Guest guest Posted February 11, 2008 Report Share Posted February 11, 2008 Prior to my last bronch I asked the nurse to move the IV tubing in front of me. I was determined to watch him push that wonderful cocktail into the line so I could "see" the moment it hit me........Yeah right, NOT, LOL, What I saw, when it was over, was the pulmo's face as me told me "get your butt off the table, I've got patients waiting". Cool Guy. I've described him as an "arrogant little bugger, and I really like him". He's done the lavage with every bronch......like 6 or 7 times maybe. This is done at Providence in Anchorage. (which is a great facility BTW) They have a very clever method of billing for this procedure. They bill my insurance as if it were 2 separate procedures.....one for lavage and one for collecting samples, when in fact what he does is squirts in the saline then sucks it back up. Thankfully insurance pays both $1250.00 procedures. We're in the wrong business.......well, maybe not. Speaking of which, Friday the 15th is my last day, I'm retiring after 22 years. Should improve not only the way I feel but my attitude, too. Everyone asks "what are you going to do?" My favorite answer is ......"sit in my recliner and breath". jim IPF 05 alaskaPeggy wrote: One more thing about the bronc. as they were ready to give me that wonderful sleep stuff, I told the Dr. I would like a face lift and a boob job while he had me out.. he just said put her out.. lol.Love and Prayers, Peggyipf 6/04Worry looks around.Sorry looks back,Faith looks up.I'm surprised I haven't heard more here having bronchoscopy lavage.Its widely listed as a method of diagnosis but sure was nevermentioned to me as a choice.>> Jumping into the middle of this....>> My PF was diagnosed using CT scan, PFT's, 6 min. walk-test, and a> bronchoscopy lavage, outpatient.> I'm told that the samples from this are often too small to give a> clear picture to the pathologist, but mine were apparently large> enough as they could tell from the samples that I have PF.>> So, in my case, especially having auto-immune diseases, the less> invasive procedure made sense. I went in at 7:30 a.m. and went home> late afternoon and had no problems at all.> However, I'm not an otherwise healthy person, so the VATS may be the> best answer for some. I personally don't think digging into a sick> persons lungs is a good idea. That's just MY opinion...>> Whatever is decided needs to be discussed and researched, and you> should always ask the doctor about viable alternatives...>> Babs in Texas> Never miss a thing. Make Yahoo your homepage. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 12, 2008 Report Share Posted February 12, 2008 Hi Jim, Where do you live ? got a map for me and I have forgotten..DUH.. not surprising with the OD going on.. and BLOND to boot. Love and Prayers, Peggy ipf 6/04 Worry looks around. Sorry looks back, Faith looks up. Prior to my last bronch I asked the nurse to move the IV tubing in front of me. I was determined to watch him push that wonderful cocktail into the line so I could " see " the moment it hit me........Yeah right, NOT, LOL, What I saw, when it was over, was the pulmo's face as me told me " get your butt off the table, I've got patients waiting " . Cool Guy. I've described him as an " arrogant little bugger, and I really like him " . He's done the lavage with every bronch......like 6 or 7 times maybe. This is done at Providence in Anchorage. (which is a great facility BTW) They have a very clever method of billing for this procedure. They bill my insurance as if it were 2 separate procedures.....one for lavage and one for collecting samples, when in fact what he does is squirts in the saline then sucks it back up. Thankfully insurance pays both $1250.00 procedures. We're in the wrong business.......well, maybe not. Speaking of which, Friday the 15th is my last day, I'm retiring after 22 years. Should improve not only the way I feel but my attitude, too. Everyone asks " what are you going to do? " My favorite answer is ...... " sit in my recliner and breath " . jim IPF 05 alaska Peggy wrote: One more thing about the bronc. as they were ready to give me that wonderful sleep stuff, I told the Dr. I would like a face lift and a boob job while he had me out.. he just said put her out.. lol. Love and Prayers, Peggy ipf 6/04 Worry looks around. Sorry looks back, Faith looks up. I'm surprised I haven't heard more here having bronchoscopy lavage. Its widely listed as a method of diagnosis but sure was never mentioned to me as a choice. > > Jumping into the middle of this.... > > My PF was diagnosed using CT scan, PFT's, 6 min. walk-test, and a > bronchoscopy lavage, outpatient. > I'm told that the samples from this are often too small to give a > clear picture to the pathologist, but mine were apparently large > enough as they could tell from the samples that I have PF. > > So, in my case, especially having auto-immune diseases, the less > invasive procedure made sense. I went in at 7:30 a.m. and went home > late afternoon and had no problems at all. > However, I'm not an otherwise healthy person, so the VATS may be the > best answer for some. I personally don't think digging into a sick > persons lungs is a good idea. That's just MY opinion... > > Whatever is decided needs to be discussed and researched, and you > should always ask the doctor about viable alternatives... > > Babs in Texas > Never miss a thing. Make Yahoo your homepage. Quote Link to comment Share on other sites More sharing options...
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