CF Foundation | Emerging Genetic-Based Therapies for CF

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  • เผยแพร่เมื่อ 19 ต.ค. 2024

ความคิดเห็น • 17

  • @BellaThePomeranian
    @BellaThePomeranian 4 ปีที่แล้ว +3

    This is awesome, hope there would be a cure soon.

  • @flameboy2651
    @flameboy2651 ปีที่แล้ว

    「もっと多くの人が必要なので、このビデオをもっと

  • @maciejligus1689
    @maciejligus1689 4 ปีที่แล้ว +1

    Hi CFF, I wonder, many foundations have t-shirts, caps and other little things with their logo, that people can buy and support them this way. I couldn't find anything like this on your www page. Do you consider anything like this?

  • @user-tj8qs8oq7n
    @user-tj8qs8oq7n 2 ปีที่แล้ว

    video anda sangat bagus dan mempunyai mesej yang luas terima kasih

  • @zacharysbrennan5376
    @zacharysbrennan5376 5 หลายเดือนก่อน +1

    Still waiting 5/15/24...

  • @MuhammadAkbar-gj1we
    @MuhammadAkbar-gj1we 4 ปีที่แล้ว

    Awaited your response.

  • @ЛераСтарикова-к3ж
    @ЛераСтарикова-к3ж 2 ปีที่แล้ว

    how did you do it can you share with me , thank you

  • @mariazaman9398
    @mariazaman9398 ปีที่แล้ว

    How to contact with your Foundation.?

    • @CysticFibrosisFoundation
      @CysticFibrosisFoundation  ปีที่แล้ว

      Hi Maria,
      Thank you for your message. We encourage you to visit our website for more information: on.cff.org/3V6ebVj

  • @MuhammadAkbar-gj1we
    @MuhammadAkbar-gj1we 4 ปีที่แล้ว +1

    My third kids is suffering in cf. Is there any country have complete treatment.

    • @BellaThePomeranian
      @BellaThePomeranian 4 ปีที่แล้ว

      The United States of america

    • @CysticFibrosisFoundation
      @CysticFibrosisFoundation  4 ปีที่แล้ว +3

      Hi, Muhammad - While we've made incredible progress in moving our mission forward, there is no cure for cystic fibrosis. Because CF is unique to every individual with the disease, we encourage you to speak with your child's doctor or care team about finding the best treatment plan for your child.

  • @alexisfuhr1846
    @alexisfuhr1846 4 ปีที่แล้ว +1

    How can i come move involved with this

    • @CysticFibrosisFoundation
      @CysticFibrosisFoundation  4 ปีที่แล้ว +1

      Hi, Alexis - There are many ways to support and connect with people with CF and their family. We encourage to explore all the different ways you can get involved here: www.cff.org/Get-Involved/

    • @alexisfuhr1846
      @alexisfuhr1846 4 ปีที่แล้ว

      @@CysticFibrosisFoundation
      Do you any support group on Facebook cf

  • @colleenshaw3481
    @colleenshaw3481 2 วันที่ผ่านมา

    I hope they hurry!