Cystic Fibrosis Forum (EXP)

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  1. C

    Hmmm...cold Tobi

    I know pulmozyme is ok at room temp for like 24 hours as long as it doesn't get cloudy so you can leave that out to warm up. I don't know about tobi. I use the eflow tobra stuff. They assume you know how to use it and don't include info every delivery. I used 7% HTS without any problem for...
  2. C

    Hmmm...cold Tobi

    I know pulmozyme is ok at room temp for like 24 hours as long as it doesn't get cloudy so you can leave that out to warm up. I don't know about tobi. I use the eflow tobra stuff. They assume you know how to use it and don't include info every delivery. I used 7% HTS without any problem for...
  3. C

    Hmmm...cold Tobi

    I know pulmozyme is ok at room temp for like 24 hours as long as it doesn't get cloudy so you can leave that out to warm up. I don't know about tobi. I use the eflow tobra stuff. They assume you know how to use it and don't include info every delivery. I used 7% HTS without any problem for...
  4. C

    Hmmm...cold Tobi

    I know pulmozyme is ok at room temp for like 24 hours as long as it doesn't get cloudy so you can leave that out to warm up. I don't know about tobi. I use the eflow tobra stuff. They assume you know how to use it and don't include info every delivery. I used 7% HTS without any problem for...
  5. C

    Hmmm...cold Tobi

    I know pulmozyme is ok at room temp for like 24 hours as long as it doesn't get cloudy so you can leave that out to warm up. I don't know about tobi. I use the eflow tobra stuff. They assume you know how to use it and don't include info every delivery. <br /> <br />I used 7% HTS without any...
  6. C

    eflow and Hypertonic Saline?

    I do 7% in my eflow and have for awhile now. I've found that if I mix my xopenex in with the HTS I feel ok, and then I don't have to do two separate nebs. It does hurt my throat, though, so I sip on water throughout the treatment. One problem I've noticed is that the HTS gunks up the metal...
  7. C

    eflow and Hypertonic Saline?

    I do 7% in my eflow and have for awhile now. I've found that if I mix my xopenex in with the HTS I feel ok, and then I don't have to do two separate nebs. It does hurt my throat, though, so I sip on water throughout the treatment. One problem I've noticed is that the HTS gunks up the metal...
  8. C

    eflow and Hypertonic Saline?

    I do 7% in my eflow and have for awhile now. I've found that if I mix my xopenex in with the HTS I feel ok, and then I don't have to do two separate nebs. It does hurt my throat, though, so I sip on water throughout the treatment. One problem I've noticed is that the HTS gunks up the metal...
  9. C

    eflow and Hypertonic Saline?

    I do 7% in my eflow and have for awhile now. I've found that if I mix my xopenex in with the HTS I feel ok, and then I don't have to do two separate nebs. It does hurt my throat, though, so I sip on water throughout the treatment. One problem I've noticed is that the HTS gunks up the metal...
  10. C

    eflow and Hypertonic Saline?

    I do 7% in my eflow and have for awhile now. I've found that if I mix my xopenex in with the HTS I feel ok, and then I don't have to do two separate nebs. It does hurt my throat, though, so I sip on water throughout the treatment. One problem I've noticed is that the HTS gunks up the metal...
  11. C

    nasal /head colds and loss in fev1

    It's not uncommon for a head cold to turn into a chest cold for me. The lower my baseline FEV1 gets, the more effect a head cold seems to have on my FEV1 (aka it's more likely to spiral into something serious over a couple weeks)
  12. C

    nasal /head colds and loss in fev1

    It's not uncommon for a head cold to turn into a chest cold for me. The lower my baseline FEV1 gets, the more effect a head cold seems to have on my FEV1 (aka it's more likely to spiral into something serious over a couple weeks)
  13. C

    nasal /head colds and loss in fev1

    It's not uncommon for a head cold to turn into a chest cold for me. The lower my baseline FEV1 gets, the more effect a head cold seems to have on my FEV1 (aka it's more likely to spiral into something serious over a couple weeks)
  14. C

    nasal /head colds and loss in fev1

    It's not uncommon for a head cold to turn into a chest cold for me. The lower my baseline FEV1 gets, the more effect a head cold seems to have on my FEV1 (aka it's more likely to spiral into something serious over a couple weeks)
  15. C

    nasal /head colds and loss in fev1

    It's not uncommon for a head cold to turn into a chest cold for me. The lower my baseline FEV1 gets, the more effect a head cold seems to have on my FEV1 (aka it's more likely to spiral into something serious over a couple weeks)
  16. C

    College and Cystic Fibrosis

    I would totally recommend living on campus. I don't know how your parents are, but my being 5 hours away and having to get myself to the doctor, pick up meds, and set my own treatment schedule was pretty much the only thing that got my parents let me have some control over my CF. Also, it's a...
  17. C

    College and Cystic Fibrosis

    I would totally recommend living on campus. I don't know how your parents are, but my being 5 hours away and having to get myself to the doctor, pick up meds, and set my own treatment schedule was pretty much the only thing that got my parents let me have some control over my CF. Also, it's a...
  18. C

    College and Cystic Fibrosis

    I would totally recommend living on campus. I don't know how your parents are, but my being 5 hours away and having to get myself to the doctor, pick up meds, and set my own treatment schedule was pretty much the only thing that got my parents let me have some control over my CF. Also, it's a...
  19. C

    College and Cystic Fibrosis

    I would totally recommend living on campus. I don't know how your parents are, but my being 5 hours away and having to get myself to the doctor, pick up meds, and set my own treatment schedule was pretty much the only thing that got my parents let me have some control over my CF. Also, it's a...
  20. C

    College and Cystic Fibrosis

    I would totally recommend living on campus. I don't know how your parents are, but my being 5 hours away and having to get myself to the doctor, pick up meds, and set my own treatment schedule was pretty much the only thing that got my parents let me have some control over my CF. Also, it's a...
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