• Sí, exacto, tienes razón. G542X

    🙂

  • Hi, I don’t know about which is my main mutation, but the ones I have are dF508 and GX542.

    I was diagnosed with CF in 1995, when I was seven years old.

    I think the gx542 mutation is the rarest because there are less documentation about it in the Internet than the others.

  • Luisa Palazola and Profile picture of UlisesUlises are now friends 6 months ago

  • Ulises changed their profile picture 7 months, 1 week ago

  • Ulises posted a new activity comment 7 months, 1 week ago

    Hi! Thank you very much

  • Ulises posted a new activity comment 7 months, 1 week ago

    Hi Michael, I’ve been reading the CF posts from this site since a few months, and I really appreciate your work. Articles about treatments for CF give me hope (to me, my brother – with CF too – and my family).

    Thank you very much.

  • Ulises posted a new activity comment 7 months, 1 week ago

    Me atienden aquí mismo en el Hospital Universitario de Canarias. También hay una asociación que hace una labor excelente, la Fundación Oliver Mayor contra la Fibrosis Quística.

  • Ulises posted a new activity comment 7 months, 1 week ago

    Hola, muchas gracias! Poco a poco creo que lo conseguiré 🙂

    Enhorabuena por el foro, nos va a ser de mucha ayuda para todos.

    Together we are stronger!!!

    • Amen! Chamo — en los islas canarias, tienen una clinica de FQ o tienes que ir a Madrid?

      • Me atienden aquí mismo en el Hospital Universitario de Canarias. También hay una asociación que hace una labor excelente, la Fundación Oliver Mayor contra la Fibrosis Quística.

  • Ulises became a registered member 7 months, 1 week ago

    • Ulises – My name is Michael Morale, and I’m the Forums and Multimedia Director for Cystic Fibrosis News Today. I want to thank you for taking the time out of your day and becoming a member of our Cystic Fibrosis forum. Our job is to make sure that we provide you with the information that you’re looking for, and to try to assist you in any way p…[Read more]

      • Hi Michael, I’ve been reading the CF posts from this site since a few months, and I really appreciate your work. Articles about treatments for CF give me hope (to me, my brother – with CF too – and my family).

        Thank you very much.

    • Hi Ulises! My name is Tré LaRosa and I’m one of the Forum Moderators. Thanks for becoming a member! I’m excited about what this forum could become as a place for quality discussion and a welcoming place for the community. Looking forward to your contributions!

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