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I went from bad to worse. At UNM in Albuquerque
they diagnosed me with CYSTIC FIBROSIS. I had to stay there right away.
Mom and I "dead asleep" ~ exhausted by all the tests and diagnoses...
Here they took a CT of my lungs.
Home at last. The inhaling is my daily routine from now on for the rest of my life
!
From now on I have to visit the Hospital every 3 month.
I don't like taking the throat-culture. But it is a MUST for every 3 month, to check
if I caught a bad "bug". In September 2004 they unfortunately found out, that I'm MRSA and Pseudomonas pos.
I absolutely hate getting blood drawn....
Twice a year they take a x-ray picture of my lungs.
When my coughing is getting worse and I don't gain
weight, I have to get admit to the hospitel for a "Tune up" (Antibiotic IV)
I have to do a lot of treatment daily to feel better (Inhaling and "The Vest")
In October 2005 I had a "Liverbiopsy". Unfortunatly they found out,
that I have Liverzirrhoses and I need a new liver :(
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