Monday, April 12, 2004

my whole athsma story gets shittier:
i now have to use a peak meter to gauge the flow of my breathing capacity three times a day and record the data in a little graph book for months so we can see if there's a pattern. when i'm feeling unable to breathe, that is. i was also strongly encouraged to keep a diary of the things i do everyday like exercise, how much, what kind, work, exposure to cold air, rain, dust, bugs, whatever so we can check the activities against the graph info, AND keep a little tabulature somewhere of how many times i use my different inhalers so i can have an idea of how empty the canisters are so that i can get my prescriptions refilled before they run out. whoa nelly! i'm suddenly feeling really frail. my doctor assigned me these tasks and i guess i just sort of google eyed him because he then explained that plenty of people my age still die from not taking athsma seriously. now everytime i feel a rattle in my chest i feel like i'm about to go into a victorian swoon, like my dress is cinched up too tightly. I have to admit though, after a couple of days of recording my breathing strength, it is interesting to see how different times of the day are the same everyday, and yet so different from other times, AND YET I DON'T FEEL ANY DIFFERENT! oh, and if anyone knows how to get around the albuterol shakes, please please please let me know: ohthedrama2003@yahoo.com

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