It is the most serious genetic disease. It’s recessive and chronic. It’s a disorder that affects many organs, mostly the lungs, pancreas, liver, kidneys and intestine. It’s due to the mutation in the CFTR gene that causes an overproduction of mucus. That leads to a respiratory infection, it blocks pancreas preventing the enzymes to reach the intestine. That’s why food cannot be digested and assimilated. Even if there are many different degrees of symptoms, the casting lung infection is the main cause of death.
The typical manifestation of this disease are:
- Difficulty of digestion
- Difficulty of breathing and too much cough
- Overproduction of mucus
- Production of swet
- Poor growth
- Chronic diarrhea
- Emotional difficulties such as depression
Avarage CF incidence in Italy
Nowadays there are 6000 affected people in Italy. It is estimated that every 2500-3000 children born in Italy, 1 is struck by CF. Thanks to treatment progress, the living expectancy can overcome 36 years of life.
CF causes
CF appears in a child when both parents are carries. In Italy one out of 25/26 people is carrier. The two carrier parents have ove in four chance to give birth to a CF baby.
Claire Wineland
Claire Wineland, a youtuber affected by Cystic Fibrosis, tells her fight in front of the camera. “…so grateful for everything this month. I’m grateful for all the people who donated to help me get through transplant. I’m grateful for the doctors that’ll be scooping out these lungs and giving me some more life to work with. I’m grateful for the change to keep being a person. I’m grateful for my own had and for all the weird things in it. I’m just really overwhelmingly grateful for all of this. There is no passionate rant to be had here I am just happy and thought I would let you all know”. With this quotation Claire says bye to her followers before getting a lung transplant. The surgery was successful, but unfortunately a complication came into being that forever ended her life. In her youtube channel she always uses a direct and carefree language, daring to be ironic about her disease and death.
The story of Claire has inspired the film “Five Feet Apart”

Five Feet Apart
Stella is a Cystic Fibrosis patient who uses social media to cope illness and tries to live a normal life. She meets Will, another CF patient , who is at the hospital in order to get rid of his lungs infection (B. Cepacia). Little by little they fall in love. CF patient are kept six feet apart to reduce the risk of the cross-infection at first Stella stick to the rules, but as soon his best friend Poe dies, she decides to live her life less strictly. There for she leaves the hospital with Will and grabs his hand, but with her gloves on. As they are working on a frozen lake, she gets to know that a lung transplant is available for her but she ignore it is suddenly she falls into the water and despite the risk of infection, will helps her with the mouth-to-mouth and she wakes up! An ambulance takes them back to the hospital. Will learns that Stella did not contract his infection. When Stella wakes up from the surgery, they must say goodbye.


Interview with my cousin Marco, who is fighting with CF
Marco is a 20-yer-old kid, tall and very thin, he’s got a beautiful and always smiling face, ready with jokes, but he i salso reserved and solitary.
Hi Marco, i’ve never asked you about your desease… do you feel like talking about it?
Me: When have you learnt to be affected by Cystic Fibrosis?
Marco: Good or bed, since i was a child i always knew about my desease, as i had to do specific checks for my health. I indeed realized what it was, when i was about 10/11 years old.
Me: How did you feel when you became aware of your desease?
Marco: Well, actually i don’t know because i was grown with what this desease concerns. There was not a real shock when i discovered my condition… it’s something i worked out little by little
Me: What are the CF symptoms and which are the treatments you need to receive?
Marco: The main symptoms are my intestinal difficulties such as severe stomachaches and breathing problems. For example when i get shortness of breath, when i walk faster or when i do some sports. Plus, i get easily sick as i catch colds or flu
As regards therapies, i have aerosol and also a kind of physical therapy called “autogenic drainage” which consist in a forced respiration, while opening my throat and pressing down my rib cage with my hands in order to squeeze my lungs and expel mucus. Obviously i have to take many medicines like antibiotics, vitamins and lactic ferments and so on…
Me: How did you describe your relationship to CF? do you hate it? Do you ignore it? Do you fight it?
Marco: I do not hate it because it’s not a person, it’s something i have in my body and i have to deal with it. Ican’t ignore it because symptoms are always there, even if i don’t do anything! It would be wrong if i ognore it because that would mean to feel even worse. I fight it every day by therapies. That’s it!
Me: have you ever thought about the positive aspects of CF?
Marco: Knowing me, i’m a very lazy person, so actually CF helps me to be more active. In fact i go to the gym since 1 year already and i have a hard work out. All that it’s something positive because it helps to start stepping me up!
Me: What is your typical daily routine?
Marco: I wake up early in the morning; after breakfast i have my aerosol for about 20 minutes; after that, i go on with my physical therapy which takes about 30/40 minutes. In total i spend an hour an half. Next, i study or i go out for some errands. Later, i have my lunch and than i go to the gym. At night i have my physical therapy and aerosol again.
Me: What do you do to keep the right weight?
Marco: First of all i eat a lot, trying to do it even if i don’t feel like; i try to eat many times a day, especially at lunch and dinner, i eat a big quantity of food that i like the most, in order to be faster since i’m very slow at eating!
Me: how much CF has influenced your life?
Marco: Of course a lot! Everytime i do something i have to put out with collateral difficulties like:
- When i go out i have to pay attention to charge my oxygen and i have to be careful not to stay without it or at list to make sure there is a place to charge it
- Everytime i make commitment, i have to take into account the time necessary to the therapies
- When i go to sleep at friend’s home, i have to remember al the stuff for the therapies
So there are many constraints, it’s only a matter of handling them!
Me: How are your relationship with your friends, relatives and school? How far has CF influenced them?
Marco: Actually my relationships are great. Being sick, has never affected them in a negative way. But instead, I was always supported by my relatives and friends. In this respect, I count myself lucky and grateful.
Me: Are there things you really would like to do but you can’t?
Marco: Actually there is nothing i can’t do as a normal person. Things are only more difficult for me. For example i like to go for excursion in the mountains buti t is too much complicated both for the breathing effort and for the oxygen handing.
Me: What’s your secret drem or your future project?
Marco: Now, my plains are obviously to finish university and then to work in the word of cinema.
Me: What are your hobbies?
Marco: I like cinema very much, in particular i prefer horror films, science fiction and western
Me: Do you trust the research to treat your desease?
Marco: Kind of yes… there are always new medicina products in commerce but I don’t believe in an ultimate drug to heal CF…

DAI RESPIRO ALLA RICERCA (give breath to the research), is the slogan sponsored by the CF research centers in order to raise awareness in people to donate their contribution. The focus is to develop research projects with the aim to find solutions to this disease. Moreover the research stands to provide CF patients to live a normal life.
Una tua donazione oggi, può cambiare il domani di molte persone (your donation today, can change the future of many people)










