Thank you all for you opinions/experience. I am still so unsure about nebs. We go back to the clinic tomorrow, so I'll bring it up again (I have read prior posts about Dr. Warwick and looked around on-line; which is another reason that I haven't been pushing pulmozyme). I religiously perform chest pt at least 2 times per day (and give him extra pats at burp time) but I of course want to do anything else to prolong Max's health/life. I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.
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Neb treatments
- Thread starter sdavis227
- Start date
Thank you all for you opinions/experience. I am still so unsure about nebs. We go back to the clinic tomorrow, so I'll bring it up again (I have read prior posts about Dr. Warwick and looked around on-line; which is another reason that I haven't been pushing pulmozyme). I religiously perform chest pt at least 2 times per day (and give him extra pats at burp time) but I of course want to do anything else to prolong Max's health/life. I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.
Thank you all for you opinions/experience. I am still so unsure about nebs. We go back to the clinic tomorrow, so I'll bring it up again (I have read prior posts about Dr. Warwick and looked around on-line; which is another reason that I haven't been pushing pulmozyme). I religiously perform chest pt at least 2 times per day (and give him extra pats at burp time) but I of course want to do anything else to prolong Max's health/life. I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.
Thank you all for you opinions/experience. I am still so unsure about nebs. We go back to the clinic tomorrow, so I'll bring it up again (I have read prior posts about Dr. Warwick and looked around on-line; which is another reason that I haven't been pushing pulmozyme). I religiously perform chest pt at least 2 times per day (and give him extra pats at burp time) but I of course want to do anything else to prolong Max's health/life. I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.
Thank you all for you opinions/experience. I am still so unsure about nebs. We go back to the clinic tomorrow, so I'll bring it up again (I have read prior posts about Dr. Warwick and looked around on-line; which is another reason that I haven't been pushing pulmozyme). I religiously perform chest pt at least 2 times per day (and give him extra pats at burp time) but I of course want to do anything else to prolong Max's health/life. I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.
Another concern I have on this is that since DS has been doing his CPT/Vest and meds since birth, it's like second nature to him. But whenever we do nebs, it's such a fight. I know that he'll fight me as he gets older anyways, but I think that if he did have that neb treatment more often, that he would just accept it like he does with other things.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
Another concern I have on this is that since DS has been doing his CPT/Vest and meds since birth, it's like second nature to him. But whenever we do nebs, it's such a fight. I know that he'll fight me as he gets older anyways, but I think that if he did have that neb treatment more often, that he would just accept it like he does with other things.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
Another concern I have on this is that since DS has been doing his CPT/Vest and meds since birth, it's like second nature to him. But whenever we do nebs, it's such a fight. I know that he'll fight me as he gets older anyways, but I think that if he did have that neb treatment more often, that he would just accept it like he does with other things.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
Another concern I have on this is that since DS has been doing his CPT/Vest and meds since birth, it's like second nature to him. But whenever we do nebs, it's such a fight. I know that he'll fight me as he gets older anyways, but I think that if he did have that neb treatment more often, that he would just accept it like he does with other things.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
Thank you everyone for all your opinions and stating what your children are on.
Another concern I have on this is that since DS has been doing his CPT/Vest and meds since birth, it's like second nature to him. But whenever we do nebs, it's such a fight. I know that he'll fight me as he gets older anyways, but I think that if he did have that neb treatment more often, that he would just accept it like he does with other things.
<br />
<br />It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
<br />
<br />Thank you everyone for all your opinions and stating what your children are on.
<br />
<br />It's definitely something I'll bring up in clinic, I'm still not sure how hard to push, though.
<br />
<br />Thank you everyone for all your opinions and stating what your children are on.
MargaritaChic
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Mom2Max</b></i>
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote></div>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote></div>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
MargaritaChic
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Mom2Max</b></i>
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote></div>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote></div>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
MargaritaChic
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Mom2Max</b></i>
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote></div>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote></div>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
MargaritaChic
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Mom2Max</b></i>
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote>
I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
MargaritaChic
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Mom2Max</b></i>
<br />
<br />I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote>
<br />
<br />I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
<br />
<br />I wish that it was much more clear cut but what I wish for most of all is that my beautiful baby boy didn't have cf.</end quote>
<br />
<br />I think this is a wish that we all share! <img src="i/expressions/heart.gif" border="0">
grassisgreener
New member
Definately with you on that wish too!
BTW, your boys are gorgeous!
BTW, your boys are gorgeous!
grassisgreener
New member
Definately with you on that wish too!
BTW, your boys are gorgeous!
BTW, your boys are gorgeous!
grassisgreener
New member
Definately with you on that wish too!
BTW, your boys are gorgeous!
BTW, your boys are gorgeous!
grassisgreener
New member
Definately with you on that wish too!
BTW, your boys are gorgeous!
BTW, your boys are gorgeous!
grassisgreener
New member
Definately with you on that wish too!
<br />
<br />BTW, your boys are gorgeous!
<br />
<br />BTW, your boys are gorgeous!