We Did It: Over $150,000 Raised for the Cystic Fibrosis Foundation!
June 04, 2018
When your alarm rings at 5 AM and all you can think about is staying in bed instead of getting up for your morning run, remember; it may seem hard, but "hard" is all about perspective. Imagine if your 5 AM alarm was for pills, enzymes, breathing and vest treatments... 5 AM wake ups would be a matter of trying to survive - not trying to squeeze in a run before work. Running with Team CF is about supporting patients who wake up everyday JUST to survive.
Our Run To Cure CF team in Pittsburgh grows each year - as do our research efforts, drug and therapy developments, and progress we’ve made in the search for a cure to cystic fibrosis. Our community has celebrated many recent successes in research, but the lives of young people are still being cut far too short. Will you join us as we run to raise awareness and funds to search for a cure? Accept the challenge today to help add tomorrows to the lives of those living with CF. Consider registering to run, putting together a relay team, or making a donation to one of our dedicated team members. We will train hard to see that our team AND CF cross the finish line one day!
All Run To Cure CF team members receive:
- FREE bib for race of your choice
- Run To Cure CF gender specific performance tank or shirt
- Group training runs and other events
- Personal support from running coaches and mentors
- Race specific training plans and tips
- Fundraising incentives from Fleet Feet, Pro Bike + Run, & more!
Thank you, Fleet Feet Pittsburgh, for also supporting Team CF!
2018 Race Fundraising Minimums:
Kid's Marathon - $100
5K - $200
Relay Team - $1,500 (per team)
Half Marathon - $400
Full Marathon - $500
Fundraising minimums must be met by May 4th, 2018. Don't think you can meet your fundraising minimum or have any questions? Contact Alanna Figurelli at firstname.lastname@example.org or (412) 321-4422 to set up a fundraising plan!Cystic fibrosis is a rare genetic disease affecting the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene causes the body to produce unusually thick, sticky mucus that clogs the lungs, leading to life-threatening lung infections.
In the 1950s, few children with CF lived to attend elementary school. Today, because of advances in research and medical treatments, the can now expect to live into their 30s, 40s, and beyond.
Learn more about Cystic Fibrosis and our chapter: www.cff.org/WesternPA