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My name is and I am the mother of Lexie, almost 9, with CF.

She takes TOBI, vest therapy twice a day, albuterol and cromolyn

twice a day, Sporanox, Zantac, Zyrtec, and of course enzymes

(Lipram). I think I am still in denial about her CF sometimes, but

after reading this board I am getting a huge wake-up call. I just

wish we could be normal -- not having to take machines

everywhere, " have you taken your enzymes " , etc., etc. Lexie actually

does very well, although it seems like when she is off TOBI for 28

days she gets a cold or something. I am a medical transcriptionist

who works at home so at least I am here with her. I guess I am just

feeling overwhelmed like everyone else and need to vent to people who

might understand. Non-CF parents try, but they don't really know. I

guess because for the most part I try to be cheery about everything.

I am rambling. I just want to introduce myself and become a part of

the board.

-- Findlay, Illinois

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