Pulmozyme

[anonymous]

Just curious when you all do your Pulmozyme treatment. My daughter started a few months ago (she is only 5) to be proactive with her CF because she hasn't had many problems and we want to stay on top of things. I have noticed a difference and she is doing even better than before, but I am just wondering if there is a difference between morning and night treatments.

Thanks!!<img src="i/expressions/rose.gif" border="0">

 

[Emily65Roses]

I don't know if there's any difference, but I've always done mine at night before I go to bed.

 

[anonymous]

my boyfriend does his Pulmozyme twice a day. It used to be once daily until a year ago when the doc recommended twice daily therapy. So he does it with his vest treatments... anyone else?

~L~

 

[anonymous]

Thank you for replying! I had one mother tell me that it is better to do in the morning but I keep forgetting to ask my daughter's doctor because I have so many other questions.
All other replys are also welcomed!

 

[anonymous]

We do it 2x a day with CPT but our cf doc said to do it in the morning after her xopenex/intal so that way when she is up and moving it will loosen the mucus up thru out the day

 

[anonymous]

My 4 year old son always does his pulmozyme in the morning, right after his first breathing treatment with his vest.

 

[anonymous]

my son did it 2 x day but now does something else similar to pulmozyne but he did it oen in morning and one at night before bed . The new one I do just before the vest each time.

 

[kathiel]

Our doc said do in morning because it helps to loosen the mucous that accumulated during the night. I was doing it at night, but the doc said that it was not doing the best it could being given at night.
kathie

 

[NoDayButToday]

Q]I was doing it at night, but the doc said that it was not doing the best it could being given at night. <hr></blockquote>


Kathie, do you and Samantha both have CF?

 

[kathiel]

no just Samantha. But, I provide 99% of her care because her biological father has nothing to with her and my husband works so I can stay home with her. I have many of the symptoms, but i am only a carrier, but caring for samantha as much as i do sometimes makes me feel as though i do have just because i suffer with her.

 

[CFTEENAGERAKADAVID]

I do mine at night

 

[cfgirl2008]

I do mine about an hour or two before I go to bed.


Tiffany 15 w/cf

 

[NoDayButToday]

I do Pulmozyme 2x/day, monring and night

 

[NoDayButToday]

I do Pulmozyme 2x/day, monring and night

 

[Anonymous1]

I do calebs pulmozyme at night after he falls asleep. i feel he gets all of it that way. durring the day he fights me doing it and keeps pulling the mask off. so after he goes to sleep i put the mask on him and do it that way, so i know he is getting it all.. its expensive stuff, so i dont want any to go to waste <img src="i/expressions/face-icon-small-tongue.gif" border="0">




melissa mom to dylan 6 no cf and caleb 4cf