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Author Topic: Fluid leaking into abdomen?  (Read 4399 times)
cloud393
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« on: July 22, 2009, 09:53:21 PM »
I started PD 2/16/09 and have had a "knot" between my navel and exit site since mid March.  The surgeon said no hernia, probably just scar tissue.  Well now it is much larger, gets hard when I stand very long and when I fill during my exchanges and I have to do gymnastics in order to drain.  Needless to say I had a few sleepless nights.  Anyway, I saw my neph today and we are gonna do a CAT Scan with the dye being inserted in a daytime solution bag and and then into my peritoneum to look for leaks.  Anyone ever had this problem? And did they use the dye in this way?  Thanks.
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May you live as long as you want and never want as long as you live.
KICKSTART
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In da House.
« Reply #1 on: July 23, 2009, 04:57:14 AM »
I dont think its common but im sure someone else on here had this problem , try doing a search in this section ..sorry i cant be of more help.
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09
« Reply #2 on: July 23, 2009, 03:19:21 PM »
No, I haven't had this problem either.  Good luck.
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
george40
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« Reply #3 on: July 28, 2009, 05:43:41 PM »
Wheww! I had a tough time in the beginning of June with this fluid leaking situation. Here is the thread....

http://ihatedialysis.com/forum/index.php?topic=14233.0
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8/2000 - Diagnosed ESRD / Hemo begins with perm cath
1/2002 - Transplant No. 1
4/2006 - Transplant failed due to CMV virus/ Back to Hemo
11/2008 - Moved to PD Modality
9/2012 - Transplanted!
cloud393
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« Reply #4 on: August 14, 2009, 09:45:36 AM »
Well I'm home again.  I went for CT scan and found out PD Cath had come out of it's "track".  Most of my fluids were going under my skin, not in the peritoneum.  Spent 4 days in hospital getting a new PD cath, a perma cath for hemo, small hernia repair and removal of scar tissue.  I came home for three days and ended up in the ER with vomiting, severe stomach pain & cramping.  After all kinds of tests, found out I was just constipated (big time). I spent a week in the hospital getting cleaned out.  Now doing hemo until abdomen is healed.  I was told 4 to 6 weeks of it.  Boy do I like PD better.  Hemo has not been the easiest. 
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May you live as long as you want and never want as long as you live.
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09
« Reply #5 on: August 14, 2009, 03:33:31 PM »
Oh dear - what a time you've had.  Hopefully it'll be all up from here.  I like how you said 'just' constipated!  We all know there's no 'just' about it.  Hang in there - it's only a few weeks and you'll be back on PD.  Makes you appreciate it eh?  You might have to make a sign saying I DON"T hate dialysis - only haemo!
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
sico
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wheres my bike gone?
« Reply #6 on: August 15, 2009, 05:20:39 AM »
I hate constipation. Was using laxatives for quite a while after my PD catheter procedures, takes time for your body to get over it.
The haemo knocked me around a bit in the beginning too, i was wheeled in in my hospital bed for my first few sessions.
But i think that was because of the catheter in my groin upper/thigh.
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Brad      "Got myself a one way ticket, going the wrong way" - Bon Scott

6/11/08 diagnosed with ESRF, dialysis that day

HD and PD

8th of April 2010 Live kidney transplant from my father.
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