Pierre was born 21 years ago in France and I remember his birth as if it were yesterday, overwhelmed with happiness.
The day after he was born, Pierre was rushed to hospital and diagnosed with Cystic Fibrosis (mucoviscidose in French) 10 days later.. The sky was falling on my head !  After being operated on at just one day old, Pierre went through intensive care and then paediatrics.

After two months, we were finally able to take our little Prince home, to the great delight of his parents and Camille, his sister.
Cystic Fibrosis is a rare and fatal genetic disease.

For 21 years, Pierre has been fighting this disease with ups and downs. This disease slowly destroys the lungs and digestive system.
He is very strong and never complains.

There is no cure to CF for now but regular treatments help improving the lifestyle of the patients. Life expectancy continues to increase with the remarkable advances in treatment and care, thanks to the research and donations.

CF presents daily compromise and challenges but with careful
management and the right treatment, people with CF can live full and happy lives !

I am taking part in this challenge to advance research and give hope to all those affected by this disease.
I dedicate this walk to Pierre and to all the patients in order to give my breath to those who don't have any.

I thank you warmly in advance.