May The Funds be With You

This year our CF Foundation employee Great Strides team adopted a “Star Wars” theme and, believe me, we went all out to make the experience extra special and out of this world. See for yourself!

Aug. 5, 2015 | 2 min read
Peter Knockstead Cropped
Peter Knockstead
IMG_0239

I feel fortunate to work at a place where passion and hard work are the norm and not the exception.

I really got to thinking about this last Thursday as I joined my colleagues here at the Cystic Fibrosis Foundation's national office to celebrate the results of our staff Great Strides team. It's an annual favorite for the office because we raise a heck of a lot of money for cystic fibrosis and have a lot of fun along the way. 

Yes, I work at the Cystic Fibrosis Foundation, but you may not know that, like other corporate and family teams across America, our employee walk team is personal, voluntary and something for which we get excited and feel great pride.

I am pumped that this year I was able to raise over $1,000 from the generous support of my family and friends. Actually that pales in comparison to what others on our team raised but I think I did good nonetheless.

This year our CF Foundation employee Great Strides team adopted a “Star Wars” theme and, believe me, we went all out to make the experience extra special and out of this world.

I could go on and on about what Great Strides means to me and our office team but, as they say, a picture says a thousand words so enjoy these special photos I took at our celebration.

IMG_0239
IMG_0233

I don't want to leave you feeling jealous, but what other Great Strides team has Dr. Beall and Dr. Campbell dressed in character as Yoda and Darth Vader -- just to convey their thanks and gratitude to all of us? Simply amazing.

On behalf of all of us at the CF Foundation, thank you for all you do and “may the funds be with you!”

This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited to people with CF and their families, belong solely to the blog post author and do not represent those of the Cystic Fibrosis Foundation, unless explicitly stated. In addition, the site is not intended as a substitute for treatment advice from a medical professional. Consult your doctor before making any changes to your treatment.

Share this article
Topics
Great Strides | Get Involved | Fundraising
Peter Knockstead Cropped

Peter lives in the heart of Washington, D.C. He is passionate about work, life, Apple products, books, history, Redskins, family, God, his two schnauzers -- George and Weezy -- and other passionate people making an everyday difference in the world. As the former senior director of corporate engagement at the Foundation, Peter worked on national corporate and donor cultivation, and with national sponsors and chapter staff. Follow @knockstead on Twitter.

Recent Community Posts
Optimism in the Face of Transplants
Blog | 6 min read
Focusing on the Future Without My G-Tube
Blog | 3 min read
How College Helped Me Open Up About My CF
Blog | 5 min read