P
pencf
Guest
My daughter just started using Fortaz for inhalation. It tastes like crap but she does it, so I am thankful for that!
This morning is coughed up a bit of blood, emailed team right away. Since we were Just in for Annual Clinic 10 days ago, they know how we are doing overall, which is way better then where we were in the Fall. Everything looks good. Cultures good, just a few of usual things you dont' want, weight up 18pds, blood work, excellent compared to fall. And she feels good.
CF Team agrees, after calling specialist in U of PITT ( who really ordered the use of Fortaz) that sometime starting a new antibiotic in the airway will do that. Cause irritation.
Just want to hear from other folks who have used Fortaz for inhalation, how it is working for you, what type of side effects if anything, just what your experiences have been.
Thanks. I read a lot of what comes up in my emails. I think this community overall is positive and helpful. I appreciate each of your journey's, and just wish we would all get our prayers answered, and see a drug that will help our entire population with every mutation!!!
~Bethann
Mom of Patrick (20) no/CF, and Madeline (soon to be 17) w/ B. cepacia and PA, o2 at night, FEV1 30%
This morning is coughed up a bit of blood, emailed team right away. Since we were Just in for Annual Clinic 10 days ago, they know how we are doing overall, which is way better then where we were in the Fall. Everything looks good. Cultures good, just a few of usual things you dont' want, weight up 18pds, blood work, excellent compared to fall. And she feels good.
CF Team agrees, after calling specialist in U of PITT ( who really ordered the use of Fortaz) that sometime starting a new antibiotic in the airway will do that. Cause irritation.
Just want to hear from other folks who have used Fortaz for inhalation, how it is working for you, what type of side effects if anything, just what your experiences have been.
Thanks. I read a lot of what comes up in my emails. I think this community overall is positive and helpful. I appreciate each of your journey's, and just wish we would all get our prayers answered, and see a drug that will help our entire population with every mutation!!!
~Bethann
Mom of Patrick (20) no/CF, and Madeline (soon to be 17) w/ B. cepacia and PA, o2 at night, FEV1 30%