I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 24, 2024, 08:06:18 AM

Login with username, password and session length
Search:     Advanced search
532606 Posts in 33561 Topics by 12678 Members
Latest Member: astrobridge
* Home Help Search Login Register
+  I Hate Dialysis Message Board
|-+  Introduction
| |-+  Introduce Yourself
| | |-+  New to PD for the past 3 weeks..
0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: New to PD for the past 3 weeks..  (Read 2850 times)
Noahsmum
Newbie
*
Offline Offline

Posts: 3


« on: October 07, 2008, 01:06:10 PM »

Hi All
My son had his PD catheter fitted just over 3 weeks ago (he's 12) and we are still riding the rollercoaster that is now our lives!
He has already had his first bout of peritionitis, then had an allergic reaction to the antibiotics (gentamycin & vancomycin) that they used to treat him, we finally came out of hospital last week and he still isn't 100%.
He has had a negative UF 300+ the last 2 nights and he had a large bit of fibrin in his drain bag after his initial drain tonight, bit of a tummy ache (although he has been a bit constipated), no temperatures , his weight and BP are normal...we have clinic tomorrow, so will check all this out with the docs then, just really worried he'll have to go on heamo....

Thanks for listening!  Amy-Noahs Mum x
Logged
okarol
Administrator
Member for Life
*****
Offline Offline

Gender: Female
Posts: 100933


Photo is Jenna - after Disneyland - 1988

WWW
« Reply #1 on: October 07, 2008, 01:10:46 PM »


Welcome Amy.  :welcomesign;

Sorry about Noah's problems. I hope they can sort them out.
My daughter began hemo at 18 years old - she couldn't do PD due to prior urinary/abdominal surgery.
It worked fine for her.
Hang in there.  :cuddle;
Logged


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 -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
willieandwinnie
Elite Member
*****
Offline Offline

Gender: Female
Posts: 3957


« Reply #2 on: October 07, 2008, 01:21:00 PM »

:welcomesign; Amy. I'm so sorry about your sons problems. I hope you get answers tomorrow. This is a great site for information and support and we hope to hear more from you. Have Noah join us.  :cuddle;
Logged

"I know there's nothing to it, but I want to know what it is there's nothing to"
monrein
Member for Life
******
Offline Offline

Gender: Female
Posts: 8323


Might as well smile

« Reply #3 on: October 07, 2008, 02:28:34 PM »

I'm so sorry that Noah is having such a tough time and I really hope that things get themselves sorted out soon.
Logged

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
pelagia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2991


« Reply #4 on: October 07, 2008, 03:42:40 PM »

 :grouphug;
Logged

As for me, I'll borrow this thought: "Having never experienced kidney disease, I had no idea how crucial kidney function is to the rest of the body." - KD
rookiegirl
Sr. Member
****
Offline Offline

Gender: Female
Posts: 724


« Reply #5 on: October 07, 2008, 04:18:13 PM »

Hi Noahsmum,

I've been on PD going on 1 year this coming October 22, 2008.  The 1st 4 weeks was very hard.  The 1st time I drained during the PD Training, I had lots and lots of fibrin. The PD Nurse injected in my solution Heparin and that helped.  I haven't had any problem with fibrin since then.

I pray that Noah will get better with PD as I did because now, I'm really doing well with the treatment.  I wish you both the best.
Logged

2000-Diagnosed IGA Nephropathy
2002-1st biopsy (complications)
2004-2nd biopsy
10/03/07-Tenckhoff Catheter Placement
10/22/07-Started Peritoneal Dialysis
03/2008-Transplant team meeting
04/2008-Transplant workup
05/2008-Active Transplant list
3/20/09-Cadaver Kidney Transplant
4/07/09-Tenckhoff Catheter removed
4/20/09-New kidney biopsy
paris
Member for Life
******
Offline Offline

Gender: Female
Posts: 8859


« Reply #6 on: October 07, 2008, 08:44:17 PM »

Hi Noah's Mom,   First, I am so very sorry that Noah is dealing with this at age 12.   Children shouldn't have to worry about their health.   Second, I am glad you joined us.  You will find so much information here.  And everyone is always ready to help when you have a question.   On days when it all seems to much to handle, members will quickly give a shoulder to cry on.  We are all here for each other.  Welcome to our family  :grouphug;





Paris,moderator
Logged



It's not what you gather, but what you scatter that tells what kind of life you have lived.
Joe Paul
Elite Member
*****
Offline Offline

Gender: Male
Posts: 4841


« Reply #7 on: October 08, 2008, 12:10:19 AM »

Welcome Noahsmum, good to have you aboard.
Logged

"The history of discovery is completed by those who don't follow rules"
Angels are with us, but don't take GOD for granted
Transplant Jan. 8, 2010
Romona
Elite Member
*****
Offline Offline

Gender: Female
Posts: 3777

« Reply #8 on: October 08, 2008, 04:46:37 AM »

 :welcomesign; Amy.
Logged
devon
Sr. Member
****
Offline Offline

Gender: Female
Posts: 677

« Reply #9 on: October 08, 2008, 06:08:52 AM »

Welcome Amy and Noah!

I'm am sorry y'all have to be going through this! Being 12 is not the time one would pick to be on PD!  I hope you find comfort and peace here.  We'll be happy to do what we can to help.

-Devon
Logged
peleroja
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1585


I have 16 hats, all the same style!

« Reply #10 on: October 08, 2008, 07:58:42 AM »

Welcome aboard, Amy.  I've been on PD for 5 years  Hang in there and keep us posted about Noah.
Logged
boxman55
Elite Member
*****
Offline Offline

Gender: Male
Posts: 3635


« Reply #11 on: October 08, 2008, 04:58:05 PM »

Welcome Amy, please keep the faith. We all want your son to get past the troubles and do better. Please post so we know how you all are doing

Boxman, Moderator
Logged


"Be the change you wished to be"
Started Hemodialysis 8/14/06
Lost lower right leg 5/16/08 due to Diabetes
Sister was denied donation to me for medical reasons 1/2008
Noahsmum
Newbie
*
Offline Offline

Posts: 3


« Reply #12 on: October 11, 2008, 10:52:17 AM »

I'd first like to say a very BIG Thankyou for making me (us) feel so welcome, we have had another rollercoaster week, after clinic on Wednseday Noahs white cell count had shot up again to 28, 000!
He still has symptons of peritonitis with yucky coloured fluid on his initial drain so they have started him on a 10 days course of cefataxin..fingers crossed this will knock the bug on the head!
Otherwise he may have to have his catheter removed  :(
Luckily he still has some kidney function left to go a few weeks without any dialysis but then they would have to put him on hemo which is going to be a nightmare travelling 50 miles 3 days a week, not to mention what i'll do about work and my other son....

Once again, thanks for being able to rant to people who know exactly how we feel
Amy & Noah
xxx

Logged
monrein
Member for Life
******
Offline Offline

Gender: Female
Posts: 8323


Might as well smile

« Reply #13 on: October 11, 2008, 12:29:34 PM »

Sending you and your boys hugs today.  I really hope they can get Noah's infection cleared up so he can get back on track.  :grouphug;
Logged

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
Ang
Elite Member
*****
Offline Offline

Gender: Male
Posts: 3314


« Reply #14 on: October 11, 2008, 11:31:23 PM »

 :welcomesign;



Logged

live  life  to  the  full  and you won't  die  wondering
Bajanne
Member for Life
******
Offline Offline

Gender: Female
Posts: 5337


Goofynina and Epoman - Gone But Not Forgotten

WWW
« Reply #15 on: October 18, 2008, 07:55:05 AM »

welcome to our community!  so sorry for the great challenge you and  your family are facing.  You gave your son a good name.  I trust he will make it through the flood and come out victorious.  Please consider this  your new extended family.  We are here for you all. :grouphug;  My caring thoughts and prayers are with you at this demanding time.  Feel free to rant, vent, rage as much as you need to.
Looking forward to hearing from you.


Bajanne, Moderator
Logged

"To be found in Him, not having a righteousness of my own ...but that which is based on faith"



I LOVE  my IHD family! :grouphug;
Pages: [1] Go Up Print 
« previous next »
 

Powered by MySQL Powered by PHP SMF 2.0.17 | SMF © 2019, Simple Machines | Terms and Policies Valid XHTML 1.0! Valid CSS!