23. 1. 2014

Febiofest helps “salty children”. We support the Club of Cystic Fibrosis Patients.

Klub nemocných cystickou fibrózou

IFF Prague – Febiofest is establishing the institution of charity partnership this year. The 21st edition will substantially support the Club of Cystic Fibrosis Patients.

The Club of Cystic Fibrosis Patients takes care of people with this serious hereditary disease that primarily affects respiratory and digestive systems. The children with Cystic Fibrosis are called “salty children” because their sweat is markedly saltier. Patients suffering from CF need intense treatment every day for their entire life and their disease is, unfortunately, incurable. With treatment, however, their lives can be improved.

Febiofest will donate the profit of a series of screenings to the Club of Cystic Fibrosis Patients. Furthermore, the Festival will organize a special screening for the Club and will spread information about this rather unknown disease among the audience. The Club of Cystic Fibrosis Patients will name one of its members to the festival's main jury.

Come to one of these six screenings and thus contribute to a good cause !

  • Friday, March 21 at 8:15pm - Hall 4:    Free Fall - Another Shore
  • Saturday, March 22 at 6:30pm - Hall 11:    Hotel - Nothern Lights 
  • Sunday, March 23 at 12 noon - Hall 9:    Life Feels Good - New Europe Competition
  • Sunday, March 23 at 6:30pm - Hall 11:    Chasing the Wind - Northern Lights
  • Monday, March 24 at 7:15pm - Hall 10:    Living is Easy with Eyes Closed - World Cinema Panorama
  • Thursday, March 27 at 6:45pm - Hall 3:    Marina - World Cinema Panorama

Thank you for supporting this worthy cause! You can find more about the Club of Cystic Fibrosis Patients here

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