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Our son Mason was diagnosed with Cystic Fibrosis through prenatal blood work and amniocentesis. This makes his life a little bit different that you and I.
He has to
- take enzymes before every snack and meal
- do his vibration vest for 40 minutes every day
- take various medications through his nebulizer to keep mucus loose in his lungs.
- if he gets a cold, he goes on liquid anti-biotics
- takes extra gummy and liquid vitamins since his body struggles to get the nutrients out of food
But through all of this, he has really inspired the whole family. His favorite things to do right now are riding his dirt bike, playing soccer and going to school.
Meaghan and I can't believe the support we've received from friends and family over the last 10 years. It's really inspiring to see how everyone has rallied around this great cause to find a cure.
Let's keep the momentum going in 2023.
With gratitude,
Jason and Meaghan Phipps
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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.