<P>A friend of mine is a Pediatric Nurse Practicioner in a pediatrician practice and she recently gave me great advice I wanted to share. She suggested that I ask my pediatician for a copy of the letters that he receives from each specialist my DD goes to. It is amazing how much concise information that the specialist sends to the referring doctor. I don't think that the CF specialist tried to hide anything from me, but he clearly states her current diagnosis, medications, short term plan for exacerbations, short term plan for further testing, long term plan for treatment, and long term plan for testing. Maybe I am still so overwhelmed at these appointments that I don't "hear" all that is said, or maybe after the doctor goes to dictate his notes he summarizes it better. Maybe he just doesn't state the long term plan so I am not alarmed, but this summary is so beneficial for me. The summary also shows how much of my parent report was received and respected. I hope that helps others trying to do the best for their children. </P>
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<P>Through this letter I learned today that my DDs diagnosis is "mucus clearing disorder of unkown etiology". </P>
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<P>Through this letter I learned today that my DDs diagnosis is "mucus clearing disorder of unkown etiology". </P>