I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 23, 2024, 11:04:32 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
|-+  Dialysis Discussion
| |-+  Dialysis: General Discussion
| | |-+  First day
0 Members and 2 Guests are viewing this topic. « previous next »
Pages: [1] 2 Go Down Print
Author Topic: First day  (Read 6150 times)
mamagemini
Full Member
***
Offline Offline

Gender: Female
Posts: 124


It's all me.

« on: September 08, 2012, 02:13:06 AM »

I had my first treatment today. They did a slow one and only ran it at 200? That may mean more to you all...lol. I left on my own but when I got home I was wiped. I just woke up awhile ago with a major muscle cramp in my thigh. Wile there my whole right leg camped up and they had to slow it down and put in more saline? same leg tonight too. Also weird pain in my jaws sometimes like they are cramping too....anyone ever have that? So many questions......
Logged

FSGS/Nephrotic syndrome 2005
AV Fistula placed right arm inside elbow 4/2012
Started HD 9/7/2012
Started PD Oct 2015
Parathyroid removed 6/2019
Cellulitis in Fistula 8/2019
RT arm Fistula removed 9/2019
jeannea
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1955

« Reply #1 on: September 08, 2012, 03:09:57 AM »

The first few times can be rough. Your body needs to do some adjusting and the people at the dialysis center have to figure out what works for you. Ask lots of questions and get plenty of rest. I would consider getting a ride rather than driving the first few times just to be safe. I hope you start to feel better soon.
Logged
SteveK87
Jr. Member
**
Offline Offline

Gender: Male
Posts: 94

« Reply #2 on: September 08, 2012, 08:02:00 AM »

Cramping is probably caused by removing too much fluid...which could be why they gave you some saline.  Keep an eye on your BP when they check it too.  When it gets too low they'll usually give saline.  Once they figure your "dry weight" (actual weight without fluid) the cramping should be more controlled and less frequent.
Logged
Big E
Full Member
***
Offline Offline

Gender: Female
Posts: 176


« Reply #3 on: September 08, 2012, 04:11:34 PM »

 :cheer: to you, mamagemini, for getting through your first session. I used to cramp a lot at first, but that got a lot better after the first few months.  It you do get leg cramps, I find it's helpful to push your foot against something--the floor if you can stand, or the seat of your chair if it happens during a treatment.
Logged

PKD diagnosed June 1996
Started in-center hemodialysis May 2010
Rerun
Member for Life
******
Offline Offline

Gender: Female
Posts: 12242


Going through life tied to a chair!

« Reply #4 on: September 08, 2012, 04:18:45 PM »

I drink some Tonic Water everyday.  It has quinine in it which is a natural muscle relaxer.  It works for me.  If they get really bad for you and you are willing to try anything..... try some Tonic Water everyday.  At least a 1/4 cup or maybe 1/2 cup.
Logged

YellowRose
Jr. Member
**
Offline Offline

Gender: Female
Posts: 51

« Reply #5 on: September 08, 2012, 08:04:04 PM »

The first few months are very difficult. One time ( I think it was within the first few weeks), they try to take 2.5Kg off me and I cramp all over and felt really bad, I thought maybe standing up will help with the cramp but while trying to stand up, I passed out. Tech was scold because they were not supposed to take that much off a new patient. But now, one year later,
I am able to have 4kg take off of me, no problem.

Besides giving  saline, normally, in our center, they do not want us to stand up if cramp, fear of low blood pressure.... they will have tech or nurse to press against the leg that you feel cramp or message the muscle until you are better.

Remember you have the final say about how much to take off, so if some tech want to take off too much, speak up. You may reach your dry weight more slower but cramping really wipe you out, so give your body the time to get used to it.

Hang in there and good luck!
Logged

Dec 1993 start with CAPD
May 1995 1st transplant
Jan 2007 start with CCPD
April 2011 start with Hemo
Sept 2012 2nd transplant
YellowRose
Jr. Member
**
Offline Offline

Gender: Female
Posts: 51

« Reply #6 on: September 08, 2012, 08:09:18 PM »

200 is pretty slow. It mean 200cc each minute of blood get dialysis.

Logged

Dec 1993 start with CAPD
May 1995 1st transplant
Jan 2007 start with CCPD
April 2011 start with Hemo
Sept 2012 2nd transplant
natnnnat
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1281


WWW
« Reply #7 on: September 09, 2012, 07:04:22 AM »

 I wrote an answer to this and then lost it because our internet is so bad right now.  GAAHH >:(
I said something like this: 
Starting at 200 is slow, and slow is good.  Also people may start with short treatments, like an hour or so, to allow the body to get used to the treatments (and it probably helps you to get used to it mentally and emotionally too).  I'm a bit freaked to hear that you have started, because you and Gregory seemed to be on a similar sort of trajectory into D.  He is still not on dialysis.  His numbers are shaky, but he is still working, walking every day, eating, and so on.  He has quite a capacity to eke things out.  Also his fistula is still too small.

Also weird pain in my jaws sometimes like they are cramping too....anyone ever have that? So many questions......

Gregory gets that sometimes now, and he used to get it back when he was on D before.  He doesn't get it a whole lot though, he mainly gets it in the hands at the moment.   I guess that its part of the 'way you cramp', people cramp in different places.  And as the others have said, when you are more settled into a routine and your body has adjusted, you should cramp less.

I guess you'll be going in for your second treatment on the 10th.  Good luck, I hope you get a smooth transition into a nice easy routine.  Let know how you go.   :cuddle;
Logged

Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
AnnieB
Sr. Member
****
Offline Offline

Gender: Female
Posts: 578


« Reply #8 on: September 09, 2012, 03:29:30 PM »

You are really doing great with this. I hope when my turn comes I handle it as well.  :thumbup;
Logged
boswife
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2644


us and fam easter 2013

« Reply #9 on: September 09, 2012, 04:16:30 PM »

there seems to be so many "normal" things that happen at first... Bo really didnt have much goen on but he really didnt have much to take off so that part is what seems to be what causes the 'issues' .  Im glad they're taking it easy with you (that was something ours did great with as well) and sounds like with you helping out,,,,ie, letting them know mabie too much fluid off, you may just have a nice smooth start.  The cramping is hell i know.  though im not the crampee, i am on my feet with massage goen at the near thought of him cramping.  Even now, (at home) we go for months w/0 any cramps, and then boom, they seem this summer to be a bit of a problem.  Not during D, but at night when sleeping...  THAT is crap!!  not only ouch, but the waking up from much needed sleep... But,,, this too will smooth out.  Wishing you the best.. Glad the 'starting' is over, somethimes thats the worst of it  :2thumbsup;
Logged

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
mamagemini
Full Member
***
Offline Offline

Gender: Female
Posts: 124


It's all me.

« Reply #10 on: September 09, 2012, 09:35:09 PM »

Thank you for th great words and information! Yes I go again tomorrow and I hope Ron is there. He is the one who got my fistula to go without a Chest cath!  :yahoo;
The cramping has been for the past 2years but bad the past year. The cramp I had there was my whole Fricking leg! Never have had that. Was weak yesterday but today much better. It looks like a rough week is ahead...keep me in your positive thoughts. :waving;
« Last Edit: September 09, 2012, 09:42:48 PM by mamagemini » Logged

FSGS/Nephrotic syndrome 2005
AV Fistula placed right arm inside elbow 4/2012
Started HD 9/7/2012
Started PD Oct 2015
Parathyroid removed 6/2019
Cellulitis in Fistula 8/2019
RT arm Fistula removed 9/2019
M3Riddler
Full Member
***
Offline Offline

Gender: Male
Posts: 385


WWW
« Reply #11 on: September 09, 2012, 10:39:49 PM »

I had my first treatment today. They did a slow one and only ran it at 200? That may mean more to you all...lol. I left on my own but when I got home I was wiped. I just woke up awhile ago with a major muscle cramp in my thigh. Wile there my whole right leg camped up and they had to slow it down and put in more saline? same leg tonight too. Also weird pain in my jaws sometimes like they are cramping too....anyone ever have that? So many questions......

mamagemini,

If you are cramping, they may be drawing too much fluid off during the treatment.  At your next treatment, pay particular attention to your blood pressure and pulse towards the end of the treatment. If your bp is on the low side and your pulse is above 90 or 95. then this is a good indication that you may have reached your dry weight and need to hold back on the amount of fluid removed.

//M3R
Logged

____________________________________
Peritoneal - 13 years
NxStage Since 4/06
3 Transplants
Admin of Dialysis Discussion Uncensored on Facebook  
___________________________________
Whamo
Elite Member
*****
Offline Offline

Posts: 1028

« Reply #12 on: September 10, 2012, 10:51:41 AM »

This is how you feel for the first two months.   :Kit n Stik; :Kit n Stik; :Kit n Stik; :Kit n Stik; :puke;
Logged
mamagemini
Full Member
***
Offline Offline

Gender: Female
Posts: 124


It's all me.

« Reply #13 on: September 10, 2012, 11:31:17 AM »

BP was 140/something and my pulse was 95
Logged

FSGS/Nephrotic syndrome 2005
AV Fistula placed right arm inside elbow 4/2012
Started HD 9/7/2012
Started PD Oct 2015
Parathyroid removed 6/2019
Cellulitis in Fistula 8/2019
RT arm Fistula removed 9/2019
boswife
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2644


us and fam easter 2013

« Reply #14 on: September 10, 2012, 09:25:48 PM »

Wishing you all goodness tomorrow ;)   Your in my prayers  :pray;
Logged

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
mamagemini
Full Member
***
Offline Offline

Gender: Female
Posts: 124


It's all me.

« Reply #15 on: September 11, 2012, 12:01:58 PM »

2nd treatment...all night had muscle cramps in legs and feet. Today weak but good spirits. Silver lining...10lbs - gone!  ;D
Logged

FSGS/Nephrotic syndrome 2005
AV Fistula placed right arm inside elbow 4/2012
Started HD 9/7/2012
Started PD Oct 2015
Parathyroid removed 6/2019
Cellulitis in Fistula 8/2019
RT arm Fistula removed 9/2019
AnnieB
Sr. Member
****
Offline Offline

Gender: Female
Posts: 578


« Reply #16 on: September 11, 2012, 03:35:50 PM »

That's a rough way to lose the weight though...you have my sympathy. I get cramps in my feet sometimes at night, it really sucks. Did you try the quinine water? I'll have to see if that works.

Anne
Logged
MooseMom
Member for Life
******
Offline Offline

Gender: Female
Posts: 11325


« Reply #17 on: September 11, 2012, 03:52:46 PM »

 :cuddle;  I'm glad you are in good spirits.  That's very important (and not always easy).  You have been very brave, and I admire you for that.
Logged

"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
mamagemini
Full Member
***
Offline Offline

Gender: Female
Posts: 124


It's all me.

« Reply #18 on: September 11, 2012, 08:39:14 PM »

I wrote an answer to this and then lost it because our internet is so bad right now.  GAAHH >:(
I said something like this: 
Starting at 200 is slow, and slow is good.  Also people may start with short treatments, like an hour or so, to allow the body to get used to the treatments (and it probably helps you to get used to it mentally and emotionally too).  I'm a bit freaked to hear that you have started, because you and Gregory seemed to be on a similar sort of trajectory into D.  He is still not on dialysis.  His numbers are shaky, but he is still working, walking every day, eating, and so on.  He has quite a capacity to eke things out.  Also his fistula is still too small.

Also weird pain in my jaws sometimes like they are cramping too....anyone ever have that? So many questions......

Gregory gets that sometimes now, and he used to get it back when he was on D before.  He doesn't get it a whole lot though, he mainly gets it in the hands at the moment.   I guess that its part of the 'way you cramp', people cramp in different places.  And as the others have said, when you are more settled into a routine and your body has adjusted, you should cramp less.

I guess you'll be going in for your second treatment on the 10th.  Good luck, I hope you get a smooth transition into a nice easy routine.  Let know how you go.   :cuddle;

You know my doctor wanted me on before I stopped urinating. To help preserve what I have.
I was having a nausea/vomiting once a week, swollen ankles (painful) and exhausted walking. I hope he made the right choice and so far I feel ok with the decision. I hope things work out better for him....and I. Transplants all around~
Logged

FSGS/Nephrotic syndrome 2005
AV Fistula placed right arm inside elbow 4/2012
Started HD 9/7/2012
Started PD Oct 2015
Parathyroid removed 6/2019
Cellulitis in Fistula 8/2019
RT arm Fistula removed 9/2019
natnnnat
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1281


WWW
« Reply #19 on: September 11, 2012, 08:42:01 PM »

Transplants all around~

Hear hear! 
I'm glad you seem to be keeping on at present.  Thinking of you and watching this space to hear how you are going, so thank you for reporting back.
Logged

Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
mamagemini
Full Member
***
Offline Offline

Gender: Female
Posts: 124


It's all me.

« Reply #20 on: September 13, 2012, 10:51:20 AM »

I went in yesterday and told them about the severe cramping at night after D. Also my feet were not swollen! So they only took off 1liter? I had no cramping during D and none until I woke up this morning. It was only a minor one and I got it to go away. A little nausea and almost tossed up but stopped it...lol. :P
Was prescribed a phosphate binder? This is a must have for those on D?  ???
Logged

FSGS/Nephrotic syndrome 2005
AV Fistula placed right arm inside elbow 4/2012
Started HD 9/7/2012
Started PD Oct 2015
Parathyroid removed 6/2019
Cellulitis in Fistula 8/2019
RT arm Fistula removed 9/2019
Joe
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1166


« Reply #21 on: September 13, 2012, 11:38:05 AM »

Sounds like you are getting things under control, and that's great!

As for the phosphorous binder; yes, it's a must for those of us that don't have kidney function. The kidneys process excess phosphorous out of your system, too much can cause your heart to stop - that's a bad thing. And unfortunately, it's in just about everything you put in your mouth. So the binders help process it out of your system and pass it out through the bowel.

Good luck!
Logged

Live simply. Love generously. Care deeply. Speak kindly.
Leave the rest to God...
Wat76
Full Member
***
Offline Offline

Gender: Female
Posts: 185


This Too Shall Pass

« Reply #22 on: September 13, 2012, 12:30:50 PM »

Wow, I have been going to D for 2 months now and I am just beginning to feel a little better. My face still cramps when I eat something after D and I requested more saline when i start to cramp and I feel better.  I have a written order in my file to give me saline when asked.  I learn if the tech gives me saline, I feel 90 percent better.  I am still using the bathroom and I drink a lot of water.  They told me to drink extra daily because I am always under my dry weight.  I have no outwards signs of swelling, so they only pull .5 liters of fluid and give it back to me at the end, which also stopped the headaches.  Hope you feel better soon.  You are the first person I have seen complained about the pain in the jaws/face.  I though i was going crazy.
Logged

PKD: PD started in February 2011.
Live, Laugh and Love daily.
gothiclovemonkey
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1659


« Reply #23 on: September 14, 2012, 03:37:12 AM »

i still struggle with taking those darn binders, and ive been on d for 5 years LOL

i cramp in some very odd places! Mostly hands and feet though, but ive had them in my chin, cheek, forehead, neck, back, boob, butt... yeaaaa....

Logged

"Imagine how important death must be to have a prerequisite such as life" Unknown
HemoDialysis since 2007
TX listed 8/1/11 inactive
LISTED ACTIVE! 11/14/11 !!!
chinksnicky
Jr. Member
**
Offline Offline

Gender: Male
Posts: 75


« Reply #24 on: September 15, 2012, 06:49:03 PM »

Yeah remembering to take those binders is hard for me too, I've found that always keeping some on my place mat at all times helps me remember.
Logged
Pages: [1] 2 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!