My Xtreme Hike Story

My Hike Story

This year marks my second incredible journey with the Cystic Fibrosis Foundation, and I'm reaching out to you once again for your support. Last year, the trek brought me from South Carolina to Lake Placid/ the Adirondacks, NY- this year, I'm lacing up my shoes to conquer the Zion Xtreme Hike. A challenge fueled by love, loss, and unwavering hope for a future free from cystic fibrosis (CF).

Many of you know that in 2011, I lost my best friend, Jackie "Jo" Rodgers, to CF at the young age of 27. Her unwavering spirit and determination inspire me every day. She fought tirelessly against this debilitating disease, reminding me of the countless individuals worldwide who continue to face similar challenges. Last year, I hiked on what would have been Jo's 40th birthday weekend. This year, I hike not only in her memory, but for all those battling CF.

Every step I take on this hike signifies a step closer to finding a cure. The funds raised will directly benefit the Cystic Fibrosis Foundation, an organization dedicated to finding a cure and supporting those living with CF.

My goal is to raise $6,000 to empower the foundation and bring us closer to a world where CF no longer stands for "chronic frustration," but for "Cure Found." While Jackie's absence leaves a void, her memory fuels my passion to make a difference. Together, we can honor her memory, bring hope to countless families, and fight for a future where everyone can breathe freely.

Your contribution, no matter the size, can make a real difference. support makes a difference. 

Every dollar raised will go towards crucial research, advocacy efforts, and support programs that empower individuals with CF to live longer, healthier lives. I hope you will consider making a tax-deductible donation to support the mission of the CF Foundation.

This isn't just a personal journey; it's a collective effort to conquer CF. With your support, we can climb mountains, both literally and figuratively, in the fight against CF. Every donation brings us closer to our goal. Please consider contributing today and help me reach the summit for CF! 

Thank you for your time and consideration. 

There is currently no cure for cystic fibrosis. 

Cystic fibrosis affects the lungs, pancreas, and other organs. The symptoms can vary from person to person, and as people with CF live longer than ever before, their disease can become more complicated, leading to serious health issues. 

The Cystic Fibrosis Foundation has made extraordinary progress — including fostering the development of more than a dozen CF treatments — but these treatments are not a cure and not everyone can benefit from them. We must keep going.