Print A Wish For Wendy Charity Event is being held on November 10th at North Park this year. Mark your calendars for this fun annual event full of family activities, ways for local sports teams to participate and a chance to meet celebrities!!
This is the 13th annual event benefiting the Cystic Fibrosis Foundation. Registration, Sponsorship and Pledge Forms are now available! Thanks to everyone who helped make the 12th Annual Wish for Wendy Softball Tournament a huge success. The support of sponsors, players, donors, volunteers and friends helped raise $150,000, the most ever donated in a single year for this event. A generous $100,000 challenge match from the Zucker Family Foundation was added to this year’s total. Andy Lipman, his family and the Wish for Wendy Foundation are grateful for all the wonderful people who are helping make CF 
stand for Cure Found.
stand for Cure Found. For more information, to register a team, volunteer, or provide sponsorship support in the fight against cystic fibrosis, go to: www.wishforwendy.org or andy@andylipman.com.
AlpharettaMoms.Org will keep you updated on all the latest information regarding the event! Cystic Fibrosis (CF) is a genetic disease affecting approximately 30,000 children and young adults in the US. CF causes the body to produce an abnormally thick mucus that clogs the lungs and leads to life-threatening lung infectins. This mucus also obstructs the pancreas and interferes with digestion. The median life expectancy for a CF patient is 37 years. Information from Georgia Chapter of the Cystic Fibrosis Foundation.
AlpharettaMoms.Org will keep you updated on all the latest information regarding the event! Cystic Fibrosis (CF) is a genetic disease affecting approximately 30,000 children and young adults in the US. CF causes the body to produce an abnormally thick mucus that clogs the lungs and leads to life-threatening lung infectins. This mucus also obstructs the pancreas and interferes with digestion. The median life expectancy for a CF patient is 37 years. Information from Georgia Chapter of the Cystic Fibrosis Foundation.
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