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Author Topic: Another seizure  (Read 1886 times)
karen547
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« on: April 10, 2010, 12:33:25 PM »

I am goiing crazy! I just can't take dialysis anymore. I want to try and see if I can go down to 2x a week. I am hardly gaining weight between treatments, thus my seizures happen. They try and take off to much fluids. I understand that I NEED dialysis, but I am thinking that going 2x a week at 3.5 hours would be better. I am going to talk to them about it monday.
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monrein
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« Reply #1 on: April 10, 2010, 12:42:20 PM »

Has the doctor said that your seizures are the result of trying to take off too much fluid Karen?  Cramping, yeah for sure, but I've never heard of seizures associated with D like this.  Let us know what your doc says.
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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
okarol
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« Reply #2 on: April 10, 2010, 04:11:18 PM »

Found this on the following PDF:
Other less common side-effects - Seizures: These are rare and are usually only seen in someone who has had seizures before. 
"In-Patient Hemodialysis Information Sheet"
http://www.rush.edu/Rush_Document/Hemodialysis and Hemofiltration Information Sheet_Final.pdf

I only read the overview of this article, but it might be helpful:
"Seizures in patients undergoing hemodialysis" http://www.uptodate.com/patients/content/topic.do?topicKey=~IIOItricih9Qca/
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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 -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
monrein
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« Reply #3 on: April 10, 2010, 04:50:23 PM »

Thanks for that Karol.  This is new to me and of some interest since I have epilepsy (first grand mal seizure at 11 years old) but haven't had a seizure in almost 40 years.

Hope they can stop this from happening to you Karen.
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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
galvo
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« Reply #4 on: April 10, 2010, 11:24:41 PM »

Sorry for your troubles, Karen. I would suggest that you find out as much as you can, before reducing D.
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Galvo
aharris2
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Volcan Pacaya, Guatemala

« Reply #5 on: April 11, 2010, 04:50:34 AM »

Karen, We have firsthand experience with this. For my brother, it happened because his blood pressure crashed severely at the beginning of dialysis. After leaving the unit by ambulance, the hospital confirmed seizure and we were told what okarol says, that there has to be a predisposition to seizures. We were not aware of such a predisposition in my brother...

As you said, you need dialysis - to remove toxins from your blood and to maintain you at your "dry weight". If you walk in at your dry weight, then no fluid should be being removed. PERIOD.

Karen, start screaming! Be heard, tell your neph, tell the charge nurse that you don't want fluid removed. Even if there is a minimum amount that must be removed, the fluid can be put back (saline) at half hour intervals so that you are never dry enough for your blood pressure to drop. Insist that they do it and get your nephrologist to back you up. Sullidog recently fought this battle and won:

http://ihatedialysis.com/forum/index.php?topic=18356.msg316510#msg316510
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Life is like a box of chocolates...the more you eat the messier it gets - Epofriend

Epofriend - April 7, 1963 - May 24, 2013
My dear Rolando, I miss you so much!
Rest in peace my dear brother...
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