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Tracy
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Loved the Movie!

« on: May 19, 2010, 12:39:52 PM »

Today is my first day for in center D.  I was in the hospital for 5 days and got out yesterday.  They wanted me in the hospital to watch me as they gradually started me on D.  I have had 3 treatments so far and my BUN went from 116 to 49.  So, I am already feeling better.  So much to learn.  I am a little nervous about today, just because it is all new.  I loved my nurse that did my D all three times in the hospital.  He was excellent.  I hope the nurses at the center are as good.

Wish me luck!  Tracy :)
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9/1990 Found out I have Type 1 Diabetes
7/2008 Told I have GFR 30
2/2009 Kidney/Pancreas Transplant
5 days later, both removed due to massive rejection
Back on List
2/26/10 Fistula placed
3/11/10 Told GFR 9
5/14/10 Started in center Hemo
Waiting on another Transplant
Jean
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« Reply #1 on: May 19, 2010, 03:03:18 PM »

Sure do wish you lots of luck on your new journey. Glad your visit to the dialysis center worked out well. That is so encouraging to those of us who are still waiting.
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One day at a time, thats all I can do.
monrein
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Might as well smile

« Reply #2 on: May 19, 2010, 03:41:11 PM »

Wishing you luck and also wishing you good, competent and caring nurses and doctors.  We're here to give whatever support you might need.  :grouphug;
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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
sullidog
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« Reply #3 on: May 19, 2010, 05:04:46 PM »

Good luck! Let us know how it goes.
Troy
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May 13, 2009, went to urgent care with shortness of breath
May 19, 2009, went to doctor for severe nausea
May 20, 2009, admited to hospital for kidney failure
May 20, 2009, started dialysis with a groin cath
May 25, 2009, permacath was placed
august 24, 2009, was suppose to have access placement but instead was admited to hospital for low potassium
august 25, 2009, access placement
January 16, 2010 thrombectomy was done on access
Tracy
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Loved the Movie!

« Reply #4 on: May 20, 2010, 11:47:21 AM »

Today is the day after my first in center treatment.  Basicallhy it was a nightmare.  The lady that stuck me said she had been doing it for 7 years, so I felt confident that she knew what she was doing.  Thirty minutes later and 4 sticks later, she finally got the needles in with two other nurses to come help.  Luckily, the emla cream had me numb enough that I couldn't really feel what she was doing.  My blood pressure dropped and they stopped pulling water off of me the last 30 minutes.  They had to keep me 30  extra minutes because my blood pressure was so low.  Then, I realized I hadn't eaten since 11am and it was now 8 pm.  I was so dizzy and had such a bad headache and was exhausted.  In the hospital, I was energetic and the nurse had no trouble sticking me.  This lady was telling me my fistula was not big enough and that I should excercise it.  The nurse that stuck me in the hospital didn't have one bit of problem.  Well, today I wasn't able to go to work because i woke up so dizzy and head hurting.  I have a HUGE knot on my fistula and it hurts like crazy.  I don't look forward to going back at all, but what choice do I have.  I will ask that a different nurse do it tomorrow.  btw, I am feeling better now.  But after missing 5 days  of work for bieing in the hospital and now another day, it has me a little freaked out.    Thanks for letting me rant! :)  :rant;
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9/1990 Found out I have Type 1 Diabetes
7/2008 Told I have GFR 30
2/2009 Kidney/Pancreas Transplant
5 days later, both removed due to massive rejection
Back on List
2/26/10 Fistula placed
3/11/10 Told GFR 9
5/14/10 Started in center Hemo
Waiting on another Transplant
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #5 on: May 20, 2010, 01:06:32 PM »

Oh man, thats awful. Did you ice your arm? So sorry you had a bad experience. They need to be really careful about taking fluid off if your weight is stable and you are still urinating. I hope next time goes better.  :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 -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
KICKSTART
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In da House.

« Reply #6 on: May 20, 2010, 02:47:38 PM »

This is the problem with hemo , you dont get 2 days the same or so it seems! Hopefully you will get a run of good days , so the odd bad day that crops up wont feel so bad.
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
cloud393
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« Reply #7 on: May 20, 2010, 02:49:59 PM »

Oh, I'm so sorry you had such a bad experience at your clinic.  I just recently started using my fistula and felt the same way you are feeling.  I am still nervous about who sticks me.  One of the most experienced nurses at my clinic infiltrated mine last week.  I guess it happens but, it sure does stink.  Hopefully things will go better next time.      :flower;
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May you live as long as you want and never want as long as you live.
tyefly
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This will be me...... Next spring.... I earned it.

« Reply #8 on: May 20, 2010, 09:30:10 PM »

Oh  Yes....... I certainly remember my first time   just a few months ago.......  Infiltration  a few times....cramps......low BP........  a baby fistula......  I am glad I am pass those days.......   Be strong and learn how to do as much your self.....that way it will be done the same way each day.......  you will be in control and no one can hurt you....... I now do my own needles and do hemo at home.......   It workd way better  ...... 
   no cramps,,,,, no low BP......  feel like normal.......  works great....

  stay with us    and let us know how you are doing each day.......  there is so much to learn......... :welcomesign;
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IgA Nephropathy   April 2009
CKD    May 2009
AV Fistula  June 2009
In-Center Dialysis   Sept 2009
Nxstage    Feb 2010
Extended Nxstage March 2011

Transplant Sept 2, 2011

  Hello from the Oregon Coast.....

I am learning to live close to the lives of my friends without ever seeing them. No miles of any measurement can separate your soul from mine.
- John Muir

The clearest way into the Universe is through a forest wilderness.
- John Muir
jamoman
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« Reply #9 on: May 21, 2010, 12:28:21 AM »

i had same problems also, but i started buttonholes from first week, now no infiltrations even if tech can`t get it right the first time, but i have watched enough that i can tell them what angle & what degree of pitch. like it`s already been said pay close attention   all aspects, stick ,machine settings etc. i`m very sorry for your pain & suffering, best of luck & hang in . :grouphug;
« Last Edit: May 21, 2010, 12:30:28 AM by jamoman » Logged
texasstyle
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« Reply #10 on: May 21, 2010, 06:02:31 AM »

I'm sorry things didn't go well. One important thing I feel, is to learn all you and be your own best advocate regarding your health and your dialysis treatments. When my husband had it done in the hosp. They were quite attentive to him. In center though there's a number of people to take care of.You're just starting you'll understand what to expect as time goes by.  For your new fistula & "excessing" it. There are little rubber balls you can use to drip on to and release which you will do several times to help build up the fistula. We kept one on our coffee table so he could always grab while watching tv. There's an awful lot of pressure that will be going through your new vein. It's your lifeline now. Maybe ask your clinic if they have one of those "ball" things there. One day at a time.
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caregiver to husband using in-center dialysis 4 years
peleroja
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« Reply #11 on: May 21, 2010, 11:06:49 AM »

Best of luck in getting everything you want out of dialysis, including excellent nurses and techs.
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billybags
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« Reply #12 on: May 21, 2010, 11:27:35 AM »

Tracy that sounds awful, hope it is better for you the next time.
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kitkatz
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« Reply #13 on: May 23, 2010, 05:30:31 PM »

I hope things get better for you in center as the days progress.
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
lola
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I can fly!!!

« Reply #14 on: May 23, 2010, 05:36:15 PM »

Tracy hope things get better for you. Will your center do buttonholes???? Otto does his own needles since they were having problems.
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Tracy
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Loved the Movie!

« Reply #15 on: May 24, 2010, 07:17:01 AM »

Friday wasn't much better.  They stuck me 3 times and you should see my arm. It is a HUGE bruise.  Thank goodness for the numbing cream.  I have a question though, how do they know how long to run you.  I had to go 3 1/2 hours on Friday, that was my first time to go that long.  I have had severe headaches with each treatment, but I seem to get them right after I get my meds shot into the lines.  One lady whispered to me that they need to do them slower.  The nurse just stands there with the meds in the syringe and pushes them in.  It seems to be slow, but the lady that spoke to me, sat across from me and watched the whole thing.  The nurse said I was probably reacting to that brand of iron and that today they will switch me.

By the way, do you feel better soon?  Cause it is very hard for me to get up the next day after dialysis.  I work full time and do D after work.  I get home about 9:30pm at night and up at 5:15am the next day.  But I tell ya, I'm pooped.  This was my first time to go 2 days without D and I feel exhausted.  I am just curious to know if I will have more energy or not.

Thank you so much for all the support.  I sure do need it!

 :grouphug;
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9/1990 Found out I have Type 1 Diabetes
7/2008 Told I have GFR 30
2/2009 Kidney/Pancreas Transplant
5 days later, both removed due to massive rejection
Back on List
2/26/10 Fistula placed
3/11/10 Told GFR 9
5/14/10 Started in center Hemo
Waiting on another Transplant
jdwills83
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LOVE will fix ANYTHING.

« Reply #16 on: May 24, 2010, 10:30:15 PM »

Tracy,

Don't be afraid to ask for someone else to stick you.  Once you feel comfortable with the people who get it right, ask for them to stick you every time.  I think it is always a battle for the nurses and techs to get used to someone's new fistula, but the ones who remember how to stick it where it won't hurt you and get it right... are the good ones.  If you want to boost your energy think : PROTEIN PROTEIN PROTEIN.  I always either drink a protein shake before and after, or drink a gatorade protein recovery.   

good luck!
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chiefsfan301
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Fish, Duck Hunt, Fish, DuckHunt, Golf and Football

« Reply #17 on: May 25, 2010, 06:23:55 AM »

My center injects the iron very slow, they said it will cause problems if they inject the entire amount all at once.
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IGA 1994
Fistula August 2009
Dialysis October 2009
Approved for Transplant January 2010
Turned down ECK kidney January 2011
RichardMEL
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« Reply #18 on: May 25, 2010, 08:18:40 PM »

Tracy - regarding feeling better - it will take maybe 2-3 months while you stabalise on dialysis before the full effects come through and you probably will find that you will have more energy and be able to function better between treatments(obviously it varies for everyone). For me I usually need a nap after a D session and then the next day I do really well. Yesterday though after D I had to go to a dinner function straight away, but I was going fine till after midnight, so some days are better than others.

Re Iron at our unit what they do is first of all they do a test dose to see if you react to it, so they keep a close watch on BP and reaction. Iron is given over the last hour of treatment so it is quite slow. If you pass the test with no reactions then it's just given as normal, again via slow release during the last hour of treatment(usually through the heparin pump once the heparin is finished).
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
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