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Thank you for joining us in this fight.

 

Andy was a lot of things to a lot of people but to me he was my brother. I don't know how I/We/My Family are going to do this but I am committed to honoring Andy's legacy and finding a cure for Cystic Fibrosis (CF).  This is going to be really tough but I know deep in my heart and gut, this is what I am supposed to do. It is what we have been doing for 20+ years and it all started with him when he created "A Wish for Wendy". Our mission since then has been to make CF stand for cure found and it doesn't stop here -- there is still work to do. Andy always said “ I may have CF, but it will never have me.” And he was right- it did not. Andy passed unexpectedly, leaving our family and this community heartbroken. However, we will carry on this mission to cure CF in honor of Andy. I would do anything for him and I know he would have for me too so now I am called to do this for him. 

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With all that said, Andy set the date for "Wish for Wendy" to come back as a pickleball tournament this year on September 20th that was going to be called "Eva's Wish for Wendy" to honor our mom who passed at the end of 2020. I cannot let the date he set go by without trying my hardest to kick this out of the park and honor him on September 20th. Please save the date for a day where we will tell our stories about Andy and close the chapter on my fundraiser. 

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I hope you will join me in this fight to cure CF in honor of my brother, Andy. All donations are 100% tax-deductible and support the critical work being done by the CF Foundation.

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ALL in for a cure for Andy Lipman's Legacy. 

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