Emily :-)
This is Emily, my cousin's smart, sassy and awesome daughter. I'm her Teta Momo and when we get together we play hard, get very silly and messy and we love dancing to Go Danny.
Em is one of the approximately 30,000 Americans living with cystic fibrosis. She was diagnosed with Cystic Fibrosis shortly after her birth. And since her diagnosis, I am in awe of the care and support that she (and her mom and dad) receive from the CF Clinic and from the CF community. While real progress has been made towards a cure, there still is none for this devastating disease. Our family is participating as “Emily’s Entourage” in the Great Strides walk in May (but fundraising starts now!) We are all working toward making CF stand for Cure Found.
Will you help me reach my fundraising goal ?
Or you can also participate and join our team!
Thank you! :-)
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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.