saveferris2009
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>LeneSouthAfrica</b></i>
I remember you posting on this topic some while back. This is very interesting. I am just curious, how on earth did you figure out this was the cause? Was it just trial and error with the Proton Pump Inhibitors (meds to reduce the stomach acid right?) or were you having other signs or symptoms related to aspirating, or is there a special test they do to diagnose this?
</end quote></div>
Being the obnoxious and aggressive CF patient that I am, I went to get a 2nd opinion at Stanford.
I was so lucky that the Dr. there was very up on the fact that many CFer's suffer from nocturnal aspiration of gastric juice and don't even know it. The only symptom they show is lower lung function (which most CF patients & docs chalk up to lung damage or infection).
He outlined a plan, and 1st on the plan was to increase my PPI dose. Luckily, it worked! <img src="i/expressions/face-icon-small-smile.gif" border="0">
<div class="FTQUOTE"><begin quote>
I don't suffer from night sweats while on IV's but I can say that most antibiotics (oral or IV) increases my heartburn from occasional to ongoing while on them, perhaps it could be that IV's aggravate your initial problem. Of course there could be hundreds of other causes too. Some side effects from IV's I have had are rashes, peeling skin, once my one pupil dilated...but no night sweats.
Either way, glad your resolved your problem.</end quote></div>
Thanks! Ya I'm trying to dig around to see if I might have worse heart burn, sugars, or just the meds giving me side effects.
thanks for the post <img src="i/expressions/face-icon-small-smile.gif" border="0">
I remember you posting on this topic some while back. This is very interesting. I am just curious, how on earth did you figure out this was the cause? Was it just trial and error with the Proton Pump Inhibitors (meds to reduce the stomach acid right?) or were you having other signs or symptoms related to aspirating, or is there a special test they do to diagnose this?
</end quote></div>
Being the obnoxious and aggressive CF patient that I am, I went to get a 2nd opinion at Stanford.
I was so lucky that the Dr. there was very up on the fact that many CFer's suffer from nocturnal aspiration of gastric juice and don't even know it. The only symptom they show is lower lung function (which most CF patients & docs chalk up to lung damage or infection).
He outlined a plan, and 1st on the plan was to increase my PPI dose. Luckily, it worked! <img src="i/expressions/face-icon-small-smile.gif" border="0">
<div class="FTQUOTE"><begin quote>
I don't suffer from night sweats while on IV's but I can say that most antibiotics (oral or IV) increases my heartburn from occasional to ongoing while on them, perhaps it could be that IV's aggravate your initial problem. Of course there could be hundreds of other causes too. Some side effects from IV's I have had are rashes, peeling skin, once my one pupil dilated...but no night sweats.
Either way, glad your resolved your problem.</end quote></div>
Thanks! Ya I'm trying to dig around to see if I might have worse heart burn, sugars, or just the meds giving me side effects.
thanks for the post <img src="i/expressions/face-icon-small-smile.gif" border="0">