I just signed up for a blog, but it says it will be ready in 1-2 days so I'm going to put this here but it might be pretty long, SORRY!
Anyway, I am 26 and my FEV1 usually sits right at 70% (has been for years). In clinic in August just two months ago it was 69%. I caught a cold almost a month ago that the doctors first tried treating w/ 2 weeks of Levaquin and then when that didn't work we switched and did a week of Zithro and Prednisone. When I still didn't feel better I came in and my FEV1 was 52%. They have me on IV Tobra and Cefepime, but six days later my FEV1 is only up to 55%. I am starting to freak a little. I have never had to stay in for more than 5 days because my PFT's usually rebound enough for me to go home and finish IV's there. They will redo PFT's on Thursday, but if there is still no improvement they will switch antibiotics. I guess my question is has anyone had something similar happen and another drug was really effective? And have you recovered from this big of a drop in lung function? These 2 have always worked for me but I guess maybe it is time to switch. They said my culture didn't show resistance to either one but who knows!!
I guess I'm just really nervous because this is the lowest my PFT's have ever been, and they are not showing any improvement. Just a little scary and depressing. Any experiences anyone has had that they could share would be helpful. Thanks so much for reading!
Anyway, I am 26 and my FEV1 usually sits right at 70% (has been for years). In clinic in August just two months ago it was 69%. I caught a cold almost a month ago that the doctors first tried treating w/ 2 weeks of Levaquin and then when that didn't work we switched and did a week of Zithro and Prednisone. When I still didn't feel better I came in and my FEV1 was 52%. They have me on IV Tobra and Cefepime, but six days later my FEV1 is only up to 55%. I am starting to freak a little. I have never had to stay in for more than 5 days because my PFT's usually rebound enough for me to go home and finish IV's there. They will redo PFT's on Thursday, but if there is still no improvement they will switch antibiotics. I guess my question is has anyone had something similar happen and another drug was really effective? And have you recovered from this big of a drop in lung function? These 2 have always worked for me but I guess maybe it is time to switch. They said my culture didn't show resistance to either one but who knows!!
I guess I'm just really nervous because this is the lowest my PFT's have ever been, and they are not showing any improvement. Just a little scary and depressing. Any experiences anyone has had that they could share would be helpful. Thanks so much for reading!