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My Great Strides Story

Maria Brown

Fundraising for Nashua Great Strides 2026

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Maria Brown

Alexandria was born in 1988; she was diagnosed with Cystic Fibrosis (CF) and had surgery when she was 4 days old.  After time in the Neonatal Intensive Care Unit at Children’s Hospital Boston, she came home with a feeding tube.  In 1989, the gene for CF was discovered. 

Thanks to the CF Foundation and donors such as yourself, Alex is now 37 years old and is thriving.  She has been married to Matthew for 13 years and works on a part-time basis for the National Park Service.

In order to stay healthy:
•Alex takes 30 pills a day, including digestive enzymes every time she eats
•Spends 2 hours a day on breathing treatments
•Uses a monitor to track sugars due to Cystic-Fibrosis-related Diabetes.

Trikafta has been a miracle drug for patients who have the most popular genetic mutation,  F508del.  However, Alex has a rare mutation, also known as a nonsense mutation.  Please help to fund the research to find the drug that will help patients such as Alex.
 

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The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.