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Celebrating Dylan and Jenn's Marriage

December 30, 2017     6:00 PM | Saturday

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Thank you for joining us in celebrating our new life together!  We are blessed to have so many friends and family to share it with us.

With our two families coming together, we want to do everything we can to keep us together for a long time.

For those of you who don’t know, our nephew, Fischer Abrams was born with cystic fibrosis.  It is a progressive genetic disease that causes persistent lung infections and limits the ability to breathe over time.  There is currently no cure.  The Cystic Fibrosis Foundation is working to change that.  And we are doing everything we can to help them.  In lieu of wedding gifts, please consider donating to the CFF and help us ensure Fischer has a long and healthy life.

We want to be able to go to his own wedding and have him be there for our 20, 30 and even 50th anniversary.

Again, thank you for celebrating our special day with us and thank you for your generosity to CFF.



Dylan & Jenn

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Beth Saladino  
What a lovely, generous way to fight for a cure!