A MONTH IN EUROPE WITH CYSTIC FIBROSIS | Chelsea Rose

Поделиться
HTML-код
  • Опубликовано: 17 окт 2024

Комментарии • 5

  • @hannahs3121
    @hannahs3121 7 лет назад +1

    To carry on living life and choosing how you want to spend your life shows how strong you are. Good for you girl, keep going and hold on to opportunities with both hands. I haven't got CF but I live with chronic illness and you have inspired me to not stay inside feeling sorry for myself and you have inspired me to keep going. Thank you so much 💜

  • @MsCrystal1980
    @MsCrystal1980 7 лет назад

    Wow!! That is awesome that you spent so much time in Europe. It is sometime I have always wanted to do and even though I don't have cf I have other invisible illness and for me I know it would be difficult traveling with TPN and fluids, but still want to find a way to travel the world. Just wondering did you go through a travel agent or how did you plan it all?

    • @paigemarie9307
      @paigemarie9307 7 лет назад

      You do all your breathing treatments with an eflow!? I'll have to talk to my docs about that. I still do mine with a regular compressor and they take forever!

  • @kattieanderson5809
    @kattieanderson5809 7 лет назад

    amazing!!!!

  • @richardleal1354
    @richardleal1354 7 лет назад

    What a great video so beautiful places thanks for sharing you did great at the end of the video I got a little teary haha 😊 don't let c.f. stop us