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For Sarah, the sky is the limit

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Sarah is both a patient (see: Story of Sara) and an enthusiastic supporter of the CF Bridge of Hope and shows how she accepts no limitations in living her life with Cystic Fibrosis. Watch as she reaches to the sky to test her will and overcome any trepidation and, in the process, experiences what is hidden from many.

In her own words, she says:

Jump!
With your eyes open, or with your eyes closed!

Dare!
To dream, to fly, to hope!
Dare to create, to laugh, to do, to feel, to love!
Take on challenges, do what scares you, expand your comfort zone, learn to breathe, be present, be here!

Live!
Live everyday to the fullest, life is here and is now, so do not let one day pass by without feeling alive!

June 4, 2019 News and Updates

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Five Feet Apart – A Review → ← Cystic Fibrosis International Congress In Ecuador

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Recent Posts

  • COVID-19 Global Pandemic and Cystic Fibrosis Webinar
  • COVID-19 Global Pandemic and Cystic Fibrosis Webinar by Dr. Sadeghi
  • Five Feet Apart – A Review
  • For Sarah, the sky is the limit
  • Cystic Fibrosis International Congress In Ecuador

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Your generous donations help provide medicine and care for children in developing countries afflicted with Cystic Fibrosis. The CF Bridge of Hope is an initiative of the Cystic Fibrosis Project, Inc., a 501(3)(c) registered charity organization whose mission is to provide care and life-saving medicine to children in countries where patient care for CF patients is severely limited or not available.

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