This is my favorite little human, Mabel, who also happens with my niece and goddaughter. She has Cystic Fibrosis, a genetic disease with a defective gene that causes a thick buildup of mucus and impacts the lungs, pancreas, and digestive system.

This year is going to look a little different because I am unable to participate in the Xtreme Hike Event for 2026. Therefore, my fundraising will focus on the Great Strides event that happens in Buffalo, New York on May 17. That's only a month away! I look forward to raising awareness about Cystic Fibrosis, even though it will be in more condensed fashion!

All of the money raised for the Cystic Fibrosis Foundation will fund research, clinical trials, and other medical assistance that will help give Mabel, and over 40,000 people in the US alone, a fighting chance against this disease.

Significant advances have been made in the treatment of common mutations of Cystic Fibrosis! In 1955, when the Cystic Fibrosis Foundation was founded, children living with CF barely made it through Elementary school. Today, people with CF are attending college, getting married, and even having children! I personally met a family who participates in the Xtreme Hike event where this is true. I wish this whole heartedly for Mabel. There are now five drugs which help 90% of those who have the most common mutations. This is such incredible news! Mabel's mutation, however, is a combination of two rare mutations, and not all of these drugs help her. This means that the fight to find a treatment and or cure for her is more difficult.

Your donationwill help support my effort to raise $1000 and bring us all closer to the day that "CF" stands for CURE FOUND.

Thank you so very much for your support! It means so much to me and my family!

With love,

Debbie Smith