Can you live an “ordinary” adolescence when you have cystic fibrosis?

A teenager with cystic fibrosis testifies that her adolescence is not “ordinary”, but that by accepting her difference, she found strength, identity and pride in her journey.

November 18, 2020

By Amélie Payment, 16 years old.

My name is Amélie and I am 16 years old. I was diagnosed with cystic fibrosis when I was nine months old. My first year of life was very hectic, as I was hospitalized for the duration of my life. Today I want to share with you my opinion on how I see the adolescence of a person living with cystic fibrosis.

How can we live an “ordinary” adolescence when we are affected by cystic fibrosis? This is a question I asked myself for a long time before drawing these conclusions.

First, because we are sick, we have to follow a routine, take and inhale medications or antibiotics on a daily basis. We also need to do sports, do respiratory physiotherapy and go to all of our medical follow-up appointments. Let's face it... it's a lot! Health is not the only thing we need to take care of. There is school, our social and family life and even more for some.

Personally, I found that my illness and adolescence were not a very good mix. Adolescence is a great phase of questioning, sometimes of rebellion, and in my case of great anxiety.

But despite this difficult stage in my life, I decided that at 16, instead of seeing my illness as something negative, I was going to accept it. By that, I mean to live one day at a time and above all to accept myself as I am. I have no control over the bacteria that enter my system, that's for sure. But what I can do is make every effort to successfully complete my treatments.

I am basically a girl like the others. I have qualities, faults, dreams and goals like speaking out about my illness. The main difference between me and other teenage girls is that I have a bit more responsibility and I can't make decisions spontaneously. For example, I can't decide to go sleep at a friend's house on a whim because I wouldn't have my PEP and my medication. I also miss school more often than normal, which is why I have already been bullied because other students did not understand my situation.

In short, even though having cystic fibrosis has already caused me problems, I realize that being different is a good thing, because it makes me unique and that is extraordinary. I am happy to be who I am and to have the life that I have right now.

Finally, to answer the question How can you live an “ordinary” adolescence with cystic fibrosis? In my opinion, we simply cannot! Hihi! And I think it's okay to be different and unique. Having cystic fibrosis has made me a warrior and I enjoy every day that goes by. I am not just a sick girl, I am a survivor!

In the same category

Interviews and testimonies

See the category
Interviews and testimonies

Interview with Jean Christophe Réhel: L'air d'aller

An interview with Jean-Christophe Réhel on L'Air d'aller, a bright and daring series that addresses cystic fibrosis with humor, friendship and sensitivity.

March 21, 2023
Interviews and testimonies

Testimonial: My adjustment disorder, CF special

A young adult living with cystic fibrosis shares her adjustment disorder, the anxiety associated with multiple diagnoses, and the importance of recognizing mental health as well as physical health.

February 1, 2023
Interviews and testimonies

Testimonial: Having a sick child

A mother's testimony frankly describing the exhaustion, emotional rollercoasters, and lack of support experienced when caring for a child with cystic fibrosis.

February 1, 2023

Thanks to Our Partners