Cystic Fibrosis Team Magee

My best friend and beautiful wife Christine Ann Nov 21,1984 - May 16 2014

This is Christine Ann Magee, (November 21, 1984 – May 16, 2014) friend, sister, daughter, wife and love of my life.  Christine  lived her life with the courage and strength of a lion and the heart of a giant.  She gave all of herself to be the best person/human being that she could be and it showed in the brightness of her eternal light, her work as a teacher with her students and to all that had crossed her path.  Cystic Fibrosis can and is being fought.  Every day new advancements in drug development, medications and treatments are being made to give our loved ones who’ve been affected by CF another moment however brief it may be with us.  Christine, in her heart of hearts would never want another family or person to endure what we and she have and will continue to endure.  So please help Christine and Team Magee in this fight by joining the team, donating or by simply sharing our team page with a friend.  With Courage, strength and heart, we thank you.

TEAM MAGEE  click to join the team, donate or share.                                                

What is Cystic Fibrosis?  Cystic fibrosis (CF) is a life-threatening genetic disease that primarily affects the lungs and digestive system. An estimated 30,000 children and adults in the United States (70,000 worldwide) have CF.


Quick Facts about CFIn the United States:

  • About 1,000 new cases of CF are diagnosed each year.
  • More than 75 percent of people with CF are
    diagnosed by age 2.
  • Nearly half of the CF population is age 18 or older.

In people with CF, a defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:

  • Clogs the lungs and leads to life-threatening lung infections.
  • Obstructs the pancreas and stops natural enzymes from helping the body break down food and absorb vital nutrients.

In the 1950s, few children with CF lived to attend elementary school. Since then, tremendous progress in understanding and treating CF has led to dramatic improvements in the length and quality of life for those with CF. Many people with the disease can now expect to live into their 30s, 40s and beyond.

Symptoms of CF

People with CF can have a variety of symptoms, including:

  • Very salty-tasting skin
  • Persistent coughing, at times with phlegm
  • Frequent lung infections
  • Wheezing or shortness of breath
  • Poor growth and slow weight gain, in spite of a good appetite
  • Frequent greasy, bulky stools or difficulty in bowel movements

The Cystic Fibrosis Foundation

A nonprofit, donor-supported organization, the Cystic Fibrosis Foundation is the world’s leader in the search for a cure for CF. The Foundation funds lifesaving research and works to provide access to quality, specialized care and effective treatments for people with CF.

Nearly every CF drug available today was made possible because of Foundation support. Through its efforts, the life expectancy of a child with CF has doubled in the last 30 years, and research to find a cure is more promising than ever before.

Find a ChapterThe Cystic Fibrosis Foundation has 70 chapters and branch offices across the country that work diligently to raise funds to help support the search for a cure. Each chapter hosts multiple fun and exciting fundraising events aimed at bringing local communities together in support of the Foundation’s mission.Click on a state to find a chapter near you, or enter your zip code in the field provided to find a chapter office within a specific radius.

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