It's official! The 7th Annual Amy's Ride for CF will be Saturday, June 25, 2011. Save the date. More details about the event will be posted as they become available.
Thank you! 6th Annual Ride Raises $23,000!
Thank you to all who supported the Sixth Annual Amy's Ride for CF on Saturday, June 26, 2010. The numbers are in, and we raised over $23,000 for the Cystic Fibrosis Foundation at this event, which will be used to fund research for treatments and a cure for cystic fibrosis. Stay tuned for details about the 2011 ride to be posted here soon!
Amy's Ride is on Facebook
Become a fan of Amy's Ride for CF on Facebook and share the link with all your friends to help promote our fight for a cure to Cystic Fibrosis. The page features news updates and also offers a chance for our family of supporters to connect and discuss events. Please join us on Facebook!
Watch this video of Amy and keep hope alive for a cure to CF
The Cystic Fibrosis Foundation has created the following video of Amy to remind us that every dollar you donate and every dollar we raise together gives hopes to CF families like ours for a cure. We encourage you to share this video with anyone and everyone you know who is interested in helping us win this fight. Thank you to Cystic Fibrosis Foundation for putting this together. (View the video.)
By the numbers: Amy's Ride Raises More Than $133,000 in First Six Years
In its first six years, Amy's Ride for CF has raised more than $133,000 for a cure to cystic fibrosis. A deep and heartfelt thank you goes out to each and every person who has contributed to our success!
We ride for a cure to Cystic Fibrosis. We ride for Amy.
Amy Miller of Hanover, PA, (pictured below) has Cystic Fibrosis, a disease in which a defective gene produces abnormally thick mucus that clogs the airwaves, causing lung infections and making breathing difficult. Amy's family and friends organized this event to raise money for a cure in the hopes that Amy and others like her can live a long and happy life. All the money raised from this event will be donated to the Cystic Fibrosis Foundation for research to find a cure for Cystic Fibrosis.
Last year, for the first time ever the Cystic Fibrosis Foundation did not have enough money to fund all of the research requests it received. With your help, we can make sure every study with the potential to find a cure is funded.