The daily ponderings of Beth Peters as she writes about Cystic Fibrosis and lung trasnplant.
Saturday, August 7, 2010
Another Day... Another Procedure
In order to attempt to further reduce the amount of lymphatic fluid in CysticGal's pleural space (Chylothorax), today they are sending her down to radiology where they will place a small chest tube that can move around and drain out the extra fluid. I really hope this helps her. Don't forget your postcards!!
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Hello Cystic girl, came across your blog from another Fibro. Keep up the good work. You will be home soon enough and be able to enjoy those new lungs...every cfers dream :)
ReplyDeleteTake care froma fellow Fibro
thinking about you. much love and light to you. all of my best. ~juli
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