Tiffany Ann Morgan was born on November 3, 1993 as the youngest daughter of Tammy and Terry Morgan. They brought home this bundle of joy to big sister Brittany, who was 3 at the time. Little did they know, in about 18 months, their lives would change. Tiffany received the diagnosis of cystic fibrosis at the WVU CF Center. Tiffany fought a hard battle against CF, but never complained and always had a smile on her face. Her smile was contagious and she never wanted anyone to think she was sick. Her life was full of trips back and forth to Morgantown, hospital stays, feeding tubes, breathing treatments, home IVs, surgeries, you name it. She was the strongest girl with a hard battle to fight. Sadly, in March 2007, at just age 13, she lost the battle against this horrible disease and is now watching from heaven above. We remember her laugh, her smile, her endless hours of watching Gilmore Girls, dancing to Usher, hunting, fishing, and just loving the life she was given. Every day we are reminded of her and everyday we miss her a little bit more. We have participated in the Great Strides walks every year since her passing in hopes to help others living with CF live healthier, longer, happier lives. Everything came full circle in 2017, when Tiffany's sister Brittany became the respiratory therapist for the WVU Mountain State CF Center, with some of the same team that cared for Tiffany during her life. Brittany is now deeply committed to helping those with CF, as well as helping the legacy live on of those loved ones who are no longer with us. Thank you for any and all support. Team Tiff is composed of friends and family of Tiffany, some who never even met her, but feel like they know her because we have continued to let her live through us. Let's make CF stand for Cure Found once and for ALL.
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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.