9

What is the life expectancy of someone with Cystic Fibrosis?

Life expectancy of people with Cystic Fibrosis and recent progresses and researches in Cystic Fibrosis

Cystic Fibrosis life expectancy
11 answers
Impossible question to answer. I was very ill as a child, wasn’t expected to have a long life. I’m currently 33 typing this and probably the healthiest of my life.

Posted Oct 2, 2017 by Andrew 1800
Honestly this cannot be answered with one number, you can die from CF by age 1 or 16 or 18 or 29. It's all dependent on the overall health of the person, CF will take your life. When is dependent on how you care for yourself and how compliant you are with your care. You can live pass 60. The average age is 36.7, but overall it depends on the person.

Posted Jan 18, 2018 by Marieliz Landa 4060
Translated from portuguese Improve translation
There are studies for new drugs, however, there is still no cure, but there are significant advances. The prospect of life in increasing with the passing of the years.

Posted May 27, 2017 by Maria Betânia 1170
Translated from portuguese Improve translation
The medications that are increasingly more potent , physical therapy, inhalation

Posted May 28, 2017 by Leonardo 1110
Translated from portuguese Improve translation
There are cases and cases, depend on the clinical condition of the patient. There is a drug in test called Orkambi, serving for some mutations, from what I understand it can prevent the progression of the disease, but still do not heal.

Posted Aug 20, 2017 by Patty 1000
Translated from portuguese Improve translation
Currently the life expectancy for CF has increased, since new studies and medicines have advanced, in addition to the information be greater than before.

Posted Aug 20, 2017 by Cláudia 1100
Translated from spanish Improve translation
Brazil 20 years
Europe more than 30
USA 40
Canada 50

Posted Sep 14, 2017 by Glauco 2000
Translated from spanish Improve translation
Every day increases more. She is currently an average of between 30-40 years.

Posted Sep 16, 2017 by Sole 1000
Translated from portuguese Improve translation
Not have a cure, but with treatment the estimated life is long

Posted Sep 27, 2017 by Kammily 1000
Translated from spanish Improve translation
37 years and also of the type of gene mutation as it progresses

Posted Sep 27, 2017 by Hilda María Mex Tun 1100
Translated from portuguese Improve translation
Many still lack knowledge and diciplina end up dying finger by the lack of adequate treatment because it is not a disease physically apparent people end up deixande and make the treatment stopping taking the inalacoes. The more I get to know people who are carriers of CF and hj is living very well with more than 30 years work have kids and do not leave the treatment..

Posted Sep 28, 2017 by Thais 1500

Cystic Fibrosis life expectancy

Celebrities with Cystic Fibrosis

Celebrities with Cystic Fibrosis

2 answers
Is Cystic Fibrosis hereditary?

Is Cystic Fibrosis hereditary?

8 answers
Is Cystic Fibrosis contagious?

Is Cystic Fibrosis contagious?

7 answers
ICD9 and ICD10 codes of Cystic Fibrosis

ICD10 code of Cystic Fibrosis and ICD9 code

6 answers
Natural treatment of Cystic Fibrosis

Is there any natural treatment for Cystic Fibrosis?

4 answers
Living with Cystic Fibrosis

Living with Cystic Fibrosis. How to live with Cystic Fibrosis?

11 answers
Cystic Fibrosis diet

Cystic Fibrosis diet. Is there a diet which improves the quality of life of...

12 answers
History of Cystic Fibrosis

What is the history of Cystic Fibrosis?

5 answers

World map of Cystic Fibrosis

Find people with Cystic Fibrosis through the map. Connect with them and share experiences. Join the Cystic Fibrosis community.

Stories of Cystic Fibrosis

CYSTIC FIBROSIS STORIES
Cystic Fibrosis stories
I was diagnosed with Cystic Fibrosis a few weeks after my birth, my mum was devastated she had no idea what this terrible illness was. They told her that I probably wouldn't reach adult hood and would not be able to do the same things as my peers.  ...
Cystic Fibrosis stories
My son was born in 2011, happy and seemingly healthy. He had had his routine screeners when he was two days old in the hospital and nothing was picked up as being abnormal. It wasn't until my husband and I decided to donate our three embryos being st...
Cystic Fibrosis stories
Misdiagnosed for many years. Diagnosed at age 50. Am now in the 54-60 age range.
Cystic Fibrosis stories
Howdy! My name is Lizzie and I was a cranky baby for the first year of my life! My mom diagnosed me when I was one, based on a commercial with Mary Tyler Moore which mentioned salty tasting skin being a symptom. She noticed that I had salty skin whe...
Cystic Fibrosis stories
I was 5 months old when I got diagnosed with Cystic fibrosis later when I was 8 I was diagnosed with cf related diabetes and when I was around 14 I was diagnosed with CF liver disease. When I was 12 I was diagnosed with 5 blood disorders

Tell your story and help others

Tell my story

Cystic Fibrosis forum

CYSTIC FIBROSIS FORUM

Ask a question and get answers from other users.

Ask a question

Find your symptoms soulmates

From now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Symptoms soulmates are people with similar symptoms to you.

Symptoms soulmates

Add your symptoms and discover your soulmates map

Soulmates map