About Xtreme Hike
Online registration has closed for this year's Oregon Xtreme Hike. Please contact Jenny Anderson at janderson@cff.org with any questions.
Celebrate our 5th Annual Oregon Xtreme Hike on Mt. Hood!
The CF Foundation’s Xtreme Hike requires sacrifice and determination and challenges each hiker to reach personal and philanthropic milestones which celebrate and support those living with cystic fibrosis. The Oregon & SW Washington Chapter is thrilled to celebrate our 5th annual Xtreme Hike in the beautiful Pacific Northwest. Join us for a bucket list experience as we tackle up to 20.3 miles in the Mt. Hood National Forest while raising awareness and funds to support those living with CF.
This year’s Oregon Xtreme Hike base will be the iconic Timberline Lodge where participants will enjoy lodging and meals for 3 days/ 2 nights. This year’s hike will celebrate the full splendor of Mt. Hood, the highest mountain peak in Oregon and the second most climbed mountain in the world. The trail itself will once again feature sections of the famed PCT (Pacific Crest Trail) and highlight Mt. Hood favorites including Split Rock, Paradise Park & Ramona Falls.
In addition to the physical commitment, each registered hiker takes on the challenge of fundraising a minimum of $2,500 or more!
The Hiker's Journey
We invite all participants to embrace this full weekend experience including lodging and most meals from August 9th-11th. Hikers will enjoy comfortable accommodations at the iconic Timberline Lodge for three days and two nights in Government Camp, Oregon.
Hikers can check in on Friday, 8/9 starting at 4pm, followed by a safety meeting and hearty dinner starting at 6:30 pm.
On early Saturday morning, 8/10, hikers will enjoy a grab-n-go breakfast before hitting the Pacific Crest Trail directly behind the lodge. During the hike, participants will be rewarded with beautiful scenery and multiple rest stops promoting hydration, aid, and sustenance. We are thrilled to offer 2 route options for this year- a 20.3 mile stretch starting at Timberline Lodge or a 12.5 mile route starting at the Ramona Falls Trailhead. Upon completing either route, hikers can toast to their efforts at the Lolo Pass Trailhead before being shuttled back to Timberline Lodge. Saturday’s dinner will be on your own.
On Sunday morning, August 11th at 10:00 am, we will join again for an Awards & Celebration brunch to honor our efforts. Please plan to stay for the celebration brunch as it is the culmination to a weekend of friendship, community, and camaraderie as we move forward on this shared path to cure CF.
Your Hike Journey includes:
- Detailed Hiker Packet with welcome guide, training schedule, fundraising tips, apparel/gear list, FAQs
- Calendar of regional training hikes
- Lodging for two nights at Timberline Lodge (based on double occupancy of two hikers)
- Transportation to and from the trail on hike day
- Rest stops and aid stations along the trail
- Official Xtreme Hike wicking t-shirt
- Grab and go breakfast, lunch, and trail snacks for hike day
- Victory brunch and awards ceremony on Sunday
- Kick off dinner on Friday
Fundraise: Fundraising is easier than ever before. You can use the participant center, the Fight CF mobile app, or fundraise on Facebook to reach your goal. You can also create a passion fundraising event or see if your employer has a matching gift program.
Share your story: Life with cystic fibrosis is different for every person living with the disease. Share your story to help others understand the realities of life with CF and why your participation in Hike is important.
Hike with us: Join the CF community on event day to celebrate our progress and commitment to finding a cure for every person with cystic fibrosis.
Sponsor the 2024 Oregon Xtreme Hike
Would you like to join a select group of sponsors for Oregon's Xtreme Hike? Funds raised will support the mission of the Cystic Fibrosis Foundation to cure cystic fibrosis and to provide all people with CF the opportunity to lead long fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care. Despite tremendous progress, we are not yet done. View our Sponsorship Opportunities!
At the Cystic Fibrosis Foundation, we commit to equity, racial justice, diversity, and inclusion as core principles guiding our efforts to provide all people with CF the opportunity to live long, fulfilling lives. We strive to host inclusive and accessible events that enable all individuals to engage fully. Please be aware that a 3-week notice is requested as some accommodations may require time for the Foundation to arrange. If you have a disability and require accommodations to fully participate in this activity, please go to www.cff.org/chapters and email or call your local chapter office.
Pet Policy
For events where pets are welcome: be respectful of other event attendees and only bring well-behaved pets; keep pets on leash at all times; follow the pet policies of the local park or venue; and clean-up after your pet. Pets must be current on all required vaccinations. Pet owners assume full responsibility for their pets.
A thank you to our sponsors.
Our events wouldn’t be possible without the support of our National Peer-to-Peer sponsors: AbbVie and Vertex. We also recognize American Airlines, our outstanding corporate supporter.
We also want to thank our local sponsors who continue to help advance our mission.
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Note: Please make all payments/contributions to the CF Foundation with a credit card or check. We accept all major credit cards.
Events may be subject to change based on health or safety concerns. If an event is moved to virtual, sponsorship benefits may be adjusted to fit that format. If an event is cancelled your local contact will reach out to discuss options.
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.
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