Hi Amy,
We have had the same experience as Jessi and Debbi. Andrew has been on pulmozyme for I think three years now, and has never had what I would call amazing results. It was not until he went on hts this summer that I even realized he had mucus in his lungs to cough up. I asked if we could stop the pulmozyme, but his doc wants us to keep it for now.
We upped his hts from 3% to 7% in the hospital. Last Monday night he started coughing up blood, so clinic told us to stop the 7% and do no hts for awhile. His lungs were obviously not doing well with the 7% because he has not bled since. However, now that we are back to doing just the pulmozyme, I am noticing that he is not coughing anything up again, he's coughing and I can hear it in there, but he's not getting it up easily. I think this weekend I'm going to go ahead and start his 3% back up and see what happens.
So, for us, HTS definitely works better. I would be so interested to find out why pulmozyme seems so ineffective for some, but so helpful for others. This thread is a great one!
Keep us posted on how you are doing with it when it comes in. I hope you are able to feel a difference and regain some of your energy! Good luck, Amy!