Climb with team DPF to Cure Cystic Fibrosis - In memory of Michele Held

Team DPF

Fundraising for Philadelphia CF Climb 2026

Donate

Team DPF

We invite you to take part in CF Climb by joining team DPF in memory of Michele Held. 
 

Michele (Shelly) was my wife Amanda’s best friend, and she tragically lost her battle with cystic fibrosis (CF) in 2012 at just 28 years old. Amanda remembers Shelly as someone who maintained an incredibly positive outlook on life, despite the challenges of the disease she was fighting. She was the life of every party and never allowed CF to prevent her from making the most of every single day.
 

Although Shelly was born and raised in Ohio, she became a passionate Philadelphia sports fan—most likely thanks to Amanda’s influence. She was always by Amanda’s side, cheering on the Phillies, Eagles, and Flyers. Shelly also loved all things Disney, the show Friends, and, of course, singing along to car karaoke.
 

Amanda describes Shelly as “the person always smiling, no matter what the occasion, and the person who told it like it is, no matter what.” She was, and continues to be, an inspiration and guiding light to everyone who had the privilege of knowing her.


While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies and we still need a cure. This will require time, funding, and persistence – but with you on our team – we are ready to go the distance.

Our team is committed to providing every person with CF the opportunity to live a long, healthy life. Will you join us?


To learn more about Cystic Fibrosis, click the link below:
https://www.cff.org/intro-cf

Comments

$125
raised of $1,000 goal
 

4 Participants

recruited
Join Our Team

Achievements

Recent Donations

Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.