a team, volunteering or fundraising, please contact
Wendy Lipman, namesake of the Wish for Wendy Softball Challenge, lived only 16 days, yet every year for 16 years family, friends and supports have gathered to honor her by raising money to help find a cure for cystic fibrosis, the genetic disease that took her life.
16 teams will yet again battle for the 2018 championship both on the field and off of it, cheered on by 16 young CF Ambassadors from around Georgia. Who will win on the field? More importantly, who will win off of it?
Click on "The Event" to get all the necessary paperwork to sign up.
The Drive at 35, Alive at 25 and A Superhero Needs No Cape are available at www.andylipman.org/books.cfm.
Want to volunteer? Please fill this out:
In addition to being the founder of Wish for Wendy, Andy Lipman is a fabulous motivational speaker. Please call 404-512-9473 if you know of a business, civic, religious, or social organization, school group or club that might be interested in hearing Andy's remarkable story. Click here to read testimonials about some of Andy's past appearances, or for speech descriptions and booking information.
Wish for Wendy will have a matching sponsor once again in 2018 as we once again shoot for raising $500,000 and reaching a 19 year total of 4 million dollars!
* All contributions to the Wish for Wendy Softball Challenge received up to or on 12/31/18 will be eligible for this 1:1 match. Donations received in excess of the matching goal will be credited to the Wish for Wendy event and would be used to support the mission of the Cystic Fibrosis Foundation.
Come hungry because the AMAZING Ray & Pam Shelor will be manning the grill!
Honoring Wendy's Memory
Wendy Carol Lipman was born December 18, 1970 and passed away January 2, 1971. She died from complications of cystic fibrosis. Back then, there weren't many treatments for cystic fibrosis. Thanks to events like A Wish for Wendy, donations are leading to treatments and are moving us even closer to a cure. The Wish for Wendy Softball Challenge is dedicated to the memory of the sister of founder Andy Lipman, and our wish for Wendy is that people with cystic fibrosis no longer have to struggle with this disease.
COMING SOON! The 19th Annual WISH FOR WENDY
Saturday, October 20, 2018 at Alpharetta's North Park!