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I would get an eFlow if your concern is time spent doing treatments and do both. The "certain type of mucus" is bunk as far as I know because it breaks down white blood cells in the mucus, which is present in every CFer as far as I know. eFlow info: <a target=_blank...

I would get an eFlow if your concern is time spent doing treatments and do both. The "certain type of mucus" is bunk as far as I know because it breaks down white blood cells in the mucus, which is present in every CFer as far as I know. eFlow info: <a target=_blank...

I would get an eFlow if your concern is time spent doing treatments and do both. The "certain type of mucus" is bunk as far as I know because it breaks down white blood cells in the mucus, which is present in every CFer as far as I know. eFlow info: <a target=_blank...

Did you call your insurance company to ask them if they cover it and at what percentage/co-pay? I should think they would have a better answer for your particular insurance than any of us not knowing what insurance you have. You can't just switch insurances because of one medication - that's not...

Did you call your insurance company to ask them if they cover it and at what percentage/co-pay? I should think they would have a better answer for your particular insurance than any of us not knowing what insurance you have. You can't just switch insurances because of one medication - that's not...

Did you call your insurance company to ask them if they cover it and at what percentage/co-pay? I should think they would have a better answer for your particular insurance than any of us not knowing what insurance you have. You can't just switch insurances because of one medication - that's not...

I doubt there is more than 1 accredited/certified CF center in the city, but if there is, they should both be good. Check the CF Foundation site for their center locations.

I doubt there is more than 1 accredited/certified CF center in the city, but if there is, they should both be good. Check the CF Foundation site for their center locations.

I doubt there is more than 1 accredited/certified CF center in the city, but if there is, they should both be good. Check the CF Foundation site for their center locations.

a) do a full-panel genetic blood test b) run him around like a wild animal outside before another sweat test Since sweat tests aren't 100% correct either way, might as well get the genetic test.

a) do a full-panel genetic blood test b) run him around like a wild animal outside before another sweat test Since sweat tests aren't 100% correct either way, might as well get the genetic test.

a) do a full-panel genetic blood test <br />b) run him around like a wild animal outside before another sweat test <br /> <br />Since sweat tests aren't 100% correct either way, might as well get the genetic test.

Now I remember: It's Doribax (doripenum) that makes that taste for me - same family: <a target=_blank class=ftalternatingbarlinklarge href="http://www.rxlist.com/doribax-drug.htm">http://www.rxlist.com/doribax-drug.htm</a>

Now I remember: It's Doribax (doripenum) that makes that taste for me - same family: <a target=_blank class=ftalternatingbarlinklarge href="http://www.rxlist.com/doribax-drug.htm">http://www.rxlist.com/doribax-drug.htm</a>

Now I remember: It's Doribax (doripenum) that makes that taste for me - same family: <a target=_blank class=ftalternatingbarlinklarge href="http://www.rxlist.com/doribax-drug.htm">http://www.rxlist.com/doribax-drug.htm</a>

My highest PFTs in over 3 years was on my 30 minutes post-Cayston PFT during the trial after 28 days on Cayston, which took me from about 31% to 38% in a month, but then I bombed on the next drug trial I tried and had to start my PFT build-up all over again. Expect it to go down on the off month...

My highest PFTs in over 3 years was on my 30 minutes post-Cayston PFT during the trial after 28 days on Cayston, which took me from about 31% to 38% in a month, but then I bombed on the next drug trial I tried and had to start my PFT build-up all over again. Expect it to go down on the off month...

My highest PFTs in over 3 years was on my 30 minutes post-Cayston PFT during the trial after 28 days on Cayston, which took me from about 31% to 38% in a month, but then I bombed on the next drug trial I tried and had to start my PFT build-up all over again. Expect it to go down on the off month...

Yes, IV meds have a tendency to affect things like that, but the oral would be the first thing I'd look at as a cause. I just can't remember which IV causes metallic taste, but I don't think it's Tobra because I'm on that one every time and we alternate second drugs and I don't get bad taste...

Yes, IV meds have a tendency to affect things like that, but the oral would be the first thing I'd look at as a cause. I just can't remember which IV causes metallic taste, but I don't think it's Tobra because I'm on that one every time and we alternate second drugs and I don't get bad taste...