I"m really concerned about Mark right now. It's been a tough 6 weeks for us, I got sick first then two the boys, then Mark then Cassie. We were all on the mend about 2 weeks later and then the kids got sick again, the Mark and then me. Ryland is on ear infection #5 (I don't think they've ever really cleared up) and Tristan is on ear infection #2.
I am finally feeling better, as are all the kids. However Mark still has this really nasty awful cough.
He normally coughs a fair amount, usually having a lot of sputum to spit out. However, he is coughing more, louder and for longer stretches and told me tonight that he is having a hard time catching his breath. The cough actaully makes me cringe because of how it sounds (sounds like it must hurt a lot!)
He saw a non CF doctor a few weeks ago and was given Cipro because he was culturing Pseudo. and Staph (normal for him)
He's scheduled for the CF clinic on the 11th of Feb and we can't get in before that.... What do you recommend we do. I've suggested to him we go see the doctor, but he keeps saying they aren't going to do anything for him and it's a waste of time.
I'm feeling a little frustrated that he doesn't want to take any action, but I'm also worried about him and wonder if you all have any suggestions? He is using his albuterol a lot more too (puffer, not nebulizer).
Thanks....
I am finally feeling better, as are all the kids. However Mark still has this really nasty awful cough.
He normally coughs a fair amount, usually having a lot of sputum to spit out. However, he is coughing more, louder and for longer stretches and told me tonight that he is having a hard time catching his breath. The cough actaully makes me cringe because of how it sounds (sounds like it must hurt a lot!)
He saw a non CF doctor a few weeks ago and was given Cipro because he was culturing Pseudo. and Staph (normal for him)
He's scheduled for the CF clinic on the 11th of Feb and we can't get in before that.... What do you recommend we do. I've suggested to him we go see the doctor, but he keeps saying they aren't going to do anything for him and it's a waste of time.
I'm feeling a little frustrated that he doesn't want to take any action, but I'm also worried about him and wonder if you all have any suggestions? He is using his albuterol a lot more too (puffer, not nebulizer).
Thanks....