Well I am back from the hospital. My doctor had got me to agree to a week in the hospital. Then to see how I felt about stopping treatment. Well the doctors in the hospital didn't want me to go home today. My pfts were the same as they were a week ago. But my mom and my cf doctors assistant pointed out I was getting the wrong version of ultrase which I had no clue pancreas and ultrase were different. Then they weren't sending me ensures daily and yesterday they told me that the IV they had me on this past week I was resistant to it. So that whole week was a waste.

It was called zycom(spelling?). But today I just wanted to go home on IV antibiotics but the doctors at Emory didn't want that. So it frustrate me I don't like Emory you don't get physical therapists like at the CF center and sottish rite. So all that just made me go ahead and leave. So I am home now, I feel a little better from taking the effexor but I can't say how I really feel for sure.

welcome home

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~ Diane 44 / cf / diabetes / b.cepacia

Glad you're home, but now what?

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**terri--grannie to Kaylee, 6 w/cf, and Jaykub, 10 wo/cf

OK, What's the next move for you? joni

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Joni 58 y/o f w c/f Married 19 years, Mother of 4 sons, Mima to a 3 y/o grandson & another grandson on the way !!

Hi Snowcone, Did you get the opportunity to discuss your desires with the doctors and make them known to your family? ~Juliet

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44 w/ CF, DX @ 43. Married, 1 daughter. Engineer. Hobbies: Beadmaking, Sailing, Knitting, Corvette Restoration.