Cystic Fibrosis Forum (EXP)

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Recent content by jfarel

  1. J

    coming up on 5 years

    I celebrated 9 years this past June. Am doing well!
  2. J

    coming up on 5 years

    Haven't posted in a while, but for those of you still waiting, keep hoping. I will be 5 years post this June and things have gone really well. I've been working fulltime, traveling and exploring new hobbies. I've also met my donor family on several occasions---which was amazing experience.
  3. J

    mycelex troche

    I think we take it forever. But I am not positive. I have been on for 14 months. Every day post transplant.
  4. J

    mycelex troche

    I think we take it forever. But I am not positive. I have been on for 14 months. Every day post transplant.
  5. J

    mycelex troche

    I think we take it forever. But I am not positive. I have been on for 14 months. Every day post transplant.
  6. J

    Scuba Diving and Transplant

    I have heard stories of people doing it, but off hand I do not know anyone.
  7. J

    Scuba Diving and Transplant

    I have heard stories of people doing it, but off hand I do not know anyone.
  8. J

    Scuba Diving and Transplant

    I have heard stories of people doing it, but off hand I do not know anyone.
  9. J

    What do you do for hemoptysis?

    I agree, adding ice or frozen veggies does seem to help. Before my transplant I would get bad bleeds from time to time, but taking ADEKS vitamins (Since they have a lot of K, for clotting) regularly, reduced the severity of the bleeding.
  10. J

    What do you do for hemoptysis?

    I agree, adding ice or frozen veggies does seem to help. Before my transplant I would get bad bleeds from time to time, but taking ADEKS vitamins (Since they have a lot of K, for clotting) regularly, reduced the severity of the bleeding.
  11. J

    What do you do for hemoptysis?

    I agree, adding ice or frozen veggies does seem to help. Before my transplant I would get bad bleeds from time to time, but taking ADEKS vitamins (Since they have a lot of K, for clotting) regularly, reduced the severity of the bleeding.
  12. J

    PFTs after transplant

    @ mCHRISTofSUBURB.. Mine Fev1 was similar to yours. I didn't even get mine measured until 3 or 4 weeks post tx. I had some minor issues and they didn't want me blowing hard for a few weeks. My first PFT was in the 40's. After that it continued to rise and now at 12 months post I am 85-95 percent.
  13. J

    PFTs after transplant

    @ mCHRISTofSUBURB.. Mine Fev1 was similar to yours. I didn't even get mine measured until 3 or 4 weeks post tx. I had some minor issues and they didn't want me blowing hard for a few weeks. My first PFT was in the 40's. After that it continued to rise and now at 12 months post I am 85-95 percent.
  14. J

    PFTs after transplant

    @ mCHRISTofSUBURB.. <br /> <br />Mine Fev1 was similar to yours. I didn't even get mine measured until 3 or 4 weeks post tx. I had some minor issues and they didn't want me blowing hard for a few weeks. My first PFT was in the 40's. After that it continued to rise and now at 12 months post I am...
  15. J

    Worried about resistance

    I agree with Anna, with CF, resistance is pretty par for the course. B. Cepacia, is really the only one that some transplant programs will refuse.
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