Dear Friends and Family
We would again like you to consider making a donation to spellbound for a cure
We couldn't be happier to tell you that Judah turns 13 this June! The world of Cystic Fibrosis has changed a tremendous amount since he and Ellie were born. The lifespan then was only to late teens early twenties NOW IT IS 44 years and growing !! There are 35 major industry programs focused on early-stage genetic therapies that are the key to curing CF, and 12 treatments available to people with CF — four of which address the underlying cause of the disease. We feel blessed and empowered to have raised money in honor of Ellie, Judah and all who suffer from Cystic Fibrosis and together, we have made remarkable progress. But our work isn't done. Your donations are huge-the funds we raise will continue to drive research forward.
With your strong support our goal is to make CF stand for CURE FOUND and it is beginning to look closer to reality!
*Below only the date changes!
All the celebratory shenanigans remain the same!
PLEASE JOIN US On Sunday May 21st -Let's have a meet and greet at 1505 Wilmette Ave. 9:00AM and will board the bus for Montrose Harbor - Grove 16 where we will enjoy the festivities and then we will hightail it back to the bus for Bloody Marys while heading back to our house for food and festivities to celebrate our achievements!
Thank You all for your loving support and your generous donations.
We are grateful to you all!
With So Much Love,
We are - Spellbound for a Cure
Jack & Judi Spellman Family
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.