quality of life and the future they deserve.

How can you help? A couple of ways...

  1. Sponsor a rider by the mile or with a one time donation. - OR -
  2. Join Team CFC. If you are an AERC endurance rider you can look for generous supporters to sponsor your miles and have fun riding your horse knowing you are doing it for a great cause.

To sponsor a rider simply email or call one of our riders to fill out our form and your rider will provide you with updates on how Team CFC is doing throughout the riding season. Team CFC is not taking any of the proceeds. We are just proud to ride for such an honorable cause. 100% of your contributions will go directly to the Cystic Fibrosis Foundation.

Stephanie Pfeiffer 541-592-4160 blackie@cavenet.com
Allen Cress 541-592-3266 acress@cavenet.com
Skip Leahy 541-592-2149 lizleahy@frontiernet.net
Marc Bowen

Click Here to download the Brochure

Click Here to download Sponsor Form

Mail completed forms to:

Team CFC
Attn: Stephanie Pfeiffer
545 Hummingbird Rd
Cave Junction, OR 97523

Already an AERC participant? To join the Team all you need to do is contact Stephanie Pfeiffer at 541-592-4160 or at blackie@cavenet.com to register as a rider. Then get your sponsors and Ride, Ride, Ride!

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CF IS A LIFE-THREATENING GENETIC DISEASE THAT AFFECTS THE LUNGS AND DIGESTIVE SYSTEM. MORE THAN 10 MILLION AMERICANS ARE SYMPTOMLESS CARRIERS OF THE DEFECTIVE CF GENE. HELP THE CF FOUNDATION CONTINUE OUR QUEST TO FIND A CURE.

WHY SHOULD YOU GET INVOLVED?

The CF Foundation is Efficient. Almost 90 cents of every dollar raised goes directly toward vital CF research and programs. According to SmartMoney, the CF Foundation is "a charity that won't waste your money." The CF Foundation also meets extensive standards of the Better Business Bureau, America's most experienced charity evaluator.

The CF Foundation is Innovative. Forbes and USAToday have recognized the CF Foundation's innovative approach to research. By offering milestone-driven research awards, the CF Foundation stimulates the development of new CF therapies that can have a profound impact on thousands of young lives.

The CF Foundation is Results-Driven. When the CF Foundation was founded, few patients lived to attend elementary school. Thanks to research and care supported by the CF Foundation, the median age of survival is now 37 years.

Working together, we can continue to add tomorrows every day to the lives of all people with CF!

Fast Facts

ABOUT CYSTIC FIBROSIS

  • CF is a life-threatening genetic disease that affects the lungs and digestive systems of approximately 30,000 children and adults in the United States.
  • A defective gene causes the body to produce unusually thick, sticky mucus that clogs the airways and leads to life-threatening lung infections, obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.
  • More than 10 million Americans are unknowingly, symptomless carriers of the defective CF gene.
  • The disease occurs in one of every 3,500 live births of all Americans and about 1,000 new cases of CF are diagnosed each year.
FOR MORE INFORMATION CONTACT THE OREGON CYSTIC FIBROSIS FOUNDATION CHAPTER: (503) 226-3435 9320 SW Barbur Blvd.
(800) 448-8404 Suite 210
(503) 226-4165 Fax Portland, OR 97219
oregon@cff.org
http://www.cff.org

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Team CFC: Ride for the CF Cure

Team CFC (meaning Team CF Challenge) was created from one simple question. How could we make a difference in the fight against CF when we were not scientists, and without direct access to copious amounts of money? We decided that we could make our love of endurance riding work for us. We felt that endurance riding and fighting Cystic Fibrosis have a lot in common. Both endurance riding and the fight against CF require that we endure the mental, physical and emotional strength to see both the next step and the finish line. Sometimes, during an endurance ride, when our lings, our hears or our will are about to call it a day, our horses seem to muster up strength enough for each of us to make it over the next hill. That's the beauty of having teammates like our horses. As you read on you'll meet Keira Rae. We're proud to be part of her team as she fights to make it "over the next hill," all the way to the finish line.

The endurance community becomes something like a second family, whose members support each other and want each other to succeed.

"As I ride with this group of committed athletes, it is great knowing that every step my horse makes puts me closer to, not just helping my daughter, but helping everyone who has ever been affected by the devastating results of CF. Something that was just a fun hobby now has a direct purpose." - Stephanie Pfeiffer (Keira's mom and Team CFC Founder)


Stephanie Pfeiffer

Allen Cress

Brian Pfeiffer

Skip Leahy

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Team CFC's Ride Schedule

May 10th Prineville 25 miles Completed
June 21st Hat Creek Hustle 25 miles Completed
July 19th Bandit Springs 30 miles
August 2nd Redwood Ride II 25 miles
August 23rd Headwaters of the Rogue 25 miles
September 6th Oakland Hills Elevator Ride 25/50 miles
October 11th Limestone Challenge 30/50 miles

TOTAL: 230 miles

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Meet Keira Rae!

Keira's story is not much different than the thousands of other families living with CF. Outside and with the animals is where this energetic seven month old wants to be. She always has a constant smile, even when the situation may not be a happy one. She has an easy-going nature and the ability to adjust and accept all the medications, shots and procedures she has to endure.

We found out that Keira had Cystic Fibrosis when she was three weeks old. When Keira came home from the hospital she was unable to gain weight, yet she was hungry as a horse. Our pediatrician saw the red flags after receiving the results of the Oregon heel prick test and recommended we have Keira genetic tested. It was a sad and overwhelming day to find out your child has a life-threatening disease for which there is not a cure.

The advantage Keira has is that she was diagnosed so young. We were able to get her set up with a CF center and start working with a staff of pulmonologists, nutritionists, nurses and our pediatrician to ensure Keira has the best chance of living as long and fulfilling a life that is possible. Knowing that the CF Foundation is working hard to find a cure gives me hope that Keira may one day see her own children grow up.

Thank You!

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Last revised: Thursday, July 10, 2008 at 02:25 PM


Circle S Ranch & Outfitters

Brian & Stephanie Pfeiffer

545 Hummingbird Rd. Cave Junction, OR 97523

Phone: 541-592-4160

URL: http://www.CircleSRanchandOutfitters.com