Cystic Fibrosis Foundation - Click here for homepage
Stay Informed  |  Volunteer  |  Clinical Trials

In This Section

Quick Links

Find a Chapter

Get Assistance

Get Assistance - Cox Boys
We are here to help people with CF get the insurance coverage they need. Hear how the Foundation helped the Cox family.

Join us on Facebook!  Facebook 
Follow us on Twitter!   Twitter
Follow us on Instagram!  Instagram 
Add us to your circle in Google+!


Subscribe to our channel on YouTube!  YouTube  




In the Spotlight

Andy Lipman

Andy Lipman speaking

In addition to founding and chairing the Wish for Wendy softball tournament, Andy is a motivational speaker. He has been invited to share his story about CF with communities around the world.

Andy Lipman always knew he had a sister — Wendy – but never knew much about her.

He knew she died as a baby, but it wasn’t until he turned 25 that he found the courage to ask his parents about the sister he never met. He learned that Wendy had died from cystic fibrosis — the same disease Andy was diagnosed with at birth.

“My parents kept those details from me because they didn’t want to scare me,” said Andy, who is now 40. “Growing up, I didn’t think I would live to be an adult. So when I learned that my sister also had CF, it was life changing. It gave me the resolve I needed to continue fighting for myself and for all people who have CF.”

Andy with kids

Andy says his biggest accomplishment in life is marrying his best friend, Andrea, and raising a family. Together, Andy and Andrea have two children.

A Wish for Wendy

Not long after having that difficult conversation with his parents, Andy wrote a book about his struggles with CF. He donated some of the proceeds to the Cystic Fibrosis Foundation, but he wanted to do more. So in 2000, he decided to combine his love for sports, his family and his community by creating a city-wide softball tournament named in honor of his sister. He calls it A Wish for Wendy.

“I wanted something to remember her by. I want people to know who she was and for her to have some kind of existence on this Earth,” Andy said.

He worked with the Georgia Chapter of the CF Foundation to promote the event and attract sponsors, growing it into one of the largest charity softball tournaments in the country.

A Wish for Wendy has generated $1.9 million in support of the Cystic Fibrosis Foundation’s mission to find a cure for CF. Sixteen teams complete in the day-long, double-elimination tournament for top prizes. Thanks to help and support from Andy’s family, the Atlanta community and celebrities like the Atlanta Falcons cheerleaders, the event continues to grow year after year.

“Every dollar we raise is going to help people live longer — and there’s nothing better than that,” Andy said.

Inspiring others

Chairing the softball tournament isn’t the only way Andy gives back to his community. When he isn’t spending time with his family, working full time or planning for the next year’s tournament, Andy can be found in schools, churches, hospitals and community centers across the world sharing his inspiring story with others.

Wish for Wendy Warriors

The Warriors are one of 16 teams that compete each year at the Wish for Wendy Softball Tournament, started by Andy Lipman, who has CF. Each year, teams compete in a day-long, double-elimination tournament to raise funds in support of the Cystic Fibrosis Foundation.

As a motivational speaker, he isn’t afraid to talk about the 40 pills, the hour-long vest therapy and aerosol treatments he must complete every day just to stay healthy. Nor is he afraid to talk about the anger and depression he has struggled with most of his life.

“Thinking I wasn’t going to live a long life was really depressing and it seemed so unfair. I blamed my parents, I blamed God, I blamed everyone for this disease,” Andy said. “Today, I look at things differently. I live with CF, but I don’t let it limit what I can do.”

Andy hopes his actions and his words encourage more people to get involved in the search for a cure. He wants to inspire all people — especially those with CF — to reach for their dreams. After all, Andy has reached many of his. He says his biggest accomplishments are marrying his best friend Andrea and having two children through in vitro fertilization.

“My goal is to help cure this disease — not only for me, but for kids who are scared to death because they have CF, and for their parents who are scared to death for them,” Andy said. “I have the ability to help other people, and that’s what I strive to do.”

Posted: 2/20/2014

The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.