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The Newman Family

Debra Newman
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Debra Newman

Most of you have been with us on this journey since Bailey was born with Cystic Fibrosis in 2016. Since then, you have shown your support both with your presence and your financial support, for which we are unbelievably grateful. This year is very special for our family. We are being honored at the GALA with the Angela Warner, Friend of the Foundation Award. Recipients are those who show unwavering dedication, generosity, intelligence, and spirit in furthering the mission of the CF Foundation.
When I visited the CF research laboratory in Lexington, Massachusetts, one of the scientists declared that she had cured Cystic Fibrosis in a petri dish. Of course, with my limited scientific background, I blurted out, "Then get on with it!!" That's the hard part, apparently! Delivering a new gene to the lungs remains a big hurdle, but with incremental advance, it will lead to a breakthrough.
 

Scott and my wish is that we see that breakthrough in our lifetimes. So, in honor of this award, I am asking you once again to donate so that Bailey and all living with CF will be able to say, "I used to have Cystic Fibrosis."
 

We will support as many tables for all of you willing to join us in person on October 11th  5:00pm Mystic Lake Hotel and Casino 2400 Mystic Lake Center NW Prior Lake.  We just ask that you donate a suggested gift of $125 per person.   


PLEASE DO NOT CLICK THE BUY TICKETS BUTTON BUT RATHER THE DONATE BUTTON. There will be an add a donation message for you to write your name and the names of your guests so that we are able to all celebrate together!

 If you are not attending we welcome any donation you wish to make!!

Thank you in advance!!
Deb and Scott

Cystic Fibrosis Foundation Charity ID No: 13-1930701

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$1,000
raised of $15,000 goal
 

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