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Author Topic: More Complications...  (Read 2531 times)
Lovebelle
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« on: November 20, 2010, 07:26:05 PM »

Well the last time I wrote I believe I had mentioned that the Revision Surgery on the 5th went well and my initial flush after that was a success. Well unfortunately a lot changes in a couple days. Well anyway, Tuesday I went in for the 2nd flush of my PD cath and Lo and behold the darn thing didnt work. The nurse didnt have any resisitance manually pushing with a syringe but once the bag went up nothing would happen. You can imagine how upset I was considering I just went through all that and Just had a 2nd surgery to fix this problem and here I am again.

So anyway She wanted to to come in the next day to try the activase routine again. But when I left I began to experience the severe abdominal cramping again and high fever 102.9. I of course put off the inevitable all night and then finally decided to go to the ER in the morning since my temp still was high.

So here I am in the hospital. I have been here since Wednesday Morning and am so miserable. They tried everything they could to try to get the PD cath to work but it just caused more cramping and more fevers and so yesterday I went to Surgery a 3rd time and had to have the Catheter removed. They are saying it was a case of peritonitis which so bizarre to me because I never really used the catheter at all.

I was pretty upset at having to have it removed though because I was looking forward to getting trained and finally going back to work but now another setback. So it seems I am stuck with Haemodialysis through my tunnel cath for now.

Anyway just wanted to share. Thanks.
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okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #1 on: November 21, 2010, 12:13:58 AM »


Wow that sounds awful. I hope you can get this straightened out. I have heard of people getting peritonitis because there's random bacteria in our systems and it can happen to anyone. It seems unfair that you've been through so much and cannot get a working catheter. Best wishes and hugs.  :cuddle; :cuddle; :cuddle;
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
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billybags
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« Reply #2 on: November 21, 2010, 04:00:49 AM »

Lovebelle. Don't dispare this is just a set back. Give it a few weeks and see if they will try again. I know it is not nice going through all this, at the end of the day it it will be better for you to go on to APD, that's my thought any way. Have you asked why this is happening? My husbands second go when he had a flush there was so much sh*t  came out from the operation, you do not know do you.
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VintageVera
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« Reply #3 on: November 23, 2010, 09:52:57 PM »

It took me 2 tries/operations to get my pd tubing right but it's been working fine now for 6 months. First time in, it kinked and second operation was to correct that. Hang in there -- home pd with the cycler is a better option that in-center hemo.
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Lovebelle
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« Reply #4 on: November 26, 2010, 11:45:59 AM »

Yeah Im trying to keep my head up about it. I know my doctors would like to place a new PD cath in a few weeks so I am hoping that will work. Im just frustrated because I had plans to go out of town for the holidays and now I am not so sure how that is going to work. This is all so sudden since I just found out I had kidney failure and started Hemodialysis all in October. When I first learned about Peritoneal at that time I was hopeful I would be up and trained by the time christmas rolled around so I could still travel. But with these complications things look grim. I suppose travel is still possible on Hemo (with some planning) but if they are doing this surgery around Christmas then Im not sure if Ill be up to the trip.

I am so thankful to come across this sitr though because I feel better knowing others have experienced the same things and this contains a wealth of info.
Thanks everyone :)
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rsudock
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will of the healthy makes up the fate of the sick.

« Reply #5 on: November 26, 2010, 03:13:42 PM »

Lovebelle it is a journey with its up and downs just keep putting one foot in front of the other. You can do it!! You know you can train for home hemodialysis as well. Be careful with the pertonitis. There is a patient in my center who got it some bad that now he has a big gaping hole in his stomach...he told me he can see his intestines...eek! i would rather get poked with needles for hemo.
take care,
xo,
R
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Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
Dec 7, 1999 cadaver transplant saved me from childhood dialysis!
10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
June 21, 2011 2nd kidney nonrelated living donor
September 2013 Liver Cancer tumor.
October 2013 Ablation of liver tumor.
Now scans every 3 months to watch for new tumors.
Now Status 7 on the wait list for a liver.
How about another decade of solid health?
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