Wednesday, March 11, 2009

update on david

Hey everyone I have not been here in a little while so I thought that I would stop by and talk with you all for a min. Im sick at this time and have been put on cipro and im being watched by the dr s in wi However at this time the cf floor does not have a bed for me so no tune up for me this month ... However im going to have a tune up this june for sure and if I get worse before then or the cipro just does not work then ill have to go in  sooner but as it stands right now im waiting for a bed in june. My pfts are down by 5 percent and my weitght is down by 3 lb and my nose is swallon as well so were going to keep an eye on thangs for awile.. Im going to stay on all the meds that I was taking and will add cipro for now and then admit in june I can say that they were ready to admit me if they did have a bed but they were full and had turned others away as well so I was not the only one this time... My left lung hurts some but thats norm when you have a infection well ill  keep you all updated talk with you all very soon

david

Monday, February 16, 2009

waiting results from CT

Hey everyone this is david just wanted to let you all know that tuesday ill be hearing the results of the ct scan of my stomach were hoping that they do somthing with the stones and that there is not over 100 this time that would be only  hope by the way well got to run have a wonderful day and friends stay warm its cold today

david

Tuesday, February 10, 2009

ct scan in the afternoon tommarow

ct scan will be at 1:00pm tommarrow ill let you all know as soon as i get the results they are looking for more kidney stones and to see what they would like to do next with this issue due to my cystic fibrosis kidney stone condion ill talk with you all soon

david 

Ct scan tommarrow

http://cfpenpals.blogspot.com/

Monday, February 9, 2009

support group introduction

Welcome to the cystic fibrosis pen pal club and support group. My name is David and im the founder of this group. Im 33 years old and I live in mn.This group is to give support to anyone needing information about cystic fibrosis including those that have cf as well.I also run the cystic fibrosis hotline that is open 24 hr a day 7 days a week . That number is 612-282-1211 or 612-331-0152 please fill free to call any time. This group is open to all but I do ask that there be no swearing here please . Hope that you injoy this web page as much as I do. Have a wonderful new year 08 The qustion was brought to my attition. Am I a cystic fibrosis patient ? The answer is Yes. I also have many family members with cystic fibrosis as well