Wednesday, December 10, 2014
Down but Not Out
My initial reaction was total frustration, and I had trouble keeping back the tears. I have worked so hard the past six months, and it is so hard to not see it pay off in the numbers. Just like I mentioned in my last post, I keep reminding myself that it's truly how I feel that matters.
When the doctor came in, we discussed how I've been feeling congested and how the weather changes seem to make it worse. She was concerned about the drop in lung function and asked a lot of questions about how I've been feeling, how I've been doing with my treatments, and how I'm doing all that I'm doing and still having time to sleep at night. After all of that, she decided to put me on an antibiotic for two weeks. I'll be doing a follow up PFT the week after Christmas. If we don't see some positive movement, I will probably have to get a PICC line. It's been two years since I've had to be on IV antibiotics, and I am not a fan. You better believe that I will be doing everything in my power these next few weeks to knock this in the butt.
Something that my doctor said today, really stuck with me though. She was telling me not to get too frustrated and not to let this stop all of my hard work. She pointed out that this is the nature of cystic fibrosis. You can do everything right, but sometimes, the bacteria growing in your lungs gets a little out of control, and we have to do something to push it back down. CF is a disease that does not care how hard you are working or how much you want to see improvement. It's unfair, and it's difficult, but it's the card I have been dealt. So that is where I am at right now. I'm working to push my bacteria back down so that my hard work can start showing again.
I have faith that this will work and that things will start looking up again. All I know is that I'm not giving up, and I am going to be pushing myself even harder.