Guest guest Posted December 6, 2007 Report Share Posted December 6, 2007 The doctors have come through to look Barby over & are again saying that everything is going as well as they can go for a liver transplant patient. Her adema is slowly receding - starting with hands & arms & slowly receding downwars. The doctors expect that it should be mostly gone within the next week or so. Her pain is under control & considered routine. She is fully independent at this time....not requiring help to get out of bed, use the restroom, walk or wash her hair. I've pulled up a Christian praise music site & have had it playing all day in the background from the computer. Barby has really enjoyed it. We've enjoyed watching the snow from the sixth floor penthouse suite - that's what we call this room. It's a corner room with windows on each corner looking over a beautiful KC panorama reaching from downtown southwards to the Plaza....very pretty....especially shrouded in snow. The lights at night are pretty as well. Barby & I stood together & just looked at the lights for awhile this evening. Her apetite is growing. Another backup IV was removed. Soon they will remove the central line - her final tube. She began with over a dozen wires & lines potruding from her body & is now down to one. Her walks do not require assistance. We hold hands for pleasure rather than need! On our last walk we visited another liver patient who Barby knows through her online support group. He has been here in KC for almost two months. He lives in another region where livers are less redily available. Where he lived he could expect to wait for well over a year. By coming and living in KC, he only had to wait a few weeks. However, he had a problem duiring surgery & has had to have an extended hospital stay of over 1.5 mos. We are very thankful that Barby has had such a short and successful stay. Barby's cousin had a liver transplant several years ago & lost his first liver immediately and had to be retransplanted - along with multiple setbacks along the way. Please continue to bathe Barby's recovery in prayer. We appreciate it deeply and God obviously cares for the details of His children. The current plan is for Barby to leave KU Med Ctr tomorrow afternoon. We plan on eating dinner at home in Topeka. My mom will be coming over to fix dinner for us. Extra meals throughout the week are welcome. We can either freeze them or use them for that day's meal. Barby & I will return to KU Med Ctr on Monday & Thursday for the next two weeks. Then once a week for several months. After that, she can arrange to have labs drawn in Topeka, or on vacation, wherever we happen to be - for the rest of her life. KU Med Ctr will continue to monitor her labs & make any adjustments that are needed to protect her new liver. She has very few restrictions when she goes home. For the next four months Barby cannot lift more than 10#'s. She'll be restricted on any housework which requires lifting or pushing of any degree approaching the 10# limit. Persons with active infections & coughs should avoid her. However, her immune system will continue to gain strength and handle common viruses. The first few weeks she needs to avoid persons who are sick. As you pray, please remember that there is a family out there that is greeving the early loss of their child. Please pray for that family as well. Thanks! & Barby Quote Link to comment Share on other sites More sharing options...
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