KrazyKat ~ I emailed Dr. Bishop about the cepacia issue with GSH and he said it is only theory. But he advised to do so with caution since they just dont know yet. I told him i was just using it orally and he said that shbouldnt be a problem. That was almost 5 years ago. Most of what i read about GSH was from people who were inhaling it and taking it orally. I wondered if it would benefit me if i tried it orally only and spoke to a few people who were using it orally only and decided to give it a try. It made a huge difference for me. Im not sure but ,maybe if i didnt have hemoptysis problems, i might be more apt to try inhaling it. But since i do have hemoptysis problems i will stick to taking it orally. I talked to my Doctor years ago about the theory of GSH causing the inflammation to go down and that being a problem and she had said to me in cf they want the inflammation to go down and that includes cepacia patients. She said if that were an issue they would never give cepacia patients steriods to reduce inflammation. Either way she recommended i never inhale it mainly because of my hemoptysis problems. There are however some petients with cepacia that do inhale it and are doing well. You may want to post on the Glutathine and cystic fibrosis message board and ask about it. My Best wishes <img src="i/expressions/face-icon-small-smile.gif" border="0">
<a target=_blank class=ftalternatingbarlinklarge href="http://members5.boardhost.com/CFGSH/
">http://members5.boardhost.com/CFGSH/
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://members5.boardhost.com/CFGSH/
">http://members5.boardhost.com/CFGSH/
</a>