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Author Topic: Fluid on the lungs  (Read 2732 times)
billybags
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« on: August 16, 2011, 02:08:59 AM »

Husband has now got fluid on the lungs, it was picked up by a nuero specialist and they want to do a lung tap. Has any one had this procedure done. He has had fluid on the lungs a few months ago but the neph did not feel concerned about it. I know about the fluid build up, he is on PD and using bags accordingly but he is so out of breath.
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monrein
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« Reply #1 on: August 16, 2011, 04:30:48 AM »

I've never had it done but I was in a hospital once for a week and my "roommate" had that done.  She was in a lot of distress at the time and the procedure helped her enormously.  She had a long-standing liver transplant and was in her early 70's and had this done on more than one occasion when the fluid buildup became too much.

I think it's a bit uncomfortable like so many procedures but she didn't complain about that since the relief was well worth it for her.  I hope the tap will help your husband.
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
Adam_W
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Me with Baron von Fresenius

« Reply #2 on: August 16, 2011, 04:40:15 AM »

A few weeks ago, I had a lot of fluid on my lungs. It was bad enough that that I had to spend a night in ICU and be on oxygen for about 24 hours. I was coughing violently and was very short of breath. Thought I was gonna die!
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-Diagnosed with ESRD (born with one kidney, hypertension killed it) Jan 21st, 2007
-Started dialysis four days later in hospital (Baxter 1550-I think, then Gambro Phoenix)
-Started in-centre dialysis Feb 6th 2007 (Fres. 2008H)
-Started home hemo June 5th 2007 (NxStage/Pureflow)
-PD catheter placed June 6th 2008 (Bye bye NxStage, at least for now)
-Started CAPD July 4th, 2008
-PD catheter removed Dec 2, 2008-PD just wouldn't work, so I'm back on NxStage
-Kidney function improved enough to go off dialysis, Feb. 2011!!!!!
-Back on dialysis (still NxStage) July 2011 :(
-In-centre self-care dialysis March 2012 (Fresenius 2008K)
-Not on transplant list yet.


"Don't live for dialysis, use dialysis to LIVE"
jbeany
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« Reply #3 on: August 16, 2011, 02:19:52 PM »

Hope it helps him feel better!
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

boswife
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us and fam easter 2013

« Reply #4 on: August 16, 2011, 04:55:51 PM »

how awful.  Bo did have fluid on his lungs just reciently and we just got to get agressive with his hemo.  It only took us 3x of taking more fluid off when he Dialysised.  He got REAL good all of a sudden when they mentioned the 'tap'.  Dont know that you can do anything like that with PD but i suppose that they'ed give that a try first if available  :(
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
lmunchkin
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"There Is No Place Like Home!"

« Reply #5 on: August 16, 2011, 05:20:37 PM »

BB, have they said how this fluid got there?  I know when J. was doing PD, he did absorb some of the fluid!  But they just backed off on his fills!  Dont know about this "tap".  Sorry, Im not much help here.  Do ask if they may have an idea where this fluid is coming from.

So sorry about this!  You have been through alot with him!  Praying for you both, Ann!

lmunchkin     :kickstart;
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
del
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« Reply #6 on: August 16, 2011, 06:50:16 PM »

BB have they checked to see how well the PD is working for him. The peritoneal can stop working and your body will start absorbing the fluid instead of removing it from your body like it is supposed to.  Hubby had fluid on his lungs (although an x ray didn't show it) when PD stopped working for him.  He gained 25 lbs of fluid and he wasn't even swollen.  He switched to hemo and in a few treatments the fluid was removed and he felt fine. 

I think the procedure is uncomfortable but well worth the discomfort.
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Don't take your organs to heaven.  Heaven knows we need them here.
billybags
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« Reply #7 on: August 17, 2011, 03:09:47 AM »

Thanks every body, I had to call the paramedics out yesterday at tea time he could not get his breath and he was admitted to the renal ward. the doctor said his right lung has lots of fluid and the left one was crackly and wet, what ever that means.  This is Thursday morning and he has just phoned to say he is waiting for a renal doctor to sort him out.
I also would like to know where the fluid is coming from. He has been on PD for 3 years now and up to now had no problems. The thing is , is it his heart or is it renal, I just wish to God they would sort it out once and for all. Heom would not be a good idea because it would put such a lot of strain on his dicky heart and I don't think it could cope with it. I will keep you informed.
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lmunchkin
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"There Is No Place Like Home!"

« Reply #8 on: August 17, 2011, 04:54:46 PM »

 :grouphug;  &   :pray;  to you BB!

lmunchkin      :kickstart;

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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
billybags
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« Reply #9 on: August 18, 2011, 11:07:22 AM »

Hubby released from hospital this afternoon after 3 nights and 3 different wards. They took a sample of fluid off his lungs on Wednesday to check it out. he has had a couple of x-rays and scans  on his lungs.  To-day Thursday he was told that it is probably his heart because his peritoneal is in tact. They drew a litre and half off his left lung. We have to go back in two weeks time because they are to discuss a different regime for his dialysis.We can not get into see the cardiologist for another month. He said he can breath a lot easier.
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boswife
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us and fam easter 2013

« Reply #10 on: August 18, 2011, 05:10:11 PM »

I hope he will feel well until then and yu get some peace.  I just want to remind you that many who have gone from PD have been surprised that they are so comfortable with it and come to feel better so it's worth it.  I hope you get to keep your PD, but dont let the possibility of hemo worry you.   :grouphug; and be well..
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
lmunchkin
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"There Is No Place Like Home!"

« Reply #11 on: August 18, 2011, 05:55:52 PM »

Well said, Boswife!  Just hang in there BB and know that we are here for you!  We do understand that this is hard for you to see your husband going through all this "Krap"!  You are his Rock!

Praying for you,   :pray; and   :grouphug;

Lee     :kickstart;
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
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