Cystic Fibrosis Forum (EXP)

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Recent content by kadomnik

  1. K

    does anyone do this?

    my daughter Kylie,7 does both HTS 7% and pulmozyme. The HTS is done morning and night. And the pulmozyme night. If we increase her treatments for any reason we always add the HTS. She started using HTS 2 years ago and it did take her awhile to get used to it. I think it really helps a lot.
  2. K

    does anyone do this?

    my daughter Kylie,7 does both HTS 7% and pulmozyme. The HTS is done morning and night. And the pulmozyme night. If we increase her treatments for any reason we always add the HTS. She started using HTS 2 years ago and it did take her awhile to get used to it. I think it really helps a lot.
  3. K

    does anyone do this?

    my daughter Kylie,7 does both HTS 7% and pulmozyme. The HTS is done morning and night. And the pulmozyme night. If we increase her treatments for any reason we always add the HTS. She started using HTS 2 years ago and it did take her awhile to get used to it. I think it really helps a lot.
  4. K

    does anyone do this?

    my daughter Kylie,7 does both HTS 7% and pulmozyme. The HTS is done morning and night. And the pulmozyme night. If we increase her treatments for any reason we always add the HTS. She started using HTS 2 years ago and it did take her awhile to get used to it. I think it really helps a lot.
  5. K

    does anyone do this?

    my daughter Kylie,7 does both HTS 7% and pulmozyme. The HTS is done morning and night. And the pulmozyme night. If we increase her treatments for any reason we always add the HTS. She started using HTS 2 years ago and it did take her awhile to get used to it. I think it really helps a lot.
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