21 days of IVs done

I did 2 weeks of IV Zosyn and was still not back to baseline. My lung functions had dropped from 35% at the beginning go IVs to 31% at the 2 week mark. We decided to do another week hoping to get over the hump. IV Zosyn is a bit daunting at every 6 hours but I manage. It wears me out to say the least. I sleep at every chance I get. I am able to “bump” my doses an hour either way which helps me get a little more sleep at one time. I’ve mastered it over the last few decades. At the end of 21 days/3 weeks my lung functions hadn’t come back up to where they were when I started IVs. I was at 32% at the end of IVs. With all that said, I am feeling better for the most part. I am however coughing a little more and coughing more up. I say better out than in! So it’s a good thing.

We had talked about putting me inpatient for IV colistin which was the one that messes with my kidneys and sent me into acute kidney failure a few years ago. That being said that is the reason they want me in the hospital for it because they would want labs everyday and be at the ready for extra IV fluids if needed. We decided against that for now. I may have to revisit that in the future when I get sick the next time (have a CF exacerbation). Yes, I say WHEN because it’s inevitable…it’s life with CF. I have another chest x-ray on February 16th to see if the pneumonia is gone. Hoping it is. If it’s not we will have to revisit IVs again I’m sure.

I barely made it through January emotionally speaking. This year my mom’s passing anniversary was harder for some reason. I found myself in bed more. Being sick on top of it didn’t not help either. I hope I’m coming out the other side of it now. My birthday is Monday which I always celebrate gladly unlike others. haha. I love getting older! Every birthday is a great milestone in my life. Especially since I am now past the “life expectancy” for CFers. I am always happy I made it another year. I might post on my birthday, I might not. Just depends on how nostalgic I am feeling…haha.

Until next time…

Hawaii

Well I survived the trip…hahaha.  I had a great time with my family and celebrating my great uncles 90th birthday.  We went to 7 or 8 beaches, I lost count.   Another one of my must haves when in Hawaii is shave ice, we got shaved ice 5 times, yummy!  No it is not a snow cone…it’s completely different.  It is shaved ice from an ice block, not ice pellets.  Anyway that is your Hawaiian lesson for the day…haha. Continue reading

Impromptu CF clinic appointment

Saturday will be 14 days of IVs so I called my nurse to let her know how I am feeling.  I am still having the pain in my lower right side (just at the bottom of my ribs) that has been there for a few weeks.  I’m convinced that my right lung has it out for me.  It seems to be where most of my infection is, I fracture ribs from coughing on that side and I also get random pains on that side.  Maybe it’s my special party trick. Continue reading

1 week follow up on chest x-ray

Wednesday I had a chest x-ray to check the progress of the upper right lobe where I was having the slight pain, which is where the x-ray showed the atelectasis (air trapping).  My x-ray was unchanged.  The prednisone didn’t do much if anything for the atelectasis.  The next step is a chest CT.  I am scheduled for the CT Thursday the 17th.  After they get the results from the CT we will then figure out what the next step will be and if there needs to be.  The atelectasis could simply be more shadowing and not as prominent as it appears which the CT will give us a more definite answer. Continue reading