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The Cystic Fibrosis Project is organizing a second round of Freestyles or clip against the Muco, which I recall is a therapeutic and non-profit organization, from 3 October 2015 to this time support the small Wylfrid which is 8 years old and its parents.Actually when you see this little guy like that, at first sight it does not look that he is sick yet.Since his birth, he is met by a rare genetic disease which is called Cystic Fibrosis, deceitful, invisible, it does not show his pain, heavy to wear every day for him but also for his parents, to put it simply it primarily affects three organs the human body, lungs, and therefore breathing capacity, liver and pancreas.It is at the time still incurable.For you to understand what it is, I invite you to take 5 minutes of your time and watch the video below where children and their families explained simply with their own words what Cystic Fibrosis.

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