It's not over.
After the doctor declared Anna's lungs clear during the appointment on Tuesday, I still had questions. Was it a virus? Could all of her coughing be from post-nasal drip? Probably, was the answer. Could be, was the other answer. We were told to check in with them on Friday to report how she was doing.
By Friday her nose had dried up somewhat, but her cough had gotten worse, especially at night. So, that is what I reported to the CF nurse. She called me back hours later with another antibiotic prescription- 14 days worth. But if it is a virus, why are we giving her another antibiotic? Well, says the nurse, she should have started getting better by now. Is the throat culture back from the lab? Not yet, was the answer. But, she continued, it might be that the staph that showed up on the January culture may be acting up. What staph? I don't have any recollection of staph being mentioned at all. Neither does Steve.
I am very confused and now also alarmed. What is going on inside my little girl's body? What is lurking in her airways? Are they sure they are looking at the right patient chart? Why didn't we wait to see what the throat culture showed? Wasn't the reason for getting the throat culture to better pick a medicine to fight the specific offender? Could it be allergies? Why is she still coughing?
Saturday, April 7, 2012
Tuesday, April 3, 2012
After the appointment
It's good news!! The doctor detected no problems in her lungs- they were completely clear! How can this be possible when she has that horrible cough? I am so surprised and so grateful. Once the doctor determined that her lungs were clear it is like he dismissed the cold completely... so should I also dismiss my fears? I will say that I feel so much relief. He said she probably has a virus (why she did not respond to the antibiotic) and it will run its course. We are to keep up the extra therapy treatments to help her keep it loose. Also we got a nasal spray to help with the runny nose.
Thank you for all who have been concerned and have added Anna to your prayers. We are so appreciative. I wonder if it hasn't been those very prayers that have brought us to the good results that we got today. Please continue to keep her in prayer as she faces the challenges of her CF.
Thank you for all who have been concerned and have added Anna to your prayers. We are so appreciative. I wonder if it hasn't been those very prayers that have brought us to the good results that we got today. Please continue to keep her in prayer as she faces the challenges of her CF.
Anna Update
We went through her first round of antibiotics. It did nothing. Her nose is running like a fountain and her cough has become so bad that it shakes her whole little body. I had so hoped, believed, that this antibiotic would help her... and I am so disappointed. And now I am starting to get scared. I am trying to keep my emotions in check, one day at a time right? I know that because of her cystic fibrosis, that we will probably be facing many instances like this, and that I ought to buckle down, face it, and be brave- but my heart still grieves and my mother-worry is on overload.
We have an appointment this afternoon at the CF clinic. They will listen to her lungs, check her blood-oxygen levels, and do a throat culture. Then they will decide what the next step will be...
We have an appointment this afternoon at the CF clinic. They will listen to her lungs, check her blood-oxygen levels, and do a throat culture. Then they will decide what the next step will be...
Thursday, March 29, 2012
Prayers, please.
We have been blessed the past 3 months to have no issues. Last Sunday, Anna suddenly developed chest congestion with a wet and heavy cough. We have upped her therapy and today she started an antibiotic. She is not eating well either. Needless to say we are worried and asking that you please pray she get over this quickly. .
Wednesday, March 21, 2012
She’s outside and I am going crazy.
It has been a beautiful and early spring but having Anna
outside and playing causes me so much worry.
It is in the dirt and mud and water, I am told, that the evil “pseudos”
lurk, waiting for a chance to invade her lungs. How does one avoid these things
that will make her sick for the rest of her life?
Every time she falls I want to wash her hands. I want to
yank her fingers out of her mouth as she chews on them. I want to strap her in
a stroller and never let her out. I want
to slather her in hands sanitizer…..
I want her to be happy. I want her to play. I want to see
her curls bounce in the sunlight. I want
her to bounce the ball she loves so much.
I want her to live… for a long time.
Tuesday, February 21, 2012
Update
I just wanted to pass on that Anna is eating better these last few days. I was so happy the first night that she decided to eat that I almost jumped up and down. I thought maybe it was just a fluke but she ate better the next meal and the next. I had put into practice some of the suggestions that the nurse and nutritionist had made, plus Anna had also at the same time worked through her constipation. Anyway, I am very grateful to have her eating better (though she still throws a good deal of food!)
Friday, February 17, 2012
Anna
I am beside myself.
Anna has decided that she no longer likes food. It started about two or
three weeks ago and has gradually gotten worse. Now at a meal she regularly
hits the food off the spoon as it is offered to her. She won’t try anything
that is put on the tray. Foods she once liked she won’t open her mouth for. And
forget trying anything new. When I have
tried that she will scream in her chair- often through the entire mealtime.
Now, I know this sounds like a typical toddler- and I suppose
that it is a common behavior for this age, but I have had four other children
and I am sure that none of them took it as far as Anna has. So, she will grow
out of it, right? Perhaps. But in the meantime her weight will probably drop
and then what will we do? See, people with CF have difficulty absorbing fats
and protein and that is why we have to give her pancreatic enzymes with every
food containing fat. And we are
encouraged to give her a lot of extra
fat and calories- heavy cream, butter, oils etc. If she is not eating, where is she going to
get the calories that she needs to maintain her weight? How many enzymes do you
give if she takes three bites an entire meal? If you give her too much enzymes
then she will have problems moving her bowels.
And that causes her to be uncomfortable and even have pain.
I called the nurse today and also talked to the nutritionist
on her CF team. They each had
suggestions. I still feel confused… and very worried.
Subscribe to:
Posts (Atom)